geneid | 121793 |
---|---|
ensemblid | ENSG00000153495.11 |
hgncid | 20370 |
symbol | TEX29 |
name | testis expressed 29 |
refseq_nuc | NM_152324.3 |
refseq_prot | NP_689537.1 |
ensembl_nuc | ENST00000283547.2 |
ensembl_prot | ENSP00000283547.1 |
mane_status | MANE Select |
chr | chr13 |
start | 111320642 |
end | 111344248 |
strand | + |
ver | v1.2 |
region | chr13:111320642-111344248 |
region5000 | chr13:111315642-111349248 |
regionname0 | TEX29_chr13_111320642_111344248 |
regionname5000 | TEX29_chr13_111315642_111349248 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 151 | 410 | 88 | 78 | 184 | 16 | 42 | 138 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0002 | 0/0 | 151 | 4 | 3 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0003 | 0/0 | 151 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0004 | 0/0 | 151 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 456 | 219 | 21 | 41 | 118 | 9 | 30 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
c0002 | 1/1 | 456 | 164 | 63 | 30 | 52 | 7 | 10 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
c0003 | 0/0 | 456 | 21 | 0 | 6 | 13 | 0 | 2 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
c0004 | 0/0 | 456 | 4 | 3 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
c0005 | 0/0 | 456 | 3 | 2 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
c0006 | 0/0 | 456 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
c0007 | 0/0 | 456 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
c0008 | 0/0 | 456 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
c0009 | 0/0 | 456 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
c0010 | 0/0 | 456 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 281 | 195 | 46 | 44 | 61 | 9 | 34 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
t0002 | 0/0 | 281 | 154 | 1 | 26 | 116 | 5 | 6 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
t0003 | 0/1 | 281 | 39 | 21 | 7 | 7 | 2 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
t0004 | 0/0 | 281 | 9 | 9 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
t0005 | 0/0 | 278 | 5 | 5 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
t0006 | 0/0 | 281 | 4 | 4 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
t0007 | 0/0 | 281 | 3 | 0 | 1 | 0 | 0 | 2 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
t0008 | 0/0 | 281 | 3 | 3 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
t0009 | 0/0 | 281 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
t0010 | 0/0 | 281 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
t0011 | 0/0 | 281 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 18 | 0 | 4 | 13 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0003 | 0/0 | 8 | 0 | 0 | 5 | 2 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0006 | 0/0 | 6 | 1 | 5 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0007 | 0/0 | 5 | 0 | 1 | 2 | 1 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0008 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0010 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0015 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0053 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0054 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0061 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0135 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 456 | 219 | 21 | 41 | 118 | 9 | 30 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0001c0002 | 1/1 | 456 | 164 | 63 | 30 | 52 | 7 | 10 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0001c0003 | 0/0 | 456 | 21 | 0 | 6 | 13 | 0 | 2 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0001c0005 | 0/0 | 456 | 3 | 2 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0001c0006 | 0/0 | 456 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0001c0008 | 0/0 | 456 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0001c0010 | 0/0 | 456 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0002c0004 | 0/0 | 456 | 4 | 3 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0003c0009 | 0/0 | 456 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0004c0007 | 0/0 | 456 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 736 | 74 | 11 | 20 | 17 | 5 | 21 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0001c0001t0002 | 0/0 | 736 | 132 | 1 | 20 | 101 | 4 | 6 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0001c0001t0003 | 0/0 | 736 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0001c0001t0006 | 0/0 | 736 | 3 | 3 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0001c0001t0007 | 0/0 | 736 | 3 | 0 | 1 | 0 | 0 | 2 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0001c0001t0008 | 0/0 | 736 | 3 | 3 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0001c0001t0010 | 0/0 | 736 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0001c0001t0011 | 0/0 | 736 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0001c0002t0001 | 1/0 | 736 | 102 | 29 | 18 | 41 | 4 | 9 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0001c0002t0002 | 0/0 | 736 | 11 | 0 | 6 | 4 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0001c0002t0003 | 0/1 | 736 | 35 | 18 | 6 | 7 | 2 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0001c0002t0004 | 0/0 | 736 | 9 | 9 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0001c0002t0005 | 0/0 | 733 | 5 | 5 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0001c0002t0009 | 0/0 | 736 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0001c0003t0001 | 0/0 | 736 | 11 | 0 | 6 | 3 | 0 | 2 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0001c0003t0002 | 0/0 | 736 | 10 | 0 | 0 | 10 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0001c0005t0001 | 0/0 | 736 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0001c0005t0003 | 0/0 | 736 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0001c0006t0002 | 0/0 | 736 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0001c0008t0006 | 0/0 | 736 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0001c0010t0001 | 0/0 | 736 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0002c0004t0001 | 0/0 | 736 | 4 | 3 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0003c0009t0001 | 0/0 | 736 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
a0004c0007t0003 | 0/0 | 736 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | copy fasta | chr13 | 111315642 | 111349248 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0001 | 0/0 | 18 | 0 | 4 | 13 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0003 | 0/0 | 7 | 0 | 0 | 5 | 2 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0015 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0003g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0006g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0006g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0007g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0007g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0008g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0008g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0010g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0001t0011g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0006 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0007 | 0/0 | 5 | 0 | 1 | 2 | 1 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0008 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0135 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0002g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0053 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0054 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0061 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0003g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0004g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0004g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0005g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0009g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0002t0009g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0003t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0003t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0003t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0003t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0003t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0003t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0003t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0003t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0003t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0003t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0003t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0005t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0005t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0005t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0006t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0008t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0001c0010t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0002c0004t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0002c0004t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0002c0004t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0003c0009t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
a0004c0007t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0101 | EUR | GBR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0269 | EUR | GBR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0154 | EUR | GBR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0007 | EUR | FIN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00280 | hp2 | a0001 | c0002 | t0003 | g0053 | EUR | FIN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00323 | hp1 | a0001 | c0002 | t0003 | g0053 | EUR | FIN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00323 | hp2 | a0001 | c0002 | t0002 | g0229 | EUR | FIN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00544 | hp2 | a0001 | c0003 | t0002 | g0044 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0274 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00639 | hp1 | a0001 | c0002 | t0003 | g0062 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0155 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0121 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00735 | hp1 | a0001 | c0003 | t0001 | g0026 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG00738 | hp2 | a0001 | c0002 | t0003 | g0259 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01070 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01070 | hp2 | a0001 | c0003 | t0001 | g0125 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0099 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01081 | hp1 | a0001 | c0005 | t0003 | g0137 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01081 | hp2 | a0001 | c0003 | t0001 | g0105 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01106 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01106 | hp2 | a0001 | c0002 | t0003 | g0289 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01167 | hp1 | a0001 | c0002 | t0002 | g0166 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0162 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01168 | hp1 | a0001 | c0003 | t0001 | g0124 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0100 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0096 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01192 | hp1 | a0001 | c0002 | t0002 | g0164 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01243 | hp2 | a0001 | c0002 | t0003 | g0063 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01255 | hp2 | a0001 | c0001 | t0007 | g0025 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01256 | hp2 | a0001 | c0003 | t0001 | g0109 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01261 | hp1 | a0001 | c0002 | t0003 | g0293 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0035 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0235 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0086 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0084 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01496 | hp1 | a0001 | c0003 | t0001 | g0026 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0102 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | IBS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | IBS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01884 | hp1 | a0002 | c0004 | t0001 | g0030 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01884 | hp2 | a0001 | c0002 | t0004 | g0034 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0022 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0268 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0098 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0097 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0267 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0277 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02055 | hp2 | a0001 | c0002 | t0004 | g0139 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02132 | hp1 | a0001 | c0006 | t0002 | g0284 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02145 | hp1 | a0001 | c0005 | t0001 | g0159 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02148 | hp2 | a0001 | c0002 | t0003 | g0054 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | CDX | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | CDX | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | CDX | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02257 | hp2 | a0001 | c0002 | t0003 | g0255 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02258 | hp1 | a0002 | c0004 | t0001 | g0030 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02258 | hp2 | a0001 | c0002 | t0004 | g0014 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02280 | hp1 | a0001 | c0002 | t0009 | g0281 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02451 | hp1 | a0001 | c0002 | t0003 | g0256 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0266 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02523 | hp2 | a0001 | c0003 | t0002 | g0044 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02572 | hp1 | a0001 | c0005 | t0001 | g0160 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02615 | hp1 | a0001 | c0002 | t0003 | g0052 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0088 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02622 | hp2 | a0001 | c0001 | t0011 | g0131 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02630 | hp1 | a0001 | c0001 | t0006 | g0296 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0260 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02647 | hp1 | a0001 | c0002 | t0005 | g0066 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02647 | hp2 | a0001 | c0002 | t0003 | g0052 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02698 | hp2 | a0001 | c0001 | t0007 | g0025 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0263 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02723 | hp1 | a0004 | c0007 | t0003 | g0257 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02735 | hp1 | a0001 | c0002 | t0003 | g0288 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02738 | hp2 | a0002 | c0004 | t0001 | g0280 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0262 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0095 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0264 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02895 | hp2 | a0002 | c0004 | t0001 | g0163 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02896 | hp2 | a0001 | c0002 | t0003 | g0051 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02897 | hp1 | a0001 | c0002 | t0003 | g0051 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0261 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02965 | hp1 | a0001 | c0002 | t0003 | g0047 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0022 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02970 | hp1 | a0001 | c0002 | t0004 | g0034 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02970 | hp2 | a0001 | c0002 | t0003 | g0156 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02976 | hp1 | a0001 | c0002 | t0003 | g0047 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0059 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03041 | hp2 | a0001 | c0002 | t0004 | g0140 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03098 | hp1 | a0001 | c0002 | t0005 | g0067 | AFR | MSL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | MSL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03130 | hp2 | a0001 | c0002 | t0003 | g0258 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03139 | hp1 | a0001 | c0002 | t0004 | g0014 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03209 | hp1 | a0001 | c0002 | t0005 | g0068 | AFR | MSL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03209 | hp2 | a0001 | c0002 | t0003 | g0141 | AFR | MSL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03225 | hp1 | a0001 | c0002 | t0003 | g0283 | AFR | MSL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | MSL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | MSL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03490 | hp1 | a0001 | c0003 | t0001 | g0027 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03492 | hp1 | a0001 | c0003 | t0001 | g0027 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03516 | hp1 | a0001 | c0002 | t0003 | g0048 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03516 | hp2 | a0001 | c0008 | t0006 | g0091 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03540 | hp1 | a0001 | c0002 | t0004 | g0138 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0103 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03579 | hp1 | a0001 | c0002 | t0003 | g0285 | AFR | MSL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | MSL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03654 | hp2 | a0001 | c0001 | t0007 | g0104 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0152 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | STU | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0252 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0273 | SAS | BEB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | BEB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0270 | SAS | BEB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0007 | SAS | STU | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG04115 | hp2 | a0003 | c0009 | t0001 | g0248 | SAS | STU | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0271 | SAS | BEB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0247 | SAS | BEB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0272 | SAS | STU | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | STU | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | STU | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | STU | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0202 | SAS | STU | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | STU | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18522 | hp1 | a0001 | c0001 | t0008 | g0077 | AFR | YRI | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | YRI | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | CHB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | CHB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18906 | hp1 | a0001 | c0002 | t0009 | g0282 | AFR | YRI | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0060 | AFR | YRI | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18954 | hp2 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18959 | hp1 | a0001 | c0003 | t0002 | g0196 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18962 | hp1 | a0001 | c0003 | t0002 | g0238 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18967 | hp1 | a0001 | c0003 | t0002 | g0041 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18968 | hp1 | a0001 | c0002 | t0003 | g0290 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18971 | hp1 | a0001 | c0002 | t0003 | g0291 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18974 | hp2 | a0001 | c0003 | t0001 | g0020 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18987 | hp1 | a0001 | c0002 | t0003 | g0287 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18993 | hp1 | a0001 | c0003 | t0002 | g0232 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18997 | hp1 | a0001 | c0002 | t0003 | g0018 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19005 | hp2 | a0001 | c0003 | t0002 | g0017 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19009 | hp1 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19030 | hp1 | a0001 | c0002 | t0005 | g0069 | AFR | LWK | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19030 | hp2 | a0001 | c0002 | t0003 | g0286 | AFR | LWK | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19066 | hp2 | a0001 | c0002 | t0003 | g0050 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19068 | hp1 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19070 | hp1 | a0001 | c0003 | t0002 | g0041 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19075 | hp2 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19077 | hp1 | a0001 | c0003 | t0002 | g0017 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19077 | hp2 | a0001 | c0003 | t0001 | g0020 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19079 | hp1 | a0001 | c0002 | t0003 | g0050 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19083 | hp1 | a0001 | c0003 | t0002 | g0017 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19085 | hp1 | a0001 | c0003 | t0001 | g0079 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19088 | hp1 | a0001 | c0002 | t0003 | g0158 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19240 | hp1 | a0001 | c0001 | t0008 | g0029 | AFR | YRI | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | YRI | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | ASW | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA20129 | hp2 | a0001 | c0001 | t0008 | g0029 | AFR | ASW | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0085 | EUR | TSI | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | TSI | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA20905 | hp1 | a0001 | c0001 | t0010 | g0292 | SAS | GIH | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | GIH | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02109 | hp1 | a0001 | c0002 | t0003 | g0054 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02109 | hp2 | a0001 | c0002 | t0003 | g0254 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0279 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02486 | hp2 | a0001 | c0002 | t0003 | g0048 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0253 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG02559 | hp2 | a0001 | c0002 | t0004 | g0014 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | MSL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG06807 | hp1 | a0001 | c0010 | t0001 | g0126 | AFR | USA | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | USA | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA20300 | hp1 | a0001 | c0002 | t0004 | g0014 | AFR | USA | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0058 | AFR | USA | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | LWK | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
NA21309 | hp2 | a0001 | c0002 | t0005 | g0065 | AFR | LWK | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0003 | g0061 | REF | REF | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0135 | REF | REF | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:111342757
|
G | A | 1 | a0002 | 4 | HG01884.hp1 HG02258.hp1 HG02738.hp2 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.241G>A | p.Val81Ile | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/6 | 396/736 | 241/456 | 81/151 | chr13 | 111342757 | ||
chr13:111342802
|
G | A | 1 | a0003 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.286G>A | p.Ala96Thr | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/6 | 441/736 | 286/456 | 96/151 | chr13 | 111342802 | ||
chr13:111342803
|
C | T | 1 | a0004 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.287C>T | p.Ala96Val | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/6 | 442/736 | 287/456 | 96/151 | chr13 | 111342803 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:111328190
|
C | T | 5 | a0001c0001a0001c0003a0001c0010others(2): Show | 246 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(243): Show |
synonymous_variant | LOW | c.66C>T | p.Asp22Asp | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/6 | 221/736 | 66/456 | 22/151 | chr13 | 111328190 | ||
chr13:111339900
|
C | A | 2 | a0001c0003a0001c0005 | 24 | HG00544.hp2 HG00735.hp1 HG01070.hp2 others(21): Show |
synonymous_variant | LOW | c.207C>A | p.Ile69Ile | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/6 | 362/736 | 207/456 | 69/151 | chr13 | 111339900 | ||
chr13:111339912
|
C | T | 1 | a0001c0008 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.219C>T | p.Phe73Phe | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/6 | 374/736 | 219/456 | 73/151 | chr13 | 111339912 | ||
chr13:111342822
|
C | T | 1 | a0001c0010 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.306C>T | p.Ser102Ser | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/6 | 461/736 | 306/456 | 102/151 | chr13 | 111342822 | ||
chr13:111342903
|
G | A | 1 | a0001c0006 | 1 | HG02132.hp1 | synonymous_variant | LOW | c.387G>A | p.Ser129Ser | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/6 | 542/736 | 387/456 | 129/151 | chr13 | 111342903 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:111320650
|
C | T | 1 | a0001c0002t0005 | 5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-147C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 1/6 | 241 | chr13 | 111320650 | |||||
chr13:111320672
|
TTTG | T | 1 | a0001c0002t0005 | 5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-119_-117delGTT | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 1/6 | 211 | INFO_REALIGN_3_PRIME | chr13 | 111320672 | ||||
chr13:111320703
|
G | A | 7 | a0001c0001t0003a0001c0001t0010a0001c0002t0003others(4): Show | 51 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(48): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-94G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 1/6 | chr13 | 111320703 | ||||||
chr13:111320751
|
T | C | 11 | a0001c0001t0002a0001c0001t0003a0001c0001t0010others(8): Show | 205 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(202): Show |
5_prime_UTR_variant | MODIFIER | c.-46T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 1/6 | 140 | chr13 | 111320751 | |||||
chr13:111344130
|
C | T | 1 | a0001c0001t0011 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 6/6 | 7 | chr13 | 111344130 | |||||
chr13:111344172
|
G | C | 2 | a0001c0001t0007a0001c0001t0010 | 4 | HG01255.hp2 HG02698.hp2 HG03654.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*49G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 6/6 | 49 | chr13 | 111344172 | |||||
chr13:111344201
|
A | G | 2 | a0001c0001t0008a0001c0002t0004 | 12 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*78A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 6/6 | 78 | chr13 | 111344201 | |||||
chr13:111344221
|
G | A | 3 | a0001c0001t0006a0001c0002t0009a0001c0008t0006 | 6 | HG02280.hp1 HG02630.hp1 HG03139.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*98G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 6/6 | 98 | chr13 | 111344221 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:111320850
|
T | G | 1 | a0001c0001t0002g0056 | 1 | HG00408.hp1 | splice_region_variant&intron_variant | LOW | c.-34-7T>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 1/5 | chr13 | 111320850 | ||||||
chr13:111320974
|
C | T | 3 | a0001c0001t0001g0055a0001c0001t0001g0295a0001c0001t0006g0296 | 4 | HG01891.hp1 HG02630.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+26C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111320974 | ||||||
chr13:111320983
|
T | C | 1 | a0001c0002t0001g0057 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.58+35T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111320983 | ||||||
chr13:111320995
|
T | TG | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0049others(167): Show | 235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.58+56dupG | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111320995 | |||||
chr13:111321006
|
A | G | 191 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0049others(188): Show | 261 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.58+58A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321006 | ||||||
chr13:111321072
|
G | A | 1 | a0001c0002t0003g0158 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.58+124G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321072 | ||||||
chr13:111321107
|
G | A | 7 | a0001c0002t0003g0141a0001c0002t0004g0014a0001c0002t0004g0034others(4): Show | 11 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.58+159G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321107 | ||||||
chr13:111321115
|
G | A | 2 | a0001c0005t0001g0159a0001c0005t0001g0160 | 2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.58+167G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321115 | ||||||
chr13:111321198
|
A | G | 1 | a0001c0001t0002g0294 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.58+250A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321198 | ||||||
chr13:111321241
|
C | T | 28 | a0001c0001t0003g0033a0001c0001t0010g0292a0001c0002t0003g0050others(25): Show | 38 | HG00280.hp2 HG00323.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.58+293C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321241 | ||||||
chr13:111321242
|
G | A | 1 | a0001c0001t0002g0161 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.58+294G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321242 | ||||||
chr13:111321334
|
A | C | 85 | a0001c0001t0001g0049a0001c0001t0001g0153a0001c0001t0001g0154others(82): Show | 104 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.58+386A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321334 | ||||||
chr13:111321365
|
C | T | 2 | a0001c0002t0001g0031a0001c0002t0001g0032 | 4 | NA18950.hp1 NA18957.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+417C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321365 | ||||||
chr13:111321433
|
G | A | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0058others(2): Show | 11 | HG01109.hp2 HG01243.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.58+485G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321433 | ||||||
chr13:111321442
|
G | T | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0165others(102): Show | 157 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.58+494G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321442 | ||||||
chr13:111321444
|
G | A | 1 | a0001c0002t0001g0239 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.58+496G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321444 | ||||||
chr13:111321469
|
T | G | 3 | a0001c0002t0003g0061a0001c0002t0003g0062a0001c0002t0003g0063 | 3 | HG00639.hp1 HG01243.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.58+521T>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321469 | ||||||
chr13:111321625
|
C | CAA | 84 | a0001c0001t0001g0049a0001c0001t0001g0153a0001c0001t0001g0154others(81): Show | 103 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.58+685_58+686dupAA | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111321625 | |||||
chr13:111321635
|
C | A | 3 | a0001c0002t0003g0061a0001c0002t0003g0062a0001c0002t0003g0063 | 3 | HG00639.hp1 HG01243.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.58+687C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321635 | ||||||
chr13:111321646
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.58+698C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321646 | ||||||
chr13:111321648
|
G | A | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0058others(2): Show | 11 | HG01109.hp2 HG01243.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.58+700G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321648 | ||||||
chr13:111321654
|
C | T | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0165others(102): Show | 157 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.58+706C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321654 | ||||||
chr13:111321700
|
G | A | 84 | a0001c0001t0001g0049a0001c0001t0001g0153a0001c0001t0001g0154others(81): Show | 103 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.58+752G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321700 | ||||||
chr13:111321701
|
C | T | 84 | a0001c0001t0001g0049a0001c0001t0001g0153a0001c0001t0001g0154others(81): Show | 103 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.58+753C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321701 | ||||||
chr13:111321798
|
C | T | 2 | a0001c0005t0001g0159a0001c0005t0001g0160 | 2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.58+850C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321798 | ||||||
chr13:111321848
|
C | T | 1 | a0001c0003t0002g0238 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.58+900C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321848 | ||||||
chr13:111321903
|
G | A | 3 | a0001c0002t0003g0061a0001c0002t0003g0062a0001c0002t0003g0063 | 3 | HG00639.hp1 HG01243.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.58+955G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321903 | ||||||
chr13:111321919
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.58+971G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321919 | ||||||
chr13:111321973
|
G | C | 18 | a0001c0001t0001g0241a0001c0001t0001g0249a0001c0001t0001g0250others(15): Show | 19 | HG02135.hp1 HG03704.hp2 HG04115.hp2 others(16): Show |
intron_variant | MODIFIER | c.58+1025G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321973 | ||||||
chr13:111322049
|
GAGCACCT others(9): Show |
G | 3 | a0001c0002t0003g0061a0001c0002t0003g0062a0001c0002t0003g0063 | 3 | HG00639.hp1 HG01243.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.58+1110_58+1125del others(16): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111322049 | |||||
chr13:111322084
|
T | A | 5 | a0001c0002t0005g0065a0001c0002t0005g0066a0001c0002t0005g0067others(2): Show | 5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+1136T>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111322084 | ||||||
chr13:111322102
|
C | T | 88 | a0001c0001t0001g0049a0001c0001t0001g0064a0001c0001t0001g0153others(85): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.58+1154C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111322102 | ||||||
chr13:111322188
|
G | T | 18 | a0001c0001t0003g0033a0001c0001t0010g0292a0001c0002t0003g0050others(15): Show | 24 | HG00280.hp2 HG00323.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.58+1240G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111322188 | ||||||
chr13:111322287
|
TGGG | T | 22 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0070others(19): Show | 27 | HG00140.hp1 HG00642.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.58+1341_58+1343del others(3): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111322287 | |||||
chr13:111322308
|
C | T | 2 | a0001c0002t0003g0054a0001c0002t0003g0293 | 3 | HG01261.hp1 HG02109.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.58+1360C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111322308 | ||||||
chr13:111322309
|
G | A | 1 | a0001c0002t0001g0253 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.58+1361G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111322309 | ||||||
chr13:111322356
|
G | GC | 285 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(282): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.58+1410dupC | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111322356 | |||||
chr13:111322388
|
C | T | 2 | a0001c0002t0001g0253a0001c0002t0003g0254 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.58+1440C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111322388 | ||||||
chr13:111322459
|
T | C | 1 | a0001c0001t0001g0128 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.58+1511T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111322459 | ||||||
chr13:111322497
|
G | A | 50 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0003g0033others(47): Show | 73 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.58+1549G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111322497 | ||||||
chr13:111322543
|
C | T | 1 | a0001c0002t0001g0252 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.58+1595C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111322543 | ||||||
chr13:111322546
|
G | C | 1 | a0001c0002t0001g0094 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.58+1598G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111322546 | ||||||
chr13:111322860
|
T | C | 30 | a0001c0001t0003g0033a0001c0001t0010g0292a0001c0002t0003g0050others(27): Show | 40 | HG00280.hp2 HG00323.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.58+1912T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111322860 | ||||||
chr13:111322883
|
G | A | 1 | a0001c0002t0001g0162 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.58+1935G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111322883 | ||||||
chr13:111322966
|
A | G | 34 | a0001c0001t0003g0033a0001c0001t0010g0292a0001c0002t0003g0047others(31): Show | 45 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.58+2018A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111322966 | ||||||
chr13:111323054
|
T | C | 13 | a0001c0001t0001g0023a0001c0002t0001g0006a0001c0002t0001g0012others(10): Show | 22 | HG00099.hp1 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.58+2106T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323054 | ||||||
chr13:111323308
|
C | A | 1 | a0001c0002t0002g0164 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.58+2360C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323308 | ||||||
chr13:111323309
|
G | A | 31 | a0001c0001t0003g0033a0001c0001t0010g0292a0001c0002t0001g0088others(28): Show | 41 | HG00280.hp2 HG00323.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.58+2361G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323309 | ||||||
chr13:111323354
|
G | A | 48 | a0001c0001t0001g0049a0001c0001t0001g0153a0001c0001t0001g0154others(45): Show | 56 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.58+2406G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323354 | ||||||
chr13:111323354
|
G | C | 1 | a0001c0002t0001g0094 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.58+2406G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323354 | ||||||
chr13:111323441
|
G | T | 31 | a0001c0001t0003g0033a0001c0001t0010g0292a0001c0002t0001g0088others(28): Show | 41 | HG00280.hp2 HG00323.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.58+2493G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323441 | ||||||
chr13:111323453
|
T | C | 298 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(295): Show | 414 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(411): Show |
intron_variant | MODIFIER | c.58+2505T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323453 | ||||||
chr13:111323562
|
C | T | 5 | a0001c0002t0001g0155a0001c0002t0001g0279a0001c0002t0003g0283others(2): Show | 5 | HG00642.hp2 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+2614C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323562 | ||||||
chr13:111323645
|
T | C | 1 | a0001c0002t0001g0103 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.58+2697T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323645 | ||||||
chr13:111323652
|
C | A | 3 | a0001c0002t0003g0061a0001c0002t0003g0062a0001c0002t0003g0063 | 3 | HG00639.hp1 HG01243.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.58+2704C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323652 | ||||||
chr13:111323670
|
G | A | 20 | a0001c0001t0001g0064a0001c0001t0001g0092a0001c0001t0001g0093others(17): Show | 33 | HG00558.hp2 HG02145.hp2 HG02257.hp1 others(30): Show |
intron_variant | MODIFIER | c.58+2722G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323670 | ||||||
chr13:111323682
|
T | C | 1 | a0001c0002t0001g0103 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.58+2734T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323682 | ||||||
chr13:111323774
|
C | T | 18 | a0001c0001t0001g0064a0001c0001t0001g0092a0001c0001t0001g0093others(15): Show | 31 | HG00558.hp2 HG00738.hp2 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.58+2826C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323774 | ||||||
chr13:111323853
|
A | G | 1 | a0001c0001t0002g0237 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.58+2905A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323853 | ||||||
chr13:111324135
|
G | A | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0070others(96): Show | 148 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.58+3187G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111324135 | ||||||
chr13:111324234
|
T | C | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0049others(196): Show | 275 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.58+3286T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111324234 | ||||||
chr13:111324458
|
G | A | 1 | a0001c0002t0001g0103 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.58+3510G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111324458 | ||||||
chr13:111324462
|
A | G | 1 | a0001c0002t0003g0254 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.58+3514A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111324462 | ||||||
chr13:111324547
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.58+3599C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111324547 | ||||||
chr13:111324564
|
C | A | 1 | a0001c0002t0001g0103 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.58+3616C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111324564 | ||||||
chr13:111324598
|
T | G | 1 | a0001c0002t0001g0162 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.59-3585T>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111324598 | ||||||
chr13:111324615
|
C | CAG | 28 | a0001c0001t0003g0033a0001c0001t0010g0292a0001c0002t0001g0088others(25): Show | 38 | HG00280.hp2 HG00323.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.59-3561_59-3560dup others(2): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111324615 | |||||
chr13:111324719
|
A | G | 1 | a0001c0002t0005g0069 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.59-3464A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111324719 | ||||||
chr13:111324748
|
G | A | 1 | a0001c0002t0001g0094 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.59-3435G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111324748 | ||||||
chr13:111324752
|
C | T | 1 | a0001c0001t0002g0230 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.59-3431C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111324752 | ||||||
chr13:111324933
|
G | T | 67 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0019others(64): Show | 87 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.59-3250G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111324933 | ||||||
chr13:111324951
|
C | T | 1 | a0001c0002t0003g0047 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.59-3232C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111324951 | ||||||
chr13:111324976
|
G | T | 1 | a0001c0001t0002g0056 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.59-3207G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111324976 | ||||||
chr13:111325001
|
G | T | 1 | a0001c0001t0001g0087 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.59-3182G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111325001 | ||||||
chr13:111325021
|
C | T | 14 | a0001c0001t0002g0045a0001c0001t0002g0227a0001c0001t0002g0228others(11): Show | 19 | HG00438.hp1 HG01081.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.59-3162C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111325021 | ||||||
chr13:111325147
|
G | A | 9 | a0001c0001t0001g0064a0001c0002t0001g0088a0001c0002t0003g0141others(6): Show | 13 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.59-3036G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111325147 | ||||||
chr13:111325225
|
C | T | 1 | a0001c0002t0001g0094 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.59-2958C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111325225 | ||||||
chr13:111325323
|
C | T | 1 | a0001c0002t0001g0021 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.59-2860C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111325323 | ||||||
chr13:111325350
|
G | A | 1 | a0001c0003t0001g0105 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.59-2833G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111325350 | ||||||
chr13:111325430
|
A | T | 2 | a0001c0002t0002g0226a0001c0002t0002g0236 | 2 | NA19009.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.59-2753A>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111325430 | ||||||
chr13:111325640
|
C | A | 8 | a0001c0002t0001g0088a0001c0002t0003g0141a0001c0002t0004g0014others(5): Show | 12 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-2543C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111325640 | ||||||
chr13:111325662
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.59-2521G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111325662 | ||||||
chr13:111325863
|
T | C | 18 | a0001c0002t0001g0006a0001c0002t0001g0012a0001c0002t0001g0022others(15): Show | 27 | HG00099.hp1 HG00323.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.59-2320T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111325863 | ||||||
chr13:111325868
|
C | T | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02280.hp2 HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.59-2315C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111325868 | ||||||
chr13:111325917
|
C | T | 8 | a0001c0002t0001g0088a0001c0002t0003g0141a0001c0002t0004g0014others(5): Show | 12 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-2266C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111325917 | ||||||
chr13:111325918
|
G | A | 64 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0019others(61): Show | 79 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.59-2265G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111325918 | ||||||
chr13:111326015
|
C | T | 18 | a0001c0002t0001g0085a0001c0002t0001g0240a0001c0002t0002g0086others(15): Show | 23 | HG00280.hp2 HG00323.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.59-2168C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326015 | ||||||
chr13:111326163
|
C | T | 8 | a0001c0002t0001g0088a0001c0002t0003g0141a0001c0002t0004g0014others(5): Show | 12 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-2020C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326163 | ||||||
chr13:111326206
|
C | T | 1 | a0001c0002t0005g0068 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.59-1977C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326206 | ||||||
chr13:111326242
|
C | T | 1 | a0001c0001t0002g0225 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.59-1941C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326242 | ||||||
chr13:111326251
|
C | CGAGCCCG others(123): Show |
2 | a0001c0001t0001g0295a0001c0001t0006g0296 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.59-1927_59-1926ins others(130): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326251 | |||||
chr13:111326251
|
C | T | 1 | a0001c0002t0003g0047 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.59-1932C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326251 | ||||||
chr13:111326257
|
T | C | 45 | a0001c0001t0001g0055a0001c0002t0001g0004a0001c0002t0001g0006others(42): Show | 76 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.59-1926T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326257 | ||||||
chr13:111326259
|
G | C | 2 | a0001c0001t0001g0295a0001c0001t0006g0296 | 2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.59-1924G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326259 | ||||||
chr13:111326259
|
G | GCGCTGGT others(123): Show |
1 | a0001c0001t0003g0033 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.59-1898_59-1897ins others(130): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326259 | |||||
chr13:111326259
|
G | GCGCTGGT others(123): Show |
80 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(77): Show | 98 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.59-1898_59-1897ins others(130): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326259 | |||||
chr13:111326259
|
G | GCGCTGGT others(302): Show |
3 | a0001c0001t0001g0010a0001c0001t0001g0082a0001c0001t0001g0120 | 6 | HG01099.hp2 HG01358.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-1898_59-1897ins others(309): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326259 | |||||
chr13:111326260
|
CGCTGGTG others(81): Show |
C | 51 | a0001c0002t0001g0004a0001c0002t0001g0006a0001c0002t0001g0011others(48): Show | 78 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.59-1897_59-1810del others(88): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326260 | |||||
chr13:111326286
|
A | G | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(113): Show | 175 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.59-1897A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326286 | ||||||
chr13:111326292
|
T | C | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(113): Show | 175 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.59-1891T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326292 | ||||||
chr13:111326301
|
T | C | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(113): Show | 175 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.59-1882T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326301 | ||||||
chr13:111326305
|
AGCCTGTC others(42): Show |
A | 2 | a0001c0001t0002g0015a0001c0001t0002g0224 | 5 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-1876_59-1828del others(49): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326305 | |||||
chr13:111326306
|
G | A | 1 | a0001c0001t0002g0170 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.59-1877G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326306 | ||||||
chr13:111326307
|
C | G | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(111): Show | 170 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.59-1876C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326307 | ||||||
chr13:111326321
|
T | TGGAGGAG others(35): Show |
112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(109): Show | 168 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.59-1858_59-1857ins others(42): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326321 | |||||
chr13:111326328
|
T | G | 1 | a0001c0002t0003g0061 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.59-1855T>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326328 | ||||||
chr13:111326330
|
C | T | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0064others(112): Show | 171 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.59-1853C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326330 | ||||||
chr13:111326336
|
A | G | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(111): Show | 170 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.59-1847A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326336 | ||||||
chr13:111326337
|
C | T | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(110): Show | 169 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.59-1846C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326337 | ||||||
chr13:111326339
|
C | T | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(111): Show | 170 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.59-1844C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326339 | ||||||
chr13:111326347
|
G | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(110): Show | 169 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.59-1836G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326347 | ||||||
chr13:111326348
|
G | C | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0049others(115): Show | 175 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.59-1835G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326348 | ||||||
chr13:111326354
|
T | C | 8 | a0001c0002t0001g0088a0001c0002t0003g0141a0001c0002t0004g0014others(5): Show | 12 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-1829T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326354 | ||||||
chr13:111326357
|
G | C | 2 | a0001c0001t0002g0015a0001c0001t0002g0224 | 5 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-1826G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326357 | ||||||
chr13:111326374
|
G | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(111): Show | 170 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.59-1809G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326374 | ||||||
chr13:111326380
|
C | T | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(115): Show | 174 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.59-1803C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326380 | ||||||
chr13:111326389
|
C | T | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(111): Show | 170 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.59-1794C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326389 | ||||||
chr13:111326391
|
T | C | 2 | a0001c0001t0003g0033a0001c0002t0003g0061 | 3 | HG03486.hp1 HG03579.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.59-1792T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326391 | ||||||
chr13:111326395
|
G | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(111): Show | 170 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.59-1788G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326395 | ||||||
chr13:111326409
|
TGGA | T | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(110): Show | 169 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.59-1769_59-1767del others(3): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326409 | |||||
chr13:111326412
|
A | AGGAGACC others(29): Show |
1 | a0001c0002t0003g0061 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.59-1765_59-1764ins others(36): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326412 | |||||
chr13:111326419
|
G | C | 4 | a0001c0001t0001g0049a0001c0001t0001g0122a0001c0001t0001g0265others(1): Show | 5 | HG01255.hp1 HG01943.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-1764G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326419 | ||||||
chr13:111326419
|
G | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(113): Show | 175 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.59-1764G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326419 | ||||||
chr13:111326421
|
T | C | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0049others(115): Show | 175 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.59-1762T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326421 | ||||||
chr13:111326427
|
G | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(111): Show | 170 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.59-1756G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326427 | ||||||
chr13:111326428
|
C | T | 2 | a0001c0001t0002g0015a0001c0001t0002g0224 | 5 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-1755C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326428 | ||||||
chr13:111326430
|
T | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(111): Show | 170 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.59-1753T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326430 | ||||||
chr13:111326430
|
T | TGAGGCTG others(120): Show |
4 | a0001c0001t0001g0049a0001c0001t0001g0122a0001c0001t0001g0265others(1): Show | 5 | HG01255.hp1 HG01943.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-1750_59-1749ins others(127): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326430 | |||||
chr13:111326431
|
G | C | 1 | a0001c0002t0001g0103 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.59-1752G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326431 | ||||||
chr13:111326432
|
A | C | 1 | a0001c0001t0001g0064 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.59-1751A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326432 | ||||||
chr13:111326438
|
G | C | 2 | a0001c0001t0002g0015a0001c0001t0002g0224 | 5 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-1745G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326438 | ||||||
chr13:111326439
|
C | T | 1 | a0001c0002t0003g0061 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.59-1744C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326439 | ||||||
chr13:111326445
|
T | C | 1 | a0001c0002t0003g0061 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.59-1738T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326445 | ||||||
chr13:111326457
|
G | C | 1 | a0001c0002t0003g0061 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.59-1726G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326457 | ||||||
chr13:111326482
|
C | T | 2 | a0001c0001t0002g0015a0001c0001t0002g0224 | 5 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-1701C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326482 | ||||||
chr13:111326486
|
CCTGTCTG others(32): Show |
C | 1 | a0001c0001t0002g0224 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.59-1678_59-1640del others(39): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326486 | |||||
chr13:111326500
|
TGGA | T | 1 | a0001c0001t0002g0015 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1678_59-1676del others(3): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326500 | |||||
chr13:111326510
|
C | T | 1 | a0001c0001t0002g0015 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1673C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326510 | ||||||
chr13:111326511
|
A | G | 1 | a0001c0001t0002g0015 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1672A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326511 | ||||||
chr13:111326518
|
G | A | 1 | a0001c0001t0002g0015 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1665G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326518 | ||||||
chr13:111326523
|
A | AGCCTGGC others(6): Show |
1 | a0001c0001t0002g0015 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1659_59-1658ins others(13): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326523 | |||||
chr13:111326526
|
C | G | 1 | a0001c0001t0002g0015 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1657C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326526 | ||||||
chr13:111326540
|
G | GGAA | 1 | a0001c0001t0002g0015 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1641_59-1640ins others(3): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326540 | |||||
chr13:111326548
|
C | T | 1 | a0001c0001t0002g0223 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.59-1635C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326548 | ||||||
chr13:111326553
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.59-1630A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326553 | ||||||
chr13:111326554
|
A | G | 1 | a0001c0001t0002g0015 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1629A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326554 | ||||||
chr13:111326555
|
C | T | 1 | a0001c0001t0002g0015 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1628C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326555 | ||||||
chr13:111326558
|
G | A | 2 | a0001c0001t0001g0122a0001c0001t0002g0172 | 2 | HG02004.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.59-1625G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326558 | ||||||
chr13:111326562
|
CTGGTGCT others(6): Show |
C | 1 | a0001c0001t0002g0015 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1618_59-1606del others(13): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326562 | |||||
chr13:111326566
|
T | C | 1 | a0001c0001t0002g0224 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.59-1617T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326566 | ||||||
chr13:111326566
|
TGCTGGCG others(120): Show |
T | 1 | a0001c0002t0003g0254 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.59-1599_59-1473del | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326566 | |||||
chr13:111326572
|
C | T | 1 | a0001c0001t0002g0224 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.59-1611C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326572 | ||||||
chr13:111326573
|
G | A | 59 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0019others(56): Show | 74 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.59-1610G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326573 | ||||||
chr13:111326584
|
C | G | 2 | a0001c0001t0002g0015a0001c0001t0002g0224 | 5 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-1599C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326584 | ||||||
chr13:111326592
|
A | G | 1 | a0001c0001t0002g0015 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1591A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326592 | ||||||
chr13:111326598
|
T | C | 1 | a0001c0001t0002g0015 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1585T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326598 | ||||||
chr13:111326599
|
G | A | 1 | a0001c0001t0002g0015 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1584G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326599 | ||||||
chr13:111326623
|
G | A | 1 | a0001c0001t0002g0015 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1560G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326623 | ||||||
chr13:111326623
|
G | GGGGTGGA others(32): Show |
5 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(2): Show | 5 | HG02630.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-1522_59-1521ins others(39): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326623 | |||||
chr13:111326637
|
C | T | 1 | a0001c0001t0002g0015 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1546C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326637 | ||||||
chr13:111326638
|
A | G | 1 | a0001c0001t0002g0015 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1545A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326638 | ||||||
chr13:111326646
|
T | C | 1 | a0001c0001t0002g0224 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.59-1537T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326646 | ||||||
chr13:111326647
|
G | A | 1 | a0001c0001t0002g0015 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1536G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326647 | ||||||
chr13:111326648
|
C | CGAGCCTG others(32): Show |
227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(224): Show | 324 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.59-1522_59-1521ins others(39): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326648 | |||||
chr13:111326648
|
C | T | 1 | a0001c0001t0002g0015 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1535C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326648 | ||||||
chr13:111326651
|
G | T | 1 | a0001c0001t0002g0224 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.59-1532G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326651 | ||||||
chr13:111326652
|
C | G | 1 | a0001c0001t0002g0224 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.59-1531C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326652 | ||||||
chr13:111326682
|
CGTGAGCC others(45): Show |
C | 1 | a0001c0001t0002g0224 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.59-1499_59-1448del others(52): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326682 | |||||
chr13:111326739
|
T | G | 237 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(234): Show | 341 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.59-1444T>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326739 | ||||||
chr13:111326745
|
C | G | 1 | a0001c0002t0001g0276 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.59-1438C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326745 | ||||||
chr13:111326745
|
C | T | 3 | a0001c0001t0001g0055a0001c0001t0002g0224a0001c0001t0006g0296 | 4 | HG01891.hp1 HG02630.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1438C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326745 | ||||||
chr13:111326823
|
T | C | 1 | a0001c0002t0003g0050 | 2 | NA19066.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.59-1360T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326823 | ||||||
chr13:111326924
|
C | T | 1 | a0001c0001t0002g0222 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.59-1259C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326924 | ||||||
chr13:111326945
|
C | T | 1 | a0001c0002t0001g0032 | 2 | NA18950.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.59-1238C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326945 | ||||||
chr13:111327056
|
G | A | 45 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0019others(42): Show | 58 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.59-1127G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327056 | ||||||
chr13:111327066
|
G | A | 8 | a0001c0002t0001g0088a0001c0002t0003g0141a0001c0002t0004g0014others(5): Show | 12 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-1117G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327066 | ||||||
chr13:111327073
|
C | T | 1 | a0001c0001t0001g0028 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.59-1110C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327073 | ||||||
chr13:111327175
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.59-1008G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327175 | ||||||
chr13:111327344
|
G | A | 5 | a0001c0001t0002g0036a0001c0001t0002g0174a0001c0001t0002g0231others(2): Show | 6 | HG00673.hp1 HG02056.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-839G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327344 | ||||||
chr13:111327348
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.59-835A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327348 | ||||||
chr13:111327593
|
G | A | 8 | a0001c0002t0001g0088a0001c0002t0003g0141a0001c0002t0004g0014others(5): Show | 12 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-590G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327593 | ||||||
chr13:111327599
|
G | A | 1 | a0001c0001t0002g0227 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.59-584G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327599 | ||||||
chr13:111327643
|
C | T | 1 | a0002c0004t0001g0030 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.59-540C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327643 | ||||||
chr13:111327689
|
G | A | 5 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0021others(2): Show | 12 | HG01109.hp2 HG01243.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-494G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327689 | ||||||
chr13:111327749
|
C | T | 1 | a0001c0002t0005g0069 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.59-434C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327749 | ||||||
chr13:111327803
|
T | C | 60 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0019others(57): Show | 75 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.59-380T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327803 | ||||||
chr13:111327882
|
G | A | 1 | a0001c0001t0002g0142 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.59-301G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327882 | ||||||
chr13:111327924
|
G | A | 1 | a0001c0002t0001g0094 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.59-259G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327924 | ||||||
chr13:111328131
|
A | G | 238 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(235): Show | 342 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.59-52A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111328131 | ||||||
chr13:111328437
|
C | T | 1 | a0001c0002t0001g0103 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.169+144C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328437 | ||||||
chr13:111328473
|
G | A | 1 | a0001c0002t0001g0103 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.169+180G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328473 | ||||||
chr13:111328497
|
C | T | 5 | a0001c0002t0001g0240a0001c0002t0003g0053a0001c0002t0003g0158others(2): Show | 6 | HG00280.hp2 HG00323.hp1 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+204C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328497 | ||||||
chr13:111328647
|
C | T | 1 | a0001c0002t0001g0103 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.169+354C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328647 | ||||||
chr13:111328649
|
G | T | 10 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(7): Show | 12 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.169+356G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328649 | ||||||
chr13:111328676
|
G | C | 218 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(215): Show | 311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.169+383G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328676 | ||||||
chr13:111328686
|
C | T | 1 | a0001c0001t0002g0220 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.169+393C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328686 | ||||||
chr13:111328740
|
T | A | 4 | a0001c0001t0001g0055a0001c0001t0001g0064a0001c0001t0001g0295others(1): Show | 5 | HG01891.hp1 HG02257.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+447T>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328740 | ||||||
chr13:111328750
|
G | C | 5 | a0001c0002t0001g0121a0001c0002t0002g0166a0001c0002t0003g0061others(2): Show | 5 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+457G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328750 | ||||||
chr13:111328846
|
A | C | 8 | a0001c0002t0001g0088a0001c0002t0003g0141a0001c0002t0004g0014others(5): Show | 12 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.169+553A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328846 | ||||||
chr13:111328868
|
C | G | 6 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0021others(3): Show | 13 | HG01109.hp2 HG01243.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.169+575C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328868 | ||||||
chr13:111328875
|
G | A | 214 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(211): Show | 305 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.169+582G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328875 | ||||||
chr13:111328893
|
C | T | 2 | a0001c0005t0001g0159a0001c0005t0001g0160 | 2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.169+600C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328893 | ||||||
chr13:111328915
|
C | T | 19 | a0001c0002t0001g0084a0001c0002t0001g0085a0001c0002t0001g0240others(16): Show | 24 | HG00280.hp2 HG00323.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.169+622C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328915 | ||||||
chr13:111328917
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.169+624C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328917 | ||||||
chr13:111329009
|
T | A | 1 | a0001c0003t0001g0124 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.169+716T>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329009 | ||||||
chr13:111329014
|
C | G | 1 | a0001c0003t0001g0124 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.169+721C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329014 | ||||||
chr13:111329052
|
T | C | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(227): Show | 330 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.169+759T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329052 | ||||||
chr13:111329138
|
C | G | 1 | a0001c0002t0001g0253 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.169+845C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329138 | ||||||
chr13:111329254
|
C | A | 8 | a0001c0002t0001g0088a0001c0002t0003g0141a0001c0002t0004g0014others(5): Show | 12 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.169+961C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329254 | ||||||
chr13:111329360
|
C | G | 139 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0019others(136): Show | 195 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.169+1067C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329360 | ||||||
chr13:111329397
|
G | T | 8 | a0001c0002t0001g0088a0001c0002t0003g0141a0001c0002t0004g0014others(5): Show | 12 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.169+1104G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329397 | ||||||
chr13:111329454
|
A | G | 8 | a0001c0002t0001g0088a0001c0002t0003g0141a0001c0002t0004g0014others(5): Show | 12 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.169+1161A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329454 | ||||||
chr13:111329505
|
G | A | 5 | a0001c0002t0001g0121a0001c0002t0002g0166a0001c0002t0003g0061others(2): Show | 5 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+1212G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329505 | ||||||
chr13:111329699
|
A | G | 1 | a0002c0004t0001g0280 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.169+1406A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329699 | ||||||
chr13:111329763
|
A | G | 1 | a0001c0001t0002g0216 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.169+1470A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329763 | ||||||
chr13:111329775
|
G | A | 18 | a0001c0002t0001g0084a0001c0002t0001g0085a0001c0002t0001g0240others(15): Show | 23 | HG00280.hp2 HG00323.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.169+1482G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329775 | ||||||
chr13:111329781
|
G | C | 1 | a0001c0002t0001g0094 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.169+1488G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329781 | ||||||
chr13:111329944
|
C | T | 61 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0019others(58): Show | 76 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.169+1651C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329944 | ||||||
chr13:111330038
|
C | CA | 3 | a0001c0001t0001g0055a0001c0001t0001g0295a0001c0001t0006g0296 | 4 | HG01891.hp1 HG02630.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+1746dupA | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 111330038 | |||||
chr13:111330043
|
CA | C | 6 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0021others(3): Show | 13 | HG01109.hp2 HG01167.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.169+1752delA | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 111330043 | |||||
chr13:111330119
|
A | G | 11 | a0001c0001t0001g0064a0001c0002t0001g0008a0001c0002t0001g0009others(8): Show | 18 | HG00639.hp1 HG00733.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.169+1826A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330119 | ||||||
chr13:111330129
|
GA | G | 9 | a0001c0002t0001g0088a0001c0002t0001g0103a0001c0002t0003g0141others(6): Show | 13 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.169+1845delA | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 111330129 | |||||
chr13:111330176
|
C | T | 18 | a0001c0001t0001g0002a0001c0001t0001g0071a0001c0001t0001g0173others(15): Show | 25 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.169+1883C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330176 | ||||||
chr13:111330209
|
C | T | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0071others(97): Show | 148 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.169+1916C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330209 | ||||||
chr13:111330268
|
A | G | 110 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0019others(107): Show | 149 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.169+1975A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330268 | ||||||
chr13:111330327
|
G | A | 5 | a0001c0002t0001g0121a0001c0002t0002g0166a0001c0002t0003g0061others(2): Show | 5 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+2034G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330327 | ||||||
chr13:111330497
|
A | C | 1 | a0001c0002t0001g0247 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.169+2204A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330497 | ||||||
chr13:111330525
|
C | T | 33 | a0001c0002t0001g0007a0001c0002t0001g0018a0001c0002t0001g0035others(30): Show | 39 | HG00099.hp2 HG00280.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.169+2232C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330525 | ||||||
chr13:111330551
|
C | T | 8 | a0001c0002t0001g0088a0001c0002t0003g0141a0001c0002t0004g0014others(5): Show | 12 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.169+2258C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330551 | ||||||
chr13:111330603
|
T | C | 1 | a0001c0001t0002g0149 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.169+2310T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330603 | ||||||
chr13:111330764
|
A | G | 2 | a0002c0004t0001g0030a0002c0004t0001g0163 | 3 | HG01884.hp1 HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.169+2471A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330764 | ||||||
chr13:111330853
|
C | T | 1 | a0001c0002t0002g0164 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.169+2560C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330853 | ||||||
chr13:111330865
|
A | G | 2 | a0001c0001t0002g0043a0001c0001t0002g0206 | 3 | NA18947.hp1 NA19075.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.169+2572A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330865 | ||||||
chr13:111330895
|
T | C | 1 | a0001c0005t0003g0137 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.169+2602T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330895 | ||||||
chr13:111330898
|
G | A | 8 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0031others(5): Show | 19 | HG00558.hp2 NA18939.hp2 NA18950.hp1 others(16): Show |
intron_variant | MODIFIER | c.169+2605G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330898 | ||||||
chr13:111330914
|
G | C | 5 | a0001c0002t0001g0121a0001c0002t0002g0166a0001c0002t0003g0061others(2): Show | 5 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+2621G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330914 | ||||||
chr13:111330986
|
A | G | 1 | a0001c0002t0001g0102 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.169+2693A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330986 | ||||||
chr13:111331000
|
T | A | 4 | a0001c0002t0004g0014a0001c0002t0004g0034a0001c0002t0004g0138others(1): Show | 8 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.169+2707T>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331000 | ||||||
chr13:111331171
|
G | A | 1 | a0001c0002t0001g0004 | 7 | NA18953.hp1 NA18972.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.169+2878G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331171 | ||||||
chr13:111331202
|
C | T | 14 | a0001c0001t0001g0093a0001c0002t0001g0006a0001c0002t0001g0012others(11): Show | 22 | HG00099.hp1 HG00323.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.169+2909C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331202 | ||||||
chr13:111331263
|
T | C | 1 | a0001c0002t0001g0162 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.169+2970T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331263 | ||||||
chr13:111331312
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.169+3019T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331312 | ||||||
chr13:111331316
|
AT | A | 12 | a0001c0002t0001g0009a0001c0002t0001g0021a0001c0002t0001g0059others(9): Show | 18 | HG01106.hp2 HG01109.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.169+3043delT | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 111331316 | |||||
chr13:111331316
|
ATT | A | 14 | a0001c0002t0001g0008a0001c0002t0001g0058a0001c0002t0001g0084others(11): Show | 20 | HG00280.hp2 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.169+3042_169+3043d others(4): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 111331316 | |||||
chr13:111331316
|
ATTT | A | 9 | a0001c0001t0001g0134a0001c0001t0002g0203a0001c0001t0002g0204others(6): Show | 9 | HG02080.hp1 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.169+3041_169+3043d others(5): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 111331316 | |||||
chr13:111331316
|
ATTTT | A | 192 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(189): Show | 276 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(273): Show |
intron_variant | MODIFIER | c.169+3040_169+3043d others(6): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 111331316 | |||||
chr13:111331316
|
ATTTTT | A | 29 | a0001c0001t0001g0055a0001c0001t0001g0093a0001c0001t0001g0106others(26): Show | 42 | HG00099.hp1 HG00323.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.169+3039_169+3043d others(7): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 111331316 | |||||
chr13:111331380
|
C | T | 2 | a0001c0002t0003g0255a0001c0002t0003g0256 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.169+3087C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331380 | ||||||
chr13:111331420
|
T | C | 5 | a0001c0002t0001g0121a0001c0002t0002g0166a0001c0002t0003g0061others(2): Show | 5 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+3127T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331420 | ||||||
chr13:111331569
|
C | T | 1 | a0001c0002t0003g0258 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.169+3276C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331569 | ||||||
chr13:111331656
|
C | A | 5 | a0001c0002t0001g0121a0001c0002t0002g0166a0001c0002t0003g0061others(2): Show | 5 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+3363C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331656 | ||||||
chr13:111331788
|
G | T | 1 | a0001c0002t0001g0162 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.169+3495G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331788 | ||||||
chr13:111331865
|
A | C | 1 | a0001c0002t0001g0094 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.169+3572A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331865 | ||||||
chr13:111331890
|
C | T | 1 | a0001c0002t0003g0156 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.169+3597C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331890 | ||||||
chr13:111331897
|
A | G | 104 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0019others(101): Show | 143 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.169+3604A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331897 | ||||||
chr13:111331995
|
C | T | 5 | a0001c0002t0001g0121a0001c0002t0002g0166a0001c0002t0003g0061others(2): Show | 5 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+3702C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331995 | ||||||
chr13:111332031
|
T | C | 1 | a0001c0001t0002g0175 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.169+3738T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111332031 | ||||||
chr13:111332032
|
G | A | 1 | a0001c0001t0003g0033 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.169+3739G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111332032 | ||||||
chr13:111332060
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.169+3767A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111332060 | ||||||
chr13:111332396
|
C | A | 3 | a0001c0001t0001g0055a0001c0001t0001g0295a0001c0001t0006g0296 | 4 | HG01891.hp1 HG02630.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+4103C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111332396 | ||||||
chr13:111332412
|
G | T | 1 | a0001c0001t0001g0070 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.169+4119G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111332412 | ||||||
chr13:111332598
|
T | G | 2 | a0001c0002t0004g0034a0001c0002t0004g0138 | 3 | HG01884.hp2 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.169+4305T>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111332598 | ||||||
chr13:111332768
|
A | G | 1 | a0001c0002t0001g0094 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.169+4475A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111332768 | ||||||
chr13:111332803
|
T | C | 1 | a0001c0002t0001g0103 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.169+4510T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111332803 | ||||||
chr13:111332858
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0006g0296 | 3 | HG01891.hp1 HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.169+4565C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111332858 | ||||||
chr13:111332884
|
A | C | 2 | a0001c0001t0002g0043a0001c0001t0002g0206 | 3 | NA18947.hp1 NA19075.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.169+4591A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111332884 | ||||||
chr13:111332911
|
G | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0049others(109): Show | 165 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.169+4618G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111332911 | ||||||
chr13:111333006
|
A | G | 1 | a0001c0001t0002g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.169+4713A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333006 | ||||||
chr13:111333025
|
G | A | 1 | a0001c0001t0002g0225 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.169+4732G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333025 | ||||||
chr13:111333141
|
A | G | 5 | a0001c0002t0005g0065a0001c0002t0005g0066a0001c0002t0005g0067others(2): Show | 5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+4848A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333141 | ||||||
chr13:111333185
|
G | A | 1 | a0001c0002t0001g0150 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.169+4892G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333185 | ||||||
chr13:111333527
|
A | G | 6 | a0001c0001t0001g0119a0001c0002t0001g0121a0001c0002t0002g0166others(3): Show | 6 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+5234A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333527 | ||||||
chr13:111333573
|
A | G | 1 | a0001c0002t0001g0094 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.169+5280A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333573 | ||||||
chr13:111333589
|
C | T | 231 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(228): Show | 326 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.169+5296C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333589 | ||||||
chr13:111333729
|
C | G | 1 | a0001c0001t0002g0201 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.169+5436C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333729 | ||||||
chr13:111333731
|
A | G | 1 | a0001c0001t0002g0201 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.169+5438A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333731 | ||||||
chr13:111333737
|
C | T | 5 | a0001c0002t0005g0065a0001c0002t0005g0066a0001c0002t0005g0067others(2): Show | 5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5444C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333737 | ||||||
chr13:111333738
|
A | C | 1 | a0001c0001t0011g0131 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.169+5445A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333738 | ||||||
chr13:111333738
|
A | G | 5 | a0001c0002t0005g0065a0001c0002t0005g0066a0001c0002t0005g0067others(2): Show | 5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5445A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333738 | ||||||
chr13:111333743
|
T | G | 25 | a0001c0001t0001g0072a0001c0001t0001g0082a0001c0001t0001g0083others(22): Show | 26 | HG00673.hp1 HG00735.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.169+5450T>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333743 | ||||||
chr13:111333746
|
A | G | 5 | a0001c0002t0005g0065a0001c0002t0005g0066a0001c0002t0005g0067others(2): Show | 5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5453A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333746 | ||||||
chr13:111333752
|
A | G | 5 | a0001c0002t0005g0065a0001c0002t0005g0066a0001c0002t0005g0067others(2): Show | 5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5459A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333752 | ||||||
chr13:111333755
|
T | C | 5 | a0001c0002t0005g0065a0001c0002t0005g0066a0001c0002t0005g0067others(2): Show | 5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5462T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333755 | ||||||
chr13:111333763
|
G | A | 5 | a0001c0002t0005g0065a0001c0002t0005g0066a0001c0002t0005g0067others(2): Show | 5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5470G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333763 | ||||||
chr13:111333766
|
G | GTGTCAGG others(5): Show |
5 | a0001c0002t0005g0065a0001c0002t0005g0066a0001c0002t0005g0067others(2): Show | 5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5473_169+5474i others(14): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333766 | ||||||
chr13:111333767
|
C | G | 5 | a0001c0002t0005g0065a0001c0002t0005g0066a0001c0002t0005g0067others(2): Show | 5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5474C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333767 | ||||||
chr13:111333776
|
T | G | 5 | a0001c0002t0005g0065a0001c0002t0005g0066a0001c0002t0005g0067others(2): Show | 5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5483T>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333776 | ||||||
chr13:111333777
|
GTGGGAA | G | 5 | a0001c0002t0005g0065a0001c0002t0005g0066a0001c0002t0005g0067others(2): Show | 5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5485_169+5490d others(8): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333777 | ||||||
chr13:111333792
|
C | T | 5 | a0001c0002t0005g0065a0001c0002t0005g0066a0001c0002t0005g0067others(2): Show | 5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5499C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333792 | ||||||
chr13:111333795
|
A | C | 5 | a0001c0002t0005g0065a0001c0002t0005g0066a0001c0002t0005g0067others(2): Show | 5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5502A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333795 | ||||||
chr13:111333809
|
A | G | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(159): Show | 231 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.169+5516A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333809 | ||||||
chr13:111333969
|
T | A | 254 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(251): Show | 358 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(355): Show |
intron_variant | MODIFIER | c.169+5676T>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333969 | ||||||
chr13:111334031
|
A | C | 1 | a0001c0002t0001g0094 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.169+5738A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111334031 | ||||||
chr13:111334034
|
G | A | 222 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(219): Show | 314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.169+5741G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111334034 | ||||||
chr13:111334121
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.170-5742C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111334121 | ||||||
chr13:111334181
|
A | G | 3 | a0001c0001t0001g0128a0001c0002t0003g0255a0001c0002t0003g0256 | 3 | HG02257.hp2 HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.170-5682A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111334181 | ||||||
chr13:111334189
|
T | C | 1 | a0004c0007t0003g0257 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.170-5674T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111334189 | ||||||
chr13:111334211
|
G | A | 1 | a0001c0001t0008g0029 | 2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.170-5652G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111334211 | ||||||
chr13:111334415
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0110 | 2 | HG00733.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.170-5448G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111334415 | ||||||
chr13:111334483
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.170-5380T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111334483 | ||||||
chr13:111334621
|
C | T | 1 | a0001c0001t0002g0225 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.170-5242C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111334621 | ||||||
chr13:111334879
|
G | C | 167 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(164): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.170-4984G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111334879 | ||||||
chr13:111335093
|
G | A | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(205): Show | 303 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.170-4770G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111335093 | ||||||
chr13:111335124
|
T | A | 1 | a0001c0002t0001g0266 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.170-4739T>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111335124 | ||||||
chr13:111335271
|
G | C | 1 | a0001c0001t0001g0129 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.170-4592G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111335271 | ||||||
chr13:111335340
|
T | C | 6 | a0001c0001t0008g0077a0001c0002t0005g0065a0001c0002t0005g0066others(3): Show | 6 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-4523T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111335340 | ||||||
chr13:111335442
|
A | G | 1 | a0001c0002t0001g0244 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.170-4421A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111335442 | ||||||
chr13:111335507
|
T | A | 1 | a0001c0001t0002g0178 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.170-4356T>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111335507 | ||||||
chr13:111335598
|
CAT | C | 10 | a0001c0001t0001g0130a0001c0001t0002g0179a0001c0001t0002g0208others(7): Show | 21 | HG00558.hp2 HG02895.hp1 HG02896.hp1 others(18): Show |
intron_variant | MODIFIER | c.170-4263_170-4262d others(4): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 111335598 | |||||
chr13:111335698
|
G | A | 42 | a0001c0001t0001g0070a0001c0001t0001g0087a0001c0001t0002g0042others(39): Show | 52 | HG00544.hp2 HG00597.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.170-4165G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111335698 | ||||||
chr13:111335759
|
T | A | 2 | a0001c0001t0002g0200a0001c0002t0001g0268 | 2 | HG01928.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.170-4104T>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111335759 | ||||||
chr13:111335825
|
C | A | 29 | a0001c0001t0001g0016a0001c0001t0001g0093a0001c0001t0001g0106others(26): Show | 38 | HG00099.hp1 HG00323.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.170-4038C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111335825 | ||||||
chr13:111335840
|
C | T | 1 | a0001c0002t0001g0273 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.170-4023C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111335840 | ||||||
chr13:111336050
|
G | C | 1 | a0001c0001t0002g0180 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.170-3813G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111336050 | ||||||
chr13:111336487
|
A | T | 1 | a0001c0002t0003g0051 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.170-3376A>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111336487 | ||||||
chr13:111336549
|
A | G | 2 | a0002c0004t0001g0030a0002c0004t0001g0163 | 3 | HG01884.hp1 HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.170-3314A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111336549 | ||||||
chr13:111336559
|
C | CT | 49 | a0001c0001t0001g0016a0001c0001t0001g0070a0001c0001t0001g0087others(46): Show | 61 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.170-3302dupT | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 111336559 | |||||
chr13:111336904
|
C | T | 1 | a0001c0002t0001g0058 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.170-2959C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111336904 | ||||||
chr13:111336920
|
G | A | 3 | a0001c0001t0011g0131a0001c0002t0003g0051a0001c0002t0003g0285 | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-2943G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111336920 | ||||||
chr13:111336950
|
G | T | 1 | a0001c0001t0002g0215 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.170-2913G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111336950 | ||||||
chr13:111336962
|
C | T | 1 | a0001c0002t0001g0101 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.170-2901C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111336962 | ||||||
chr13:111337043
|
G | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(136): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.170-2820G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111337043 | ||||||
chr13:111337123
|
G | A | 201 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(198): Show | 290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.170-2740G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111337123 | ||||||
chr13:111337319
|
C | T | 29 | a0001c0001t0001g0016a0001c0001t0001g0093a0001c0001t0001g0106others(26): Show | 38 | HG00099.hp1 HG00323.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.170-2544C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111337319 | ||||||
chr13:111337377
|
A | G | 3 | a0002c0004t0001g0030a0002c0004t0001g0163a0002c0004t0001g0280 | 4 | HG01884.hp1 HG02258.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-2486A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111337377 | ||||||
chr13:111337530
|
G | T | 1 | a0001c0001t0001g0019 | 2 | HG00140.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.170-2333G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111337530 | ||||||
chr13:111337571
|
G | A | 1 | a0001c0001t0001g0028 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.170-2292G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111337571 | ||||||
chr13:111337618
|
G | A | 2 | a0001c0002t0009g0281a0001c0002t0009g0282 | 2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.170-2245G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111337618 | ||||||
chr13:111337706
|
A | C | 8 | a0001c0001t0001g0023a0001c0001t0001g0107a0001c0001t0001g0119others(5): Show | 9 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.170-2157A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111337706 | ||||||
chr13:111337772
|
A | C | 1 | a0001c0001t0001g0070 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.170-2091A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111337772 | ||||||
chr13:111337883
|
C | T | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(140): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.170-1980C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111337883 | ||||||
chr13:111337941
|
G | A | 8 | a0001c0001t0001g0023a0001c0001t0001g0107a0001c0001t0001g0119others(5): Show | 9 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.170-1922G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111337941 | ||||||
chr13:111338022
|
C | T | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(141): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.170-1841C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338022 | ||||||
chr13:111338025
|
C | T | 1 | a0001c0002t0002g0164 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.170-1838C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338025 | ||||||
chr13:111338074
|
C | T | 3 | a0001c0001t0011g0131a0001c0002t0003g0051a0001c0002t0003g0285 | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-1789C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338074 | ||||||
chr13:111338117
|
TGCG | T | 29 | a0001c0001t0001g0016a0001c0001t0001g0093a0001c0001t0001g0106others(26): Show | 38 | HG00099.hp1 HG00323.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.170-1743_170-1741d others(5): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 111338117 | |||||
chr13:111338118
|
G | A | 3 | a0001c0001t0001g0119a0001c0002t0003g0062a0001c0002t0003g0063 | 3 | HG00639.hp1 HG01243.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.170-1745G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338118 | ||||||
chr13:111338120
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.170-1743G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338120 | ||||||
chr13:111338185
|
G | A | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(141): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.170-1678G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338185 | ||||||
chr13:111338305
|
G | C | 3 | a0001c0002t0009g0281a0001c0002t0009g0282a0001c0008t0006g0091 | 3 | HG02280.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.170-1558G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338305 | ||||||
chr13:111338440
|
C | T | 1 | a0001c0001t0003g0033 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.170-1423C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338440 | ||||||
chr13:111338441
|
T | A | 1 | a0001c0001t0003g0033 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.170-1422T>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338441 | ||||||
chr13:111338493
|
C | T | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(165): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.170-1370C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338493 | ||||||
chr13:111338584
|
C | T | 4 | a0001c0001t0001g0106a0001c0001t0001g0117a0001c0002t0001g0252others(1): Show | 4 | HG02735.hp2 HG03516.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-1279C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338584 | ||||||
chr13:111338743
|
C | G | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(138): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.170-1120C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338743 | ||||||
chr13:111338751
|
GTGATTAG others(36): Show |
G | 1 | a0001c0002t0002g0229 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.170-1111_170-1069d others(45): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338751 | ||||||
chr13:111338848
|
G | T | 2 | a0001c0001t0002g0040a0001c0001t0002g0223 | 3 | HG00621.hp2 NA18979.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.170-1015G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338848 | ||||||
chr13:111338937
|
G | A | 18 | a0001c0001t0001g0023a0001c0001t0001g0064a0001c0001t0001g0107others(15): Show | 24 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.170-926G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338937 | ||||||
chr13:111338962
|
G | A | 1 | a0001c0001t0002g0201 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.170-901G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338962 | ||||||
chr13:111339116
|
G | C | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(166): Show | 237 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.170-747G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111339116 | ||||||
chr13:111339414
|
A | G | 2 | a0001c0001t0002g0147a0001c0001t0002g0214 | 2 | NA18946.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.170-449A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111339414 | ||||||
chr13:111339490
|
G | A | 1 | a0001c0001t0002g0181 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.170-373G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111339490 | ||||||
chr13:111339528
|
G | A | 1 | a0001c0002t0003g0047 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.170-335G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111339528 | ||||||
chr13:111339535
|
T | TTCCATGC others(31): Show |
1 | a0001c0001t0001g0108 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.170-304_170-267dup others(38): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 111339535 | |||||
chr13:111339545
|
T | C | 1 | a0001c0002t0003g0141 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.170-318T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111339545 | ||||||
chr13:111339663
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.170-200C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111339663 | ||||||
chr13:111339716
|
C | T | 8 | a0001c0001t0001g0023a0001c0001t0001g0107a0001c0001t0001g0119others(5): Show | 9 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.170-147C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111339716 | ||||||
chr13:111339735
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.170-128G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111339735 | ||||||
chr13:111339779
|
A | T | 5 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(2): Show | 5 | HG02630.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.170-84A>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111339779 | ||||||
chr13:111339941
|
C | T | 36 | a0001c0001t0001g0023a0001c0001t0001g0064a0001c0001t0001g0119others(33): Show | 54 | HG00639.hp1 HG00733.hp1 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.239+9C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111339941 | ||||||
chr13:111339967
|
A | G | 20 | a0001c0001t0001g0023a0001c0001t0001g0064a0001c0001t0001g0119others(17): Show | 31 | HG00639.hp1 HG00733.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.239+35A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111339967 | ||||||
chr13:111339998
|
TCCTGCCT others(32): Show |
T | 1 | a0001c0002t0002g0169 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.239+67_239+105delC others(38): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111339998 | ||||||
chr13:111340019
|
C | T | 1 | a0001c0001t0002g0039 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.239+87C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340019 | ||||||
chr13:111340040
|
G | A | 10 | a0001c0001t0001g0165a0001c0001t0001g0218a0001c0001t0002g0046others(7): Show | 11 | HG00438.hp1 NA18612.hp1 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.239+108G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340040 | ||||||
chr13:111340064
|
C | A | 1 | a0001c0002t0002g0169 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.239+132C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340064 | ||||||
chr13:111340088
|
C | G | 1 | a0001c0002t0001g0100 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.239+156C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340088 | ||||||
chr13:111340116
|
AGTGCTTG others(79): Show |
A | 7 | a0001c0001t0001g0064a0001c0001t0011g0131a0001c0002t0001g0013others(4): Show | 12 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.239+254_239+339del others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340116 | |||||
chr13:111340136
|
A | G | 2 | a0001c0001t0001g0295a0001c0001t0003g0033 | 3 | HG03486.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.239+204A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340136 | ||||||
chr13:111340143
|
A | ATGTTTAG others(122): Show |
1 | a0001c0002t0003g0141 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.239+254_239+382dup others(129): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340143 | |||||
chr13:111340146
|
T | TTAGTGAG others(248): Show |
1 | a0001c0002t0002g0169 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.239+215_239+216ins others(255): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340146 | |||||
chr13:111340171
|
T | G | 1 | a0001c0003t0001g0079 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.239+239T>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340171 | ||||||
chr13:111340171
|
T | TGAAAATC others(160): Show |
1 | a0001c0002t0001g0099 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.239+253_239+254ins others(167): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340171 | |||||
chr13:111340175
|
A | C | 1 | a0001c0002t0002g0169 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.239+243A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340175 | ||||||
chr13:111340175
|
AATCATAA others(380): Show |
A | 1 | a0001c0002t0001g0162 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.239+254_239+640del | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340175 | |||||
chr13:111340175
|
AATCATAA others(509): Show |
A | 1 | a0001c0002t0001g0103 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.239+254_239+769del | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340175 | |||||
chr13:111340186
|
A | ATGTTTAG others(380): Show |
6 | a0001c0001t0008g0029a0001c0001t0008g0077a0001c0002t0004g0014others(3): Show | 11 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.239+296_239+297ins others(387): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340186 | |||||
chr13:111340186
|
A | G | 12 | a0001c0001t0001g0023a0001c0001t0001g0107a0001c0001t0001g0119others(9): Show | 14 | HG00639.hp1 HG00733.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.239+254A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340186 | ||||||
chr13:111340186
|
ATGTTTAG others(79): Show |
A | 2 | a0001c0001t0001g0073a0001c0001t0001g0110 | 2 | HG00733.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.239+297_239+382del others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340186 | |||||
chr13:111340186
|
ATGTTTAG others(337): Show |
A | 1 | a0001c0001t0001g0132 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.239+286_239+629del | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340186 | |||||
chr13:111340186
|
ATGTTTAG others(380): Show |
A | 6 | a0001c0001t0001g0129a0001c0001t0001g0134a0001c0002t0001g0008others(3): Show | 12 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.239+297_239+683del | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340186 | |||||
chr13:111340218
|
A | AATCATAA others(79): Show |
8 | a0001c0001t0001g0023a0001c0001t0001g0107a0001c0001t0001g0119others(5): Show | 9 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.239+296_239+297ins others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340218 | |||||
chr13:111340218
|
A | C | 1 | a0001c0002t0002g0169 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.239+286A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340218 | ||||||
chr13:111340229
|
A | ATGTTTAG others(36): Show |
3 | a0001c0002t0001g0095a0001c0002t0003g0052a0001c0002t0003g0156 | 4 | HG02615.hp1 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+458_239+500dup others(43): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340229 | |||||
chr13:111340229
|
A | ATGTTTAG others(1283): Show |
1 | a0001c0001t0001g0115 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.239+382_239+383ins others(1290): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340229 | |||||
chr13:111340229
|
A | ATGTTTAG others(337): Show |
1 | a0001c0001t0003g0033 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.239+382_239+383ins others(344): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340229 | |||||
chr13:111340229
|
A | ATGTTTAG others(1154): Show |
1 | a0001c0002t0001g0021 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.239+501_240-1163du others(1162): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340229 | |||||
chr13:111340229
|
A | ATGTTTAG others(1369): Show |
2 | a0001c0001t0001g0081a0001c0001t0001g0118 | 2 | HG03491.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.239+457_239+458ins others(1376): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340229 | |||||
chr13:111340229
|
A | ATGTTTAG others(1842): Show |
1 | a0001c0001t0001g0080 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.239+457_239+458ins others(1849): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340229 | |||||
chr13:111340229
|
A | G | 67 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0070others(64): Show | 85 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.239+297A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340229 | ||||||
chr13:111340229
|
ATGTTTAG others(36): Show |
A | 2 | a0001c0001t0002g0042a0001c0001t0002g0197 | 3 | HG02027.hp1 NA19074.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.239+458_239+500del others(43): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340229 | |||||
chr13:111340229
|
ATGTTTAG others(79): Show |
A | 1 | a0001c0001t0001g0106 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.239+415_239+500del others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340229 | |||||
chr13:111340260
|
A | C | 1 | a0001c0002t0001g0099 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.239+328A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340260 | ||||||
chr13:111340261
|
A | AATCATAA others(123): Show |
1 | a0001c0001t0002g0209 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.239+363_239+364ins others(130): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340261 | |||||
chr13:111340261
|
A | AATCATAA others(1154): Show |
1 | a0001c0002t0002g0086 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.239+382_239+383ins others(1161): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340261 | |||||
chr13:111340261
|
A | AATCATAA others(1111): Show |
1 | a0001c0010t0001g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.239+382_239+383ins others(1118): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340261 | |||||
chr13:111340261
|
A | AATCATAA others(1111): Show |
3 | a0001c0001t0001g0016a0001c0001t0001g0114a0001c0001t0001g0117 | 5 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.239+382_239+383ins others(1118): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340261 | |||||
chr13:111340261
|
A | AATCATAA others(466): Show |
1 | a0001c0002t0001g0060 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.239+382_239+383ins others(473): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340261 | |||||
chr13:111340261
|
A | AATCATAA others(1111): Show |
1 | a0001c0001t0001g0116 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.239+382_239+383ins others(1118): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340261 | |||||
chr13:111340261
|
A | AATCATAA others(1111): Show |
3 | a0001c0001t0001g0123a0001c0002t0001g0006a0001c0002t0002g0006 | 7 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.239+382_239+383ins others(1118): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340261 | |||||
chr13:111340261
|
A | AATCATAA others(1111): Show |
2 | a0001c0002t0001g0102a0001c0002t0003g0259 | 2 | HG00738.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.239+382_239+383ins others(1118): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340261 | |||||
chr13:111340261
|
A | AATCATAA others(1198): Show |
1 | a0001c0002t0001g0096 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.239+382_239+383ins others(1205): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340261 | |||||
chr13:111340261
|
A | AATCATAA others(1068): Show |
1 | a0001c0001t0001g0136 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.239+382_239+383ins others(1075): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340261 | |||||
chr13:111340272
|
G | GTGTTTAG others(79): Show |
6 | a0001c0001t0001g0093a0001c0001t0001g0112a0001c0001t0001g0113others(3): Show | 9 | HG01192.hp2 HG03239.hp2 NA18968.hp2 others(6): Show |
intron_variant | MODIFIER | c.239+382_239+383ins others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340272 | |||||
chr13:111340272
|
G | GTGTTTAG others(79): Show |
2 | a0001c0002t0001g0098a0001c0002t0001g0100 | 2 | HG01168.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.239+425_239+426ins others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340272 | |||||
chr13:111340272
|
G | GTGTTTAG others(79): Show |
1 | a0001c0002t0001g0252 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.239+371_239+372ins others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340272 | |||||
chr13:111340304
|
A | AATCATAA others(1068): Show |
1 | a0001c0002t0001g0101 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.239+382_239+383ins others(1075): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340304 | |||||
chr13:111340304
|
A | AATCATAA others(1068): Show |
1 | a0001c0002t0002g0229 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.239+382_239+383ins others(1075): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340304 | |||||
chr13:111340304
|
A | AATCATAA others(1369): Show |
1 | a0001c0001t0001g0177 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.239+382_239+383ins others(1376): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340304 | |||||
chr13:111340304
|
A | AATCATAA others(466): Show |
1 | a0001c0002t0001g0097 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.239+382_239+383ins others(473): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340304 | |||||
chr13:111340304
|
A | AATCATAA others(251): Show |
1 | a0001c0002t0009g0281 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.239+458_239+715dup others(258): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340304 | |||||
chr13:111340304
|
A | AATCATAA others(122): Show |
57 | a0001c0001t0001g0002a0001c0001t0001g0092a0001c0001t0001g0165others(54): Show | 87 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.239+457_239+458ins others(129): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340304 | |||||
chr13:111340304
|
A | C | 4 | a0001c0001t0002g0209a0001c0002t0001g0252a0001c0002t0002g0169others(1): Show | 4 | HG02083.hp1 HG03704.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+372A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340304 | ||||||
chr13:111340315
|
G | C | 1 | a0001c0002t0004g0140 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.239+383G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340315 | ||||||
chr13:111340324
|
G | GAGCACCT others(251): Show |
1 | a0001c0008t0006g0091 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.239+649_239+650ins others(258): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340324 | |||||
chr13:111340347
|
A | AATCATAA others(332): Show |
1 | a0001c0002t0001g0099 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.239+450_239+451ins others(339): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340347 | |||||
chr13:111340347
|
A | AATCATAA others(36): Show |
4 | a0001c0001t0002g0220a0001c0002t0001g0057a0001c0002t0001g0090others(1): Show | 4 | HG00558.hp2 HG02027.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+457_239+458ins others(43): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340347 | |||||
chr13:111340347
|
A | AATCATAA others(79): Show |
1 | a0003c0009t0001g0248 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.239+457_239+458ins others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340347 | |||||
chr13:111340347
|
A | C | 5 | a0001c0001t0001g0115a0001c0001t0001g0177a0001c0001t0002g0149others(2): Show | 5 | HG01975.hp2 HG03688.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.239+415A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340347 | ||||||
chr13:111340357
|
C | T | 2 | a0002c0004t0001g0030a0002c0004t0001g0163 | 3 | HG01884.hp1 HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.239+425C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340357 | ||||||
chr13:111340358
|
G | C | 2 | a0001c0001t0001g0295a0001c0002t0004g0140 | 2 | HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.239+426G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340358 | ||||||
chr13:111340358
|
GTGTTTAG others(724): Show |
G | 3 | a0001c0002t0001g0013a0001c0002t0003g0051a0001c0002t0003g0285 | 7 | HG02895.hp1 HG02896.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.239+501_239+1231de others(1): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340358 | |||||
chr13:111340358
|
GTGTTTAG others(982): Show |
G | 5 | a0001c0001t0007g0025a0001c0001t0007g0104a0001c0001t0010g0292others(2): Show | 6 | HG01255.hp2 HG02698.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.239+501_240-1335de others(1): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340358 | |||||
chr13:111340372
|
C | T | 2 | a0001c0002t0001g0098a0001c0002t0001g0100 | 2 | HG01168.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.239+440C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340372 | ||||||
chr13:111340389
|
A | C | 1 | a0001c0002t0001g0099 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.239+457A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340389 | ||||||
chr13:111340390
|
A | AATCATAA others(36): Show |
1 | a0001c0001t0001g0130 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.239+501_239+543dup others(43): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340390 | |||||
chr13:111340390
|
A | AATCATAA others(122): Show |
1 | a0001c0002t0001g0084 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.239+716_239+844dup others(129): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340390 | |||||
chr13:111340390
|
A | C | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(140): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.239+458A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340390 | ||||||
chr13:111340390
|
AATCATAA others(294): Show |
A | 1 | a0001c0001t0001g0064 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.239+501_239+801del | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340390 | |||||
chr13:111340401
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.239+469G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340401 | ||||||
chr13:111340401
|
GTGTTTAG others(939): Show |
G | 1 | a0002c0004t0001g0280 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.239+501_240-1378de others(1): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340401 | |||||
chr13:111340433
|
C | A | 43 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0093others(40): Show | 59 | HG00099.hp2 HG00639.hp1 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.239+501C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340433 | ||||||
chr13:111340433
|
C | CATCATAA others(36): Show |
1 | a0001c0001t0003g0033 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.239+544_239+586dup others(43): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340433 | |||||
chr13:111340444
|
G | C | 6 | a0001c0001t0008g0029a0001c0001t0008g0077a0001c0002t0004g0014others(3): Show | 11 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.239+512G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340444 | ||||||
chr13:111340465
|
T | C | 1 | a0001c0002t0001g0252 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.239+533T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340465 | ||||||
chr13:111340476
|
A | AATCATAA others(79): Show |
1 | a0001c0002t0001g0252 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.239+618_239+619ins others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340476 | |||||
chr13:111340476
|
A | C | 14 | a0001c0001t0001g0115a0001c0001t0001g0123a0001c0001t0002g0194others(11): Show | 23 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.239+544A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340476 | ||||||
chr13:111340476
|
AATCATAA others(208): Show |
A | 2 | a0002c0004t0001g0030a0002c0004t0001g0163 | 3 | HG01884.hp1 HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.239+587_239+801del | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340476 | |||||
chr13:111340487
|
G | C | 3 | a0001c0001t0001g0128a0001c0002t0003g0255a0001c0002t0003g0256 | 3 | HG02257.hp2 HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.239+555G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340487 | ||||||
chr13:111340519
|
C | A | 20 | a0001c0001t0001g0093a0001c0001t0001g0112a0001c0001t0001g0113others(17): Show | 28 | HG01168.hp2 HG01192.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.239+587C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340519 | ||||||
chr13:111340551
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.239+619T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340551 | ||||||
chr13:111340562
|
C | A | 20 | a0001c0001t0001g0093a0001c0001t0001g0112a0001c0001t0001g0113others(17): Show | 29 | HG01168.hp2 HG01192.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.239+630C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340562 | ||||||
chr13:111340562
|
C | CATCATAA others(36): Show |
1 | a0001c0001t0002g0213 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.239+673_239+715dup others(43): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340562 | |||||
chr13:111340562
|
C | CATCATAA others(79): Show |
55 | a0001c0001t0001g0002a0001c0001t0001g0092a0001c0001t0001g0165others(52): Show | 85 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.239+715_239+716ins others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340562 | |||||
chr13:111340562
|
C | CATCATAA others(208): Show |
8 | a0001c0001t0001g0218a0001c0001t0002g0005a0001c0001t0002g0036others(5): Show | 11 | HG03927.hp2 HG04115.hp2 NA18952.hp1 others(8): Show |
intron_variant | MODIFIER | c.239+716_239+930dup others(215): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340562 | |||||
chr13:111340562
|
C | CATCATAA others(79): Show |
2 | a0001c0001t0002g0170a0001c0001t0002g0193 | 2 | NA18970.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.239+672_239+673ins others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340562 | |||||
chr13:111340562
|
C | CATCATAA others(122): Show |
1 | a0001c0001t0002g0194 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.239+672_239+673ins others(129): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340562 | |||||
chr13:111340568
|
A | AACCCGTG others(36): Show |
1 | a0001c0002t0001g0060 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.239+672_239+673ins others(43): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340568 | |||||
chr13:111340568
|
A | T | 2 | a0001c0001t0011g0131a0001c0002t0001g0252 | 2 | HG02622.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.239+636A>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340568 | ||||||
chr13:111340582
|
G | A | 4 | a0001c0001t0006g0024a0001c0001t0006g0296a0001c0002t0001g0253others(1): Show | 5 | HG02559.hp1 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.239+650G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340582 | ||||||
chr13:111340605
|
A | C | 46 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0078others(43): Show | 60 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.239+673A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340605 | ||||||
chr13:111340605
|
AATCATAA others(595): Show |
A | 1 | a0001c0002t0001g0253 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.239+802_239+1403de others(1): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340605 | |||||
chr13:111340648
|
C | A | 44 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0072others(41): Show | 58 | HG00140.hp1 HG00558.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.239+716C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340648 | ||||||
chr13:111340648
|
C | CATCATAA others(79): Show |
5 | a0001c0002t0001g0121a0001c0002t0002g0166a0001c0002t0003g0061others(2): Show | 5 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.239+759_239+844dup others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340648 | |||||
chr13:111340648
|
CATCATAA others(509): Show |
C | 1 | a0001c0001t0001g0106 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.239+802_239+1317de others(1): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340648 | |||||
chr13:111340648
|
CATCATAA others(767): Show |
C | 1 | a0001c0001t0011g0131 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.239+759_240-1292de others(1): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340648 | |||||
chr13:111340658
|
C | CGTGTTTA others(165): Show |
1 | a0001c0001t0003g0033 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.239+801_239+802ins others(172): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340658 | |||||
chr13:111340659
|
G | GTGTTTAG others(79): Show |
1 | a0001c0001t0001g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.239+758_239+759ins others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340659 | |||||
chr13:111340691
|
C | A | 8 | a0001c0001t0001g0115a0001c0001t0001g0177a0001c0001t0001g0295others(5): Show | 9 | HG01167.hp2 HG02027.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.239+759C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340691 | ||||||
chr13:111340691
|
C | CATCATAA others(1240): Show |
1 | a0001c0001t0001g0112 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.239+801_239+802ins others(1247): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340691 | |||||
chr13:111340691
|
CATCATAA others(724): Show |
C | 1 | a0001c0002t0001g0151 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.239+956_240-1138de others(1): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340691 | |||||
chr13:111340702
|
GTGTTTAG others(638): Show |
G | 2 | a0002c0004t0001g0030a0002c0004t0001g0163 | 3 | HG01884.hp1 HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.239+956_240-1224de others(1): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340702 | |||||
chr13:111340705
|
T | TTTAGTGA others(802): Show |
1 | a0001c0002t0001g0099 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.239+801_239+802ins others(809): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340705 | |||||
chr13:111340734
|
A | AATCATAA others(122): Show |
1 | a0001c0002t0004g0140 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.239+898_239+899ins others(129): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340734 | |||||
chr13:111340734
|
A | AATCATAA others(638): Show |
1 | a0001c0002t0003g0258 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.239+1274_239+1275i others(647): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340734 | |||||
chr13:111340734
|
A | AATCATAA others(165): Show |
2 | a0001c0001t0002g0176a0001c0001t0002g0222 | 2 | HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.239+930_239+931ins others(172): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340734 | |||||
chr13:111340734
|
A | AATCATAA others(208): Show |
1 | a0001c0001t0002g0146 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.239+930_239+931ins others(215): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340734 | |||||
chr13:111340734
|
A | AATCATAA others(36): Show |
3 | a0001c0001t0001g0023a0001c0001t0001g0107a0001c0001t0001g0119 | 4 | HG01258.hp1 HG01361.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+844_239+845ins others(43): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340734 | |||||
chr13:111340734
|
A | C | 12 | a0001c0001t0001g0093a0001c0001t0001g0113a0001c0001t0001g0127others(9): Show | 15 | HG00099.hp1 HG00323.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.239+802A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340734 | ||||||
chr13:111340759
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.239+827C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340759 | ||||||
chr13:111340777
|
A | AATCATAA others(939): Show |
2 | a0001c0002t0001g0098a0001c0002t0001g0100 | 2 | HG01168.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.239+930_239+931ins others(946): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340777 | |||||
chr13:111340777
|
A | AATCATAA others(552): Show |
1 | a0001c0002t0001g0060 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.239+887_239+888ins others(559): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340777 | |||||
chr13:111340777
|
A | C | 2 | a0001c0001t0002g0220a0001c0002t0001g0252 | 2 | HG02027.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.239+845A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340777 | ||||||
chr13:111340820
|
A | AATCATAA others(79): Show |
3 | a0001c0001t0001g0023a0001c0001t0001g0107a0001c0001t0001g0119 | 4 | HG01258.hp1 HG01361.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+955_239+956ins others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340820 | |||||
chr13:111340820
|
A | AATCATAA others(79): Show |
3 | a0001c0001t0001g0071a0001c0001t0002g0144a0001c0002t0003g0053 | 4 | HG00280.hp2 HG00323.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+930_239+931ins others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340820 | |||||
chr13:111340820
|
A | AATCATAA others(208): Show |
5 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0265others(2): Show | 7 | HG00140.hp2 HG01099.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.239+930_239+931ins others(215): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340820 | |||||
chr13:111340820
|
A | C | 2 | a0001c0001t0002g0220a0001c0001t0003g0033 | 3 | HG02027.hp2 HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.239+888A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340820 | ||||||
chr13:111340823
|
CATAACCC others(165): Show |
C | 1 | a0001c0002t0002g0164 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.239+956_239+1127de others(1): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340823 | |||||
chr13:111340831
|
G | A | 1 | a0001c0001t0002g0175 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.239+899G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340831 | ||||||
chr13:111340831
|
GTGTTTAG others(509): Show |
G | 1 | a0001c0001t0002g0192 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.239+956_240-1353de others(1): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340831 | |||||
chr13:111340845
|
CCTGTGCT others(36): Show |
C | 1 | a0001c0002t0001g0032 | 2 | NA18950.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.239+956_239+998del others(43): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340845 | |||||
chr13:111340863
|
A | C | 14 | a0001c0001t0001g0028a0001c0001t0001g0093a0001c0001t0001g0113others(11): Show | 18 | HG00609.hp1 HG00639.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.239+931A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340863 | ||||||
chr13:111340866
|
CATAACCC others(122): Show |
C | 6 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0001g0134others(3): Show | 12 | HG01109.hp2 HG01243.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.239+956_239+1084de others(1): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340866 | |||||
chr13:111340869
|
A | AACCCGTG others(208): Show |
1 | a0001c0001t0001g0127 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.239+955_239+956ins others(215): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340869 | |||||
chr13:111340888
|
T | C | 59 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0028others(56): Show | 77 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.239+956T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340888 | ||||||
chr13:111340888
|
TCTGTGCT others(552): Show |
T | 2 | a0001c0001t0001g0064a0001c0002t0001g0162 | 2 | HG01167.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.239+1063_240-1203d others(2): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340888 | |||||
chr13:111340906
|
A | AATCATAA others(79): Show |
1 | a0001c0001t0003g0033 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.239+1059_239+1060i others(88): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340906 | |||||
chr13:111340906
|
A | AATCATAA others(36): Show |
1 | a0001c0002t0004g0014 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.239+1016_239+1017i others(45): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340906 | |||||
chr13:111340906
|
A | AATCATAA others(1240): Show |
4 | a0001c0001t0001g0093a0001c0001t0001g0113a0001c0001t0002g0171others(1): Show | 7 | HG03239.hp2 NA18968.hp2 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.239+1016_239+1017i others(1249): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340906 | |||||
chr13:111340906
|
A | C | 7 | a0001c0001t0001g0112a0001c0001t0001g0115a0001c0001t0001g0249others(4): Show | 7 | HG00609.hp1 HG01071.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.239+974A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340906 | ||||||
chr13:111340931
|
C | T | 2 | a0001c0001t0002g0176a0001c0001t0002g0222 | 2 | HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.239+999C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340931 | ||||||
chr13:111340949
|
A | AATCATAA others(208): Show |
1 | a0001c0001t0001g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.239+1062_239+1063i others(217): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340949 | |||||
chr13:111340949
|
A | C | 9 | a0001c0001t0001g0127a0001c0001t0008g0029a0001c0001t0008g0077others(6): Show | 14 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.239+1017A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340949 | ||||||
chr13:111340952
|
C | A | 1 | a0001c0002t0001g0247 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.239+1020C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340952 | ||||||
chr13:111340959
|
C | T | 1 | a0001c0001t0002g0208 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.239+1027C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340959 | ||||||
chr13:111340974
|
C | CCTGTGCT others(36): Show |
1 | a0001c0001t0002g0220 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.239+1062_239+1063i others(45): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340974 | |||||
chr13:111340992
|
A | AATCATAA others(1111): Show |
1 | a0001c0002t0001g0252 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.239+1062_239+1063i others(1120): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340992 | |||||
chr13:111340992
|
A | C | 8 | a0001c0001t0001g0127a0001c0001t0008g0029a0001c0001t0008g0077others(5): Show | 12 | HG00738.hp2 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.239+1060A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340992 | ||||||
chr13:111340995
|
A | C | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0010others(185): Show | 271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.239+1063A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340995 | ||||||
chr13:111341003
|
G | C | 3 | a0001c0001t0001g0023a0001c0001t0001g0107a0001c0001t0001g0119 | 4 | HG01258.hp1 HG01361.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+1071G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341003 | ||||||
chr13:111341003
|
G | GTGTTTAG others(36): Show |
5 | a0001c0002t0001g0121a0001c0002t0002g0166a0001c0002t0003g0061others(2): Show | 5 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.239+1113_239+1114i others(45): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341003 | |||||
chr13:111341017
|
C | CCTGTGCT others(79): Show |
1 | a0001c0001t0001g0249 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.239+1113_239+1114i others(88): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341017 | |||||
chr13:111341035
|
A | AATCATAA others(595): Show |
1 | a0001c0001t0001g0116 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.239+1145_239+1146i others(604): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341035 | |||||
chr13:111341035
|
A | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0127a0001c0002t0001g0252 | 4 | HG03491.hp1 HG03492.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+1103A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341035 | ||||||
chr13:111341078
|
A | AATCATAA others(79): Show |
1 | a0001c0001t0001g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.239+1156_239+1157i others(88): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341078 | |||||
chr13:111341078
|
A | AATCATAA others(638): Show |
2 | a0001c0002t0001g0097a0001c0002t0001g0101 | 2 | HG00099.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.239+1156_239+1157i others(647): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341078 | |||||
chr13:111341078
|
A | AATCATAA others(681): Show |
1 | a0001c0002t0002g0229 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.239+1156_239+1157i others(690): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341078 | |||||
chr13:111341078
|
A | AATCATAA others(595): Show |
10 | a0001c0001t0001g0016a0001c0001t0001g0123a0001c0001t0001g0136others(7): Show | 15 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.239+1156_239+1157i others(604): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341078 | |||||
chr13:111341078
|
A | C | 4 | a0001c0001t0001g0116a0001c0001t0001g0127a0001c0001t0002g0191others(1): Show | 4 | HG01123.hp1 HG02040.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+1146A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341078 | ||||||
chr13:111341086
|
C | A | 1 | a0001c0002t0009g0281 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.239+1154C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341086 | ||||||
chr13:111341089
|
C | CTGTTTAG others(380): Show |
1 | a0001c0002t0001g0271 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.239+1274_239+1275i others(389): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341089 | |||||
chr13:111341089
|
C | G | 63 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0093others(60): Show | 85 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.239+1157C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341089 | ||||||
chr13:111341089
|
CTGTTTAG others(595): Show |
C | 1 | a0004c0007t0003g0257 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.239+1232_240-991de others(1): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341089 | |||||
chr13:111341103
|
C | T | 1 | a0001c0001t0002g0212 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.239+1171C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341103 | ||||||
chr13:111341121
|
A | AATCATAA others(79): Show |
1 | a0001c0002t0004g0014 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.239+1231_239+1232i others(88): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341121 | |||||
chr13:111341121
|
A | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0117a0001c0001t0001g0132others(1): Show | 4 | HG01934.hp2 HG02165.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+1189A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341121 | ||||||
chr13:111341132
|
G | C | 2 | a0001c0001t0002g0176a0001c0001t0002g0222 | 2 | HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.239+1200G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341132 | ||||||
chr13:111341156
|
T | G | 1 | a0001c0002t0001g0247 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.239+1224T>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341156 | ||||||
chr13:111341164
|
A | AATCATAA others(294): Show |
1 | a0001c0001t0001g0016 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.239+1274_239+1275i others(303): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341164 | |||||
chr13:111341164
|
A | AATCATAA others(337): Show |
1 | a0001c0001t0001g0117 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.239+1274_239+1275i others(346): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341164 | |||||
chr13:111341164
|
A | AATCATAA others(79): Show |
1 | a0001c0002t0001g0060 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.239+1329_240-1410d others(88): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341164 | |||||
chr13:111341164
|
A | AATCATAA others(122): Show |
2 | a0001c0001t0001g0114a0001c0001t0003g0033 | 3 | HG02615.hp2 HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.239+1286_240-1410d others(131): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341164 | |||||
chr13:111341164
|
A | C | 10 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0001g0134others(7): Show | 16 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.239+1232A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341164 | ||||||
chr13:111341164
|
AATCATAA others(36): Show |
A | 1 | a0001c0001t0002g0212 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.239+1372_240-1410d others(45): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341164 | |||||
chr13:111341169
|
T | C | 1 | a0001c0002t0001g0247 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.239+1237T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341169 | ||||||
chr13:111341170
|
A | T | 1 | a0001c0001t0001g0106 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.239+1238A>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341170 | ||||||
chr13:111341175
|
G | GTGTTTAG others(36): Show |
1 | a0001c0001t0002g0144 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.239+1274_239+1275i others(45): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341175 | |||||
chr13:111341207
|
C | A | 104 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0001g0070others(101): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.239+1275C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341207 | ||||||
chr13:111341207
|
C | CATCATAA others(681): Show |
2 | a0001c0002t0001g0098a0001c0002t0001g0100 | 2 | HG01168.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.239+1317_239+1318i others(690): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341207 | |||||
chr13:111341207
|
C | CATCATAA others(294): Show |
1 | a0001c0001t0001g0016 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.240-1410_240-1409i others(303): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341207 | |||||
chr13:111341207
|
C | CATCATAA others(1283): Show |
1 | a0001c0002t0003g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.239+1366_239+1367i others(1292): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341207 | |||||
chr13:111341216
|
C | G | 1 | a0001c0002t0001g0240 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.239+1284C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341216 | ||||||
chr13:111341218
|
G | C | 1 | a0001c0001t0001g0249 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.239+1286G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341218 | ||||||
chr13:111341250
|
C | A | 22 | a0001c0001t0001g0116a0001c0001t0001g0123a0001c0001t0001g0127others(19): Show | 26 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.239+1318C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341250 | ||||||
chr13:111341250
|
C | CATCATAA others(509): Show |
5 | a0001c0001t0008g0029a0001c0001t0008g0077a0001c0002t0004g0014others(2): Show | 9 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.239+1360_239+1361i others(518): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341250 | |||||
chr13:111341250
|
C | CATCATAA others(380): Show |
7 | a0001c0001t0001g0093a0001c0001t0001g0112a0001c0001t0001g0113others(4): Show | 10 | HG01071.hp2 HG01192.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.240-1410_240-1409i others(389): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341250 | |||||
chr13:111341250
|
C | CATCATAA others(122): Show |
6 | a0001c0001t0001g0023a0001c0001t0001g0119a0001c0002t0001g0121others(3): Show | 7 | HG00733.hp1 HG01167.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.239+1366_239+1367i others(131): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341250 | |||||
chr13:111341261
|
G | A | 1 | a0001c0003t0001g0027 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.239+1329G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341261 | ||||||
chr13:111341293
|
C | A | 5 | a0001c0001t0001g0127a0001c0001t0001g0249a0001c0001t0001g0295others(2): Show | 5 | HG00609.hp1 HG02559.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.239+1361C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341293 | ||||||
chr13:111341293
|
C | CATCATAA others(337): Show |
1 | a0001c0001t0001g0177 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.240-1410_240-1409i others(346): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341293 | |||||
chr13:111341299
|
A | T | 1 | a0001c0001t0001g0107 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.239+1367A>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341299 | ||||||
chr13:111341336
|
C | A | 6 | a0001c0001t0001g0107a0001c0001t0002g0212a0001c0001t0002g0217others(3): Show | 7 | HG00609.hp1 HG01891.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.239+1404C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341336 | ||||||
chr13:111341336
|
C | CATCATAA others(36): Show |
1 | a0001c0001t0001g0074 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.240-1410_240-1409i others(45): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341336 | |||||
chr13:111341342
|
A | AACCCGTG others(509): Show |
1 | a0001c0002t0004g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.240-1410_240-1409i others(518): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341342 | |||||
chr13:111341342
|
A | T | 17 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0001g0134others(14): Show | 31 | HG00639.hp1 HG01109.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.239+1410A>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341342 | ||||||
chr13:111341347
|
A | ATGTTTAG others(36): Show |
2 | a0001c0001t0001g0265a0001c0002t0001g0275 | 2 | HG01993.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.240-1033_240-991du others(44): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341347 | |||||
chr13:111341347
|
A | G | 111 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0019others(108): Show | 150 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.240-1409A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341347 | ||||||
chr13:111341347
|
ATGTTTAG others(36): Show |
A | 1 | a0001c0002t0002g0164 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.240-1033_240-991de others(44): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341347 | |||||
chr13:111341347
|
ATGTTTAG others(79): Show |
A | 1 | a0001c0001t0002g0212 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.240-1076_240-991de others(87): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341347 | |||||
chr13:111341379
|
A | AATCATAA others(1068): Show |
1 | a0001c0002t0001g0060 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.240-1249_240-1248i others(1077): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341379 | |||||
chr13:111341379
|
A | C | 26 | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0132others(23): Show | 39 | HG01109.hp2 HG01243.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.240-1377A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341379 | ||||||
chr13:111341390
|
G | A | 2 | a0001c0001t0002g0176a0001c0001t0002g0222 | 2 | HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.240-1366G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341390 | ||||||
chr13:111341390
|
G | GTGTTTAG others(36): Show |
1 | a0001c0001t0002g0144 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.240-1335_240-1334i others(45): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341390 | |||||
chr13:111341422
|
A | AATCATAA others(36): Show |
1 | a0001c0001t0002g0219 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.240-1292_240-1291i others(45): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341422 | |||||
chr13:111341422
|
A | C | 7 | a0001c0001t0001g0107a0001c0001t0001g0249a0001c0001t0002g0183others(4): Show | 11 | HG02155.hp2 HG02895.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.240-1334A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341422 | ||||||
chr13:111341465
|
A | AATCATAA others(122): Show |
1 | a0001c0001t0001g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.240-1206_240-1205i others(131): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341465 | |||||
chr13:111341465
|
A | C | 10 | a0001c0001t0001g0107a0001c0001t0001g0249a0001c0001t0008g0029others(7): Show | 14 | HG00639.hp1 HG01884.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.240-1291A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341465 | ||||||
chr13:111341476
|
G | A | 1 | a0001c0001t0001g0249 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.240-1280G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341476 | ||||||
chr13:111341476
|
G | GTGTTTAG others(36): Show |
1 | a0001c0001t0001g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.240-1238_240-1237i others(45): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341476 | |||||
chr13:111341477
|
T | TGTTTAGT others(208): Show |
1 | a0001c0001t0001g0107 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.240-1131_240-1130i others(217): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341477 | |||||
chr13:111341490
|
C | T | 1 | a0001c0002t0001g0253 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.240-1266C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341490 | ||||||
chr13:111341500
|
T | C | 1 | a0002c0004t0001g0280 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.240-1256T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341500 | ||||||
chr13:111341508
|
A | AATCATAA others(1070): Show |
1 | a0001c0001t0001g0107 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.240-1076_240-1075i others(1079): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341508 | |||||
chr13:111341508
|
A | AATCATAA others(380): Show |
2 | a0001c0002t0004g0014a0001c0002t0004g0140 | 2 | HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.240-1077_240-1076i others(389): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341508 | |||||
chr13:111341508
|
A | AATCATAA others(380): Show |
1 | a0001c0001t0001g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.240-1077_240-1076i others(389): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341508 | |||||
chr13:111341508
|
A | AATCATAA others(1154): Show |
6 | a0001c0001t0001g0023a0001c0001t0001g0119a0001c0002t0001g0121others(3): Show | 7 | HG00733.hp1 HG01167.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.240-1163_240-1162i others(1163): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341508 | |||||
chr13:111341508
|
A | C | 11 | a0001c0001t0007g0025a0001c0001t0007g0104a0001c0001t0008g0029others(8): Show | 16 | HG00639.hp1 HG01255.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.240-1248A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341508 | ||||||
chr13:111341518
|
C | T | 1 | a0001c0001t0002g0043 | 2 | NA18947.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.240-1238C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341518 | ||||||
chr13:111341530
|
G | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0106a0001c0002t0001g0252others(2): Show | 7 | HG01346.hp2 HG01934.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.240-1226G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341530 | ||||||
chr13:111341530
|
G | GCACCTGT others(122): Show |
1 | a0001c0001t0001g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.240-1098_240-1097i others(131): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341530 | |||||
chr13:111341530
|
G | GCACCTGT others(251): Show |
1 | a0001c0001t0001g0117 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.240-1206_240-1205i others(260): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341530 | |||||
chr13:111341551
|
A | AATCATAA others(165): Show |
1 | a0001c0001t0002g0219 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.240-1034_240-1033i others(174): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341551 | |||||
chr13:111341551
|
A | C | 7 | a0001c0001t0002g0212a0001c0001t0011g0131a0001c0002t0001g0013others(4): Show | 11 | HG00609.hp1 HG01071.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.240-1205A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341551 | ||||||
chr13:111341562
|
G | C | 1 | a0001c0001t0002g0187 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.240-1194G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341562 | ||||||
chr13:111341594
|
A | C | 10 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0001g0134others(7): Show | 16 | HG00609.hp1 HG01109.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.240-1162A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341594 | ||||||
chr13:111341605
|
G | A | 1 | a0001c0002t0001g0060 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.240-1151G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341605 | ||||||
chr13:111341622
|
G | A | 4 | a0001c0002t0005g0065a0001c0002t0005g0066a0001c0002t0005g0067others(1): Show | 4 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.240-1134G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341622 | ||||||
chr13:111341637
|
A | C | 14 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0001g0134others(11): Show | 24 | HG00609.hp1 HG01109.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.240-1119A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341637 | ||||||
chr13:111341691
|
G | C | 1 | a0001c0002t0001g0253 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.240-1065G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341691 | ||||||
chr13:111341723
|
A | C | 14 | a0001c0001t0001g0023a0001c0001t0001g0064a0001c0001t0001g0107others(11): Show | 16 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.240-1033A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341723 | ||||||
chr13:111341777
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.240-979G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341777 | ||||||
chr13:111341868
|
G | A | 43 | a0001c0001t0001g0016a0001c0001t0001g0093a0001c0001t0001g0106others(40): Show | 63 | HG00099.hp1 HG00323.hp2 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.240-888G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341868 | ||||||
chr13:111341874
|
G | T | 1 | a0001c0001t0002g0185 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.240-882G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341874 | ||||||
chr13:111342247
|
A | T | 1 | a0001c0002t0001g0060 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.240-509A>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111342247 | ||||||
chr13:111342289
|
G | A | 1 | a0001c0001t0001g0023 | 2 | HG01258.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.240-467G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111342289 | ||||||
chr13:111342299
|
C | T | 8 | a0001c0001t0001g0023a0001c0001t0001g0107a0001c0001t0001g0119others(5): Show | 9 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.240-457C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111342299 | ||||||
chr13:111342328
|
T | C | 4 | a0001c0001t0011g0131a0001c0002t0001g0013a0001c0002t0003g0051others(1): Show | 8 | HG02622.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.240-428T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111342328 | ||||||
chr13:111342334
|
C | T | 8 | a0001c0001t0001g0295a0001c0001t0008g0029a0001c0001t0008g0077others(5): Show | 13 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.240-422C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111342334 | ||||||
chr13:111342501
|
A | C | 1 | a0001c0002t0001g0267 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.240-255A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111342501 | ||||||
chr13:111342509
|
G | A | 2 | a0001c0002t0001g0253a0004c0007t0003g0257 | 2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.240-247G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111342509 | ||||||
chr13:111342557
|
C | CA | 22 | a0001c0001t0001g0075a0001c0001t0001g0113a0001c0001t0001g0118others(19): Show | 25 | HG00621.hp1 HG00642.hp1 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.240-179dupA | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111342557 | |||||
chr13:111342557
|
C | CAA | 43 | a0001c0001t0001g0016a0001c0001t0001g0064a0001c0001t0001g0093others(40): Show | 59 | HG00099.hp1 HG00323.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.240-180_240-179dup others(2): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111342557 | |||||
chr13:111342557
|
C | CAAA | 22 | a0001c0001t0001g0023a0001c0001t0001g0107a0001c0001t0001g0119others(19): Show | 33 | HG00639.hp1 HG00733.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.240-181_240-179dup others(3): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111342557 | |||||
chr13:111342557
|
CA | C | 15 | a0001c0001t0001g0070a0001c0001t0001g0128a0001c0001t0002g0037others(12): Show | 16 | HG01243.hp2 HG02083.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.240-179delA | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111342557 | |||||
chr13:111342576
|
A | G | 1 | a0001c0002t0001g0011 | 4 | NA18952.hp2 NA18957.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.240-180A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111342576 | ||||||
chr13:111342595
|
G | A | 1 | a0001c0002t0001g0097 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.240-161G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111342595 | ||||||
chr13:111342610
|
T | G | 2 | a0001c0001t0002g0180a0001c0001t0002g0189 | 2 | NA19063.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.240-146T>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111342610 | ||||||
chr13:111342741
|
C | T | 1 | a0001c0001t0002g0178 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.240-15C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111342741 | ||||||
chr13:111342750
|
C | T | 1 | a0001c0002t0003g0283 | 1 | HG03225.hp1 | splice_region_variant&intron_variant | LOW | c.240-6C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111342750 | ||||||
chr13:111342973
|
C | T | 1 | a0001c0002t0002g0164 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.415+42C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111342973 | ||||||
chr13:111343032
|
C | T | 1 | a0001c0001t0002g0178 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.415+101C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343032 | ||||||
chr13:111343097
|
A | C | 1 | a0001c0002t0001g0242 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.415+166A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343097 | ||||||
chr13:111343103
|
G | T | 1 | a0001c0001t0002g0178 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.415+172G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343103 | ||||||
chr13:111343171
|
T | G | 1 | a0001c0003t0001g0027 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.415+240T>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343171 | ||||||
chr13:111343184
|
C | T | 1 | a0001c0001t0003g0033 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.415+253C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343184 | ||||||
chr13:111343333
|
A | C | 6 | a0001c0003t0001g0026a0001c0003t0001g0027a0001c0003t0001g0105others(3): Show | 8 | HG00735.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+402A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343333 | ||||||
chr13:111343334
|
CGTGGTGG | C | 6 | a0001c0003t0001g0026a0001c0003t0001g0027a0001c0003t0001g0105others(3): Show | 8 | HG00735.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+404_415+410del others(7): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343334 | ||||||
chr13:111343335
|
G | A | 3 | a0001c0002t0001g0095a0001c0002t0003g0052a0001c0002t0003g0156 | 4 | HG02615.hp1 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.415+404G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343335 | ||||||
chr13:111343342
|
T | A | 6 | a0001c0003t0001g0026a0001c0003t0001g0027a0001c0003t0001g0105others(3): Show | 8 | HG00735.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+411T>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343342 | ||||||
chr13:111343345
|
TG | T | 6 | a0001c0003t0001g0026a0001c0003t0001g0027a0001c0003t0001g0105others(3): Show | 8 | HG00735.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+416delG | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr13 | 111343345 | |||||
chr13:111343347
|
G | C | 6 | a0001c0003t0001g0026a0001c0003t0001g0027a0001c0003t0001g0105others(3): Show | 8 | HG00735.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+416G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343347 | ||||||
chr13:111343348
|
T | C | 6 | a0001c0003t0001g0026a0001c0003t0001g0027a0001c0003t0001g0105others(3): Show | 8 | HG00735.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+417T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343348 | ||||||
chr13:111343352
|
GCA | G | 6 | a0001c0003t0001g0026a0001c0003t0001g0027a0001c0003t0001g0105others(3): Show | 8 | HG00735.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+422_415+423del others(2): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343352 | ||||||
chr13:111343401
|
G | A | 52 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0064others(49): Show | 69 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.415+470G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343401 | ||||||
chr13:111343499
|
A | T | 1 | a0001c0001t0002g0190 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.415+568A>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343499 | ||||||
chr13:111343577
|
G | A | 2 | a0001c0002t0001g0262a0001c0002t0001g0264 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.416-506G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343577 | ||||||
chr13:111343582
|
C | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0110 | 2 | HG00733.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.416-501C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343582 | ||||||
chr13:111343593
|
C | T | 1 | a0001c0001t0007g0104 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.416-490C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343593 | ||||||
chr13:111343685
|
G | A | 1 | a0001c0001t0002g0215 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.416-398G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343685 | ||||||
chr13:111343687
|
C | T | 8 | a0001c0001t0001g0295a0001c0001t0008g0029a0001c0001t0008g0077others(5): Show | 13 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.416-396C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343687 | ||||||
chr13:111343809
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.416-274G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343809 | ||||||
chr13:111344028
|
C | T | 1 | a0001c0002t0001g0266 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.416-55C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111344028 | ||||||
chr13:111344070
|
T | G | 1 | a0001c0002t0001g0267 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.416-13T>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111344070 |