geneid | 166012 |
---|---|
ensemblid | ENSG00000180767.11 |
hgncid | 21755 |
symbol | CHST13 |
name | carbohydrate sulfotransferase 13 |
refseq_nuc | NM_152889.3 |
refseq_prot | NP_690849.1 |
ensembl_nuc | ENST00000319340.7 |
ensembl_prot | ENSP00000317404.2 |
mane_status | MANE Select |
chr | chr3 |
start | 126524155 |
end | 126543291 |
strand | + |
ver | v1.2 |
region | chr3:126524155-126543291 |
region5000 | chr3:126519155-126548291 |
regionname0 | CHST13_chr3_126524155_126543291 |
regionname5000 | CHST13_chr3_126519155_126548291 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 341 | 185 | 36 | 43 | 76 | 8 | 21 | 62 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0002 | 0/1 | 341 | 73 | 3 | 17 | 45 | 5 | 2 | 37 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0003 | 0/0 | 341 | 56 | 38 | 11 | 0 | 1 | 6 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0004 | 0/0 | 341 | 30 | 5 | 3 | 16 | 2 | 4 | 13 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0005 | 0/0 | 341 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0006 | 0/0 | 341 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0007 | 0/0 | 341 | 4 | 0 | 3 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0008 | 0/0 | 341 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0009 | 0/0 | 341 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1026 | 185 | 36 | 43 | 76 | 8 | 21 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
c0002 | 0/1 | 1026 | 73 | 3 | 17 | 45 | 5 | 2 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
c0003 | 0/0 | 1026 | 30 | 5 | 3 | 16 | 2 | 4 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
c0004 | 0/0 | 1026 | 27 | 20 | 7 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
c0005 | 0/0 | 1026 | 21 | 12 | 3 | 0 | 0 | 6 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
c0006 | 0/0 | 1026 | 8 | 7 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
c0007 | 0/0 | 1026 | 7 | 5 | 1 | 0 | 1 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
c0008 | 0/0 | 1026 | 6 | 6 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
c0009 | 0/0 | 1026 | 4 | 0 | 3 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
c0010 | 0/0 | 1026 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
c0011 | 0/0 | 1026 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
c0012 | 0/0 | 1026 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 892 | 326 | 90 | 70 | 120 | 14 | 30 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
t0002 | 0/0 | 892 | 34 | 5 | 6 | 17 | 2 | 4 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
t0003 | 0/0 | 892 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
t0004 | 0/0 | 892 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
t0005 | 0/0 | 892 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
t0006 | 0/0 | 892 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 61 | 3 | 11 | 38 | 2 | 7 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0002 | 0/1 | 30 | 0 | 3 | 24 | 1 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0003 | 0/0 | 21 | 1 | 1 | 14 | 2 | 3 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0004 | 0/0 | 18 | 11 | 0 | 3 | 0 | 4 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0005 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0006 | 0/0 | 8 | 0 | 6 | 0 | 2 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0007 | 0/0 | 8 | 0 | 8 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0008 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0009 | 0/0 | 7 | 0 | 2 | 0 | 1 | 4 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0010 | 0/0 | 6 | 1 | 4 | 0 | 1 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0011 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0014 | 0/0 | 5 | 2 | 2 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0016 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0018 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0019 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0020 | 0/0 | 4 | 0 | 1 | 0 | 3 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0021 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0024 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0027 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0046 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1026 | 185 | 36 | 43 | 76 | 8 | 21 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0002c0002 | 0/1 | 1026 | 73 | 3 | 17 | 45 | 5 | 2 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0003c0004 | 0/0 | 1026 | 27 | 20 | 7 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0003c0005 | 0/0 | 1026 | 21 | 12 | 3 | 0 | 0 | 6 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0003c0007 | 0/0 | 1026 | 7 | 5 | 1 | 0 | 1 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0003c0010 | 0/0 | 1026 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0004c0003 | 0/0 | 1026 | 30 | 5 | 3 | 16 | 2 | 4 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0005c0006 | 0/0 | 1026 | 8 | 7 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0006c0008 | 0/0 | 1026 | 6 | 6 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0007c0009 | 0/0 | 1026 | 4 | 0 | 3 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0008c0012 | 0/0 | 1026 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0009c0011 | 0/0 | 1026 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1917 | 183 | 36 | 42 | 75 | 8 | 21 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0001c0001t0003 | 0/0 | 1917 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0001c0001t0005 | 0/0 | 1917 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0002c0002t0001 | 0/1 | 1917 | 73 | 3 | 17 | 45 | 5 | 2 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0003c0004t0001 | 0/0 | 1917 | 27 | 20 | 7 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0003c0005t0001 | 0/0 | 1917 | 21 | 12 | 3 | 0 | 0 | 6 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0003c0007t0001 | 0/0 | 1917 | 6 | 5 | 0 | 0 | 1 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0003c0007t0006 | 0/0 | 1917 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0003c0010t0001 | 0/0 | 1917 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0004c0003t0002 | 0/0 | 1917 | 30 | 5 | 3 | 16 | 2 | 4 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0005c0006t0001 | 0/0 | 1917 | 8 | 7 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0006c0008t0001 | 0/0 | 1917 | 6 | 6 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0007c0009t0002 | 0/0 | 1917 | 4 | 0 | 3 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0008c0012t0001 | 0/0 | 1917 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
a0009c0011t0004 | 0/0 | 1917 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | copy fasta | chr3 | 126519155 | 126548291 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 61 | 3 | 11 | 38 | 2 | 7 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0004 | 0/0 | 18 | 11 | 0 | 3 | 0 | 4 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0006 | 0/0 | 8 | 0 | 6 | 0 | 2 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0009 | 0/0 | 7 | 0 | 2 | 0 | 1 | 4 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0010 | 0/0 | 6 | 1 | 4 | 0 | 1 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0018 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0024 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0027 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0046 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0002c0002t0001g0002 | 0/1 | 30 | 0 | 3 | 24 | 1 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0002c0002t0001g0007 | 0/0 | 8 | 0 | 8 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0002c0002t0001g0008 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0002c0002t0001g0014 | 0/0 | 5 | 2 | 2 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0002c0002t0001g0020 | 0/0 | 4 | 0 | 1 | 0 | 3 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0002c0002t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0002c0002t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0002c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0002c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0004t0001g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0004t0001g0016 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0004t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0004t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0004t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0004t0001g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0004t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0004t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0004t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0004t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0004t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0004t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0004t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0004t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0005t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0005t0001g0019 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0005t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0005t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0005t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0005t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0005t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0005t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0005t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0005t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0005t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0005t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0005t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0007t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0007t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0007t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0007t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0007t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0007t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0007t0006g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0003c0010t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0004c0003t0002g0003 | 0/0 | 19 | 1 | 0 | 13 | 2 | 3 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0004c0003t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0004c0003t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0004c0003t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0004c0003t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0004c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0004c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0004c0003t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0004c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0004c0003t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0005c0006t0001g0005 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0006c0008t0001g0011 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0007c0009t0002g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0007c0009t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0007c0009t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0008c0012t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
a0009c0011t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0102 | EUR | GBR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | FIN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG00323 | hp1 | a0003 | c0007 | t0001 | g0098 | EUR | FIN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG00323 | hp2 | a0004 | c0003 | t0002 | g0003 | EUR | FIN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG00639 | hp2 | a0005 | c0006 | t0001 | g0005 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG00733 | hp2 | a0003 | c0004 | t0001 | g0034 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG00735 | hp1 | a0003 | c0005 | t0001 | g0032 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0040 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01099 | hp1 | a0003 | c0007 | t0006 | g0114 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0040 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01109 | hp1 | a0003 | c0004 | t0001 | g0016 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01109 | hp2 | a0003 | c0004 | t0001 | g0119 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01167 | hp2 | a0004 | c0003 | t0002 | g0037 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01169 | hp2 | a0004 | c0003 | t0002 | g0037 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01175 | hp1 | a0003 | c0004 | t0001 | g0034 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01243 | hp2 | a0003 | c0004 | t0001 | g0016 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01255 | hp2 | a0003 | c0004 | t0001 | g0039 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01261 | hp1 | a0004 | c0003 | t0002 | g0132 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01346 | hp2 | a0003 | c0004 | t0001 | g0086 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01358 | hp1 | a0003 | c0005 | t0001 | g0032 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01358 | hp2 | a0003 | c0005 | t0001 | g0019 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01516 | hp1 | a0004 | c0003 | t0002 | g0003 | EUR | IBS | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0020 | EUR | IBS | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0020 | EUR | IBS | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01884 | hp2 | a0004 | c0003 | t0002 | g0003 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0014 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01891 | hp2 | a0003 | c0004 | t0001 | g0100 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01928 | hp1 | a0007 | c0009 | t0002 | g0003 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0065 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0133 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01975 | hp1 | a0007 | c0009 | t0002 | g0104 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01981 | hp1 | a0007 | c0009 | t0002 | g0103 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02055 | hp1 | a0004 | c0003 | t0002 | g0091 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02055 | hp2 | a0003 | c0007 | t0001 | g0092 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02056 | hp1 | a0004 | c0003 | t0002 | g0099 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02083 | hp1 | a0004 | c0003 | t0002 | g0003 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02132 | hp1 | a0007 | c0009 | t0002 | g0003 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02135 | hp1 | a0004 | c0003 | t0002 | g0107 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02145 | hp1 | a0003 | c0004 | t0001 | g0022 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02258 | hp1 | a0003 | c0005 | t0001 | g0113 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02280 | hp2 | a0003 | c0004 | t0001 | g0124 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02572 | hp1 | a0003 | c0007 | t0001 | g0116 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02602 | hp1 | a0003 | c0005 | t0001 | g0019 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02622 | hp1 | a0003 | c0004 | t0001 | g0087 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02647 | hp1 | a0003 | c0005 | t0001 | g0110 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02647 | hp2 | a0003 | c0004 | t0001 | g0012 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02683 | hp1 | a0003 | c0005 | t0001 | g0019 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02698 | hp1 | a0008 | c0012 | t0001 | g0076 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02698 | hp2 | a0003 | c0005 | t0001 | g0019 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02723 | hp1 | a0003 | c0004 | t0001 | g0025 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02723 | hp2 | a0003 | c0004 | t0001 | g0039 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02818 | hp1 | a0003 | c0004 | t0001 | g0123 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02818 | hp2 | a0006 | c0008 | t0001 | g0011 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02886 | hp1 | a0003 | c0004 | t0001 | g0120 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02886 | hp2 | a0005 | c0006 | t0001 | g0005 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02895 | hp1 | a0006 | c0008 | t0001 | g0011 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02895 | hp2 | a0003 | c0005 | t0001 | g0017 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02896 | hp1 | a0003 | c0004 | t0001 | g0022 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02896 | hp2 | a0003 | c0005 | t0001 | g0080 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02897 | hp1 | a0003 | c0005 | t0001 | g0017 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02897 | hp2 | a0003 | c0005 | t0001 | g0077 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02922 | hp2 | a0003 | c0004 | t0001 | g0022 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02965 | hp1 | a0003 | c0004 | t0001 | g0012 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02965 | hp2 | a0003 | c0010 | t0001 | g0089 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02970 | hp2 | a0006 | c0008 | t0001 | g0011 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02976 | hp1 | a0005 | c0006 | t0001 | g0005 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03098 | hp1 | a0005 | c0006 | t0001 | g0005 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03098 | hp2 | a0003 | c0004 | t0001 | g0025 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03139 | hp1 | a0003 | c0004 | t0001 | g0012 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03195 | hp1 | a0005 | c0006 | t0001 | g0005 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03195 | hp2 | a0003 | c0004 | t0001 | g0012 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03209 | hp1 | a0004 | c0003 | t0002 | g0036 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03209 | hp2 | a0003 | c0005 | t0001 | g0038 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03225 | hp1 | a0003 | c0005 | t0001 | g0017 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03225 | hp2 | a0003 | c0007 | t0001 | g0043 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03490 | hp1 | a0003 | c0005 | t0001 | g0082 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03516 | hp1 | a0003 | c0004 | t0001 | g0121 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03516 | hp2 | a0004 | c0003 | t0002 | g0106 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03540 | hp1 | a0003 | c0007 | t0001 | g0115 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0130 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03579 | hp1 | a0003 | c0004 | t0001 | g0016 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03579 | hp2 | a0006 | c0008 | t0001 | g0011 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03654 | hp1 | a0004 | c0003 | t0002 | g0003 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03654 | hp2 | a0003 | c0005 | t0001 | g0081 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0014 | SAS | STU | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03688 | hp2 | a0004 | c0003 | t0002 | g0003 | SAS | STU | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03942 | hp2 | a0003 | c0005 | t0001 | g0111 | SAS | BEB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG04228 | hp2 | a0004 | c0003 | t0002 | g0003 | SAS | STU | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18522 | hp1 | a0003 | c0005 | t0001 | g0038 | AFR | YRI | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18522 | hp2 | a0005 | c0006 | t0001 | g0005 | AFR | YRI | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18906 | hp1 | a0006 | c0008 | t0001 | g0011 | AFR | YRI | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18906 | hp2 | a0005 | c0006 | t0001 | g0005 | AFR | YRI | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18947 | hp2 | a0004 | c0003 | t0002 | g0003 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18949 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18957 | hp2 | a0004 | c0003 | t0002 | g0003 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18968 | hp1 | a0004 | c0003 | t0002 | g0003 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18969 | hp2 | a0004 | c0003 | t0002 | g0003 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18974 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18983 | hp1 | a0001 | c0001 | t0005 | g0079 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18992 | hp1 | a0004 | c0003 | t0002 | g0003 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18997 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA18999 | hp2 | a0004 | c0003 | t0002 | g0003 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19005 | hp2 | a0004 | c0003 | t0002 | g0003 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19007 | hp1 | a0004 | c0003 | t0002 | g0003 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | LWK | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | LWK | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19043 | hp1 | a0004 | c0003 | t0002 | g0036 | AFR | LWK | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19043 | hp2 | a0003 | c0005 | t0001 | g0117 | AFR | LWK | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19059 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19063 | hp2 | a0004 | c0003 | t0002 | g0105 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19074 | hp2 | a0004 | c0003 | t0002 | g0003 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19079 | hp2 | a0004 | c0003 | t0002 | g0003 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19083 | hp1 | a0004 | c0003 | t0002 | g0003 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19089 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA19091 | hp2 | a0004 | c0003 | t0002 | g0003 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ASW | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA20129 | hp2 | a0005 | c0006 | t0001 | g0005 | AFR | ASW | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | TSI | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | TSI | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0020 | EUR | TSI | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | GIH | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA20905 | hp2 | a0004 | c0003 | t0002 | g0093 | SAS | GIH | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02109 | hp1 | a0003 | c0007 | t0001 | g0108 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02486 | hp2 | a0003 | c0005 | t0001 | g0112 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02559 | hp1 | a0003 | c0005 | t0001 | g0017 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG02559 | hp2 | a0003 | c0004 | t0001 | g0016 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG06807 | hp1 | a0003 | c0004 | t0001 | g0012 | AFR | USA | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
HG06807 | hp2 | a0003 | c0004 | t0001 | g0025 | AFR | USA | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA20300 | hp2 | a0006 | c0008 | t0001 | g0011 | AFR | USA | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA21309 | hp1 | a0009 | c0011 | t0004 | g0084 | AFR | LWK | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0002 | REF | REF | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0046 | REF | REF | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:126536303
|
C | T | 1 | a0008 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.130C>T | p.Leu44Phe | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/3 | 308/1917 | 130/1026 | 44/341 | chr3 | 126536303 | ||
chr3:126536323
|
C | G | 1 | a0009 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.150C>G | p.Ser50Arg | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/3 | 328/1917 | 150/1026 | 50/341 | chr3 | 126536323 | ||
chr3:126541787
|
A | G | 2 | a0004a0007 | 34 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(31): Show |
missense_variant | MODERATE | c.235A>G | p.Ser79Gly | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 413/1917 | 235/1026 | 79/341 | chr3 | 126541787 | ||
chr3:126541929
|
C | T | 1 | a0005 | 8 | HG00639.hp2 HG02886.hp2 HG02976.hp1 others(5): Show |
missense_variant | MODERATE | c.377C>T | p.Ala126Val | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 555/1917 | 377/1026 | 126/341 | chr3 | 126541929 | ||
chr3:126541988
|
C | T | 1 | a0006 | 6 | HG02818.hp2 HG02895.hp1 HG02970.hp2 others(3): Show |
missense_variant | MODERATE | c.436C>T | p.Pro146Ser | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 614/1917 | 436/1026 | 146/341 | chr3 | 126541988 | ||
chr3:126542048
|
G | A | 1 | a0007 | 4 | HG01928.hp1 HG01975.hp1 HG01981.hp1 others(1): Show |
missense_variant | MODERATE | c.496G>A | p.Ala166Thr | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 674/1917 | 496/1026 | 166/341 | chr3 | 126542048 | ||
chr3:126542364
|
C | T | 2 | a0002a0008 | 74 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(71): Show |
missense_variant | MODERATE | c.812C>T | p.Ala271Val | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 990/1917 | 812/1026 | 271/341 | chr3 | 126542364 | ||
chr3:126542502
|
G | A | 4 | a0002a0003a0008others(1): Show | 131 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(128): Show |
missense_variant | MODERATE | c.950G>A | p.Arg317Gln | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 1128/1917 | 950/1026 | 317/341 | chr3 | 126542502 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:126541765
|
G | T | 3 | a0002c0002a0003c0004a0008c0012 | 101 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(98): Show |
synonymous_variant | LOW | c.213G>T | p.Arg71Arg | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 391/1917 | 213/1026 | 71/341 | chr3 | 126541765 | ||
chr3:126542014
|
C | T | 1 | a0006c0008 | 6 | HG02818.hp2 HG02895.hp1 HG02970.hp2 others(3): Show |
synonymous_variant | LOW | c.462C>T | p.Asp154Asp | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 640/1917 | 462/1026 | 154/341 | chr3 | 126542014 | ||
chr3:126542152
|
C | T | 1 | a0003c0005 | 21 | HG00735.hp1 HG01358.hp1 HG01358.hp2 others(18): Show |
synonymous_variant | LOW | c.600C>T | p.Tyr200Tyr | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 778/1917 | 600/1026 | 200/341 | chr3 | 126542152 | ||
chr3:126542359
|
G | A | 6 | a0002c0002a0003c0004a0003c0005others(3): Show | 130 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(127): Show |
synonymous_variant | LOW | c.807G>A | p.Thr269Thr | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 985/1917 | 807/1026 | 269/341 | chr3 | 126542359 | ||
chr3:126542383
|
G | A | 1 | a0003c0010 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.831G>A | p.Val277Val | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 1009/1917 | 831/1026 | 277/341 | chr3 | 126542383 | ||
chr3:126542470
|
C | T | 1 | a0006c0008 | 6 | HG02818.hp2 HG02895.hp1 HG02970.hp2 others(3): Show |
synonymous_variant | LOW | c.918C>T | p.Arg306Arg | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 1096/1917 | 918/1026 | 306/341 | chr3 | 126542470 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:126542702
|
C | T | 1 | a0003c0007t0006 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*124C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 124 | chr3 | 126542702 | |||||
chr3:126542747
|
C | A | 1 | a0001c0001t0003 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*169C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 169 | chr3 | 126542747 | |||||
chr3:126542810
|
C | T | 1 | a0001c0001t0005 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*232C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 232 | chr3 | 126542810 | |||||
chr3:126543249
|
G | C | 2 | a0004c0003t0002a0007c0009t0002 | 34 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*671G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 671 | chr3 | 126543249 | |||||
chr3:126543250
|
G | A | 1 | a0009c0011t0004 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*672G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 672 | chr3 | 126543250 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:126524576
|
A | C | 91 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(88): Show | 224 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.97+147A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126524576 | ||||||
chr3:126524774
|
A | T | 1 | a0001c0001t0001g0027 | 3 | HG02300.hp1 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.97+345A>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126524774 | ||||||
chr3:126524836
|
C | A | 1 | a0003c0005t0001g0077 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.97+407C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126524836 | ||||||
chr3:126524837
|
A | C | 1 | a0003c0005t0001g0077 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.97+408A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126524837 | ||||||
chr3:126524846
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.97+417G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126524846 | ||||||
chr3:126524982
|
G | A | 1 | a0002c0002t0001g0078 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.97+553G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126524982 | ||||||
chr3:126525012
|
G | A | 1 | a0001c0001t0005g0079 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.97+583G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126525012 | ||||||
chr3:126525208
|
T | C | 2 | a0003c0005t0001g0077a0003c0005t0001g0080 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.97+779T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126525208 | ||||||
chr3:126525491
|
G | T | 21 | a0001c0001t0001g0128a0001c0001t0001g0134a0002c0002t0001g0002others(18): Show | 75 | HG00408.hp2 HG00558.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.97+1062G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126525491 | ||||||
chr3:126525633
|
G | A | 1 | a0002c0002t0001g0125 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.97+1204G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126525633 | ||||||
chr3:126525748
|
G | A | 24 | a0001c0001t0001g0128a0001c0001t0001g0134a0002c0002t0001g0002others(21): Show | 79 | HG00408.hp2 HG00558.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.97+1319G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126525748 | ||||||
chr3:126525969
|
C | T | 1 | a0003c0005t0001g0077 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.97+1540C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126525969 | ||||||
chr3:126526007
|
T | C | 93 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(90): Show | 233 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.97+1578T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126526007 | ||||||
chr3:126526086
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.97+1657G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126526086 | ||||||
chr3:126526233
|
T | G | 2 | a0001c0001t0001g0033a0009c0011t0004g0084 | 3 | HG01081.hp1 HG01496.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.97+1804T>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126526233 | ||||||
chr3:126526311
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.97+1882G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126526311 | ||||||
chr3:126526349
|
G | A | 1 | a0001c0001t0001g0027 | 3 | HG02300.hp1 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.97+1920G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126526349 | ||||||
chr3:126526404
|
C | A | 5 | a0003c0004t0001g0012a0003c0004t0001g0022a0003c0004t0001g0034others(2): Show | 12 | HG00733.hp2 HG01175.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.97+1975C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126526404 | ||||||
chr3:126526664
|
C | A | 1 | a0001c0001t0001g0088 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.97+2235C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126526664 | ||||||
chr3:126526902
|
C | T | 15 | a0001c0001t0001g0033a0001c0001t0001g0122a0003c0004t0001g0012others(12): Show | 26 | HG00733.hp2 HG01081.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.97+2473C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126526902 | ||||||
chr3:126527068
|
C | G | 1 | a0003c0005t0001g0077 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.97+2639C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527068 | ||||||
chr3:126527071
|
G | C | 1 | a0003c0005t0001g0077 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.97+2642G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527071 | ||||||
chr3:126527072
|
A | T | 1 | a0002c0002t0001g0136 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.97+2643A>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527072 | ||||||
chr3:126527113
|
C | T | 74 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(71): Show | 193 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.97+2684C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527113 | ||||||
chr3:126527257
|
C | T | 2 | a0001c0001t0001g0033a0009c0011t0004g0084 | 3 | HG01081.hp1 HG01496.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.97+2828C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527257 | ||||||
chr3:126527407
|
T | A | 1 | a0004c0003t0002g0091 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.97+2978T>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527407 | ||||||
chr3:126527470
|
C | T | 1 | a0002c0002t0001g0135 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.97+3041C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527470 | ||||||
chr3:126527527
|
G | A | 21 | a0001c0001t0001g0128a0002c0002t0001g0002a0002c0002t0001g0007others(18): Show | 75 | HG00408.hp2 HG00558.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.97+3098G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527527 | ||||||
chr3:126527531
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | NA19009.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.97+3102G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527531 | ||||||
chr3:126527561
|
C | T | 17 | a0001c0001t0001g0033a0001c0001t0001g0122a0003c0004t0001g0012others(14): Show | 35 | HG00639.hp2 HG00733.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.97+3132C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527561 | ||||||
chr3:126527640
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.97+3211C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527640 | ||||||
chr3:126527646
|
G | A | 2 | a0003c0007t0001g0043a0005c0006t0001g0005 | 9 | HG00639.hp2 HG02886.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.97+3217G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527646 | ||||||
chr3:126527650
|
C | A | 1 | a0003c0007t0001g0092 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.97+3221C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527650 | ||||||
chr3:126527680
|
G | A | 1 | a0004c0003t0002g0093 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.97+3251G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527680 | ||||||
chr3:126527684
|
G | C | 76 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(73): Show | 198 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.97+3255G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527684 | ||||||
chr3:126527735
|
AAATTGGT others(15): Show |
A | 1 | a0001c0001t0001g0075 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.97+3307_97+3328del others(22): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527735 | ||||||
chr3:126527752
|
C | G | 2 | a0001c0001t0001g0090a0003c0010t0001g0089 | 2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.97+3323C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527752 | ||||||
chr3:126527792
|
G | A | 72 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(69): Show | 194 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.97+3363G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527792 | ||||||
chr3:126528324
|
C | G | 15 | a0003c0005t0001g0019a0003c0005t0001g0032a0003c0005t0001g0038others(12): Show | 20 | HG00735.hp1 HG01099.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.97+3895C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126528324 | ||||||
chr3:126528352
|
A | G | 1 | a0001c0001t0001g0018 | 4 | HG00735.hp2 HG01074.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+3923A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126528352 | ||||||
chr3:126528355
|
T | A | 80 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(77): Show | 206 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.97+3926T>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126528355 | ||||||
chr3:126528472
|
G | C | 4 | a0001c0001t0001g0033a0003c0007t0001g0043a0005c0006t0001g0005others(1): Show | 12 | HG00639.hp2 HG01081.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.97+4043G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126528472 | ||||||
chr3:126528615
|
G | A | 50 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(47): Show | 146 | HG00408.hp2 HG00558.hp1 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.97+4186G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126528615 | ||||||
chr3:126528621
|
G | A | 1 | a0003c0007t0001g0098 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.97+4192G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126528621 | ||||||
chr3:126528626
|
T | G | 2 | a0002c0002t0001g0007a0002c0002t0001g0133 | 9 | HG01346.hp1 HG01361.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.97+4197T>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126528626 | ||||||
chr3:126528675
|
G | A | 1 | a0004c0003t0002g0099 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.97+4246G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126528675 | ||||||
chr3:126528767
|
C | T | 1 | a0001c0001t0001g0074 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.97+4338C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126528767 | ||||||
chr3:126528772
|
A | C | 1 | a0004c0003t0002g0132 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.97+4343A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126528772 | ||||||
chr3:126528952
|
C | T | 46 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(43): Show | 136 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.97+4523C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126528952 | ||||||
chr3:126528954
|
C | G | 1 | a0002c0002t0001g0131 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.97+4525C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126528954 | ||||||
chr3:126528979
|
G | A | 1 | a0003c0004t0001g0016 | 4 | HG01109.hp1 HG01243.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+4550G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126528979 | ||||||
chr3:126529005
|
C | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(56): Show | 157 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.97+4576C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126529005 | ||||||
chr3:126529130
|
ACCCTGCA others(11): Show |
A | 21 | a0002c0002t0001g0102a0003c0007t0001g0043a0003c0007t0001g0092others(18): Show | 49 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.97+4708_97+4725del others(18): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126529130 | |||||
chr3:126529142
|
GCGCGAGC others(11): Show |
G | 3 | a0001c0001t0001g0083a0001c0001t0001g0101a0006c0008t0001g0011 | 8 | HG02630.hp1 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+4714_97+4731del others(18): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126529142 | ||||||
chr3:126529165
|
G | A | 13 | a0002c0002t0001g0102a0004c0003t0002g0003a0004c0003t0002g0036others(10): Show | 34 | HG00099.hp2 HG00323.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.97+4736G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126529165 | ||||||
chr3:126529384
|
G | A | 2 | a0003c0004t0001g0025a0003c0004t0001g0119 | 4 | HG01109.hp2 HG02723.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+4955G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126529384 | ||||||
chr3:126529464
|
G | A | 2 | a0001c0001t0001g0083a0001c0001t0001g0101 | 2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.97+5035G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126529464 | ||||||
chr3:126529673
|
C | T | 13 | a0003c0005t0001g0017a0003c0005t0001g0019a0003c0005t0001g0032others(10): Show | 21 | HG00735.hp1 HG01358.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.97+5244C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126529673 | ||||||
chr3:126529760
|
C | T | 1 | a0003c0010t0001g0089 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.97+5331C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126529760 | ||||||
chr3:126529782
|
C | G | 23 | a0002c0002t0001g0102a0003c0007t0001g0043a0003c0007t0001g0092others(20): Show | 51 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.97+5353C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126529782 | ||||||
chr3:126529930
|
C | T | 4 | a0003c0007t0001g0043a0003c0007t0001g0092a0003c0007t0001g0098others(1): Show | 4 | HG00323.hp1 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+5501C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126529930 | ||||||
chr3:126530061
|
C | T | 1 | a0009c0011t0004g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.97+5632C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530061 | ||||||
chr3:126530079
|
A | C | 13 | a0002c0002t0001g0102a0004c0003t0002g0003a0004c0003t0002g0036others(10): Show | 34 | HG00099.hp2 HG00323.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.97+5650A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530079 | ||||||
chr3:126530107
|
C | A | 1 | a0003c0005t0001g0081 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.97+5678C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530107 | ||||||
chr3:126530172
|
G | T | 35 | a0001c0001t0001g0122a0001c0001t0001g0128a0002c0002t0001g0002others(32): Show | 102 | HG00408.hp2 HG00558.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.97+5743G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530172 | ||||||
chr3:126530187
|
G | T | 1 | a0003c0004t0001g0012 | 5 | HG02647.hp2 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.97+5758G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530187 | ||||||
chr3:126530377
|
C | T | 5 | a0003c0007t0001g0043a0003c0007t0001g0092a0003c0007t0001g0098others(2): Show | 12 | HG00323.hp1 HG00639.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.98-5894C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530377 | ||||||
chr3:126530383
|
C | T | 1 | a0002c0002t0001g0130 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.98-5888C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530383 | ||||||
chr3:126530422
|
G | A | 52 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0122others(49): Show | 145 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.98-5849G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530422 | ||||||
chr3:126530438
|
C | T | 1 | a0002c0002t0001g0133 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.98-5833C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530438 | ||||||
chr3:126530439
|
G | A | 1 | a0002c0002t0001g0040 | 2 | HG01074.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.98-5832G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530439 | ||||||
chr3:126530464
|
C | T | 3 | a0003c0007t0001g0115a0003c0007t0001g0116a0003c0007t0006g0114 | 3 | HG01099.hp1 HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.98-5807C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530464 | ||||||
chr3:126530467
|
C | A | 2 | a0003c0007t0001g0043a0003c0007t0001g0092 | 2 | HG02055.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.98-5804C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530467 | ||||||
chr3:126530566
|
G | A | 1 | a0003c0004t0001g0016 | 4 | HG01109.hp1 HG01243.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-5705G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530566 | ||||||
chr3:126530594
|
G | T | 1 | a0001c0001t0001g0073 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.98-5677G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530594 | ||||||
chr3:126530601
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.98-5670C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530601 | ||||||
chr3:126530745
|
G | A | 1 | a0002c0002t0001g0020 | 4 | HG01175.hp2 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-5526G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530745 | ||||||
chr3:126530837
|
T | G | 4 | a0003c0007t0001g0043a0003c0007t0001g0092a0003c0007t0001g0098others(1): Show | 4 | HG00323.hp1 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-5434T>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530837 | ||||||
chr3:126530838
|
G | A | 1 | a0008c0012t0001g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.98-5433G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530838 | ||||||
chr3:126530925
|
G | A | 1 | a0001c0001t0001g0048 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.98-5346G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530925 | ||||||
chr3:126530944
|
G | A | 4 | a0003c0004t0001g0025a0003c0004t0001g0039a0003c0004t0001g0119others(1): Show | 7 | HG01109.hp2 HG01255.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-5327G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530944 | ||||||
chr3:126530981
|
T | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(132): Show | 362 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.98-5290T>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530981 | ||||||
chr3:126531034
|
A | C | 39 | a0001c0001t0001g0122a0001c0001t0001g0128a0002c0002t0001g0002others(36): Show | 106 | HG00408.hp2 HG00558.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.98-5237A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531034 | ||||||
chr3:126531035
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.98-5236A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531035 | ||||||
chr3:126531037
|
G | T | 5 | a0003c0007t0001g0043a0003c0007t0001g0092a0003c0007t0001g0098others(2): Show | 12 | HG00323.hp1 HG00639.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.98-5234G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531037 | ||||||
chr3:126531193
|
C | T | 18 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(15): Show | 52 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.98-5078C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531193 | ||||||
chr3:126531244
|
C | A | 19 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(16): Show | 53 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.98-5027C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531244 | ||||||
chr3:126531261
|
A | G | 1 | a0001c0001t0001g0071 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.98-5010A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531261 | ||||||
chr3:126531292
|
G | A | 19 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(16): Show | 53 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.98-4979G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531292 | ||||||
chr3:126531596
|
T | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(1): Show | 11 | HG00642.hp1 HG01069.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-4675T>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531596 | ||||||
chr3:126531604
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.98-4667C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531604 | ||||||
chr3:126531625
|
C | T | 1 | a0009c0011t0004g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.98-4646C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531625 | ||||||
chr3:126531744
|
G | T | 1 | a0009c0011t0004g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.98-4527G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531744 | ||||||
chr3:126531775
|
G | C | 1 | a0001c0001t0001g0051 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.98-4496G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531775 | ||||||
chr3:126531878
|
A | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(132): Show | 362 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.98-4393A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531878 | ||||||
chr3:126531926
|
A | G | 3 | a0003c0004t0001g0016a0003c0004t0001g0123a0003c0004t0001g0124 | 6 | HG01109.hp1 HG01243.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-4345A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531926 | ||||||
chr3:126531955
|
C | A | 7 | a0003c0004t0001g0012a0003c0004t0001g0022a0003c0004t0001g0034others(4): Show | 14 | HG00733.hp2 HG01175.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.98-4316C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531955 | ||||||
chr3:126532032
|
G | A | 4 | a0003c0004t0001g0025a0003c0004t0001g0039a0003c0004t0001g0119others(1): Show | 7 | HG01109.hp2 HG01255.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-4239G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126532032 | ||||||
chr3:126532055
|
T | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(132): Show | 362 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.98-4216T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126532055 | ||||||
chr3:126532151
|
G | A | 2 | a0001c0001t0001g0083a0001c0001t0001g0101 | 2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.98-4120G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126532151 | ||||||
chr3:126532292
|
T | A | 1 | a0001c0001t0001g0052 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.98-3979T>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126532292 | ||||||
chr3:126532370
|
G | A | 10 | a0003c0005t0001g0019a0003c0005t0001g0032a0003c0005t0001g0077others(7): Show | 14 | HG00735.hp1 HG01358.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.98-3901G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126532370 | ||||||
chr3:126532442
|
T | TGTATGTG | 13 | a0003c0005t0001g0017a0003c0005t0001g0019a0003c0005t0001g0032others(10): Show | 21 | HG00735.hp1 HG01358.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.98-3823_98-3817dup others(7): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126532442 | |||||
chr3:126532562
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.98-3709A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126532562 | ||||||
chr3:126532606
|
C | G | 3 | a0002c0002t0001g0007a0002c0002t0001g0014a0002c0002t0001g0133 | 14 | HG01256.hp2 HG01258.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.98-3665C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126532606 | ||||||
chr3:126532637
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.98-3634C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126532637 | ||||||
chr3:126532649
|
A | G | 1 | a0009c0011t0004g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.98-3622A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126532649 | ||||||
chr3:126532664
|
T | C | 1 | a0006c0008t0001g0011 | 6 | HG02818.hp2 HG02895.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-3607T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126532664 | ||||||
chr3:126532975
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.98-3296T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126532975 | ||||||
chr3:126533038
|
A | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(73): Show | 221 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.98-3233A>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126533038 | ||||||
chr3:126533160
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0095 | 4 | HG02280.hp1 HG02622.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-3111G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126533160 | ||||||
chr3:126533355
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.98-2916G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126533355 | ||||||
chr3:126533532
|
T | TTTGTGTA others(16): Show |
1 | a0008c0012t0001g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.98-2738_98-2716dup others(23): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126533532 | |||||
chr3:126533582
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.98-2689C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126533582 | ||||||
chr3:126533662
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.98-2609G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126533662 | ||||||
chr3:126533663
|
G | T | 21 | a0001c0001t0001g0128a0002c0002t0001g0002a0002c0002t0001g0007others(18): Show | 75 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.98-2608G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126533663 | ||||||
chr3:126533684
|
T | C | 17 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(14): Show | 51 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.98-2587T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126533684 | ||||||
chr3:126533804
|
T | G | 7 | a0003c0004t0001g0012a0003c0004t0001g0022a0003c0004t0001g0034others(4): Show | 14 | HG00733.hp2 HG01175.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.98-2467T>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126533804 | ||||||
chr3:126533867
|
T | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(128): Show | 358 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.98-2404T>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126533867 | ||||||
chr3:126533868
|
T | A | 4 | a0003c0007t0001g0043a0003c0007t0001g0092a0003c0007t0001g0098others(1): Show | 4 | HG00323.hp1 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-2403T>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126533868 | ||||||
chr3:126533909
|
T | A | 1 | a0001c0001t0001g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.98-2362T>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126533909 | ||||||
chr3:126534032
|
T | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0054 | 3 | HG00741.hp1 HG02135.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.98-2239T>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126534032 | ||||||
chr3:126534041
|
G | A | 13 | a0003c0005t0001g0017a0003c0005t0001g0019a0003c0005t0001g0032others(10): Show | 21 | HG00735.hp1 HG01358.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.98-2230G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126534041 | ||||||
chr3:126534262
|
C | T | 13 | a0003c0005t0001g0017a0003c0005t0001g0019a0003c0005t0001g0032others(10): Show | 21 | HG00735.hp1 HG01358.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.98-2009C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126534262 | ||||||
chr3:126534279
|
A | T | 2 | a0003c0004t0001g0012a0003c0004t0001g0100 | 6 | HG01891.hp2 HG02647.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.98-1992A>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126534279 | ||||||
chr3:126534330
|
T | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(131): Show | 354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.98-1941T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126534330 | ||||||
chr3:126534342
|
C | T | 1 | a0005c0006t0001g0005 | 8 | HG00639.hp2 HG02886.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.98-1929C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126534342 | ||||||
chr3:126534354
|
T | C | 7 | a0003c0007t0001g0043a0003c0007t0001g0092a0003c0007t0001g0098others(4): Show | 7 | HG00323.hp1 HG01099.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.98-1917T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126534354 | ||||||
chr3:126534390
|
GAGAC | G | 17 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(14): Show | 51 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.98-1862_98-1859del others(4): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126534390 | |||||
chr3:126534475
|
A | G | 1 | a0001c0001t0001g0013 | 5 | NA18942.hp1 NA18963.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.98-1796A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126534475 | ||||||
chr3:126534644
|
G | A | 1 | a0005c0006t0001g0005 | 8 | HG00639.hp2 HG02886.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.98-1627G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126534644 | ||||||
chr3:126534914
|
C | T | 1 | a0001c0001t0001g0067 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.98-1357C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126534914 | ||||||
chr3:126534961
|
G | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(14): Show | 51 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.98-1310G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126534961 | ||||||
chr3:126535061
|
C | CACACAGA others(23): Show |
34 | a0001c0001t0001g0122a0001c0001t0001g0128a0002c0002t0001g0002others(31): Show | 101 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.98-1209_98-1208ins others(30): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126535061 | |||||
chr3:126535063
|
G | C | 2 | a0002c0002t0001g0129a0002c0002t0001g0136 | 2 | NA18953.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.98-1208G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535063 | ||||||
chr3:126535083
|
C | CCAGCCGG others(23): Show |
97 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(94): Show | 249 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.98-1173_98-1172ins others(30): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126535083 | |||||
chr3:126535083
|
C | T | 34 | a0001c0001t0001g0122a0001c0001t0001g0128a0002c0002t0001g0002others(31): Show | 101 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.98-1188C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535083 | ||||||
chr3:126535088
|
C | CGGGAGAC others(23): Show |
2 | a0002c0002t0001g0129a0002c0002t0001g0136 | 2 | NA18953.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.98-1173_98-1172ins others(30): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126535088 | |||||
chr3:126535091
|
GAGACAGA others(293): Show |
G | 1 | a0001c0001t0001g0035 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.98-1172_98-873del | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126535091 | |||||
chr3:126535123
|
G | A | 1 | a0001c0001t0001g0018 | 4 | HG00735.hp2 HG01074.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-1148G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535123 | ||||||
chr3:126535158
|
G | GAGACAGA others(27): Show |
1 | a0001c0001t0001g0018 | 4 | HG00735.hp2 HG01074.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-1098_98-1065dup others(34): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126535158 | |||||
chr3:126535186
|
G | A | 1 | a0009c0011t0004g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.98-1085G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535186 | ||||||
chr3:126535207
|
G | A | 13 | a0003c0005t0001g0017a0003c0005t0001g0019a0003c0005t0001g0032others(10): Show | 21 | HG00735.hp1 HG01358.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.98-1064G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535207 | ||||||
chr3:126535219
|
C | T | 2 | a0002c0002t0001g0129a0002c0002t0001g0136 | 2 | NA18953.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.98-1052C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535219 | ||||||
chr3:126535319
|
G | GAGACAGA others(61): Show |
1 | a0003c0007t0001g0116 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.98-923_98-856dupGC others(66): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126535319 | |||||
chr3:126535351
|
G | A | 1 | a0009c0011t0004g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.98-920G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535351 | ||||||
chr3:126535416
|
A | G | 1 | a0001c0001t0001g0035 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.98-855A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535416 | ||||||
chr3:126535421
|
GAGAC | G | 16 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(13): Show | 49 | HG00735.hp2 HG01074.hp2 HG01496.hp1 others(46): Show |
intron_variant | MODIFIER | c.98-839_98-836delAC others(2): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126535421 | |||||
chr3:126535436
|
C | T | 1 | a0001c0001t0001g0035 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.98-835C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535436 | ||||||
chr3:126535440
|
C | G | 1 | a0001c0001t0001g0035 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.98-831C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535440 | ||||||
chr3:126535461
|
G | C | 1 | a0001c0001t0001g0035 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.98-810G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535461 | ||||||
chr3:126535470
|
T | C | 1 | a0001c0001t0001g0035 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.98-801T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535470 | ||||||
chr3:126535473
|
C | T | 2 | a0002c0002t0001g0008a0002c0002t0001g0135 | 9 | NA18949.hp1 NA18959.hp2 NA18968.hp2 others(6): Show |
intron_variant | MODIFIER | c.98-798C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535473 | ||||||
chr3:126535477
|
G | T | 1 | a0001c0001t0001g0035 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.98-794G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535477 | ||||||
chr3:126535487
|
G | A | 1 | a0001c0001t0001g0035 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.98-784G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535487 | ||||||
chr3:126535504
|
T | C | 18 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(15): Show | 52 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.98-767T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535504 | ||||||
chr3:126535508
|
G | C | 1 | a0001c0001t0001g0035 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.98-763G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535508 | ||||||
chr3:126535511
|
G | T | 16 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(13): Show | 49 | HG00735.hp2 HG01074.hp2 HG01496.hp1 others(46): Show |
intron_variant | MODIFIER | c.98-760G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535511 | ||||||
chr3:126535521
|
G | A | 16 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(13): Show | 49 | HG00735.hp2 HG01074.hp2 HG01496.hp1 others(46): Show |
intron_variant | MODIFIER | c.98-750G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535521 | ||||||
chr3:126535525
|
GAC | G | 16 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(13): Show | 49 | HG00735.hp2 HG01074.hp2 HG01496.hp1 others(46): Show |
intron_variant | MODIFIER | c.98-740_98-739delCA | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126535525 | |||||
chr3:126535529
|
C | G | 1 | a0001c0001t0001g0035 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.98-742C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535529 | ||||||
chr3:126535531
|
C | T | 1 | a0001c0001t0001g0035 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.98-740C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535531 | ||||||
chr3:126535542
|
C | G | 1 | a0001c0001t0001g0035 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.98-729C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535542 | ||||||
chr3:126535545
|
G | GTCCCCAG others(523): Show |
1 | a0003c0010t0001g0089 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.98-723_98-722insCC others(528): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126535545 | |||||
chr3:126535545
|
G | T | 1 | a0001c0001t0001g0035 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.98-726G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535545 | ||||||
chr3:126535551
|
A | AGCAGGGA others(27): Show |
1 | a0003c0004t0001g0120 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.98-718_98-717insAG others(32): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126535551 | |||||
chr3:126535551
|
A | AGCCGGGA others(27): Show |
115 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(112): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.98-700_98-699insCA others(32): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126535551 | |||||
chr3:126535551
|
A | AGCCGGGA others(27): Show |
16 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(13): Show | 49 | HG00735.hp2 HG01074.hp2 HG01496.hp1 others(46): Show |
intron_variant | MODIFIER | c.98-707_98-706insTA others(32): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126535551 | |||||
chr3:126535551
|
A | G | 2 | a0001c0001t0001g0035a0003c0010t0001g0089 | 3 | HG01070.hp2 HG01071.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.98-720A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535551 | ||||||
chr3:126535580
|
A | G | 1 | a0002c0002t0001g0126 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.98-691A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535580 | ||||||
chr3:126535589
|
A | G | 1 | a0002c0002t0001g0126 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.98-682A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535589 | ||||||
chr3:126535591
|
T | C | 1 | a0002c0002t0001g0126 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.98-680T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535591 | ||||||
chr3:126535602
|
C | A | 1 | a0002c0002t0001g0126 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.98-669C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535602 | ||||||
chr3:126535604
|
G | A | 1 | a0002c0002t0001g0126 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.98-667G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535604 | ||||||
chr3:126535619
|
T | C | 1 | a0002c0002t0001g0126 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.98-652T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535619 | ||||||
chr3:126535625
|
C | T | 1 | a0002c0002t0001g0126 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.98-646C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535625 | ||||||
chr3:126535627
|
A | G | 1 | a0002c0002t0001g0126 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.98-644A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535627 | ||||||
chr3:126535636
|
A | C | 1 | a0002c0002t0001g0126 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.98-635A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535636 | ||||||
chr3:126535638
|
A | G | 1 | a0002c0002t0001g0126 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.98-633A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535638 | ||||||
chr3:126535648
|
A | G | 1 | a0005c0006t0001g0005 | 8 | HG00639.hp2 HG02886.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.98-623A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535648 | ||||||
chr3:126535651
|
G | T | 1 | a0002c0002t0001g0126 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.98-620G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535651 | ||||||
chr3:126535653
|
C | T | 1 | a0002c0002t0001g0126 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.98-618C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535653 | ||||||
chr3:126535670
|
C | G | 1 | a0002c0002t0001g0126 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.98-601C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535670 | ||||||
chr3:126535720
|
G | T | 1 | a0009c0011t0004g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.98-551G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535720 | ||||||
chr3:126535724
|
C | T | 58 | a0001c0001t0001g0122a0001c0001t0001g0128a0002c0002t0001g0002others(55): Show | 133 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.98-547C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535724 | ||||||
chr3:126535849
|
G | A | 36 | a0001c0001t0001g0122a0001c0001t0001g0128a0002c0002t0001g0002others(33): Show | 103 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.98-422G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535849 | ||||||
chr3:126535852
|
T | C | 2 | a0003c0004t0001g0012a0003c0004t0001g0100 | 6 | HG01891.hp2 HG02647.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.98-419T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535852 | ||||||
chr3:126535897
|
G | C | 1 | a0001c0001t0001g0018 | 4 | HG00735.hp2 HG01074.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-374G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535897 | ||||||
chr3:126536029
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0085 | 2 | NA19067.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.98-242C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126536029 | ||||||
chr3:126536046
|
G | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(14): Show | 51 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.98-225G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126536046 | ||||||
chr3:126536252
|
T | G | 1 | a0001c0001t0001g0029 | 2 | NA18997.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.98-19T>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126536252 | ||||||
chr3:126536526
|
T | G | 7 | a0003c0004t0001g0012a0003c0004t0001g0022a0003c0004t0001g0034others(4): Show | 14 | HG00733.hp2 HG01175.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.180+173T>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126536526 | ||||||
chr3:126536601
|
G | C | 1 | a0007c0009t0002g0103 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.180+248G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126536601 | ||||||
chr3:126536710
|
G | C | 1 | a0001c0001t0001g0109 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.180+357G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126536710 | ||||||
chr3:126536786
|
G | A | 1 | a0001c0001t0001g0018 | 4 | HG00735.hp2 HG01074.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+433G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126536786 | ||||||
chr3:126536790
|
G | C | 1 | a0003c0004t0001g0119 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.180+437G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126536790 | ||||||
chr3:126536863
|
GCT | G | 58 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(55): Show | 169 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.180+523_180+524del others(2): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126536863 | |||||
chr3:126536882
|
C | CACACACA others(3): Show |
1 | a0003c0005t0001g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.180+538_180+539ins others(10): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126536882 | |||||
chr3:126536895
|
AAACACAC others(6): Show |
A | 1 | a0004c0003t0002g0105 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.180+544_180+556del others(13): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126536895 | |||||
chr3:126536896
|
A | AAC | 25 | a0001c0001t0001g0049a0001c0001t0001g0056a0001c0001t0001g0096others(22): Show | 81 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.180+570_180+571dup others(2): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126536896 | |||||
chr3:126536896
|
A | AACAC | 9 | a0002c0002t0001g0026a0002c0002t0001g0126a0003c0004t0001g0016others(6): Show | 16 | HG00733.hp2 HG01109.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.180+568_180+571dup others(4): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126536896 | |||||
chr3:126536896
|
A | AACACAC | 5 | a0001c0001t0001g0122a0003c0004t0001g0012a0003c0004t0001g0022others(2): Show | 11 | HG01346.hp2 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.180+566_180+571dup others(6): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126536896 | |||||
chr3:126536896
|
A | AACACACA others(1): Show |
2 | a0003c0005t0001g0017a0003c0005t0001g0082 | 5 | HG02559.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.180+564_180+571dup others(8): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126536896 | |||||
chr3:126536896
|
A | AACACACA others(3): Show |
8 | a0003c0005t0001g0019a0003c0005t0001g0032a0003c0005t0001g0038others(5): Show | 13 | HG00735.hp1 HG01358.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.180+562_180+571dup others(10): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126536896 | |||||
chr3:126536896
|
A | AACACACA others(5): Show |
1 | a0003c0005t0001g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.180+560_180+571dup others(12): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126536896 | |||||
chr3:126536896
|
A | C | 1 | a0003c0005t0001g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.180+543A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126536896 | ||||||
chr3:126536896
|
AAC | A | 18 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(15): Show | 56 | HG00639.hp2 HG00735.hp2 HG01070.hp2 others(53): Show |
intron_variant | MODIFIER | c.180+570_180+571del others(2): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126536896 | |||||
chr3:126536896
|
AACACAC | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0031 | 8 | HG00738.hp2 HG01168.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.180+566_180+571del others(6): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126536896 | |||||
chr3:126536921
|
A | C | 1 | a0005c0006t0001g0005 | 8 | HG00639.hp2 HG02886.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.180+568A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126536921 | ||||||
chr3:126536923
|
A | C | 2 | a0003c0007t0001g0098a0003c0007t0001g0115 | 2 | HG00323.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.180+570A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126536923 | ||||||
chr3:126536924
|
C | CACACACA others(4): Show |
1 | a0003c0005t0001g0110 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.180+571_180+572ins others(11): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126536924 | ||||||
chr3:126536928
|
A | C | 1 | a0003c0007t0001g0116 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.180+575A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126536928 | ||||||
chr3:126537017
|
G | A | 1 | a0002c0002t0001g0020 | 4 | HG01175.hp2 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+664G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537017 | ||||||
chr3:126537035
|
C | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(56): Show | 170 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.180+682C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537035 | ||||||
chr3:126537041
|
G | T | 17 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(14): Show | 51 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.180+688G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537041 | ||||||
chr3:126537110
|
C | G | 1 | a0009c0011t0004g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.180+757C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537110 | ||||||
chr3:126537149
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.180+796A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537149 | ||||||
chr3:126537289
|
G | A | 1 | a0001c0001t0001g0030 | 2 | NA18945.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.180+936G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537289 | ||||||
chr3:126537297
|
G | A | 2 | a0001c0001t0001g0083a0001c0001t0001g0101 | 2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.180+944G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537297 | ||||||
chr3:126537373
|
G | A | 34 | a0001c0001t0001g0122a0002c0002t0001g0002a0002c0002t0001g0007others(31): Show | 100 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.180+1020G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537373 | ||||||
chr3:126537459
|
A | G | 1 | a0009c0011t0004g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.180+1106A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537459 | ||||||
chr3:126537568
|
G | A | 1 | a0005c0006t0001g0005 | 8 | HG00639.hp2 HG02886.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.180+1215G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537568 | ||||||
chr3:126537705
|
G | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(14): Show | 51 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.180+1352G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537705 | ||||||
chr3:126537755
|
CAT | C | 17 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(14): Show | 51 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.180+1404_180+1405d others(4): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126537755 | |||||
chr3:126537812
|
G | A | 1 | a0001c0001t0001g0057 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.180+1459G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537812 | ||||||
chr3:126537826
|
T | G | 74 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(71): Show | 183 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.180+1473T>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537826 | ||||||
chr3:126537932
|
A | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(132): Show | 362 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.180+1579A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537932 | ||||||
chr3:126538138
|
G | A | 18 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(15): Show | 52 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.180+1785G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538138 | ||||||
chr3:126538168
|
A | G | 1 | a0001c0001t0001g0021 | 3 | HG01258.hp1 HG01361.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.180+1815A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538168 | ||||||
chr3:126538172
|
A | G | 1 | a0003c0007t0001g0108 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.180+1819A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538172 | ||||||
chr3:126538205
|
C | A | 7 | a0003c0004t0001g0012a0003c0004t0001g0022a0003c0004t0001g0034others(4): Show | 14 | HG00733.hp2 HG01175.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.180+1852C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538205 | ||||||
chr3:126538236
|
C | T | 35 | a0002c0002t0001g0002a0002c0002t0001g0007a0002c0002t0001g0008others(32): Show | 102 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.180+1883C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538236 | ||||||
chr3:126538323
|
C | T | 19 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(16): Show | 53 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.180+1970C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538323 | ||||||
chr3:126538362
|
G | C | 1 | a0001c0001t0001g0097 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.180+2009G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538362 | ||||||
chr3:126538383
|
T | G | 1 | a0003c0005t0001g0111 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.180+2030T>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538383 | ||||||
chr3:126538393
|
G | A | 55 | a0002c0002t0001g0002a0002c0002t0001g0007a0002c0002t0001g0008others(52): Show | 130 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.180+2040G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538393 | ||||||
chr3:126538435
|
G | A | 1 | a0002c0002t0001g0133 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.180+2082G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538435 | ||||||
chr3:126538513
|
A | C | 19 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(16): Show | 53 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.180+2160A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538513 | ||||||
chr3:126538528
|
TGGGCTCA others(15): Show |
T | 1 | a0001c0001t0005g0079 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.180+2179_180+2200d others(24): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126538528 | |||||
chr3:126538592
|
G | A | 1 | a0009c0011t0004g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.180+2239G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538592 | ||||||
chr3:126538668
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.180+2315C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538668 | ||||||
chr3:126538725
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.180+2372C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538725 | ||||||
chr3:126538738
|
G | A | 7 | a0003c0007t0001g0043a0003c0007t0001g0092a0003c0007t0001g0098others(4): Show | 7 | HG00323.hp1 HG01099.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.180+2385G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538738 | ||||||
chr3:126538764
|
T | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(132): Show | 362 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.180+2411T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538764 | ||||||
chr3:126538765
|
G | A | 1 | a0002c0002t0001g0127 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.180+2412G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538765 | ||||||
chr3:126538903
|
T | C | 3 | a0001c0001t0001g0083a0001c0001t0001g0101a0001c0001t0001g0122 | 3 | HG02630.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.180+2550T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538903 | ||||||
chr3:126538948
|
C | T | 1 | a0002c0002t0001g0102 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.180+2595C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538948 | ||||||
chr3:126539009
|
C | T | 7 | a0003c0007t0001g0043a0003c0007t0001g0092a0003c0007t0001g0098others(4): Show | 7 | HG00323.hp1 HG01099.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.180+2656C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539009 | ||||||
chr3:126539010
|
G | A | 1 | a0006c0008t0001g0011 | 6 | HG02818.hp2 HG02895.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.180+2657G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539010 | ||||||
chr3:126539029
|
C | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(56): Show | 170 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.180+2676C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539029 | ||||||
chr3:126539034
|
C | A | 1 | a0006c0008t0001g0011 | 6 | HG02818.hp2 HG02895.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.180+2681C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539034 | ||||||
chr3:126539037
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.180+2684T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539037 | ||||||
chr3:126539073
|
G | A | 19 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(16): Show | 53 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.181-2660G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539073 | ||||||
chr3:126539183
|
C | T | 19 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(16): Show | 53 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.181-2550C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539183 | ||||||
chr3:126539202
|
C | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(56): Show | 170 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.181-2531C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539202 | ||||||
chr3:126539442
|
C | A | 20 | a0002c0002t0001g0002a0002c0002t0001g0007a0002c0002t0001g0008others(17): Show | 74 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.181-2291C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539442 | ||||||
chr3:126539486
|
CAT | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0051a0001c0001t0001g0056others(1): Show | 17 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.181-2244_181-2243d others(4): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539486 | |||||
chr3:126539512
|
C | A | 1 | a0008c0012t0001g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.181-2221C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539512 | ||||||
chr3:126539520
|
C | A | 1 | a0008c0012t0001g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.181-2213C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539520 | ||||||
chr3:126539541
|
A | C | 1 | a0008c0012t0001g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.181-2192A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539541 | ||||||
chr3:126539569
|
A | C | 1 | a0008c0012t0001g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.181-2164A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539569 | ||||||
chr3:126539598
|
C | A | 1 | a0008c0012t0001g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.181-2135C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539598 | ||||||
chr3:126539602
|
A | T | 1 | a0008c0012t0001g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.181-2131A>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539602 | ||||||
chr3:126539722
|
C | A | 2 | a0001c0001t0001g0083a0001c0001t0001g0101 | 2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.181-2011C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539722 | ||||||
chr3:126539748
|
C | CCACA | 19 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(16): Show | 53 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.181-1981_181-1978d others(6): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539748 | |||||
chr3:126539777
|
A | ACACACAC | 17 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(14): Show | 49 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.181-1944_181-1938d others(9): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539777 | |||||
chr3:126539797
|
ACAC | A | 34 | a0002c0002t0001g0002a0002c0002t0001g0007a0002c0002t0001g0008others(31): Show | 101 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.181-1932_181-1930d others(5): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539797 | |||||
chr3:126539810
|
C | T | 2 | a0003c0004t0001g0025a0003c0004t0001g0119 | 4 | HG01109.hp2 HG02723.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.181-1923C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539810 | ||||||
chr3:126539829
|
ACACACAC others(2): Show |
A | 3 | a0001c0001t0001g0027a0001c0001t0001g0083a0006c0008t0001g0011 | 6 | HG02451.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.181-1895_181-1887d others(11): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539829 | |||||
chr3:126539838
|
C | T | 18 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(15): Show | 47 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.181-1895C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539838 | ||||||
chr3:126539842
|
A | ACACACAC others(4): Show |
18 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(15): Show | 47 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.181-1887_181-1886i others(13): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539842 | |||||
chr3:126539847
|
T | C | 18 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(15): Show | 47 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.181-1886T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539847 | ||||||
chr3:126539862
|
C | CCAAACCA others(427): Show |
5 | a0001c0001t0001g0027a0001c0001t0001g0090a0001c0001t0001g0101others(2): Show | 7 | HG01884.hp1 HG02300.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.181-1869_181-1868i others(436): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539862 | |||||
chr3:126539862
|
C | CCAAACCA others(427): Show |
13 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(10): Show | 40 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.181-1869_181-1868i others(436): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539862 | |||||
chr3:126539868
|
C | A | 18 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(15): Show | 47 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.181-1865C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539868 | ||||||
chr3:126539874
|
C | CACACACC others(445): Show |
1 | a0001c0001t0001g0060 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.181-1853_181-1852i others(454): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539874 | |||||
chr3:126539875
|
A | AC | 18 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(15): Show | 47 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.181-1857dupC | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539875 | |||||
chr3:126539875
|
A | ACACACCC others(451): Show |
1 | a0001c0001t0001g0059 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.181-1853_181-1852i others(460): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539875 | |||||
chr3:126539875
|
A | ACACACCC others(447): Show |
1 | a0003c0005t0001g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.181-1853_181-1852i others(456): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539875 | |||||
chr3:126539875
|
A | ACACACCC others(448): Show |
3 | a0001c0001t0001g0027a0001c0001t0001g0083a0006c0008t0001g0011 | 6 | HG02451.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.181-1853_181-1852i others(457): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539875 | |||||
chr3:126539875
|
A | ACACACCC others(452): Show |
1 | a0009c0011t0004g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.181-1853_181-1852i others(461): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539875 | |||||
chr3:126539875
|
A | ACACACCC others(452): Show |
62 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(59): Show | 180 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.181-1853_181-1852i others(461): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539875 | |||||
chr3:126539875
|
A | ACACACCC others(450): Show |
1 | a0001c0001t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.181-1853_181-1852i others(459): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539875 | |||||
chr3:126539875
|
A | ACACACCC others(450): Show |
1 | a0003c0007t0001g0115 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.181-1853_181-1852i others(459): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539875 | |||||
chr3:126539875
|
A | ACACACCC others(452): Show |
1 | a0001c0001t0001g0064 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.181-1853_181-1852i others(461): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539875 | |||||
chr3:126539875
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A | ACACACCC others(450): Show |
12 | a0003c0005t0001g0017a0003c0005t0001g0019a0003c0005t0001g0032others(9): Show | 20 | HG00735.hp1 HG01358.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.181-1853_181-1852i others(459): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539875 | |||||
chr3:126539875
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A | ACACACCC others(443): Show |
35 | a0002c0002t0001g0002a0002c0002t0001g0007a0002c0002t0001g0008others(32): Show | 102 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.181-1853_181-1852i others(452): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539875 | |||||
chr3:126539875
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A | ACACACCC others(452): Show |
1 | a0001c0001t0003g0065 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.181-1853_181-1852i others(461): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539875 | |||||
chr3:126539896
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A | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(112): Show | 301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.181-1837A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539896 | ||||||
chr3:126539972
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A | G | 6 | a0003c0004t0001g0012a0003c0004t0001g0022a0003c0004t0001g0034others(3): Show | 13 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.181-1761A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539972 | ||||||
chr3:126539989
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A | C | 1 | a0003c0004t0001g0087 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.181-1744A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539989 | ||||||
chr3:126540028
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C | T | 19 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(16): Show | 53 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.181-1705C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540028 | ||||||
chr3:126540080
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G | A | 1 | a0001c0001t0001g0010 | 6 | HG00738.hp2 HG01168.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.181-1653G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540080 | ||||||
chr3:126540100
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G | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(131): Show | 354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.181-1633G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540100 | ||||||
chr3:126540177
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G | A | 1 | a0001c0001t0001g0015 | 4 | NA18944.hp2 NA18974.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.181-1556G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540177 | ||||||
chr3:126540355
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A | T | 19 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(16): Show | 53 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.181-1378A>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540355 | ||||||
chr3:126540422
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G | C | 1 | a0007c0009t0002g0104 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.181-1311G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540422 | ||||||
chr3:126540526
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G | A | 56 | a0002c0002t0001g0002a0002c0002t0001g0007a0002c0002t0001g0008others(53): Show | 131 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.181-1207G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540526 | ||||||
chr3:126540548
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G | T | 19 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0018others(16): Show | 53 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.181-1185G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540548 | ||||||
chr3:126540589
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T | C | 1 | a0003c0010t0001g0089 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.181-1144T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540589 | ||||||
chr3:126540615
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C | T | 7 | a0003c0004t0001g0012a0003c0004t0001g0022a0003c0004t0001g0034others(4): Show | 14 | HG00733.hp2 HG01175.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.181-1118C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540615 | ||||||
chr3:126540642
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G | C | 2 | a0003c0007t0001g0043a0003c0007t0001g0092 | 2 | HG02055.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.181-1091G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540642 | ||||||
chr3:126540760
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T | C | 2 | a0004c0003t0002g0036a0004c0003t0002g0106 | 3 | HG03209.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.181-973T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540760 | ||||||
chr3:126540862
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C | G | 1 | a0001c0001t0001g0063 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.181-871C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540862 | ||||||
chr3:126540957
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A | G | 5 | a0003c0005t0001g0077a0003c0005t0001g0080a0003c0005t0001g0110others(2): Show | 5 | HG02486.hp2 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.181-776A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540957 | ||||||
chr3:126540968
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G | T | 1 | a0003c0007t0001g0116 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.181-765G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540968 | ||||||
chr3:126541057
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C | A | 1 | a0004c0003t0002g0037 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.181-676C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126541057 | ||||||
chr3:126541064
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T | C | 13 | a0003c0005t0001g0017a0003c0005t0001g0019a0003c0005t0001g0032others(10): Show | 21 | HG00735.hp1 HG01358.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.181-669T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126541064 | ||||||
chr3:126541320
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C | T | 35 | a0002c0002t0001g0002a0002c0002t0001g0007a0002c0002t0001g0008others(32): Show | 102 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.181-413C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126541320 | ||||||
chr3:126541340
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T | C | 4 | a0003c0004t0001g0025a0003c0004t0001g0039a0003c0004t0001g0119others(1): Show | 7 | HG01109.hp2 HG01255.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.181-393T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126541340 | ||||||
chr3:126541354
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A | C | 1 | a0001c0001t0001g0062 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.181-379A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126541354 | ||||||
chr3:126541417
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C | T | 1 | a0001c0001t0001g0061 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.181-316C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126541417 | ||||||
chr3:126541602
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G | C | 1 | a0001c0001t0001g0095 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.181-131G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126541602 | ||||||
chr3:126541686
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C | T | 1 | a0004c0003t0002g0099 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.181-47C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126541686 |