CA2392948A1 - Nucleic acids containing single nucleotide polymorphisms and methods of use thereof - Google Patents

Abstract

The invention provides nucleic acids containing single-nucleotide polymorphisms identified for transcribed human sequences, as well as methods of using the nucleic acids.

Description

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NUCLEIC ACIDS CONTAINING SINGLE NUCLEOTIDE
POLYMORPHISMS AND METHODS OF USE THEREOF
BACKGROUND OF THE INVENTION
Sequence polymorphism-based analysis of nucleic acid sequences can augment or replace previously known methods for determining the identity and relatedness of individuals.
The approach is generally based on alterations in nucleic acid sequences between related individuals. This analysis has been widely used in a variety of genetic, diagnostic, and forensic applications. For example, polymorphism analyses are used in identity and paternity analysis, and in genetic mapping studies.
One such type of variation is a restriction fragment length polymorphism (RFLP).
RFLPS can create or delete a recognition sequence for a restriction endonuclease in one nucleic acid relative to a second nucleic acid. The result of the variation is an alteration in the relative length of restriction enzyme generated DNA fragments in the two nucleic acids.
Other polymorphisms take the form of short tandem repeats (STR) sequences, which are also referred to as variable numbers of tandem repeat (VNTR) sequences.
STR sequences typically include tandem repeats of 2, 3, or 4 nucleotide sequences that are present in a nucleic acid from one individual but absent from a second, related individual at the corresponding genomic location.
Other polymorphisms take the form of single nucleotide variations, termed single nucleotide polymorphisms (SNPs), between individuals. A SNP can, in some instances, be referred to as a "cSNP" to denote that the nucleotide sequence containing the SNP originates as a cDNA.
SNPs can arise in several ways. A single nucleotide polymorphism may arise due to a substitution of one nucleotide for another at the polymorphic site.
Substitutions can be transitions or transversions. A transition is the replacement of one purine nucleotide by another purine nucleotide, or one pyrimidine by another pyrimidine. A
transversion is the replacement of a purine by a pyrimidine, or the converse.
Single nucleotide polymorphisms can also arise from a deletion of a nucleotide or an insertion of a nucleotide relative to a reference allele. Thus, the polymorphic site is a site at which one allele bears a gap with respect to a single nucleotide in another allele. Some SNPs occur within, or near genes. One such class includes SNPs falling within regions of genes encoding for a polypeptide product. These SNPs may result in an alteration of the amino acid sequence of the polypeptide product and give rise to the expression of a defective or other variant protein. Such variant products can, in some cases result in a pathological condition, e.g., genetic disease. Examples of genes in which a polymorphism within a coding sequence gives rise to genetic disease include sickle cell anemia and cystic fibrosis.
Other SNPs do not result in alteration of the polypeptide product. Of course, SNPs can also occur in noncoding regions of genes.
SNPs tend to occur with great frequency and are spaced uniformly throughout the genome. The frequency and uniformity of SNPs means that there is a greater probability that such a polymorphism will be found in close proximity to a genetic locus of interest.
SUMMARY OF THE INVENTION
The invention is based in part on the discovery of novel single nucleotide polymorphisms (SNPs) in regions of human DNA.
Accordingly, in one aspect, the invention provides an isolated polynucleotide which includes one or more of the SNPs described herein. The polynucleotide can be, e.g., a nucleotide sequence which includes one or more of the polymorphic sequences shown in Table 1 and the Sequence Listing (SEQ ID NOS: 1 - 7024) and which includes a polymorphic sequence, or a fragment of the polymorphic sequence, as long as it includes the polymorphic site. The polynucleotide may alternatively contain a nucleotide sequence which includes a sequence complementary to one or more of the sequences (SEQ ID NOS: 1-7024), or a fragment of the complementary nucleotide sequence, provided that the fragment includes a polymorphic site in the polymorphic sequence.
The polynucleotide can be, e.g., DNA or RNA, and can be between about 10 and about 100 nucleotides, e.g, 10-90, 10-75, 10-51, 10-40, or 10-30, nucleotides in length.
In some embodiments, the polymorphic site in the polymorphic sequence includes a nucleotide other than the nucleotide listed in Table 1, column 5 for the polymorphic sequence, e.g., the polymorphic site includes the nucleotide listed in Table l, column 6 for the polymorphic sequence.
In other embodiments, the complement of the polymorphic site includes a nucleotide other than the complement of the nucleotide listed in Table l, column 5 for the complement of the polymorphic sequence, e.g., the complement of the nucleotide listed in Table 1, column 6 for the polymorphic sequence.
In some embodiments, the polymorphic sequence is associated with a polypeptide related to one of the protein families disclosed herein. For example, the nucleic acid may be associated with a polypeptide related to an ATPase associated protein, a cadherin, or any of the other proteins identified in Table 1, column 10.
In another aspect, the invention provides an isolated allele-specific oligonucleotide that hybridizes to a first polynucleotide containing a polymorphic site. The first polynucleotide can be, e.g., a nucleotide sequence comprising one or more polymorphic sequences (SEQ ID
NOS:1 - 7024), provided that the polymorphic sequence includes a nucleotide other than the nucleotide recited in Table 1, column 5 for the polymorphic sequence.
Alternatively, the first polynucleotide can be a nucleotide sequence that is a fragment of the polymorphic sequence, provided that the fragment includes a polymorphic site in the polymorphic sequence, or a complementary nucleotide sequence which includes a sequence complementary to one or more polymorphic sequences (SEQ ID NOS:1 - 7024), provided that the complementary nucleotide sequence includes a nucleotide other than the complement of the nucleotide recited in Table 1, column 5. The first polynucleotide may in addition include a nucleotide sequence that is a fragment of the complementary sequence, provided that the fragment includes a polymorphic site in the polymorphic sequence.
In some embodiments, the oligonucleotide does not hybridize under stringent conditions to a second polynucleotide. The second polynucleotide can be, e.g., (a) a nucleotide sequence comprising one or more polymorphic sequences (SEQ ID NOS:1 - 7024), wherein the polymorphic sequence includes the nucleotide listed in Table 1, column 5 for the polymorphic sequence; (b) a nucleotide sequence that is a fragment of any of the polymorphic sequences; (c) a complementary nucleotide sequence including a sequence complementary to one or more polymorphic sequences (SEQ ID NOS:1 - 7024), wherein the polymorphic sequence includes the complement of the nucleotide listed in Table 1, column 5; and (d) a nucleotide sequence that is a fragment of the complementary sequence, provided that the fragment includes a polymorphic site in the polymorphic sequence.
The oligonucleotide can be, e.g., between about 10 and about 100 bases in length. In some embodiments, the oligonucleotide is between about 10 and 75 bases, 10 and 51 bases, 10 and about 40 bases, or about 15 and 30 bases in length.

The invention also provides a method of detecting a polymorphic site in a nucleic acid.
The method includes contacting the nucleic acid with an oligonucleotide that hybridizes to a polymorphic sequence selected from the group consisting of SEQ ID NOS: 1-7024, or its complement, provided that the polymorphic sequence includes a nucleotide other than the nucleotide recited in Table 1, column 5 for the polymorphic sequence, or the complement includes a nucleotide other than the complement of the nucleotide recited in Table 1, column S. The method also includes determining whether the nucleic acid and the oligonucleotide hybridize. Hybridization of the oligonucleotide to the nucleic acid sequence indicates the presence of the polymorphic site in the nucleic acid.
In preferred embodiments, the oligonucleotide does not hybridize to the polymorphic sequence when the polymorphic sequence includes the nucleotide recited in Table 1, column 5 for the polymorphic sequence, or when the complement of the polymorphic sequence includes the complement of the nucleotide recited in Table 1, column 5 for the polymorphic sequence.
The oligonucleotide can be, e.g., between about 10 and about 100 bases in length. In some embodiments, the oligonucleotide is between about 10 and 75 bases, 10 and S 1 bases, 10 and about 40 bases, or about 15 and 30 bases in length.
In some embodiments, the polymorphic sequence identified by the oligonucleotide is associated with a polypeptide related to one of the protein families disclosed herein. For example, the nucleic acid may be associated polypeptide related to an ATPase associated protein, cadherin, or any of the other protein families identified in Table 1, column 10.
In another aspect, the method includes determining if a sequence polymorphism is the present in a subject, such as a human. The method includes providing a nucleic acid from the subject and contacting the nucleic acid with an oligonucleotide that hybridizes to a polymorphic sequence selected from the group consisting of SEQ ID NOS: 1-7024, or its complement, provided that the polymorphic sequence includes a nucleotide other than the nucleotide recited in Table 1, column 5 for said polymorphic sequence, or the complement includes a nucleotide other than the complement of the nucleotide recited in Table 1, column 5. Hybridization between the nucleic acid and the oligonucleotide is then determined.
Hybridization of the oligonucleotide to the nucleic acid sequence indicates the presence of the polymorphism in said subject.
In a further aspect, the invention provides a method of determining the relatedness of a first and second nucleic acid. The method includes providing a first nucleic acid and a second nucleic acid and contacting the first nucleic acid and the second nucleic acid with an oligonucleotide that hybridizes to a polymorphic sequence selected from the group consisting of SEQ ID NOS: 1-7024, or its complement, provided that the polymorphic sequence includes a nucleotide other than the nucleotide recited in Table 1, column 5 for the polymorphic sequence, or the complement includes a nucleotide other than the complement of the nucleotide recited in Table 1, column S. The method also includes determining whether the first nucleic acid and the second nucleic acid hybridize to the oligonucleotide, and comparing hybridization of the first and second nucleic acids to the oligonucleotide.
Hybridization of first and second nucleic acids to the nucleic acid indicates the first and second subjects are related.
In preferred embodiments, the oligonucleotide does not hybridize to the polymorphic sequence when the polymorphic sequence includes the nucleotide recited in Table 1, column 5 for the polymorphic sequence, or when the complement of the polymorphic sequence includes the complement of the nucleotide recited in Table 1, column 5 for the polymorphic sequence.
The oligonucleotide can be, e.g., between about 10 and about 100 bases in length. In some embodiments, the oligonucleotide is between about 10 and 75 bases, 10 and S 1 bases, 10 and about 40 bases, or about 15 and 30 bases in length.
The method can be used in a variety of applications. For example, the first nucleic acid may be isolated from physical evidence gathered at a crime scene, and the second nucleic acid may be obtained from a person suspected of having committed the crime.
Matching the two nucleic acids using the method can establish whether the physical evidence originated from the person.
In another example, the first sample may be from a human male suspected of being the father of a child and the second sample may be from the child. Establishing a match using the described method can establish whether the male is the father of the child.
In another aspect, the invention provides an isolated polypeptide comprising a polymorphic site at one or more amino acid residues, and wherein the protein is encoded by a polynucleotide including one of the polymorphic sequences SEQ ID NOS:1-7024, or their complement, provided that the polymorphic sequence includes a nucleotide other than the nucleotide recited in Table 1, column S for the polymorphic sequence, or the complement includes a nucleotide other than the complement of the nucleotide recited in Table 1, column 5.

The polypeptide can be, e.g., related to one of the protein families disclosed herein.
For example, polypeptide can be related to an ATPase associated protein, cadherin, or any of the other proteins provided in Table 1, column 10.
In some embodiments, the polypeptide is translated in the same open reading frame as is a wild type protein whose amino acid sequence is identical to the amino acid sequence of the polymorphic protein except at the site of the polymorphism.
In some embodiments, the polypeptide encoded by the polymorphic sequence, or its complement, includes the nucleotide listed in Table l, column 6 for the polymorphic sequence, or the complement includes the complement of the nucleotide listed in Table 1, column 6.
The invention also provides an antibody that binds specifically to a polypeptide encoded by a polynucleotide comprising a nucleotide sequence encoded by a polynucleotide selected from the group consisting of polymorphic sequences SEQ ID NOS:1-7024, or its complement. The polymorphic sequence includes a nucleotide other than the nucleotide recited in Table l, column S for the polymorphic sequence, or the complement includes a nucleotide other than the complement of the nucleotide recited in Table 1, column 5.
In some embodiments, the antibody binds specifically to a polypeptide encoded by a polymorphic sequence which includes the nucleotide listed in Table 1, column 6 for the polymorphic sequence.
Preferably, the antibody does not bind specifically to a polypeptide encoded by a polymorphic sequence which includes the nucleotide listed in Table 1, column S
for the polymorphic sequence.
The invention further provides a method of detecting the presence of a polypeptide having one or more amino acid residue polymorphisms in a subject. The method includes providing a protein sample from the subject and contacting the sample with the above-described antibody under conditions that allow for the formation of antibody-antigen complexes. The antibody-antigen complexes are then detected. The presence of the complexes indicates the presence of the polypeptide.
The invention also provides a method of treating a subject suffering from, at risk for, or suspected of, suffering from a pathology ascribed to the presence of a sequence polymorphism in a subject, e.g., a human, non-human primate, cat, dog, rat, mouse, cow, pig, goat, or rabbit.
The method includes providing a subject suffering from a pathology associated with aberrant expression of a first nucleic acid comprising a polymorphic sequence selected from the group consisting of SEQ ID NOS:1 - 7024, or its complement, and treating the subject by administering to the subject an effective dose of a therapeutic agent.
Aberrant expression can include qualitative alterations in expression of a gene, e.g., expression of a gene encoding a polypeptide having an altered amino acid sequence with respect to its wild-type counterpart.
Qualitatively different polypeptides can include, shorter, longer, or altered polypeptides relative to the amino acid sequence of the wild-type polypeptide. Aberrant expression can also include quantitative alterations in expression of a gene. Examples of quantitative alterations in gene expression include lower or higher levels of expression of the gene relative to its wild-type counterpart, or alterations in the temporal or tissue-specific expression pattern of a gene.
Finally, aberrant expression may also include a combination of qualitative and quantitative alterations in gene expression.
The therapeutic agent can include, e.g., second nucleic acid comprising the polymorphic sequence, provided that the second nucleic acid comprises the nucleotide present in the wild type allele. In some embodiments, the second nucleic acid sequence comprises a polymorphic sequence which includes nucleotide listed in Table 1, column 5 for the polymorphic sequence.
Alternatively, the therapeutic agent can be a polypeptide encoded by a polynucleotide comprising polymorphic sequence selected from the group consisting of SEQ ID
NOS:1 -7024, or by a polynucleotide comprising a nucleotide sequence that is complementary to any one of polymorphic sequences SEQ ID NOS:1 - 7024, provided that the polymorphic sequence includes the nucleotide listed in Table 1, column 6 for the polymorphic sequence.
The therapeutic agent may further include an antibody as herein described, or an oligonucleotide comprising a polymorphic sequence selected from the group consisting of SEQ ID NOS:1 - 7024, or by a polynucleotide comprising a nucleotide sequence that is complementary to any one of polymorphic sequences SEQ ID NOS:1 - 7024, provided that the polymorphic sequence includes the nucleotide listed in Table 1, column 5 or Table l, column 6 for the polymorphic sequence.
In another aspect, the invention provides an oligonucleotide array comprising one or more oligonucleotides hybridizing to a first polynucleotide at a polymorphic site encompassed therein. The first polynucleotide can be, e.g., a nucleotide sequence comprising one or more polymorphic sequences (SEQ ID NOS:1 - 7024); a nucleotide sequence that is a fragment of any of the nucleotide sequences, provided that the fragment includes a polymorphic site in the polymorphic sequence; a complementary nucleotide sequence comprising a sequence complementary to one or more polymorphic sequences (SEQ ID NOS:1 - 7024); or a nucleotide sequence that is a fragment of the complementary sequence, provided that the fragment includes a polymorphic site in the polymorphic sequence.
In preferred embodiments, the array comprises 10; 100; 1,000; 10,000; 100,000 or more oligonucleotides.
The invention also provides a kit comprising one or more of the herein-described nucleic acids. The kit can include, e.g., a polynucleotide which includes one or more of the SNPs described herein. The polynucleotide can be, e.g., a nucleotide sequence which includes one or more of the polymorphic sequences shown in Table 1 and the Sequence Listing (SEQ
ID NOS: 1 - 7024) and which includes a polymorphic sequence, or a fragment of the polymorphic sequence, as long as it includes the polymorphic site. The polynucleotide may alternatively contain a nucleotide sequence which includes a sequence complementary to one or more of the sequences (SEQ ID NOS:1-7024), or a fragment of the complementary nucleotide sequence, provided that the fragment includes a polymorphic site in the polymorphic sequence. The invention provides an isolated allele-specific oligonucleotide that hybridizes to a first polynucleotide containing a polymorphic site. The first polynucleotide can be, e.g., a nucleotide sequence comprising one or more polymorphic sequences (SEQ ID
NOS: l - 7024), provided that the polymorphic sequence includes a nucleotide other than the nucleotide recited in Table 1, column 5 for the polymorphic sequence.
Alternatively, the first polynucleotide can be a nucleotide sequence that is a fragment of the polymorphic sequence, provided that the fragment includes a polymorphic site in the polymorphic sequence, or a complementary nucleotide sequence which includes a sequence complementary to one or more polymorphic sequences (SEQ ID NOS:1 - 7024), provided that the complementary nucleotide sequence includes a nucleotide other than the complement of the nucleotide recited in Table 1, column 5. The first polynucleotide may in addition include a nucleotide sequence that is a fragment of the complementary sequence, provided that the fragment includes a polymorphic site in the polymorphic sequence.
Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Although methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, suitable methods and materials are described below. All publications, patent applications, patents, and other references mentioned herein are incorporated by reference in their entirety. In the case of conflict, the present specification, including definitions, will control. In addition, the materials, methods, and examples are illustrative only and not intended to be limiting.
Other features and advantages of the invention will be apparent from the following detailed description and claims.
DETAILED DESCRIPTION OF THE INVENTION
The present invention provides 3,404 distinct polymorphic sites (i.e., human cSNP's) based on genes that have not yet been previously identified. They are described in the Table included with this application for patent. The instant application presents only polymorphisms in nucleic acid sequences that have not previously been identified. For this reason, both nucleotide sequences for a reference-polymorphic pair are presented in the instant application.
Since neither sequence was known prior to this invention, the choice of designating one sequence of the cognate pair as a "reference" sequence and the second cognate of the pair as a "polymorphic" sequence is arbitrary.
The SNPs are shown in Table 1 and the Sequence Listing. Both provide a summary of_ the polymorphic sequences disclosed herein. In the Table, a "SNP" is a polymorphic site embedded in a polymorphic sequence. The polymorphic site is occupied by a single nucleotide, which is the position of nucleotide variation between the wild type and polymorphic allelic sequences. The site is usually preceded by and followed by relatively highly conserved sequences of the allele (e.g., sequences that vary in less than 1/100 or 1/1000 members of the populations). Thus, a polymorphic sequence can include one or more of the following sequences: (1) a sequence having the nucleotide denoted in Table 1, column 5 at the polymorphic site in the polymorphic sequence; or (2) a sequence having a nucleotide other than the nucleotide denoted in Table 1, column 5 at the polymorphic site in the polymorphic sequence. An example of the latter sequence is a polymorphic sequence having the nucleotide denoted in Table 1, column 6 at the polymorphic site in the polymorphic sequence.

Nucleotide sequences for a referenced-polymorphic pair are presented in Table 1.
Each cSNP entry provides information concerning the wild type nucleotide sequence as well as the corresponding sequence that includes the SNP at the polymorphic site.
Since the wild type sequence is already known, the Sequence Listing accompanying this application provides only the sequence of the polymorphic allele; its SEQ ID NO: is also cross referenced in the Table 1. A reference to the SEQ ID NO: giving the translated amino acid sequence is also given if appropriate. The Table includes thirteen columns that provide descriptive information for each cSNP, each of which occupies one row in the Table. The column headings, and an explanation for each, are given below.
"SEQ ID" provides the cross-references to the two nucleotide SEQ ID NOs: for the cognate pair, which are numbered consecutively, and, as explained below, amino acid SEQ ID
NOs: as well, in the Sequence Listing of the application. Conversely, each sequence entry in the Sequence Listing also includes a cross-reference to the CuraGen sequence ID, under the label "CuraGen sequence ID". The first pair of SEQ ID NOs: given in the first column of each row of the Table are the SEQ ID NOs: identifying the nucleic acid sequences for the polymorphisms. If a polymorphism carries an entry for the amino acid portion of the row, a third SEQ ID NO: appears in parentheses in the column "Amino acid before" (see below) for the reference amino acid sequence, and a fourth SEQ ID NO: appears in parentheses in the column "Amino acid after" (see below) for the polymorphic amino acid sequence . The latter SEQ ID NOs: refer to amino acid sequences giving the cognate reference and polymorphic amino acid sequences that are the translation of the nucleotide polymorphism.
If a polymorphism carries no entry for the protein portion of the row, only one pair SEQ ID NOs:
is provided, in the first column.
"Base pos. of SNP" gives the numerical position of the nucleotide in the nucleic acid at which the cSNP is found, as identified in this invention.
"Polymorphic sequence" provides a S 1-base sequence with the polymorphic site at the 26th base in the sequence, as well as 25 bases from the reference sequence on the 5' side and the 3' side of the polymorphic site. The designation at the polymorphic site is enclosed in square brackets, and provides first, the reference nucleotide; second, a "slash (/)"; and third, the polymorphic nucleotide. In certain cases the polymorphism is an insertion or a deletion.
In that case, the position which is "unfilled" (i.e., the reference or the polymorphic position) is indicated by the word "gap".

"Base before" provides the nucleotide present in the reference sequence at the position at which the polymorphism is found.
"Base after" provides the altered nucleotide at the position of the polymorphism.
"Amino acid before" provides the amino acid in the reference protein, if the polymorphism occurs in a coding region. This column also includes the SEQ ID
NO: in parentheses for the translated reference amino acid sequence if the polymorphism occurs in a coding region.
"Amino acid after" provides the amino acid in the polymorphic protein, if the polymorphism occurs in a coding region. This column also includes the SEQ ID
NO: in parentheses for the translated polymorphic amino acid sequence if the polymorphism occurs in a coding region.
"Type of change" provides information on the nature of the polymorphism.
"SILENT-NONCODING" is used if the polymorphism occurs in a noncoding region of a nucleic acid.
"SILENT-CODING" is used if the polymorphism occurs in a coding region of a nucleic acid of a nucleic acid and results in no change of amino acid in the translated polymorphic protein.
"CONSERVATIVE" is used if the polymorphism occurs in a coding region of a nucleic acid and provides a change in which the altered amino acid falls in the same class as the reference amino acid. The classes are:
Aliphatic: Gly, Ala, Val, Leu, Ile;
Aromatic: Phe, Tyr, Trp;
Sulfur-containing: Cys, Met;
Aliphatic OH: Ser, Thr;
Basic: Lys, Arg, His;
Acidic: Asp, Glu, Asn, Gln;

Pro falls in none of the other classes; and End defines a termination codon.
"NONCONSERVATIVE" is used if the polymorphism occurs in a coding region of a nucleic acid and provides a change in which the altered amino acid falls in a different class than the reference amino acid.
"FRAMESHIFT" relates to an insertion or a deletion. If the frameshift occurs in a coding region, the Table provides the translation of the frameshifted codons 3' to the polymorphic site.
"Protein classification of CuraGen gene" provides a generic class into which the protein is classified. During the course of the work leading to the filing of the four applications identified above, approximately 100 classes of proteins were identified. They are described further below.
"Name of protein identified following a BLASTX analysis of the CuraGen sequence"
provides the database reference for the protein found to resemble the novel reference-polymorphism cognate pair most closely. (The next paragraph explains how a sequence was determined to be "novel").
"Similarity (pvalue) following a BLASTX analysis" provides the pvalue, a statistical measure from the BLASTX analysis that the polymorphic sequence is similar to, and therefore an allele of, the reference, or wild-type, sequence. In the present application, a cutoff of pvalue > 1 x 10-5° (entered, for example, as 1.0E-50 in the Table) is used to establish that the reference-polymorphic cognate pairs are novel.
"Map location" provides any information available at the time of filing related to localization of a gene on a chromosome.
The polymorphisms are arranged in the Table in the following order.
SEQ ID NOs: 1-6592, in consecutive pairs, are SNPs that are silent.
SEQ ID NOs: 6593-6648, in consecutive pairs, are SNPs that lead to conservative amino acid changes.

SEQ ID NOs: 6649-7024, in consecutive pairs, are SNPs that lead to nonconservative amino acid changes.
SEQ ID NOs: 6809-6864, in consecutive pairs, are the amino acid sequences centered at the polymorphic amino acid residue for the protein products provided by SNPs that lead to conservative amino acid changes between the reference and the polymorphic sequences.
These amino acid SEQ ID NOs: are derived from the corresponding nucleotide SEQ
ID NOs:
44335-44850, as described in U.S.S.N. 60/168,138, filed November 30, 1999. 7 or 8 amino acids on either side of the polymorphic site are shown. The order in which these sequences appear mirrors the order of presentation of the cognate nucleotide sequences, and is set forth in the Table.
SEQ ID NOs: 6865-7024, in consecutive pairs, are the amino acid sequences centered at the polymorphic amino acid residue for the protein products provided by SNPs that lead to nonconservative amino acid changes between the reference and the polymorphic sequences.
These amino acid SEQ ID NOs: are derived from the corresponding nucleotide SEQ
ID NOs:
44851-46464, as described in U.S.S.N. 60/168,138, filed November 30, 1999. 7 or 8 amino acids on either side of the polymorphic site are shown. The order in which these sequences appear mirrors the order of presentation of the cognate nucleotide sequences, and is set forth in the Table.
Provided herein are compositions which include, or are capable of detecting, nucleic acid sequences having these polymorphisms, as well as methods of using nucleic acids.

Individuals carrying polymorphic alleles of the invention may be detected at either the DNA, the RNA, or the protein level using a variety of techniques that are well known in the art. Strategies for identification and detection are described in e.g., EP
730,663, EP 717,113, and PCT US97/02102. The present methods usually employ pre-characterized polymorphisms. That is, the genotyping location and nature of polymorphic forms present at a site have already been determined. The availability of this information allows sets of probes to be designed for specific identification of the known polymorphic forms.
Many of the methods described below require amplification of DNA from target samples. This can be accomplished by e.g., PCR. See generally PCR Technology:
Principles and Applications for DNA Amplification (ed. H.A. Erlich, Freeman Press, NY, NY, 1992);

PCR Protocols: A Guide to Methods and Applications (eds. Innis, et al., Academic Press, San Diego, CA, 1990); Manila et al., Nucleic Acids Res. 19, 4967 (1991);
Eckert et al., PCR
Methods and Applications l, 17 (1991); PCR (eds. McPherson et al., IRL Press, Oxford);
and U.S. Patent 4,683,202.
The phrase "recombinant protein" or "recombinantly produced protein'.' refers to a peptide or protein produced using non-native cells that do not have an endogenous copy of DNA able to express the protein. In particular, as used herein, a recombinantly produced protein relates to the gene product of a polymorphic allele, i.e., a "polymorphic protein"
containing an altered amino acid at the site of translation of the nucleotide polymorphism.
The cells produce the protein because they have been genetically altered by the introduction of the appropriate nucleic acid sequence. The recombinant protein will not be found in association with proteins and other subcellular components normally associated with the cells producing the protein. The terms "protein" and "polypeptide" are used interchangeably herein.
The phrase "substantially purified" or "isolated" when refernng to a nucleic acid, peptide or protein, means that the chemical composition is in a milieu containing fewer, or preferably, essentially none, of other cellular components with which it is naturally associated. Thus, the phrase "isolated" or "substantially pure" refers to nucleic acid preparations that lack at least one protein or nucleic acid normally associated with the nucleic acid in a host cell. It is preferably in a homogeneous state although it can be in either a dry or aqueous solution. Purity and homogeneity are typically determined using analytical chemistry techniques such as gel electrophoresis or high performance liquid chromatography. Generally, a substantially purified or isolated nucleic acid or protein will comprise more than 80% of all macromolecular species present in the preparation. Preferably, the nucleic acid or protein is purified to represent greater than 90% of all macromolecular species present.
More preferably the nucleic acid or protein is purified to greater than 95%, and most preferably the nucleic acid or protein is purified to essential homogeneity, wherein other macromolecular species are not detected by conventional analytical procedures.
The genomic DNA used for the diagnosis may be obtained from any nucleated cells of the body, such as those present in peripheral blood, urine, saliva, buccal samples, surgical specimen, and autopsy specimens. The DNA may be used directly or may be amplified enzymatically in vitro through use of PCR (Saiki et al. Science 239:487-491 (1988)) or other in vitro amplification methods such as the ligase chain reaction (LCR) (Wu and Wallace Genomics 4:560-569 (1989)), strand displacement amplification (SDA) (Walker et al. Proc.
Natl. Acad. Sci. U.S.A, 89:392-396 (1992)), self sustained sequence replication (35R) (Fahy et al. PCR Methods P&J& 1:25-33 (1992)), prior to mutation analysis.
The method for preparing nucleic acids in a form that is suitable for mutation detection is well known in the art. A "nucleic acid" is a deoxyribonucleotide or ribonucleotide polymer in either single-or double-stranded form, including known analogs of natural nucleotides unless otherwise indicated. The term "nucleic acids", as used herein, refers to either DNA or RNA. "Nucleic acid sequence" or "polynucleotide sequence" refers to a single-stranded sequence of deoxyribonucleotide or ribonucleotide bases read from the 5' end to the 3' end.
The direction of 5' to 3' addition of nascent RNA transcripts is referred to as the transcription direction; sequence regions on the DNA strand having the same sequence as the RNA and which are beyond the 5' end of the RNA transcript in the 5' direction are referred to as "upstream sequences"; sequence regions on the DNA strand having the same sequence as the RNA and which are beyond the 3' end of the RNA transcript in the 3' direction are referred to as "downstream sequences". The term includes both self replicating plasmids, infectious polymers of DNA or RNA and nonfunctional DNA or RNA. The complement of any nucleic acid sequence of the invention is understood to be included in the definition of that sequence.
"Nucleic acid probes" may be DNA or RNA fragments.
The detection of polymorphisms in specific DNA sequences, can be accomplished by a variety of methods including, but not limited to, restriction-fragment-length-polymorphism detection based on allele-specific restriction-endonuclease cleavage (Kan and Dozy Lancet ii:910-912 (1978)), hybridization with allele-specific oligonucleotide probes (Wallace et al.
Nucl. Acids Res. 6:3543-3557 (1978)), including immobilized oligonucleotides (Saiki et al.
Proc. Natl. Acad. SCI. USA, 86:6230-6234 (1969)) or oligonucleotide arrays (Maskos and Southern Nucl. Acids Res 21:2269-2270 (1993)), allele-specific PCR (Newton et al. Nucl Acids Res 17:2503 _2516 (1989)), mismatch-repair detection (MRD) (Faham and Cox Genome Res 5:474-482 (1995)), binding of MutS protein (Wagner et al. Nucl Acids Res 23:3944-3948 (1995), denaturing-gradient gel electrophoresis (DGGE) (Fisher and Lerman et al. Proc. Natl. Acad. Sci. U.S.A. 80:1579-l 583 (1983)), single-strand-conformation-polymorphism detection (Orita et al. Genomics 5:874-879 (1983)), RNAase cleavage at mismatched base-pairs (Myers et al. Science 230:1242 (1985)), chemical (Cotton et al. Proc.
Natl. w Sci. U.S.A, 824397-4401 (1988)) or enzymatic (Youil et al. Proc. Natl.
Acad. Sci.
U.S.A. 92:87-91 (1995)) cleavage of heteroduplex DNA, methods based on allele specific primer extension (Syvanen et al. Genomics 8:684-692 (1990)), genetic bit analysis (GBA) (Nikiforov et al. &&I Acids 22:4167-4175 (1994)), the oligonucleotide-ligation assay (OLA) (Landegren et al. Science 241:1077 (1988)), the allele-specific ligation chain reaction (LCR) (Barrany Proc. Natl. Acad. Sci. U.S.A. 88:189-193 (1991)), gap-LCR (Abravaya et al.
Nucl Acids Res 23:675-682 (1995)), radioactive and/or fluorescent DNA
sequencing using standard procedures well known in the art, and peptide nucleic acid (PNA) assays (Drum et al., Nucl. Acids Res, 21:5332-5356 (1993); Thiede et al., Nucl. Acids Res.
24:983-984 (1996)).
"Specific hybridization" or "selective hybridization" refers to the binding, or duplexing, of a nucleic acid molecule only to a second particular nucleotide sequence to which the nucleic acid is complementary, under suitably stringent conditions when that sequence is present in a complex mixture (e.g., total cellular DNA or RNA).
"Stringent conditions" are conditions under which a probe will hybridize to its target subsequence, but to no other sequences. Stringent conditions are sequence-dependent and are different in different circumstances. Longer sequences hybridize specifically at higher temperatures than shorter ones. Generally, stringent conditions are selected such that the temperature is about 5°C lower than the thermal melting point (Tm) for the specific sequence to which hybridization is intended to occur at a defined ionic strength and pH. The Tm is the temperature (under defined ionic strength, pH, and nucleic acid concentration) at which 50% of the target sequence hybridizes to the complementary probe at equilibrium. Typically, stringent conditions include a salt concentration of at least about 0.01 to about 1.0 M
Na ion concentration (or other salts), at pH 7.0 to 8.3. The temperature is at least about 30°C for short probes (e.g., 10 to 50 nucleotides) . Stringent conditions can also be achieved with the addition of destabilizing agents such as formamide. For example, conditions of 5X SSPE (750 mM NaCI, 50 mM NaPhosphate, 5 mM EDTA, pH 7.4) and a temperature of 25-30°C are suitable for allele-specific probe hybridization.
"Complementary" or "target" nucleic acid sequences refer to those nucleic acid sequences which selectively hybridize to a nucleic acid probe. Proper annealing conditions depend, for example, upon a probe's length, base composition, and the number of mismatches and their position on the probe, and must often be determined empirically. For discussions of nucleic acid probe design and annealing conditions, see, for example, Sambrook et al., or Current Protocols in Molecular Biology, F. Ausubel et al., ed., Greene Publishing and Wiley-Interscience, New York (1987).

A perfectly matched probe has a sequence perfectly complementary to a particular target sequence. The test probe is typically perfectly complementary to a portion of the target sequence. A "polymorphic" marker or site is the locus at which a sequence difference occurs with respect to a reference sequence. Polymorphic markers include restriction fragment length polymorphisms, variable number of tandem repeats (VNTR's), hypervariable regions, minisatellites, dinucleotide repeats, trinucleotide repeats, tetranucleotide repeats, simple sequence repeats, and insertion elements such as Alu. The reference allelic form may be, for example, the most abundant form in a population, or the first allelic form to be identified, and other allelic forms are designated as alternative, variant or polymorphic alleles. The allelic form occurnng most frequently in a selected population is sometimes referred to as the "wild type" form, and herein may also be referred to as the "reference" form.
Diploid organisms may be homozygous or heterozygous for allelic forms. A diallelic polymorphism has two distinguishable forms (i.e., base sequences), and a triallelic polymorphism has three such forms.
As used herein an "oligonucleotide" is a single-stranded nucleic acid ranging in length from 2 to about 60 bases. Oligonucleotides are often synthetic but can also be produced from naturally occurring polynucleotides. A probe is an oligonucleotide capable of binding to a target nucleic acid of a complementary sequence through one or more types of chemical bonds, usually through complementary base pairing via hydrogen bond formation.
Oligonucleotides probes are often between 5 and 60 bases, and, in specific embodiments, may be between 10-40, or 15-30 bases long. An oligonucleotide probe may include natural (i.e. A, G, C, or T) or modified bases (7-deazaguanosine, inosine, etc.). In addition, the bases in an oligonucleotide probe may be joined by a linkage other than a phosphodiester bond, such as a phosphoramidite linkage or a phosphorothioate linkage, or they may be peptide nucleic acids in which the constituent bases are joined by peptide bonds rather than by phosphodiester bonds, so long as it does not interfere with hybridization.
As used herein, the term "primer" refers to a single-stranded oligonucleotide which acts as a point of initiation of template-directed DNA synthesis under appropriate conditions (e.g., in the presence of four different nucleoside triphosphates and a polymerization agent, such as DNA polymerase, RNA polymerase or reverse transcriptase) in an appropriate buffer and at a suitable temperature. The appropriate length of a primer depends on the intended use of the primer, but typically ranges from 1 S to 30 nucleotides. Short primer molecules generally require cooler temperatures to form sufficiently stable hybrid complexes with the template. A primer need not be perfectly complementary to the exact sequence of the template, but should be sufficiently complementary to hybridize with it. The term "primer site" refers to the sequence of the target DNA to which a primer hybridizes.
The term "primer pair" refers to a set of primers including a 5' (upstream) primer that hybridizes with the 5' end of the DNA sequence to be amplified and a 3' (downstream) primer that hybridizes with the complement of the 3' end of the sequence to be amplified.
DNA fragments can be prepared, for example, by digesting plasmid DNA, or by use of PCR. Oligonucleotides for use as primers or probes are chemically synthesized by methods known in the field of the chemical synthesis of polynucleotides, including by way of non-limiting example the phosphoramidite method described by Beaucage and Carruthers, Tetrahedron Lett 22:1859-1 862 (1981) and the triester method provided by Matteucci, et al., J. Am. Chem. Soc., 103:3185 (1981) both incorporated herein by reference.
These syntheses may employ an automated synthesizer, as described in Needham-VanDevanter, D.R., et al., Nucleic Acids Res. 12:61596168 (1984). Purification of oligonucleotides may be carried out by either native acrylamide gel electrophoresis or by anion-exchange HPLC as described in Pearson, J.D. and Regnier, F.E., ,J. Chrom" 255:137-149 (1983). A double stranded fragment may then be obtained, if desired, by annealing appropriate complementary single strands together under suitable conditions or by synthesizing the complementary strand using a DNA polymerase with an appropriate primer sequence. Where a specific sequence for a nucleic acid probe is given, it is understood that the complementary strand is also identified and included. The complementary strand will work equally well in situations where the target is a double-stranded nucleic acid.
The sequence of the synthetic oligonucleotide or of any nucleic acid fragment can be can be obtained using either the dideoxy chain termination method or the Maxam-Gilbert method (see Sambrook et al. Molecular Cloning - a Laboratory Manual (2nd Ed.), Vols. 1-3, Cold Spring Harbor Laboratory, Cold Spring Harbor, New York, (1989), which is incorporated herein by reference. This manual is hereinafter referred to as "Sambrook et al." ;
Zyskind et al., (1988)). Recombinant DNA Laboratory Manual, (Acad. Press, New York).
Oligonucleotides useful in diagnostic assays are typically at least 8 consecutive nucleotides in length, and may range upwards of 18 nucleotides in length to greater than 100 or more consecutive nucleotides.
Another aspect of the invention pertains to isolated antisense nucleic acid molecules that are hybridizable to or complementary to the nucleic acid molecule comprising the SNP-containing nucleotide sequences of the invention, or fragments, analogs or derivatives thereof.
An "antisense" nucleic acid comprises a nucleotide sequence that is complementary to a "sense" nucleic acid encoding a protein, e.g., complementary to the coding strand of a double-stranded cDNA molecule or complementary to an mRNA sequence. In specific aspects, antisense nucleic acid molecules are provided that comprise a sequence complementary to at least about 10, about 25, about 50, or about 60 nucleotides or an entire SNP coding strand, or to only a portion thereof.
In one embodiment, an antisense nucleic acid molecule is antisense to a "coding region" of the coding strand of a polymorphic nucleotide sequence of the invention. The term "coding region" refers to the region of the nucleotide sequence comprising codons which are translated into amino acid. In another embodiment, the antisense nucleic acid molecule is antisense to a "noncoding region" of the coding strand of a nucleotide sequence of the invention. The term "noncoding region" refers to 5' and 3' sequences which flank the coding region that are not translated into amino acids (i. e., also referred to as 5' and 3' untranslated regions).
Given the coding strand sequences disclosed herein, antisense nucleic acids of the invention can be designed according to the rules of Watson and Crick or Hoogsteen base pairing. For example, the antisense nucleic acid molecule can generally be complementary to the entire coding region of an mRNA, but more preferably as embodied herein, it is an oligonucleotide that is antisense to only a portion of the coding or noncoding region of the mRNA. An antisense oligonucleotide can range in length between about 5 and about 60 nucleotides, preferably between about 10 and about 45 nucleotides, more preferably between about 15 and 40 nucleotides, and still more preferably between about 1 S and 30 in length. An antisense nucleic acid of the invention can be constructed using chemical synthesis or enzymatic ligation reactions using procedures known in the art. For example, an antisense nucleic acid (e.g., an antisense oligonucleotide) can be chemically synthesized using naturally occurring nucleotides or variously modified nucleotides designed to increase the biological stability of the molecules or to increase the physical stability of the duplex formed between the antisense and sense nucleic acids, e.g., phosphorothioate derivatives and acridine substituted nucleotides can be used.
Examples of modified nucleotides that can be used to generate the antisense nucleic acid include: 5-fluorouracil, 5-bromouracil, 5-chlorouracil, 5-iodouracil, hypoxanthine, xanthine, 4-acetylcytosine, 5-(carboxyhydroxylmethyl) uracil, 5-carboxymethylaminomethyl-2-thiouridine, 5-carboxymethylaminomethyluracil, dihydrouracil, beta-D-galactosylqueosine, inosine, N6-isopentenyladenine, 1-methylguanine, 1-methylinosine, 2,2-dimethylguanine, 2-methyladenine, 2-methylguanine, 3-methylcytosine, 5-methylcytosine, N6-adenine, 7-methylguanine, 5-methylaminomethyluracil, 5-methoxyaminomethyl-2-thiouracil, beta-D-mannosylqueosine, 5'-methoxycarboxymethyluracil, S-methoxyuracil, 2-methylthio-N6-isopentenyladenine, uracil-5-oxyacetic acid (v), wybutoxosine, pseudouracil, queosine, 2-thiocytosine, S-methyl-2-thiouracil, 2-thiouracil, 4-thiouracil, 5-methyluracil, uracil-5-oxyacetic acid methylester, uracil-5-oxyacetic acid (v), 5-methyl-2-thiouracil, 3-(3-amino-3-N-2-carboxypropyl) uracil, (acp3)w, and 2,6-diaminopurine.
Alternatively, the antisense nucleic acid can be produced biologically using an expression vector into which a nucleic acid has been subcloned in an antisense orientation (i.e., RNA
transcribed from the inserted nucleic acid will be of an antisense orientation to a target nucleic acid of interest, described further in the following section).
The antisense nucleic acid molecules of the invention are typically administered to a subject or generated in situ such that they hybridize with or bind to cellular mRNA and/or genomic DNA encoding a polymorphic protein to thereby inhibit expression of the protein, e.g., by inhibiting transcription and/or translation. The hybridization can be by conventional nucleotide complementary to form a stable duplex, or, for example, in the case of an antisense nucleic acid molecule that binds to DNA duplexes, through specific interactions in the major groove of the double helix. An example of a route of administration of antisense nucleic acid molecules of the invention includes direct injection at a tissue site.
Alternatively, antisense nucleic acid molecules can be modified to target selected cells and then administered systemically. For example, for systemic administration, antisense molecules can be modified such that they specifically bind to receptors or antigens expressed on a selected cell surface, e.g., by linking the antisense nucleic acid molecules to peptides or antibodies that bind to cell surface receptors or antigens. The antisense nucleic acid molecules can also be delivered to cells using the vectors described herein. To achieve sufficient intracellular concentrations of antisense molecules, vector constructs in which the antisense nucleic acid molecule is placed under the control of a strong pol II or pol III promoter are preferred.
In yet another embodiment, the antisense nucleic acid molecule of the invention is an a-anomeric nucleic acid molecule. An a-anomeric nucleic acid molecule forms specific double-stranded hybrids with complementary RNA in which, contrary to the usual -units, the strands run parallel to each other (Gaultier et al. (1987) Nucleic Acids Res 15: 6625-6641). The antisense nucleic acid molecule can also comprise a 2'-o-methylribonucleotide (moue et al.
(1987) Nucleic Acids Res 15: 6131-6148) or a chimeric RNA -DNA analogue (moue et al.
(1987) FEBSLett 215: 327-330).
The following terms are used to describe the sequence relationships between two or more nucleic acids or polynucleotides: "reference sequence", "comparison window", "sequence identity", "percentage of sequence identity", and "substantial identity". A
"reference sequence" is a defined sequence used as a basis for a sequence comparison; a reference sequence may be a subset of a larger sequence, for example, as a segment of a full-length cDNA or gene sequence given in a sequence listing, or may comprise a complete cDNA or gene sequence. Optimal alignment of sequences for aligning a comparison window may, for example, be conducted by the local homology algorithm of Smith and Waterman Adv. AppI. Math, 2482 (1981), by the homology alignment algorithm of Needleman and Wunsch J. Mol. Biol. 48:443 (1970), by the search for similarity method of Pearson and Lipman Proc. Natl. Acad. Sci. U.S.A. 852444 (1988), or by computerized implementations of these algorithms (for example, GAP, BESTFIT, FASTA, and TFASTA in the Wisconsin Genetics Software Package Release 7.0, Genetics Computer Group, 575 Science Dr., Madison, WI).
Techniques for nucleic acid manipulation of the nucleic acid sequences harboring the cSNP's of the invention, such as subcloning nucleic acid sequences encoding polypeptides into expression vectors, labeling probes, DNA hybridization, and the like, are described generally in Sambrook et al., The phrase "nucleic acid sequence encoding"
refers to a nucleic acid which directs the expression of a specific protein, peptide or amino acid sequence. The nucleic acid sequences include both the DNA strand sequence that is transcribed into RNA
and the RNA sequence that is translated into protein, peptide or amino acid sequence. The nucleic acid sequences include both the full length nucleic acid sequences disclosed herein as well as non-full length sequences derived from the full length protein. It being further understood that the sequence includes the degenerate codons of the native sequence or sequences which may be introduced to provide codon preference in a specific host cell.
Consequently, the principles of probe selection and array design can readily be extended to analyze more complex polymorphisms (see EP 730,663). For example, to characterize a triallelic SNP polymorphism, three groups of probes can be designed tiled on the three polymorphic forms as described above. As a further example, to analyze a diallelic polymorphism involving a deletion of a nucleotide, one can tile a first group of probes based on the undeleted polymorphic form as the reference sequence and a second group of probes based on the deleted form as the reference sequence.
For assays of genomic DNA, virtually any biological convenient tissue sample can be used. Suitable samples include whole blood, semen, saliva, tears, urine, fecal material, sweat, buccal, skin and hair. Genomic DNA is typically amplified before analysis.
Amplification is usually effected by PCR using primers flanking a suitable fragment e.g., of 50-500 nucleotides containing the locus of the polymorphism to be analyzed. Target is usually labeled in the course of amplification. The amplification product can be RNA or DNA, single stranded or double stranded. If double stranded, the amplification product is typically denatured before application to an array. If genomic DNA is analyzed without amplification, it may be desirable to remove RNA from the sample before applying it to the array. Such can be accomplished by digestion with DNase-free RNase.
DETECTION OF POLYMORPHISMS IN A NUCLEIC ACID SAMPLE
The SNPs disclosed herein can be used to determine which forms of a characterized polymorphism are present in individuals under analysis.
The design and use of allele-specific probes for analyzing polymorphisms is described by e.g., Saiki et al., Nature 324, 163-166 (1986); Dattagupta, EP 235,726, Saiki, WO
89/11548. Allele-specific probes can be designed that hybridize to a segment of target DNA
from one individual but do not hybridize to the corresponding segment from another individual due to the presence of different polymorphic forms in the respective segments from the two individuals. Hybridization conditions should be sufficiently stringent that there is a significant difference in hybridization intensity between alleles, and preferably an essentially binary response, whereby a probe hybridizes to only one of the alleles. Some probes are designed to hybridize to a segment of target DNA such that the polymorphic site aligns with a central position (e.g., in a 15-mer at the 7 position; in a 16-mer, at either the 7, 8 or 9 position) of the probe. This design of probe achieves good discrimination in hybridization between different allelic forms.
Allele-specific probes are often used in pairs, one member of a pair showing a perfect match to a reference form of a target sequence and the other member showing a perfect match to a variant form. Several pairs of probes can then be immobilized on the same support for simultaneous analysis of multiple polymorphisms within the same target sequence.

The polymorphisms can also be identified by hybridization to nucleic acid arrays, some examples of which are described in published PCT application WO 95/11995. WO

also describes subarrays that are optimized for detection of a variant form of a precharacterized polymorphism. Such a subarray contains probes designed to be complementary to a second reference sequence, which is an allelic variant of the first reference sequence. The second group of probes is designed by the same principles, except that the probes exhibit complementarity to the second reference sequence. The inclusion of a second group (or further groups) can be particularly useful for analyzing short subsequences of the primary reference sequence in which multiple mutations are expected to occur within a short distance commensurate with the length of the probes (e.g., two or more mutations within 9 to 21 bases).
An allele-specific primer hybridizes to a site on a target DNA overlapping a polymorphism and only primes amplification of an allelic form to which the primer exhibits perfect complementarity. See Gibbs, Nucleic Acid Res. 17 2427-2448 (1989).
This primer is used in conjunction with a second primer which hybridizes at a distal site.
Amplification proceeds from the two-primers, resulting in a detectable product which indicates the particular allelic form is present. A control is usually performed with a second pair of primers, one of which shows a single base mismatch at the polymorphic site and the other of which exhibits perfect complementarity to a distal site. The single-base mismatch prevents amplification and no detectable product is formed. The method works best when the mismatch is included in the 3'-most position of the oligonucleotide aligned with the polymorphism because this position is most destabilizing to elongation from the primer (see, e.g., WO
93/22456).
Amplification products generated using the polymerase chain reaction can be analyzed by the use of denaturing gradient gel electrophoresis. Different alleles can be identified based on the different sequence-dependent melting properties and electrophoretic migration of DNA
in solution. Erlich, ed., PCR Technology, Principles and Applications for DNA
Amplification, (W.H. Freeman and Co New York, 1992, Chapter 7).
Alleles of target sequences can be differentiated using single-strand conformation polymorphism analysis, which identifies base differences by alteration in electrophoretic migration of single stranded PCR products, as described in Orita et al., Proc.
Nat. Acad.
Sci. 86, 2766-2770 (1989). Amplified PCR products can be generated and heated or otherwise denatured, to form single stranded amplification products. Single-stranded nucleic acids may refold or form secondary structures which are partially dependent on the base sequence. The different electrophoretic mobilities of single-stranded amplification products can be related to base-sequence differences between alleles of target sequences.
The genotype of an individual with respect to a pathology suspected of being caused by a genetic polymorphism may be assessed by association analysis. Phenotypic traits suitable for association analysis include diseases that have known but hitherto unmapped genetic components (e.g., agammaglobulinemia, diabetes insipidus, Lesch-Nyhan syndrome, muscular dystrophy, Wiskott-Aldrich syndrome, Fabry's disease, familial hypercholesterolemia, polycystic kidney disease, hereditary spherocytosis, von Willebrand's disease, tuberous sclerosis, hereditary hemorrhagic telangiectasia, familial colonic polyposis, Ehlers-Danlos syndrome, osteogenesis imperfecta, and acute intermittent porphyria).
Phenotypic traits also include symptoms of, or susceptibility to, multifactorial diseases of which a component is or may be genetic, such as autoimmune diseases, inflammation, cancer, diseases of the nervous system, and infection by pathogenic microorganisms. Some examples of autoimmune diseases include rheumatoid arthritis, multiple sclerosis, diabetes (insulin-dependent and non- independent), systemic lupus erythematosus and Graves disease.
Some examples of cancers include cancers of the bladder, brain, breast, colon, esophagus, kidney, oral cavity, ovary, pancreas, prostate, skin, stomach, leukemia, liver, lung, and uterus.
Phenotypic traits also include characteristics such as longevity, appearance (e.g., baldness, obesity), strength, speed, endurance, fertility, and susceptibility or receptivity to particular drugs or therapeutic treatments.
Determination of which polymorphic forms occupy a set of polymorphic sites in an individual identifies a set of polymorphic forms that distinguishes the individual. See generally National Research Council, The Evaluation of Forensic DNA Evidence (Eds.
Pollard et al., National Academy Press, DC, 1996). Since the polymorphic sites are within a 50,000 by region in the human genome, the probability of recombination between these polymorphic sites is low. That low probability means the haplotype (the set of all 10 polymorphic sites) set forth in this application should be inherited without change for at least several generations.
The more sites that are analyzed the lower the probability that the set of polymorphic forms in one individual is the same as that in an unrelated individual. Preferably, if multiple sites are analyzed, the sites are unlinked. Thus, polymorphisms of the invention are often used in conjunction with polymorphisms in distal genes. Preferred polymorphisms for use in forensics are diallelic because the population frequencies of two polymorphic forms can usually be determined with greater accuracy than those of multiple polymorphic forms at multi-allelic loci.
The capacity to identify a distinguishing or unique set of forensic markers in an individual is useful for forensic analysis. For example, one can determine whether a blood sample from a suspect matches a blood or other tissue sample from a crime scene by determining whether the set of polymorphic forms occupying selected polymorphic sites is the same in the suspect and the sample. If the set of polymorphic markers does not match between a suspect and a sample, it can be concluded (barnng experimental error) that the suspect was not the source of the sample. If the set of markers does match, one can conclude that the DNA
from the suspect is consistent with that found at the crime scene. If frequencies of the polymorphic forms at the loci tested have been determined (e.g., by analysis of a suitable population of individuals), one can perform a statistical analysis to determine the probability that a match of suspect and crime scene sample would occur by chance.
p(ID) is the probability that two random individuals have the same polymorphic or allelic form at a given polymorphic site. In diallelic loci, four genotypes are possible: AA, AB, BA, and BB. If alleles A and B occur in a haploid genome of the organism with frequencies x and y, the probability of each genotype in a diploid organism are (see WO
95/12607):
Homozygote: p(AA)=x2 Homozygote: p(BB)=y2=(1-x)2 Single Heterozygote: p(AB)=p(BA)=xy=x(1-x) Both Heterozygotes: p(AB+ BA)=2xy=2x(1-x) The probability of identity at one locus (i.e, the probability that two individuals, picked at random from a population will have identical polymorphic forms at a given locus) is given by the equation:
P(ID)=(x2)2+ (2x3,)2+ (Y2)2.
These calculations can be extended for any number of polymorphic forms at a given locus. For example, the probability of identity p(ID) for a 3-allele system where the alleles have the frequencies in the population of x, y and z, respectively, is equal to the sum of the squares of the genotype frequencies:

p(ID) ~+ (~y)2+ (2yZ)2+ (2xz)2+ z4+ y4 In a locus of n alleles, the appropriate binomial expansion is used to calculate p(ID) and p(exc).
The cumulative probability of identity (cum p(ID)) for each of multiple unlinked loci is determined by multiplying the probabilities provided by each locus:
cum p(ID) p(ID1)p(ID2)p(ID3) . . . p(IDn) The cumulative probability of non-identity for n loci (i.e. the probability that two random individuals will be different at 1 or more loci) is given by the equation:
cum p(nonlD)=1-cum p(ID).
If several polymorphic loci are tested, the cumulative probability of non-identity for random individuals becomes very high (e.g., one billion to one). Such probabilities can be taken into account together with other evidence in determining the guilt or innocence of the suspect.
The object of paternity testing is usually to determine whether a male is the father of a child. In most cases, the mother of the child is known and thus, the mother's contribution to the child's genotype can be traced. Paternity testing investigates whether the part of the child's genotype not attributable to the mother is consistent with that of the putative father. Paternity testing can be performed by analyzing sets of polymorphisms in the putative father and the child.
If the set of polymorphisms in the child attributable to the father does not match the putative father, it can be concluded, barnng experimental error, that the putative father is not the real father. If the set of polymorphisms in the child attributable to the father does match the set of polymorphisms of the putative father, a statistical calculation can be performed to determine the probability of coincidental match.
The probability of parentage exclusion (representing the probability that a random male will have a polymorphic form at a given polymorphic site that makes him incompatible as the father) is given by the equation (see WO 95/12607):
p(exc) xy(1-xy) where x and y are the population frequencies of alleles A and B of a diallelic polymorphic site.

(At a triallelic site p(exc)=xy(1-xy)+ yz(1-yz)+ xz(1-xz)+ 3xyz(1-xyz))), where x, y and z and the respective population frequencies of alleles A, B and C). The probability of non-exclusion is:
p(non-exc)=1 p(exc) The cumulative probability of non-exclusion (representing the value obtained when n loci are used) is thus:
cum p(non-exc) p(non-excl)p(non-exc2)p(non-exc3) . . . p(non-excn) The cumulative probability of exclusion for n loci (representing the probability that a random male will be excluded) is:
cum p(exc)=1-cum p(non-exc).
If several polymorphic loci are included in the analysis, the cumulative probability of exclusion of a random male is very high. This probability can be taken into account in assessing the liability of a putative father whose polymorphic marker set matches the child's polymorphic marker set attributable to his/her father.
The polymorphisms of the invention may contribute to the phenotype of an organism in different ways. Some polymorphisms occur within a protein coding sequence and contribute to phenotype by affecting protein structure. The effect may be neutral, beneficial or detrimental, or both beneficial and detrimental, depending on the circumstances. For example, a heterozygous sickle cell mutation confers resistance to malaria, but a homozygous sickle cell mutation is usually lethal. Other polymorphisms occur in noncoding regions but may exert phenotypic effects indirectly via influence on replication, transcription, and translation. A
single polymorphism may affect more than one phenotypic trait. Likewise, a single phenotypic trait may be affected by polymorphisms in different genes. Further, some polymorphisms predispose an individual to a distinct mutation that is causally related to a certain phenotype.
Phenotypic traits include diseases that have known but hitherto unmapped genetic components. Phenotypic traits also include symptoms of, or susceptibility to, multifactorial diseases of which a component is or may be genetic, such as autoimmune diseases, inflammation, cancer, diseases of the nervous system, and infection by pathogenic microorganisms. Some examples of autoimmune diseases include rheumatoid arthritis, multiple sclerosis, diabetes (insulin-dependent and non-independent), systemic lupus erythematosus and Graves disease. Some examples of cancers include cancers of the bladder, brain, breast, colon, esophagus, kidney, leukemia, liver, lung, oral cavity, ovary, pancreas, prostate, skin, stomach and uterus. Phenotypic traits also include characteristics such as longevity, appearance (e.g., baldness, obesity), strength, speed, endurance, fertility, and susceptibility or receptivity to particular drugs or therapeutic treatments.
Correlation is performed for a population of individuals who have been tested for the presence or absence of a phenotypic trait of interest and for polymorphic marker sets. To perform such analysis, the presence or absence of a set of polymorphisms (i.e.
a polymorphic set) is determined for a set of the individuals, some of whom exhibit a particular trait, and some of whom exhibit lack of the trait. The alleles of each polymorphism of the set are then reviewed to determine whether the presence or absence of a particular allele is associated with the trait of interest. Correlation can be performed by standard statistical methods and statistically significant correlations between polymorphic forms) and phenotypic characteristics are noted. For example, it might be found that the presence of allele A1 at polymorphism A correlates with heart disease. As a further example, it might be found that the combined presence of allele A1 at polymorphism A and allele B 1 at polymorphism B
correlates with increased milk production of a farm animal.
Such correlations can be exploited in several ways. In the case of a strong correlation between a set of one or more polymorphic forms and a disease for which treatment is available, detection of the polymorphic form set in a human or animal patient may justify immediate administration of treatment, or at least the institution of regular monitoring of the patient. Detection of a polymorphic form correlated with serious disease in a couple contemplating a family may also be valuable to the couple in their reproductive decisions. For example, the female partner might elect to undergo in vitro fertilization to avoid the possibility of transmitting such a polymorphism from her husband to her offspring. In the case of a weaker, but still statistically significant correlation between a polymorphic set and human disease, immediate therapeutic intervention or monitoring may not be justified. Nevertheless, the patient can be motivated to begin simple life-style changes (e.g., diet, exercise) that can be accomplished at little cost to the patient but confer potential benefits in reducing the risk of conditions to which the patient may have increased susceptibility by virtue of variant alleles.
Identification of a polymorphic set in a patient correlated with enhanced receptiveness to one of several treatment regimes for a disease indicates that this treatment regime should be followed.

For animals and plants, correlations between characteristics and phenotype are useful for breeding for desired characteristics. For example, Beitz et al., U.S. Pat.
No. 5,292,639 discuss use of bovine mitochondria) polymorphisms in a breeding program to improve milk production in cows. To evaluate the effect of mtDNA D-loop sequence polymorphism on milk production, each cow was assigned a value of 1 if variant or 0 if wild type with respect to a prototypical mitochondria) DNA sequence at each of 17 locations considered.
The previous section concerns identifying correlations between phenotypic traits and polymorphisms that directly or indirectly contribute to those traits. The present section describes identification of a physical linkage between a genetic locus associated with a trait of interest and polymorphic markers that are not associated with the trait, but are in physical proximity with the genetic locus responsible for the trait and co-segregate with it. Such analysis is useful for mapping a genetic locus associated with a phenotypic trait to a chromosomal position, and thereby cloning genes) responsible for the trait.
See Lander et al., Proc. Nat). Acad. Sci. (USA) 83, 7353-7357 (1986); Lander et al., Proc. Nat).
Acad. Sci.
(USA) 84, 2363-2367 (1987); Donis-Keller et al., Cell 51, 319-337 (1987);
Lander et al., Genetics 121, 185-199 (1989)). Genes localized by linkage can be cloned by a process known as directional cloning. See Wainwright, Med. J. Australia 159, 170-174 (1993);
Collins, Nature Genetics 1, 3-6 (1992) (each of which is incorporated by reference in its entirety for all purposes).
Linkage studies are typically performed on members of a family. Available members of the family are characterized for the presence or absence of a phenotypic trait and for a set of polymorphic markers. The distribution of polymorphic markers in an informative meiosis is then analyzed to determine which polymorphic markers co-segregate with a phenotypic trait.
See, e.g., Kerem et al., Science 245, 1073-1080 (1989); Monaco et al., Nature 316, 842 (1985); Yamoka et al., Neurology 40, 222-226 (1990); Rossiter et al., FASEB
Journal 5, 21-27 (1991).
Linkage is analyzed by calculation of LOD (log of the odds) values. A lod value is the relative likelihood of obtaining observed segregation data for a marker and a genetic locus when the two are located at a recombination fraction RF, versus the situation in which the two are not linked, and thus segregating independently (Thompson & Thompson, Genetics in Medicine (5th ed, W.B. Saunders Company, Philadelphia, 1991); Strachan, "Mapping the human genome" in The Human Genome (BIOS Scientific Publishers Ltd, Oxford), Chapter 4).
A series of likelihood ratios are calculated at various recombination fractions (RF), ranging from RF--0.0 (coincident loci) to RF--0.50 (unlinked). Thus, the likelihood at a given value of RF is: probability of data if loci linked at RF to probability of data if loci unlinked. The computed likelihood is usually expressed as the logl0 of this ratio (i.e., a lod score). For example, a lod score of 3 indicates 1000:1 odds against an apparent observed linkage being a coincidence. The use of logarithms allows data collected from different families to be combined by simple addition. Computer programs are available for the calculation of lod scores for differing values of RF (e.g., LIPED, MLINK (Lathrop, Proc. Nat.
Acad. Sci. (USA) 81, 3443-3446 (1984)). For any particular lod score, a recombination fraction may be determined from mathematical tables. See Smith et al., Mathematical tables for research workers in human genetics (Churchill, London, 1961); Smith, Ann. Hum. Genet.
32, 127-150 (1968). The value of RF at which the lod score is the highest is considered to be the best estimate of the recombination fraction.
Positive lod score values suggest that the two loci are linked, whereas negative values suggest that linkage is less likely (at that value of RF) than the possibility that the two loci are unlinked. By convention, a combined lod score of + 3 or greater (equivalent to greater than 1000:1 odds in favor of linkage) is considered definitive evidence that two loci are linked.
Similarly, by convention, a negative lod score of -2 or less is taken as definitive evidence against linkage of the two loci being compared. Negative linkage data are useful in excluding a chromosome or a segment thereof from consideration. The search focuses on the remaining non-excluded chromosomal locations.
The invention further provides transgenic nonhuman animals capable of expressing an exogenous variant gene and/or having one or both alleles of an endogenous variant gene inactivated. Expression of an exogenous variant gene is usually achieved by operably linking the gene to a promoter and optionally an enhancer, and microinjecting the construct into a zygote. See Hogan et al., "Manipulating the Mouse Embryo, A Laboratory Manual," Cold Spring Harbor Laboratory. (1989). Inactivation of endogenous variant genes can be achieved by forming a transgene in which a cloned variant gene is inactivated by insertion of a positive selection marker. See Capecchi, Science 244, 1288-1292 The transgene is then introduced into an embryonic stem cell, where it undergoes homologous recombination with an endogenous variant gene. Mice and other rodents are preferred animals. Such animals provide useful drug screening systems.
The invention further provides methods for assessing the pharmacogenomic susceptibility of a subject harboring a single nucleotide polymorphism to a particular pharmaceutical compound, or to a class of such compounds. Genetic polymorphism in drug-metabolizing enzymes, drug transporters, receptors for pharmaceutical agents, and other drug targets have been correlated with individual differences based on distinction in the efficacy and toxicity of the pharmaceutical agent administered to a subject.
Pharmocogenomic characterization of a subjects susceptibility to a drug enhances the ability to tailor a dosing regimen to the particular genetic constitution of the subject, thereby enhancing and optimizing the therapeutic effectiveness of the therapy.
In cases in which a cSNP leads to a polymorphic protein that is ascribed to be the cause of a pathological condition, method of treating such a condition includes administering to a subject experiencing the pathology the wild type cognate of the polymorphic protein. Once administered in an effective dosing regimen, the wild type cognate provides complementation or remediation of the defect due to the polymorphic protein. The subject's condition is ameliorated by this protein therapy.
A subject suspected of suffering from a pathology ascribable to a polymorphic protein that arises from a cSNP is to be diagnosed using any of a variety of diagnostic methods capable of identifying the presence of the cSNP in the nucleic acid, or of the cognate polymorphic protein, in a suitable clinical sample taken from the subject.
Once the presence of the cSNP has been ascertained, and the pathology is correctable by administering a normal or wild-type gene, the subject is treated with a pharmaceutical composition that includes a nucleic acid that harbors the correcting wild-type gene, or a fragment containing a correcting sequence of the wild-type gene. Non-limiting examples of ways in which such a nucleic acid may be administered include incorporating the wild-type gene in a viral vector, such as an adenovirus or adeno associated virus, and administration of a naked DNA in a pharmaceutical composition that promotes intracellular uptake of the administered nucleic acid. Once the nucleic acid that includes the gene coding for the wild-type allele of the polymorphism is incorporated within a cell of the subject, it will initiate de novo biosynthesis of the wild-type gene product. If the nucleic acid is further incorporated into the genome of the subject, the treatment will have long-term effects, providing de novo synthesis of the wild-type protein for a prolonged duration. The synthesis of the wild-type protein in the cells of the subject will contribute to a therapeutic enhancement of the clinical condition of the subject.
A subject suffering from a pathology ascribed to a SNP may be treated so as to correct the genetic defect. (See Kren et al., Proc. Natl. Acad. Sci. USA 96:10349-10354 (1999)).
Such a subject is identified by any method that can detect the polymorphism in a sample drawn from the subject. Such a genetic defect may be permanently corrected by administering to such a subject a nucleic acid fragment incorporating a repair sequence that supplies the wild-type nucleotide at the position of the SNP. This site-specific repair sequence encompasses an RNA/DNA oligonucleotide which operates to promote endogenous repair of a subject's genomic DNA. Upon administration in an appropriate vehicle, such as a complex with polyethylenimine or encapsulated in anionic liposomes, a genetic defect leading to an inborn pathology may be overcome, as the chimeric oligonucleotides induces incorporation of the wild-type sequence into the subject's genome. Upon incorporation, the wild-type gene -product is expressed, and the replacement is propagated, thereby engendering a permanent repair.
The invention further provides kits comprising at least one allele-specific oligonucleotide as described above. Often, the kits contain one or more pairs of allele-specific oligonucleotides hybridizing to different forms of a polymorphism. In some kits, the allele-specific oligonucleotides are provided immobilized to a substrate.
For example, the same substrate can comprise allele-specific oligonucleotide probes for detecting at least 10, 100, 1000 or all of the polymorphisms shown in the Table. Optional additional components of the kit include, for example, restriction enzymes, reverse-transcriptase or polymerise, the substrate nucleoside triphosphates, means used to label (for example, an avidin-enzyme conjugate and enzyme substrate and chromogen if the label is biotin), and the appropriate buffers for reverse transcription, PCR, or hybridization reactions. Usually, the kit also contains instructions for carrying out the hybridizing methods.
Several aspects of the present invention rely on having available the polymorphic proteins encoded by the nucleic acids comprising a SNP of the inventions.
There are various methods of isolating these nucleic acid sequences. For example, DNA is isolated from a genomic or cDNA library using labeled oligonucleotide probes having sequences complementary to the sequences disclosed herein.
Such probes can be used directly in hybridization assays. Alternatively probes can be designed for use in amplification techniques such as PCR.
To prepare a cDNA library, mRNA is isolated from tissue such as heart or pancreas, preferably a tissue wherein expression of the gene or gene family is likely to occur. cDNA is prepared from the mRNA and ligated into a recombinant vector. The vector is transfected into a recombinant host for propagation, screening and cloning. Methods for making and screening cDNA libraries are well known, See Gubler, U. and Hoffman, B.J. Gene 25:263-269 (1983) and Sambrook et al.
For a genomic library, for example, the DNA is extracted from tissue and either mechanically sheared or enzymatically digested to yield fragments of about 12-20 kb. The fragments are then separated by gradient centrifugation from undesired sizes and are constructed in bacteriophage lambda vectors. These vectors and phage are packaged in vitro, as described in Sambrook, et al. Recombinant phage are analyzed by plaque hybridization as described in Benton and Davis, Science 196:180-1 82 (1977). Colony hybridization is carned out as generally described in M. Grunstein et al. Proc. Natl. Acid. Sci. USA.
72:3961-3965 (1975). DNA of interest is identified in either cDNA or genomic libraries by its ability to hybridize with nucleic acid probes, for example on Southern blots, and these DNA regions are isolated by standard methods familiar to those of skill in the art. See Sambrook, et al.
In PCR techniques, oligonucleotide primers complementary to the two 3' borders of the DNA region to be amplified are synthesized. The polymerise chain reaction is then carried out using the two primers. See PCR Protocols: a Guide to Methods and Applications (Innis, M, Gelfand, D., Sninsky, J. and White, T., eds.), Academic Press, San Diego (1990).
Primers can be selected to amplify the entire regions encoding a full-length sequence of interest or to amplify smaller DNA segments as desired. PCR can be used in a variety of protocols to isolate cDNAs encoding a sequence of interest. In these protocols, appropriate primers and probes for amplifying DNA encoding a sequence of interest are generated from analysis of the DNA sequences listed herein. Once such regions are PCR-amplified, they can be sequenced and oligonucleotide probes can be prepared from the sequence.
Once DNA encoding a sequence comprising a cSNP is isolated and cloned, one can express the encoded polymorphic proteins in a variety of recombinantly engineered cells. It is expected that those of skill in the art are knowledgeable in the numerous expression systems available for expression of DNA encoding a sequence of interest. No attempt to describe in detail the various methods known for the expression of proteins in prokaryotes or eukaryotes is made here.
In brief summary, the expression of natural or synthetic nucleic acids encoding a sequence of interest will typically be achieved by operably linking the DNA or cDNA to a promoter (which is either constitutive or inducible), followed by incorporation into an expression vector. The vectors can be suitable for replication and integration in either prokaryotes or eukaryotes. Typical expression vectors contain initiation sequences, transcription and translation terminators, and promoters useful for regulation of the expression of a polynucleotide sequence of interest. To obtain high level expression of a cloned gene, it is desirable to construct expression plasmids which contain, at the minimum, a strong promoter to direct transcription, a ribosome binding site for translational initiation, and a transcription/translation terminator. The expression vectors may also comprise generic expression cassettes containing at least one independent terminator sequence, sequences permitting replication of the plasmid in both eukaryotes and prokaryotes, i.e., shuttle vectors, and selection markers for both prokaryotic and eukaryotic systems. See Sambrook et al.
A variety of prokaryotic expression systems may be used to express the polymorphic proteins of the invention. Examples include E. coli, Bacillus, Streptomyces, and the like.
It is preferred to construct expression plasmids which contain, at the minimum, a strong promoter to direct transcription, a ribosome binding site for translational initiation, and a transcription/translation terminator. Examples of regulatory regions suitable for this purpose in E. coli are the promoter and operator region of the E. coli tryptophan biosynthetic pathway as described by Yanofsky, C., J. Bacterial. 158:1018-1024 (1984) and the leftward promoter of phage lambda as described by A, I. and Hagen, D., Ann. Rev. Genet. 14:399-445 (1980).
The inclusion of selection markers in DNA vectors transformed in E. coli is also useful.
Examples of such markers include genes specifying resistance to ampicillin, tetracycline, or chloramphenicol. See Sambrook et al. for details concerning selection markers for use in E.
coli.
To enhance proper folding of the expressed recombinant protein, during purification from E. coli, the expressed protein may first be denatured and then renatured.
This can be accomplished by solubilizing the bacterially produced proteins in a chaotropic agent such as guanidine HCI and reducing all the cysteine residues with a reducing agent such as beta-mercaptoethanol. The protein is then renatured, either by slow dialysis or by gel filtration.
See U.S. Patent No. 4,511,503. Detection of the expressed antigen is achieved by methods known in the art as radioimmunoassay, or Western blotting techniques or immunoprecipitation. Purification from E. coli can be achieved following procedures such as those described in U.S. Patent No. 4,511,503.
Any of a variety of eukaryotic expression systems such as yeast, insect cell lines, bird, fish, and mammalian cells, may also be used to express a polymorphic protein of the invention. As explained briefly below, a nucleotide sequence harboring a cSNP
may be expressed in these eukaryotic systems. Synthesis of heterologous proteins in yeast is well known. Methods in Yeast Genetics, Sherman, F., et al., Cold Spring Harbor Laboratory, (1982) is a well recognized work describing the various methods available to produce the protein in yeast. Suitable vectors usually have expression control sequences, such as promoters, including 3-phosphogtycerate kinase or other glycolytic enzymes, and an origin of replication, termination sequences and the like as desired. For instance, suitable vectors are described in the literature (Botstein, et al., Gene 8:17-24 (1979); Broach, et al., Gene 8:121-133 (1979)).
Two procedures are used in transforming yeast cells. In one case, yeast cells are first converted into protoplasts using zymolyase, lyticase or glusulase, followed by addition of DNA and polyethylene glycol (PEG). The PEG-treated protoplasts are then regenerated in a 3% agar medium under selective conditions. Details of this procedure are given in the papers by J.D. Beggs, Nature (London) 275:104-109 (1978); and Hinnen, A., et al., Proc. Natl.
Acad. Sci. USA, 75:1929-1933 (1978). The second procedure does not involve removal of the cell wall. Instead the cells are treated with lithium chloride or acetate and PEG and put on selective plates (Ito, H., et al., J. Bact, 153163-168 (1983)) cells and applying standard protein isolation techniques to the lysates:.
The purification process can be monitored by using Western blot techniques or radioimmunoassay or other standard techniques. The sequences encoding the proteins of the invention can also be ligated to various immunoassay expression vectors for use in transforming cell cultures of, for instance, mammalian, insect, bird or fish origin. Illustrative of cell cultures useful for the production of the polypeptides are mammalian cells.
Mammalian cell systems often will be in the form of monolayers of cells although mammalian cell suspensions may also be used. A number of suitable host cell lines capable of expressing intact proteins have been developed in the art, and include the HEK293, BHK21, and CHO
cell lines, and various human cells such as COS cell lines, HeLa cells, myeloma cell lines, Jurkat cells, etc. Expression vectors for these cells can include expression control sequences, such as an origin of replication, a promoter (e.g., the CMV promoter, a HSV tk promoter or pgk (phosphoglycerate kinase) promoter), an enhancer (Queen et al. Immunol.
Rev, 89:49 (1986)) and necessary processing information sites, such as ribosome binding sites, RNA
splice sites, polyadenylation sites (e.g., an SV40 large T Ag poly A addition site), and transcriptional terminator sequences.

Other animal cells are available, for instance, from the American Type Culture Collection Catalogue of Cell Lines and Hybridomas (7th edition, (1992)).
Appropriate vectors for expressing the proteins of the invention in insect cells are usually derived from baculovirus. Insect cell lines include mosquito larvae, silkworm, armyworm, moth and Drosophila cell lines such as a Schneider cell line (See Schneider J. Embryol.
Exp. Morphol., 27:353-365 (1987). As indicated above, the vector, e.g., a plasmid, which is used to transform the host cell, preferably contains DNA sequences to initiate transcription and sequences to control the translation of the protein. These sequences are referred to as expression control sequences. As with yeast, when higher animal host cells are employed, polyadenylation or transcription terminator sequences from known mammalian genes need to be incorporated into the vector. An example of a terminator sequence is the polyadenylation sequence from the bovine growth hormone gene. Sequences for accurate splicing of the transcript may also be included. An example of a splicing sequence is the VP1 intron from SV40 (Sprague, J. et a/., J. Virol. 45: 773-781 (1983)). Additionally, gene sequences to control replication in the host cell may be Saveria-Campo, M., 1985, "Bovine Papilloma virus DNA a Eukaryotic Cloning Vector" in DNA Cloning Vol. II a Practical Approach Ed. D.M. Glover, IRL
Press, Arlington, Virginia pp. 213-238. The host cells are competent or rendered competent for transformation by various means. There are several well-known methods of introducing DNA
into animal cells. These include: calcium phosphate precipitation, fusion of the recipient cells with bacterial protoplasts containing the DNA, treatment of the recipient cells with liposomes containing the DNA, DEAE dextran, electroporation and micro-injection of the DNA directly into the cells.
The transformed cells are cultured by means well known in the art (Biochemical Methods in Cell Culture and Virology, Kuchler, R.J., Dowden, Hutchinson and Ross, Inc., (1977)). The expressed polypeptides are isolated from cells grown as suspensions or as monolayers. The latter are recovered by well known mechanical, chemical or enzymatic means.
General methods of expressing recombinant proteins are also known and are exemplified in R. Kaufinan, Methods in Enzymology 185, 537-566 (1990). As defined herein "operably linked" refers to linkage of a promoter upstream from a DNA sequence such that the promoter mediates transcription of the DNA sequence. Specifically, "operably linked" means that the isolated polynucleotide of the invention and an expression control sequence are situated within a vector or cell in such a way that the gene encoding the protein is expressed by a host cell which has been transformed (transfected) with the ligated polynucleotide/expression sequence. The term "vector", refers to viral expression systems, autonomous self replicating circular DNA (plasmids), and includes both expression and nonexpression plasmids.
The term "gene" as used herein is intended to refer to a nucleic acid sequence which encodes a polypeptide. This definition includes various sequence polymorphisms, mutations, and/or sequence variants wherein such alterations do not affect the function of the gene product. The term "gene" is intended to include not only coding sequences but also regulatory regions such as promoters, enhancers, termination regions and similar untranslated nucleotide sequences. The term further includes all introns and other DNA sequences spliced from the mRNA transcript, along with variants resulting from alternative splice sites.
A number of types of cells may act as suitable host cells for expression of the protein.
Mammalian host cells include, for example, monkey COS cells, Chinese Hamster Ovary (CHO) cells, human kidney 293 cells, human epidermal A43 1 cells, human Co10205 cells, 3T3 cells, CV-1 cells, other transformed primate cell lines, normal diploid cells, cell strains derived from in vitro culture of primary tissue, primary explants, HeLa cells, mouse L cells, BHK, HL- 60, U937, HaK or Jurkat cells. Alternatively, it may be possible to produce the protein in lower eukaryotes such as yeast or in prokaryotes such as bacteria.
Potentially suitable yeast strains include Saccharomyces cerevisiae, Schizosaccharomyces pombe, Kluyveromyces strains, Candida or any yeast strain capable of expressing heterologous proteins. Potentially suitable bacterial strains include Escherichia coli, Bacillus subtilis, Salmonella typhimurium, or any bacterial strain capable of expressing heterologous proteins.
If the protein is made in yeast or bacteria, it may be necessary to modify the protein produced therein, for example by phosphorylation or glycosylation of the appropriate sites, in order to obtain the functional protein.
The protein may also be produced by operably linking the isolated polynucleotide of the invention to suitable control sequences in one or more insect expression vectors, and employing an insect expression system. Materials and methods for baculovirus/insect cell expression systems are commercially available in kit form from, e.g., Invitrogen, San Diego, California, U.S.A. (the MaxBac~ kit), and such methods are well known in the art, as described in Summers and Smith, Texas Agricultural Experiment Station Bulletin No. 1555 1987 incorporated herein by reference. As used herein, an insect cell capable of expressing a polynucleotide of the present invention is "transformed." The protein of the invention may be prepared by culturing transformed host cells under culture conditions suitable to express the recombinant protein.
The polymorphic protein of the invention may also be expressed as a product of transgenic animals, e.g., as a component of the milk of transgenic cows, goats, pigs, or sheep which are characterized by somatic or germ cells containing a nucleotide sequence encoding the protein. The protein may also be produced by known conventional chemical synthesis. Methods for constructing the proteins of the present invention by synthetic means are known to those skilled in the art.
The polymorphic proteins produced by recombinant DNA technology may be purified by techniques commonly employed to isolate or purify recombinant proteins.
Recombinantly produced proteins can be directly expressed or expressed as a fusion protein.
The protein is then purified by a combination of cell lysis (e.g., sonication) and affinity chromatography. For fusion products, subsequent digestion of the fusion protein with an appropriate proteolytic enzyme releases the desired polypeptide. The polypeptides of this invention may be purified to substantial purity by standard techniques well known in the art, including selective precipitation with such substances as ammonium sulfate, column chromatography, immunopurification methods, and others. See, for instance, R. Scopes, Protein Purification:
Principles and Practice, Springer-Verlag: New York (1982), incorporated herein by reference.
For example, in an embodiment, antibodies may be raised to the proteins of the invention as described herein. Cell membranes are isolated from a cell line expressing the recombinant protein, the protein is extracted from the membranes and immunoprecipitated.
The proteins may then be further purified by standard protein chemistry techniques as described above.
The resulting expressed protein may then be purified from such culture (i.e., from culture medium or cell extracts) using known purification processes, such as gel filtration and ion exchange chromatography. The purification of the protein may also include an affinity column containing agents which will bind to the protein; one or more column steps over such affinity resins as concanavalin A-agarose, heparin-Toyopearl@ or Cibacrom blue 3GA Sepharose B; one or more steps involving hydrophobic interaction chromatography using such resins as phenyl ether, butyl ether, or propyl ether; or immunoaffmity chromatography.
Alternatively, the protein of the invention may also be expressed in a form which will facilitate purification. For example, it may be expressed as a fusion protein, such as those of maltose binding protein (MBP), glutathione-S-transferase (GST) or thioredoxin (TRX). Kits for expression and purification of such fusion proteins are commercially available from New England BioLab (Beverly, MA), Pharmacia (Piscataway, NJ) and InVitrogen, respectively.
The protein can also be tagged with an epitope and subsequently purified by using a specific antibody directed to such epitope. One such epitope ("Flag") is commercially available from Kodak (New Haven, CT). Finally, one or more reverse-phase high performance liquid chromatography (RP- HPLC) steps employing hydrophobic RP-HPLC media, e.g., silica gel having pendant methyl or other aliphatic groups, can be employed to further purify the protein.
Some or all of the foregoing purification steps, in various combinations, can also be employed to provide a substantially homogeneous isolated recombinant protein. The protein thus purified is substantially free of other mammalian proteins and is defined in accordance with the present invention as an "isolated protein."
The term "antibody" as used herein refers to immunoglobulin molecules and immunologically active portions of immunoglobulin molecules, i.e., molecules that contain an antigen binding site that specifically binds (immunoreacts with) an antigen, such as polymorphic. Such antibodies include, but are not limited to, polyclonal, monoclonal, chimeric, single chain, Fab and F~ab')2 fragments, and an Fab expression library. In a specific embodiment, antibodies to human polymorphic proteins are disclosed.
The phrase "specifically binds to", "immunospecifically binds to" or is "specifically immunoreactive with", an antibody when referring to a protein or peptide, refers to a binding reaction which is determinative of the presence of the protein in the presence of a heterogeneous population of proteins and other biological materials. Thus, for example, under designated immunoassay conditions, the specified antibodies bind to a particular protein and do not bind in a significant amount to other proteins present in the sample.
Specific binding to an antibody under such conditions may require an antibody that is selected for its specificity for a particular protein. Of particular interest in the present invention is an antibody that binds immunospecifically to a polymorphic protein but not to its cognate wild type allelic protein, or vice versa. A variety of immunoassay formats may be used to select antibodies specifically immunoreactive with a particular protein. For example, solid-phase ELISA
immunoassays are routinely used to select monoclonal antibodies specifically immunoreactive with a protein.
See Harlow and Lane (1988) Antibodies, a Laboratory Manual, Cold Spring Harbor Publications, New York, for a description of immunoassay formats and conditions that can be used to determine specific immunoreactivity.
Polyclonal and/or monoclonal antibodies that immunospecifically bind to polymorphic gene products but not to the corresponding prototypical or "wild-type" gene products are also provided. Antibodies can be made by injecting mice or other animals with the variant gene product or synthetic peptide. Monoclonal antibodies are screened as are described, for example, in Harlow & Lane, Antibodies, A Laboratory Manual, Cold Spring Harbor Press, New York (1988); Goding, Monoclonal antibodies, Principles and Practice (2d ed.) Academic Press, New York (1986). Monoclonal antibodies are tested for specific immunoreactivity with a variant gene product and lack of immunoreactivity to the corresponding prototypical gene product.
An isolated polymorphic protein, or a portion or fragment thereof, can be used as an immunogen to generate the antibody that binds the polymorphic protein using standard techniques for polyclonal and monoclonal antibody preparation. The full-length polymorphic protein can be used or, alternatively, the invention provides antigenic peptide fragments of polymorphic for use as immunogens. The antigenic peptide of a polymorphic protein of the invention comprises at least 8 amino acid residues of the amino acid sequence encompassing the polymorphic amino acid and encompasses an epitope of the polymorphic protein such that an antibody raised against the peptide forms a specific immune complex with the polymorphic protein. Preferably, the antigenic peptide comprises at least 10 amino acid residues, more preferably at least 15 amino acid residues, even more preferably at least 20 amino acid residues, and most preferably at least 30 amino acid residues. Preferred epitopes encompassed by the antigenic peptide are regions of polymorphic that are located on the surface of the protein, e.g., hydrophilic regions.
For the production of polyclonal antibodies, various suitable host animals (e.g., rabbit, goat, mouse or other mammal) may be immunized by injection with the polymorphic protein.
An appropriate immunogenic preparation can contain, for example, recombinantly expressed polymorphic protein or a chemically synthesized polymorphic polypeptide. The preparation can further include an adjuvant. Various adjuvants used to increase the immunological response include, but are not limited to, Freund's (complete and incomplete), mineral gels (e.g., aluminum hydroxide), surface active substances (e.g., lysolecithin, pluronic polyols, polyanions, peptides, oil emulsions, dinitrophenol, etc.), human adjuvants such as Bacille Calmette-Guerin and Corynebacterium parvum, or similar immunostimulatory agents. If desired, the antibody molecules directed against polymorphic proteins can be isolated from the mammal (e.g., from the blood) and further purified by well known techniques, such as protein A chromatography, to obtain the IgG fraction.

The term "monoclonal antibody" or "monoclonal antibody composition", as used herein, refers to a population of antibody molecules that originates from the clone of a singly hybridoma cell, and that contains only one type of antigen binding site capable of immunoreacting with a particular epitope of a polymorphic protein. A
monoclonal antibody composition thus typically displays a single binding affinity for a particular polymorphic protein with which it immunoreacts. For preparation of monoclonal antibodies directed towards a particular polymorphic protein, or derivatives, fragments, analogs or homologs thereof, any technique that provides for the production of antibody molecules by continuous cell line culture may be utilized. Such techniques include, but are not limited to, the hybridoma technique (see Kohler & Milstein, 1975 Nature 256: 495-497); the trioma technique; the human B-cell hybridoma technique (see Kozbor, et al., 1983 Immunol Today 4:
72) and the EBV hybridoma technique to produce human monoclonal antibodies (see Cole, et al., 1985 In: MONOCLONAL ANTIBODIES AND CANCER THERAPY, Alan R. Liss, Inc., pp. 77-96).
Human monoclonal antibodies may be utilized in the practice of the present invention and may be produced by using human hybridomas (see Cote, et al., 1983. Proc Natl Acad Sci USA 80:
2026-2030) or by transforming human B-cells with Epstein Barr Virus in vitro (see Cole, et al., 1985 In: MONOCLONAL ANTIBODIES AND CANCER THERAPY, Alan R. Liss, Inc., pp. 77-96).
According to the invention, techniques can be adapted for the production of single-chain antibodies specific to a polymorphic protein (see e.g., U.S.
Patent No. 4,946,778).
In addition, methodologies can be adapted for the construction of Fab expression libraries (see e.g., Huse, et al., 1989 Science 246: 1275-1281) to allow rapid and effective identification of monoclonal Fab fragments with the desired specificity for a polymorphic protein or derivatives, fragments, analogs or homologs thereof. Non-human antibodies can be "humanized" by techniques well known in the art. See e.g., U.S. Patent No. 5,225,539.
Antibody fragments that contain the idiotypes to a polymorphic protein may be produced by techniques known in the art including, but not limited to: (i) an F~ab~~2 fragment produced by pepsin digestion of an antibody molecule; (ii) an Fab fragment generated by reducing the disulfide bridges of an F(ab')2 fragment; (iii) an Fab fragment generated by the treatment of the antibody molecule with papain and a reducing agent and (iv) F,, fragments.
Additionally, recombinant anti-polymorphic protein antibodies, such as chimeric and humanized monoclonal antibodies, comprising both human and non-human portions, which can be made using standard recombinant DNA techniques, are within the scope of the invention. Such chimeric and humanized monoclonal antibodies can be produced by recombinant DNA techniques known in the art, for example using methods described in PCT
International Application No. PCT/LJS86/02269; European Patent Application No.
184,187;
European Patent Application No. 171,496; European Patent Application No.
173,494; PCT
International Publication No. WO 86/01533; U.S. Pat. No. 4,816,567; European Patent Application No. 125,023; Better et al. (1988) Science 240:1041-1043; Liu et al. (1987) PNAS
84:3439-3443; Liu et al. (1987) Jlmmunol. 139:3521-3526; Sun et al. (1987) PNAS
84:214-218; Nishimura et al. (1987) Cancer Res 47:999-1005; Wood et al. (1985) Nature 314:446-449; Shaw et al. (1988) JNatl Cancer Inst 80:1553-1559); Mornson(1985) Science 229:1202-1207; Oi et al. (1986) BioTechniques 4:214; U.S. Pat. No. 5,225,539;
Jones et al.
(1986) Nature 321:552-525; Verhoeyan et al. (1988) Science 239:1534; and Beidler et al.
(1988) Jlmmunol 141:4053-4060.
In one embodiment, methodologies for the screening of antibodies that possess the desired specificity include, but are not limited to, enzyme-linked immunosorbent assay (ELISA) and other immunologically-mediated techniques known within the art.
Anti-polymorphic protein antibodies may be used in methods known within the art relating to the detection, quantitation and/or cellular or tissue localization of a polymorphic protein (e.g., for use in measuring levels of the polymorphic protein within appropriate physiological samples, for use in diagnostic methods, for use in imaging the protein, and the like). In a given embodiment, antibodies for polymorphic proteins, or derivatives, fragments, analogs or homologs thereof, that contain the antibody-derived CDR, are utilized as pharmacologically-active compounds in therapeutic applications intended to treat a pathology in a subject that arises from the presence of the cSNP allele in the subject.
An anti-polymorphic protein antibody (e.g., monoclonal antibody) can be used to isolate polymorphic proteins by a variety of immunochemical techniques, such as immunoaffinity chromatography or immunoprecipitation. An anti-polymorphic protein antibody can facilitate the purification of natural polymorphic protein from cells and of recombinantly produced polymorphic proteins expressed in host cells. Moreover, an anti-polymorphic protein antibody can be used to detect polymorphic protein (e.g., in a cellular lysate or cell supernatant) in order to evaluate the abundance and pattern of expression of the polymorphic protein. Anti-polymorphic antibodies can be used diagnostically to monitor protein levels in tissue as part of a clinical testing procedure, e.g., to, for example, determine the efficacy of a given treatment regimen. Detection can be facilitated by coupling (i.e., physically linking) the antibody to a detectable substance. Examples of detectable substances include various enzymes, prosthetic groups, fluorescent materials, luminescent materials, bioluminescent materials, and radioactive materials. Examples of suitable enzymes include horseradish peroxidase, alkaline phosphatase, -galactosidase, or acetylcholinesterase;
examples of suitable prosthetic group complexes include streptavidin/biotin and avidin/biotin;
examples of suitable fluorescent materials include umbelliferone, fluorescein, fluorescein isothiocyanate, rhodamine, dichlorotriazinylamine fluorescein, dansyl chloride or phycoerythrin; an example of a luminescent material includes luminol; examples of bioluminescent materials include luciferase, luciferin, and aequorin, and examples of suitable radioactive material include lzsh ~31h ass or 3H.
EQUIVALENTS
From the foregoing detailed description of the specific embodiments of the invention, it should be apparent that unique compositions and methods of use thereof in SNPs in known genes have been described. Although particular embodiments have been disclosed herein in detail, this has been done by way of example for purposes of illustration only, and is not intended to be limiting with respect to the scope of the appended claims which follow. In particular, it is contemplated by the inventor that various substitutions, alterations, and modifications may be made to the invention without departing from the spirit and scope of the invention as defined by the claims.

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<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (4 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg42918213 <400> 3 ctgaggcagg agaatcgctt gaacccagga ggcggaggtt gcagtgagcc g 51 <210> 4 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (3 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg42918213 <400> 4 ctgaggcagg agaatcgctt gaacctagga ggcggaggtt gcagtgagcc g 51 <210> 5 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (6 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg42918213 <400> 5 ggagaatcgc ttgaacccag gaggcagagg ttgcagtgag ccgagattgc a 51 <210> 6 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (5 is other entry) <221> misc feature <2zz> (o>...(o) <223> Accession number cg42918213 <400> 6 ggagaatcgc ttgaacccag gaggcggagg ttgcagtgag ccgagattgc a 51 <210> 7 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (8 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg42918213 <400> 7 ggaggttgca gtgagccgag attgcgccac tgcactccag cctgggcgac a 51 <210> 8 -<211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (7 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg42918213 <400> 8 ggaggttgca gtgagccgag attgcaccac tgcactccag cctgggcgac a 51 <210> 9 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (10 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg42918213 <400> 9 ctgcactcca gcctgggcga cagagtgaga ctctgtctca aaaaaaagaa a 51 <210> 10 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (9 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg42918213 <400> 10 ctgcactcca gcctgggcga cagagcgaga ctctgtctca aaaaaaagaa a 51 <210> 11 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (12 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg42918213 <400> 11 tgcactccag cctgggcgac agagtgagac tctgtctcaa aaaaaagaaa a 51 <210> 12 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (11 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg42918213 <400> 12 tgcactccag cctgggcgac agagtaagac tctgtctcaa aaaaaagaaa a 51 <210> 13 <211> 51 <212> DNA
<213> Homo sapiens <220>

<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (14 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44029012 <400> 13 ggaacggcca catcctcggg cagagccaag agtcaccgtc tttcgtgggc c 51 <210> 14 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (13 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg44029012 <400> 14 ggaacggcca catcctcggg cagagcaaga gtcaccgtct ttcgtgggcc 50 <210> 15 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (16 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43093113 <400> 15 gagcgccgaa atttccctgc ccattatcag agcggtggta acaaggatga a 51 <210> 16 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (15 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43093113 <400> 16 gagcgccgaa atttccctgc ccattgtcag agcggtggta acaaggatga a 51 <210> 17 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (18 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43987690 <400> 17 aagagaaaga cttaggggga aaaaagacca gagagcatcc caaggacaga c 51 <210> 18 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (17 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg43987690 <400> 18 aagagaaaga cttaggggga aaaaaaccag agagcatccc aaggacagac 50 <210> 19 <211> 51 '<212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (20 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29479549 <400> 19 gcgtaagatc gattgtggat cagcatcgat gctggtcccc ccgacgttgt t 51 <210> 20 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (19 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29479549 <400> 20 gcgtaagatc gattgtggat cagcaccgat gctggtcccc ccgacgttgt t 51 <210> 21 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (22 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29479549 <400> 21 ggatcagcat cgatgctggt ccccccgacg ttgttgttgg cgggtgttgt t 51 <210> 22 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (21 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg29479549 <400> 22 ggatcagcat cgatgctggt cccccgacgt tgttgttggc gggtgttgtt 50 <210> 23 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (24 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43299481 <400> 23 cagagctggg agcggggtcc cgaaggcggg tcagtcccgg tcagggtggg c 51 <210> 24 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26)...(0) <223> 2 of 2 allelic variants (23 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg43299481 <400> 24 cagagctggg agcggggtcc cgaagcgggt cagtcccggt cagggtgggc 50 <210> 25 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (26 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43299481 <400> 25 caccttcaca gccacccctt tcgccatctc cttccatgtc gggatcttct t 51 <210> 26 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (25 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43299481 <400> 26 caccttcaca gccacccctt tcgccgtctc cttccatgtc gggatcttct t 51 <210> 27 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (28 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43941958 <400> 27 ggaaatgcca cattccatag cgcagcttgc actgcacact gctatgaatt c 51 <210> 28 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (27 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43941958 <400> 28 ggaaatgcca cattccatag cgcagtttgc actgcacact gctatgaatt c 51 <210> 29 <211> 51 <212> DNA

<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (30 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27363108 <400> 29 gtgcaatgca gttcacacat acctggaatt tatgcagatg ttcagatata g 51 <210> 30 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (29 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27363108 <400> 30 gtgcaatgca gttcacacat acctgaaatt tatgcagatg ttcagatata g 51 <210> 31 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) -<223> 1 of 2 allelic variants (32 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921820 <400> 31 tgggtaaagg ggattctggg agttgagagc tctgccaggg tgagatgttt c 51 <210> 32 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (31 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921820 <400> 32 tgggtaaagg ggattctggg agttgggagc tctgccaggg tgagatgttt c 51 <210> 33 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (34 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43988115 <400> 33 atgcttagat gtggtgctgt ggtgctgtgc atttatctaa aatattttaa a 51 <210> 34 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (33 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43988115 <400> 34 atgcttagat gtggtgctgt ggtgcagtgc atttatctaa aatattttaa a 51 <210> 35 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (36 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27783345 <400> 35 tcatgagaca tgcacagccc gcatcccatg ctccgggcgg ggatcgggag c 51 <210> 36 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (35 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27783345 <400> 36 tcatgagaca tgcacagccc gcatcacatg ctccgggcgg ggatcgggag c 51 <210> 37 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (38 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27783345 <400> 37 ccatgctccg ggcggggatc gggagcgtcc gctcaccgac gtggggcgcc g 51 <210> 38 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (37 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg27783345 <400> 38 ccatgctccg ggcggggatc gggaggtccg ctcaccgacg tggggcgccg 50 <210> 39 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (40 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43256113 <400> 39 cctcagcttc ctgagtagct gggactacag gtatatacca ctgcacccag c 51 <210> 40 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (39 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43256113 <400> 40 cctcagcttc ctgagtagct gggaccacag gtatatacca ctgcacccag c 51 <210> 41 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (42 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg43256113 <400> 41 cttcctgagt agctgggact acaggtatat accactgcac ccagctgtaa g 51 <210> 42 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (41 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43256113 <400> 42 cttcctgagt agctgggact acaggcatat accactgcac ccagctgtaa g 51 <210> 43 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (44 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44023415 <400> 43 ggaccggaga tggcgccgcc agcggcgcgg gcggcggcgg cggcctcgga c 51 <210> 44 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (43 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44023415 <400> 44 ggaccggaga tggcgccgcc agcggggcgg gcggcggcgg cggcctcgga c 51 <210> 45 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (46 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44023415 <400> 45 accggagatg gcgccgccag cggcgcgggc ggcggcggcg gcctcggact t 51 <210> 46 <211> 51 <212> DNA -<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (45 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44023415 <400> 46 accggagatg gcgccgccag cggcgggggc ggcggcggcg gcctcggact t 51 <210> 47 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (48 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44929662 <400> 47 agcactttgg gaggccgagg caggcggatc accggaggtc aggagatcga g 51 <210> 48 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (47 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44929662 <400> 48 agcactttgg gaggccgagg caggcagatc accggaggtc aggagatcga g 51 <210> 49 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (50 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44929662 <400> 49 gcggatcacc ggaggtcagg agatcgagac catcctggcc aacatggtga a 51 <210> 50 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (49 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44929662 <400> 50 gcggatcacc ggaggtcagg agatcaagac catcctggcc aacatggtga a 51 <210> 51 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (52 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg29691725 <400> 51 gggcatgggc cggccctctg tggcgtcccg gaacttttcg caatcggccc c 51 <210> 52 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26)...(0) <223> 2 of 2 allelic variants (51 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29691725 <400> 52 gggcatgggc cggccctctg tggcggcccg gaacttttcg caatcggccc c 51 <210> 53 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (54 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29691725 <400> 53 aggcggccat caccgcgccg aaaacgttca tccccctcat cgacgcggct c 51 <210> 54 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (53 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29691725 <400> 54 aggcggccat caccgcgccg aaaaccttca tccccctcat cgacgcggct c 51 <210> 55 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (56 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43985676 <400> 55 aataaaagta tcatgaaaaa acctattttt ttttccactg tccttccact a 51 <210> 56 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (55 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg43985676 <400> 56 aataaaagta tcatgaaaaa acctattttt tttccactgt ccttccacta 50 <210> 57 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (58 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44010970 <400> 57 tcctggtccc gaagatgggg ggggggggca gagtgagatc ttcacagttt c 51 <210> 58 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (57 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc feature <222> (0)...(0) <223> Accession number cg44010970 <400> 58 tcctggtccc gaagatgggg gggggggcag agtgagatct tcacagtttc 50 <210> 59 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (60 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44010970 <400> 59 cctggtcccg aagatggggg gggggggcag agtgagatct tcacagtttc c 51 <210> 60 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (59 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg44010970 <400> 60 cctggtcccg aagatggggg ggggggcaga gtgagatctt cacagtttcc 50 <210> 61 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic.variants (62 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44010970 <400> 61 ctggtcccga agatgggggg ggggggcaga gtgagatctt cacagtttcc a 51 <210> 62 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (61 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg44010970 <400> 62 ctggtcccga agatgggggg gggggcagag tgagatcttc acagtttcca 50 <210> 63 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (64 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg42718385 <400> 63 tattttgtag agatggggtt ttgccgtgtt atccaggctg gttttgaact c 51 <210> 64 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (63 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg42718385 <400> 64 tattttgtag agatggggtt ttgccttgtt atccaggctg gttttgaact c 51 <210> 65 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (66 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43263821 <400> 65 aaacagcact cctcttctaa aaagatacac aggccgcctt tctcggcagt g 51 <210> 66 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (65 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43263821 <400> 66 aaacagcact cctcttctaa aaagacacac aggccgcctt tctcggcagt g 51 <210> 67 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (68 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg41644093 <400> 67 aagaccagcc tgggcaacat ggggaaaccc catctctaca aaaatacaaa a 51 <210> 68 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (67 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg41644093 <400> 68 aagaccagcc tgggcaacat ggggagaccc catctctaca aaaatacaaa a 51 <210> 69 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (70 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43284479 <400> 69 cagtcgcatt taaaaaaatc aacaacaatg atgataatga aaaaatctga a 51 <210> 70 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (69 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43284479 <400> 70 cagtcgcatt taaaaaaatc aacaagaatg atgataatga aaaaatctga a 51 <210> 71 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (72 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg43284479 <400> 71 ggaatgaaga gagaaagcag ctccccaact tcaaaaccat tttggtacct g 51 <210> 72 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (71 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg43284479 <400> 72 ggaatgaaga gagaaagcag ctccctaact tcaaaaccat tttggtacct g 51 <210> 73 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (74 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43971784 <400> 73 gcacagctag gtaaaggggg aaaaaatcag atctcaagac agactctttg a 51 <210> 74 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (73 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg43971784 <400>74 gcacagctag gtaaaggggg aaaaatcagatctcaagacagactctttga 50 <210>75 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ . . (0) <223>1 2 allelic variants is other entry) of (76 <221>miscfeature <222>(0)._ .(0) <223>Accession number cg43971784 <400>75 accggcacca aggcatgtct gccctacccaagaagggagacaggccctgg g 51 <210>76 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants is other entry) of (75 <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg43971784 <400>76 accggcacca aggcatgtct gccctgcccaagaagggagacaggccctgg g 51 <210>77 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants is other entry) of (78 <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg42719787 <400>77 tcaggctccc tagaattacc ccaaaggtcaacactatctcagtgccagcc c 51 <210> 78 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (77 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg42719787 <400> 78 tcaggctccc tagaattacc ccaaatgtca acactatctc agtgccagcc c 51 <210> 79 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (80 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44938005 <400> 79 gcccagaggg aggccatctc agtctgtcca ctgtggtttc agctggtgca t 51 <210> 80 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (79 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44938005 <400> 80 gcccagaggg aggccatctc agtctctcca ctgtggtttc agctggtgca t 51 <210> 81 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> mist feature <222> (26)...(0) <223> 1 of 2 allelic variants (82 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43983675 <400> 81 agcctcatta ttaaaactga aggcattttt tttttctgct gcctttccca a 51 <210> 82 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (81 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg43983675 <400> 82 agcctcatta ttaaaactga aggcattttt ttttctgctg cctttcccaa 50 <210> 83 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (84 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43983675 <400> 83 attaaaactg aaggcatttt ttttttctgc tgcctttccc aaagtggtta g 51 <210> 84 <211> 50 <212> DNA
<213> Homo sapiens , <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (83 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg43983675 <400> 84 attaaaactg aaggcatttt tttttctgct gcctttccca aagtggttag 50 <210> 85 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (86 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43983675 <400> 85 tttatttgtg ctttttaagc catttcccca aatgggacta gcatgcttgt t 51 <210> 86 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (85 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43983675 <400> 86 tttatttgtg ctttttaagc cattttccca aatgggacta gcatgcttgt t 51 <210> 87 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (88 is other entry) <221> misc feature <222> (0)...(0) <223> Accession number cg43330621 <400> 87 ccagggaata ctgagagcac taactatgca ctaacctaga ttttcatttc g 51 <210> 88 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (87 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43330621 <400> 88 ccagggaata ctgagagcac taactgtgca ctaacctaga ttttcatttc g 51 <210> 89 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (90 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44021993 <400> 89 ccatgaagct aatggatgca gcagaactgg taaaacagcc tccggatgtc a 51 <210> 90 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (89 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44021993 <400> 90 ccatgaagct aatggatgca gcagagctgg,taaaacagcc tccggatgtc a 51 <210> 91 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (92 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44021993 <400> 91 attcttgccc ctgtggaaga atcagcctgt cagtttttct ttgatttaaa t 51 <210> 92 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (91 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44021993 <400> 92 attcttgccc ctgtggaaga atcagactgt cagtttttct ttgatttaaa t 51 <210> 93 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (94 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44012362 <400> 93 gcaagacaca tgaaaaaaaa aaaaaaactc aagtcccaac tgaatcttta c 51 <210> 94 <211> 50 <212> DNA
<213> Homo sapiens <220>

<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (93 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg44012362 <400> 94 gcaagacaca tgaaaaaaaa aaaaaactca agtcccaact gaatctttac 50 <210> 95 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (96 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44012362 <400> 95 caagacacat gaaaaaaaaa aaaaaactca agtcccaact gaatctttac t 51 <210> 96 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (95 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg44012362 <400> 96 caagacacat gaaaaaaaaa aaaaactcaa gtcccaactg aatctttact 50 <210> 97 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (98 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43309765 <400> 97 cctcagactt tcacagatgc gggcggcatc gccagctggt tcacctgctg c 51 <210> 98 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (97 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg43309765 <400> 98 cctcagactt tcacagatgc gggcgcatcg ccagctggtt cacctgctgc 50 <210> 99 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (100 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43309765 <400> 99 ctttcacaga tgcgggcggc atcgccagct ggttcacctg ctgctcagcc c 51 <210> 100 <211> 50 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (99 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg43309765 <400> 100 ctttcacaga tgcgggcggc atcgcagctg gttcacctgc tgctcagccc 50 <210> 101 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (102 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43294390 <400> 101 ttcttgcttt ctttttcttt ttttttcaat aaacaaagtt ttctcgcttc t 51 <210> 102 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (101 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg43294390 <400> 102 ttcttgcttt ctttttcttt tttttcaata aacaaagttt tctcgcttct 50 <210> 103 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (104 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg39570730 <400> 103 cgatgaagag gacgatggcc gtggccgggg cctgctgcgc tgggacagct t 51 <210> 104 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (103 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) , <223> Accession number cg39570730 <400> 104 cgatgaagag gacgatggcc gtggcggggc ctgctgcgct gggacagctt 50 <210> 105 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (106 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44011255 <400> 105 atcatggcag ctgcgttgtt caaaaggaag tttcattgag cttcatcttg g 51 <210> 106 <211> 51 <212> DNA
<213> Homo sapiens <220>

<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (105 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44011255 <400> 106 atcatggcag ctgcgttgtt caaaaagaag tttcattgag cttcatcttg g 51 <210> 107 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (108 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43926454 <400> 107 ggatgggagg agggatagca ggggaggccc cctgaacggt caaatctggg t 51 <210> 108 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (107 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43926454 <400> 108 ggatgggagg agggatagca ggggaagccc cctgaacggt caaatctggg t 51 <210> 109 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (110 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43993127 <400> 109 ctgtaaactt gcccttgact ggggagatac catctcctta aaaatactct t 51 <210> 110 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (109 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43993127 <400> 110 ctgtaaactt gcccttgact ggggaaatac catctcctta aaaatactct t 51 <210> 111 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (112 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43993127 <400> 111 cttcatgcac cagtgcagcg tgaacagggg ctttattgat ggggcttggg a 51 <210> 112 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (111 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43993127 <400> 112 cttcatgcac cagtgcagcg tgaactgggg ctttattgat ggggcttggg a 51 <210> 113 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (114 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg43054187 <400> 113 gttggagact cagcattggg gttcgccctg cccgtagcac agccaagccc 50 <210> 114 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (113 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43054187 <400> 114 gttggagact cagcattggg gttcggccct gcccgtagca cagccaagcc c 51 <210> 115 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (116 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44911042 <400> 115 tccccttagg tccctcccac aacacgtggg aattatggga gtacaattca a 51 <210> 116 <211> 51 <212> DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (115 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44911042 <400> 116 tccccttagg tccctcccac aacacatggg aattatggga gtacaattca a 51 <210> 117 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (118 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg39722830 <400> 117 aatggccggc cattatcagt tcttcctgcg gttcgggttt tggcagtaac a 51 <210> 118 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (117 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg39722830 <400> 118 aatggccggc cattatcagt tcttctgcgg ttcgggtttt ggcagtaaca 50 <210> 119 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (120 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg39570416 <400> 119 cctgcggagc taaaaccaga ttctgaggac ttatcctccc agtcctcagc t 51 <210> 120 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (119 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg39570416 <400> 120 cctgcggagc taaaaccaga ttctggggac ttatcctccc agtcctcagc t 51 <210> 121 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (122 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg43281110 <400> 121 cgttgtgacc ttgtctcaaa aaaaactaaa aaataaagca gttgcatctt 50 <210> 122 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26) . . . (0) <223> 2 of 2 allelic variants (121 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43281110 <400> 122 cgttgtgacc ttgtctcaaa aaaaaactaa aaaataaagc agttgcatct t S1 <210> 123 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (124 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg43933032 <400> 123 gtattattgc acagatctga agatcaaaaa aagctcaagg aaatacagat 50 <210> 124 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (123 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg43933032 <400> 124 gtattattgc acagatctga agatcaaaaa aaagctcaag gaaatacaga t 51 <210> 125 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (126 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43965698 <400> 125 cccaaagctt ccagagtgct ggctgatcag ggagtgtaca gtcagtcctg g 51 <210> 126 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (125 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43965698 <400> 126 cccaaagctt ccagagtgct ggctggtcag ggagtgtaca gtcagtcctg g 51 <210> 127 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (128 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg42719279 <400> 127 aagcctttac attcccactg gcagaaaatg agtacccaca agtgccccaa g 51 <210> 128 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (127 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg42719279 <400> 128 aagcctttac attcccactg gcagagaatg agtacccaca agtgccccaa g 51 <210> 129 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (130 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43142151 <400> 129 actcaaaggc caaaccttct tgcccaaggt gaaagtggtc aggcttcgat t 51 <210> 130 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (129 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43142151 <400> 130 actcaaaggc caaaccttct tgcccgaggt gaaagtggtc aggcttcgat t 51 <210> 131 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (132 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg42538578 <400> 131 ttcaggaact ggggagaggc tggctccttt ggaggctgag ctgacagagg c 51 <210> 132 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (131 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg42538578 <400> 132 ttcaggaact ggggagaggc tggcttcttt ggaggctgag ctgacagagg c 51 <210> 133 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (134 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg42481111 <400> 133 gcaagactcc acctcaaaaa aaaaaaccac aaaaaaacac aaaaggattc t 51 <210> 134 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (133 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg42481111 <400> 134 gcaagactcc acctcaaaaa aaaaaccaca aaaaaacaca aaaggattct 50 <210> 135 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (136 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg39710199 <400> 135 caaactcgac tcagcggtga gctctagcac agttccatga gttgcgaccc t 51 <210> 136 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (135 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg39710199 <400> 136 caaactcgac tcagcggtga gctctggcac agttccatga gttgcgaccc t 51 <210> 137 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (138 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg38821538 <400> 137 aaaaaataat aataataata ataatttttt taaaaagagg tgtttttgag 50 <210> 138 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (137 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38821538 <400> 138 aaaaaataat aataataata ataatatttt ttaaaaagag gtgtttttga g 51 <210> 139 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (140 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg38821538 <400> 139 aaaaaataat aataataata ataatttttt taaaaagagg tgtttttgag 50 <210> 140 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (139 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38821538 <400> 140 aaaaaataat aataataata ataatatttt ttaaaaagag gtgtttttga g 51 , <210> 141 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (142 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg38821538 <400> 141 taataataat aataataatt tttttaaaaa gaggtgtttt tgaggtctta 50 <210> 142 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (141 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38821538 <400> 142 taataataat aataataatt ttttttaaaa agaggtgttt ttgaggtctt a 51 <210> 143 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (144 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg40038435 <400> 143 tgatcctgca gaggagccaa aaaaaatctt aggtatagaa ctaatacaat t 51 <210> 144 <211> 50 <212> DNA
<213> Homo saoiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (143 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg40038435 <400> 144 tgatcctgca gaggagccaa aaaaatctta ggtatagaac taatacaatt 50 <210> 145 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (146 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg43963046 <400> 145 ggccctgtgg ttagcatccc ccacacccat atcagccact agcattttaa a 51 <210> 146 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (145 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg43963046 <400> 146 ggccctgtgg ttagcatccc ccacaccata tcagccacta gcattttaaa 50 <210> 147 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (148 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43963046 <400> 147 ccctgtggtt agcatccccc acacccatat cagccactag cattttaaag a 51 <210> 148 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (147 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg43963046 <400> 148 ccctgtggtt agcatccccc acaccatatc agccactagc attttaaaga 50 <210> 149 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (150 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43979733 <400> 149 aaaatgtatg atcaagtccc agaaaacttt gccttcccaa ggaatgtgtt t 51 <210> 150 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (149 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg43979733 <400> 150 aaaatgtatg atcaagtccc agaaactttg ccttcccaag gaatgtgttt 50 <210> 151 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (152 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43979733 <400> 151 ccaaaaatca cattctctct ctctctcctc tcctctctac cattctcctc a 51 <210> 152 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (151 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg43979733 <400> 152 ccaaaaatca cattctctct ctctccctct cctctctacc attctcctca 50 <210> 153 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (154 is other entry) <221>miscfeature <222>_ (0) .
.
(0) <223>Accession number cg43979733 <400>153 cagtaagaaa accaggagac tccttctgaa aggcttccacctgggaggaa a 51 <210>154 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>2 2 allelic variants (153 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg43979733 <400>154 cagtaagaaa accaggagac tccttatgaa aggcttccacctgggaggaa a 51 <210>155 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ . . (0) <223>1 2 allelic variants (156 is entry) of other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg42286566 <400>155 ctgggattac aggcatgagc caccgtgcct ggccagaaaattgtaaacac a 51 <210>156 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (155 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg42286566 <400>156 ctgggattac aggcatgagc caccgggcct ggccagaaaattgtaaacac a 51 <210> 157 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (158 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg42286566 <400> 157 gattacaggc atgagccacc gtgcctggcc agaaaattgt aaacacacac a 51 <210> 158 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (157 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg42286566 <400> 158 gattacaggc atgagccacc gtgcccggcc agaaaattgt aaacacacac a 51 <210> 159 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (160 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg42286566 <400> 159 tgcctggcca gaaaattgta aacacacaca aactctcaag tggcctaatt c 51 <210> 160 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (159 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg42286566 <400> 160 tgcctggcca gaaaattgta aacacgcaca aactctcaag tggcctaatt c 51 <210> 161 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (162 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg42286566 <400> 161 ctctcaccaa accaatcaca atacagataa aagagaataa cttgtgttca t 51 <210> 162 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (161 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg42286566 <400> 162 ctctcaccaa accaatcaca atacaaataa aagagaataa cttgtgttca t 51 <210> 163 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (164 is other entry) <221> misc feature <222>(0)...(0) <223>Accession number cg42286566 <400>163 caatacagat aaaagagaat aacttgtgtt catttttgtacaaacaaaaa a 51 <210>164 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (163 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg42286566 <400>164 caatacagat aaaagagaat aacttatgtt catttttgtacaaacaaaaa a 51 <210>165 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>1 2 allelic variants (166 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg42286566 <400>165 atacagataa aagagaataa cttgtgttca tttttgtacaaacaaaaaag a 51 <210>166 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>2 2 allelic variants (165 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg42286566 <400>166 atacagataa aagagaataa cttgtattca tttttgtacaaacaaaaaag a 51 <210> 167 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (168 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg42286566 <400> 167 cagataaaag agaataactt gtgttcattt ttgtacaaac aaaaaagata t 51 <210> 168 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (167 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg42286566 <400> 168 cagataaaag agaataactt gtgttaattt ttgtacaaac aaaaaagata t 51 <210> 169 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (170 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg42286566 <400> 169 ttcatttttg tacaaacaaa aaagatataa attgtgaatg atgcatgatt 50 <210> 170 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (169 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg42286566 <400> 170 ttcatttttg tacaaacaaa aaagactata aattgtgaat gatgcatgat t 51 <210> 171 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (172 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg42468290 <400> 171 caaaccaaac aacccaacaa aaaaaatccc tcacttttgt tttctgttta t 51 <210> 172 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (171 is other entry).
<221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg42468290 <400> 172 caaaccaaac aacccaacaa aaaaatccct cacttttgtt ttctgtttat 50 <210> 173 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (174 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44010179 <400> 173 tcccataggt agcagtgcct gtgggcaggt ggaaggtgcc cgtccctcta g 51 <210> 174 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (173 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg44010179 <400> 174 tcccataggt agcagtgcct gtgggaggtg gaaggtgccc gtccctctag 50 <210> 175 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (176 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg42927851 <400> 175 cctaggagga agacaagctt gaaggacgac ccttaataaa gagcttctag g 51 <210> 176 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (175 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg42927851 <400> 176 cctaggagga agacaagctt gaagggcgac ccttaataaa gagcttctag g 51 <210> 177 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (178 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43998776 <400> 177 tgatggggag ttttagagga gcaataaaaa acttccttct ttgtgcttgt g 51 <210> 178 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (177 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43998776 <400> 178 tgatggggag ttttagagga gcaatcaaaa acttccttct ttgtgcttgt g 51 <210> 179 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (180 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43923142 <400> 179 cccactcgcg ttctgagccc cgagagcgtc ccgcacgctc agtttggctg a 51 <210> 180 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (179 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg43923142 <400> 180 cccactcgcg ttctgagccc cgagaccgtc ccgcacgctc agtttggctg a 51 <210> 181 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (182 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg10053419 <400> 181 gggggaggta ggcagtaccc ccccctgctc ctgtggggaa ataggggctt a 51 <210> 182 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (181 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg10053419 <400>182 gggggaggta ggcagtaccc cccccgctcc tgtggggaaataggggctta 50 <210>183 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (184 is entry) of other <221>miscfeature <222>(0) _ . . (0) , <223>Accession number cg10333107 <400>183 tgcccctgag gtcaagcaga cccacaccgt cgacccggttgtcgtcgtaa c 51 <210>184 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>2 2 allelic variants (183 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg10333107 <400>184 tgcccctgag gtcaagcaga cccaccccgt cgacccggttgtcgtcgtaa c 51 <210>185 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (186 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg10353763 <400>185 tggcaggctt tgtcagtgtt tcagcgggta agaaatcttgactagtagga a 51 <210>186 <211>51 <212>DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (185 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg10353763 <400> 186 tggcaggctt tgtcagtgtt tcagcaggta agaaatcttg actagtagga a 51 <210> 187 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (188 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg10854402 <400> 187 ttgtgatctc aacaacaaca ttgaaaacag caggagcacc aggaccgatc t 51 <210> 188 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (187 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg10854402 <400> 188 ttgtgatctc aacaacaaca ttgaatacag caggagcacc aggaccgatc t 51 <210> 189 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (190 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg11763542 <400> 189 aggctgaggc aggagaatcg cttgagcctg ggaggcagag gttgcagtga g 51 <210> 190 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (189 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg11763542 <400> 190 aggctgaggc aggagaatcg cttgaacctg ggaggcagag gttgcagtga g 51 <210> 191 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (192 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg11763542 <400> 191 cgcttgagcc tgggaggcag aggttgcagt gagccaagat catgccactg c 51 <210> 192 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (191 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg11763542 <400> 192 cgcttgagcc tgggaggcag aggtttcagt gagccaagat catgccactg c 51 <210> 193 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (194 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg11794373 <400> 193 ccggaatacc ttatactttt tccccctttt ttttggggga aggaatgtgt g 51 <210> 194 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (193 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg11794373 <400> 194 ccggaatacc ttatactttt tccccttttt ttttggggga aggaatgtgt g 51 <210> 195 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (196 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg11801777 <400> 195 accctatcaa cccattaaaa tggattttaa tgaattgata ataggggctc a 51 <210> 196 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (195 is other entry) <221> misC_feature <222> (0) . . (0) <223> Accession number cg11801777 <400> 196 accctatcaa cccattaaaa tggatattaa tgaattgata ataggggctc a 51 <210> 197 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (198 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg11801777 <400> 197 tcaatcagct gataaacccc ctaaaaaagt tgcggaaacc caattgttac a 51 <210> 198 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (197 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg11801777 <400> 198 tcaatcagct gataaacccc ctaaagaagt tgcggaaacc caattgttac a 51 <210> 199 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (200 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg12991942 <400> 199 agagttttat tcctttgagg gccacagaag aaagtagtct agctctcttc a S1 <210> 200 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (199 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg12991942 <400> 200 agagttttat tcctttgagg gccactgaag aaagtagtct agctctcttc a 51 <210> 201 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (202 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg13084930 <400> 201 ttgttgtgcg tgtggtcaag atgctgactc acgatcacag tgggctcttc g 51 <210> 202 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (201 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg13084930 <400> 202 ttgttgtgcg tgtggtcaag atgctaactc acgatcacag tgggctcttc g 51 <210> 203 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (204 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg13086160 <400> 203 actaagcaca ggctcagccc cggtcgccat gcgcccaggc tcggttatca g 51 <210> 204 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2-allelic variants (203 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg13086160 <400> 204 actaagcaca ggctcagccc cggtcaccat gcgcccaggc tcggttatca g 51 <210> 205 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (206 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg13502101 <400> 205 gcggggttaa cgggtcagga gacaagaagg tggtggtagt tgggtcgtag a 51 <210> 206 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (205 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg13502101 <400> 206 gcggggttaa cgggtcagga gacaaaaagg tggtggtagt tgggtcgtag a 51 <210> 207 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (208 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg14203037 <400> 207 agtaacagaa atataacaaa attggcataa acatttgggt atctgttaac c 51 <210> 208 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (207 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg14203037 <400> 208 agtaacagaa atataacaaa attggaataa acatttgggt atctgttaac c 51 <210> 209 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (210 is other entry) <221> misc feature <222>(0) .
.
.
(0) <223>Accession number cg14203037 <400>209 agaaatataa caaaattggc ataaacattt gggtatctgttaaccaagag t 51 <210>210 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (209 is entry) of other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg14203037 <400>210 agaaatataa caaaattggc ataaaaattt gggtatctgttaaccaagag t 51 <210>211 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (212 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg14203037 <400>211 cataaacatt tgggtatctg ttaaccaaga gtgtgaagataaggtagttc c 51 <210>212 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>2 2 allelic variants (211 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg14203037 <400>212 cataaacatt tgggtatctg ttaacaaaga gtgtgaagataaggtagttc c 51 <210> 213 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (214 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg14369904 <400> 213 gcggaacctc gcgcttcgcc cgggggacaa tccgaagtcc gcgctatgga a 51 i <210> 214 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (213 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg14369904 <400> 214 gcggaacctc gcgcttcgcc cggggacaat ccgaagtccg cgctatggaa 50 <210> 215 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (216 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg14395282 <400> 215 cacccctgat gccggcctgg ctgggaatgg gcccgtcctg cacctcgagc t 51 <210> 216 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (215 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg14395282 <400> 216 cacccctgat gccggcctgg ctggggatgg gcccgtcctg cacctcgagc t 51 <210> 217 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (218 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg14395282 <400> 217 cacctcgagc tagggcaaga agaggcagag ctggaggagt tcctgtgccc 50 <210> 218 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (217 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg14395282 <400> 218 cacctcgagc tagggcaaga agaggacaga gctggaggag ttcctgtgcc c 51 <210> 219 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (220 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg14396111 <400> 219 tcagatatgg aactacatga gatctgtagc gaactgcgga ggatcagaca c 51 <210> 220 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (219 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg14396111 <400> 220 tcagatatgg aactacatga gatcttagcg aactgcggag gatcagacac 50 <210> 221 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (222 is other entry) <221> misc_feature <222> (0)...(0) <223> Accession number cg16311688 <400> 221 gttctcgggt gccgtcgctg tgcgcttcgc tgtcgtgacg ctcactgggc g 51 <210> 222 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (221 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg16311688 <400> 222 gttctcgggt gccgtcgctg tgcgcctcgc tgtcgtgacg ctcactgggc g 51 <210> 223 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (224 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg16311688 <400> 223 gcgtccagtc ccacagttcg accacatccg gcggctccgt gcccgcgacc a 51 <210> 224 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (223 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg16311688 <400> 224 gcgtccagtc ccacagttcg accacttccg gcggctccgt gcccgcgacc a 51 <210> 225 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (226 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg16311688 <400> 225 tgtccattgc gggtgagttt cggggcgcgc gaagccgggg gttccactag g 51 <210> 226 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (225 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg16311688 <400> 226 tgtccattgc gggtgagttt cggggtgcgc gaagccgggg gttccactag g 51 <210> 227 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (228 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg16311688 <400> 227 gggcgcgcga agccgggggt tccactaggg ctgggagccc gacaccgagc g 51 <210> 228 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (227 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg16311688 <400> 228 gggcgcgcga agccgggggt tccacgaggg ctgggagccc gacaccgagc g 51 <210> 229 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (230 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg16392609 <400> 229 tgctcattga tccctacgac aaggttgtca tggctcatga cagggtggtc g 51 <210> 230 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (229 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg16392609 <400> 230 tgctcattga tccctacgac aaggtcgtca tggctcatga cagggtggtc g 51 <210> 231 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (232 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg16392609 <400> 231 cctacgacaa ggttgtcatg gctcatgaca gggtggtcgc ggttcccact g 51 <210> 232 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26) . . . (0) <223> 2 of 2 allelic variants (231 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg16392609 <400> 232 cctacgacaa ggttgtcatg gctcaagaca gggtggtcgc ggttcccact g 51 <210> 233 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (234 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg16392609 <400> 233 acaaggttgt catggctcat gacagggtgg tcgcggttcc cactgagggt g 51 <210> 234 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (233 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg16392609 <400> 234 acaaggttgt catggctcat gacagagtgg tcgcggttcc cactgagggt g 51 <210> 235 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (236 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg16697187 <400> 235 atgtgttcat tgccatcggg tcgatcctgc tcatcactgg attcgttgac g 51 <210> 236 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (235 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg16697187 <400> 236 atgtgttcat tgccatcggg tcgattctgc tcatcactgg attcgttgac g 51 <210> 237 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (238 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg16843354 <400> 237 aaaagactag taacggcgaa gccgacgaga cagttatctg ccacgttgct g 51 <210> 238 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (237 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg16843354 <400> 238 aaaagactag taacggcgaa gccgatgaga cagttatctg ccacgttgct g 51 <210> 239 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (240 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg16845019 <400> 239 cctctctgat atttgggtgg ggaagggggg ttgggggtcc tctttcttca a 51 <210> 240 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (239 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg16845019 <400> 240 cctctctgat atttgggtgg ggaagtgggg ttgggggtcc tctttcttca a 51 <210> 241 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (242 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg17201640 <400> 241 ccagttcata ttgatccaat ttctagaaaa caaatgctga agttcattgc a 51 <210> 242 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (241 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg17201640 <400> 242 ccagttcata ttgatccaat ttctaaaaaa caaatgctga agttcattgc a 51 <210> 243 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (244 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg17872027 <400> 243 tgacttcaag tgatcctcct gcctcggcct ctcaaagtgc tgggattaca g 51 <210> 244 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (243 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg17872027 <400> 244 tgacttcaag tgatcctcct gcctcagcct ctcaaagtgc tgggattaca g 51 <210> 245 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (246 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg17872027 <400>245 caagtgatcc tcctgcctcg gcctctcaaa gtgctgggattacagatatg a 51 <210>246 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (245 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg17872027 <400>246 caagtgatcc tcctgcctcg gcctcccaaa gtgctgggat~tacagatatg a 51 <210>247 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>1 2 allelic variants (248 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg17964567 <400>247 gccctgtcca cactcagctc ccacagcctc accctgtcccaccagacaca c 51 <210>248 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (247 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg17964567 <400>248 gccctgtcca cactcagctc ccacatcctc accctgtcccaccagacaca c 51 <210>249 <211>46 <212>DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (250 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg17964567 <400> 249 gtcccaccag acacacacag cttagtgaca cagattctgg aagctt 46 <210> 250 <211> 46 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (249 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg17964567 <400> 250 gtcccaccag acacacacag cttagcgaca cagattctgg aagctt 46 <210> 251 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (252 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg17964567 <400> 251 gctgaggcct gagcccatca aagacgagaa ctgactgagc acacctgggc a 51 <210> 252 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (251 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg17964567 <400> 252 gctgaggcct gagcccatca aagacaagaa ctgactgagc acacctgggc a 51 <210> 253 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (254 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg19426737 <400> 253 cgttcagctc tgccaatggg aagccggagg cgcctccttc agcgagaagg t 51 <210> 254 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (253 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg19426737 <400> 254 cgttcagctc tgccaatggg aagccagagg cgcctccttc agcgagaagg t 51 <210> 255 <211> 40 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (15) ..(0) <223> 1 of 2 allelic variants (256 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg19540358 <400> 255 nggagagacg acaagggtga agggaaagaa tgactgatgg 40 <210> 256 <211> 40 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (15) ..(0) <223> 2 of 2 allelic variants (255 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg19540358 <400> 256 nggagagacg acaacggtga agggaaagaa tgactgatgg 40 <210> 257 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (258 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg19636928 <400> 257 ctatcagagg gctccatcac tccatcgtaa ggaggcagct ggtggcgagt c 51 <210> 258 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (257 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg19636928 <400> 258 ctatcagagg gctccatcac tccattgtaa ggaggcagct ggtggcgagt c 51 <210> 259 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature c222> (26) ..(0) c223> 1 of 2 allelic variants (260 is other entry) c221> misc_feature c222> (0) . . (0) <223> Accession number cg19650073 <400> 259 agctttggca gaggaccctc tgcacgcttc ctctcctcta gccagagctt c 51 c210> 260 <211> 51 <212> DNA
<213> Homo Sapiens c220>
c221> misc_feature <222> (26) .. (0) c223> 2 of 2 allelic variants (259 is other entry) c221> misc_feature <222> (0) . . (0) <223> Accession number cg19650073 <400> 260 agctttggca gaggaccctc tgcacacttc ctctcctcta gccagagctt c 51 <210> 261 c211> 51 <212> DNA
c213> Homo Sapiens c220>
<221> misc_feature c222> (26) ..(0) <223> 1 of 2 allelic variants (262 is other entry) <221> misc_feature c222> (0) . . (0) c223> Accession number cg19847826 c400> 261 acgccgaccg gatcgtcgat cccattactc gggatctgct ggaatccctg g 51 c210> 262 <211> 51 <212> DNA
c213> Homo Sapiens c220>
<221> misc_feature <222> (26) ..(0) c223> 2 of 2 allelic variants (261 is other entry) <221>miscfeature <222>(0)._ .(0) <223>Accession number cg19847826 <400>262 acgccgaccg gatcgtcgat cccatcactc gggatctgctggaatccctg g 51 <210>263 <211>39 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(14)_ . . (0) <223>1 2 allelic variants (264 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg19847826 <400>263 acgcgtccgc tccggatttc gttgacgagc tgcgctcag 39 <210>264 <211>39 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(14)_ . . (0) <223>2 2 allelic variants (263 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg19847826 <400>264 acgcgtccgc tcccgatttc gttgacgagc tgcgctcag 39 <210>265 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (266 is entry) of other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg19847826 <400>265 ctcgggatct gctggaatcc ctggttcgcg aagccggcgaggctgcggtg a 51 <210> 266 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (265 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg19847826 <400> 266 ctcgggatct gctggaatcc ctggtccgcg aagccggcga ggctgcggtg a 51 <210> 267 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (268 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg19847826 <400> 267 ctgctggaat ccctggttcg cgaagccggc gaggctgcgg tgatcttggg t 51 <210> 268 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (267 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg19847826 <400> 268 ctgctggaat ccctggttcg cgaagtcggc gaggctgcgg tgatcttggg t 51 <210> 269 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (270 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg19847826 <400> 269 tcacccatct gccccgacga cccagtaaac gtccccggct gttcctcatt g 51 <210> 270 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (269 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg19847826 <400> 270 tcacccatct gccccgacga cccagcaaac gtccccggct gttcctcatt g 51 <210> 271 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (272 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg19848544 <400> 271 accgcgacgc gattctggcc ttccccgttg agacggtgta taccgccgac c 51 <210> 272 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (271 is other entry) <221> misc feature <222> (0)...(0) <223> Accession number cg19848544 <400> 272 accgcgacgc gattctggcc ttccctgttg agacggtgta taccgccgac c 51 <210> 273 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (274 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg19848544 <400> 273 tctggccttc cccgttgaga cggtgtatac cgccgaccgc cccgtgcagc g 51 <210> 274 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (273 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg19848544 <400> 274 tctggccttc cccgttgaga cggtgcatac cgccgaccgc cccgtgcagc g 51 <210> 275 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (276 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg19848544 <400> 275 taccgccgac cgccccgtgc agcgcctggc cgaaatcgtt gccgagtacg a 51 <210> 276 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (275 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg19848544 <400> 276 taccgccgac cgccccgtgc agcgcttggc cgaaatcgtt gccgagtacg a 51 <210> 277 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (278 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg19848544 <400> 277 acgaaccggt tgaagtcatc atgggacttc cggtcgccct taacgggact g 51 <210> 278 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (277 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg19848544 <400> 278 acgaaccggt tgaagtcatc atggggcttc cggtcgccct taacgggact g 51 <210> 279 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (280 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg19848544 <400> 279 ttgaagtcat catgggactt ccggtcgccc ttaacgggac tgagcagttg g 51 <210> 280 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (279 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg19848544 <400> 280 ttgaagtcat catgggactt ccggttgccc ttaacgggac tgagcagttg g 51 <210> 281 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (282 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg19848544 <400> 281 cggacacgtg tctgtgcggt gtgaggcttg ccatcgactg gggaaaggca c 51 <210> 282 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (281 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg19848544 <400> 282 cggacacgtg tctgtgcggt gtgagacttg ccatcgactg gggaaaggca c 51 <210> 283 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (284 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg19869623 <400> 283 cagagtctgt gagcggccag gaggccacct gctcgactgg cccgtcctct c 51 <210> 284 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (283 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg19869623 <400> 284 cagagtctgt gagcggccag gaggcacctg ctcgactggc ccgtcctctc 50 <210> 285 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (286 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg19891431 <400>285 cttcaggagg ccaaggaggg aggatagact aaggtgagttcaagaccagc c 51 <210>286 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (285 entry) of is other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg19891431 <400>286 cttcaggagg ccaaggaggg aggatggact aaggtgagttcaagaccagc c 51 <210>287 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (288 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg19891431 <400>287 caagaccagc ctgggcaata cagtgagacc ctgcctctataaaaaaaaat t 51 <210>288 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (287 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg19891431 <400>288 caagaccagc ctgggcaata cagtgggacc ctgcctctataaaaaaaaat t 51 <210>289 <211>51 <212>DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (290 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg19906230 <400> 289 cagactgaca agcaagggat tttttccact caccgtcagt gggatggttc t 51 <210> 290 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (289 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg19906230 <400> 290 cagactgaca agcaagggat ttttttcact caccgtcagt gggatggttc t 51 <210> 291 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (292 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg19906230 <400> 291 acacgattat ttcacaaaaa gaaactttct gtgggacgtg cctgggcgac t 51 <210> 292 <211> 51 <212> DNA
<213> Homo Sapiens , <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (291 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg19906230 <400> 292 acacgattat ttcacaaaaa gaaaccttct gtgggacgtg cctgggcgac t 51 <210> 293 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) , <223> 1 of 2 allelic variants (294 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg19906230 <400> 293 gccagcaaaa ctgagaacct tgttcgcaaa tccgtaccct ctcccaaggc a 51 <210> 294 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (293 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg19906230 <400> 294 gccagcaaaa ctgagaacct tgttctcaaa tccgtaccct ctcccaaggc a 51 <210> 295 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (296 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg19906230 <400> 295 aaactgagaa ccttgttcgc aaatccgtac cctctcccaa ggcagcctca g 51 <210> 296 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (295 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg19906230 <400> 296 aaactgagaa ccttgttcgc aaatctgtac cctctcccaa ggcagcctca g 51 <210> 297 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (298 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20177119 <400> 297 ctcagaacct ggagatcagg ttttgaccgg tgagccagcc cgggaccttc c 51 <210> 298 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (297 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20177119 <400> 298 ctcagaacct ggagatcagg ttttggccgg tgagccagcc cgggaccttc c 51 <210> 299 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (300 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20177119 <400> 299 cagccgacgt cgcggctgac gacgtccccc ccaaatccgt tgggcgatac c 51 <210> 300 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (299 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg20177119 <400> 300 cagccgacgt cgcggctgac gacgtccccc caaatccgtt gggcgatacc 50 <210> 301 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (302 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20177119 <400> 301 acgtcgcggc tgacgacgtc ccccccaaat ccgttgggcg atacccgcct c 51 <210> 302 <211> 50 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (301 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg20177119 <400> 302 acgtcgcggc tgacgacgtc cccccaaatc cgttgggcga tacccgcctc 50 <210> 303 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (304 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20177119 <400> 303 tcccccccaa atccgttggg cgatacccgc ctcgaaccaa cccgggattg a 51 <210> 304 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (303 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20177119 <400> 304 tcccccccaa atccgttggg cgatatccgc ctcgaaccaa cccgggattg a 51 <210> 305 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (306 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20177119 <400> 305 ttgggcgata cccgcctcga accaacccgg gattgacccc gggagatcca a 51 <210> 306 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (305 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20177119 <400> 306 ttgggcgata cccgcctcga accaatccgg gattgacccc gggagatcca a 51 <210> 307 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (308 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20283978 <400> 307 aggaaacacc agatttgccc aggaagacag tgggatggct ttgatatctc t 51 <210> 308 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (307 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20283978 <400>308 aggaaacacc agatttgccc aggaatacag tgggatggctttgatatctc t 51 <210>309 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (310 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg20287156 <400>309 cggcggccca atctgccgga cgtgacgccg ggatgtcgctgggacttatg t 51 <210>310 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (309 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg20287156 <400>310 cggcggccca atctgccgga cgtgatgccg ggatgtcgctgggacttatg t 51 <210>311 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (312 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg20287300 <400>311 ttgccggccg atttcgactt tatcagtctc ttccacggagtcgacgagag a 51 <210>312 <211>51 <212>DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (311 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20287300 <400> 312 ttgccggccg atttcgactt tatcaatctc ttccacggag tcgacgagag a 51 <210> 313 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (314 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20289946 <400> 313 tccaggctgt gagcgtgcaa gaacagcacg gcggcgaaag agaacccggt a , 51 <210> 314 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (313 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20289946 <400> 314 tccaggctgt gagcgtgcaa gaacaccacg gcggcgaaag agaacccggt a 51 <210> 315 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (316 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20289946 <400> 315 gagcgtgcaa gaacagcacg gcggcgaaag agaacccggt acgcggtgcg g 51 <210> 316 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (315 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20289946 <400> 316 gagcgtgcaa gaacagcacg gcggccaaag agaacccggt acgcggtgcg g 51 <210> 317 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (318 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20375502 <400> 317 ggatctgtgg ccacctcctc aagggttgcc acacgcacca ggtcctgact g 51 <210> 318 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (317 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20375502 <400> 318 ggatctgtgg ccacctcctc aaggggtgcc acacgcacca ggtcctgact g 51 <210> 319 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (320 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20375502 <400> 319 cgcaccaggt cctgactggg agtccggccc ccagggcctg tggatggctg g 51 <210> 320 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (319 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20375502 <400> 320 cgcaccaggt cctgactggg agtccagccc ccagggcctg tggatggctg g 51 <210> 321 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (322 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20436198 <400> 321 aagttttcct cgagaagcct gcgcagcatc tccgagaggg cgcctggagc g 51 <210> 322 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (321 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg20436198 <400> 322 aagttttcct cgagaagcct gcgcacatct ccgagagggc gcctggagcg 50 <210> 323 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (324 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20436198 <400> 323 gggcccggtg gggtcctgcg gggacgcggg cgaggacggc gcggacgagg c 51 <210> 324 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (323 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg20436198 <400> 324 gggcccggtg gggtcctgcg gggaccgggc gaggacggcg cggacgaggc 50 <210> 325 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (326 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20436638 <400> 325 ctaccaggcc gccgccttcg ccggatcccg tcccgacctt gagttggttc a 51 <210> 326 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (325 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20436638 <400> 326 ctaccaggcc gccgccttcg ccggaacccg tcccgacctt gagttggttc a 51 <210> 327 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (328 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20436638 <400> 327 ccgccgcctt cgccggatcc cgtcccgacc ttgagttggt tcagctgaat t 51 <210> 328 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (327 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20436638 <400> 328 ccgccgcctt cgccggatcc cgtccagacc ttgagttggt tcagctgaat t 51 <210> 329 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (330 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20440553 <400> 329 tgagggtccc ctcttcttcc tctccgtgag ctgaaatgtt tcccttttct t 51 <210> 330 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (329 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20440553 <400> 330 tgagggtccc ctcttcttcc tctccatgag ctgaaatgtt tcccttttct t 51 <210> 331 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (332 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20442259 <400> 331 cggccactcc ccatcgccta tgaggcgacc atcatcacct tcaccgaaca a 51 <210> 332 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (331 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg20442259 <400> 332 cggccactcc ccatcgccta tgagggacca tcatcacctt caccgaacaa 50 <210> 333 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (334 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20452710 <400> 333 ggggagagag gcgggaggga cactggcctg gagagaggcg ggagggacgc t 51 <210> 334 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (333 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20452710 <400> 334 ggggagagag gcgggaggga cactgacctg gagagaggcg ggagggacgc t 51 <210> 335 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (336 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20457127 <400> 335 cgaggaaatg acctccttcg cggtagccga ccagcgatcc accgacgaga c 51 <210> 336 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (335 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg20457127 <400> 336 cgaggaaatg acctccttcg cggtaccgac cagcgatcca ccgacgagac 50 <210> 337 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (338 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20549295 <400> 337 ttagagggac aaggaagaag ccaggaagcc gccccaggcc cattgccatt g 51 <210> 338 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (337 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20549295 <400> 338 ttagagggac aaggaagaag ccagggagcc gccccaggcc cattgccatt g 51 <210> 339 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (340 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20562029 <400> 339 ttggtctttt gagatggttt tcagactttt gcattatggc aaccaactga c 51 <210> 340 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (339 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20562029 <400> 340 ttggtctttt gagatggttt tcagattttt gcattatggc aaccaactga c 51 <210> 341 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc feature <222> (26) . . . (0) <223> 1 of 2 allelic variants (342 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg20562607 <400> 341 tgagcttgtt cacaccctct ggcaggaagt tcagaaggga acacagaacc a 51 <210> 342 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (341 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg20562607 <400> 342 tgagcttgtt cacaccctct ggcagaaagt tcagaaggga acacagaacc a 51 <210> 343 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (344 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921008 <400> 343 aaacccaagt gtggcaaagg aactcattgc tctcgaaatg catatatgtt g 51 <210> 344 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (343 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921008 <400>344 aaacccaagt gtggcaaagg aactcgttgc tctcgaaatgcatatatgtt g 51 <210>345 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>1 2 allelic variants (346 is entry) of other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg44921017 <400>345 acatctgttt agccacagaa agcattgggc catactcactgcagaagata a 51 <210>346 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (345 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg44921017 <400>346 acatctgttt agccacagaa agcatcgggc catactcactgcagaagata a 51 <210>347 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>1 2 allelic variants (348 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg44921017 <400>347 gataagactt cctcagaatc ttattcgttt agtgcactcaattttacttc a 51 <210>348 <211>51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (347 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921017 <400> 348 gataagactt cctcagaatc ttatttgttt agtgcactca attttacttc a 51 <210> 349 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (350 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921180 <400> 349 ggatgcggac atcgacaagg ccttgcagga tctgctgggg caccttgaag c 51 <210> 350 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (349 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921180 <400> 350 ggatgcggac atcgacaagg ccttgaagga tctgctgggg caccttgaag c 51 <210> 351 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (352 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921180 <400> 351 tctgctgggg caccttgaag cggacatagg agcagagctg aagcatttca c 51 <210> 352 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (351 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921180 <400> 352 tctgctgggg caccttgaag cggacgtagg agcagagctg aagcatttca c 51 <210> 353 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (354 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44921180 <400> 353 tgaagcggac ataggagcag agctgaagca tttcactcat ctcttctggg g 51 <210> 354 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (353 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44921180 <400>

tgaagcggacataggagcag agctgcagca tttcactcatctcttctgggg 51 <210>

<211>

<212>
DNA

<213> sapiens Homo <220>

<221> feature misc <222> _ (26) .. (0) <223> 2 allelic variants (356 is entry) 1 of other <221> feature misc <222> _ (0) . (0) .

<223>
Accession number cg44921180 <400>

ggacataggagcagagctga agcatttcac tcatctcttctggggtagacg 51 <210>

<211>

<212>
DNA

<213> sapiens Homo <220>

<221> feature misc <222> _ (26) .. (0) <223> 2 allelic variants (355 is entry) 2 of other <221> feature misc <222> _ (0) . (0) .

<223> ssion number cg44921180 Acce <400>

ggacataggagcagagctga agcatctcac tcatctcttctggggtagacg 51 <210>

<211>

<212>
DNA

<213> sapiens Homo <220>

<221> feature misc <222> _ (26) ..(0) <223> 2 allelic variants (358 is entry) 1 of other <221> feature misc <222> _ (0). .(0) <223> ssion number cg44921180 Acce <400>

gctgaagcatttcactcatc tcttctgggg tagacgggatcaagggaatct 51 <210>

<211>

<212>
DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (357 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921180 <400> 358 gctgaagcat ttcactcatc tcttccgggg tagacgggat caagggaatc t 51 <210> 359 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (360 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921180 <400> 359 gcatttcact catctcttct ggggtagacg ggatcaaggg aatcttctcc a 51 <210> 360 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (359 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921180 <400> 360 gcatttcact catctcttct ggggtggacg ggatcaaggg aatcttctcc a 51 <210> 361 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (362 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921180 <400> 361 tctcttctgg ggtagacggg atcaagggaa tcttctccac ggcggcagag c 51 <210> 362 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (361 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44921180 <400> 362 tctcttctgg ggtagacggg atcaaaggaa tcttctccac ggcggcagag c 51 <210> 363 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (364 is other entry) <221> misc_feature <222> (0)...(0) <223> Accession number cg44921180 <400> 363 tcctccctgg tcttgcagcc aatgggctgc agtcatacat gggtctctat g 51 <210> 364 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (363 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921180 <400> 364 tcctccctgg tcttgcagcc aatggactgc agtcatacat gggtctctat g 51 <210> 365 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (366 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921801 <400> 365 gcctgggcaa caagagtgaa actccatctc aaaaaaaaaa aaaaaaaaag a 51 <210> 366 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (365 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921801 <400> 366 gcctgggcaa caagagtgaa actccgtctc aaaaaaaaaa aaaaaaaaag a 51 <210> 367 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (368 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921847 <400> 367 aataatatgt taacataaac ataacaacac acatattatt tttctacccc t 51 <210> 368 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (367 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44921847 <400> 368 aataatatgt taacataaac ataacgacac acatattatt tttctacccc t 51 <210> 369 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (370 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921882 <400> 369 aaaacttgaa ctcttctaga cagataccga gtggcaatct gggtatgttt g 51 <210> 370 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (369 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44921882 <400> 370 aaaacttgaa ctcttctaga cagatcccga gtggcaatct gggtatgttt g 51 <210> 371 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (372 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921882 <400> 371 acagataccg agtggcaatc tgggtatgtt tggcaatagc ggagcagcac a 51 <210> 372 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (371 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921882 <400> 372 acagataccg agtggcaatc tgggtgtgtt tggcaatagc ggagcagcac a 51 <210> 373 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (374 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921986 <400> 373 cctgaatggg gtggtagatt ttttttctta aaaaaatttt tttgtttttt t 51 <210> 374 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (373 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921986 <400> 374 cctgaatggg gtggtagatt tttttcttaa aaaaattttt ttgttttttt 50 <210> 375 <211> 51 <212> DNA
<213> Homo sapiens <220'>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (376 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921986 <400> 375 attttttttc ttaaaaaaat ttttttgttt tttttaatac tcagaggaga g 51 <210> 376 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (375 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921986 <400> 376 attttttttc ttaaaaaaat tttttgtttt ttttaatact cagaggagag 50 <210> 377 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (378 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921986 <400> 377 tttttttctt aaaaaaattt ttttgttttt tttaatactc agaggagagg g 51 <210> 378 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (377 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921986 <400> 378 tttttttctt aaaaaaattt ttttgttttt ttaatactca gaggagaggg 50 <210> 379 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (380 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44921986 <400> 379 cttaaaaaaa tttttttgtt ttttttaata ctcagaggag agggacatag g 51 <210> 380 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (379 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg44921986 <400>380 cttaaaaaaa tttttttgtt tttttaatac tcagaggagagggacatagg 50 <210>381 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ . . (0) <223>1 2 allelic variants (382 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg44922032 <400>381 acgtggagac catcctgggc ctcacaggag cgaccatgggaagcctcatc t 51 <210>382 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ . . (0) <223>2 2 allelic variants (381 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg44922032 <400>382 acgtggagac catcctgggc ctcacgggag cgaccatgggaagcctcatc t 51 <210>383 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (384 is entry) of other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg44922119 <400>383 cagcccaggc ccagtatgat accccgaaag ctgggaagccaggtctacct g 51 <210> 384 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (383 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44922119 <400> 384 cagcccaggc ccagtatgat accccaaaag ctgggaagcc aggtctacct g 51 <210> 385 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (386 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg44922119 <400> 385 aagcatcgtt ttaaagcaca tggccttttt tttttaatta ttagtggtag 50 <210> 386 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (385 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44922119 <400> 386 aagcatcgtt ttaaagcaca tggccttttt ttttttaatt attagtggta g 51 <210> 387 <211> 51 <212> DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (388 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44922119 <400> 387 tttaaagcac atggcctttt ttttttaatt attagtggta gtaatatata g 51 <210> 388 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (387 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg44922119 <400> 388 tttaaagcac atggcctttt tttttaatta ttagtggtag taatatatag 50 <210> 389 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (390 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44922119 <400> 389 -atgtggtgac tgaggtacag gaaactacta atcttgccat cttgctttaa g 51 <210> 390 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (389 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44922119 <400> 390 atgtggtgac tgaggtacag gaaaccacta atcttgccat cttgctttaa g 51 <210> 391 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (392 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44922173 <400> 391 tggctataaa ttctcaatta tgatacgaac atttatttta caaattctac a 51 <210> 392 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (391 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44922173 <400> 392 tggctataaa ttctcaatta tgatatgaac atttatttta caaattctac a 51 <210> 393 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (394 is other entry) <221> misc feature <222>(0)...(0) <223>Accession number cg44923068 <400>393 ataaaaaccg gcacagcccg tctggcatgt ttgattatgactttgagattg 51 <210>394 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (393 is entry) of other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg44923068 <400>394 ataaaaaccg gcacagcccg tctgggatgt ttgattatgactttgagattg 51 <210>395 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (396 is entry) of other <221>miscfeature <222>(0)_ . . (0) <223>Accession number cg44923491 <400>395 gtaagcagag gtaccaaaga aagtactggg aggtgcagactttgttaaaag 51 <210>396 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (395 is entry) of other <221>miscfeature <222>(0)_ . . (0) <223>Accession number cg44923491 <400>396 gtaagcagag gtaccaaaga aagtattggg aggtgcagactttgttaaaag 51 <210> 397 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (398 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44923661 <400> 397 atcacttagg accatcaaaa aaatgtgtac ctttctccaa acgacaactg a 51 <210> 398 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (397 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44923661 <400> 398 atcacttagg accatcaaaa aaatgcgtac ctttctccaa acgacaactg a 51 <210> 399 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (400 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44923666 <400> 399 attggtagca tgggttcact tggctacaac tgagcaaaat agatgcaact t 51 <210> 400 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (399 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44923666 <400> 400 attggtagca tgggttcact tggctgcaac tgagcaaaat agatgcaact t 51 <210> 401 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (402 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44923675 <400> 401 aagatttgaa gcaattggtg gagtcaacag aatgggaggt tagagaaaga t 51 <210> 402 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (401 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44923675 <400> 402 aagatttgaa gcaattggtg gagtcgacag aatgggaggt tagagaaaga t 51 <210> 403 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (404 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44923675 <400>403 gagattaagt acaaagtgag gaagatggaa gatggttgaatagtgctgaa t 51 <210>404 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (403 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg44923675 <400>404 gagattaagt acaaagtgag gaagacggaa gatggttgaatagtgctgaa t 51 <210>405 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (406 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg44923758 <400>405 acttaaataa cgccatgttt aatactgaca attatttgctaaccttaaga c 51 <210>406 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>2 2 allelic variants (405 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg44923758 <400>406 acttaaataa cgccatgttt aatacagaca attatttgctaaccttaaga c 51 <210> 407 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (408 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44923987 <400> 407 ccactctttg gagaccatta tgatactatg accagagtac aggcaaaagg c 51 <210> 408 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (407 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44923987 <400> 408 ccactctttg gagaccatta tgatattatg accagagtac aggcaaaagg c 51 <210> 409 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (410 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44924189 <400> 409 aggatgcact gagtcagagc taagggaggg tggacaagcg ctgaactctg c 51 <210> 410 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> mist feature <222> (26)...(0) <223> 2 of 2 allelic variants (409 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44924189 <400> 410 aggatgcact gagtcagagc taaggaaggg tggacaagcg ctgaactctg c 51 <210> 411 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (412 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44924398 <400> 411 ctgaggagcc aggagacagg ggaccggcca agggtcaccg gcaatcacat c 51 <210> 412 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (411 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44924398 <400> 412 ctgaggagcc aggagacagg ggacccgcca agggtcaccg gcaatcacat c 51 <210> 413 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (414 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44924398 <400>413 agacagggga ccggccaagg gtcaccggca atcacatccttaaagctgccg 51 <210>414 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>2 2 allelic variants (413 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg44924398 <400>414 agacagggga ccggccaagg gtcacgggca atcacatccttaaagctgccg 51 <210>415 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>1 2 allelic variants (416 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg44924398 <400>415 gacaggggac attcctcctc ctcacgggtg aggacagttatcccaccaggt 51 <210>416 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (415 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg44924398 <400>416 gacaggggac attcctcctc ctcacaggtg aggacagttatcccaccaggt 51 <210>417 <211>51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (418 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44924574 <400> 417 aagacgaact gatccagccc cagctcggag agctctcagg agagaagctt c 51 <210> 418 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (417 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44924574 <400> 418 aagacgaact gatccagccc cagcttggag agctctcagg agagaagctt c 51 <210> 419 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (420 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44924623 <400> 419 gtgctgagat tacaggcatg aaccactgcc cttggacaag gcagggtttt a- 51 <210> 420 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (419 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44924623 <400> 420 gtgctgagat tacaggcatg aaccattgcc cttggacaag gcagggtttt a 51 <210> 421 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (422 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44924630 <400> 421 gcttttgggt gaagggtgat ttctactaga cacatctgtg cttcagtcat a 51 <210> 422 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (421 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44924630 <400> 422 gcttttgggt gaagggtgat ttctattaga cacatctgtg cttcagtcat a 51 <210> 423 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (424 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44924824 <400>423 ggggaggctg gagagtctgg gtggataccc tctcaatagcccattccaagg 51 <210>424 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (423 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg44924824 <400>424 ggggaggctg gagagtctgg gtggacaccc tctcaatagcccattccaagg 51 <210>425 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (426 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg44924824 <400>425 ccctctcaat agcccattcc aaggtcactt atgaagctcataaggaatacc 51 <210>426 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (425 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg44924824 <400>426 ccctctcaat agcccattcc aaggttactt atgaagctcataaggaatacc 51 <210>427 <211>51 <212>DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (428 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44924824 <400> 427 cccattccaa ggtcacttat gaagctcata aggaatacct agccaaaatg t 51 <210> 428 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (427 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44924824 <400> 428 cccattccaa ggtcacttat gaagcacata aggaatacct agccaaaatg t 51 <210> 429 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (430 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44924824 <400> 429 cttatgaagc tcataaggaa tacctagcca aaatgtatga ggaatatcaa a 51 <210> 430 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (429 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44924824 <400> 430 cttatgaagc tcataaggaa tacctggcca aaatgtatga ggaatatcaa a 51 <210> 431 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (432 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44924824 <400> 431 ggaatgtgag caccatctct ggtctttcat cacagacaac aggagcaaaa g 51 <210> 432 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (431 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44924824 <400> 432 ggaatgtgag caccatctct ggtctctcat cacagacaac aggagcaaaa g 51 <210> 433 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (434 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44924961 <400> 433 aactcctggc ctcaagctat cctcccgcct cagcctccca aagtgctgag a 51 <210> 434 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (433 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44924961 <400> 434 aactcctggc ctcaagctat cctcctgcct cagcctccca aagtgctgag a 51 <210> 435 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (436 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44925079 <400> 435 cttgggctcc cccttcatgg cctctgcacc tccacactcc caaccactga c 51 <210> 436 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (435 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44925079 <400> 436 cttgggctcc cccttcatgg cctctacacc tccacactcc caaccactga c 51 <210> 437 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (438 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44925235 <400> 437 tcgtgttaaa ctgatgtggc agtaaaccaa gggactaagc acatgattat t 51 <210> 438 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (437 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44925235 <400> 438 tcgtgttaaa ctgatgtggc agtaatccaa gggactaagc acatgattat t 51 <210> 439 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (440 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44925358 <400> 439 cggaactcgc tatatgcacg tgtgtgtgtc cgtatgtaag aaagtgtgca c 51 <210> 440 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (439 is other entry) <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg44925358 <400>440 cggaactcgc tatatgcacg tgtgtatgtc cgtatgtaagaaagtgtgca c 51 <210>441 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (442 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg44925402 <400>441 acagaagatg ctaggtttgc acgctgatga gatcctggctaacactgctg c 51 <210>442 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (441 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg44925402 <400>442 acagaagatg ctaggtttgc acgctaatga gatcctggctaacactgctg c 51 <210>443 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ . . (0) <223>1 2 allelic variants (444 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg44925402 <400>443 ttcaagactt cgagttagac agaaacccag ggggctgcggctctggtggt t 51 <210> 444 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (443 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44925402 <400> 444 ttcaagactt cgagttagac agaaatccag ggggctgcgg ctctggtggt t 51 <210> 445 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (446 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44925406 <400> 445 aaagagccaa ggcgctggac cagtccgaca acgatatgtc cgccgtgtac c 51 <210> 446 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (445 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44925406 <400> 446 aaagagccaa ggcgctggac cagtctgaca acgatatgtc cgccgtgtac c 51 <210> 447 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (448 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44925534 <400> 447 cttctataac ttacttgcca ctgccttttt tttttgatag aatcttgctc t 51 <210> 448 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (447 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg44925534 <400> 448 cttctataac ttacttgcca ctgccttttt ttttgataga atcttgctct 50 <210> 449 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (450 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44925534 <400> 449 ttgccactgc cttttttttt tgatagaatc ttgctctgtc gcccagggtg g 51 <210> 450 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> mist feature <222> (26) . . . (0) <223> 2 of 2 allelic variants (449 is other entry) <221> misc_feature <222> (0). .(0) ' <223> Accession number cg44925534 <400> 450 ttgccactgc cttttttttt tgataaaatc ttgctctgtc gcccagggtg g 51 <210> 451 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (452 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44925849 <400> 451 gaatgccact tggatgacag ttctccctaa gacccccttt tcagcatggt t 51 <210> 452 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (451 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44925849 <400> 452 gaatgccact tggatgacag ttctctctaa gacccccttt tcagcatggt t 51 <210> 453 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (454 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44925849 <400> 453 gctggtgtcc tcctttggga tactctcacc ccttggttcc tcagatgaaa g 51 <210> 454 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (453 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44925849 <400> 454 gctggtgtcc tcctttggga tactcccacc ccttggttcc tcagatgaaa g 51 <210> 455 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (456 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg44926335 <400> 455 cacacacaca cacacacaca cacaccctta cacgaatggt aatgaaatga 50 <210> 456 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (455 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44926335 <400> 456 cacacacaca cacacacaca cacacacctt acacgaatgg taatgaaatg a 51 <210> 457 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (458 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44927187 <400> 457 ggctgggggg ctaagaagga gatcttgaga aggatggacc tgagctaaag a 51 <210> 458 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (457 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44927187 <400> 458 ggctgggggg ctaagaagga gatctcgaga aggatggacc tgagctaaag a 51 <210> 459 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (460 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44927553 <400> 459 actacaggca tgcaccacca cacccagcta atttttgtat ttttagtaga g 51 <210> 460 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (459 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44927553 <400> 460 actacaggca tgcaccacca cacccggcta atttttgtat ttttagtaga g 51 <210> 461 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (462 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44927553 <400> 461 cacccagcta atttttgtat ttttagtaga gacggggttt catcatgttg g 51 <210> 462 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (461 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44927553 <400> 462 cacccagcta atttttgtat ttttaataga gacggggttt catcatgttg g 51 <210> 463 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (464 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44927553 <400> 463 acccagctaa tttttgtatt tttagtagag acggggtttc atcatgttgg c 51 <210> 464 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (463 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg44927553 <400> 464 acccagctaa tttttgtatt tttagagaga cggggtttca tcatgttggc 50 <210> 465 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (466 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44927553 <400> 465 acggggtttc atcatgttgg ccaggctggt ctcaaactcc tgacctcatg a 51 <210> 466 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (465 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44927553 <400> 466 acggggtttc atcatgttgg ccaggttggt ctcaaactcc tgacctcatg a 51 <210> 467 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (468 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44928037 <400> 467 aaaaaagaaa agaaaagcaa aaaagaaaaa aaaaaggatt gggtgggggg a 51 <210> 468 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (467 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg44928037 <400> 468 aaaaaagaaa agaaaagcaa aaaagaaaaa aaaaggattg ggtgggggga 50 <210> 469 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (470 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44928037 <400> 469 aagaaaagca aaaaagaaaa aaaaaaggat tgggtggggg gaaggaggtg g 51 <210> 470 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (469 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg44928037 <400> 470 aagaaaagca aaaaagaaaa aaaaaggatt gggtgggggg aaggaggtgg 50 <210> 471 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) ' <223> 1 of 2 allelic variants (472 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44928037 <400> 471 tagatttcaa agatgaacct ggctctccat cactgagcca gacattcatt c 51 <210> 472 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (471 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44928037 <400> 472 tagatttcaa agatgaacct ggctccccat cactgagcca gacattcatt c 51 <210> 473 <211> 51 <212> DNA
<213>~ Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (474 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44928115 <400> 473 catggtgact caagcctgta atcccagcac tttgggaggc cgaggcgggc g 51 <210> 474 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (473 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44928115 <400> 474 catggtgact caagcctgta atcccggcac tttgggaggc cgaggcgggc g 51 <210> 475 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (476 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44928274 <400> 475 tgcagtgcac acgtggtatg catgtccggc attgatcaag tccatctggg.cl 51 <210> 476 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (475 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44928274 <400> 476 tgcagtgcac acgtggtatg catgttcggc attgatcaag tccatctggg c 51 <210> 477 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (478 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44928274 <400> 477 gtccggcatt gatcaagtcc atctgggcta tggccataag ccaacaccag t 51 <210> 478 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (477 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44928274 <400> 478 gtccggcatt gatcaagtcc atctgagcta tggccataag ccaacaccag t 51 <210> 479 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (480 is other entry) <221> misc feature <222>(0)...(0) <223>Accession number cg44928274 <400>479 gcagagtaag tccaaaatcc atgcagcacg cagcctgagtgagatcgcca t 51 <210>480 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (479 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg44928274 <400>480 gcagagtaag tccaaaatcc atgcaacacg cagcctgagtgagatcgcca t 51 <210>481 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (482 is entry) of other <221>misc_feature <222>(0)...(0) <223>Accession number cg44928274 <400>481 agacctcgaa gctggccaac atgggtagca aggggaagatcatcagcggc a 51 <210>482 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (481 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg44928274 <400>482 agacctcgaa gctggccaac atgggcagca aggggaagatcatcagcggc a 51 <210> 483 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (484 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44928274 <400> 483 aagatcatca gcggcagcag cggcagcctg ctgtcttcag gttctcagga a 51 <210> 484 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (483 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg44928274 <400> 484 aagatcatca gcggcagcag cggcacctgc tgtcttcagg ttctcaggaa 50 <210> 485 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (486 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature' <222> (0) . . (0) <223> Accession number cg44928329 <400> 485 ttaagaagtg taaaaaacaa caacgaaaaa aaaccccaaa tcatggagaa 50 <210> 486 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (485 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44928329 <400> 486 ttaagaagtg taaaaaacaa caacgaaaaa aaaaccccaa atcatggaga a 51 <210> 487 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (488 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44928356 <400> 487 ccccaacgtg tacaagaaat ccaggaggaa aggccgtcaa ggtaaaaaat g 51 <210> 488 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (487 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44928356 <400> 488 ccccaacgtg tacaagaaat ccagggggaa aggccgtcaa ggtaaaaaat g 51 <210> 489 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (490 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44928356 <400> 489 caacgtgtac aagaaatcca ggaggaaagg ccgtcaaggt aaaaaatgga a 51 <210> 490 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (489 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44928356 <400> 490 caacgtgtac aagaaatcca ggagggaagg ccgtcaaggt aaaaaatgga a 51 <210> 491 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (492 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44928356 <400> 491 gtcaaggtaa aaaatggaaa ttccctctgt tccaacgctg attgagtctg t 51 <210> 492 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (491 is other entry) <221>miscfeature <222>_ (0).
.(0) <223>Accession number cg44928356 <400>492 gtcaaggtaa aaaatggaaa ttcccgctgt tccaacgctgattgagtctgt 51 <210>493 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>1 2 allelic variants (494 is entry) of other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg44928356 <400>493 atggaaattc cctctgttcc aacgctgatt gagtctgttgtcttaaaagag 51 <210>494 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>2 2 allelic variants (493 is entry) of other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg44928356 <400>494 atggaaattc cctctgttcc aacgccgatt gagtctgttgtcttaaaagag 51 <210>495 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (496 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg44928356 <400>495 gaaattccct ctgttccaac gctgattgag tctgttgtcttaaaagagctt 51 <210> 496 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (495 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44928356 <400> 496 gaaattccct ctgttccaac gctgactgag tctgttgtct taaaagagct t 51 <210> 497 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (498 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44928356 <400> 497 gttccaacgc tgattgagtc tgttgtctta aaagagcttt aaagggcccc c 51 <210> 498 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (497 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44928356 <400> 498 gttccaacgc tgattgagtc tgttgcctta aaagagcttt aaagggcccc c 51 <210> 499 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (500 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44928356 <400> 499 ctgattgagt ctgttgtctt aaaagagctt taaagggccc cccttctttt c 51 <210> 500 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (499 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44928356 <400> 500 ctgattgagt ctgttgtctt aaaagggctt taaagggccc cccttctttt c 51 <210> 501 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (502 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44928356 <400> 501 agggcccccc ttcttttcca gcactaccac tgcccattcc agtcttgggt g 51 <210> 502 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (501 is other entry) <221> misc feature <222> (0)...(0) <223> Accession number cg44928356 <400> 502 agggcccccc ttcttttcca gcactcccac tgcccattcc agtcttgggt g 51 <210> 503 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (504 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44928665 <400> 503 caaagccaaa cttgcaccaa aaaaaaggtc atggtcactg ttcggtggtc t 51 <210> 504 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (503 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg44928665 <400> 504 caaagccaaa cttgcaccaa aaaaaggtca tggtcactgt tcggtggtct 50 <210> 505 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (506 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44928771 <400> 505 agctggccag gcacttaatt tggggaaaga gaaggatttt gaggtaaact a 51 <210> 506 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (505 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44928771 <400> 506 agctggccag gcacttaatt tgggggaaga gaaggatttt gaggtaaact a 51 <210> 507 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (508 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44929331 <400> 507 gatgacagca actataaagg agagaagttt tcgttgaagt acactggaaa t 51 <210> 508 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (507 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44929331 <400> 508 gatgacagca actataaagg agagaggttt tcgttgaagt acactggaaa t 51 <210> 509 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (510 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44930314 <400> 509 tgggcgtgtc ggtggtgacg caccctgggg gctgccgggg ccatgaggtg g 51 <210> 510 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ...(0) <223> 2 of 2 allelic variants (509 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44930314 <400> 510 tgggcgtgtc ggtggtgacg caccccgggg gctgccgggg ccatgaggtg g 51 <210> 511 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (512 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44930892 <400> 511 gtgtacatat tccttgcatt ttttttagtt gttgtcttaa aaaaaaaaaa a 51 <210> 512 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (511 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg44930892 <400> 512 gtgtacatat tccttgcatt tttttagttg ttgtcttaaa aaaaaaaaaa 50 <210> 513 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (514 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44931317 <400> 513 aaaagtttag tagagacatg gaagacgtaa aggggacccc aagcaagcct c 51 <210> 514 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (513 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44931317 <400> 514 aaaagtttag tagagacatg gaagatgtaa aggggacccc aagcaagcct c 51 <210> 515 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (516 is other entry) <221>miscfeature <222>(0)._ .(0) <223>Accession number cg44931528 <400>515 tctaccagct gctcatagtc ctcatcatag gtaacatagggaatctggaag 51 <210>516 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (515 is entry) of other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg44931528 <400>516 tctaccagct gctcatagtc ctcatgatag gtaacatagggaatctggaag 51 <210>517 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (518 is entry) of other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg44932156 <400>517 gcgcggcagc ccccaggtcc cggggggcct cgtcacaggctgtaggccgtg 51 <210>518 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (517 is entry) of other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg44932156 <400>518 gcgcggcagc ccccaggtcc cggggcgcct cgtcacaggctgtaggccgtg 51 <210> 519 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (520 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44932430 <400> 519 atgtcacatt aaaagtgcat catcgacact caatagagat taggttttac c 51 <210> 520 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (519 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44932430 <400> 520 atgtcacatt aaaagtgcat catcggcact caatagagat taggttttac c 51 <210> 521 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (522 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44932430 <400> 521 attcttggca gatgctgcag ataacgtgga gagcatacga aaggcacatg t 51 <210> 522 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (521 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44932430 <400> 522 attcttggca gatgctgcag ataacatgga gagcatacga aaggcacatg t 51 <210> 523 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (524 is other entry) <223> misc_feature <222> (0) . . (0) <223> Accession number cg44932430 <400> 523 agataacgtg gagagcatac gaaaggcaca tgtttgaacc aatagtgaca t 51 <210> 524 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (523 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44932430 <400> 524 agataacgtg gagagcatac gaaagacaca tgtttgaacc aatagtgaca t 51 <210> 525 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (526 is other entry) <221> misc feature <222> (0)...(0) <223> Accession number cg44932430 <400> 525 taacgtggag agcatacgaa aggcacatgt ttgaaccaat agtgacatac a 51 <210> 526 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (525 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44932430 <400> 526 taacgtggag agcatacgaa aggcatatgt ttgaaccaat agtgacatac a 51 <210> 527 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (528 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44932430 <400> 527 gagagcatac gaaaggcaca tgtttgaacc aatagtgaca tacaggtgct a 51 <210> 528 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (527 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44932430 <400> 528 gagagcatac gaaaggcaca tgttttaacc aatagtgaca tacaggtgct a 51 <210> 529 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (530 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44932430 <400> 529 cgaaaggcac atgtttgaac caatagtgac atacaggtgc taagttctgc a 51 <210> 530 .
<211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (529 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44932430 <400> 530 cgaaaggcac atgtttgaac caatactgac atacaggtgc taagttctgc a 51 <210> 531 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (532 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44932430 <400> 531 atgtttgaac caatagtgac atacaggtgc taagttctgc agtaggggaa g 51 <210> 532 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (531 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44932430 <400> 532 atgtttgaac caatagtgac atacaagtgc taagttctgc agtaggggaa g 51 <210> 533 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (534 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44932430 <400> 533 tgtttgaacc aatagtgaca tacaggtgct aagttctgca gtaggggaag g 51 <210> 534 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (533 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44932430 <400> 534 tgtttgaacc aatagtgaca tacagatgct aagttctgca gtaggggaag g 51 <210> 535 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (536 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44932430 <400> 535 tgacatacag gtgctaagtt.ctgcagtagg ggaagggcag agagccatgg a 51 <210> 536 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (535 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44932430 <400> 536 tgacatacag gtgctaagtt ctgcattagg ggaagggcag agagccatgg a 51 <210> 537 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (538 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44932430 <400> 537 agcctcagaa aaaagttccc gttgaattgc tgttttagct gagacttgtg g 51 <210> 538 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (537 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44932430 <400> 538 agcctcagaa aaaagttccc gttgatttgc tgttttagct gagacttgtg g 51 <210> 539 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (540 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44932430 <400> 539 ggtagtagtt ggagatccca gacaggaggt gaccgagtta gccagggaaa a 51 <210> 540 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (539 is other entry) <221> misc_feature <222> (0) . . (0) , <223> Accession number cg44932430 <400> 540 ggtagtagtt ggagatccca gacagcaggt gaccgagtta gccagggaaa a 51 <210> 541 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (542 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44932430 <400> 541 tcctggcacc catggcagag ttgagtgatc cagtctttct gtctcctctg g 51 <210> 542 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26)...(0) <223> 2 of 2 allelic variants (541 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44932430 <400> 542 tcctggcacc catggcagag ttgagcgatc cagtctttct gtctcctctg g 51 <210> 543 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (544 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44932430 <400> 543 cagatctggg aatgtccagt tgggggaggg ggctgacaat gatcatgacc t 51 <210> 544 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (543 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44932430 <400> 544 cagatctggg aatgtccagt tggggaaggg ggctgacaat gatcatgacc t 51 <210> 545 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (546 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44932719 <400> 545 taggccttgt tcctcttcca gggaaaaaaa gccaaatcct tatcaaggaa a 51 <210> 546 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (545 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44932719 <400> 546 taggccttgt tcctcttcca gggaagaaaa gccaaatcct tatcaaggaa a 51 <210> 547 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (548 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44938377 <400> 547 tcaaaatgtc aaaagactca gagccggggg gcaccagtgc agtgactgcg g 51 <210> 548 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (547 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44938377 <400> 548 tcaaaatgtc aaaagactca gagccagggg gcaccagtgc agtgactgcg g 51 <210> 549 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (550 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44938377 <400> 549 actcagagcc ggggggcacc agtgcagtga ctgcggattc atgggaaatg a 51 <210> 550 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (549 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44938377 <400> 550 actcagagcc ggggggcacc agtgcggtga ctgcggattc atgggaaatg a 51 <210> 551 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (552 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44938828 <400> 551 cacctcctgg tgagtaaatg tgtaaacgcg tgaagggtca gggatgtgtt t 51 <210> 552 <211> 51 <212> DNA ' <213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (551 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44938828 <400> 552 cacctcctgg tgagtaaatg tgtaagcgcg tgaagggtca gggatgtgtt t 51 <210> 553 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (554 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44938869 <400> 553 taatttggtg taataaaaat gatgcaaaaa aaaaaaaaat cagggttgtt t 51 <210> 554 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (553 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg44938869 <400> 554 taatttggtg taataaaaat gatgcaaaaa aaaaaaaatc agggttgttt 50 <210> 555 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (556 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44938869 <400> 555 ataaaaatga tgcaaaaaaa aaaaaaatca gggttgtttg acaccttttt t 51 <210> 556 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (555 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg44938869 <400> 556 ataaaaatga tgcaaaaaaa aaaaaatcag ggttgtttga cacctttttt 50 <210> 557 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (558 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44938869 <400> 557 taaaaatgat gcaaaaaaaa aaaaaatcag ggttgtttga cacctttttt c 51 <210> 558 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (557 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg44938869 <400> 558 taaaaatgat gcaaaaaaaa aaaaatcagg gttgtttgac accttttttc 50 <210> 559 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (560 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44938869 <400> 559 aaaccttcac caaaagggga taaaagattt aaaggcaaaa tgagtaaaca a 51 <210> 560 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (559 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44938869 <400> 560 aaaccttcac caaaagggga taaaaaattt aaaggcaaaa tgagtaaaca a 51 <210> 561 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (562 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44939935 <400>561 acagtgtggc ctcacaggta tggcagcgga agcagctccggtggaagaaat 51 <210>562 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>2 2 allelic variants (561 is entry) of other <221>miscfeature <222>(0)_ . . (0) <223>Accession number cg44939935 <400>562 acagtgtggc ctcacaggta tggcaacgga agcagctccggtggaagaaat 51 <210>563 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (564 is entry) of other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg44939935 <400>563 cccacaaagt gcacacaggt ccccagcacc ggcctcctggtgttgggatgg 51 <210>564 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (563 is entry) of other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg44939935 <400>564 cccacaaagt gcacacaggt ccccaacacc ggcctcctggtgttgggatgg 51 <210>565 <211>44 <212>DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (19) ..(0) <223> 1 of 2 allelic variants (566 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44939948 <400> 565 ntgcagcgga ggagagaggg ggggccaccg tggggcggtc gcac 44 <210> 566 <211> 44 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (19) ..(0) <223> 2 of 2 allelic variants (565 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44939948 <400> 566 ntgcagcgga ggagagagtg ggggccaccg tggggcggtc gcac 44 <210> 567 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (568 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44963511 <400> 567 tgtgtcttta ggctgaggca gtgcccatag ctgcagtgcc tcgagtttcc g 51 <210> 568 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (567 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg44963511 <400> 568 tgtgtcttta ggctgaggca gtgccatagc tgcagtgcct cgagtttccg 50 <210> 569 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (570 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44963787 <400> 569 tggtaagggg atttttgtat aagtcaatta gttgttgaat cattttctca t 51 <210> 570 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (569 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg44963787 <400> 570 tggtaagggg atttttgtat aagtcattag ttgttgaatc attttctcat 50 <210> 571 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26) . . . (0) <223> 1 of 2 allelic variants (572 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44963787 <400> 571 caggattcta tgaattaatt tttaagtagc ttagtatcat tcaatagtat t 51 <210> 572 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (571 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44963787 <400> 572 caggattcta tgaattaatt tttaactagc ttagtatcat tcaatagtat t 51 <210> 573 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (574 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44963787 <400> 573 aataccaggt tacttatact acctattcat gtatgacatt tgtgttagta t 51 <210> 574 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (573 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44963787 <400> 574 aataccaggt tacttatact acctactcat gtatgacatt tgtgttagta t 51 <210> 575 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (576 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44963787 <400> 575 tcatcaaagg ggctatgagc tagacctgca gattaacacg cagatgtggc c 51 <210> 576 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (575 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg44963787 <400> 576 tcatcaaagg ggctatgagc tagactgcag attaacacgc agatgtggcc 50 <210> 577 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (578 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44963787 <400> 577 cacgcagatg tggccttaaa aaaaaatcag ttaatctggg atccagagaa g 51 <210> 578 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (577 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg44963787 <400> 578 cacgcagatg tggccttaaa aaaaatcagt taatctggga tccagagaag 50 <210> 579 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (580 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44964193 <400> 579 ccttagcctt ccataatgga gaagtcgggc aggggatgtc tgcatgcaat a 51 <210> 580 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (579 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44964193 <400> 580 ccttagcctt ccataatgga gaagttgggc aggggatgtc tgcatgcaat a 51 <210> 581 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (582 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44964193 <400> 581 gggcagggga tgtctgcatg caatagacaa ctgaattaga aagagcagaa a 51 <210> 582 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (581 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44964193 <400> 582 gggcagggga tgtctgcatg caataaacaa ctgaattaga aagagcagaa a 51 <210> 583 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (584 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44964193 <400> 583 ttagaaagag cagaaatgta aaccagcagt gcttccctat cttgggcctg g 51 <210> 584 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (583 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44964193 <400> 584 ttagaaagag cagaaatgta aaccaacagt gcttccctat cttgggcctg g 51 <210> 585 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (586 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44965051 <400> 585 tgtcccaaca tttactggct ttgggtccag tggcacagat gcagcatcag a 51 <210> 586 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (585 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44965051 <400> 586 tgtcccaaca tttactggct ttgggcccag tggcacagat gcagcatcag a 51 <210> 587 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (588 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44965051 <400>

tgggtccagtggcacagatg cagcatcaga accctccctcccatcctcaa g 51 <210>

<211>

<212>
DNA

<213> Sapiens Homo <220>

<221> feature misc <222> _ (26) .. (0) <223> 2 allelic variants (587 is entry) 2 of other <221> feature misc <222> _ (0) . (0) .

<223>
Accession number cg44965051 <400>

tgggtccagtggcacagatg cagcagcaga accctccctcccatcctcaa g 51 <210>

<211>

<212>
DNA

<213> Sapiens Homo <220>

<221> feature misc <222> _ (26) ..(0) <223> 2 allelic variants (590 is entry) 1 of other <221> feature misc <222> _ (0) . (0) .

<223> ssion number cg44965597 Acce <400>

cctgaccttaacctatatac tgatggaagt tcatttgtggagaatgggat a 51 <210>

<211>

<212>
DNA

<213> Sapiens Homo <220>

<221> feature misc <222> _ (26) ..(0) <223> 2 allelic variants (589 is entry) 2 of other <221> feature misc <222> _ (0) . (0) .

<223> ssion number cg44965597 Acce <400>

cctgaccttaacctatatac tgatgaaagt tcatttgtggagaatgggat a 51 <210> 591 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (592 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44965597 <400> 591 ggatacaaag ggcaggttat gccatagtta gtgatgtaac catacttgaa a 51 <210> 592 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (591 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44965597 <400> 592 ggatacaaag ggcaggttat gccatggtta gtgatgtaac catacttgaa a 51 <210> 593 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (594 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg44965597 <400> 593 ccccagggac cagtgcccag ttagcggaac tagtggcact tacccgagcc t 51 <210> 594 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26) . . . (0) <223> 2 of 2 allelic variants (593 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg44965597 <400> 594 ccccagggac cagtgcccag ttagcagaac tagtggcact tacccgagcc t 51 <210> 595 <211> 45 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (20) ..(0) <223> 1 of 2 allelic variants (596 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg5621185 <400> 595 tcctaggatt gctagcgcag caaacgccat tgtttgagag cttgt 45 <210> 596 <211> 44 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (20) ..(0) <223> 2 of 2 allelic variants (595 is other entry) <221> misc_feature <222> (19) ..(20) <223> Nucleotide deleted between bases 19 and 20 <221> misc_feature <222> (0) . . (0) <223> Accession number cg5621185 <400> 596 tcctaggatt gctagcgcac aaacgccatt gtttgagagc ttgt 44 <210> 597 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (598 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg5738781 <400> 597 aatagaaagg tatgagtctc aggacgggtt ctctgcaaag cagccatcgg c 51 <210> 598 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (597 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg5738781 <400> 598 aatagaaagg tatgagtctc aggactggtt ctctgcaaag cagccatcgg c 51 <210> 599 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (600 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg6370826 <400> 599 gttctcttct tttgtctttt ttttttcttt agagacgggg tctagctatg t 51 <210> 600 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (599 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc feature <222> (0)...(0) <223> Accession number cg6370826 <400> 600 gttctcttct tttgtctttt tttttcttta gagacggggt ctagctatgt 50 <210> 601 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (602 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg6586279 <400> 601 gcgggaatgt gactgagggg cagggcccag cggctccctg cagccatcag g 51 <210> 602 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (601 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg6586279 <400> 602 gcgggaatgt gactgagggg cagggccagc ggctccctgc agccatcagg 50 <210> 603 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (604 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg8754307 <400> 603 ttgtatgcta gggctttcaa ggggccttcg gagtggctgt tgattgtagc a 51 <210> 604 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (603 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg8754307 <400> 604 ttgtatgcta gggctttcaa ggggcttcgg agtggctgtt gattgtagca 50 <210> 605 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (606 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg9886159 <400> 605 aaaacatggt atatctcgat ttatcacata aagatccaca tgaattagac g 51 <210> 606 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (605 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg9886159 <400> 606 aaaacatggt atatctcgat ttatctcata aagatccaca tgaattagac g 51 <210> 607 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (608 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg9886159 <400> 607 ataaagatcc acatgaatta gacgtaaaac taggtggtat cattgaaatc t 51 <210> 608 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (607 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg9886159 <400> 608 ataaagatcc acatgaatta gacgttaaac taggtggtat cattgaaatc t 51 <210> 609 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (610 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20595730 <400> 609 aaattgaaca gagagccaaa taaacatgag aaactttatt tctccaaaga c 51 <210> 610 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (609 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20595730 <400> 610 aaattgaaca gagagccaaa taaacctgag aaactttatt tctccaaaga c 51 <210> 611 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (612 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20611295 <400> 611 agcaaggtgg acctggtgcc tgggcacacc atgccatgct ctggagccct g 51 <210> 612 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (611 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg20611295 <400> 612 agcaaggtgg acctggtgcc tgggccacca tgccatgctc tggagccctg 50 <210> 613 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (614 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20614578 <400> 613 attctctggg ttggagcgtg atggcgtcat ctatggttgg ggcacactgg a 51 <210> 614 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (613 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg20614578 <400> 614 attctctggg ttggagcgtg atggcatcat ctatggttgg ggcacactgg a 51 <210> 615 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (616 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20614578 <400> 615 ggagcgtgat ggcgtcatct atggttgggg cacactggac gacaagaact c 51 <210> 616 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (615 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20614578 <400> 616 ggagcgtgat ggcgtcatct atggtcgggg cacactggac gacaagaact c 51 <210> 617 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (618 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20615101 <400> 617 attattaatt tgtaatcatt ttaacagcct ttcttccact gtaaaaaggg t 51 <210> 618 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (617 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20615101 <400> 618 attattaatt tgtaatcatt ttaacggcct ttcttccact gtaaaaaggg t 51 <210> 619 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (620 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20622181 <400> 619 ccatcttgat gaagagcgga cgtaccgcga acaccacggc gacagccagg a 51 <210> 620 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (619 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20622181 <400> 620 ccatcttgat gaagagcgga cgtacagcga acaccacggc gacagccagg a 51 <210> 621 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (622 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20627797 <400> 621 ccttcgttaa aactgtcagt gtgggggata ccatcggcta cggcagaaca t 51 <210> 622 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (621 is other entry) i <221> misc_feature <222> (0) . . (0) <223> Accession number cg20627797 <400> 622 ccttcgttaa aactgtcagt gtgggtgata ccatcggcta cggcagaaca t 51 <210> 623 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26)...(0) <223> 1 of 2 allelic variants (624 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20627797 <400> 623 ccatcggcta cggcagaaca tggacagcca gcgaaacgac aaaaatcgcc a 51 <210> 624 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (623 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20627797 <400> 624 ccatcggcta cggcagaaca tggaccgcca gcgaaacgac aaaaatcgcc a 51 <210> 625 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (626 is other entry) <221> misc_feature _ <222> (0) . . (0) <223> Accession number cg20628068 <400> 625 ttcgcatggc ttcgtgggcg atttcagtgg catcggactt cgatgtgccc t 51 <210> 626 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (625 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20628068 <400>626 ttcgcatggc ttcgtgggcg atttcggtgg catcggacttcgatgtgccc t 51 <210>627 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>1 2 allelic variants (628 entry) of is other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg20628068 <400>627 gggcgatttc agtggcatcg gacttcgatg tgccctgcgcccacaggggt a 51 <210>628 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (627 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg20628068 <400>628 gggcgatttc agtggcatcg gactttgatg tgccctgcgcccacaggggt a 51 <210>629 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>1 2 allelic variants (630 entry) of is other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg20628068 <400>629 aatattctcg gtattggtca actcagcgat gaggttgtcgtcctggaaga t 51 <210>630 <211>51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (629 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20628068 <400> 630 aatattctcg gtattggtca actcaacgat gaggttgtcg tcctggaaga t 51 <210> 631 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (632 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg20628068 <400> 631 tggccacccg agacctcgcc ggggtggcgt ctgcccaatg actcgattcc t 51 <210> 632 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (631 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20628068 <400> 632 tggccacccg agacctcgcc ggggtagcgt ctgcccaatg actcgattcc t 51 <210> 633 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (634 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20631839 <400> 633 aggtggaagc caggatggag ggcaggcctc gccttctgtc cgggatccgc c 51 <210> 634 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (633 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20631839 <400> 634 aggtggaagc caggatggag ggcagccctc gccttctgtc cgggatccgc c 51 <210> 635 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (636 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20635329 <400> 635 gtgttacatc aaatgcagtt tgttcttttt acgttgctgt gttgtatttc c 51 <210> 636 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (635 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20635329 <400> 636 gtgttacatc aaatgcagtt tgttcctttt acgttgctgt gttgtatttc c 51 <210> 637 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (638 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20635664 <400> 637 ctagtggtgc agttttgtgt gtgtgtggac gtgctggccc agtggtgcag g 51 <210> 638 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (637 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg20635664 <400> 638 ctagtggtgc agttttgtgt gtgtgggacg tgctggccca gtggtgcagg 50 <210> 639 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (640 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20636603 <400> 639 gctgtaggca caatccatgg cttttcactt gaagccaatg tggcctctga a 51 <210> 640 <211> 51 <212> DNA
c213> Homo sapiens c220>
<221> misc_feature <222> (26) ..(0) c223> 2 of 2 allelic variants (639 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20636603 <400> 640 gctgtaggca caatccatgg ctttttactt gaagccaatg tggcctctga a 51 c210> 641 c211> 51 c212> DNA
c213> Homo sapiens c220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (642 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20638203 <400> 641 cgcatagtac gtgtggggcg gtggccagct catcagcagg gagcgcggct c 51 <210> 642 c211> 50 c212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (641 is other entry) c221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) c223> Accession number cg20638203 <400> 642 cgcatagtac gtgtggggcg gtggcagctc atcagcaggg agcgcggctc 50 <210> 643 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (644 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20705188 <400> 643 tcccctcttg aatctcaagg cctggcctgt ttgggggcct gtttgggctt c 51 <210> 644 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (643 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg20705188 <400> 644 tcccctcttg aatctcaagg cctggctgtt tgggggcctg tttgggcttc 50 <210> 645 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (646 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20705880 <400> 645 ccggcccggc tatcaaccag ggaggttcat tcctgtctat cccggccggc g 51 <210> 646 <211> 51 <212> DNA

<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (645 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20705880 <400> 646 ccggcccggc tatcaaccag ggaggctcat tcctgtctat cccggccggc g 51 <210> 647 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (648 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20709811 <400> 647 agtggagtga tctcaactca ctgcagcctc tacctcctgg tctcaagcag t 51 <210> 648 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (647 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20709811 <400> 648 agtggagtga tctcaactca ctgcaacctc tacctcctgg tctcaagcag t 51 <210> 649 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (650 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20710663 <400> 649 caaaaaccag tgcggagacg actaccgacg tccagcaccc ggctttttcc g 51 <210> 650 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (649 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20710663 <400> 650 caaaaaccag tgcggagacg actactgacg tccagcaccc ggctttttcc g 51 <210> 651 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (652 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20719026 <400> 651 cgtgttcttc ccaaagcggc gggagctcca gatccatgac gaggaggtcc t 51.
<210> 652 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (651 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc feature <222> (0)...(0) <223> Accession number cg20719026 <400> 652 cgtgttcttc ccaaagcggc gggagtccag atccatgacg aggaggtcct 50 <210> 653 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (654 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20721343 <400> 653 gcccgcaacg tgttaggtcg ttggtatttg tgacttgtgc tcggcgcgag c 51 <210> 654 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (653 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20721343 <400> 654 gcccgcaacg tgttaggtcg ttggtgtttg tgacttgtgc tcggcgcgag c 51 <210> 655 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (656 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20721343 <400> 655 acgtgttagg tcgttggtat ttgtgacttg tgctcggcgc gagcaaacct c 51 <210> 656 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (655 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20721343 <400> 656 acgtgttagg tcgttggtat ttgtggcttg tgctcggcgc gagcaaacct c 51 <210> 657 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (658 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20721343 <400> 657 aggtcgttgg tatttgtgac ttgtgctcgg cgcgagcaaa cctcctgcca g 51 <210> 658 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (657 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20721343 <400> 658 aggtcgttgg tatttgtgac ttgtgttcgg cgcgagcaaa cctcctgcca g 51 <210> 659 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (660 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg20721343 <400> 659 ggtatttgtg acttgtgctc ggcgcgagca aacctcctgc caggatgacg t 51 <210> 660 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (659 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20721343 <400> 660 ggtatttgtg acttgtgctc ggcgcaagca aacctcctgc caggatgacg t 51 <210> 661 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (662 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20721343 <400> 661 tatttgtgac ttgtgctcgg cgcgagcaaa cctcctgcca ggatgacgtg c 51 <210> 662 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (661 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg20721343 <400> 662 tatttgtgac ttgtgctcgg cgcgacaaac ctcctgccag gatgacgtgc 50 <210> 663 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (664 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg20721343 <400> 663 ggatgacgtg ctcagcacca acacttctca cggtcgtcac cagctccgat g 51 <210> 664 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (663 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg20721343 <400> 664 ggatgacgtg ctcagcacca acactcctca cggtcgtcac cagctccgat g 51 <210> 665 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (666 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg20723457 <400>665 ctttgaaaat cacacacaac ccatccgggt tttctgctatggaaaggctc t 51 <210>666 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>2 2 allelic variants (665 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg20723457 <400>666 ctttgaaaat cacacacaac ccatctgggt tttctgctatggaaaggctc t 51 <210>667 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (668 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg20724478 <400>667 gaggctgggg agctcggcct ggctgggata cgcgatgtcgtcaacgccag c 51 <210>668 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (667 is entry) of other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg20724478 <400>668 gaggctgggg agctcggcct ggctgagata cgcgatgtcgtcaacgccag c 51 <210>669 <211>51 <212>DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (670 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg20724478 <400> 669 ctggggagct cggcctggct gggatacgcg atgtcgtcaa cgccagcccg t 51 <210> 670 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (669 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20724478 <400> 670 ctggggagct cggcctggct gggattcgcg atgtcgtcaa cgccagcccg t 51 <210> 671 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (672 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg20724478 <400> 671 aagacgtagc ccgggtggga tgtgacggcc tgagcgtcgt ctcggcgatt t 51 <210> 672 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (671 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20724478 <400> 672 aagacgtagc ccgggtggga tgtgatggcc tgagcgtcgt ctcggcgatt t 51 <210> 673 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (674 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20724478 <400> 673 gaggggtgcc cctcatcatt gatgatcgcg tacatctcgt tgccgaaatt g 51 <210> 674 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (673 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20724478 <400> 674 gaggggtgcc cctcatcatt gatgaccgcg tacatctcgt tgccgaaatt g 51 <210> 675 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (676 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg20727018 <400> 675 cacgtgcaca tctgcggtga ggttgagggc tgcagtgata ttgaaagtct c 51 <210> 676 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (675 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg20727018 <400> 676 cacgtgcaca tctgcggtga ggttgggggc tgcagtgata ttgaaagtct c 51 <210> 677 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (678 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20728358 <400> 677 gatgaaaccc cgtctctact aaaaatacaa aaattagccg ggtg.tgatgg c 51 <210> 678 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (677 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20728358 <400> 678 gatgaaaccc cgtctctact aaaaacacaa aaattagccg ggtgtgatgg c 51 <210> 679 <211> 36 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (11) ..(0) <223> 1 of 2 allelic variants (680 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20730743 <400> 679 acgcgtactg gcggatctca gtacgataac ccacca 36 <210> 680 <211> 36 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (11) ..(0) <223> 2 of 2 allelic variants (679 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg20730743 <400> 680 acgcgtactg acggatctca gtacgataac ccacca 36 <210> 681 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (682 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20730927 <400> 681 atctgaacat ctttttatcg actactggcc ccagtgaacc tatgcaacgt c 51 <210> 682 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (681 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg20730927 <400> 682 atctgaacat ctttttatcg actaccggcc ccagtgaacc tatgcaacgt c 51 <210> 683 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (684 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg20738127 <400> 683 tcgatgtcga agttcgcttc gatgggcccg gaggatagcg cgtcaggtgg c 51 <210> 684 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (683 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg20738127 <400> 684 tcgatgtcga agttcgcttc gatggccccg gaggatagcg cgtcaggtgg c 51 <210> 685 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (686 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20744814 <400> 685 ccatggccac ccacgaagct ctccctgccc cctccgtcgc ccaactcctg g 51 <210> 686 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (685 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20744814 <400> 686 ccatggccac ccacgaagct ctccccgccc cctccgtcgc ccaactcctg g 51 <210> 687 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (688 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20744814 <400> 687 gaggggcacc cgggtgctgc tggccatggc cacccacgaa gctctccctg c 51 <210> 688 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (687 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20744814 <400> 688 gaggggcacc cgggtgctgc tggccgtggc cacccacgaa gctctccctg c 51 <210> 689 <211> 46 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (21) . . (0) <223> 1 of 2 allelic variants (690 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20745811 <400> 689 nacgcgtggg gcatgtcaga gcttcagatg tgcattgcga acatgc 46 <210> 690 <211> 46 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (21) ..(0) <223> 2 of 2 allelic variants (689 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg20745811 <400> 690 nacgcgtggg gcatgtcaga acttcagatg tgcattgcga acatgc 46 <210> 691 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (692 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21132570 <400> 691 gtatgtacga gtgtgcacgt gtgtgcgtgt gcacagaggg tgtggtgcca g 51 <210> 692 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (691 is other entry) <221> misc feature <222> (25)...(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg21132570 <400> 692 gtatgtacga gtgtgcacgt gtgtggtgtg cacagagggt gtggtgccag 50 <210> 693 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (694 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21132570 <400> 693 cgagtgtgca cgtgtgtgcg tgtgcacaga gggtgtggtg ccagcttgag t 51 <210> 694 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (693 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg21132570 <400> 694 cgagtgtgca cgtgtgtgcg tgtgccagag ggtgtggtgc cagcttgagt 50 <210> 695 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (696 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21147609 <400> 695 agtgcagagc caggatccac ctgagtcccc cggctggctc cagatcccac a 51 <210> 696 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (695 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21147609 <400> 696 agtgcagagc caggatccac ctgagccccc cggctggctc cagatcccac a 51 <210> 697 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (698 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21147771 <400> 697 gactggctta ttccacttag cataatgtcc tcaaggtgtg ttcacccatg t 51 <210> 698 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (697 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg21147771 <400> 698 gactggctta ttccacttag cataacgtcc tcaaggtgtg ttcacccatg t 51 <210> 699 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (700 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21147771 <400> 699 gtttgacaga gtatcactct gtcacccagg ctggagtgca gtgatgcaat c 51 <210> 700 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (699 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21147771 <400> 700 gtttgacaga gtatcactct gtcactcagg ctggagtgca gtgatgcaat c 51 <210> 701 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (702 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21147771 <400> 701 gctggagtgc agtgatgcaa tctcggctca ctgcaacctc cgcctcccag c 51 <210> 702 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (701 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21147771 <400> 702 gctggagtgc agtgatgcaa tctcgactca ctgcaacctc cgcctcccag c 51 <210> 703 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (704 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg21148047 <400> 703 tgcttatatt cctgttggtg ggaatataaa accgtacatc tagtatggaa a 51 <210> 704 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (703 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21148047 <400> 704 tgcttatatt cctgttggtg ggaatgtaaa accgtacatc tagtatggaa a 51 <210> 705 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (706 is other entry) <221>miscfeature <222>_ (0).
.(0) <223>Accession number cg21148047 <400>705 attgagggat gaatggaaaa acaaaatctg acatatacatacatacagtgg 51 <210>706 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (705 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg21148047 <400>706 attgagggat gaatggaaaa acaaagtctg acatatacatacatacagtgg 51 <210>707 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (708 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg21148047 <400>707 catatagaca tatgctataa catggatgca ccttgagtacattatgctagg 51 <210>708 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (707 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg21148047 <400>708 catatagaca tatgctataa catggctgca ccttgagtacattatgctagg 51 <210> 709 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (710 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg21148047 <400> 709 ggatgcacct tgagtacatt atgctaggtg aaataagcct gtcacaaaaa c 51 <210> 710 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (709 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21148047 <400> 710 ggatgcacct tgagtacatt atgctgggtg aaataagcct gtcacaaaaa c 51 <210> 711 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (712 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg21148047 <400> 711 tgagtacatt atgctaggtg aaataagcct gtcacaaaaa caaatactgc a 51 <210> 712 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (711 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg21148047 <400> 712 tgagtacatt atgctaggtg aaataggcct gtcacaaaaa caaatactgc a 51 <210> 713 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (714 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21148047 <400> 713 aaacaaatac tgcatgattc catttaaatg aggggcctag aatattcaac t 51 <210> 714 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (713 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg21148047 <400> 714 aaacaaatac tgcatgattc catttgaatg aggggcctag aatattcaac t 51 <210> 715 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (716 is other entry) <221> misc feature <222>(0)...(0) <223>Accession number cg21148047 <400>715 aacaaatact gcatgattcc atttaaatga ggggcctagaatattcaactt 51 <210>716 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (715 is entry) of other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg21148047 <400>716 aacaaatact gcatgattcc atttagatga ggggcctagaatattcaactt 51 <210>717 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (718 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg21150410 <400>717 ggcggaggtt tcagagtaga aggtgatgtc agctccagctcccctctgtcg 51 <210>718 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>2 2 allelic variants (717 is entry) of other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg21150410 <400>718 ggcggaggtt tcagagtaga aggtggtgtc agctccagctcccctctgtcg 51 <210> 719 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (720 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21150410 <400> 719 gaataagaag atgaagtttg cagtcgaatt catgttctcc tacccctgct c 51 <210> 720 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (719 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21150410 <400> 720 gaataagaag atgaagtttg cagtcaaatt catgttctcc tacccctgct c 51 <210> 721 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (722 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21405503 <400> 721 gaaagacttc tagttcacag gggctgtatc tgaaccctaa aacaggccca g 51 <210> 722 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (721 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21405503 <400> 722 gaaagacttc tagttcacag gggctctatc tgaaccctaa aacaggccca g 51 <210> 723 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (724 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21415668 <400> 723 ggactggtca gggaggagtt agggcaggag gactggtcag ggaggagtta g 51 <210> 724 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (723 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21415668 <400> 724 ggactggtca gggaggagtt agggctggag gactggtcag ggaggagtta g 51 <210> 725 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (726 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21415668 <400> 725 ggactggtca gggaggagtt agggcaggag gactggtcag ggaggagtta g 51 <210> 726 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (725 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21415668 <400> 726 ggactggtca gggaggagtt agggctggag gactggtcag ggaggagtta g 51 <210> 727 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (728 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21417734 <400> 727 tcctggccgt tctcgacagg agcgcatcat ggaccagccc agcaatctgt t 51 <210> 728 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (727 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg21417734 <400>728 tcctggccgt tctcgacagg agcgctcatg gaccagcccagcaatctgtt 50 <210>729 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (730 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg21424662 <400>729 tgaggaagag gaaatacaga actcagctgt cccgggggtgcgcgcgtgtg t 51 <210>730 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (729 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg21424662 <400>730 tgaggaagag gaaatacaga actcacctgt cccgggggtgcgcgcgtgtg t 51 <210>731 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (732 is entry) of other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg21424662 <400>731 gtgctgtgcc gcgagcgcgc gcgaggcggc gtgtgtgtgtgtgtgtgtgt g 51 <210>732 <211>51 <212>DNA

<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (731 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21424662 <400> 732 gtgctgtgcc gcgagcgcgc gcgagacggc gtgtgtgtgt gtgtgtgtgt g 51 <210> 733 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (734 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg21424662 <400> 733 gtgtgtgtgt gtgtgtgtgt gtgtggtgtg tgcgcgcgcg cgtatgtatg 50 <210> 734 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (733 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21424662 <400> 734 gtgtgtgtgt gtgtgtgtgt gtgtgtgtgt gtgcgcgcgc gcgtatgtat g 51 <210> 735 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (736 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21424662 <400> 735 tgtgtgtgtg tgtgtgtggt gtgtgcgcgc gcgcgtatgt atgtgtgtgt g 51 <210> 736 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (735 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21424662 <400> 736 tgtgtgtgtg tgtgtgtggt gtgtgtgcgc gcgcgtatgt atgtgtgtgt g 51 <210> 737 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (738 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21424863 <400> 737 ggaccgttcg cgtcgacctg ggctcgttgg agggcattat gcctccggcg g 51 <210> 738 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (737 is other entry) <221> misc feature <222> (0) . . . (0) <223> Accession number cg21424863 <400> 738 ggaccgttcg cgtcgacctg ggctcattgg agggcattat gcctccggcg g 51 <210> 739 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (740 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21424863 <400> 739 tcgttggagg gcattatgcc tccggcggaa caggttcccg gggagaaata t 51 <210> 740 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (739 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg21424863 <400> 740 tcgttggagg gcattatgcc tccggggaac aggttcccgg ggagaaatat 50 <210> 741 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (742 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21424863 <400> 741 caactgcccg gcaggtcatt ttccaacggc tgcgcgaggc cgaggacgag c 51 <210> 742 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (741 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21424863 <400> 742 caactgcccg gcaggtcatt ttccagcggc tgcgcgaggc cgaggacgag c 51 <210> 743 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (744 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21424863 <400> 743 ggacgagcag aaatacggtc atttttccgc cgttgagggt gacgtcatca c 51 <210> 744 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (743 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21424863 <400> 744 ggacgagcag aaatacggtc attttgccgc cgttgagggt gacgtcatca c 51 <210> 745 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (746 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21424863 <400> 745 agcagaaata cggtcatttt tccgccgttg agggtgacgt catcaccgga g 51 <210> 746 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (745 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21424863 <400> 746 agcagaaata cggtcatttt tccgcggttg agggtgacgt catcaccgga g 51 <210> 747 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (748 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21424863 <400> 747 aatacggtca tttttccgcc gttgagggtg acgtcatcac cggagtcgtc c 51 <210> 748 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (747 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21424863 <400> 748 aatacggtca tttttccgcc gttgaaggtg acgtcatcac cggagtcgtc c 51 <210> 749 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (750 is other entry) <221> misc_feature <222> (0) . . (0) .
<223> Accession number cg21425684 <400> 749 tgcacctgac gcggttcgac gtgcagatcg aggccttcga agagcccctc c 51 <210> 750 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (749 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21425684 <400> 750 tgcacctgac gcggttcgac gtgcatatcg aggccttcga agagcccctc c 51 <210> 751 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (752 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21425684 <400>751 agaaggcatc cgtgaggatc ccgacagcca gggccagggcgatttccttg a 51 <210>752 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (751 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg21425684 <400>752 agaaggcatc cgtgaggatc ccgacggcca gggccagggcgatttccttg a 51 <210>753 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>1 2 allelic variants (754 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg21425687 <400>753 ccccagaaga gggagggcgc tctctgccca ggagacctgctgtgctccca t 51 <210>754 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (753 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg21425687 <400>754 ccccagaaga gggagggcgc tctcttccca ggagacctgctgtgctccca t 51 <210>755 <211>51 <212>DNA

<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (756 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21428753 <400> 755 ccttccctct gtacctgtgt cctgaccccc tcttcttata aggacaccgg t 51 <210> 756 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (755 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21428753 <400> 756 ccttccctct gtacctgtgt cctgaacccc tcttcttata aggacaccgg t 51 <210> 757 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (758 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg21428762 <400> 757 catcagaggt gaaaacgatg agcggggtgc tcggacgcag acgagcgata c 51 <210> 758 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (757 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21428762 <400> 758 catcagaggt gaaaacgatg agcggtgtgc tcggacgcag acgagcgata c 51 <210> 759 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (760 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21428762 <400> 759 acaccggggt aacgacggcg tgagcgcccc agacccaggc gagggtcttg g 51 <210> 760 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (759 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg21428762 <400> 760 acaccggggt aacgacggcg tgagccccca gacccaggcg agggtcttgg 50 <210> 761 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (762 is other entry) <221> misc feature <222> (0)...(0) <223> Accession number cg21433543 <400> 761 tacgcctccc tcaccactcc gacgcgtacc ttcgtcgtcg ccgtgacagc a 51 <210> 762 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (761 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21433543 <400> 762 tacgcctccc tcaccactcc gacgcatacc ttcgtcgtcg ccgtgacagc a 51 <210> 763 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> l~of 2 allelic variants (764 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21433543 <400> 763 tccgacgcgt accttcgtcg tcgccgtgac agcagccgta tgcggggccg c 51 <210> 764 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (763 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg21433543 <400> 764 tccgacgcgt accttcgtcg tcgccatgac agcagccgta tgcggggccg c 51 <210> 765 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (766 is other entry) <221> misc_feature .
<222> (0). .(0) <223> Accession number cg21433543 <400> 765 cactgaagtt atggcgtcgc tgcgtagccg aggctggggt agcgctcctg g 51 <210> 766 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (765 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg21433543 <400> 766 cactgaagtt atggcgtcgc tgcgtcgccg aggctggggt agcgctcctg g 51 <210> 767 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (768 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21435343 <400> 767 cggggcctct ggcctggcag ccgcaggacc caatggatcg ggcgctcacg c 51 <210> 768 <211> 50 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (767 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg21435343 <400> 768 cggggcctct ggcctggcag ccgcagaccc aatggatcgg gcgctcacgc 50 <210> 769 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (770 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21435589 <400> 769 tcattttgtg ccaagataca ctgtcggtgc ctgatccgga atggtctgtg t 51 <210> 770 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (769 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg21435589 <400> 770 tcattttgtg ccaagataca ctgtcagtgc ctgatccgga atggtctgtg t 51 <210> 771 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (772 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21628871 <400> 771 gcccggaccc tgtacccgca ccaggacaca gcccatcact aatcaatgat a 51 <210> 772 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (771 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21628871 <400> 772 gcccggaccc tgtacccgca ccagggcaca gcccatcact aatcaatgat a 51 <210> 773 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (774 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21628871 <400> 773 ggacacagcc catcactaat caatgatatt tccataaacc aaagagaatt c 51 <210> 774 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (773 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21628871 <400> 774 ggacacagcc catcactaat caatggtatt tccataaacc aaagagaatt c 51 <210> 775 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (776 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21632268 <400> 775 aagaacaccc gtgacaaaag aaggagggcc ggcagaatga cccgccggcc c 51 <210> 776 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (775 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg21632268 <400> 776 aagaacaccc gtgacaaaag aaggaggccg gcagaatgac ccgccggccc 50 <210> 777 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (778 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21632268 <400> 777 gacggtcgtc acttctcctc tttgggcagc cgccactggt cgtgctcggt g 51 <210> 778 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (777 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg21632268 <400> 778 gacggtcgtc acttctcctc tttggcagcc gccactggtc gtgctcggtg 50 <210> 779 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (780 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg21632268 <400> 779 gcggacgcgg gccgtgataa tcagggccgt aggctcccgg agcggggcga c 51 <210> 780 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (779 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg21632268 <400>780 gcggacgcgg gccgtgataa tcaggccgta ggctcccggagcggggcgac 50 <210>.781 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (782 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg21632288 <400>781 gtgtgagggg cgcggcgccc cctagccggc cctgcgccggggtctcagag g 51 <210>782 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (781 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg21632288 <400>782 gtgtgagggg cgcggcgccc cctaggcggc cctgcgccggggtctcagag g 51 <210>783 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>1 2 allelic variants (784 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg21632288 <400>783 gccggggtct cagagggccg gcccggcggg gggcgccgcggggccaggac t 51 <210>784 <211>50 <212>DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (783 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg21632288 <400> 784 gccggggtct cagagggccg gcccgcgggg ggcgccgcgg ggccaggact 50 <210> 785 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (786 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21632288 <400> 785 gagggccggc ccggcggggg gcgccgcggg gccaggactg cgctcaggat c 51 <210> 786 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (785 is other entry) <221> misc_~feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg21632288 <400> 786 gagggccggc ccggcggggg gcgcccgggg ccaggactgc gctcaggatc 50 <210> 787 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (788 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21634562 <400> 787 cctggctcag cagagccgcc ttcctgctgc agaagctgat gtcgccccac c 51 <210> 788 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (787 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21634562 <400> 788 cctggctcag cagagccgcc ttcctactgc agaagctgat gtcgccccac c 51 <210> 789 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (790 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg21638303 <400> 789 caagcctgtt atacaaccag atctcatgag aactcactat cacaaggtca g 51 <210> 790 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26)...(0) <223> 2 of 2 allelic variants (789 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg21638303 <400> 790 caagcctgtt atacaaccag atctcctgag aactcactat cacaaggtca g 51 <210> 791 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (792 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg21638303 <400> 791 tgagaactca ctatcacaag gtcagcatca agaagatggt gcttaaccat t 51 <210> 792 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (791 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21638303 <400> 792 tgagaactca ctatcacaag gtcagtatca agaagatggt gcttaaccat t 51 <210> 793 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (794 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg21638303 <400>793 tcacaaggtc agcatcaaga agatggtgct taaccattggtgaaagatcc g 51 <210>794 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (793 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg21638303 <400>794 tcacaaggtc agcatcaaga agatgttgct taaccattggtgaaagatcc g 51 <210>795 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>1 2 allelic variants (796 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg21638638 <400>795 gagggaaggc ctcccatgta cccgtcactc ctctcttctccatcaaggcc a 51 <210>796 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (795 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg21638638 <400>796 gagggaaggc ctcccatgta cccgttactc ctctcttctccatcaaggcc a 51 <210>797 <211>51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (798 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21639240 <400> 797 ttgccacgtt gcctaggctg gtctcaaact cctgggctca gatgatccac c 51 <210> 798 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (797 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21639240 <400> 798 ttgccacgtt gcctaggctg gtctcgaact cctgggctca gatgatccac c 51 <210> 799 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (800 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21639652 <400> 799 aaaacccatg cactcctgtg ggattgcccc tgagctccac agtctctccc c 51 <210> 800 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (799 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg21639652 <400> 800 aaaacccatg cactcctgtg ggattacccc tgagctccac agtctctccc c 51 <210> 801 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (802 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21640260 <400> 801 tgtcacccag gctgaactgc agtggtgtga tcttggctca ctgcaacctc c 51 <210> 802 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (801 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21640260 <400> 802 tgtcacccag gctgaactgc agtggcgtga tcttggctca ctgcaacctc c 51 <210> 803 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (804 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21640260 <400>803 tggctcactg caacctccac ctcccaggtt caagcaattctcctgcctca g 51 <210>804 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (803 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg21640260 <400>804 tggctcactg caacctccac ctcccgggtt caagcaattctcctgcctca g 51 <210>805 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (806 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg21640260 <400>805 caacctccac ctcccaggtt caagcaattc tcctgcctcagcctcagcct c 51 <210>806 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (805 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg21640260 <400>806 caacctccac ctcccaggtt caagcgattc tcctgcctcagcctcagcct c 51 <210>807 <211>51 <212>DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (808 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21642593 <400> 807 cggccacccc cgacccagcc cgcacgccca gggcgtaccc atcggtcatc g 51 <210> 808 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (807 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21642593 <400> 808 cggccacccc cgacccagcc cgcacaccca gggcgtaccc atcggtcatc g 51 <210> 809 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (810 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg21643872 <400> 809 ccgaagaccc agccaagccg tccaagatct tcgctcccag tggtctcatg c 51 <210> 810 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (809 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg21643872 <400> 810 ccgaagaccc agccaagccg tccaaaatct tcgctcccag tggtctcatg c 51 <210> 811 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (812 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg21646394 <400> 811 aggaagcaga gtctatacaa aatttaagag aatgagacag aagacgctcc t 51 <210> 812 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (811 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21646394 <400> 812 aggaagcaga gtctatacaa aatttgagag aatgagacag aagacgctcc t 51 <210> 813 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (814 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21651520 <400> 813 gcatccccgc acagcacgtg gtgtgtggac atgccacagc atccgcggga g 51 <210> 814 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (813 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21651520 <400> 814 gcatccccgc acagcacgtg gtgtgcggac atgccacagc atccgcggga g 51 <210> 815 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (816 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21652256 <400> 815 actgcagcgt gagccctggg acgcagtcga agcagagcaa agtctccccc g 51 <210> 816 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (815 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21652256 <400> 816 actgcagcgt gagccctggg acgcaatcga agcagagcaa agtctccccc g 51 <210> 817 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (818 is other entry) <221> misc_feature , <222> (0). .(0) <223> Accession number cg21655657 <400> 817 caacatacat ggcgtttgcg tcacagttgg agtcagatgt gagcccggag g 51 <210> 818 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (817 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21655657 <400> 818 caacatacat ggcgtttgcg tcacaattgg agtcagatgt gagcccggag g 51 <210> 819 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (820 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21656849 <400> 819 cacccagaac cacggattac gcaacgcacg ctgccaccag ggacgacgcg c 51 <210> 820 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (819 is other entry) <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg21656849 <400>820 cacccagaac cacggattac gcaacacacg ctgccaccagggacgacgcg c 51 <210>821 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (822 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg21656849 <400>821 aggactggtt ggtgatcccc gggatgacac ccttctgaccttgctgctcg a 51 <210>822 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (821 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg21656849 <400>822 aggactggtt ggtgatcccc gggataacac ccttctgaccttgctgctcg a 51 <210>823 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (824 is entry) of other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg21656849 <400>823 cgggatgaca cccttctgac cttgctgctc gacctcagtatcggcatgca c 51 <210> 824 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (823 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21656849 <400> 824 cgggatgaca cccttctgac cttgccgctc gacctcagta tcggcatgca c 51 <210> 825 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (826 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21659091 <400> 825 gttcaaacca aatcctgctc ctgaggagac agaaggggca ggacttccag a 51 <210> 826 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (825 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21659091 <400> 826 gttcaaacca aatcctgctc ctgagtagac agaaggggca ggacttccag a 51 <210> 827 <211> 38 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (13) ..(0) <223> 1 of 2 allelic variants (828 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21659216 <400> 827 acgcgtgtgt cctgtgacta caaaacagca ctggggtt 38 <210> 828 <211> 38 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (13) ..(0) <223> 2 of 2 allelic variants (827 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21659216 <400> 828 acgcgtgtgt cccgtgacta caaaacagca ctggggtt 38 <210> 829 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (830 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21659216 <400> 829 aaggatgctg ggacctggag tcaggcaagt tgcagccaag ctcagccttt g 51 <210> 830 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (829 is other entry) <221> misc feature <222> (0)...(0) <223> Accession number cg21659216 <400> 830 aaggatgctg ggacctggag tcaggtaagt tgcagccaag ctcagccttt g 51 <210> 831 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (832 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg21659349 <400> 831 acattcgcct caatggagac ccggtcaaac cctcccacgc cgtgaaaccc g 51 <210> 832 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (831 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg21659349 <400> 832 acattcgcct caatggagac ccggttaaac cctcccacgc cgtgaaaccc g 51 <210> 833 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (834 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21659349 <400> 833 ggagacccgg tcaaaccctc ccacgccgtg aaacccggcg ataccgtcac c 51 <210> 834 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (833 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg21659349 <400> 834 ggagacccgg tcaaaccctc ccacgacgtg aaacccggcg ataccgtcac c 51 <210> 835 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (836 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21659349 <400> 835 cgtgaaaccc ggcgataccg tcaccgtcca cacccccgga tgggaccggg t 51 <210> 836 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (835 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg21659349 <400> 836 cgtgaaaccc ggcgataccg tcaccatcca cacccccgga tgggaccggg t 51 <210> 837 <211> 51 <212> DNA
<213> Homo sapiens <220>

<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (838 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21659349 <400> 837 tccacacccc cggatgggac cgggttctcc aggtcatcaa cccgatcacg a 51 <210> 838 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (837 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21659349 <400> 838 tccacacccc cggatgggac cgggtcctcc aggtcatcaa cccgatcacg a 51 <210> 839 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (840 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21660290 <400> 839 aggtggaacg ggcactggac ctgtgcatgg cgtgcaaagg gtgcgcccga g 51 <210> 840 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (839 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21660290 <400> 840 aggtggaacg ggcactggac ctgtgtatgg cgtgcaaagg gtgcgcccga g 51 <210> 841 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (842 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21660634 <400> 841 cccacaccag gaaacagata ccaataaggg tccacgtgac gaccggaaca t 51 <210> 842 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (841 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21660634 <400> 842 cccacaccag gaaacagata ccaatgaggg tccacgtgac gaccggaaca t 51 <210> 843 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (844 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg21660687 <400>843 ctcaaccgcc tgacgcgctc gctgcccgcg cgcgcaccgtggagttgccc 50 <210>844 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (843 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg21660687 <400>844 ctcaaccgcc tgacgcgctc gctgcgccgc gcgcgcaccgtggagttgcc c 51 <210>845 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (846 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg21660975 <400>845 gcaggggcat tggggtaata gccttctagc cctttttgagggaaacacat g 51 <210>846 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (845 is entry) of other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg21660975 <400>846 gcaggggcat tggggtaata gccttttagc cctttttgagggaaacacat g 51 <210>847 <211>51 <212>DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (848 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg21661807 <400> 847 tgccttcagg agcagacccc cacacgtatg agccgtcgct gcgtgacgtt c 51 <210> 848 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (847 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg21661807 <400> 848 tgccttcagg agcagacccc cacacctatg agccgtcgct gcgtgacgtt c 51 <210> 849 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (850 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg23217486 <400> 849 gctatggctg tggatttcgg agtgcgggga agtgtggagg aggtgttggg g 51 <210> 850 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (849 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg23217486 <400> 850 gctatggctg tggatttcgg agtgctggga agtgtggagg aggtgttggg g 51 <210> 851 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (852 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg23217486 <400> 851 ggatttcgga gtgcggggaa gtgtggagga ggtgttgggg gctggagaga t 51 <210> 852 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (851 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg23217486 <400> 852 ggatttcgga gtgcggggaa gtgtgcagga ggtgttgggg gctggagaga t 51 <210> 853 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (854 is other entry) <221> misc_feature <222> (0). .(0) ' <223> Accession number cg23295774 <400> 853 gcccctcctg agtgccaagg aggcgggcgt ctacacttgc cgtgcacaca a 51 <210> 854 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (853 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg23295774 <400> 854 gcccctcctg agtgccaagg aggcgagcgt ctacacttgc cgtgcacaca a 51 <210> 855 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (856 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg23295774 <400> 855 gccaactcta-cgtcaatacg cgtggcggtg gcagcaaccg ggcccccaaa a 51 <210> 856 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (855 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg2,3295774 <400> 856 gccaactcta cgtcaatacg cgtggaggtg gcagcaaccg ggcccccaaa a 51 <210> 857 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (858 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg23298372 <400> 857 cgcgtgatag gctcaggagc ctgcctgtgt acacagacag cacacatgac a 51 <210> 858 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (857 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg23298372 <400> 858 cgcgtgatag gctcaggagc ctgcccgtgt acacagacag cacacatgac a 51 <210> 859 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (860 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg23298372 <400> 859 ctgtgtacac agacagcaca catgacaggc ccgggagcct gtctgtgtac a 51 <210> 860 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (859 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg23298372 <400> 860 ctgtgtacac agacagcaca catgataggc ccgggagcct gtctgtgtac a 51 <210> 861 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (862 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg23299043 <400> 861 agtacgacat ccgacacgct tcagaccgac cagagtgaag aatttcgcgt a 51 <210> 862 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (861 is other entry) <221> misc_feature <222> (b) . . (0) <223> Accession number cg23299043 <400> 862 agtacgacat ccgacacgct tcagagcgac cagagtgaag aatttcgcgt a 51 <210> 863 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (864 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg23299248 <400>863 ccaactatta agatatatat acccctaccc cagtgaagaacaatctgcta 50 <210>864 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (863 is entry) of other <221>miscfeature <222>(0)_ . . (0) <223>Accession number cg23299248 <400>864 ccaactatta agatatatat accccctacc ccagtgaagaacaatctgct a 51 <210>865 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (866 is entry) of other <221>miscfeature <222>(0)_ . . (0) <223>Accession number cg23305320 <400>865 tgctgcatac caggtgccaa atggcgtcct ataaatggaagctcttgtgt g 51 <210>866 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (865 is entry) of other <221>miscfeature <222>(0)_ . . (0) <223>Accession number cg23305320 <400>866 tgctgcatac caggtgccaa atggcatcct ataaatggaagctcttgtgt g 51 <210> 867 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (868 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg23306056 <400> 867 tccagtatga ctttatctcg attacacctg taaagacctt aagccatatt t 51 <210> 868 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (867 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg23306056 <400> 868 tccagtatga ctttatctcg attaccctgt aaagacctta agccatattt 50 <210> 869 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (870 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg23306056 <400> 869 actttatctc gattacacct gtaaagacct taagccatat tttaaggttc t 51 <210> 870 <211> 51 <212> DNA

<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (869 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg23306056 <400> 870 actttatctc gattacacct gtaaatacct taagccatat tttaaggttc t 51 <210> 871 <211> 48 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (23) .. (0) <223> 1 of 2 allelic variants (872 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg23309108 <400> 871 acgcgtgccc gttacgttga ccaggctggt tgtaaactcc tgggctca 48 <210> 872 <211> 48 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (23) . . (0) <223> 2 of 2 allelic variants (871 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg23309108 <400> 872 acgcgtgccc gttacgttga ccgggctggt tgtaaactcc tgggctca 48 <210> 873 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (874 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg23309108 <400> 873 tgggctcaag tgatccacct gcctcagcct ccaaaagtgc tgggattaca t 51 <210> 874 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (873 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg23309108 <400> 874 tgggctcaag tgatccacct gcctcggcct ccaaaagtgc tgggattaca t 51 <210> 875 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (876 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg23331833 <400> 875 acagcgcgta ctttgggctc cgggattcgc tccgcgcccg cggttgtagc a 51 <210> 876 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (875 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg23331833 <400> 876 acagcgcgta ctttgggctc cgggagtcgc tccgcgcccg cggttgtagc a 51 <210> 877 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (878 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg23332230 <400> 877 ttgtgggagt attaggggaa gttgccacta aggctggcag gtcctggagt t 51 <210> 878 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (877 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg23332230 <400> 878 ttgtgggagt attaggggaa gttgcactaa ggctggcagg tcctggagtt 50 <210> 879 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (880 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg23333370 <400> 879 ttgggggctc agaggcacgg ttaacgcagc agcagcgcaa acctcacact c 51 <210> 880 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (879 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg23333370 <400> 880 ttgggggctc agaggcacgg ttaacacagc agcagcgcaa acctcacact c 51 <210> 881 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (882 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg24109555 <400> 881 aatataatgg gtttatatga ctatatcaaa ggagggaaga aggcccccag c 51 <210> 882 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (881 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg24109555 <400> 882 aatataatgg gtttatatga ctataccaaa ggagggaaga aggcccccag c 51 <210> 883 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (884 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg24110526 <400> 883 gcactgagac agcatcacga ggactgtgcc tgccccgcat gcctcttgcc a 51 <210> 884 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (883 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg24110526 <400> 884 gcactgagac agcatcacga ggactatgcc tgccccgcat gcctcttgcc a 51 <210> 885 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (886 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg24113982 <400> 885 tacttagtta tgtttttaaa cacacatctg agctcaaagc caagaaaggg a 51 <210> 886 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (885 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg24113982 <400> 886 tacttagtta tgtttttaaa cacacgtctg agctcaaagc caagaaaggg a 51 <210> 887 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (888 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg24114224 <400> 887 aatgggccag gctggagcta cgttgagttt gttgagtttt ttgcttattg c 51 <210> 888 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (887 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg24114224 <400> 888 aatgggccag gctggagcta cgttgcgttt gttgagtttt ttgcttattg c 51 <210> 889 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (890 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg24114456 <400> 889 atcctgacgt gtagactcct atggagacct acttaattca caccgggtgt c 51 <210> 890 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (889 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg24114456 <400> 890 atcctgacgt gtagactcct atggatacct acttaattca caccgggtgt c 51 <210> 891 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (892 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg24114456 <400> 891 ttcacaccgg gtgtcctgat gtgtagaccc ctgtggagac ctacttaatt c 51 <210> 892 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (891 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg24114456 <400> 892 ttcacaccgg gtgtcctgat gtgtaaaccc ctgtggagac ctacttaatt c 51 <210> 893 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26) . . . (0) <223> 1 of 2 allelic variants (894 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg24115035 <400> 893 gaggtgaaag ggaagaaaag ctaaggtcga ccttagaaag cattgagtca a 51 <210> 894 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (893 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg24115035 <400> 894 gaggtgaaag ggaagaaaag ctaagatcga ccttagaaag cattgagtca a 51 <210> 895 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (896 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg24115035 <400> 895 agaactgttg ctttttgttt aacccacgtg caagtaaagt tcaataaagt t 51 <210> 896 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (895 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg24115035 <400>896 agaactgttg ctttttgttt aacccccgtg caagtaaagttcaataaagtt 51 <210>897 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (898 is entry) of other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg24121961 <400>897 acaggccaca cccccatctc agagatggca gcgacttcatccaaggggcag 51 <210>898 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>2 2 allelic variants (897 is entry) of other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg24121961 <400>898 acaggccaca cccccatctc agagaaggca gcgacttcatccaaggggcag 51 <210>899 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ . . (0) <223>1 2 allelic variants (900 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg24132746 <400>899 cctgtggtgc tgcttctcca aatgccgccc ttggctgtttcccaggagtca 51 <210>900 <211>51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (899 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg24132746 <400> 900 cctgtggtgc tgcttctcca aatgctgccc ttggctgttt cccaggagtc a 51 <210> 901 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (902 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg24141481 <400> 901 gtgtaaagaa gtataatttc tctgccgact ccatttaatc cactgcaagg c 51 <210> 902 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (901 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg24141481 <400> 902 gtgtaaagaa gtataatttc tctgctgact ccatttaatc cactgcaagg c 51 <210> 903 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (904 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg24144955 <400> 903 gcacgcgtgt tgtggctgga agggcgcagt gctctggagg gggaaactga g 51 <210> 904 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (903 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg24144955 <400> 904 gcacgcgtgt tgtggctgga agggctcagt gctctggagg gggaaactga g 51 <210> 905 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (906 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25132332 <400> 905 aagtaagttg cttaatcagg tccaagcagt aattgagaga agagagtagc t 51 <210> 906 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (905 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25132332 <400>906 aagtaagttg cttaatcagg tccaaacagt aattgagagaagagagtagc t 51 <210>907 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>1 2 allelic variants (908 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg25132807 <400>907 tgaactgtca ccattcttta tgtacgtgta gagatttgcagtttactgca c 51 <210>908 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>2 2 allelic variants (907 is entry) of other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg25132807 <400>908 tgaactgtca ccattcttta tgtacatgta gagatttgcagtttactgca c 51 <210>909 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>1 2 allelic variants (910 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg25147161 <400>909 ctgcaatatg ccaccagcgc catggcgaac cgcatctacgctccaattcc c 51 <210>910 <211>50 <212>DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (909 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg25147161 <400> 910 ctgcaatatg ccaccagcgc catgggaacc gcatctacgc tccaattccc 50 <210> 911 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221.> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (912 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25153589 <400> 911 tcccagcact tctgggaggc caaagtggga ggatcgcttg agcccaggag t 51 <210> 912 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (911 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg25153589 <400> 912 tcccagcact tctgggaggc caaagcggga ggatcgcttg agcccaggag t 51 <210> 913 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (914 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25153589 <400> 913 tctgggaggc caaagtggga ggatcgcttg agcccaggag ttcgagacca g 51 <210> 914 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (913 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25153589 <400> 914 tctgggaggc caaagtggga ggatcccttg agcccaggag ttcgagacca g 51 <210> 915 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (916 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25153589 <400> 915 ggaggatcgc ttgagcccag gagttcgaga ccagcctggg caacatagcg a 51 <210> 916 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (915 is other entry) <221> misc feature <222> (0)...(0) <223> Accession number cg25153589 <400> 916 ggaggatcgc ttgagcccag gagtttgaga ccagcctggg caacatagcg a 51 <210> 917 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (918 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25154211 <400> 917 ggccacccag ctgcctatgc tggggacggg gccgctcagg tccccaccgg g 51 <210> 918 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (917 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25154211 <400> 918 ggccacccag ctgcctatgc tggggtcggg gccgctcagg tccccaccgg g 51 <210> 919 <211> 51 <212> DNA
<213> Homo Sapiens .
<220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (920 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25154211 <400> 919 ccacccagct gcctatgctg gggacggggc cgctcaggtc cccaccgggc c 51 <210> 920 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (919 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25154211 <400> 920 ccacccagct gcctatgctg gggaccgggc cgctcaggtc cccaccgggc c 51 <210> 921 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (922 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25154211 <400> 921 gggccgctca ggtccccacc gggcctgtgc caccggctgc ggtcctctcg c 51 <210> 922 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (921 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg25154211 <400> 922 gggccgctca ggtccccacc gggccgtgcc accggctgcg gtcctctcgc 50 <210> 923 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (924 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25164916 <400> 923 gataataaaa cctgccccac aatttaaaaa aaaaaatcat gtcatgttag t 51 <210> 924 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (923 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg25164916 <400> 924 gataataaaa cctgccccac aatttaaaaa aaaaatcatg tcatgttagt 50 <210> 925 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (926 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25165258 <400> 925 tgtctgagct gagtctaaag gaggaagaaa ggggacctag gcaaagggac c 51 <210> 926 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (925 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg25165258 <400> 926 tgtctgagct gagtctaaag gaggagaaag gggacctagg caaagggacc 50 <210> 927 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (928 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg25167383 <400> 927 tgactgtgtg tccgggccac gtgtggctat gtgtccgggc cacgtgtgac t 51 <210> 928 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (927 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25167383 <400> 928 tgactgtgtg tccgggccac gtgtgactat gtgtccgggc cacgtgtgac t 51 <210> 929 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (930 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25171115 <400> 929 gaccacctcc ggtaccccgg ctgcgctgct gatatcccgc cggcctctct g ' 51 <210> 930 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (929 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25171115 <400> 930 gaccacctcc ggtaccccgg ctgcgttgct gatatcccgc cggcctctct g 51 <210> 931 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (932 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25171115 <400> 931 gccaagcgtt cacccacgcc tgctgcctgc aagacctgag gaacgcgcat g 51 <210> 932 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (931 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25171115 <400> 932 gccaagcgtt cacccacgcc tgctgtctgc aagacctgag gaacgcgcat g 51 <210> 933 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (934 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25171136 <400> 933 ttgcaggcca gtcggctggg ggaaacggat gccctgcagg gggacgggaa c 51 <210> 934 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (933 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25171136 <400> 934 ttgcaggcca gtcggctggg ggaaatggat gccctgcagg gggacgggaa c 51 <210> 935 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (936 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg25171709 <400> 935 gcattgtcaa cgaaacctgc gactctcttg ccttctgtgc ctgcagcatg g 51 <210> 936 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (935 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg25171709 <400> 936 gcattgtcaa cgaaacctgc gactcccttg ccttctgtgc ctgcagcatg g 51 <210> 937 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (938 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg25173882 <400> 937 ttgcagtcca gctttctctc accttcaccg tgttctgtgc gcaccactga g 51 <210> 938 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (937 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg25173882 <400> 938 ttgcagtcca gctttctctc acctttaccg tgttctgtgc gcaccactga g 51 <210> 939 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26)...(0) <223> 1 of 2 allelic variants (940 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25174416 <400> 939 atgctggaca cagggctcga caaacacaag agacgatcct cggaccatcc t' 51 <210> 940 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (939 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25174416 <400> 940 atgctggaca cagggctcga caaacccaag agacgatcct cggaccatcc t 51 <210> 941 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (942 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25184184 <400> 941 cagtgggagc gggaagaggc cggagctcct gccccacacg tgagcaaagg g 51 <210> 942 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (941 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25184184 <400>942 cagtgggagc gggaagaggc cggagttcct gccccacacgtgagcaaagg g 51 <210>943 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (944 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg25237193 <400>943 cttccaaaat gaatcccaac ttcacctgta ctagttttacagtccttaca c 51 <210>944 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (943 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg25237193 <400>944 cttccaaaat gaatcccaac ttcacttgta ctagttttacagtccttaca c 51 <210>945 <211>51 <212>DNA

<213>HomoSapiens , <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (946 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg25239764 <400>945 cataacctca agaagctgtg ggagcgcaac ctccaggacgatttccctca t 51 <210>946 <211>51 <212> DNA
<213> Homo~sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (945 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25239764 <400> 946 cataacctca agaagctgtg ggagcacaac ctccaggacg atttccctca t 51 <210> 947 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (948 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25244087 <400> 947 tcgtcaccac tggcgttgtc gacgttgtca aaccgaggag gttcatgcgc t 51 <210> 948 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (947 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25244087 <400> 948 tcgtcaccac tggcgttgtc gacgtcgtca aaccgaggag gttcatgcgc t 51 <210> 949 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature , <222> (26) .. (0) <223> 1 of 2 allelic variants (950 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg25244087 <400> 949 cgatcgttcc ccctcccgct ccttaagagc cttgtaggcg caccgtctgc g 51 <210> 950 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (949 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25244087 <400> 950 cgatcgttcc ccctcccgct ccttacgagc cttgtaggcg caccgtctgc g 51 <210> 951 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (952 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25244087 <400> 951 cgagccggac cgctcggcga gcatcggagt accaaacacg atgtcgcccg c 51 <210> 952 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (951 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25244087 <400>952 cgagccggac cgctcggcga gcatcagagt accaaacacgatgtcgcccg c 51 <210>953 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (954 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg25244087 <400>953 gccggaccgc tcggcgagca tcggagtacc aaacacgatgtcgcccgcct c 51 <210>954 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (953 is entry) of other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg25244087 <400>954 gccggaccgc tcggcgagca tcggaatacc aaacacgatgtcgcccgcct c 51 <210>955 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (956 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg25244087 <400>955 ctctcttgtg aatggggacc ggacgcccgc agcgaggacagcggccgtcg a 51 <210>956 <211>51 <212>DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (955 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25244087 <400> 956 ctctcttgtg aatggggacc ggacgtccgc agcgaggaca gcggccgtcg a 51 <210> 957 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (958 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25248402 <400> 957 agaaaggcac agaggaaggg caaagcccca ggggagagaa aaccagtgac c 51 <210> 958 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (957 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg25248402 <400> 958 agaaaggcac agaggaaggg caaagcccag gggagagaaa accagtgacc 50 <210> 959 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (960 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25257592 <400> 959 gaggacgaca ccgatctggc ggacgccgcc cgttcatggc gcagatacct c 51 <210> 960 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (959 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25257592 <400> 960 gaggacgaca ccgatctggc ggacgtcgcc cgttcatggc gcagatacct c 51 <210> 961 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (962 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25257592 <400> 961 ctgtcctcgg actaggcatt ttcgggtatc ttgcgtggtg gtcattgtgc g 51 <210> 962 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (961 is other entry) <221> mist feature <222>(0)...(0) <223>Accession number cg25257592 <400>962 ctgtcctcgg actaggcatt ttcggctatc ttgcgtggtggtcattgtgcg 51 <210>963 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (964 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg25257592 <400>963 tggtcacatc catgtcgatg gtgtgagcgt aatgaaggtctacatcgccct 51 <210>964 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>2 2 allelic variants (963 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg25257592 <400>964 tggtcacatc catgtcgatg gtgtgcgcgt aatgaaggtctacatcgccct 51 <210>965 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (966 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg25257592 <400>965 tcccggctgt tttcatcgtc gccggcatct ttttctggctcgccgtctaag 51 <210> 966 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (965 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25257592 <400> 966 tcccggctgt tttcatcgtc gccggtatct ttttctggct cgccgtctaa g 51 <210> 967 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (968 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25257592 <400> 967 tgtgagcgta atgaaggtct acatcgccct ggtgaaggcc tgcaccacta g 51 <210> 968 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (967 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25257592 <400> 968 tgtgagcgta atgaaggtct acatcaccct ggtgaaggcc tgcaccacta g 51 <210> 969 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (970 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25257592 <400> 969 aggtctacat cgccctggtg aaggcctgca ccactagcgt cggcaccatt t 51 <210> 970 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (969 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25257592 <400> 970 aggtctacat cgccctggtg aaggcttgca ccactagcgt cggcaccatt t 51 <210> 971 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (972 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25261577 <400> 971 tgataatagc gcttgccggt tagtggtaat acacagcttg aaatttggtg a 51 <210> 972 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (971 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25261577 <400> 972 tgataatagc gcttgccggt tagtgataat acacagcttg aaatttggtg a 51 <210> 973 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (974 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25263948 <400> 973 ggggcgattt caagcagaag ctcacgacga ccttcactgc gggctccggg c 51 <210> 974 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (973 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25263948 <400> 974 ggggcgattt caagcagaag ctcacaacga ccttcactgc gggctccggg c 51 <210> 975 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (976 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25263948 <400> 975 cgaccttcac tgcgggctcc gggctgcccg accttaccgg cgtcaagggc g 51 <210> 976 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (975 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25263948 <400> 976 cgaccttcac tgcgggctcc gggctacccg accttaccgg cgtcaagggc g 51 <210> 977 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (978 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25263948 <400> 977 ccggtgacgc taagaagctc gtcctgtgga tgtggccaga aggcttcgac a 51 <210> 978 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (977 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25263948 <400> 978 ccggtgacgc taagaagctc gtcctatgga tgtggccaga aggcttcgac a 51 <210> 979 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26) . . . (0) <223> 1 of 2 allelic variants (980 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25263948 <400> 979 gaaggcttcg acaagcagac gttagttgcc gtcgccaaag cgcagccgtc t 51 <210> 980 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (979 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25263948 <400> 980 gaaggcttcg acaagcagac gttagctgcc gtcgccaaag cgcagccgtc t 51 <210> 981 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (982 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25268662 <400> 981 cccttgagct ttgagctcag gtctagaggt gaacagagca gtcaccgggc g 51 <210> 982 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (981 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg25268662 <400> 982 cccttgagct ttgagctcag gtctaaggtg aacagagcag tcaccgggcg 50 <210> 983 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (984 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25268662 <400> 983 gagctttgag ctcaggtcta gaggtgaaca gagcagtcac cgggcgactc a 51 <210> 984 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (983 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25268662 <400> 984 gagctttgag ctcaggtcta gaggtaaaca gagcagtcac cgggcgactc a 51 <210> 985 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (986 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25268662 <400> 985 agagcagtca ccgggcgact cagacgggcc agcgctcagg gtccttggta a 51 <210> 986 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (985 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg25268662 <400> 986 agagcagtca ccgggcgact cagaccggcc agcgctcagg gtccttggta a 51 <210> 987 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (988 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25268662 <400> 987 acgggccagc gctcagggtc cttggtaata tatgcctaga gaaaggccat g 51 <210> 988 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (987 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg25268662 <400> 988 acgggccagc gctcagggtc cttggaatat atgcctagag aaaggccatg 50 <210> 989 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (990 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg25268662 <400> 989 cgggccagcg ctcagggtcc ttggtaatat atgcctagag aaaggccatg c 51 <210> 990 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (989 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg25268662 <400> 990 cgggccagcg ctcagggtcc ttggtatata tgcctagaga aaggccatgc 50 <210> 991 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (992 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25310296 <400> 991 aaactccatc tcaaaaaaaa aaaaaaatta gtttggggat accagtaatt t 51 <210> 992 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (991 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg25310296 <400> 992 aaactccatc tcaaaaaaaa aaaaaattag tttggggata ccagtaattt 50 <210> 993 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (994 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25310296 <400> 993 aactccatct caaaaaaaaa aaaaaattag tttggggata ccagtaattt c 51 <210> 994 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (993 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg25310296 <400> 994 aactccatct caaaaaaaaa aaaaattagt ttggggatac cagtaatttc 50 <210> 995 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (996 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg25311248 <400> 995 cacaggcaac ccgtccagcc aagcagaagc cgtggcgtag ccgacacgcc t 51 <210> 996 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (995 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg25311248 <400> 996 cacaggcaac ccgtccagcc aagcataagc cgtggcgtag ccgacacgcc t 51 <210> 997 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (998 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg25311248 <400> 997 gtccagccaa gcagaagccg tggcgtagcc gacacgcctt cgacccaacc c 51 <210> 998 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (997 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg25311248 <400> 998 gtccagccaa gcagaagccg tggcgcagcc gacacgcctt cgacccaacc c 51 <210> 999 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1000 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25311248 <400> 999 tcgtgttgtt cttcctcacc ctcattccat tgacggtcat tggttgggcc a 51 <210> 1000 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (999 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25311248 <400> 1000 tcgtgttgtt cttcctcacc ctcatcccat tgacggtcat tggttgggcc a 51 <210> 1001 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1002 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg25311248 <400>1001 tcaccctcat tccattgacg gtcattggtt gggccaacaacaaggacctc c 51 <210>1002 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1001 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg25311248 <400>1002 tcaccctcat tccattgacg gtcatcggtt gggccaacaacaaggacctc c 51 <210>1003 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1004 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg25311248 <400>1003 ccctcattcc attgacggtc attggttggg ccaacaacaaggacctccga t 51 <210>1004 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1003 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg25311248 <400>1004 ccctcattcc attgacggtc attgggtggg ccaacaacaaggacctccga t 51 <210> 1005 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1006 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25314764 <400> 1005 tatggaagaa aagtcactcg gaagtaccgt aaatcacccc agcgcctcat c 51 <210> 1006 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1005 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25314764 <400> 1006 tatggaagaa aagtcactcg gaagtgccgt aaatcacccc agcgcctcat c 51 <210> 1007 <211> 51 <212> DNA
<213> Homo sapi2ns <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1008 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25314764 <400> 1007 aagtcactcg gaagtaccgt aaatcacccc agcgcctcat cccccgaatc t 51 <210> 1008 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc feature <222> (26) . . . (0) <223> 2 of 2 allelic variants (1007 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25314764 <400> 1008 aagtcactcg gaagtaccgt aaatcgcccc agcgcctcat cccccgaatc t 51 <210> 1009 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1010 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg25314764 <400> 1009 gaagtaccgt aaatcacccc agcgcctcat cccccgaatc tgttcgccat c 51 <210> 1010 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1009 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25314764 <400> 1010 gaagtaccgt aaatcacccc agcgcgtcat cccccgaatc tgttcgccat c 51 <210> 1011 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1012 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25314764 <400> 1011 aatcacccca gcgcctcatc ccccgaatct gttcgccatc tgctgtcgcc c 51 <210> 1012 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1011 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25314764 <400> 1012 aatcacccca gcgcctcatc ccccggatct gttcgccatc tgctgtcgcc c 51 <210> 1013 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1014 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25314764 <400> 1013 tgttcgccat ctgctgtcgc ccctgcgctt aaggcatcac cccactagac t 51 <210> 1014 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1013 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25314764 <400> 1014 tgttcgccat ctgctgtcgc ccctgtgctt aaggcatcac cccactagac t 51 <210> 1015 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1016 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25314764 <400> 1015 gccatctgct gtcgcccctg cgcttaaggc atcaccccac tagactgacc g 51 <210> 1016 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1015 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25314764 <400> 1016 gccatctgct gtcgcccctg cgcttgaggc atcaccccac tagactgacc g 51 <210> 1017 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1018 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25314764 <400> 1017 ggcgacatca ccggtgacgg ttcaaggtgg cagcccgagg gcccgccgtg a 51 <210> 1018 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1017 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25314764 <400> 1018 ggcgacatca ccggtgacgg ttcaaagtgg cagcccgagg gcccgccgtg a 51 <210> 1019 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1020 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25314764 <400> 1019 aggtggcagc ccgagggccc gccgtgaact tattgtgtcg tcttatggaa g 51 <210> 1020 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1019 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg25314764 <400> 1020 aggtggcagc ccgagggccc gccgtcaact tattgtgtcg tcttatggaa g 51 <210> 1021 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1022 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg25314764 <400>1021 ggcagcccga gggcccgccg tgaacttatt gtgtcgtctt atggaagaaa 51 a <210>1022 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1021 is other entry) of <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg25314764 <400>1022 ggcagcccga gggcccgccg tgaacatatt gtgtcgtctt atggaagaaa 51 a <210>1023 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>1 2 allelic variants (1024 is other entry) of <221>miscfeature <222>(0)._ .(0) <223>Accession number cg27297262 <400>1023 cacacacaca cacacacaca cacacactca cccaagagtg ttcaaacaga 51 a <210>1024 <211>50 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ . . (0) <223>2 2 allelic variants (1023 is other entry) of <221>miscfeature <222>(25)_ . . (26) <223>Nucleotide deleted between bases and <221>miscfeature <222>(0)._ .(0) <223>Accession number cg27297262 <400>1024 cacacacaca cacacacaca cacacctcac ccaagagtgt tcaaacagaa 50 <210> 1025 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1026 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27355682 <400> 1025 gagacaggct tgtacataaa aaaaaatact tagattaatt cctggccctg t 51 <210> 1026 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1025 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg27355682 <400> 1026 gagacaggct tgtacataaa aaaaatactt agattaattc ctggccctgt 50 <210> 1027 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1028 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27360908 <400> 1027 gtgcggtatc cagcgtgaga agaaatgccg aaggtcacgg cgatgaccgc g 51 <210> 1028 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1027 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27360908 <400> 1028 gtgcggtatc cagcgtgaga agaaacgccg aaggtcacgg cgatgaccgc g 51 <210> 1029 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1030 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27364539 <400> 1029 cgctcactgt gttgtccttc cttgggtatg tctcgatggt tcagcgatgg a 51 <210> 1030 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1029 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg27364539 <400> 1030 cgctcactgt gttgtccttc cttggtatgt ctcgatggtt cagcgatgga 50 <210> 1031 <211> 51 <212> DNA

<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1032 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27369798 <400> 1031 cgacatcctg ttcacccagg gtgacatcat cagcagtaag tgttgcacag g 51 <210> 1032 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1031 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27369798 <400> 1032 cgacatcctg ttcacccagg gtgacgtcat cagcagtaag tgttgcacag g 51 <210> 1033 <211> 48 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1034 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27784915 <400> 1033 ccatagacac tcacctccga gtccgagatc ttctcctcgc tgcggccg 48 <210> 1034 <211> 48 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1033 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27784915 <400> 1034 ccatagacac tcacctccga gtccgggatc ttctcctcgc tgcggccg 48 <210> 1035 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1036 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27794839 <400> 1035 ccttcactcg caaatcgcct ctctccccac ctccccaggc ccctcctggg a 51 <210> 1036 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1035 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27794839 <400> 1036 ccttcactcg caaatcgcct ctctctccac ctccccaggc ccctcctggg a 51 <210> 1037 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1038 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27802892 <400> 1037 ttgctactgc taacatcctt taggcactgg gactatttct aatgcctggc a 51 <210> 1038 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1037 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg27802892 <400> 1038 ttgctactgc taacatcctt taggcctggg actatttcta atgcctggca 50 <210> 1039 <211> 46 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (21) ..(0) <223> 1 of 2 allelic variants (1040 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27804759 <400> 1039 acgcgtgccg aggcgctggg cggcggctgt gtgagttggt ggccca 46 <210> 1040 <211> 45 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (21) ..(0) <223> 2 of 2 allelic variants (1039 is other entry) <221> misc_feature <222> (20) .. (21) <223> Nucleotide deleted between bases 20 and 21 <221> misc_feature <222> (0) . . (0) <223> Accession number cg27804759 <400>1040 acgcgtgccg aggcgctggg ggcggctgtg tgagttggtg 45 gccca <210>1041 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1042 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg27804759 <400>1041 ctgtgtgagt tggtggccca gacgaacagc ttgtgcgagactctgggcat t 51 <210>1042 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>misc_feature <222>(26)...(0) <223>2 2 allelic variants (1041 is entry) of other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg27804759 <400>1042 ctgtgtgagt tggtggccca gacgagcagc ttgtgcgagactctgggcat t 51 <210>1043 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1044 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg27805688 <400>1043 ccagcaccag ttctgctggc cacgcgcctt gtcggcatgcagcacagggt c 51 <210>1044 <211>50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1043 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg27805688 <400> 1044 ccagcaccag ttctgctggc cacgcccttg tcggcatgca gcacagggtc 50 <210> 1045 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1046 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27806958 <400> 1045 agcagtggaa gggcagcggc gcacaggcat atccacagcc ccattgaccc a 51 <210> 1046 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1045 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27806958 <400> 1046 agcagtggaa gggcagcggc gcacaagcat atccacagcc ccattgaccc a 51 <210> 1047 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1048 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27807001 <400> 1047 acaatgccgt taacactgcc gctggcacca gcatcggctg aaccgtgacc a 51 <210> 1048 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) , <223> 2 of 2 allelic variants (1047 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg27807001 <400> 1048 acaatgccgt taacactgcc gctggaccag catcggctga accgtgacca 50 <210> 1049 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1050 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27807001 <400> 1049 accgacttta gccttaacct tgagatccgc cttacctttg acatcgactt c 51 <210> 1050 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1049 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27807001 <400> 1050 accgacttta gccttaacct tgagagccgc cttacctttg acatcgactt c 51 <210> 1051 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1052 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27807001 <400> 1051 cttctactgt cctcgaagtc gaagagagcc gagagttggg gacatcgggg g 51 <210> 1052 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1051 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27807001 <400> 1052 cttctactgt cctcgaagtc gaagaaagcc gagagttggg gacatcgggg g 51 <210> 1053 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1054 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27807001 <400> 1053 ctgtcctcga agtcgaagag agccgagagt tggggacatc gggggcactg c 51 <210> 1054 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1053 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27807001 <400> 1054 ctgtcctcga agtcgaagag agccgggagt tggggacatc gggggcactg c 51 <210> 1055 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1056 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27807001 <400> 1055 gagccgagag ttggggacat cgggggcact gccaagatgc atgaccgcca g 51 <210> 1056 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1055 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg27807001 <400> 1056 gagccgagag ttggggacat cggggcactg ccaagatgca tgaccgccag 50 <210> 1057 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1058 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27807001 <400> 1057 gatgcatgac cgccagcgca cgttcccgag cgtacttgtt caagttgtcc c 51 <210> 1058 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1057 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27807001 <400> 1058 gatgcatgac cgccagcgca cgttctcgag cgtacttgtt caagttgtcc c 51 <210> 1059 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1060 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27807001 <400> 1059 acgttcccga gcgtacttgt tcaagttgtc ccgatctgcg cgagcggcgg c 51 <210> 1060 <211> 51 <212> DNA

<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1059 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27807001 <400> 1060 acgttcccga gcgtacttgt tcaagctgtc ccgatctgcg cgagcggcgg c 51 <210> 1061 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1062 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27825769 <400> 1061 ctgtatcttt aacagtaaaa gcgtaggaag cacatagccc caatgtattt a 51 <210> 1062 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1061 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27825769 <400> 1062 ctgtatcttt aacagtaaaa gcgtacgaag cacatagccc caatgtattt a 51 <210> 1063 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1064 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27826716 <400> 1063 cgttggttga gaaggatgtc accaactgag gtatcgagat ctcatgccca c 51 <210> 1064 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1063 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27826716 <400> 1064 cgttggttga gaaggatgtc accaattgag gtatcgagat ctcatgccca c 51 <210> 1065 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1066 is other eritry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27831266 <400> 1065 taaggctgtg gaggagccag atggggacta gcctctggac ttctgcttag g 51 <210> 1066 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1065 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27831266 <400> 1066 taaggctgtg gaggagccag atgggaacta gcctctggac ttctgcttag g 51 <210> 1067 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1068 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27831595 <400> 1067 gggcctcagg gtaagctgga gttgcgggcc accgccccag gagttgagtg g 51 <210> 1068 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1067 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg27831595 <400> 1068 gggcctcagg gtaagctgga gttgcggcca ccgccccagg agttgagtgg 50 <210> 1069 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1070 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27834324 <400> 1069 catggagtca ctcagatcac gcatcgagga aagcactaag gtaacaccca g 51 <210> 1070 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1069 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27834324 <400> 1070 catggagtca ctcagatcac gcatcaagga aagcactaag gtaacaccca g 51 <210> 1071 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1072 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27835768 <400> 1071 cagctgttgt gtgcctggca gcgctgcttt cagccccatt catttccaac t 51 <210> 1072 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1071 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg27835768 <400> 1072 cagctgttgt gtgcctggca gcgctctttc agccccattc atttccaact 50 <210> 1073 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1074 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27837446 <400> 1073 tgtttgctat tttatttttt gagacaggtc tcattctgcc attcaggctg a 51 <210> 1074 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1073 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27837446 <400> 1074 tgtttgctat tttatttttt gagacgggtc tcattctgcc attcaggctg a 51 <210> 1075 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1076 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27837446 <400> 1075 tgtacgtgtg tgtgtgtgtg tgtgtgtaag tgtctgtgtg tacgtgtaag t 51 <210> 1076 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1075 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg27837446 <400> 1076 tgtacgtgtg tgtgtgtgtg tgtgttaagt gtctgtgtgt acgtgtaagt 50 <210> 1077 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1078 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27838870 <400> 1077 cgacaactcg atcgcaccga ggcgcgacac ccgcctgccc cgtactttcc c 51 <210> 1078 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1077 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27838870 <400> 1078 cgacaactcg atcgcaccga ggcgcaacac ccgcctgccc cgtactttcc c 51 <210> 1079 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1080 is other entry) <221>miscfeature <222>_ (0) .
.
(0) <223>Accession number cg27838870 <400>1079 actttcccgc catcccaagt caccggtgtg tcgctcgtca gcatcgcctc 51 a <210>1080 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1079 is other entry) of <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg27838870 <400>1080 actttcccgc catcccaagt caccgttgtg tcgctcgtca gcatcgcctc 51 a <210>1081 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ . . (0) <223>1 2 allelic variants (1082 is other entry) of <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg27840665 <400>1081 tgatacgaag gatgcgcaga ttgttggtct tacccggaat atccatcggg 51 g <210>1082 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>2 2 allelic variants (1081 is other entry) of <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg27840665 <400>1082 tgatacgaag gatgcgcaga ttgttagtct tacccggaat atccatcggg 51 g <210> 1083 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1084 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27840665 <400> 1083 gcagattgtt ggtcttaccc ggaatatcca tcggggaacc ggacaacacg a 51 <210> 1084 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1083 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27840665 <400> 1084 gcagattgtt ggtcttaccc ggaatgtcca tcggggaacc ggacaacacg a 51 <210> 1085 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1086 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27840665 <400> 1085 gacaacacga cgacgcggtc accgaccggc acgaaaccct tgtcgcgcag g 51 <210> 1086 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1085 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27840665 <400> 1086 gacaacacga cgacgcggtc accgatcggc acgaaaccct tgtcgcgcag g 51 <210> 1087 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1088 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg27842663 <400> 1087 ctagcctgga gtcaggagac agcaagagta ggggctgagg ttgtggggcc 50 <210> 1088 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1087 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27842663 <400> 1088 ctagcctgga gtcaggagac agcaaagagt aggggctgag gttgtggggc c 51 <210> 1089 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26)...(0) <223> 1 of 2 allelic variants (1090 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg27842663 <400> 1089 ctagcctgga gtcaggagac agcaagagta ggggctgagg ttgtggggcc 50 <210> 1090 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26)...(0) <223> 2 of 2 allelic variants (1089 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27842663 <400> 1090 ctagcctgga gtcaggagac agcaaagagt aggggctgag gttgtggggc c 51 <210> 1091 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1092 is other entry) <221> misc_feature <222> (0)...(0) <223> Accession number cg27842663 <400> 1091 gagacagcaa gagtaggggc tgaggttgtg gggcccaggg tcccagtgta g 51 <210> 1092 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1091 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27842663 <400> 1092 gagacagcaa gagtaggggc tgagggtgtg gggcccaggg tcccagtgta g 51 <210> 1093 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1094 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27843594 <400> 1093 aggtacagct cagggaaggg agcagcccct tgctcacggt cctttctggc a 51 <210> 1094 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1093 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg27843594 <400> 1094 aggtacagct cagggaaggg agcagccctt gctcacggtc ctttctggca 50 <210> 1095 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1096 is other entry) <221> misc feature <222> (0)...(0) <223> Accession number cg27843890 <400> 1095 cgtggttgac gatctcgccg gtggaggcgt ccttgacgac gatctggcca c 51 <210> 1096 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1095 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27843890 <400> 1096 cgtggttgac gatctcgccg gtggaagcgt ccttgacgac gatctggcca c 51 <210> 1097 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1098 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27843890 <400> 1097 tggacttcgt cggtctgcgg tacgacgaag ggctcaacat tgccggtggc a 51 <210> 1098 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1097 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27843890 <400> 1098 tggacttcgt cggtctgcgg tacgatgaag ggctcaacat tgccggtggc a 51 <210> 1099 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1100 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27843890 <400> 1099 acgaagggct caacattgcc ggtggcatcg atgatgagtt tgctcgcctg g 51 <210> 1100 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1099 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg27843890 <400> 1100 acgaagggct caacattgcc ggtggatcga tgatgagttt gctcgcctgg 50 <210> 1101 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1102 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27843890 <400> 1101 tgagtttgct cgcctgggca acacctagca gcaatggcat cgatagtccc t 51 <210> 1102 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1101 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27843890 <400> 1102 tgagtttgct cgcctgggca acacccagca gcaatggcat cgatagtccc t 51 <210> 1103 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1104 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27844015 <400> 1103 ggtaatgcgg aacgcacgtg cctgcgttca gactccattt atcttcaccg t 51 <210> 1104 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1103 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27844015 <400> 1104 ggtaatgcgg aacgcacgtg cctgcattca gactccattt atcttcaccg t 51 <210> 1105 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1106 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27845127 <400> 1105 gagcgtgcgc catgatgccg cgactgacac cacctgcggt ccagcccaaa a 51 <210> 1106 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1105 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27845127 <400> 1106 gagcgtgcgc catgatgccg cgactcacac cacctgcggt ccagcccaaa a 51 <210> 1107 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1108 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27845127 <400> 1107 aaaatcgggt gcttcttcat accaatcacg aggaggtcaa cgttgcccga g 51 <210> 1108 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1107 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27845127 <400> 1108 aaaatcgggt gcttcttcat accaaccacg aggaggtcaa cgttgcccga g 51 <210> 1109 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1110 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27845127 <400> 1109 cataccaatc acgaggaggt caacgttgcc cgagaggtcg actaaggcgt c 51 <210> 1110 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1109 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27845127 <400> 1110 cataccaatc acgaggaggt caacgctgcc cgagaggtcg actaaggcgt c 51 <210> 1111 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1112 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27845127 <400> 1111 caacgttgcc cgagaggtcg actaaggcgt cgacgggttc tccggacagc a 51 <210> 1112 <211> 51 <212> DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1111 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27845127 <400> 1112 caacgttgcc cgagaggtcg actaaagcgt cgacgggttc tccggacagc a 51 <210> 1113 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1114 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27845127 <400> 1113 agaggtcgac taaggcgtcg acgggttctc cggacagcac gcgggtctcg a 51 <210> 1114 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1113 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27845127 <400> 1114 agaggtcgac taaggcgtcg acgggctctc cggacagcac gcgggtctcg a 51 <210> 1115 <211> 47 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (22) ..(0) <223> 1 of 2 allelic variants (1116 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27845127 <400> 1115 acgcgtcctg aagccgccga cgcgacgaga acagcaggcc agcagct 47 <210> 1116 <211> 47 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (22) ..(0) <223> 2 of 2 allelic variants (1115 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27845127 <400> 1116 acgcgtcctg aagccgccga cacgacgaga acagcaggcc agcagct 47 <210> 1117 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1118 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27845127 <400> 1117 gttctccgga cagcacgcgg gtctcgacct cgacatgggg atgcttatta g 51 <210> 1118 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1117 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27845127 <400> 1118 gttctccgga cagcacgcgg gtctctacct cgacatgggg atgcttatta g 51 <210> 1119 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1120 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27845127 <400> 1119 gtctcgacct cgacatgggg atgcttatta gcgagcggct tgacgacctc g 51 <210> 1120 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1119 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27845127 <400> 1120 gtctcgacct cgacatgggg atgctcatta gcgagcggct tgacgacctc g 51 <210> 1121 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1122 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27845127 <400> 1121 cgacctcgac atggggatgc ttattagcga gcggcttgac gacctcgttg a 51 <210> 1122 <211> 51 <212> DNA
<213> Homo.sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1121 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27845127 <400> 1122 cgacctcgac atggggatgc ttattggcga gcggcttgac gacctcgttg a 51 <210> 1123 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1124 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27845127 <400> 1123 gatgcttatt agcgagcggc ttgacgacct cgttgagtcg tttgagggcc t 51 <210> 1124 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1123 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27845127 <400> 1124 gatgcttatt agcgagcggc ttgacaacct cgttgagtcg tttgagggcc t 51 <210> 1125 <211> 48 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (24) .. (0) <223> 1 of 2 allelic variants (1126 is other entry) <221> misc_feature <222> (23) ..(24) <223> Nucleotide deleted between bases 23 and 24 <221> misc_feature <222> (0) . . (0) <223> Accession number cg27845621 <400> 1125 ggatcctgtg ccagccgagg aggtccttcc caggctctct caagggtc 48 <210> 1126 <211> 49 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (24) ..(0) <223> 2 of 2 allelic variants (1125 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27845621 <400> 1126 ggatcctgtg ccagccgagg aggctccttc ccaggctctc tcaagggtc 49 <210> 1127 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1128 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27845788 <400> 1127 gcgttttggt aatgagcctg agcagtcatg ctggaccgcc caggctccca g 51 <210> 1128 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1127 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27845788 <400>1128 gcgttttggt aatgagcctg agcagccatg ctggaccgcccaggctcccag 51 <210>1129 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1130 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg27846188 <400>1129 ttcaaatcca gttcttccac agcaaccagc ccatagttgttctgtgttctt 51 <210>1130 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>2 2 allelic variants (1129 entry) of is other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg27846188 <400>1130 ttcaaatcca gttcttccac agcaatcagc ccatagttgttctgtgttctt 51 <210>1131 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1132 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg27846188 <400>1131 ttccacagca accagcccat agttgttctg tgttcttccacagctgtttac 51 <210> 1132 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1131 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27846188 <400> 1132 ttccacagca accagcccat agttgctctg tgttcttcca cagctgttta c 51 <210> 1133 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1134 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27846188 <400> 1133 tgttcttcca cagctgttta cggtagcctc ctagccactc tcctcagcaa g 51 <210> 1134 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1133 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27846188 <400> 1134 tgttcttcca cagctgttta cggtaacctc ctagccactc tcctcagcaa g 51 <210> 1135 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26)...(0) <223> 1 of 2 allelic variants (1136 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27846188 <400> 1135 tacctcactt cctccaccgc tcttcagccc ctttgatgtc ccctcagaga a 51 <210> 1136 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1135 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27846188 -<400> 1136 tacctcactt cctccaccgc tcttcggccc ctttgatgtc ccctcagaga a 51 <210> 1137 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1138 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27846188 <400> 1137 actagatcca ctgtgctttc cttcaaatcc agttcttcca cagcaaccag c 51 <210> 1138 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1137 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27846188 <400>1138 actagatcca ctgtgctttc cttcagatcc agttcttccacagcaaccag c 51 <210>1139 <211>46 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(21)_ ..(0) <223>1 2 allelic variants (1140 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg27847752 <400>1139 gcgcgccctc cctgggtgac aggctgtact tctttcacaaaaggac 46 <210>1140 <211>46 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(21)_ ..(0) <223>2 2 allelic variants (1139 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg27847752 <400>1140 gcgcgccctc cctgggtgac gggctgtact tctttcacaaaaggac 46 <210>1141 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1142 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg27847752 <400>1141 tgaggccatt cttgcactgc tataaagaaa tacccgagactgggtaattt a 51 <210>1142 <211>51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1141 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27847752 <400> 1142 tgaggccatt cttgcactgc tataacgaaa tacccgagac tgggtaattt a 51 <210> 1143 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1144 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27850121 <400> 1143 cgtcgccgaa aagccaggcc cggaggtgcc taagtcaggg accgagacgc a 51 <210> 1144 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1143 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg27850121 <400> 1144 cgtcgccgaa aagccaggcc cggagtgcct aagtcaggga ccgagacgca 50 <210> 1145 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1146 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27922967 <400> 1145 cgcgtggtac cagggaaggg gacaggattc tttgcacttt tacccctttc t 51 <210> 1146 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1145 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27922967 <400> 1146 cgcgtggtac cagggaaggg gacagaattc tttgcacttt tacccctttc t 51 <210> 1147 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26)...(0) <223> 1 of 2 allelic variants (1148 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27926321 <400> 1147 catcacctcc ctgactgcct ctcctaccac ctcccatcac ctccctgact g 51 <210> 1148 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1147 is other entry) <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg27926321 <400>1148 catcacctcc ctgactgcct ctcctcccac ctcccatcac 51 ctccctgact g <210>1149 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1150 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg27926378 <400>1149 atgggatgtt ctgtttttgt ctgtaaaggg aaagggatcatttatgttca a 51 <210>1150 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1149 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg27926378 <400>1150 atgggatgtt ctgtttttgt ctgtagaggg aaagggatcatttatgttca a 51 <210>1151 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1152 is entry) of other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg27926378 <400>1151 ttagggaagt aattaagagg ctgtgccctc tgtcacatccaagtttctgc c 51 <210> 1152 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1151 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg27926378 <400> 1152 ttagggaagt aattaagagg ctgtgcctct gtcacatcca agtttctgcc 50 <210> 1153 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1154 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27926378 <400> 1153 agggaagtaa ttaagaggct gtgccctctg tcacatccaa gtttctgccc a 51 <210> 1154 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1153 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg27926378 <400>1154 agggaagtaa ttaagaggct gtgcctctgt cacatccaagtttctgccca SO

<210>1155 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1156 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg27926927 <400>1155 atcttaagac cctcgatgga tgttgatgcg ggccgcccggtcggcgaagg g 51 <210>1156 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>2 2 allelic variants (1155 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg27926927 <400>1156 atcttaagac cctcgatgga tgttgttgcg ggccgcccggtcggcgaagg g 51 <210>1157 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1158 of is other entry) <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg27928117 <400>1157 gtggtggagg tcggggcatg gggtgcccca gccatgttcagattcctgta g 51 <210>1158 <211>50 <212>DNA

<213> Homo Sapiens <220>
<221> misc_'feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1157 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg27928117 <400> 1158 gtggtggagg tcggggcatg gggtgcccag ccatgttcag attcctgtag 50 <210> 1159 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1160 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27928408 <400> 1159 accttgggga gggcgggtag aggccgagga atctgcaggc gcagaggaca g 51 <210> 1160 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1159 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27928408 <400> 1160 , accttgggga gggcgggtag aggccaagga atctgcaggc gcagaggaca g 51 <210> 1161 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1162 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27930889 <400> 1161 acaattagat gtatggttag tctgacgatg tgataagaaa acctccccag c 51 <210> 1162 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1161 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27930889 <400> 1162 acaattagat gtatggttag tctgatgatg tgataagaaa acctccccag c 51 <210> 1163 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1164 is other entry) <221> misc_feature <zz2> (o) . . (o>
<223> Accession number cg27931448 <400> 1163 aaccaccacc ttcggccgcc ccgcgcgcca gccagcccgt acgcgctcac c 51 <210> 1164 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1163 is other entry) <221> misc feature <222> (0)...(0) <223> Accession number cg27931448 <400> 1164 aaccaccacc ttcggccgcc ccgcgagcca gccagcccgt acgcgctcac c 51 <210> 1165 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1166 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27931448 <400> 1165 agccagcccg tacgcgctca cccacaggaa ccccctcgtc cagtccctca c 51 <210> 1166 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1165 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27931448 <400> 1166 agccagcccg tacgcgctca cccacgggaa ccccctcgtc cagtccctca c 51 <210> 1167 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1168 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27931448 <400> 1167 ccgtacgcgc tcacccacag gaaccccctc gtccagtccc tcactacccc t 51 <210> 1168 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1167 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27931448 <400> 1168 ccgtacgcgc tcacccacag gaacctcctc gtccagtccc tcactacccc t 51 <210> 1169 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1170 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27931448 <400> 1169 gcgctcaccc acaggaaccc cctcgtccag tccctcacta cccctcaggc c 51 <210> 1170 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1169 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27931448 <400> 1170 gcgctcaccc acaggaaccc cctcgcccag tccctcacta cccctcaggc c 51 <210> 1171 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1172 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27931448 <400> 1171 acccacagga accccctcgt ccagtccctc actacccctc aggccctgtc a 51 <210> 1172 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1171 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27931448 <400> 1172 acccacagga accccctcgt ccagttcctc actacccctc aggccctgtc a 51 <210> 1173 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1174 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27931448 <400> 1173 ccacaggaac cccctcgtcc agtccctcac tacccctcag gccctgtcaa g 51 <210> 1174 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1173 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27931448 <400>1174 ccacaggaac cccctcgtcc agtccttcac tacccctcaggccctgtcaag 51 <210>1175 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1176 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg27931448 <400>1175 cgtccagtcc ctcactaccc ctcaggccct gtcaagccggcgccggcgcag 51 <210>1176 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>2 2 allelic variants (1175 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg27931448 <400>1176 cgtccagtcc ctcactaccc ctcagaccct gtcaagccggcgccggcgcag 51 <210>1177 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>1 2 allelic variants (1178 is entry) of other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg27933823 <400>1177 cgttaacctc ccacctctgc aatcttgccc gacacctagatacctgcgtgc 51 <210> 1178 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1177 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27933823 <400> 1178 cgttaacctc ccacctctgc aatctagccc gacacctaga tacctgcgtg c 51 <210> 1179 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1180 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27955069 <400> 1179 aaaaaaagaa aaaagaaaaa aaaaaagaat gcagtctgtc catttttgtg c 51 <210> 1180 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1179 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg27955069 <400> 1180 aaaaaaagaa aaaagaaaaa aaaaagaatg cagtctgtcc atttttgtgc 50 <210> 1181 <211> 51 <212> DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1182 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27957329 <400> 1181 gccgcgggct gagattttcg tcctgccccc ctccctgccg cccagcgcct a 51 <210> 1182 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1181 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg27957329 <400> 1182 gccgcgggct gagattttcg tcctgccccc tccctgccgc ccagcgccta 50 <210> 1183 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1184 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27958374 <400> 1183 gattggctgt acaggatagc gaatgctgtg gttggagggc acagtcttcc c 51 <210> 1184 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1183 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg27958374 <400> 1184 gattggctgt acaggatagc gaatgtgtgg ttggagggca cagtcttccc 50 <210> 1185 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1186 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27958800 <400> 1185 agtggcagga gagaggagat gggggcgtgg cagtgagcga tgaggtcaat c 51 <210> 1186 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1185 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27958800 <400> 1186 agtggcagga gagaggagat gggggtgtgg cagtgagcga tgaggtcaat c 51 <210> 1187 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26) . . . (0) <223> 1 of 2 allelic variants (1188 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27958800 <400> 1187 gagatggggg cgtggcagtg agcgatgagg tcaatctgac gaggcctgtg g 51 <210> 1188 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1187 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27958800 <400> 1188 gagatggggg cgtggcagtg agcgacgagg tcaatctgac gaggcctgtg g 51 <210> 1189 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1190 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27958800 <400> 1189 tttggcttca gctaagggag atggccgcca ctgtggagtt ttggggcaga g 51 <210> 1190 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1189 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27958800 <400> 1190 tttggcttca gctaagggag atggcagcca ctgtggagtt ttggggcaga g 51 <210> 1191 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1192 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27958800 <400> 1191 ccgccactgt ggagttttgg ggcagaggga catgctctga cttcccttta a 51 <210> 1192 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1191 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27958800 <400> 1192 ccgccactgt ggagttttgg ggcaggggga catgctctga cttcccttta a 51 <210> 1193 <211> 51 -<212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1194 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27958800 <400> 1193 tctgacttcc ctttaaatgg gtcatcatgg ctcctacgct gagggactac a 51 <210> 1194 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1193 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27958800 <400> 1194 tctgacttcc ctttaaatgg gtcatgatgg ctcctacgct gagggactac a 51 <210> 1195 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1196 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27958800 <400> 1195 catggctcct acgctgaggg actacagggg agaaggggag aaagaccagt t 51 <210> 1196 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1195 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg27958800 <400> 1196 catggctcct acgctgaggg actacgggga gaaggggaga aagaccagtt 50 <210> 1197 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1198 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27958800 <400> 1197 cttgagcgcg ccagggacag tggagaccag agtggcagga gagaggagat g 51 <210> 1198 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1197 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27958800 <400> 1198 cttgagcgcg ccagggacag tggaggccag agtggcagga gagaggagat g 51 <210> 1199 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1200 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27961578 <400> 1199 tatggaagag agagagagag agagagtttt tttttcacat ctgaattgat g 51 <210> 1200 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1199 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg27961578 <400> 1200 tatggaagag agagagagag agagattttt ttttcacatc tgaattgatg 50 <210> 1201 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1202 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg27962034 <400> 1201 gcccgcccga ccaagcgtcg gacgcggccc ggcgccgagc catggagcct g 51 <210> 1202 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1201 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg27962034 <400> 1202 gcccgcccga ccaagcgtcg gacgcgcccg gcgccgagcc atggagcctg 50 <210> 1203 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1204 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27963505 <400> 1203 cccttcgagg cccgggaaga cctccaaccc cgctgacaat gctgggccct c 51 <210> 1204 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1203 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg27963505 <400> 1204 cccttcgagg cccgggaaga cctccgaccc cgctgacaat gctgggccct c 51 <210> 1205 <211> 51 -<212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1206 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28098037 <400> 1205 gaatggagat aaaagggaat aacaattcaa ctagaaggag aagaagtcct g 51 <210> 1206 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1205 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28098037 <400>1206 gaatggagat aaaagggaat aacaactcaa ctagaaggag g 51 aagaagtcct <210>1207 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1208 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg28104192 <400>1207 taactaccga gagtgggtat ttatctagag agatagaggcttttggagcag 51 <210>1208 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1207 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg28104192 <400>1208 taactaccga gagtgggtat ttatcaagag agatagaggcttttggagcag 51 <210>1209 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ . . (0) <223>1 2 allelic variants (1210 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg28117507 <400>1209 aggcggaagc tgctccggtg ttgttggctc agtgtgccgatgccggcgtca 51 <210>1210 <211>51 <212>DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1209 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28117507 <400> 1210 aggcggaagc tgctccggtg ttgttagctc agtgtgccga tgccggcgtc a 51 <210> 1211 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1212 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28117507 <400> 1211 agtgtgccga tgccggcgtc aagcctttgt tggagggtcc agactggggt t 51 <210> 1212 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1211 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28117507 <400> 1212 agtgtgccga tgccggcgtc aagcccttgt tggagggtcc agactggggt t 51 <210> 1213 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1214 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg28117507 <400> 1213 ccggcgtcaa gcctttgttg gagggtccag actggggttt attggatcga c 51 <210> 1214 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1213 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28117507 <400> 1214 ccggcgtcaa gcctttgttg gagggcccag actggggttt attggatcga c 51 <210> 1215 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1216 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28350841 <400> 1215 gggacttgga caggcacggg ccctggcatg gcgggccagg tccacctcgg c 51 <210> 1216 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1215 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc feature <222> (0)...(0) <223> Accession number cg28350841 <400> 1216 gggacttgga caggcacggg ccctgcatgg cgggccaggt ccacctcggc 50 <210> 1217 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1218 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg28375854 <400> 1217 gcgggggccc agccatcttg cacttaatgg atggcacacg aggccagctg c 51 <210> 1218 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1217 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28375854 <400> 1218 gcgggggccc agccatcttg cacttgatgg atggcacacg aggccagctg c 51 <210> 1219 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1220 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28376296 <400> 1219 aacggagtaa gcgataaaga gtccgtagat gaacaccgcg ccgctgagga t 51 <210> 1220 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1219 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg28376296 <400> 1220 aacggagtaa gcgataaaga gtccgagatg aacaccgcgc cgctgaggat 50 <210> 1221 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1222 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28388611 <400> 1221 agatagatag atagatagat agatgataga tagatagata gatagataga t 51 <210> 1222 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1221 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg28388611 <400> 1222 agatagatag atagatagat agatgtagat agatagatag atagatagat 50 <210> 1223 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1224 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg28388611 <400> 1223 atagatagat agatagatag atgatagata gatagataga tagatagata g 51 <210> 1224 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1223 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg28388611 <400> 1224 atagatagat agatagatag atgatgatag atagatagat agatagatag 50 <210> 1225 -<211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1226 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28389525 <400> 1225 ttcgacctgg agtcacgaag cgtttgggag tggatgcgga aagtgtacat a 51 <210> 1226 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1225 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28389525 <400> 1226 ttcgacctgg agtcacgaag cgtttaggag tggatgcgga aagtgtacat a 51 <210> 1227 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1228 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28389525 <400> 1227 tcacgaagcg tttgggagtg gatgcggaaa gtgtacataa aaccaatccg c 51 <210> 1228 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1227 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28389525 <400> 1228 tcacgaagcg tttgggagtg gatgcagaaa gtgtacataa aaccaatccg c 51 <210> 1229 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1230 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28389525 <400> 1229 ttcggtcaag aggggccgtt ccgaaatcgt cccgcgtatg atctcattgt a 51 <210> 1230 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1229 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28389525 <400> 1230 ttcggtcaag aggggccgtt ccgaagtcgt cccgcgtatg atctcattgt a 51 <210> 1231 <211> 51 <212> DNA
<213> Homo sapiens , <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1232 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28389525 <400> 1231 taaatttcaa agatcccaag gaccatgagc gtttcatgaa gctcgttgag c 51 <210> 1232 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1231 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28389525 <400>1232 taaatttcaa agatcccaag gaccacgagc gtttcatgaa 51 gctcgttgag c <210>1233 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1234 entry) of is other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg28389807 <400>1233 accttctgta tgctggcatt gcagacccag caaggagccaaacgaatgaa a 51 <210>1234 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1233 entry) of is other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg28389807 <400>1234 accttctgta tgctggcatt gcagatccag caaggagccaaacgaatgaa a 51 <210>1235 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ . . (0) <223>1 2 allelic variants (1236 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg28396311 <400>1235 gcacgaggcc tgacactttg cgggagccct ggaggaaacaggtggttgct g 51 <210> 1236 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1235 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg28396311 <400> 1236 gcacgaggcc tgacactttg cgggaccctg gaggaaacag gtggttgctg 50 <210> 1237 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1238 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28397512 <400> 1237 ttttgctgtc agcaaccata gccacgggta taccagcttc tgcattttct g 51 <210> 1238 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1237 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28397512 <400> 1238 ttttgctgtc agcaaccata gccacaggta taccagcttc tgcattttct g 51 <210> 1239 <211> 51 <212> DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1240 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28397512 <400> 1239 gcctccacct gtgctaggtg ggcccctctg ggttctaagg catctctgta t 51 <210> 1240 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1239 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg28397512 <400> 1240 gcctccacct gtgctaggtg ggccctctgg gttctaaggc atctctgtat 50 <210> 1241 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1242 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28399769 <400> 1241 gggtccaggg aggagagcgc ggcgcgggcg gctgagcgcg aagagggagt g 51 <210> 1242 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1241 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg28399769 <400> 1242 gggtccaggg aggagagcgc ggcgcggcgg ctgagcgcga agagggagtg 50 <210> 1243 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1244 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28453626 <400> 1243 gagtggttca ccttttactt ggtcaatcag ggggtttgtg ttcccaggaa c 51 <210> 1244 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1243 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28453626 <400> 1244 gagtggttca ccttttactt ggtcagtcag ggggtttgtg ttcccaggaa c 51 <210> 1245 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26)...(0) <223> 1 of 2 allelic variants (1246 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28458642 <400> 1245 ggaaggtcag acccgcgtca cccgcgaacg aaatggcctc ggatgcgtca g 51 <210> 1246 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1245 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28458642 <400> 1246 ggaaggtcag acccgcgtca cccgcaaacg aaatggcctc ggatgcgtca g 51 <210> 1247 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1248 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28464065 <400> 1247 tgtccacgaa atacacccca aacccgaagc cttctctcca ccaagtccaa g 51 <210> 1248 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1247 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28464065 <400>1248 tgtccacgaa atacacccca aacccaaagc cttctctccaccaagtccaag 51 <210>1249 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1250 of is other entry) <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg28464080 <400>1249 gtggatggca gccagagaga ctgctgaggt tctggatgttagggccttgat 51 <210>1250 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1249 of is other entry) <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg28464080 <400>1250 gtggatggca gccagagaga ctgctcaggt tctggatgttagggccttgat 51 <210>1251 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1252 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg28464080 <400>1251 ggggacagcc gagggcgagt ggtcttggaa gcgtgccatgtgcaggacaca 51 <210>1252 <211>51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1251 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg28464080 <400> 1252 ggggacagcc gagggcgagt ggtctcggaa gcgtgccatg tgcaggacac a 51 <210> 1253 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1254 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28473092 <400> 1253 tggcgagggt cagcagtctt ctcggcgtcg tcaggtcgag catggtactc g 51 <210> 1254 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1253 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28473092 <400> 1254 tggcgagggt cagcagtctt ctcggtgtcg tcaggtcgag catggtactc g 51 <210> 1255 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1256 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28473092 <400> 1255 gacggttaag gatttgcgag ctaataacga tcggagcgtc accctcgagc a 51 <210> 1256 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1255 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28473092 <400> 1256 gacggttaag gatttgcgag ctaatgacga tcggagcgtc accctcgagc a 51 <210> 1257 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1258 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28473092 <400> 1257 ggatttgcga gctaataacg atcggagcgt caccctcgag catcgtcacc t 51 <210> 1258 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1257 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28473092 <400> 1258 ggatttgcga gctaataacg atcggggcgt caccctcgag catcgtcacc t 51 <210> 1259 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1260 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28473092 <400> 1259 gcgagctaat aacgatcgga gcgtcaccct cgagcatcgt cacctcgatg c 51 <210> 1260 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1259 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28473092 <400> 1260 gcgagctaat aacgatcgga gcgtcgccct cgagcatcgt cacctcgatg c 51 <210> 1261 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1262 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28473092 <400> 1261 cgatgctaat tagagccatg tgccgatgag tgaaggagac catccgcgag g 51 <210> 1262 <211> 51 <212> DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1261 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28473092 <400> 1262 cgatgctaat tagagccatg tgccggtgag tgaaggagac catccgcgag g 51 <210> 1263 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1264 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28473092 <400> 1263 ttgcccgccg gggtgcgcca taccaactcc cgacacagga caccctcgcg g 51 <210> 1264 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1263 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28473092 <400> 1264 ttgcccgccg gggtgcgcca taccagctcc cgacacagga caccctcgcg g 51 <210> 1265 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1266 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg28473092 <400> 1265 gtttatacga ctggatctcg ttgatactga gcaggagtgg ttcgtcatcc a 51 <210> 1266 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1265 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg28473092 <400> 1266 gtttatacga ctggatctcg ttgatgctga gcaggagtgg ttcgtcatcc a 51 <210> 1267 <211> 47 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (22) ..(0) <223> 1 of 2 allelic variants (1268 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28473115 <400> 1267 tcatgaaatg tttgttggta aggtaccatt taaccttttt ttccaat 47 <210> 1268 <211> 47 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (22) ..(0) <223> 2 of 2 allelic variants (1267 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28473115 <400> 1268 tcatgaaatg tttgttggta aagtaccatt taaccttttt ttccaat 47 <210> 1269 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1270 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28785423 <400> 1269 gggtttagct agcatgtagc aagcccttaa tgactgcagc tattatcata a 51 <210> 1270 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1269 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28785423 <400> 1270 gggtttagct agcatgtagc aagcctttaa tgactgcagc tattatcata a 51 <210> 1271 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1272 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28785423 <400> 1271 atgtagcaag cccttaatga ctgcagctat tatcataatt agctctgtat g 51 <210> 1272 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1271 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg28785423 <400> 1272 atgtagcaag cccttaatga ctgcaactat tatcataatt agctctgtat g 51 <210> 1273 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1274 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg28785423 <400> 1273 ctattatcat aattagctct gtatgacttt ttacattcat cagatccctt a 51 <210> 1274 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1273 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg28785423 <400> 1274 ctattatcat aattagctct gtatgctttt tacattcatc agatccctta 50 <210> 1275 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1276 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28786600 <400> 1275 ggatgcaccc acgctgggcg cccagcggcc tctaaccgcc gccccagccc a 51 <210> 1276 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1275 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg28786600 <400> 1276 ggatgcaccc acgctgggcg cccagggcct ctaaccgccg ccccagccca 50 <210> 1277 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1278 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28790405 <400> 1277 ggtatgcctc actacccggg gcgtagccga cgcgacttcg aggaaaacgt g 51 <210> 1278 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1277 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg28790405 <400> 1278 ggtatgcctc actacccggg gcgtaccgac gcgacttcga ggaaaacgtg 50 <210> 1279 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1280 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28814812 <400> 1279 taataacagc agagttaccc taagacatac aatctgctgc gtgtatgcta a 51 <210> 1280 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1279 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28814812 <400> 1280 taataacagc agagttaccc taagatatac aatctgctgc gtgtatgcta a 51 <210> 1281 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1282 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28821175 <400> 1281 actattgcca atattttaaa acactaattt gcctttaaac tagagattta a 51 <210> 1282 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1281 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28821175 <400> 1282 actattgcca atattttaaa acacttattt gcctttaaac tagagattta a 51 <210> 1283 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1284 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28955364 <400> 1283 caataaccgc ggtgggtgtg cagcaggaag ttttccagta cctgatagcc g 51 <210> 1284 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1283 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28955364 <400> 1284 caataaccgc ggtgggtgtg cagcaagaag ttttccagta cctgatagcc g 51 <210> 1285 <211> S1 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1286 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28955364 <400> 1285 tgtgcagcag gaagttttcc agtacctgat agccgtcacc ttcgggtgcg t 51 <210> 1286 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1285 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28955364 <400> 1286 tgtgcagcag gaagttttcc agtacttgat agccgtcacc ttcgggtgcg t 51 <210> 1287 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1288 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg28955364 <400> 1287 agccgtcacc ttcgggtgcg ttgatctcgt aatggaatcg agcgctgtca c 51 <210> 1288 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1287 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28955364 <400> 1288 agccgtcacc ttcgggtgcg ttgatgtcgt aatggaatcg agcgctgtca c 51 <210> 1289 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1290 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28955364 <400> 1289 cagttttgaa tcgcgatggc Cttggctacg ggggtagatt tccccttgat a 51 <210> 1290 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1289 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28955364 <400> 1290 cagttttgaa tcgcgatggc cttggttacg ggggtagatt tccccttgat a 51 <210> 1291 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1292 is other entry) <221> misc feature <222> (0)...(0) <223> Accession number cg28955364 <400> 1291 tccccttgat aattcggtta gttaactccc ctatgtcgga tggaacgttg g 51 <210> 1292 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1291 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28955364 <400> 1292 tccccttgat aattcggtta gttaagtccc ctatgtcgga tggaacgttg g 51 <210> 1293 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1294 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28955364 <400> 1293 ttgataattc ggttagttaa ctcccctatg tcggatggaa cgttggcagg g 51 <210> 1294 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1293 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28955364 <400> 1294 ttgataattc ggttagttaa ctcccttatg tcggatggaa cgttggcagg g 51 <210> 1295 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1296 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg28955364 <400> 1295 aattcggtta gttaactccc ctatgtcgga tggaacgttg gcagggactt c 51 <210> 1296 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221>.misc feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1295 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg28955364 <400> 1296 aattcggtta gttaactccc ctatgccgga tggaacgttg gcagggactt c 51 <210> 1297 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1298 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28955364 <400> 1297 actcccctat gtcggatgga acgttggcag ggacttcggt gtacaccgag t 51 <210> 1298 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1297 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28955364 <400> 1298 actcccctat gtcggatgga acgttagcag ggacttcggt gtacaccgag t 51 <210> 1299 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1300 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28955364 <400> 1299 gggacttcgg tgtacaccga gttatgtggg gtgccggctt tcgcgttatc g 51 <210> 1300 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1299 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28955364 <400> 1300 gggacttcgg tgtacaccga gttatttggg gtgccggctt tcgcgttatc g 51 <210> 1301 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1302 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28955364 <400>1301 acaccgagtt atgtggggtg ccggctttcg cgttatcgaaggttactgga t 51 <210>1302 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1301 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg28955364 <400>1302 acaccgagtt atgtggggtg ccggccttcg cgttatcgaaggttactgga t 51 <210>1303 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1304 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg28955364 <400>1303 acggaatacc ttcaagtcgt gccatgagtg ccattgacgccgcgaaatgg a 51 <210>1304 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1303 of is other entry) <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg28955364 <400>1304 acggaatacc ttcaagtcgt gccataagtg ccattgacgccgcgaaatgg a 51 <210> 1305 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1306 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg28955364 <400> 1305 acgccgcgaa atggatgcaa taaccgcggt gggtgtgcag caggaagttt t 51 <210> 1306 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1305 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28955364 <400> 1306 acgccgcgaa atggatgcaa taaccacggt gggtgtgcag caggaagttt t 51 <210> 1307 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1308 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28955364 <400> 1307 atggatgcaa taaccgcggt gggtgtgcag caggaagttt tccagtacct g 51 <210> 1308 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26)...(0) <223> 2 of 2 allelic variants (1307 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg28955364 <400> 1308 atggatgcaa taaccgcggt gggtgcgcag caggaagttt tccagtacct g 51 <210> 1309 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1310 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg28961882 <400> 1309 aacagaatgc aaacaatcaa aaacatagtc catttaaact atctgggcga c 51 <210> 1310 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26)...(0) <223> 2 of 2 allelic variants (1309 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg28961882 <400> 1310 aacagaatgc aaacaatcaa aaacaagtcc atttaaacta tctgggcgac 50 <210> 1311 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1312 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg28961882 <400> 1311 tggcagttct gctgagattt tttttaggac tttcctgaag cttagcttca 50 <210> 1312 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1311 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28961882 <400> 1312 tggcagttct gctgagattt ttttttagga ctttcctgaa gcttagcttc a 51 <210> 1313 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1314 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28961882 <400> 1313 acatagtcca tttaaactat ctgggcgaca aaatgggcac ttaattttac t 51 <210> 1314 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1313 is other entry) <221> misc feature <222> (0)...(0) <223> Accession number cg28961882 <400> 1314 acatagtcca tttaaactat ctgggtgaca aaatgggcac ttaattttac t 51 <210> 1315 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1316 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28970326 <400> 1315 catggcctgt catggcgtag tcttccacgt cgtaaagtat gagacaatcc a 51 <210> 1316 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1315 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg28970326 <400> 1316 catggcctgt catggcgtag tcttctacgt cgtaaagtat gagacaatcc a 51 <210> 1317 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1318 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg28970326 <400>1317 gggtccatga ggagttcgtc caaggttcga actcattacc 50 gtcgaatacg <210>1318 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1317 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg28970326 <400>1318 gggtccatga ggagttcgtc caagggttcg aactcattaccgtcgaatac g 51 <210>1319 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>1 2 allelic variants (1320 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg28972181 <400>1319 agctggttct ctccgaaatg catttgggtg cagcgtcgggtcattacgtc c 51 <210>1320 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>2 2 allelic variants (1319 is entry) of other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg28972181 <400>1320 agctggttct ctccgaaatg catttaggtg cagcgtcgggtcattacgtc c 51 <210>1321 <211>51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1322 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28972181 <400> 1321 aaatgcattt gggtgcagcg tcgggtcatt acgtcccggg ggtagagcta c 51 <210> 1322 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1321 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28972181 <400> 1322 aaatgcattt gggtgcagcg tcggggcatt acgtcccggg ggtagagcta c 51 <210> 1323 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1324 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28972181 <400> 1323 cgggggtaga gctactggat gcttgcgggc ccgtatcggg taccaacagc a 51 <210> 1324 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1323 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg28972181 <400> 1324 cgggggtaga gctactggat gcttgagggc ccgtatcggg taccaacagc a 51 <210> 1325 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1326 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg28986449 <400> 1325 agggaagagc aagttggtct ggaacacaaa aagggccggg atctcctttg g 51 <210> 1326 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1325 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg28986449 <400> 1326 agggaagagc aagttggtct ggaacgcaaa aagggccggg atctcctttg g 51 <210> 1327 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1328 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg29004129 <400> 1327 cgcaagattt cgaggcaact cggtatcact cactgtgctt gaccacgttg g 51 <210> 1328 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1327 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29004129 <400> 1328 cgcaagattt cgaggcaact cggtaccact cactgtgctt gaccacgttg g 51 <210> 1329 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1330 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29012565 <400> 1329 cccattcgga aaatcaatcc gggggcgtcg gctgggttag tcacggcggg c 51 <210> 1330 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1329 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29012565 <400> 1330 cccattcgga aaatcaatcc gggggtgtcg gctgggttag tcacggcggg c 51 <210> 1331 <211> 51 <212> DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1332 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29012565 <400> 1331 ggcaaagcca cggttgtccc tcctgaatga gctagattac cctaccctac c 51 <210> 1332 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1331 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29012565 <400> 1332 ggcaaagcca cggttgtccc tcctggatga gctagattac cctaccctac c 51 <210> 1333 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1334 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29141731 <400> 1333 atagggggga tattttgggg tggtggtagt ggtggtctgt tttccagata t 51 <210> 1334 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1333 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29141731 <400> 1334 atagggggga tattttgggg tggtgttagt ggtggtctgt tttccagata t 51 <210> 1335 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1336 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29141731 <400> 1335 aatattcagt aagctttttg aagctcctta cacatccgta aaacttctca g 51 <210> 1336 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1335 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29141731 <400> 1336 aatattcagt aagctttttg aagctactta cacatccgta aaacttctca g 51 <210> 1337 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1338 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29144273 <400> 1337 atgggataag atgtaagttt ttaatactag caatgtacac tactcttttt t 51 <210> 1338 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1337 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29144273 <400> 1338 atgggataag atgtaagttt ttaatgctag caatgtacac tactcttttt t 51 <210> 1339 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1340 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg29144339 <400> 1339 aagcaaaacc catcgggggg gggggacatc tacatgccat ctttggtgct 50 <210> 1340 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1339 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29144339 <400> 1340 aagcaaaacc catcgggggg ggggggacat ctacatgcca tctttggtgc t 51 <210> 1341 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1342 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg29195033 <400> 1341 ccgctcatag tgtcgtcagt cagaatcttc atcattgccg atacgtgatc g 51 <210> 1342 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1341 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29195033 <400> 1342 ccgctcatag tgtcgtcagt cagaaccttc atcattgccg atacgtgatc g 51 <210> 1343 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1344 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29202844 <400> 1343 ccgccacccc actctaggcc tccctgtggt tcagcatcct caaccccgct t 51 <210> 1344 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1343 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29202844 <400> 1344 ccgccacccc actctaggcc tccctatggt tcagcatcct caaccccgct t 51 <210> 1345 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1346 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29207528 <400> 1345 cgggtcaggg gcgttcgcgg cgccagctgg cacaacttcg cgaccggcga c 51 <210> 1346 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1345 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg29207528 <400> 1346 cgggtcaggg gcgttcgcgg cgccactggc acaacttcgc gaccggcgac 50 <210> 1347 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1348 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29207528 <400> 1347 cttcgacgcc aacgagcttg ccgtagctcc tgatactgac accgtcatcc a 51 <210> 1348 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1347 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg29207528 <400> 1348 cttcgacgcc aacgagcttg ccgtaactcc tgatactgac accgtcatcc a 51 <210> 1349 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1350 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29207528 <400> 1349 tactgacacc gtcatccagg gagtcgggcc cgccctagcc ctcctcgatc c 51 <210> 1350 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1349 is other entry) <221> misc_feature ' <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg29207528 <400>1350 tactgacacc gtcatccagg gagtcggccc gccctagccctcctcgatcc 50 <210>1351 <211>51 <212>DNA

<213>Homo.sapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>1 2 allelic variants (1352 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg29207528 <400>1351 cctcgtcgac acatgccgat aacccgacag cccaggcatggcgcgatttc g 51 <210>1352 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1351 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg29207528 <400>1352 cctcgtcgac acatgccgat aacccaacag cccaggcatggcgcgatttc g 51 <210>1353 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1354 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg29207528 <400>1353 ctgcgcgtcg cagatgccgc acaggcacgg gtcaggggcgttcgcggcgc c 51 <210> 1354 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1353 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg29207528 <400> 1354 ctgcgcgtcg cagatgccgc acaggacggg tcaggggcgt tcgcggcgcc 50 <210> 1355 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1356 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29210581 <400> 1355 tttttcctga gttatggaag gaatggtaat tggggaattc aggcttaaaa t 51 <210> 1356 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1355 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29210581 <400> 1356 tttttcctga gttatggaag gaatgataat tggggaattc aggcttaaaa t 51 <210> 1357 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1358 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29216983 <400> 1357 gcattctgtg aggctaccgc aggctctggc gtaaagcagt ggagccaggt c 51 <210> 1358 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1357 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29216983 <400> 1358 gcattctgtg aggctaccgc aggctttggc gtaaagcagt ggagccaggt c 51 <210> 1359 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1360 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29217243 <400> 1359 ggcgcggcgc tccatccaaa tcgatctggg catccgcccc tgtcaccgca a 51 <210> 1360 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc feature <222> (26)...(0) <223> 2 of 2 allelic variants (1359 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29217243 <400> 1360 ggcgcggcgc tccatccaaa tcgatttggg catccgcccc tgtcaccgca a 51 <210> 1361 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1362 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29217243 <400> 1361 cagcaccatt accgacgagc cgagcaccgt ccagataggc ccggcgatcc c 51 <210> 1362 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . . (0) <223> 2 of 2 allelic variants (1361 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29217243 <400> 1362 cagcaccatt accgacgagc cgagcgccgt ccagataggc ccggcgatcc c 51 <210> 1363 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1364 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29217243 <400> 1363 gccgagcacc gtccagatag gcccggcgat cccatgctcc gcagccactg a 51 <210> 1364 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1363 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg29217243 <400> 1364 gccgagcacc gtccagatag gcccgacgat cccatgctcc gcagccactg a 51 <210> 1365 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1366 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29217243 <400> 1365 ttcctagatc cgcccaaccg cgacggccag cgtcctcaat gagggttctc g 51 <210> 1366 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1365 is other entry) <221> misc_feature <222> (0)...(0) <223> Accession number cg29217243 <400> 1366 ttcctagatc cgcccaaccg cgacgtccag cgtcctcaat gagggttctc g 51 <210> 1367 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1368 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29217243 <400> 1367 cgcgacggcc agcgtcctca atgagggttc tcggcccggc tgtctctact a 51 <210> 1368 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1367 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29217243 <400> 1368 cgcgacggcc agcgtcctca atgagagttc tcggcccggc tgtctctact a 51 <210> 1369 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1370 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29234950 <400> 1369 caacccaggg gcccctctcc gagggtaccc cacaggccac acggtggcga c 51 <210> 1370 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1369 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29234950 <400> 1370 caacccaggg gcccctctcc gagggcaccc cacaggccac acggtggcga c 51 <210> 1371 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1372 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29237731 <400> 1371 ctcaatcctg acagataccg atcataaggc aatggcactc caggagtatt t 51 <210> 1372 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1371 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg2923'7731 <400> 1372 ctcaatcctg acagataccg atcatgaggc aatggcactc caggagtatt t 51 <210> 1373 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1374 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29237731 <400> 1373 aatcctgaca gataccgatc ataaggcaat ggcactccag gagtatttcc t 51 <210> 1374 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1373 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29237731 <400> 1374 aatcctgaca gataccgatc ataagccaat ggcactccag gagtatttcc t 51 <210> 1375 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1376 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29239003 <400> 1375 ggattccact ttccctgtcc cctacctccc caaactcttg caagaaaata a 51 <210> 1376 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1375 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29239003 <400> 1376 ggattccact ttccctgtcc cctacttccc caaactcttg caagaaaata a 51 <210> 1377 <211> 51 <212> DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1378 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg29250853 <400> 1377 cgtacgagat cacgttcctc acccagctcc ccaaagacct cacgtgcagc g 51 <210> 1378 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1377 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg29250853 <400> 1378 cgtacgagat cacgttcctc acccatctcc ccaaagacct cacgtgcagc g 51 <210> 1379 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1380 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29255997 <400> 1379 aaacaaggaa gagtaggatg gaatcggaat aaaacagtga aagaacatta t 51 <210> 1380 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1379 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg29255997 <400> 1380 aaacaaggaa gagtaggatg gaatcgaata aaacagtgaa agaacattat 50 <210> 1381 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1382 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg29255997 <400> 1381 aggatggaat cggaataaaa cagtgaaaga acattattct ttgtaccgtg a 51 <210> 1382 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1381 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29255997 <400> 1382 aggatggaat cggaataaaa cagtggaaga acattattct ttgtaccgtg a 51 <210> 1383 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1384 is other entry) <221> misc feature <222> (0)...(0) <223> Accession number cg29256466 <400> 1383 tgaatataag gctagataat ggagcgtttg tgatcccttg tctattctca g 51 <210> 1384 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1383 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29256466 <400> 1384 tgaatataag gctagataat ggagcatttg tgatcccttg tctattctca g 51 <210> 1385 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1386 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29260975 <400> 1385 ctgcaatgag ctgtgaccac gccactgcac tccagcctgg gcgacagagc a 51 <210> 1386 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1385 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg29260975 <400> 1386 ctgcaatgag ctgtgaccac gccaccgcac tccagcctgg gcgacagagc a 51 <210> 1387 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1388 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29260975 <400> 1387 ccagcctggg cgacagagca agaccatgat atttcaagaa aagtccttga g 51 <210> 1388 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1387 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29260975 <400> 1388 ccagcctggg cgacagagca agaccgtgat atttcaagaa aagtccttga g 51 <210> 1389 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1390 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29264501 <400> 1389 ctccccaacc cactccccag taacagaggg ttttccccga ttctcacagt g 51 <210> 1390 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1389 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29264501 <400> 1390 ctccccaacc cactccccag taacacaggg ttttccccga ttctcacagt g 51 <210> 1391 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1392 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg29337682 <400> 1391 gtggtgcatg cctgtaatcc cagcactttg ggaggctgag gcaggaggat c 51 <210> 1392 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1391 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg29337682 <400> 1392 gtggtgcatg cctgtaatcc cagcaatttg ggaggctgag gcaggaggat c 51 <210> 1393 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1394 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29345077 <400>1393 actcccgacc tcaggtgatc cgcccacctc ggcctcccaaagtgctggga t 51 <210>1394 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>2 2 allelic variants (1393 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg29345077 <400>1394 actcccgacc tcaggtgatc cgcccgcctc ggcctcccaaagtgctggga t 51 <210>1395 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1396 entry) of is other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg29345273 <400>1395 cttatggcac gggggctgca gcctggcctc ctcctccaggtgggatgcct c 51 <210>1396 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1395 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg29345273 <400>1396 cttatggcac gggggctgca gcctgccctc ctcctccaggtgggatgcct c 51 <210> 1397 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1398 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29345769 <400> 1397 ctgtattaag acttaaactc ctgccgcacc tggagtaata aacttgtggg a 51 <210> 1398 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1397 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29345769 <400> 1398 ctgtattaag acttaaactc ctgccacacc tggagtaata aacttgtggg a 51 <210> 1399 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1400 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29346973 <400> 1399 agttatctca taattaaaaa aaaaaactag ctcgttagaa ttagaatcta a 51 <210> 1400 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> mist feature <222> (26)...(0) <223> 2 of 2 allelic variants (1399 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg29346973 <400> 1400 agttatctca taattaaaaa aaaaactagc tcgttagaat tagaatctaa 50 <210> 1401 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1402 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg29348101 <400> 1401 ccgctcaggc tgctgctgcg ggcgccgtgt ggtactccgc cgaaggcgat a 51 <210> 1402 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1401 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg29348101 <400> 1402 ccgctcaggc tgctgctgcg ggcgctgtgt ggtactccgc cgaaggcgat a 51 <210> 1403 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1404 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348101 <400> 1403 ccgccgaagg cgataagtgg aaggtcgata ccaacggtga caagagcaaa g 51 <210> 1404 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1403 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348101 <400> 1404 ccgccgaagg cgataagtgg aaggttgata ccaacggtga caagagcaaa g 51 <210> 1405 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1406 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348101 <400> 1405 ataagtggaa ggtcgatacc aacggtgaca agagcaaagt tgttgccgat t 51 <210> 1406 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1405 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348101 <400> 1406 ataagtggaa ggtcgatacc aacggcgaca agagcaaagt tgttgccgat t 51 <210> 1407 <211> 44 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1408 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348101 <400> 1407 cgacgacaag agcgctgtca ctgacccccg ttggagcgac gcgt 44 <210> 1408 <211> 44 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1407 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348101 <400> 1408 cgacgacaag agcgctgtca ctgacgcccg ttggagcgac gcgt 44 <210> 1409 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1410 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348101 <400> 1409 tgctttcctc cgccaagaag gctgccgcca agggcaagta catcctcgga t 51 <210> 1410 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1409 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348101 <400> 1410 tgctttcctc cgccaagaag gctgctgcca agggcaagta catcctcgga t 51 <210> 1411 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1412 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348101 <400> 1411 tttcctccgc caagaaggct gccgccaagg gcaagtacat cctcggattt g 51 <210> 1412 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1411 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348101 <400> 1412 tttcctccgc caagaaggct gccgctaagg gcaagtacat cctcggattt g 51 <210> 1413 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1414 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348230 <400> 1413 tcagagggtg agaaagccca gagcatttta catgtttagg attttgactt t 51 <210> 1414 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1413 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348230 <400> 1414 tcagagggtg agaaagccca gagcatttac atgtttagga ttttgacttt 50 <210> 1415 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1416 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348328 <400> 1415 tgcattacca agagctgacg atctctggag gatcgaatgc cagtcgggca g 51 <210> 1416 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1415 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348328 <400> 1416 tgcattacca agagctgacg atctccggag gatcgaatgc cagtcgggca g 51 <210> 1417 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1418 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348328 <400> 1417 tctctggagg atcgaatgcc agtcgggcag acgttcaccg ggcggtcgac a 51 <210> 1418 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1417 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348328 <400> 1418 tctctggagg atcgaatgcc agtcgagcag acgttcaccg ggcggtcgac a 51 <210> 1419 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1420 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg29348328 <400> 1419 atgctcggac ggggaaatat cgacgggacc cccattgtca ctcacacttt t 51 <210> 1420 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1419 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348328 <400> 1420 atgctcggac ggggaaatat cgacgagacc cccattgtca ctcacacttt t 51 <210> 1421 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1422 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348328 <400> 1421 tgctcggacg gggaaatatc gacgggaccc ccattgtcac tcacactttt g 51 <210> 1422 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1421 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg29348328 <400> 1422 tgctcggacg gggaaatatc gacggaaccc ccattgtcac tcacactttt g 51 <210> 1423 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26)...(0) <223> 1 of 2 allelic variants (1424 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348328 <400> 1423 cttttggcct gtcccagtgg accgaggctg ttgacgccgt gcgcggtcac g 51 <210> 1424 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1423 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348328 <400> 1424 cttttggcct gtcccagtgg accgaagctg ttgacgccgt gcgcggtcac g 51 <210> 1425 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1426 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348328 <400> 1425 gctgttgacg ccgtgcgcgg tcacgccggc gtcaagatcg ctatcgatcc c 51 <210> 1426 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1425 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348328 <400>1426 gctgttgacg ccgtgcgcgg tcacgtcggc gtcaagatcgctatcgatcc c 51 <210>1427 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1428 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg29348328 <400>1427 ttgacgccgt gcgcggtcac gccggcgtca agatcgctatcgatccccgc c 51 <210>1428 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1427 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg29348328 <400>1428 ttgacgccgt gcgcggtcac gccggtgtca agatcgctatcgatccccgc c 51 <210>1429 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1430 entry) of is other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg29348328 <400>1429 gacgcgtgag ttggtttgct ggttttccca agggatcaacgacgaccatc a 51 <210>1430 <211>51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1429 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg29348328 <400> 1430 gacgcgtgag ttggtttgct ggtttcccca agggatcaac gacgaccatc a 51 <210> 1431 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1432 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348397 <400> 1431 ttatgttatt tataaaacga ccaaggaaat gaatgtaatt tggtcttcat a 51 <210> 1432 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1431 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg29348397 <400> 1432 ttatgttatt tataaaacga ccaagaaaat gaatgtaatt tggtcttcat a 51 <210> 1433 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1434 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348993 <400> 1433 gtttgtttgt tttaactttt tttttttcat tctcgctgta gatagcctga a 51 <210> 1434 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1433 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348993 <400> 1434 gtttgtttgt tttaactttt ttttttcatt ctcgctgtag atagcctgaa 50 <210> 1435 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1436 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348993 <400> 1435 tttgtttgtt ttaacttttt ttttttcatt ctcgctgtag atagcctgaa t 51 <210> 1436 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1435 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348993 <400> 1436 tttgtttgtt ttaacttttt tttttcattc tcgctgtaga tagcctgaat 50 <210> 1437 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1438 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348993 <400> 1437 tcgctgtaga tagcctgaat ccaaagaaaa ccaaaagggg ttatccaagt a 51 <210> 1438 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1437 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29348993 <400> 1438 tcgctgtaga tagcctgaat ccaaaaaaaa ccaaaagggg ttatccaagt a 51 <210> 1439 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1440 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29349829 <400> 1439 cataggcacc gcgtgaaggg caccgtaaga atcttcccga atgctcctgt c 51 <210> 1440 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1439 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg29349829 <400> 1440 cataggcacc gcgtgaaggg caccgaagaa tcttcccgaa tgctcctgtc 50 <210> 1441 <211> ~51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1442 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29349990 <400> 1441 tccgggtggg gaacggcgat cagcgccagc ttggcgcttt cgacgttggt c 51 <210> 1442 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1441 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29349990 <400> 1442 tccgggtggg gaacggcgat cagcgtcagc ttggcgcttt cgacgttggt c 51 <210> 1443 <211> 51 .
<212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1444 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29351920 <400> 1443 tcaggagttt gagaccagcc tggccagcat ggcgaaaccc catctctact a 51 <210> 1444 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1443 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29351920 <400> 1444 tcaggagttt gagaccagcc tggccggcat ggcgaaaccc catctctact a 51 <210> 1445 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1446 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29352964 <400> 1445 ggaaggtgtg cggatactta ttgtcggtgc ggcatcgtcc atccacaccg t 51 <210> 1446 <211> 51 <212> DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1445 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29352964 <400> 1446 ggaaggtgtg cggatactta ttgtcagtgc ggcatcgtcc atccacaccg t 51 <210> 1447 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1448 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29352964 <400> 1447 gccgtcactc cattgatccc cgagtccgga tccatctggc cccacacggc g 51 <210> 1448 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1447 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29352964 <400> 1448 gccgtcactc cattgatccc cgagttcgga tccatctggc cccacacggc g 51 <210> 1449 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1450 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29352964 <400> 1449 ccattgatcc ccgagtccgg atccatctgg ccccacacgg cgggaaggca a 51 <210> 1450 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1449 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg29352964 <400> 1450 ccattgatcc ccgagtccgg atccacctgg ccccacacgg cgggaaggca a 51 <210> 1451 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1452 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29352964 <400> 1451 cgaccggtta tggtctgctc gctcgtcttg cccatattga cgccccgacg c 51 <210> 1452 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1451 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg29352964 <400> 1452 cgaccggtta tggtctgctc gctcgccttg cccatattga cgccccgacg c 51 <210> 1453 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1454 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29352964 <400> 1453 ccccgacgct gctgtcggtg tgggggagtg acgtttacga ttccccccgg g 51 <210> 1454 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ...~(0) <223> 2 of 2 allelic variants (1453 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29352964 <400> 1454 ccccgacgct gctgtcggtg tggggaagtg acgtttacga ttccccccgg g 51 <210> 1455 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1456 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29354835 <400> 1455 ggggcctttc ctgttgtaca cttcccgtga gggtctcaga ccccttgcag a 51 <210> 1456 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) , <223> 2 of 2 allelic variants (1455 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29354835 <400> 1456 ggggcctttc ctgttgtaca cttcctgtga gggtctcaga ccccttgcag a 51 <210> 1457 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1458 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29357657 <400> 1457 tatccgcggg acgccgcgaa ttcgttcgcg accgcacgtt ctacgagggc g 51 <210> 1458 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1457 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg29357657 <400> 1458 tatccgcggg acgccgcgaa ttcgtcgcga ccgcacgttc tacgagggcg 50 <210> 1459 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1460 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29357938 <400> 1459 ttgctatcgc tcgcgctttc gcctctgaac ccaaaatatt gtttgcggat g 51 <210> 1460 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1459 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg29357938 <400> 1460 ttgctatcgc tcgcgctttc gcctcgaacc caaaatattg tttgcggatg 50 <210> 1461 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1462 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29360589 <400> 1461 gcccgctgtg acaccattgg tactccggtc cgtctgacct tcgacccaga a 51 <210> 1462 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1461 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg29360589 <400> 1462 gcccgctgtg acaccattgg tactcgggtc cgtctgacct tcgacccaga a 51 <210> 1463 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1464 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29360589 <400> 1463 cgatggggcg tgacgaattg cccctgccga cggcgacctc tctggctctg t 51 <210> 1464 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1463 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg29360589 <400> 1464 cgatggggcg tgacgaattg cccctccgac ggcgacctct ctggctctgt 50 <210> 1465 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1466 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg29363109 <400> 1465 taatccagtg ctcccggctg taccaccctg cctattcaca gtgggcacac t 51 <210> 1466 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1465 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29363109 <400> 1466 taatccagtg ctcccggctg taccaacctg cctattcaca gtgggcacac t 51 <210> 1467 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1468 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29495773 <400> 1467 aggagctgtc cagggttctg gagacgaaac ggagcccgct gggaactgtc c 51 <210> 1468 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1467 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29495773 <400> 1468 aggagctgtc cagggttctg gagactaaac ggagcccgct gggaactgtc.c 51 <210> 1469 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1470 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29498780 <400> 1469 agagggagcc acagaagccc cgacgttgca cagccctgca ggcaggggct g 51 <210> 1470 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1469 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29498780 <400> 1470 agagggagcc acagaagccc cgacgctgca cagccctgca ggcaggggct g 51 <210> 1471 <211> Sl <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1472 is other entry) <221> misc_feature <222> (0)'. . (0) <223> Accession number cg29513153 <400> 1471 tctcgagaaa aaaaacaacc ggagagactc tagtgaaggt ctcgacaaga c 51 <210> 1472 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1471 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29513153 <400> 1472 tctcgagaaa aaaaacaacc ggagaaactc tagtgaaggt ctcgacaaga c 51 <210> 1473 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1474 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29513153 <400> 1473 gcggcaggaa cctgccactc ctgggagcaa aaagctgctc tcgggaaccc t 51 <210> 1474 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1473 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29513153 <400> 1474 gcggcaggaa cctgccactc ctgggggcaa aaagctgctc tcgggaaccc t 51 <210> 1475 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1476 is other entry) <221> misc feature <222>(0)...(0) <223>Accession number cg29514688 <400>1475 gtagttttag tanggacggg gtttcgccat gttgcccaggctggtcttga a 51 <210>1476 _ <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1475 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg29514688 <400>1476 gtagttttag tanggacggg gtttcaccat gttgcccaggctggtcttga a 51 <210>1477 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1478 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg29514688 <400>1477 gggtttcgcc atgttgccca ggctggtctt gaactcctgggctcgagtga t 51 <210>1478 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1477 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg29514688 <400>1478 gggtttcgcc atgttgccca ggctgttctt gaactcctgggctcgagtga t 51 <210> 1479 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1480 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29514688 <400> 1479 cttgaactcc tgggctcgag tgatccacct gcctcagcct cccaatgcgc t 51 <210> 1480 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1479 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg29514688 <400> 1480 cttgaactcc tgggctcgag tgatctacct gcctcagcct cccaatgcgc t 51 <210> 1481 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1482 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg29689883 <400> 1481 ggccactttt ctttttcttg ttttgttttt tttttctttt tttctttttt t 51 <210> 1482 <211> 50 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1481 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg29689883 <400> 1482 ggccactttt ctttttcttg ttttgttttt ttttcttttt ttcttttttt 50 <210> 1483 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1484 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29689883 <400> 1483 tttttttctt tttttctttt ttttttcttc tctttttgag acattctcac t 51 <210> 1484 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1483 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg29689883 <400> 1484 tttttttctt tttttctttt tttttcttct ctttttgaga cattctcact 50 <210> 1485 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1486 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29692482 <400> 1485 tttcctccac ctccctccac tcattcaggt caggcatcga atgtcacttt c 51 <210> 1486 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1485 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg29692482 <400> 1486 tttcctccac ctccctccac tcatttaggt caggcatcga atgtcacttt c 51 <210> 1487 <211> 44 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (19) .. (0) <223> 1 of 2 allelic variants (1488 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29694531 <400> 1487 ttgcaaaaat aaccccttgg ggctctgtct ccctcaacta ttgc 44 <210> 1488 <211> 43 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (19) . . (0) <223> 2 of 2 allelic variants (1487 is other entry) <221> misc_feature <222> (18) . . (19) <223> Nucleotide deleted between bases 18 and 19 <221> misc_feature <222> (0) . . (0) <223> Accession number cg29694531 <400> 1488 ttgcaaaaat aaccccttgg gctctgtctc cctcaactat tgc 43 <210> 1489 <211> 47 <212> DNA
<213> Homo Sapiens <220> -<221> misc_feature <222> (22) .. (0) <223> 1 of 2 allelic variants (1490 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29694531 <400> 1489 ttgcaaaaat aaccccttgg ggctctgtct ccctcaacta ttgctct 47 <210> 1490 <211> 46 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (22) .. (0) <223> 2 of 2 allelic variants (1489 is other entry) <221> misc_feature <222> (21) .. (22) <223> Nucleotide deleted between bases 21 and 22 <221> misc_feature <222> (0) . . (0) <223> Accession number cg29694531 <400> 1490 ttgcaaaaat aaccccttgg gctctgtctc cctcaactat tgctct 46 <210> 1491 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1492 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg29694613 <400> 1491 agtaggtatc cccgctcccc caccaacccc caatttgaat gcacatttga 50 <210> 1492 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1491 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29694613 <400> 1492 agtaggtatc cccgctcccc caccacaccc ccaatttgaa tgcacatttg a 51 <210> 1493 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variantsW 1494 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29694613 <400> 1493 tccagtgttt ttcagtaggt atccccgctc ccccaccaac ccccaatttg a 51 <210> 1494 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1493 is other entry) <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg29694613 <400>1494 tccagtgttt ttcagtaggt atccctgctc ccccaccaacccccaatttg a 51 <210>1495 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1496 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg29694879 <400>1495 gttgcagtga gccgagatcg tgccactgca ctccagcctgggtgacagag c 51 <210>1496 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1495 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg29694879 <400>1496 gttgcagtga gccgagatcg tgccattgca ctccagcctgggtgacagag c 51 <210>1497 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1498 of is other entry) <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg29970826 <400>1497 gtttgtcctg gcacggaaca ggagacatac gtaagcagctaagtctcttc c 51 <210> 1498 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1497 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29970826 <400> 1498 gtttgtcctg gcacggaaca ggagatatac gtaagcagct aagtctcttc c 51 <210> 1499 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1500 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg29970826 <400> 1499 ctaagtctct tccaaggaac ggtggagaca ccaatcacca tgtcgaggtg a 51 <210> 1500 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1499 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg29970826 <400> 1500 ctaagtctct tccaaggaac ggtggggaca ccaatcacca tgtcgaggtg a 51 <210> 1501 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1502 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30123222 <400> 1501 ctatgacatg acactattac attttggttt ttagcatttt taaagaggaa g 51 <210> 1502 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1501 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30123222 <400> 1502 ctatgacatg acactattac attttagttt ttagcatttt taaagaggaa g 51 <210> 1503 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1504 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg30144940 <400> 1503 cccgcggaca agtcaagatc tgtgatttgg cgtcagtggc aacctagttg 50 <210> 1504 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26) . . . (0) <223> 2 of 2 allelic variants (1503 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg30144940 <400> 1504 cccgcggaca agtcaagatc tgtgattttg gcgtcagtgg caacctagtt g 51 <210> 1505 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1506 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30144940 <400> 1505 catccatcgc gacgtcaaac cgaccgatat cttggtcaac acccgcggac a 51 <210> 1506 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1505 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30144940 <400> 1506 catccatcgc gacgtcaaac cgaccaatat cttggtcaac acccgcggac a 51 <210> 1507 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1508 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30148429 <400>1507 atgacagaaa tgctacagta agggagagga gatgggggaaggcaaaagggg 51 <210>1508 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1507 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg30148429 <400>1508 atgacagaaa tgctacagta agggacagga gatgggggaaggcaaaagggg 51 <210>1509 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1510 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg30148429 <400>1509 agtaagggag aggagatggg ggaaggcaaa agggggttcctacttattaag 51 <210>1510 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1509 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg30148429 <400>1510 agtaagggag aggagatggg ggaagacaaa agggggttcctacttattaag 51 <210>1511 <211>51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1512 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30148429 <400> 1511 ggagatgggg gaaggcaaaa gggggttcct acttattaag tcaaatagat c 51 <210> 1512 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1511 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30148429 <400> 1512 ggagatgggg gaaggcaaaa gggggctcct acttattaag tcaaatagat c 51 <210> 1513 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1514 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30154402 <400> 1513 tatgtgaagt aaaacaaaaa caaaagttgt tacaattttt tcccttctaa t 51 <210> 1514 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1513 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30154402 <400> 1514 tatgtgaagt aaaacaaaaa caaaacttgt tacaattttt tcccttctaa t 51 <210> 1515 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1516 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30177428 <400> 1515 gtgtgagggt gcaggttctc cccaagggcc cattttctgc accagaaagc t 51 <210> 1516 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1515 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg30177428 <400> 1516 gtgtgagggt gcaggttctc cccaaggccc attttctgca ccagaaagct 50 <210> 1517 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1518 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg30179644 <400> 1517 cctttggtgg ggagaagtga aaaaagagga tctgaagact cattagttgt 50 <210> 1518 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1517 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg30179644 <400> 1518 cctttggtgg ggagaagtga aaaaaagagg atctgaagac tcattagttg t 51 <210> 1519 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1520 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30275403 <400> 1519 gtgggcagca ggaattggga ggaggaggtg ggggtggggc acagagcggg g 51 <210> 1520 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1519 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg30275403 <400> 1520 gtgggcagca ggaattggga ggaggggtgg gggtggggca cagagcgggg 50 <210> 1521 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1522 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30373246 <400> 1521 agccggcccc tatttccttg ccggacgcct ctcgcggcct tcagcgcgac c 51 <210> 1522 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1521 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg30373246 <400> 1522 agccggcccc tatttccttg ccggaagcct ctcgcggcct tcagcgcgac c 51 <210> 1523 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1524 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30386365 <400>1523 gaccccagtt aggcagctca ggttattatt gcagcttgat ggcccctggg 51 a <210>1524 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1523 is other entry) of <221>miscfeature <222>_ (0) .
.
(0) <223>Accession number cg30386365 <400>1524 gaccccagtt aggcagctca ggttactatt gcagcttgat ggcccctggg 51 a <210>1525 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1526 is other entry) of <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg30386365 <400>1525 aggcttcacc tcctcagtgg gctagatgca attctaacca gggggcaagt 51~
t <210>1526 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1525 is other entry) of <221>miscfeature <222>(0)._ .(0) <223>Accession number cg30386365 <400>1526 aggcttcacc tcctcagtgg gctaggtgca attctaacca gggggcaagt 51 t <210>1527 <211>51 <212>DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . '(0) <223> 1 of 2 allelic variants (1528 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30420313 <400> 1527 agtacaataa tgacccgcac cagggcacag ctgaaatggc actgactgat a 51 <210> l5za <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1527 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30420313 <400> 1528 agtacaataa tgacccgcac caggggacag ctgaaatggc actgactgat a 51 <210> 1529 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1530 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30421261 <400> 1529 tagtcccctt ctttgtcaac gctttgatgt tctgggtagt ggacaatttc c 51 <210> 1530 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1529 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30421261 <400> 1530 tagtcccctt ctttgtcaac gctttcatgt tctgggtagt ggacaatttc c 51 <210> 1531 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1532 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30421963 <400> 1531 aggcactgtc ccttgtcgcc ttcccagaca acctgtaccc tccaggccac c 51 <210> 1532 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1531 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30421963 <400> 1532 aggcactgtc ccttgtcgcc ttcccggaca acctgtaccc tccaggccac c 51 <210> 1533 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1534 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30453852 <400> 1533 cggtgcctgg attcctttga tgaaaaggca aagccttgaa cctaagtcat c 51 <210> 1534 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1533 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30453852 <400> 1534 cggtgcctgg attcctttga tgaaagggca aagccttgaa cctaagtcat c 51 <210> 1535 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1536 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30489596 <400> 1535 aataagtata gcaagtttat aaaggaaaaa gataaaatac agttccagta t 51 <210> 1536 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1535 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30489596 <400> 1536 aataagtata gcaagtttat aaagggaaaa gataaaatac agttccagta t 51 <210> 1537 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1538 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30489596 <400> 1537 gcctttaatc ctgggagata aagccaagat ctctgagttc aaggccagca t 51 <210> 1538 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1537 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30489596 <400> 1538 gcctttaatc ctgggagata aagccgagat ctctgagttc aaggccagca t 51 <210> 1539 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1540 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30490648 <400> 1539 acaggtacag cctgcggtca gacacaacca caaggcacat gaactcccca g 51 <210> 1540 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1539 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30490648 <400> 1540 acaggtacag cctgcggtca gacacgacca caaggcacat gaactcccca g 51 <210> 1541 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1542 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30575906 <400> 1541 tttttctggt aaatggtcct aaaatgaaac ctggcgttta acatggacac t 51 <210> 1542 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1541 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30575906 <400> 1542 tttttctggt aaatggtcct aaaataaaac ctggcgttta acatggacac t 51 <210> 1543 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1544 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30578763 <400> 1543 gaggtctggt tcgggttgcg catgtgaggg gcaagaggtg tctgccccct c 51 <210> 1544 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1543 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30578763 <400> 1544 gaggtctggt tcgggttgcg catgtaaggg gcaagaggtg tctgccccct c 51 <210> 1545 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1546 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30630643 <400> 1545 gttcttggct gggggtagga tgactgcaag aattgggtct gtatttaata a 51 <210> 1546 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1545 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30630643 <400> 1546 gttcttggct gggggtagga tgactccaag aattgggtct gtatttaata a 51 <210> 1547 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1548 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30748852 <400> 1547 aaccagggaa cattatggcc tgaggcccca gaggagtggg acagttaccc a 51 <210> 1548 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1547 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg30748852 <400> 1548 aaccagggaa cattatggcc tgaggcccag aggagtggga cagttaccca 50 <210> 1549 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1550 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30749846 <400> 1549 ggtcgagcag ggttttactt ttagttggat ctgtcgtgtg acttgcctct a 51 <210> 1550 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26) . . . (0) <223> 2 of 2 allelic variants (1549 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg30749846 <400> 1550 ggtcgagcag ggttttactt ttagtgggat ctgtcgtgtg acttgcctct a 51 <210> 1551 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1552 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg30750319 <400> 1551 ggcttactcc tttgatggaa agtggggaca aaaggctaga gtgcagcagt t 51 <210> 1552 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1551 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30750319 <400> 1552 ggcttactcc tttgatggaa agtggagaca aaaggctaga gtgcagcagt t 51 <210> 1553 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1554 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30750319 <400> 1553 agcatcagtg gtgcccccga cccaggcctt gccaccccag aacagatagg a 51 <210> 1554 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1553 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg30750319 <400> 1554 agcatcagtg gtgcccccga cccagccttg ccaccccaga acagatagga 50 <210> 1555 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1556 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg30750659 <400> 1555 aggactaaat gtaagagaga gggatagcaa agcttgagga aaagaaactc c 51 <210> 1556 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1555 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30750659 <400> 1556 aggactaaat gtaagagaga gggatggcaa agcttgagga aaagaaactc c 51 <210> 1557 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1558 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30750659 <400> 1557 taggacccca tgcctcaaat cgctcaacac ccatccctga ctctgaaaat c 51 <210> 1558 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1557 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30750659 <400> 1558 taggacccca tgcctcaaat cgctcgacac ccatccctga ctctgaaaat c 51 <210> 1559 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1560 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30783885 <400> 1559 gcggcccaga accttgggcc cggctactca ctggggcatt ggctgcatac c 51 <210> 1560 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1559 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30783885 <400> 1560 gcggcccaga accttgggcc cggctgctca ctggggcatt ggctgcatac c 51 <210> 1561 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1562 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30783885 <400> 1561 aaccttgggc ccggctactc actggggcat tggctgcata cctgacccac g 51 <210> 1562 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1561 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30783885 <400> 1562 aaccttgggc ccggctactc actggagcat tggctgcata cctgacccac g 51 <210> 1563 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1564 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg30784771 <400> 1563 tttatttcta tagaacaaaa aaaaaagtta agagattagt agagacgggt c 51 <210> 1564 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1563 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg30784771 <400> 1564 tttatttcta tagaacaaaa aaaaagttaa gagattagta gagacgggtc 50 <210> 1565 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1566 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30785174 <400> 1565 cgtttctctg gtttttctgg tctccgaaat tcaaggattt ctacagttag c 51 <210> 1566 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1565 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg30785174 <400> 1566 cgtttctctg gtttttctgg tctccaaaat tcaaggattt ctacagttag c 51 <210> 1567 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1568 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30785603 <400> 1567 aagttcccct agctgagaac caaagaagtg gtcccgactg tgcaggcagc t 51 <210> 1568 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misC_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1567 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg30785603 <400> 1568 aagttcccct agctgagaac caaagagtgg tcccgactgt gcaggcagct 50 <210> 1569 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1570 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg30785603 <400> 1569 agttccccta gctgagaacc aaagaagtgg tcccgactgt gcaggcagct t 51 <210> 1570 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1569 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg30785603 <400> 1570 agttccccta gctgagaacc aaagagtggt cccgactgtg caggcagctt ' S0 <210> 1571 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1572 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30785603 <400> 1571 caaagaagtg gtcccgactg tgcaggcagc ttgaaagaag aaacaggccc g 51 <210> 1572 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221>-misc feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1571 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30785603 <400> 1572 caaagaagtg gtcccgactg tgcagccagc ttgaaagaag aaacaggccc g 51 <210> 1573 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1574 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30785957 <400> 1573 ttcgcgaatg tgtgtgtggc ataccttggc cccatcgtct gtcccataat c 51 <210> 1574 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1573 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30785957 <400> 1574 ttcgcgaatg tgtgtgtggc ataccctggc cccatcgtct gtcccataat c 51 <210> 1575 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26)...(0) <223> 1 of 2 allelic variants (1576 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30786264 <400> 1575 ctcaaaccct ttgaactcct cagtggttcc ctcccccatg cagctgtact c 51 <210> 1576 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1575 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30786264 <400> 1576 ctcaaaccct ttgaactcct cagtgattcc ctcccccatg cagctgtact c 51 <210> 1577 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1578 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30786450 <400> 1577 tcacagcagc caattctttc tcccttagcc tcatcgcgtt ccagtcagcc t 51 <210> 1578 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1577 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30786450 <400> 1578 tcacagcagc caattctttc tccctcagcc tcatcgcgtt ccagtcagcc t 51 <210> 1579 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1580 is other entry) <221> misc feature <222> (25)...(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg30787589 <400> 1579 cgtctggagc cttctttttt tttttgagac aggatctcgc tccgtcctcc 50 <210> 1580 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1579 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30787589 <400> 1580 cgtctggagc cttctttttt ttttttgaga caggatctcg ctccgtcctc c 51 <210> 1581 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1582 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg30787589 <400> 1581 cgtctggagc cttctttttt tttttgagac aggatctcgc tccgtcctcc 50 <210> 1582 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1581 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30787589 <400> 1582 cgtctggagc cttctttttt ttttttgaga caggatctcg ctccgtcctc c 51 <210> 1583 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1584 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg30787705 <400> 1583 gagtaacacc ctttttcaaa aaaaaagtta ccattttctg taataggaaa a 51 <210> 1584 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1583 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg30787705 <400> 1584 gagtaacacc ctttttcaaa aaaaagttac cattttctgt aataggaaaa 50 <210> 1585 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1586 is other entry) <221> misc feature <222> (0)...(0) <223> Accession number cg30787705 <400> 1585 aaatgtgaaa gactctttag gacaaaatac caagtggaaa gaacaggaat a 51 <210> 1586 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (-0) <223> 2 of 2 allelic variants (1585 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30787705 <400> 1586 aaatgtgaaa gactctttag gacaatatac caagtggaaa gaacaggaat a 51 <210> 1587 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1588 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30787816 <400> 1587 taaaaacatc actcttggag ctgcagggaa aaggagttga gaagcatgga a 51 <210> 1588 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1587 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30787816 <400> 1588 taaaaacatc actcttggag ctgcatggaa aaggagttga gaagcatgga a 51 <210> 1589 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1590 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30788422 <400> 1589 gattgcatgg aggccccgcc ccccccaacc.aattctttga taatagcaca g 51 <210> 1590 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1589 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg30788422 <400> 1590 gattgcatgg aggccccgcc cccccaacca attctttgat aatagcacag 50 <210> 1591 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1592 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30788717 <400> 1591 atcatatcat gaaagctatc ataaaggaag aaaaataggg atttgactat c 51 <210> 1592 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1591 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30788717 <400> 1592 atcatatcat gaaagctatc ataaatgaag aaaaataggg atttgactat c 51 <210> 1593 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1594 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg30790895 <400> 1593 gtcctgggca ggaagatgag gcaaacacaa gcacatggat gcacgcacac a 51 <210> 1594 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1593 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30790895 <400> 1594 gtcctgggca ggaagatgag gcaaatacaa gcacatggat gcacgcacac a 51 <210> 1595 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1596 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg30790895 <400> 1595 caggaagatg aggcaaacac aagcacatgg atgcacgcac acactcgtgc t 51 <210> 1596 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1595 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30790895 <400> 1596 caggaagatg aggcaaacac aagcaaatgg atgcacgcac acactcgtgc t 51 <210> 1597 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1598 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30792591 <400> 1597 ttggatattg gctttaaaat gttttcattt aataccccct cccccacaca c 51 <210> 1598 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1597 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30792591 <400> 1598 ttggatattg gctttaaaat gtttttattt aataccccct cccccacaca c 51 <210> 1599 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1600 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30793374 <400> 1599 aattgaactg ctgttccctg tgtgccgggc cccatagcta gcactgggaa c 51 <210> 1600 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1599 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg30793374 <400> 1600 aattgaactg ctgttccctg tgtgctgggc cccatagcta gcactgggaa c 51 <210> 1601 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1602 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30794324 <400> 1601 tcctaaatga gtgtttagaa tagttatttc attggaaaca aggtcaaaac a 51 <210> 1602 <211> 51 <212> DNA

<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1601 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30794324 <400> 1602 tcctaaatga gtgtttagaa tagttgtttc attggaaaca aggtcaaaac a 51 <210> 1603 <211> 45 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1604 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg30794324 <400> 1603 tctaccacaa ttatttgatc aactagttat caaccctgac tgcag 45 <210> 1604 <211> 45 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1603 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg30794324 <400> 1604 tctaccacaa ttatttgatc aactaattat caaccctgac tgcag 45 <210> 1605 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1606 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32073644 <400> 1605 accctcctgg cacatctctg ctcaccctgc gagcaaccga ccccgacgtg g 51 <210> 1606 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1605 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32073644 <400> 1606 accctcctgg cacatctctg ctcactctgc gagcaaccga ccccgacgtg g 51 <210> 1607 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1608 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg32119723 <400> 1607 tggatcgcca gggctacggc cagatcaagg tggtccgcgc cgatggggac a 51 <210> 1608 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1607 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32119723 <400> 1608 tggatcgcca gggctacggc cagattaagg tggtccgcgc cgatggggac a 51 <210> 1609 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1610 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32119813 <400> 1609 gcccgtcgta cgtggggcgc tcgcgctggg tgcagacgcg cttgattggt t 51 <210> 1610 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1609 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32119813 <400> 1610 gcccgtcgta cgtggggcgc tcgcggtggg tgcagacgcg cttgattggt t 51 <210> 1611 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1612 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32120097 <400> 1611 tggcctgcac gtcccgcacg ctcagctccc gctggccccg gctgtacagg a 51 <210> 1612 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1611 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg32120097 <400> 1612 tggcctgcac gtcccgcacg ctcagtcccg ctggccccgg ctgtacagga 50 <210> 1613 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1614 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32126043 <400> 1613 cctgtggcat ccgttctgat ggaaacgtgc agttgtattt ggaagttcag a 51 <210> 1614 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1613 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32126043 <400> 1614 cctgtggcat ccgttctgat ggaaatgtgc agttgtattt ggaagttcag a 51 <210> 1615 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1616 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32149436 <400> 1615 agggcgcccg gagtggctcc aggaacgacg gaaacccctc agggcttttg g 51 <210> 1616 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1615 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg32149436 <400> 1616 agggcgcccg gagtggctcc aggaaggacg gaaacccctc agggcttttg g 51 <210> 1617 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1618 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg32149517 <400> 1617 tgtgcgtgta tgtgcgcttg ctctgcatgc gtggtgtgtg tatgtgtgtg 50 <210> 1618 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1617 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32149517 <400> 1618 tgtgcgtgta tgtgcgcttg ctctgtcatg cgtggtgtgt gtatgtgtgt g 51 <210> 1619 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1620 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg32149517 <400> 1619 tggtggtgtc gccagagagt gacctgcctg tctggggtgg aggaaaagcc a 51 <210> 1620 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1619 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32149517 <400> 1620 tggtggtgtc gccagagagt gacctccctg tctggggtgg aggaaaagcc a 51 <210> 1621 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1622 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32150747 <400> 1621 cagaacttcg gcagtaaaga ataaaaggcc agacagagag gcagcagcac a 51 <210> 1622 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1621 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg32150747 <400> 1622 cagaacttcg gcagtaaaga ataaaggcca gacagagagg cagcagcaca 50 <210> 1623 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1624 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32152942 <400> 1623 cacagctgtg catgtcgact taggtggcct gccagctcat ctccggcggc a 51 <210> 1624 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1623 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32152942 <400> 1624 cacagctgtg catgtcgact taggtagcct gccagctcat ctccggcggc a 51 <210> 1625 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1626 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32152942 <400> 1625 ggtggcctgc cagctcatct ccggcggcac ggtcaacgac gtcgagctgc c 51 <210> 1626 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1625 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32152942 <400> 1626 ggtggcctgc cagctcatct ccggcagcac ggtcaacgac gtcgagctgc c 51 <210> 1627 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1628 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32152942 <400> 1627 ggcctgccag ctcatctccg gcggcacggt caacgacgtc gagctgccgc g 51 <210> 1628 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1627 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg32152942 <400> 1628 ggcctgccag ctcatctccg gcggcccggt caacgacgtc gagctgccgc g 51 <210> 1629 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1630 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32152942 <400> 1629 tcacttgttc agattggcca tggatagtca cctgatcccc aacgatgtgg g 51 <210> 1630 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1629 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32152942 <400> 1630 tcacttgttc agattggcca tggatggtca cctgatcccc aacgatgtgg g 51 <210> 1631 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1632 is other entry) <221> misc feature <222>(0)...(0) <223>Accession number cg32152942 <400>1631 ggccatggat agtcacctga tccccaacga tgtgggctagctgactagcg g 51 <210>1632 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1631 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg32152942 <400>1632 ggccatggat agtcacctga tccccgacga tgtgggctagctgactagcg g 51 <210>1633 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1634 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg32152942 <400>1633 tcacctgatc cccaacgatg tgggctagct gactagcggtaacttgagct c 51 <210>1634 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1633 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg32152942 <400>1634 tcacctgatc cccaacgatg tgggccagct gactagcggtaacttgagct c 51 <210> 1635 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1636 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32152942 <400> 1635 cgcgatcctc gttgaggcgc tgaagacgct gggatgcagc acgaaactcc g 51 <210> 1636 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1635 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32152942 <400> 1636 cgcgatcctc gttgaggcgc tgaaggcgct gggatgcagc acgaaactcc g 51 <210> 1637 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1638 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32153241 <400> 1637 acccggctcc ggtcccgagg tcccacagca gttgaccagg catgggccgc a 51 <210> 1638 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1637 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32153241 <400> 1638 acccggctcc ggtcccgagg tcccatagca gttgaccagg catgggccgc a 51 <210> 1639 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1640 is other entry) <221> misc_feature <222> (0)...(0) <223> Accession number cg32153241 <400> 1639 gcatgggccg cagggctgcc agcgcgacag ctcgtaccgc gtgcttggtg a 51 <210> 1640 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1639 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32153241 <400> 1640 gcatgggccg cagggctgcc agcgcaacag ctcgtaccgc gtgcttggtg a 51 <210> 1641 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1642 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32153241 <400> 1641 cagctcgtac cgcgtgcttg gtgataagtc cgtcgtgggc gaaatgctcc t 51 <210> 1642 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1641 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32153241 <400> 1642 cagctcgtac cgcgtgcttg gtgatgagtc cgtcgtgggc gaaatgctcc t 51 <210> 1643 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1644 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32153241 <400> 1643 tggtgataag tccgtcgtgg gcgaaatgct cctcggccag gccgggggta c 51 <210> 1644 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1643 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32153241 <400> 1644 tggtgataag tccgtcgtgg gcgaagtgct cctcggccag gccgggggta c 51 <210> 1645 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1646 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32158391 <400> 1645 tgcataccat gctccagagg aagcagataa atctgatcct aaacctgggg t 51 <210> 1646 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1645 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg32158391 <400> 1646 tgcataccat gctccagagg aagcaataaa tctgatccta aacctggggt 50 <210> 1647 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1648 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32168122 <400> 1647 catgcgcgct ggcctccatg ggtggcggga ccgactgtgt gacgcacttg c 51 <210> 1648 <211> 51 <212> DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1647 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32168122 <400> 1648 catgcgcgct ggcctccatg ggtgggggga ccgactgtgt gacgcacttg c 51 <210> 1649 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1650 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32168828 <400> 1649 tgattcgccg cacaggtcgt ttagggcaac gccaagttcg aagacgtccc c 51 <210> 1650 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1649 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32168828 <400> 1650 tgattcgccg cacaggtcgt ttaggacaac gccaagttcg aagacgtccc c 51 <210> 1651 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1652 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32177197 <400> 1651 caccgtgttg ccgaaaaggt cgctcacctc taccacgatc cggtggttac c 51 <210> 1652 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1651 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32177197 <400> 1652 caccgtgttg ccgaaaaggt cgctcgcctc taccacgatc cggtggttac c 51 <210> 1653 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1654 is other entry) .
<221> misc_feature <222> (0) . . (0) <223> Accession number cg32177197 <400> 1653 ggggaaggaa tggaaagcgg tggggtcgtc ggtcgtcggg gcagtgcccc a 51 <210> 1654 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1653 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32177197 <400> 1654 ggggaaggaa tggaaagcgg tggggccgtc ggtcgtcggg gcagtgcccc a 51 <210> 1655 <211> 45 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (20) ..(0) <223> 1 of 2 allelic variants (1656 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32177584 <400> 1655 ccgcacgcgt gagccaccgt gcctggccca cgtgacactg ttaaa 45 <210> 1656 <211> 45 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (20) .. (0) <223> 2 of 2 allelic variants (1655 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32177584 <400> 1656 ccgcacgcgt gagccaccgc gcctggccca cgtgacactg ttaaa 45 <210> 1657 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1658 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32180618 <400> 1657 aatcagcacg gtgcgcgtga ggggcgggcg cgcttctcac acatgctgtg c 51 <210> 1658 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1657 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32180618 <400> 1658 aatcagcacg gtgcgcgtga ggggcaggcg cgcttctcac acatgctgtg c 51 <210> 1659 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1660 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32195480 <400> 1659 cctttccctt gcgtacactc tggactccag gcaggaaaat caaggcctca c 51 <210> 1660 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1659 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32195480 <400> 1660 cctttccctt gcgtacactc tggaccccag gcaggaaaat caaggcctca c 51 <210> 1661 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1662 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg32195480 <400> 1661 gcattagtcc aggacagcag acccctctgg acgctgactc gggatggggt 50 <210> 1662 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1661 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32195480 <400> 1662 gcattagtcc aggacagcag accccctctg gacgctgact cgggatgggg t 51 <210> 1663 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1664 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32308743 <400> 1663 tttccgtacg cgtgaacgtc tgtgttgtct gtggaatccc ctcgggacgt t 51 <210> 1664 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1663 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32308743 <400> 1664 tttccgtacg cgtgaacgtc tgtgtcgtct gtggaatccc ctcgggacgt t 51 <210> 1665 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1666 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32338390 <400> 1665 gagccataag ggaggacttg gcagcgtgct tgctccctga gtgacgttgt g 51 <210> 1666 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1665 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32338390 <400> 1666 gagccataag ggaggacttg gcagcatgct tgctccctga gtgacgttgt g 51 <210> 1667 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1668 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32544064 <400> 1667 caggagttca tgaccagcct ggccaacaca gtgagacccc gtctctacta a 51 <210> 1668 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1667 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32544064 <400> 1668 caggagttca tgaccagcct ggccagcaca gtgagacccc gtctctacta a 51 <210> 1669 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1670 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32544064 <400> 1669 gagttcatga ccagcctggc caacacagtg agaccccgtc tctactaaaa a 51 <210> 1670 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1669 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg32544064 <400> 1670 gagttcatga ccagcctggc caacatagtg agaccccgtc tctactaaaa a 51 <210> 1671 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26)...(0) <223> 1 of 2 allelic variants (1672 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg33193895 <400> 1671 tctctcctnt gccaagataa aaataatatt ctccctgggc tttcttaact a 51 <210> 1672 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1671 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg33193895 <400> 1672 tctctcctnt gccaagataa aaatatattc tccctgggct ttcttaacta 50 <210> 1673 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1674 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg33193895 <400> 1673 tctcctntgc caagataaaa ataatattct ccctgggctt tcttaactac a 51 <210> 1674 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1673 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg33193895 <400> 1674 tctcctntgc caagataaaa ataatttctc cctgggcttt cttaactaca 50 <210> 1675 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1676 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg33194116 <400> 1675 gtgtcactag tgtgaaaaaa gttgtagtgg agagcttggt atgtcaggca a 51 <210> 1676 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1675 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg33194116 <400> 1676 gtgtcactag tgtgaaaaaa gttgtgtgga gagcttggta tgtcaggcaa 50 <210> 1677 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26)...(0) <223> 1 of 2 allelic variants (1678 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg33199608 <400> 1677 gattctcctg tctcaacctg ccaagtagct gggactacag gcgcacgcca c 51 <210> 1678 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1677 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg33199608 <400> 1678 gattctcctg tctcaacctg ccaagcagct gggactacag gcgcacgcca c 51 <210> 1679 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1680 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg33199608 <400> 1679 cgccaccacg accggccaat ttctgcactt ttagtagaga cagggcttca c 51 <210> 1680 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1679 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg33199608 <400>1680 cgccaccacg accggccaat ttctgtactt ttagtagagacagggcttcac 51 <210>1681 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1682 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg33208319 <400>1681 ccttgatgag gctgtctttt aagctcaatt gaaggtagtaacaacaatcct 51 <210>1682 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1681 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg33208319 <400>1682 ccttgatgag gctgtctttt aagcttaatt gaaggtagtaacaacaatcct 51 <210>1683 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1684 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg33208319 <400>1683 gaaatgtgta gattctggaa cagtgcctag caggttgcagatacttactag 51 <210>1684 <211>51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1683 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg33208319 <400> 1684 gaaatgtgta gattctggaa cagtgtctag caggttgcag atacttacta g 51 <210> 1685 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1686 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg33208319 <400> 1685 aagttttctg agtgaatgaa aagtcaaaaa tgaatgtatc cttccaagca t 51 <210> 1686 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1685 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg33208319 <400> 1686 aagttttctg agtgaatgaa aagtcgaaaa tgaatgtatc cttccaagca t 51 <210> 1687 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1688 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg33265890 <400> 1687 tcgtgcttgg aatcagcagg cagggccact tccctcttga agctcacatc t 51 <210> 1688 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1687 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg33265890 <400> 1688 tcgtgcttgg aatcagcagg cagggcactt ccctcttgaa gctcacatct 50 <210> 1689 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1690 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg33271693 <400> 1689 gttcgggaga aagctacgac caagtacgcc cagctcgggc cttagaactt c 51 <210> 1690 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1689 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg33271693 <400> 1690 gttcgggaga aagctacgac caagtcgccc agctcgggcc ttagaacttc 50 <210> 1691 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1692 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg33899283 <400> 1691 cccttcggga ttggagttcg acctgaaagc atggataatt attcacattt c 51 <210> 1692 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1691 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg33899283 <400> 1692 cccttcggga ttggagttcg acctgtaagc atggataatt attcacattt c 51 <210> 1693 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1694 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34078594 <400> 1693 agagacaagg cttcctcata ggacggcaga gccaccttta ggaacagctt g 51 <210> 1694 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1693 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg34078594 <400> 1694 agagacaagg cttcctcata ggacgcagag ccacctttag gaacagcttg 50 <210> 1695 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1696 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34078594 <400> 1695 tcaaagtgaa gaagcaggag gcggggagtt ccgcctctcc cagcccaagg g 51 <210> 1696 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1695 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34078594 <400>1696 tcaaagtgaa gaagcaggag gcgggcagtt ccgcctctcccagcccaagg g 51 <210>1697 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1698 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg34078713 <400>1697 tgaaaatagt gtgctgagcc ctggaacatt aaaaatgtgttcctatgtgg a 51 <210>1698 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ . . (0) <223>2 2 allelic variants (1697 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg34078713 <400>1698 tgaaaatagt gtgctgagcc ctggagcatt aaaaatgtgttcctatgtgg a 51 <210>1699 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1700 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg34096681 <400>1699 agacttgaaa acaactggaa gagagggttc ctcaagggagaagacacgag a 51 <210>1700 <211>51 <212>DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1699 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34096681 <400> 1700 agacttgaaa acaactggaa gagagagttc ctcaagggag aagacacgag a 51 <210> 1701 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1702 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg34098766 <400> 1701 ctcagcctca tgagtagctg ggacagcaga catgtacaac cacacctggc t 51 <210> 1702 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1701 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg34098766 <400> 1702 ctcagcctca tgagtagctg ggacacagac atgtacaacc acacctggct 50 <210> 1703 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1704 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg34098766 <400> 1703 acacctggct aatttttttt tttttttggg gtggaaatag aatctcactg a 51 <210> 1704 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1703 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg34098766 <400> 1704 acacctggct aatttttttt ttttttgggg tggaaataga atctcactga 50 <210> 1705 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1706 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg34098766 <400> 1705 cacctggcta attttttttt ttttttgggg tggaaataga atctcactga t 51 <210> 1706 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> mist feature <222> (26)...(0) <223> 2 of 2 allelic variants (1705 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg34098766 <400> 1706 cacctggcta attttttttt tttttggggt ggaaatagaa tctcactgat 50 <210> 1707 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1708 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34107938 <400> 1707 cacaaatgct ctgtaggcac gtgtggctag tgactgccct acggtcggca t 51 <210> 1708 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1707 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34107938 <400> 1708 cacaaatgct ctgtaggcac gtgtgactag tgactgccct acggtcggca t 51 <210> 1709 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1710 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg34108088 <400> 1709 atattaacca ttgaatgaag tatggttatc ctcccctctt ttttgataat c 51 <210> 1710 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1709 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34108088 <400> 1710 atattaacca ttgaatgaag tatggctatc ctcccctctt ttttgataat c 51 <210> 1711 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1712 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34126415 <400> 1711 atgctaggaa gctagctcct ggggggttca gatctagtga gggtgccttt c 51 <210> 1712 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1711 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34126415 <400> 1712 atgctaggaa gctagctcct gggggattca gatctagtga gggtgccttt c 51 <210> 1713 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1714 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34126415 <400> 1713 aagtaaaaac aaacaagata actttttttt ttctgagatg aattttcact t 51 <210> 1714 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1713 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg34126415 <400> 1714 aagtaaaaac aaacaagata actttctttt ttctgagatg aattttcact t 51 <210> 1715 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1716 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34147197 <400> 1715 ggctcaagca atcctcccgc ctcagtctcc caagcagctg ggactacagg c 51 <210> 1716 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1715 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34147197 <400> 1716 ggctcaagca atcctcccgc ctcagcctcc caagcagctg ggactacagg c 51 <210> 1717 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1718 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34387835 <400> 1717 tgtattttta gtagagatgg ggttttacca tgtgggcctg gcaggtctcg a 51 <210> 1718 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1717 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34387835 <400> 1718 tgtattttta gtagagatgg ggtttcacca tgtgggcctg gcaggtctcg a 51 <210> 1719 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1720 is other entry) <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg34387835 <400>1719 cctcggcctc ccaaattcct gggactacag gcgtgagccactgcacccgg c 51 <210>1720 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>2 2 allelic variants (1719 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg34387835 <400>1720 cctcggcctc ccaaattcct gggaccacag gcgtgagccactgcacccgg c 51 <210>1721 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1722 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg34387835 <400>1721 accggtgcgt gccaccacac ccgaccaatt tttgtatttttagtagagat g 51 <210>1722 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1721 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg34387835 <400>1722 accggtgcgt gccaccacac ccgactaatt tttgtatttttagtagagat g 51 <210> 1723 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1724 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34387835 <400> 1723 tgccaccaca cccgaccaat ttttgtattt ttagtagaga tggggtttta c 51 <210> 1724 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1723 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg34387835 <400> 1724 tgccaccaca cccgaccaat ttttgcattt ttagtagaga tggggtttta c 51 <210> 1725 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1726 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg34390673 <400> 1725 taaacttcga tctttccctg tgctcaacat tcctatttgg atcccggtct 50 <210> 1726 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1725 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34390673 <400> 1726 taaacttcga tctttccctg tgctctaaca ttcctatttg gatcccggtc t 51 <210> 1727 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1728 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34405904 <400> 1727 agttcgctgt tgattgctat aattttctct ctaaaatctg gattttcatc t 51 <210> 1728 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1727 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg34405904 <400> 1728 agttcgctgt tgattgctat aatttctctc taaaatctgg attttcatct 50 <210> 1729 <211> 51 <212> DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1730 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34407516 <400> 1729 cacatatatc tcaacaaacc atgcacatca tctgttcaga actgggaaac g 51 <210> 1730 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1729 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34407516 <400> 1730 cacatatatc tcaacaaacc atgcatatca tctgttcaga actgggaaac g 51 <210> 1731 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1732 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34407558 <400> 1731 ccaagctcct gcctcgcaat tgcctttgta ggccaagatc atgccgtgaa g 51 <210> 1732 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1731 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34407558 <400> 1732 ccaagctcct gcctcgcaat tgcctctgta ggccaagatc atgccgtgaa g 51 <210> 1733 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1734 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34407558 <400> 1733 caagatcatg ccgtgaagtg gcctttccta gcctaacttt tgctttttga t 51 <210> 1734 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1733 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34407558 <400> 1734 caagatcatg ccgtgaagtg gccttcccta gcctaacttt tgctttttga t 51 <210> 1735 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1736 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34407558 <400> 1735 tcctagccta acttttgctt tttgatgcat actccagtcc caaaacttcc t 51 <210> 1736 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1735 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34407558 <400> 1736 tcctagccta acttttgctt tttgacgcat actccagtcc caaaacttcc t 51 <210> 1737 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1738 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34407558 <400> 1737 ggccaaaatc gtcgtgaagt caccctctgc aggcctagct cctgcgtccg a 51 <210> 1738 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1737 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34407558 <400> 1738 ggccaaaatc gtcgtgaagt cacccactgc aggcctagct cctgcgtccg a 51 <210> 1739 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1740 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34407558 <400> 1739 cgtcgtgaag tcaccctctg caggcctagc tcctgcgtcc gagtgctgtg t 51 <210> 1740 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1739 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34407558 <400> 1740 cgtcgtgaag tcaccctctg caggcgtagc tcctgcgtcc gagtgctgtg t 51 <210> 1741 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1742 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34407558 <400> 1741 caccctctgc aggcctagct cctgcgtccg agtgctgtgt aggccaagct a 51 <210> 1742 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1741 is other entry) <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg34407558 <400>1742 caccctctgc aggcctagct cctgcctccg agtgctgtgtaggccaagct a 51 <210>1743 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1744 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg34407558 <400>1743 ctctgcaggc ctagctcctg cgtccgagtg ctgtgtaggccaagctaatg c 51 <210>1744 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1743 entry) of is other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg34407558 <400>1744 ctctgcaggc ctagctcctg cgtccaagtg ctgtgtaggccaagctaatg c 51 <210>1745 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1746 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg34407558 <400>1745 aagctaatgc ctcacagcac acttttgagg ctgagcgtttccttttgtgc a 51 <210> 1746 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1745 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34407558 <400> 1746 aagctaatgc ctcacagcac actttcgagg ctgagcgttt ccttttgtgc a 51 <210> 1747 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1748 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34407558 <400> 1747 tcacagcaca cttttgaggc tgagcgtttc cttttgtgca tcctctccaa g 51 <210> 1748 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1747 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34407558 <400> 1748 tcacagcaca cttttgaggc tgagcatttc cttttgtgca tcctctccaa g 51 <210> 1749 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1750 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34407558 <400> 1749 caagccctga acttactcca gttggcctct ccagaccaag ctctccctcc c 51 <210> 1750 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1749 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34407558 <400> 1750 caagccctga acttactcca gttggtctct ccagaccaag ctctccctcc c 51 <210> 1751 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1752 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg34409256 <400> 1751 ttactatata tgatgtagtc taataatttt ctatcctatt ttatttcctt t 51 <210> 1752 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1751 is other entry) <221> misc feature <222> (0)...(0) <223> Accession number cg34409256 <400> 1752 ttactatata tgatgtagtc taatactttt ctatcctatt ttatttcctt t 51 <210> 1753 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1754 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg34409256 <400> 1753 tatatatgat gtagtctaat aattttctat cctattttat ttcctttttt t 51 <210> 1754 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1753 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg34409256 <400> 1754 tatatatgat gtagtctaat aatttctatc ctattttatt tccttttttt 50 <210> 1755 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1756 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34411960 <400> 1755 atggtggaga tgcttctggt ttattctgtg gctaccgctg ttactgcttg g 51 <210> 1756 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1755 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34411960 <400> 1756 atggtggaga tgcttctggt ttattttgtg gctaccgctg ttactgcttg g 51 <210> 1757 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1758 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34664360 <400> 1757 agctagacat agagccctga ccgtgtgatt ccaactgtgg aattcacaca a 51 <210> 1758 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1757 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34664360 <400> 1758 agctagacat agagccctga ccgtgcgatt ccaactgtgg aattcacaca a 51 <210> 1759 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1760 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34750113 <400> 1759 ttttattgtt ttgagacaga gtctcactct gttgcctagg ctggagtgca g 51 <210> 1760 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1759 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34750113 <400> 1760 ttttattgtt ttgagacaga gtctcgctct gttgcctagg ctggagtgca g 51 <210> 1761 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1762 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34750113 <400> 1761 ggctggagtg cagtggtgca atcacagctc actgcaactt ccacctcctg g 51 <210> 1762 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1761 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34750113 <400> 1762 ggctggagtg cagtggtgca atcacggctc actgcaactt ccacctcctg g 51 <210> 1763 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1764 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34888218 <400> 1763 aaatgttggg atcaatatct aaatcgaact ccaaattaca gcctccaggg a 51 <210> 1764 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1763 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34888218 <400> 1764 aaatgttggg atcaatatct aaatcaaact ccaaattaca gcctccaggg a 51 <210> 1765 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1766 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg34888218 <400> 1765 caggctgtat gcctgaagtc cccaagtacc aagtgcatgt actctgctct g 51 <210> 1766 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1765 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34888218 <400> 1766 caggctgtat gcctgaagtc cccaaatacc aagtgcatgt actctgctct g 51 <210> 1767 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1768 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34888218 <400> 1767 gaagtcccca agtaccaagt gcatgtactc tgctctggtc taaggatgaa a 51 <210> 1768 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1767 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34888218 <400> 1768 gaagtcccca agtaccaagt gcatgcactc tgctctggtc taaggatgaa a 51 <210> 1769 <211> 51 <212> DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1770 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34896418 <400> 1769 aaacaaggat taaatctggt cctggtggtt gtatgggata aacatggatt t 51 <210> 1770 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1769 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg34896418 <400> 1770 aaacaaggat taaatctggt cctggcggtt gtatgggata aacatggatt t 51 <210> 1771 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1772 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35001967 <400> 1771 tgagcagaga acactgacct ggtttggcag ggacaggaga tacgctgggt t 51 <210> 1772 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1771 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35001967 <400> 1772 tgagcagaga acactgacct ggttttgcag ggacaggaga tacgctgggt t 51 <210> 1773 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1774 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35001967 <400> 1773 agcagagaac actgacctgg tttggcaggg acaggagata cgctgggttg g 51 <210> 1774 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1773 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35001967 <400> 1774 agcagagaac actgacctgg tttggtaggg acaggagata cgctgggttg g 51 <210> 1775 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1776 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35001967 <400> 1775 agatacgctg ggttggtatg gatcagcaag agggtactgc taatgggaac a 51 <210> 1776 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1775 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg35001967 <400> 1776 agatacgctg ggttggtatg gatcaacaag agggtactgc taatgggaac a 51 <210> 1777 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1778 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg35001967 <400> 1777 aatgggaaca gggagggaag gctcaacccc attcccgtat ttccctgatt c 51 <210> 1778 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1777 is other entry) <221> misc_feature <222> (25) .'. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg35001967 <400> 1778 aatgggaaca gggagggaag gctcacccca ttcccgtatt tccctgattc 50 <210> 1779 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1780 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35003947 <400> 1779 tgttctggtg aatgggaact taacatgtct ttgccgttac atattctttg a 51 <210> 1780 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1779 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35003947 <400> 1780 tgttctggtg aatgggaact taacacgtct ttgccgttac atattctttg a 51 <210> 1781 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1782 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35003951 <400> 1781 ttgaactcct gacctcaagt gatccacccg cctcagcctc ctaaagtgct g 51 <210> 1782 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1781 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35003951 <400> 1782 ttgaactcct gacctcaagt gatccgcccg cctcagcctc ctaaagtgct g 51 <210> 1783 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1784 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35013956 <400> 1783 cagaatccag ccctgcttga tgcaatcctc ttcagccagg cgttcctgaa t 51 <210> 1784 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1783 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35013956 <400> 1784 cagaatccag ccctgcttga tgcaaccctc ttcagccagg cgttcctgaa t 51 <210> 1785 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1786 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35014502 <400> 1785 gagcagtttc tgtttttcta gttaagatgt actgcacatc cccctactgt t 51 <210> 1786 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1785 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35014502 <400> 1786 gagcagtttc tgtttttcta gttaatatgt actgcacatc cccctactgt t 51 <210> 1787 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1788 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35017611 <400> 1787 gcaggcagac gggcagggcc agaggcgcta ccggggtctc ctgcactgta t 51 <210> 1788 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1787 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg35017611 <400>1788 gcaggcagac gggcagggcc agagggctac cggggtctcc tgcactgtat 50 <210>1789 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1790 is other entry) of <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg35019280 <400>1789 ataaactgtg tcagacatgg gcgacgcggg gaccgctgga gggaggcgcg 51 c <210>1790 <211>50 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1789 is other entry) of <221>miscfeature <222>(25)_ ..(26) <223>Nucleotide deleted between bases and <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg35019280 <400>1790 ataaactgtg tcagacatgg gcgaccgggg accgctggag ggaggcgcgc 50 <210>1791 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1792 is other entry) of <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg35019280 <400>1791 tccgctggga gcaggagggg cggggccggg cttgaggagt ggctggccgc 51 c <210> 1792 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1791 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg35019280 <400> 1792 tccgctggga gcaggagggg cggggcgggc ttgaggagtg gctggccgcc 50 <210> 1793 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1794 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35023126 <400> 1793 agaaatacca ttctggacat aagacttggc taaaatttca tgatgaagat a 51 <210> 1794 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1793 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35023126 <400> 1794 agaaatacca ttctggacat aagacgtggc taaaatttca tgatgaagat a 51 <210> 1795 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1796 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35049067 <400> 1795 tctccctgat ggacggggaa gtcttgtttg tggaagacac tgagccacgc t 51 <210> 1796 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1795 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35049067 <400> 1796 tctccctgat ggacggggaa gtcttctttg tggaagacac tgagccacgc t 51 <210> 1797 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1798 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35049067 <400> 1797 caccaccacc ggcatccggg gaggagtgtc aaacgggtga ctcggccagg a 51 <210> 1798 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26)...(0) <223> 2 of 2 allelic variants (1797 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35049067 <400> 1798 caccaccacc ggcatccggg gaggactgtc aaacgggtga ctcggccagg a 51 <210> 1799 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1800 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35049067 <400> 1799 tgcgggcacc ctcctgcggg tggacaatga gcgcctggga ggccgttgtc c 51 <210> 1800 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1799 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35049067 <400> 1800 tgcgggcacc ctcctgcggg tggacgatga gcgcctggga ggccgttgtc c 51 <210> 1801 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1802 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35049628 <400> 1801 gctggaggat tgcttgaagc caggaattca agaccagcct gggcaacata g 51 <210> 1802 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1801 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35049628 <400> 1802 gctggaggat tgcttgaagc caggagttca agaccagcct gggcaacata g 51 <210> 1803 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1804 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35063579 <400> 1803 gcagatcact ggaggtcagg agttcaagac cagactggcc aacatggtga a 51 <210> 1804 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1803 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35063579 <400> 1804 gcagatcact ggaggtcagg agttcgagac cagactggcc aacatggtga a 51 <210> 1805 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1806 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35066497 <400> 1805 gcgtggcacg cccgtcaggg gcaggtgccc cagggtactc ctacggtgct c 51 <210> 1806 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1805 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35066497 <400> 1806 gcgtggcacg cccgtcaggg gcaggagccc cagggtactc ctacggtgct c 51 <210> 1807 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1808 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg35066497 <400> 1807 cccagggtac tcctacggtg ctcgggcttc ccaccgtggg agtgccgaga c 51 <210> 1808 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1807 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg35066497 <400> 1808 cccagggtac tcctacggtg ctcggacttc ccaccgtggg agtgccgaga c 51 <210> 1809 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1810 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35066497 <400> 1809 caccgtggga gtgccgagac actgatcgat gggtcttaca ggtatggcat t 51 <210> 1810 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1809 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35066497 <400> 1810 caccgtggga gtgccgagac actgaccgat gggtcttaca ggtatggcat t 51 <210> 1811 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1812 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35066497 <400> 1811 gggtcttaca ggtatggcat tttacggaca gtgaggaaga tagacgaggg a 51 <210> 1812 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1811 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35066497 <400> 1812 gggtcttaca ggtatggcat tttactgaca gtgaggaaga tagacgaggg a 51 <210> 1813 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1814 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35066497 <400> 1813 caggtatggc attttacgga cagtgaggaa gatagacgag ggatggcgct c 51 <210> 1814 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1813 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35066497 <400> 1814 caggtatggc attttacgga cagtggggaa gatagacgag ggatggcgct c 51 <210> 1815 <211> 51 <212> DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1816 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35066497 <400> 1815 ggcctgattc ttgatgtcgt cctggcggtc gctgatggcg tccttggcct t 51 <210> 1816 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1815 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35066497 <400> 1816 ggcctgattc ttgatgtcgt cctggtggtc gctgatggcg tccttggcct t 51 <210> 1817 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1818 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35068462 <400> 1817 tggcacagga gcccgagatc ttatttcttg acgagccgac aaatcacctt g 51 <210> 1818 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1817 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg35068462 <400> 1818 tggcacagga gcccgagatc ttattccttg acgagccgac aaatcacctt g 51 <210> 1819 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1820 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg35072832 <400> 1819 ttttggataa tatgtaactc tccacaatgt cgcttccgta gcaattgtag a 51 <210> 1820 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1819 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg35072832 <400> 1820 ttttggataa tatgtaactc tccactatgt cgcttccgta gcaattgtag a 51 <210> 1821 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1822 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg35074019 <400> 1821 tgcagaagga actggactcg ctgcagggag agaaagtaca cctgaaggag a 51 <210> 1822 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1821 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35074019 <400> 1822 tgcagaagga actggactcg ctgcatggag agaaagtaca cctgaaggag a 51 <210> 1823 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1824 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35097790 <400> 1823 tccctcagtt tgctcatctg taaagcagga ataaggctga taccttctca g 51 <210> 1824 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1823 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35097790 <400> 1824 tccctcagtt tgctcatctg taaagtagga ataaggctga taccttctca g 51 <210> 1825 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1826 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35097892 <400> 1825 gtattttcag tagagacggg gttttaccat gttggccagg ctggtctcga a 51 <210> 1826 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1825 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35097892 <400> 1826 gtattttcag tagagacggg gttttgccat gttggccagg ctggtctcga a 51 <210> 1827 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1828 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35098722 <400> 1827 tatgtcttct ttcgttggtt agtggcttgc aggatatttt gagcagcata a 51 <210> 1828 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1827 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35098722 <400> 1828 tatgtcttct ttcgttggtt agtgggttgc aggatatttt gagcagcata a 51 <210> 1829 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1830 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg35098722 <400> 1829 ctttcgttgg ttagtggctt gcaggatatt ttgagcagca taaaactgtt a 51 <210> 1830 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1829 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35098722 <400> 1830 ctttcgttgg ttagtggctt gcagggtatt ttgagcagca taaaactgtt a 51 <210> 1831 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1832 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35106817 <400> 1831 atgcaggtgc cgggtgagga cggcaccatg ccgaaactgt tcggacggat c 51 <210> 1832 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1831 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35106817 <400> 1832 atgcaggtgc cgggtgagga cggcatcatg ccgaaactgt tcggacggat c 51 <210> 1833 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1834 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35111750 <400> 1833 atattggatc tttccctgtt ttttttgtat ctagcagacc ttcatggtta t 51 <210> 1834 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1833 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg35111750 <400> 1834 atattggatc tttccctgtt tttttgtatc tagcagacct tcatggttat 50 <210> 1835 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1836 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35137271 <400> 1835 agccaatggt gcacagtgat gatacgaatg tcaatctttg ctcggtcagt g 51 <210> 1836 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1835 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35137271 <400> 1836 agccaatggt gcacagtgat gatacaaatg tcaatctttg ctcggtcagt g 51 <210> 1837 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1838 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35137271 <400> 1837 ttgctcggtc agtgaggatg tcgccctgac ccttcctgct ccccagaaag g 51 <210> 1838 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26)...(0) <223> 2 of 2 allelic variants (1837 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35137271 <400> 1838 ttgctcggtc agtgaggatg tcgccttgac ccttcctgct ccccagaaag g 51 <210> 1839 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1840 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35138283 <400> 1839 tgaagtataa gaatattctg ctgctgttga gtggtatgta atgtatatgt c 51 <210> 1840 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1839 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35138283 <400> 1840 tgaagtataa gaatattctg ctgcttttga gtggtatgta atgtatatgt c 51 <210> 1841 <211> 45 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1842 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35138283 <400>1841 gttttataca ttattgaaag tggaatatta gattctaccactagt 45 <210>1842 <211>45 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1841 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg35138283 <400>1842 gttttataca ttattgaaag tggaacatta gattctaccactagt 45 <210>1843 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1844 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg35350458 <400>1843 ttctcgtcta gcagtattca gatacccctt ctgctcagcctgcttggcgt t 51 <210>1844 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1843 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg35350458 <400>1844 ttctcgtcta gcagtattca gatactcctt ctgctcagcctgcttggcgt t 51 <210>1845 <211>51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1846 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35354409 <400> 1845 ttttccggag ttatttaaaa aaaaaacaaa cagatgcctt ttaagggtta t 51 <210> 1846 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1845 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg35354409 <400> 1846 ttttccggag ttatttaaaa aaaaacaaac agatgccttt taagggttat 50 <210> 1847 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1848 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35364749 <400> 1847 cccatcacca acgccaccct ggaccgggtg agtgcctggg ctagccctgt c 51 <210> 1848 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1847 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35364749 <400> 1848 cccatcacca acgccaccct ggaccaggtg agtgcctggg ctagccctgt c 51 <210> 1849 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1850 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35364849 <400> 1849 gttgatgctt gatttaagag taagtgttat cgtgttcagt ttttatatct c 51 <210> 1850 <211> S1 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1849 is other entry.) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35364849 <400> 1850 gttgatgctt gatttaagag taagtattat cgtgttcagt ttttatatct c 51 <210> 1851 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1852 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg35817789 <400> 1851 ctcttagcaa ccaataattt ttttttcaat aattaagtac caatttcctg c 51 <210> 1852 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1851 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg35817789 <400> 1852 ctcttagcaa ccaataattt tttttcaata attaagtacc aatttcctgc 50 <210> 1853 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1854 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35817789 <400> 1853 caatttcctg ctaatgggca ggcccacctt tatttctttt tttttccatt a 51 <210> 1854 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1853 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35817789 <400>1854 caatttcctg ctaatgggca ggcccccctt tatttctttttttttccatt a 51 <210>1855 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1856 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg35817789 <400>1855 ctaatgggca ggcccacctt tatttctttt tttttccattagaacgagca t 51 <210>1856 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ . . (0) <223>2 2 allelic variants (1855 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg35817789 <400>1856 ctaatgggca ggcccacctt tatttttttt tttttccattagaacgagca t 51 <210>1857 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1858 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg35907288 <400>1857 gaagagcact tgcagccgca tcaggtgaac atcaaactgcaaagccacct g 51 <210> 1858 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1857 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35907288 <400> 1858 gaagagcact tgcagccgca tcaggcgaac atcaaactgc aaagccacct g 51 <210> 1859 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1860 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35927209 <400> 1859 cccccttgtt agtgggcgca cgaatcagtc ttcttcgcgg tccatggtga c 51 <210> 1860 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1859 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35927209 <400> 1860 cccccttgtt agtgggcgca cgaattagtc ttcttcgcgg tccatggtga c 51 <210> 1861 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26)...(0) <223> 1 of 2 allelic variants (1862 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35927209 <400> 1861 ccacgggatc accggcatcg cgcagaccga cgaagttaac ccctttaacg a 51 <210> 1862 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1861 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35927209 <400> 1862 ccacgggatc accggcatcg cgcaggccga cgaagttaac ccctttaacg a 51 <210> 1863 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1864 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35927209 <400> 1863 gatcaccggc atcgcgcaga ccgacgaagt taaccccttt aacgacccgc c 51 <210> 1864 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1863 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg35927209 <400> 1864 gatcaccggc atcgcgcaga ccgacaaagt taaccccttt aacgacccgc c 51 <210> 1865 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1866 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35929317 <400> 1865 gccgagcatg gtggcgggca cctgtagtcc cagccacctg ggaggctgag g 51 <210> 1866 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1865 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35929317 <400> 1866 gccgagcatg gtggcgggca cctgtggtcc cagccacctg ggaggctgag g 51 <210> 1867 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1868 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35933276 <400> 1867 atgagttcct gcgataaccc ggtagtctcg aaaatctggg ctccggtata c 51 <210> 1868 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1867 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35933276 <400> 1868 atgagttcct gcgataaccc ggtagcctcg aaaatctggg ctccggtata c 51 <210> 1869 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1870 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35933276 <400> 1869 cctgcgataa cccggtagtc tcgaaaatct gggctccggt atacgacgag a 51 <210> 1870 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1869 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35933276 <400> 1870 cctgcgataa cccggtagtc tcgaagatct gggctccggt atacgacgag a 51 <210> 1871 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1872 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg35933276 <400> 1871 ccggtatacg acgagatagt ggatataccc atcttgctca tcgtcttaag g 51 <210> 1872 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1871 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg35933276 <400> 1872 ccggtatacg acgagatagt ggatacaccc atcttgctca tcgtcttaag g 51 <210> 1873 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1874 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg35933276 <400> 1873 taaggacgcc cttgccaaga gccttgtaaa cgttatggat agcagtttca g 51 <210> 1874 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1873 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35933276 <400> 1874 taaggacgcc cttgccaaga gccttataaa cgttatggat agcagtttca g 51 <210> 1875 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1876 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg35933276 <400> 1875 taaacgttat ggatagcagt ttcagggtca gtagacaccc acacctcgcg c 51 <210> 1876 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1875 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35933276 <400> 1876 taaacgttat ggatagcagt ttcagagtca gtagacaccc acacctcgcg c 51 <210> 1877 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1878 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg35933276 <400> 1877 ctgactcgaa gagcaaatac gggttgacag ccgaagcacc ataacccatg a 51 <210> 1878 <211> 51 <212> DNA

<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1877 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg35933276 <400> 1878 ctgactcgaa gagcaaatac gggttaacag ccgaagcacc ataacccatg a 51 <210> 1879 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1880 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35933276 <400> 1879 agagcaaata cgggttgaca gccgaagcac cataacccat gaggagggcg a 51 <210> 1880 <211> 51 <212> DNA
<213> Homo sapiens, <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1879 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg35933276 <400> 1880 agagcaaata cgggttgaca gccgaggcac cataacccat gaggagggcg a 51 <210> 1881 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1882 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg35933276 <400> 1881 agcgatctcg gtcaggccga ccccctcgat gcgactcgtc gttccggcga a 51 <210> 1882 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1881.is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35933276 <400> 1882 agcgatctcg gtcaggccga cccccgcgat gcgactcgtc gttccggcga a 51 <210> 1883 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1884 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35933276 <400> 1883 ccctcgatgc gactcgtcgt tccggcgaag tactcatcaa tgagttcctg c 51 <210> 1884 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1883 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg35933276 <400> 1884 ccctcgatgc gactcgtcgt tccggtgaag tactcatcaa tgagttcctg c 51 <210> 1885 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1886 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg35980513 <400> 1885 aaaatgagcc gggcgtggtg acacacgcct gtagtcccag ctacttggga g 51 <210> 1886 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1885 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg35980513 <400> 1886 aaaatgagcc gggcgtggtg acacatgcct gtagtcccag ctacttggga g 51 <210> 1887 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1888 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg36173201 <400> 1887 gcctccagaa ctgtgagaga ataaacgtcc gatgttttaa gccattcagt t 51 <210> 1888 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1887 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg36173201 <400> 1888 gcctccagaa ctgtgagaga ataaatgtcc gatgttttaa gccattcagt t 51 <210> 1889 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1890 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg36180692 <400> 1889 gaggactgct tgagcccagg agttcaagac cagcctgggc aacacagtga g 51 <210> 1890 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1889 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg36180692 <400> 1890 gaggactgct tgagcccagg agttcgagac cagcctgggc aacacagtga g 51 <210> 1891 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1892 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg36190410 <400> 1891 acaggcgtga gccaccatgc ccagccttga atactgaatc taagtatttt t 51 <210> 1892 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1891 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg36190410 <400> 1892 acaggcgtga gccaccatgc ccagctttga atactgaatc taagtatttt t 51 <210> 1893 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1894 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg36190410 <400> 1893 ccagccttga atactgaatc taagtatttt ttgctagttt taaaataatt a 51 <210> 1894 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1893 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg36190410 <400> 1894 ccagccttga atactgaatc taagtttttt ttgctagttt taaaataatt a 51 <210> 1895 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1896 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg36190410 <400> 1895 tctagcatat gttaaatgaa gtagattttt tttttaactc tccatttgat a 51 <210> 1896 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1895 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg36190410 <400> 1896 tctagcatat gttaaatgaa gtagattttt ttttaactct ccatttgata 50 <210> 1897 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1898 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg36504297 <400> 1897 cgttttcttc agtgcttcat tttatacctc aaattctgct gaagtgattt a 51 <210> 1898 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1897 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg36504297 <400> 1898 cgttttcttc agtgcttcat tttatgcctc aaattctgct gaagtgattt a 51 <210> 1899 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1900 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg36517624 <400> 1899 cctcctcgtc gcggaacggg ctctccccga agcgctcctc cagctgccgg c 51 <210> 1900 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1899 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg36517624 <400> 1900 cctcctcgtc gcggaacggg ctctcgccga agcgctcctc cagctgccgg c 51 <210> 1901 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26)...(0) <223> 1 of 2 allelic variants (1902 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg36517624 <400> 1901 ctgccggcga agcttctggg aactggccca gccaaactct tcaagctgct g 51 <210> 1902 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1901 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg36517624 <400> 1902 ctgccggcga agcttctggg aactgcccag ccaaactctt caagctgctg 50 <210> 1903 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1904 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg36588981 <400> 1903 aggagcacct caaggcctgt gacccgagca ccatgtcggg gtgtggctgc a 51 <210> 1904 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1903 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg36588981 <400> 1904 aggagcacct caaggcctgt gacccaagca ccatgtcggg gtgtggctgc a 51 <210> 1905 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1906 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg36603177 <400> 1905 tgagatcagg agttcgagac cagcccagcc aacatagtga aaccctgtct c 51 <210> 1906 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1905 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg36603177 <400> 1906 tgagatcagg agttcgagac cagcctagcc aacatagtga aaccctgtct c 51 <210> 1907 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1908 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg36618790 <400> 1907 caggcacggt ggttcacgtc tgtaacccca gcactttggg aggctgagga a 51 <210> 1908 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1907 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg36618790 <400> 1908 caggcacggt ggttcacgtc tgtaatccca gcactttggg aggctgagga a 51 <210> 1909 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1910 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg36618790 <400> 1909 cagcactttg ggaggctgag gaaggtggat gacttgagcc caggagtttg a 51 <210> 1910 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1909 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg36618790 <400> 1910 cagcactttg ggaggctgag gaaggcggat gacttgagcc caggagtttg a 51 <210> 1911 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1912 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg36618790 <400> 1911 ctttgggagg ctgaggaagg tggatgactt gagcccagga gtttgagacc a 51 <210> 1912 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1911 is other entry) <221> misc_feature <222> (.0) . . (0) <223> Accession number cg36618790 <400> 1912 ctttgggagg ctgaggaagg tggatcactt gagcccagga gtttgagacc a 51 <210> 1913 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1914 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg36618790 <400> 1913 gaaggtggat gacttgagcc caggagtttg agaccagcct gggcaacatg g 51 <210> 1914 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1913 is other entry) <221>miscfeature <222>(0)._ .(0) <223>Accession number cg36618790 <400>1914 gaaggtggat gacttgagcc caggaatttg agaccagcctgggcaacatg g 51 <210>1915 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1916 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg36623778 <400>1915 tgtgcctatc aaggttgtgg tcgaccgttg gaacgtgcccgtcaccgtca c 51 <210>1916 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ . . (0) <223>2 2 allelic variants (1915 of is other entry) <221>miscfeature <222>(0)._ .(0) <223>Accession number cg36623778 <400>1916 tgtgcctatc aaggttgtgg tcgacggttg gaacgtgcccgtcaccgtca c 51 <210>1917 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1918 of is other entry) <221>miscfeature <222>(0)._ .(0) <223>Accession number cg36733186 <400>1917 gctccacagg acaatgacct tggcccgtgg cccatcctctctggcctcca t S1 <210> 1918 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1917 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg36733186 <400> 1918 gctccacagg acaatgacct tggccggtgg cccatcctct ctggcctcca t 51 <210> 1919 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . . (0) <223> 1 of 2 allelic variants (1920 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg36753762 <400> 1919 caggagttca agaccagcct ggccaacatg atgaaaccct gtctctacta a 51 <210> 1920 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1919 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg36753762 <400> 1920 caggagttca agaccagcct ggccagcatg atgaaaccct gtctctacta a 51 <210> 1921 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1922 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg36753762 <400> 1921 ctactaaaaa tacacaaagt tagccaggcg tggtggcacg tgcctgtaat c 51 <210> 1922 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1921 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg36753762 <400> 1922 ctactaaaaa tacacaaagt tagccgggcg tggtggcacg tgcctgtaat c 51 <210> 1923 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1924 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg36999717 <400> 1923 cctgcgcctt cggatacgat cagcgtctag aggcatttgg ggccgacggc a 51 <210> 1924 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1923 is other entry) <221> misc feature <222> (0)...(0) <223> Accession number cg36999717 <400> 1924 cctgcgcctt cggatacgat cagcgcctag aggcatttgg ggccgacggc a 51 <210> 1925 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1926 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg36999717 <400> 1925 gtctagaggc atttggggcc gacggcatgc ttagtgccga caacctcacc g 51 <210> 1926 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1925 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg36999717 <400> 1926 gtctagaggc atttggggcc gacggatgct tagtgccgac aacctcaccg 50 <210> 1927 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1928 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg37003369 <400> 1927 gtgagtttca gttgatttaa ggaataaaaa aagaccattt tgctaaacac t 51 <210> 1928 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1927 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) , <223> Accession number cg37003369 <400> 1928 gtgagtttca gttgatttaa ggaataaaaa agaccatttt gctaaacact 50 <210> 1929 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1930 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg37028403 <400> 1929 caggtaaccc gcatattgtt gctggtggag tgcccaacac ggcacttgga a 51 <210> 1930 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1929 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg37028403 <400> 1930 caggtaaccc gcatattgtt gctggcggag tgcccaacac ggcacttgga a 51 <210> 1931 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1932 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg37056126 <400> 1931 ctggggctca ggccctatga cccaacggcc attggtggcc tgtcctcatg g 51 <210> 1932 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1931 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg37056126 <400> 1932 ctggggctca ggccctatga cccaatggcc attggtggcc tgtcctcatg g 51 <210> 1933 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1934 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg37056126 <400> 1933 caaaccacaa tagcagttct gggttatggg tttggtaaaa ccacctcagg g 51 <210> 1934 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1933 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg37056126 <400> 1934 caaaccacaa tagcagttct gggttttggg tttggtaaaa ccacctcagg g 51 <210> 1935 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1936 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg37418902 <400> 1935 atccacctca caaagaaatg caacacccat tagcggtcac tctcattctc c 51 <210> 1936 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1935 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg37418902 <400> 1936 atccacctca caaagaaatg caacatccat tagcggtcac tctcattctc c 51 <210> 1937 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1938 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg37418902 <400> 1937 caaagaaatg caacacccat tagcggtcac tctcattctc cttgtccagc c 51 <210> 1938 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1937 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg37418902 <400> 1938 caaagaaatg caacacccat tagcgctcac tctcattctc cttgtccagc c 51 <210> 1939 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1940 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg38034239 <400> 1939 ggcctggaac aggagagcgg gcgtagctcg ggcttctatg aagatcccag c 51 <210> 1940 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1939 is other entry) <221> misc_feature <222> (25) . . (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg38034239 <400>1940 ggcctggaac aggagagcgg gcgtactcgg gcttctatgaagatcccagc 50 <210>1941 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1942 entry) of is other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg38068769 <400>1941 ttatgctcct catctttcta gattggttca gatgccccttctaggaagcc t 51 <210>1942 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1941 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg38068769 <400>1942 ttatgctcct catctttcta gattgattca gatgccccttctaggaagcc t 51 <210>1943 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1944 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg38068769 <400>1943 tctagattgg ttcagatgcc ccttctagga agccttcccagattttcgcc c 51 <210> 1944 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1943 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38068769 <400> 1944 tctagattgg ttcagatgcc ccttccagga agccttccca gattttcgcc c 51 <210> 1945 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1946 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38070669 <400> 1945 actgttatgc cactgaaaaa aaaaaacaaa aaaacaaaac ccaaagccaa a 51 <210> 1946 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1945 is other entry) <221> misc_feature <222> (25) .. (26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg38070669 <400> 1946 actgttatgc cactgaaaaa aaaaacaaaa aaacaaaacc caaagccaaa 50 <210> 1947 <211> 51 <212> DNA

<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1948 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38206730 <400> 1947 aggtgtgcca catgttcatt ttcggttcaa ggcgtacacg tgcaggtgtg t 51 <210> 1948 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1947 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg38206730 <400> 1948 aggtgtgcca catgttcatt ttcggctcaa ggcgtacacg tgcaggtgtg t 51 <210> 1949 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1950 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38206730 <400> 1949 gttcattttc ggttcaaggc gtacacgtgc aggtgtgtta cgtgttcatt t 51 <210> 1950 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1949 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38206730 <400> 1950 gttcattttc ggttcaaggc gtacatgtgc aggtgtgtta cgtgttcatt t 51 <210> 1951 <211> 50 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1952 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0) . . (0) <223> Accession number cg38276118 <400> 1951 ttttgaaatt agccaaaaaa aaaaatcaaa ccttaaacat tgttcaattc 50 <210> 1952 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1951 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg38276118 <400> 1952 ttttgaaatt agccaaaaaa aaaaaatcaa accttaaaca ttgttcaatt c 51 <210> 1953 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1954 is other entry) <221> misc feature <zz2> (o),... (o>
<223> Accession number cg38277495 <400> 1953 cagcaccttg ggaggctgag gtgggcggat cacctgaggt tgggagttcg a 51 <210> 1954 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1953 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38277495 <400> 1954 cagcaccttg ggaggctgag gtgggtggat cacctgaggt tgggagttcg a 51 <210> 1955 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1956 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg38278604 <400> 1955 caggaatgtg atagaaagtg gctgggaaga gggagctgag gctggtgggt c 51 <210> 1956 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1955 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38278604 <400> 1956 caggaatgtg atagaaagtg gctggcaaga gggagctgag gctggtgggt c 51 <210> 1957 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1958 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg38279706 <400> 1957 tgcagctcca tggctcaaca aggtgcggat gcctgctgga cctggctgct t 51 <210> 1958 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1957 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38279706 <400> 1958 tgcagctcca tggctcaaca aggtgtggat gcctgctgga cctggctgct t 51 <210> 1959 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1960 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38318472 <400> 1959 ccacgtgtca tgactgtctg tccttctcca aggcagcatt cagacacccc g 51 <210> 1960 <211> 51 <212> DNA
<213> Homo sapiens <220>

<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1959 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg38318472 <400> 1960 ccacgtgtca tgactgtctg tccttttcca aggcagcatt cagacacccc g 51 <210> 1961 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1962 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38323872 <400> 1961 cgcccgcctc ggccaccaaa aatgctggga ccacaggctg taatttattt t 51 <210> 1962 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1961 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38323872 <400> 1962 cgcccgcctc ggccaccaaa aatgccggga ccacaggctg taatttattt t 51 <210> 1963 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1964 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38323872 <400> 1963 gcctcggcca ccaaaaatgc tgggaccaca ggctgtaatt tatttttttc a 51 <210> 1964 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1963 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38323872 <400> 1964 gcctcggcca ccaaaaatgc tgggatcaca ggctgtaatt tatttttttc a 51 <210> 1965 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1966 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38323872 <400> 1965 cctcggccac caaaaatgct gggaccacag gctgtaattt atttttttca t 51 <210> 1966 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1965 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38323872 <400> 1966 cctcggccac caaaaatgct gggactacag gctgtaattt atttttttca t 51 <210> 1967 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1968 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38326936 <400> 1967 tgcgcggcct gcgcacgctg ctggctaaga acaaccggct cggcgggccc a 51 <210> 1968 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1967 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38326936 <400> 1968 tgcgcggcct gcgcacgctg ctggccaaga acaaccggct cggcgggccc a 51 <210> 1969 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1970 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38338993 <400> 1969 ctgtagccta agcaacagag caagatgccg tctctgaaaa ggaaagaaaa c 51 <210> 1970 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26)...(0) <223> 2 of 2 allelic variants (1969 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38338993 <400> 1970 ctgtagccta agcaacagag caagacgccg tctctgaaaa ggaaagaaaa c 51 <210> 1971 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1972 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38341382 <400> 1971 ggtgcttaag acagcagact gctgctttgc tgggccaggc ctgggtttat t 51 <210> 1972 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1971 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38341382 <400> 1972 ggtgcttaag acagcagact gctgccttgc tgggccaggc ctgggtttat t 51 <210> 1973 <211> 51 - <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1974 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38345418 <400>1973 tggccgcctt ctccagttga tgggacaaat gacaagacctccagcatctt c 51 <210>1974 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1973 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg38345418 <400>1974 tggccgcctt ctccagttga tgggataaat gacaagacctccagcatctt c 51 <210>1975 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (1976 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg38350552 <400>1975 tcctgggcta ggatgacagc ttcctcctcg ttctcatctgcttctgccca g 51 <210>1976 <211>51 <212>DNA

<213>Homosapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (1975 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg38350552 <400>1976 tcctgggcta ggatgacagc ttcctactcg ttctcatctgcttctgccca g 51 <210>1977 <211>51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1978 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403226 <400> 1977 cgctgggtgg cgccatcgat aagtctcttg aagccgtcaa gatggctccc g 51 <210> 1978 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1977 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403226 <400> 1978 cgctgggtgg cgccatcgat aagtcccttg aagccgtcaa gatggctccc g 51 <210> 1979 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1980 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403226 <400> 1979 gcgccatcga taagtctctt gaagccgtca agatggctcc cggggggtct a 51 <210> 1980 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1979 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403226 <400> 1980 gcgccatcga taagtctctt gaagctgtca agatggctcc cggggggtct a 51 <210> 1981 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1982 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403226 <400> 1981 cggccgccat tgtcatgctc agtgacggga ataataccca aggcggttct c 51 <210> 1982 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1981 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403226 <400> 1982 cggccgccat tgtcatgctc agtgatggga ataataccca aggcggttct c 51 <210> 1983 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1984 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403226 <400> 1983 cgccattgtc atgctcagtg acgggaataa tacccaaggc ggttctcccc t 51 <210> 1984 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1983 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403226 <400> 1984 cgccattgtc atgctcagtg acggggataa tacccaaggc ggttctcccc t 51 <210> 1985 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1986 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg38403226 <400> 1985 tcagtgacgg gaataatacc caaggcggtt ctcccctggt ggcggccaac c 51 <210> 1986 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1985 is other entry) <221> misc_feature <222> , (0) . . (0) <223> Accession number cg38403226 <400> 1986 tcagtgacgg gaataatacc caaggtggtt ctcccctggt ggcggccaac c 51 <210> 1987 <211> 51 <212> DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1988 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg38403226 <400> 1987 caaccgagct gccgcggcca aagtctcggt gtacaccatc gcctttggta c 51 <210> 1988 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1987 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg38403226 <400> 1988 caaccgagct gccgcggcca aagtcccggt gtacaccatc gcctttggta c 51 <210> 1989 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1990 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg38403226 <400> 1989 taccgagacc gggtatgtcg accttgacgg gcagcgagag agagttgcac c 51 <210> 1990 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (1989 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403226 <400> 1990 taccgagacc gggtatgtcg accttaacgg gcagcgagag agagttgcac c 51 <210> 1991 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (1992 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403226 <400> 1991 tactgtcgcc gaccgtactc acgctaaatc gtggaccgcc gactcggcgg a 51 <210> 1992 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1991 is other entry) <221> misc_feature , <222> (0) . . (0) <223> Accession number cg38403226 <400> 1992 tactgtcgcc gaccgtactc acgctcaatc gtggaccgcc gactcggcgg a 51 <210> 1993 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1994 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403226 <400> 1993 ggatgccacc gtcgaccgac cggcctaccg tgttacgtgc tgttgacgga a 51 <210> 1994 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (1993 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403226 <400> 1994 ggatgccacc gtcgaccgac cggcccaccg tgttacgtgc tgttgacgga a 51 <210> 1995 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (1996 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403231 <400> 1995 aacggagaag ctcgaagtat caaagcggtt ggattcgtcg gatggggctc g 51 <210> 1996 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1995 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg38403231 <400> 1996 aacggagaag ctcgaagtat caaagtggtt ggattcgtcg gatggggctc g 51 <210> 1997 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (1998 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403231 <400> 1997 tggcaactgg atcggtgtca ttgggatcga cgaacggaga agctcgaagt a 51 <210> 1998 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (1997 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403231 <400> 1998 tggcaactgg atcggtgtca ttgggttcga cgaacggaga agctcgaagt a 51 <210> 1999 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (2000 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg38403266 <400> 1999 cggtatgcct ttgatggtca gtcacattga cgggcgctgg aacgctcgtg c 51 <210> 2000 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . . (0) <223> 2 of 2 allelic variants (1999 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403266 <400> 2000 cggtatgcct ttgatggtca gtcacgttga cgggcgctgg aacgctcgtg c 51 <210> 2001 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (2002 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403266 <400> 2001 acattgacgg gcgctggaac gctcgtgctg cccgctgaca cccgcaccga c 51 <210> 2002 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (2001 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403266 <400> 2002 acattgacgg gcgctggaac gctcgcgctg cccgctgaca cccgcaccga c 51 <210> 2003 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (2004 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403266 <400> 2003 acgggcgctg gaacgctcgt gctgcccgct gacacccgca ccgacgacgg g 51 <210> 2004 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (2003 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403266 <400> 2004 acgggcgctg gaacgctcgt gctgctcgct gacacccgca ccgacgacgg g 51 <210> 2005 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (2006 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403271 <400> 2005 tcaacggccc agtcggaatt tcgaaggatg atcgaaactt gctgacgaac t 51 <210> 2006 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (2005 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403271 <400> 2006 tcaacggccc agtcggaatt tcgaacgatg atcgaaactt gctgacgaac t 51 <210> 2007 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (2008 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg38403271 <400> 2007 atcgaaactt gctgacgaac tctcccatgg ttctgatgcc gggttcaagt a 51 <210> 2008 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (2007 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg38403271 <400> 2008 atcgaaactt gctgacgaac tctccgatgg ttctgatgcc gggttcaagt a 51 <210> 2009 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (2010 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403276 <400> 2009 agcagatcgc cgcatctgat ccggagcatt ccaagcggtt gttctccttt g 51 <210> 2010 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (2009 is other entry) <221> misc feature <222> (0)...(0) <223> Accession number cg38403276 <400> 2010 agcagatcgc cgcatctgat ccggaacatt ccaagcggtt gttctccttt g 51 <210> 2011 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (2012 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403276 <400> 2011 attccaagcg gttgttctcc tttgccaacc agatcgctgg tatggccagc c 51 <210> 2012 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (2011 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403276 <400> 2012 attccaagcg gttgttctcc tttgctaacc agatcgctgg tatggccagc c 51 <210> 2013 <211> 51 <212> DNA.
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (2014 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403276 <400> 2013 ctctcagatc ctcgacattc tgtctgcggg cctgattttc gtcgcgctgc t 51 <210> 2014 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (2013 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403276 <400> 2014 ctctcagatc ctcgacattc tgtctacggg cctgattttc gtcgcgctgc t 51 <210> 2015 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (2016 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403276 <400> 2015 tggaagactc gccgagaaac tcgggttggc ctctgcgagc ccgcgtggag t 51 <210> 2016 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (2015 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403276 <400> 2016 tggaagactc gccgagaaac tcgggctggc ctctgcgagc ccgcgtggag t 51 <210> 2017 <211> 51 <212> DNA
<213> Homo Sapiens <220>

<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (2018 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403276 <400> 2017 agaaactcgg gttggcctct gcgagcccgc gtggagtgat gttcgcgggg t 51 <210> 2018 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (2017 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403276 <400> 2018 agaaactcgg gttggcctct gcgagtccgc gtggagtgat gttcgcgggg t 51 <210> 2019 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (2020 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403276 <400> 2019 ctgcgagccc gcgtggagtg atgttcgcgg ggtcacctgc ttggactatc g 51 <210> 2020 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (2019 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403276 <400>2020 ctgcgagccc gcgtggagtg atgtttgcgg ggtcacctgcttggactatc g 51 <210>2021 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (2022 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg38403276 <400>2021 tcgataccgc caagacccta cgcgacctcg atgtgccgactctcatcgtc a 51 <210>2022 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (2021 entry) of is other <221>miscfeature <222>(0)._ .(0) <223>Accession number cg38403276 <400>2022 tcgataccgc caagacccta cgcgatctcg atgtgccgactctcatcgtc a 51 <210>2023 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (2024 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg38403276 <400>2023 cgataccgcc aagaccctac gcgacctcga tgtgccgactctcatcgtca c 51 <210> 2024 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (2023 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403276 <400> 2024 cgataccgcc aagaccctac gcgacttcga tgtgccgact ctcatcgtca c 51 <210> 2025 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (2026 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403276 <400> 2025 gtgcgtatga cctgtacgcg gcacgcaaag ccggtctgag atgcgaggct g 51 <210> 2026 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . .. (0) <223> 2 of 2 allelic variants (2025 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403276 <400> 2026 gtgcgtatga cctgtacgcg gcacgtaaag ccggtctgag atgcgaggct g 51 <210> 2027 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc feature <222> (26) . . . (0) <223> 1 of 2 allelic variants (2028 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403276 <400> 2027 aggctgcgga ctttctatct gaatacgcca ccgaagatat ggaccttgcc g 51 <210> 2028 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 2 of 2 allelic variants (2027 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403276 <400> 2028 aggctgcgga ctttctatct gaatatgcca ccgaagatat ggaccttgcc g 51 <210> 2029 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (2030 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403345 <400> 2029 gtgttgacgt gtaacttgga ttctccggct aagtcggcaa tcgtcactgg t 51 <210> 2030 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (2029 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403345 <400> 2030 gtgttgacgt gtaacttgga ttctctggct aagtcggcaa tcgtcactgg t 51 <210> 2031 <211> 51 <212> DNA
c213> Homo Sapiens <220>
<221> misc_feature c222> (26) ..(0) <223> 1 of 2 allelic variants (2032 is other entry) c221> misc_feature <222> (0) . . (0) c223> Accession number cg38403345 c400> 2031 aacttggatt ctccggctaa gtcggcaatc gtcactggtc ccgcgtggag c 51 <210> 2032 c211> 51 <212> DNA
<213> Homo Sapiens c220>
c221> misc_feature c222> (26) ..(0) <223> 2 of 2 allelic variants (2031 is other entry) c221> misc_feature <222> (0) . . (0) c223> Accession number cg38403345 c400> 2032 aacttggatt ctccggctaa gtcggtaatc gtcactggtc ccgcgtggag c 51 c210> 2033 <211> 51 <212> DNA
c213> Homo Sapiens c220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (2034 is other entry) c221> misc_feature c222> (0) . . (0) <223> Accession number cg38403345 <400> 2033 actggtcccg cgtggagcga tacttctttg aggactgact gctgggcagg g 51 c210> 2034 c211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (2033 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403345 <400> 2034 actggtcccg cgtggagcga tacttttttg aggactgact gctgggcagg g 51 <210> 2035 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (2036 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403345 <400> 2035 actgctgggc aggggtgagc gatgcgatga tggtgagaat ttcgcctatt c 51 <210> 2036 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (2035 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403345 <400> 2036 actgctgggc aggggtgagc gatgcaatga tggtgagaat ttcgcctatt c 51 <210> 2037 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 1 of 2 allelic variants (2038 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403345 <400> 2037 ctgggcaggg gtgagcgatg cgatgatggt gagaatttcg cctattcctt g 51 <210> 2038 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (2037 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg38403345 <400> 2038 ctgggcaggg gtgagcgatg cgatggtggt gagaatttcg cctattcctt g 51 <210> 2039 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (2040 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403345 <400> 2039 cccgctcata tcaccatccg tagtgccgcg acgaagatcc cagatggccg t 51 <210> 2040 <211> 51 <212> DNA
<213> Homo Sapiens , <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (2039 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403345 <400>2040 cccgctcata tcaccatccg tagtgtcgcg acgaagatcccagatggccgt 51 <210>2041 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>1 2 allelic variants (2042 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg38403345 <400>2041 catatcacca tccgtagtgc cgcgacgaag atcccagatggccgttcttgg 51 <210>2042 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ ..(0) <223>2 2 allelic variants (2041 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg38403345 <400>2042 catatcacca tccgtagtgc cgcgatgaag atcccagatggccgttcttgg 51 <210>2043 <211>51 <212>DNA

<213>HomoSapiens <220>

<221>miscfeature <222>(26)_ .. (0) <223>1 2 allelic variants (2044 entry) of is other <221>miscfeature <222>(0) _ . . (0) <223>Accession number cg38403345 <400>2043 tcttggacct gtatatgacg tatggtcttg tcgggtagcttactggcgcag 51 <210>2044 <211>51 <212>DNA

<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (2043 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403345 <400> 2044 tcttggacct gtatatgacg tatggccttg tcgggtagct tactggcgca g 51 <210> 2045 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (2046 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403345 <400> 2045 ccccagtatg gacggccccg gcctgttgct gggagtttct cgcgttccac c 51 <210> 2046 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (2045 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403345 <400> 2046 ccccagtatg gacggccccg gcctgctgct gggagtttct cgcgttccac c 51 <210> 2047 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (2048 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403345 <400> 2047 gctgggagtt tctcgcgttc caccagcccc aaggacacca gcacgttgag g 51 <210> 2048 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) .. (0) <223> 2 of 2 allelic variants (2047 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403345 <400> 2048 gctgggagtt tctcgcgttc caccaacccc aaggacacca gcacgttgag g 51 <210> 2049 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (2050 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403345 <400> 2049 gttccaccag ccccaaggac accagcacgt tgaggggctc ccgaatcgtg t 51 <210> 2050 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (2049 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403345 <400> 2050 gttccaccag ccccaaggac accagtacgt tgaggggctc ccgaatcgtg t 51 <210> 2051 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (2052 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403377 <400> 2051 aaatcttctt gacgatgacg tgcccttgtc tgagcgatcc ctgcttcgtc g 51 <210> 2052 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (2051 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403377 <400> 2052 aaatcttctt gacgatgacg tgcccgtgtc tgagcgatcc ctgcttcgtc g 51 <210> 2053 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (2054 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403377 <400> 2053 aatcttcttg acgatgacgt gcccttgtct gagcgatccc tgcttcgtcg t 51 <210> 2054 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (2053 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403377 <400> 2054 aatcttcttg acgatgacgt gccctggtct gagcgatccc tgcttcgtcg t 51 <210> 2055 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) . . (0) <223> 1 of 2 allelic variants (2056 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg38403377 <400> 2055 agcgatccct gcttcgtcgt tgcgtgccgt gagcgatccg gacgttgcac c 51 <210> 2056 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (2055 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403377 <400> 2056 agcgatccct gcttcgtcgt tgcgtaccgt gagcgatccg gacgttgcac c 51 <210> 2057 <211> 51 <212> DNA
<213> Homo Sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (2058 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403377 <400> 2057 cctctgcgac atatcgctgg gccgatgagg catcgacgat ctccccgcgg t 51 <210> 2058 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (2057 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38403377 <400> 2058 cctctgcgac atatcgctgg gccgacgagg catcgacgat ctccccgcgg t 51 <210> 2059 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (2060 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg38420254 <400> 2059 tccaggaaag gacaatgtcc tgcgagaaaa tcaggaggcc tccacttcct g 51 <210> 2060 <211> 50 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (2059 is other entry) <221> misc_feature <222> (25) ..(26) <223> Nucleotide deleted between bases 25 and 26 <221> misc_feature <222> (0). .(0) <223> Accession number cg38420254 <400> 2060 tccaggaaag gacaatgtcc tgcgaaaaat caggaggcct ccacttcctg 50 <210> 2061 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (2062 is other entry) <221> misc_feature <222> (0) . . (0) <223> Accession number cg38420254 <400> 2061 cagtcaataa ttgtctttgt ggatgtgata attttggaga tacacttctg g 51 <210> 2062 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 2 of 2 allelic variants (2061 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg38420254 <400> 2062 cagtcaataa ttgtctttgt ggatgcgata attttggaga tacacttctg g 51 <210> 2063 <211> 51 <212> DNA
<213> Homo sapiens <220>
<221> misc_feature <222> (26) ..(0) <223> 1 of 2 allelic variants (2064 is other entry) <221> misc_feature <222> (0). .(0) <223> Accession number cg38421034 <400> 2063 ggtgactctg agcaagttct ggagccgcac gcacaagggg ctcctgaaca g 51 <210> 2064 DEMANDE OU BREVET VOLUMINEUX
LA PRESENTE PARTIE DE CETTE DEMANDE OU CE BREVET COMPREND
PLUS D'UN TOME.

NOTE : Pour les tomes additionels, veuillez contacter 1e Bureau canadien des brevets JUMBO APPLICATIONS/PATENTS
THIS SECTION OF THE APPLICATION/PATENT CONTAINS MORE THAN ONE
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Claims (44)

WHAT IS CLAIMED IS:

1. An isolated polynucleotide selected from the group consisting of:
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a) a nucleotide sequence comprising one or more polymorphic sequences selected from the group consisting of SEQ ID NOS:1 - 7024;

b) a fragment of said nucleotide sequence, provided that the fragment includes a polymorphic site in said polymorphic sequence;

c) a complementary nucleotide sequence comprising a sequence complementary to one or more of said polymorphic sequences selected from the group consisting of SEQ ID NOS:1-7024; and d) a fragment of said complementary nucleotide sequence, provided that the fragment includes a polymorphic site in said polymorphic sequence.

2. The polynucleotide of claim 1, wherein said polynucleotide sequence is DNA.

3. The polynucleotide of claim 1, wherein said polynucleotide sequence is RNA.

4. The polynucleotide of claim 1, wherein said polynucleotide sequence is between about and about 100 nucleotides in length.

5. The polynucleotide of claim 1, wherein said polynucleotide sequence is between about 10 and about 90 nucleotides in length.

6. The polynucleotide of claim 1, wherein said polynucleotide sequence is between about 10 and about 75 nucleotides in length.

7. The polynucleotide of claim 1, wherein said polynucleotide is between about 10 and about 50 bases in length.

8. The polynucleotide of claim 1, wherein said polynucleotide is between about 10 and about 40 bases in length.

9. The polynucleotide of claim 1, wherein said polynucleotide is between about 15 and about 30 bases in length.

10. The polynucleotide of claim 1, wherein said polymorphic site includes a nucleotide other than the nucleotide listed in Table 1, column 5 for said polymorphic sequence.

11. The polynucleotide of claim 1, wherein the complement of said polymorphic site includes a nucleotide other than the complement of the nucleotide listed in Table 1, column 5 for the complement of said polymorphic sequence.

12. The polynucleotide of claim 1, wherein said polymorphic site includes the nucleotide listed in Table 1, column 6 for said polymorphic sequence.

13. The polynucleotide of claim 1, wherein the complement of said polymorphic site includes the complement of the nucleotide listed in Table 1, column 6 for said polymorphic sequence.

14. An isolated allele-specific oligonucleotide that hybridizes to a first polynucleotide at a polymorphic site encompassed therein, wherein the first polynucleotide is selected from the group consisting of:

a) a nucleotide sequence comprising one or more polymorphic sequences selected from the group consisting of SEQ ID NOS:1 - 7024 provided that the polymorphic sequence includes a nucleotide other than the nucleotide recited in Table 1, column 5 for said polymorphic sequence;

b) a nucleotide sequence that is a fragment of said polymorphic sequence, provided that the fragment includes a polymorphic site in said polymorphic sequence;

c) a complementary nucleotide sequence comprising a sequence complementary to one or more polymorphic sequences selected from the group consisting of SEQ ID NOS:1 - 7024, provided that the complementary nucleotide sequence includes a nucleotide other than the complement of the nucleotide recited in Table 1, column 5; and d) a nucleotide sequence that is a fragment of said complementary sequence, provided that the fragment includes a polymorphic site in said polymorphic sequence.

15. The oligonucleotide of claim 14, wherein the oligonucleotide does not hybridize under stringent conditions to a second polynucleotide selected from the group consisting of:

a) a nucleotide sequence comprising one or more polymorphic sequences selected from the group consisting of SEQ ID NOS:1 - 7024, wherein said polymorphic sequence includes the nucleotide listed in Table 1, column 5 for said polymorphic sequence;

b) a nucleotide sequence that is a fragment of any of said nucleotide sequences;

c) a complementary nucleotide sequence comprising a sequence complementary to one or more polymorphic sequences selected from the group consisting of SEQ ID NOS:1 - 7024, wherein said polymorphic sequence includes the complement of the nucleotide listed in Table 1, column 5; and d) a nucleotide sequence that is a fragment of said complementary sequence, provided that the fragment includes a polymorphic site in said polymorphic sequence.

16. The oligonucleotide of claim 15, wherein the oligonucleotide is between about 10 and about 51 bases in length.

17. The oligonucleotide of claim 15, wherein the oligonucleotide is between about 10 and about 40 bases in length.

18. The oligonucleotide of claim 15, wherein the oligonucleotide is between about 1 S and about 30 bases in length.

19. A method of detecting a polymorphic site in a nucleic acid, the method comprising:

a) contacting said nucleic acid with an oligonucleotide that hybridizes to a polymorphic sequence selected from the group consisting of SEQ ID NOS:

1-7024, or its complement, provided that the polymorphic sequence includes a nucleotide other than the nucleotide recited in Table 1, column 5 for said polymorphic sequence, or the complement includes a nucleotide other than the complement of the nucleotide recited in Table 1, column 5; and b) determining whether said nucleic acid and said oligonucleotide hybridize;

whereby hybridization of said oligonucleotide to said nucleic acid sequence indicates the presence of the polymorphic site in said nucleic acid.

20. The method of claim 19, wherein said oligonucleotide does not hybridize to said polymorphic sequence when said polymorphic sequence includes the nucleotide recited in Table 1, column 5 for said polymorphic sequence, or when the complement of the polymorphic sequence includes the complement of the nucleotide recited in Table 1, column 5 for said polymorphic sequence.

21. The method of claim 19, wherein said oligonucleotide is between about 10 and about 51 bases in length.

22. The method of claim 19, wherein said oligonucleotide is between about 10 and about 40 bases in length.

23. A method of detecting the presence of a sequence polymorphism in a subject, the method comprising:

a) providing a nucleic acid from said subject;

b) contacting said nucleic acid with an oligonucleotide that hybridizes to a polymorphic sequence selected from the group consisting of SEQ ID NOS:

1-7024, or its complement, provided that the polymorphic sequence includes a nucleotide other than the nucleotide recited in Table 1, column 5 for said polymorphic sequence, or the complement includes a nucleotide other than the complement of the nucleotide recited in Table 1, column 5; and c) determining whether said nucleic acid and said oligonucleotide hybridize;
whereby hybridization of said oligonucleotide to said nucleic acid sequence indicates the presence of the polymorphism in said subject.

24. A method of determining the relatedness of a first and second nucleic acid, the method comprising:

a) providing a first nucleic acid and a second nucleic acid;

b) contacting said first nucleic acid and said second nucleic acid with an oligonucleotide that hybridizes to a polymorphic sequence selected from the group consisting of SEQ ID NOS: 1-7024, or its complement, provided that the polymorphic sequence includes a nucleotide other than the nucleotide recited in Table 1, column 5 for said polymorphic sequence, or the complement includes a nucleotide other than the complement of the nucleotide recited in Table 1, column 5;

c) determining whether said first nucleic acid and said second nucleic acid hybridize to said oligonucleotide; and d) comparing hybridization of said first and second nucleic acids to said oligonucleotide, wherein hybridization of first and second nucleic acids to said nucleic acid indicates the first and second subjects are related.

25. The method of claim 24, wherein said oligonucleotide does not hybridize to said polymorphic sequence when said polymorphic sequence includes the nucleotide recited in Table 1, column 5 for said polymorphic sequence, or when the complement of the polymorphic sequence includes the complement of the nucleotide recited in Table 1, column 5 for said polymorphic sequence.

26. The method of claim 24, wherein the oligonucleotide is between about 10 and about 51 bases in length.

27. The method of claim 24, wherein the oligonucleotide is between about 10 and about 40 bases in length.

28. The method of claim 24, wherein the oligonucleotide is between about 15 and about 30 bases in length.

29. An isolated polypeptide comprising a polymorphic site at one or more amino acid residues, wherein the protein is encoded by a polynucleotide selected from the group consisting of polymorphic sequences SEQ ID NOS:1-7024, or their complement, provided that the polymorphic sequence includes a nucleotide other than the nucleotide recited in Table 1, column 5 for said polymorphic sequence, or the complement includes a nucleotide other than the complement of the nucleotide recited in Table 1, column 5.

30. The polypeptide of claim 29, wherein said polypeptide is translated in the same open reading frame as is a wild type protein whose amino acid sequence is identical to the amino acid sequence of the polymorphic protein except at the site of the polymorphism.

31. The polypeptide of claim 29, wherein the polypeptide encoded by said polymorphic sequence, or its complement, includes the nucleotide listed in Table 1, column 6 for said polymorphic sequence, or the complement includes the complement of the nucleotide listed in Table 1, column 6.

32. An antibody that binds specifically to a polypeptide encoded by a polynucleotide comprising a nucleotide sequence selected from the group consisting of polymorphic sequences SEQ ID NOS:1-7024, or its complement, provided that the polymorphic sequence includes a nucleotide other than the nucleotide recited in Table 1, column 5 for said polymorphic sequence, or the complement includes a nucleotide other than the complement of the nucleotide recited in Table 1, column 5.

33. The antibody of claim 32, wherein said antibody binds specifically to a polypeptide encoded by a polymorphic sequence which includes the nucleotide listed in Table 1, column 6 for said polymorphic sequence.

34. The antibody of claim 32, wherein said antibody does not bind specifically to a polypeptide encoded by a polymorphic sequence which includes the nucleotide listed in Table 1, column 5 for said polymorphic sequence.

35. A method of detecting the presence of a polypeptide having one or more amino acid residue polymorphisms in a subject, the method comprising a) providing a protein sample from said subject;

b) contacting said sample with the antibody of claim 34 under conditions that allow for the formation of antibody-antigen complexes; and c) detecting said antibody-antigen complexes, whereby the presence of said complexes indicates the presence of said polypeptide.

36. A method of treating a subject suffering from, at risk for, or suspected of, suffering from a pathology ascribed to the presence of a sequence polymorphism in a subject, the method comprising:

a) providing a subject suffering from a pathology associated with aberrant expression of a first nucleic acid comprising a polymorphic sequence selected from the group consisting of SEQ ID NOS:1 - 7024, or its complement; and b) administering to the subject an effective therapeutic dose of a second nucleic acid comprising the polymorphic sequence, provided that the second nucleic acid comprises the nucleotide present in the wild type allele, thereby treating said subject.

37. The method of claim 36, wherein the second nucleic acid sequence comprises a polymorphic sequence which includes the nucleotide listed in Table 1, column 5 for said polymorphic sequence.

38. A method of treating a subject suffering from, at risk for, or suspected of, suffering from a pathology ascribed to the presence of a sequence polymorphism in a subject, the method comprising:

a) providing a subject suffering from a pathology associated with aberrant expression of a polymorphic sequence selected from the group consisting of polymorphic sequences SEQ ID NOS:1 - 7024, or its complement; and b) administering to the subject an effective therapeutic dose of a polypeptide, wherein said polypeptide is encoded by a polynucleotide comprising a polymorphic sequence selected from the group consisting of SEQ ID NOS:1 - 7024, or by a polynucleotide comprising a nucleotide sequence that is complementary to any one of polymorphic sequences SEQ ID NOS:1 - 7024, provided that said polymorphic sequence includes the nucleotide listed in Table 1, column 6 for said polymorphic sequence.

39. A method of treating a subject suffering from, at risk for, or suspected of suffering from, a pathology ascribed to the presence of a sequence polymorphism in a subject, the method comprising:
a) providing a subject suffering from, at risk for, or suspected of suffering from, a pathology associated with aberrant expression of a first nucleic acid comprising a polymorphic sequence selected from the group consisting of SEQ ID NOS:1 - 7024, or its complement; and b) administering to the subject an effective dose of the antibody of claim 34, thereby treating said subject.

40. A method of treating a subject suffering from, at risk for, or suspected of suffering from, a pathology ascribed to the presence of a sequence polymorphism in a subject, the method comprising:
a) providing a subject suffering from, at risk for, or suspected of suffering from, a pathology associated with aberrant expression of a nucleic acid comprising a polymorphic sequence selected from the group consisting of SEQ ID
NOS:1 - 7024, or its complement; and b) administering to the subject an effective dose of an oligonucleotide comprising a polymorphic sequence selected from the group consisting of SEQ ID NOS:1 - 7024, or by a polynucleotide comprising a nucleotide sequence that is complementary to any one of polymorphic sequences SEQ
ID NOS:1 - 7024, provided that said polymorphic sequence includes the nucleotide listed in Table 1, column 5 or Table 1, column 6 for said polymorphic sequence, thereby treating said subject.

41. An oligonucleotide array, comprising one or more oligonucleotides hybridizing to a first polynucleotide at a polymorphic site encompassed therein, wherein the first polynucleotide is chosen from the group consisting of:
a) a nucleotide sequence comprising one or more polymorphic sequences selected from the group consisting of SEQ ID NOS:1 - 7024;
b) a nucleotide sequence that is a fragment of any of said nucleotide sequence, provided that the fragment includes a polymorphic site in said polymorphic sequence;

c) a complementary nucleotide sequence comprising a sequence complementary to one or more polymorphic sequences selected from the group consisting of SEQ ID NOS:1 - 7024; and d) a nucleotide sequence that is a fragment of said complementary sequence, provided that the fragment includes a polymorphic site in said polymorphic sequence.

42. The array of claim 41, wherein said array comprises about 10 oligonucleotides.

43. The array of claim 41, wherein said array comprises about 100 oligonucleotides.

44. The array of claim 41, wherein said array comprises about 1000 oligonucleotides.