geneid | 1638 |
---|---|
ensemblid | ENSG00000080166.16 |
hgncid | 2709 |
symbol | DCT |
name | dopachrome tautomerase |
refseq_nuc | NM_001922.5 |
refseq_prot | NP_001913.2 |
ensembl_nuc | ENST00000377028.10 |
ensembl_prot | ENSP00000366227.4 |
mane_status | MANE Select |
chr | chr13 |
start | 94436811 |
end | 94479682 |
strand | - |
ver | v1.2 |
region | chr13:94436811-94479682 |
region5000 | chr13:94431811-94484682 |
regionname0 | DCT_chr13_94436811_94479682 |
regionname5000 | DCT_chr13_94431811_94484682 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 519 | 323 | 88 | 58 | 115 | 18 | 42 | 80 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0002 | 0/0 | 519 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0003 | 0/0 | 519 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0004 | 0/0 | 519 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0005 | 0/0 | 519 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0006 | 0/0 | 519 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0007 | 0/0 | 519 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0008 | 0/0 | 519 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0009 | 0/0 | 519 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1560 | 314 | 81 | 57 | 114 | 18 | 42 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
c0002 | 0/0 | 1560 | 5 | 5 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
c0003 | 0/0 | 1560 | 4 | 4 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
c0004 | 0/0 | 1560 | 2 | 2 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
c0005 | 0/0 | 1560 | 2 | 1 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
c0006 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
c0007 | 0/0 | 1560 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
c0008 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
c0009 | 0/0 | 1560 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
c0010 | 0/0 | 1560 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
c0011 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
c0012 | 0/0 | 1560 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
c0013 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
c0014 | 0/0 | 1560 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3514 | 95 | 2 | 19 | 63 | 2 | 9 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0002 | 0/1 | 3513 | 66 | 12 | 17 | 15 | 5 | 16 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0003 | 0/0 | 3512 | 46 | 2 | 6 | 29 | 2 | 7 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0004 | 0/0 | 3513 | 24 | 8 | 6 | 1 | 5 | 4 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0005 | 0/0 | 3514 | 21 | 14 | 4 | 0 | 1 | 2 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0006 | 0/0 | 3513 | 19 | 16 | 1 | 1 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0007 | 0/0 | 3510 | 12 | 10 | 2 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0008 | 0/0 | 3512 | 9 | 8 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0009 | 0/0 | 3512 | 5 | 5 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0010 | 0/0 | 3509 | 4 | 0 | 3 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0011 | 0/0 | 3513 | 3 | 3 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0012 | 0/0 | 3513 | 2 | 0 | 0 | 2 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0013 | 0/0 | 3513 | 2 | 0 | 0 | 2 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0014 | 0/0 | 3512 | 2 | 0 | 0 | 0 | 0 | 2 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0015 | 0/0 | 3513 | 2 | 2 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0016 | 0/0 | 3513 | 2 | 1 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0017 | 0/0 | 3514 | 2 | 2 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0018 | 0/0 | 3512 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0019 | 0/0 | 3512 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0020 | 0/0 | 3512 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0021 | 0/0 | 3512 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0022 | 0/0 | 3512 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0023 | 0/0 | 3512 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0024 | 1/0 | 3515 | 1 | 0 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0025 | 0/0 | 3513 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0026 | 0/0 | 3513 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0027 | 0/0 | 3513 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0028 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0029 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0030 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0031 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0032 | 0/0 | 3581 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0033 | 0/0 | 3514 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0034 | 0/0 | 3512 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0035 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0036 | 0/0 | 3513 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
t0037 | 0/0 | 3512 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0030 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0122 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1560 | 314 | 81 | 57 | 114 | 18 | 42 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0003 | 0/0 | 1560 | 4 | 4 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0004 | 0/0 | 1560 | 2 | 2 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0007 | 0/0 | 1560 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0011 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0012 | 0/0 | 1560 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0002c0002 | 0/0 | 1560 | 5 | 5 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0003c0005 | 0/0 | 1560 | 2 | 1 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0004c0006 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0005c0008 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0006c0013 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0007c0010 | 0/0 | 1560 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0008c0009 | 0/0 | 1560 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0009c0014 | 0/0 | 1560 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5073 | 90 | 2 | 19 | 59 | 2 | 8 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0002 | 0/1 | 5072 | 63 | 11 | 16 | 15 | 5 | 15 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0003 | 0/0 | 5071 | 46 | 2 | 6 | 29 | 2 | 7 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0004 | 0/0 | 5072 | 20 | 4 | 6 | 1 | 5 | 4 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0005 | 0/0 | 5073 | 20 | 14 | 3 | 0 | 1 | 2 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0006 | 0/0 | 5072 | 13 | 10 | 1 | 1 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0007 | 0/0 | 5069 | 12 | 10 | 2 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0008 | 0/0 | 5071 | 8 | 7 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0009 | 0/0 | 5071 | 5 | 5 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0010 | 0/0 | 5068 | 4 | 0 | 3 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0011 | 0/0 | 5072 | 3 | 3 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0012 | 0/0 | 5072 | 2 | 0 | 0 | 2 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0013 | 0/0 | 5072 | 2 | 0 | 0 | 2 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0014 | 0/0 | 5071 | 2 | 0 | 0 | 0 | 0 | 2 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0015 | 0/0 | 5072 | 2 | 2 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0017 | 0/0 | 5073 | 2 | 2 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0018 | 0/0 | 5071 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0019 | 0/0 | 5071 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0020 | 0/0 | 5071 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0021 | 0/0 | 5071 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0022 | 0/0 | 5071 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0023 | 0/0 | 5071 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0024 | 1/0 | 5074 | 1 | 0 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0025 | 0/0 | 5072 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0026 | 0/0 | 5072 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0027 | 0/0 | 5072 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0028 | 0/0 | 5072 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0029 | 0/0 | 5072 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0030 | 0/0 | 5072 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0031 | 0/0 | 5072 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0032 | 0/0 | 5140 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0033 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0034 | 0/0 | 5071 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0035 | 0/0 | 5072 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0036 | 0/0 | 5072 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0001t0037 | 0/0 | 5071 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0003t0004 | 0/0 | 5072 | 4 | 4 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0004t0006 | 0/0 | 5072 | 2 | 2 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0007t0005 | 0/0 | 5073 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0011t0001 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0001c0012t0002 | 0/0 | 5072 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0002c0002t0006 | 0/0 | 5072 | 4 | 4 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0002c0002t0008 | 0/0 | 5071 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0003c0005t0016 | 0/0 | 5072 | 2 | 1 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0004c0006t0001 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0005c0008t0001 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0006c0013t0001 | 0/0 | 5073 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0007c0010t0002 | 0/0 | 5072 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0008c0009t0002 | 0/0 | 5072 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
a0009c0014t0001 | 0/0 | 5073 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | copy fasta | chr13 | 94431811 | 94484682 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0122 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0004g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0004g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0004g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0005g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0005g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0005g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0005g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0005g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0005g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0005g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0005g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0005g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0005g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0005g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0005g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0005g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0005g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0005g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0005g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0005g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0005g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0005g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0006g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0006g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0006g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0006g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0006g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0006g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0006g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0006g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0007g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0007g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0007g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0007g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0007g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0007g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0007g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0007g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0007g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0007g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0008g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0008g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0008g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0008g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0008g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0008g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0008g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0009g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0009g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0009g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0009g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0009g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0010g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0010g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0010g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0010g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0011g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0011g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0011g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0012g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0012g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0013g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0013g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0014g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0014g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0015g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0015g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0017g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0017g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0018g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0019g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0020g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0021g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0022g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0023g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0024g0030 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0025g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0026g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0027g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0028g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0029g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0030g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0031g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0032g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0033g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0034g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0035g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0036g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0001t0037g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0003t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0003t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0003t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0003t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0004t0006g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0004t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0007t0005g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0011t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0001c0012t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0002c0002t0006g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0002c0002t0006g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0002c0002t0006g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0002c0002t0006g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0002c0002t0008g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0003c0005t0016g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0003c0005t0016g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0004c0006t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0005c0008t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0006c0013t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0007c0010t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0008c0009t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
a0009c0014t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0121 | EUR | GBR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0136 | EUR | GBR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00140 | hp1 | a0001 | c0001 | t0004 | g0211 | EUR | GBR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00140 | hp2 | a0001 | c0001 | t0027 | g0113 | EUR | GBR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00280 | hp1 | a0001 | c0001 | t0026 | g0117 | EUR | FIN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0078 | EUR | FIN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0273 | EUR | FIN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00323 | hp2 | a0001 | c0001 | t0021 | g0076 | EUR | FIN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00609 | hp2 | a0006 | c0013 | t0001 | g0021 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0278 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0075 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01069 | hp1 | a0001 | c0001 | t0004 | g0074 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0209 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0190 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01074 | hp1 | a0001 | c0001 | t0004 | g0077 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0274 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01109 | hp2 | a0001 | c0001 | t0005 | g0311 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0282 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01192 | hp1 | a0001 | c0001 | t0007 | g0196 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01243 | hp1 | a0001 | c0001 | t0007 | g0198 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01243 | hp2 | a0003 | c0005 | t0016 | g0302 | AMR | PUR | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01256 | hp1 | a0001 | c0001 | t0010 | g0284 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01256 | hp2 | a0001 | c0001 | t0004 | g0233 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01257 | hp1 | a0001 | c0001 | t0010 | g0286 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0258 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0091 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01346 | hp2 | a0001 | c0001 | t0005 | g0308 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01358 | hp2 | a0001 | c0001 | t0005 | g0309 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01496 | hp2 | a0001 | c0007 | t0005 | g0307 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0101 | EUR | IBS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | IBS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01516 | hp2 | a0001 | c0001 | t0005 | g0324 | EUR | IBS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01884 | hp1 | a0001 | c0001 | t0015 | g0204 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0323 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01891 | hp1 | a0001 | c0001 | t0006 | g0145 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0325 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0265 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01952 | hp2 | a0007 | c0010 | t0002 | g0174 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01975 | hp1 | a0001 | c0001 | t0006 | g0240 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0267 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01981 | hp2 | a0001 | c0001 | t0008 | g0013 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0092 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02055 | hp1 | a0001 | c0001 | t0029 | g0280 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02055 | hp2 | a0001 | c0001 | t0034 | g0312 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02135 | hp1 | a0001 | c0001 | t0033 | g0153 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02145 | hp1 | a0001 | c0001 | t0005 | g0321 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02145 | hp2 | a0001 | c0001 | t0017 | g0293 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CDX | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | CDX | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02257 | hp2 | a0001 | c0001 | t0008 | g0143 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02280 | hp1 | a0001 | c0001 | t0007 | g0093 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02280 | hp2 | a0001 | c0001 | t0009 | g0305 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | PEL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02523 | hp2 | a0001 | c0001 | t0013 | g0036 | EAS | KHV | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02572 | hp1 | a0001 | c0001 | t0011 | g0238 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02572 | hp2 | a0001 | c0001 | t0008 | g0140 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0042 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0299 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0251 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02622 | hp2 | a0001 | c0001 | t0007 | g0214 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0326 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02630 | hp2 | a0001 | c0001 | t0030 | g0291 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0316 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02647 | hp2 | a0001 | c0001 | t0008 | g0142 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02683 | hp1 | a0001 | c0001 | t0004 | g0212 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0243 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0310 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02717 | hp2 | a0001 | c0001 | t0007 | g0085 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0083 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02723 | hp2 | a0001 | c0001 | t0018 | g0114 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0269 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02738 | hp2 | a0001 | c0001 | t0004 | g0210 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0318 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0281 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02818 | hp1 | a0001 | c0001 | t0011 | g0239 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02818 | hp2 | a0001 | c0003 | t0004 | g0100 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02886 | hp1 | a0001 | c0001 | t0007 | g0197 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02886 | hp2 | a0001 | c0001 | t0020 | g0279 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02895 | hp1 | a0002 | c0002 | t0006 | g0296 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0315 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02897 | hp1 | a0001 | c0001 | t0005 | g0319 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02897 | hp2 | a0002 | c0002 | t0006 | g0287 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02922 | hp1 | a0003 | c0005 | t0016 | g0294 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02922 | hp2 | a0001 | c0001 | t0007 | g0084 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02965 | hp1 | a0001 | c0001 | t0008 | g0014 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02965 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0208 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02970 | hp2 | a0001 | c0001 | t0007 | g0086 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0072 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02976 | hp2 | a0001 | c0001 | t0005 | g0317 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03041 | hp1 | a0001 | c0001 | t0007 | g0068 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03041 | hp2 | a0001 | c0001 | t0011 | g0103 | AFR | GWD | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0246 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03098 | hp2 | a0001 | c0001 | t0035 | g0320 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0290 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03130 | hp2 | a0001 | c0001 | t0017 | g0192 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0010 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03195 | hp1 | a0001 | c0001 | t0009 | g0304 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03195 | hp2 | a0001 | c0001 | t0008 | g0002 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03209 | hp2 | a0001 | c0001 | t0031 | g0144 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03225 | hp1 | a0001 | c0004 | t0006 | g0232 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03225 | hp2 | a0001 | c0001 | t0008 | g0012 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0272 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0080 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03453 | hp1 | a0001 | c0001 | t0015 | g0203 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03453 | hp2 | a0001 | c0001 | t0007 | g0199 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03486 | hp1 | a0001 | c0001 | t0007 | g0213 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03486 | hp2 | a0001 | c0001 | t0006 | g0292 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03490 | hp1 | a0001 | c0001 | t0014 | g0099 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0079 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03492 | hp1 | a0001 | c0001 | t0014 | g0230 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0261 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03516 | hp2 | a0001 | c0001 | t0019 | g0300 | AFR | ESN | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03579 | hp1 | a0001 | c0001 | t0028 | g0202 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0071 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0106 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0216 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | STU | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03688 | hp2 | a0008 | c0009 | t0002 | g0271 | SAS | STU | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0229 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03710 | hp1 | a0001 | c0001 | t0005 | g0314 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0172 | SAS | PJL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03831 | hp2 | a0009 | c0014 | t0001 | g0306 | SAS | BEB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0164 | SAS | BEB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03927 | hp1 | a0001 | c0001 | t0022 | g0160 | SAS | BEB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | STU | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0104 | SAS | STU | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0270 | SAS | BEB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG04184 | hp2 | a0001 | c0001 | t0010 | g0283 | SAS | BEB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0115 | SAS | STU | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0207 | SAS | STU | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG04204 | hp1 | a0001 | c0001 | t0025 | g0228 | SAS | STU | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG04204 | hp2 | a0001 | c0001 | t0005 | g0327 | SAS | STU | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0108 | SAS | STU | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0069 | SAS | STU | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18522 | hp1 | a0001 | c0012 | t0002 | g0250 | AFR | YRI | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18522 | hp2 | a0001 | c0001 | t0009 | g0295 | AFR | YRI | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | CHB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18747 | hp1 | a0001 | c0001 | t0004 | g0241 | EAS | CHB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | CHB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0011 | AFR | YRI | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18906 | hp2 | a0002 | c0002 | t0006 | g0297 | AFR | YRI | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18948 | hp1 | a0005 | c0008 | t0001 | g0161 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18975 | hp1 | a0004 | c0006 | t0001 | g0008 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18978 | hp1 | a0001 | c0001 | t0012 | g0089 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18978 | hp2 | a0001 | c0001 | t0032 | g0051 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18998 | hp1 | a0001 | c0011 | t0001 | g0015 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA18998 | hp2 | a0001 | c0001 | t0012 | g0097 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | LWK | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19030 | hp2 | a0001 | c0003 | t0004 | g0242 | AFR | LWK | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19043 | hp1 | a0001 | c0003 | t0004 | g0235 | AFR | LWK | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0007 | AFR | LWK | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19064 | hp2 | a0001 | c0001 | t0023 | g0215 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19067 | hp2 | a0001 | c0001 | t0036 | g0328 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19068 | hp1 | a0001 | c0001 | t0013 | g0044 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19078 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19080 | hp1 | a0001 | c0001 | t0037 | g0329 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19086 | hp1 | a0001 | c0001 | t0006 | g0205 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19240 | hp1 | a0001 | c0001 | t0007 | g0237 | AFR | YRI | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0141 | AFR | YRI | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0159 | EUR | TSI | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0006 | EUR | TSI | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0081 | EUR | TSI | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0095 | EUR | TSI | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA20905 | hp1 | a0001 | c0001 | t0006 | g0088 | SAS | GIH | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | GIH | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0124 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG01123 | hp2 | a0001 | c0001 | t0010 | g0285 | AMR | CLM | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0073 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02486 | hp1 | a0001 | c0004 | t0006 | g0231 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02486 | hp2 | a0001 | c0001 | t0008 | g0002 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02559 | hp1 | a0001 | c0003 | t0004 | g0234 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | ACB | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0298 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG03471 | hp2 | a0002 | c0002 | t0008 | g0289 | AFR | MSL | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG06807 | hp1 | a0002 | c0002 | t0006 | g0288 | AFR | USA | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
HG06807 | hp2 | a0001 | c0001 | t0009 | g0301 | AFR | USA | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0322 | AFR | USA | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA20300 | hp2 | a0001 | c0001 | t0009 | g0303 | AFR | USA | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | LWK | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0313 | AFR | LWK | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0122 | REF | REF | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0024 | g0030 | REF | REF | DCT_chr13_94431811_94484682 | DCT | chr13 | 94431811 | 94484682 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:94460111
|
C | T | 1 | a0007 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.1159G>A | p.Ala387Thr | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/8 | 1586/5074 | 1159/1560 | 387/519 | chr13 | 94460111 | ||
chr13:94465646
|
T | C | 1 | a0006 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.850A>G | p.Thr284Ala | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/8 | 1277/5074 | 850/1560 | 284/519 | chr13 | 94465646 | ||
chr13:94465672
|
C | T | 1 | a0002 | 5 | HG02895.hp1 HG02897.hp2 HG03471.hp2 others(2): Show |
missense_variant | MODERATE | c.824G>A | p.Arg275Gln | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/8 | 1251/5074 | 824/1560 | 275/519 | chr13 | 94465672 | ||
chr13:94465739
|
C | T | 1 | a0008 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.757G>A | p.Glu253Lys | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/8 | 1184/5074 | 757/1560 | 253/519 | chr13 | 94465739 | ||
chr13:94466616
|
C | T | 1 | a0005 | 1 | NA18948.hp1 | missense_variant | MODERATE | c.638G>A | p.Gly213Glu | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/8 | 1065/5074 | 638/1560 | 213/519 | chr13 | 94466616 | ||
chr13:94468832
|
T | C | 1 | a0003 | 2 | HG01243.hp2 HG02922.hp1 |
missense_variant | MODERATE | c.509A>G | p.Asn170Ser | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/8 | 936/5074 | 509/1560 | 170/519 | chr13 | 94468832 | ||
chr13:94479033
|
A | C | 1 | a0004 | 1 | NA18975.hp1 | missense_variant | MODERATE | c.223T>G | p.Tyr75Asp | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/8 | 650/5074 | 223/1560 | 75/519 | chr13 | 94479033 | ||
chr13:94479110
|
G | A | 1 | a0009 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.146C>T | p.Ala49Val | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/8 | 573/5074 | 146/1560 | 49/519 | chr13 | 94479110 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:94440033
|
T | G | 1 | a0001c0011 | 1 | NA18998.hp1 | synonymous_variant | LOW | c.1425A>C | p.Val475Val | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 1852/5074 | 1425/1560 | 475/519 | chr13 | 94440033 | ||
chr13:94440039
|
G | C | 1 | a0001c0012 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.1419C>G | p.Leu473Leu | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 1846/5074 | 1419/1560 | 473/519 | chr13 | 94440039 | ||
chr13:94462144
|
A | G | 1 | a0001c0004 | 2 | HG02486.hp1 HG03225.hp1 |
synonymous_variant | LOW | c.909T>C | p.Tyr303Tyr | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 5/8 | 1336/5074 | 909/1560 | 303/519 | chr13 | 94462144 | ||
chr13:94468999
|
G | A | 1 | a0001c0003 | 4 | HG02559.hp1 HG02818.hp2 NA19030.hp2 others(1): Show |
synonymous_variant | LOW | c.342C>T | p.Thr114Thr | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/8 | 769/5074 | 342/1560 | 114/519 | chr13 | 94468999 | ||
chr13:94479007
|
A | C | 1 | a0001c0007 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.249T>G | p.Arg83Arg | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/8 | 676/5074 | 249/1560 | 83/519 | chr13 | 94479007 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:94436864
|
A | G | 36 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(33): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*3034T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 3034 | chr13 | 94436864 | |||||
chr13:94436900
|
G | A | 1 | a0001c0001t0022 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2998C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 2998 | chr13 | 94436900 | |||||
chr13:94437026
|
C | T | 1 | a0001c0001t0030 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2872G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 2872 | chr13 | 94437026 | |||||
chr13:94437052
|
GA | G | 36 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(33): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*2845delT | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 2845 | chr13 | 94437052 | |||||
chr13:94437354
|
ACTT | A | 1 | a0001c0001t0007 | 12 | HG01192.hp1 HG01243.hp1 HG02280.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2541_*2543delAAG | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 2541 | chr13 | 94437354 | |||||
chr13:94437481
|
T | C | 3 | a0001c0001t0004a0001c0001t0021a0001c0003t0004 | 25 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2417A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 2417 | chr13 | 94437481 | |||||
chr13:94437753
|
A | G | 1 | a0001c0001t0007 | 12 | HG01192.hp1 HG01243.hp1 HG02280.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2145T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 2145 | chr13 | 94437753 | |||||
chr13:94437764
|
G | A | 1 | a0001c0001t0026 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2134C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 2134 | chr13 | 94437764 | |||||
chr13:94437964
|
A | G | 2 | a0001c0001t0015a0001c0001t0028 | 3 | HG01884.hp1 HG03453.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1934T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 1934 | chr13 | 94437964 | |||||
chr13:94438437
|
T | C | 1 | a0001c0001t0019 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1461A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 1461 | chr13 | 94438437 | |||||
chr13:94438438
|
T | A | 40 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(37): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
3_prime_UTR_variant | MODIFIER | c.*1460A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 1460 | chr13 | 94438438 | |||||
chr13:94438574
|
C | CCTATGCT others(60): Show |
1 | a0001c0001t0032 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1323_*1324insCTTT others(63): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 1323 | chr13 | 94438574 | |||||
chr13:94438583
|
A | T | 1 | a0001c0001t0032 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1315T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 1315 | chr13 | 94438583 | |||||
chr13:94438656
|
C | G | 1 | a0001c0001t0032 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1242G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 1242 | chr13 | 94438656 | |||||
chr13:94438679
|
T | C | 1 | a0001c0001t0031 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1219A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 1219 | chr13 | 94438679 | |||||
chr13:94438700
|
A | G | 1 | a0001c0001t0007 | 12 | HG01192.hp1 HG01243.hp1 HG02280.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1198T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 1198 | chr13 | 94438700 | |||||
chr13:94438741
|
A | G | 3 | a0001c0001t0009a0001c0001t0034a0003c0005t0016 | 8 | HG01243.hp2 HG02055.hp2 HG02280.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1157T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 1157 | chr13 | 94438741 | |||||
chr13:94438948
|
A | G | 3 | a0001c0001t0004a0001c0001t0021a0001c0003t0004 | 25 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*950T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 950 | chr13 | 94438948 | |||||
chr13:94439042
|
C | G | 7 | a0001c0001t0008a0001c0001t0009a0001c0001t0011others(4): Show | 21 | HG01243.hp2 HG01981.hp2 HG02055.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*856G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 856 | chr13 | 94439042 | |||||
chr13:94439093
|
C | T | 37 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(34): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*805G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 805 | chr13 | 94439093 | |||||
chr13:94439103
|
A | G | 1 | a0001c0001t0025 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*795T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 795 | chr13 | 94439103 | |||||
chr13:94439107
|
A | G | 2 | a0001c0001t0020a0001c0001t0029 | 2 | HG02055.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*791T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 791 | chr13 | 94439107 | |||||
chr13:94439173
|
G | C | 1 | a0001c0001t0027 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*725C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 725 | chr13 | 94439173 | |||||
chr13:94439185
|
A | G | 7 | a0001c0001t0008a0001c0001t0009a0001c0001t0011others(4): Show | 21 | HG01243.hp2 HG01981.hp2 HG02055.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*713T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 713 | chr13 | 94439185 | |||||
chr13:94439206
|
G | A | 1 | a0001c0001t0028 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*692C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 692 | chr13 | 94439206 | |||||
chr13:94439485
|
A | G | 13 | a0001c0001t0002a0001c0001t0010a0001c0001t0015others(10): Show | 79 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*413T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 413 | chr13 | 94439485 | |||||
chr13:94439554
|
G | A | 1 | a0001c0001t0023 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*344C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 344 | chr13 | 94439554 | |||||
chr13:94439579
|
GT | G | 49 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(46): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
3_prime_UTR_variant | MODIFIER | c.*318delA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 318 | chr13 | 94439579 | |||||
chr13:94439612
|
G | A | 1 | a0001c0001t0014 | 2 | HG03490.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*286C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 286 | chr13 | 94439612 | |||||
chr13:94439625
|
TG | T | 15 | a0001c0001t0003a0001c0001t0008a0001c0001t0009others(12): Show | 74 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*272delC | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 272 | chr13 | 94439625 | |||||
chr13:94439667
|
ATCTT | A | 1 | a0001c0001t0010 | 4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*227_*230delAAGA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 227 | chr13 | 94439667 | |||||
chr13:94439847
|
G | A | 1 | a0001c0001t0033 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*51C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 8/8 | 51 | chr13 | 94439847 | |||||
chr13:94479309
|
T | C | 4 | a0001c0001t0005a0001c0001t0034a0001c0001t0035others(1): Show | 23 | HG01109.hp2 HG01346.hp2 HG01358.hp2 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-54A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/8 | 54 | chr13 | 94479309 | |||||
chr13:94479437
|
T | C | 1 | a0001c0001t0036 | 1 | NA19067.hp2 | 5_prime_UTR_variant | MODIFIER | c.-182A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/8 | 182 | chr13 | 94479437 | |||||
chr13:94479536
|
G | A | 1 | a0001c0001t0037 | 1 | NA19080.hp1 | 5_prime_UTR_variant | MODIFIER | c.-281C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/8 | 281 | chr13 | 94479536 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:94440642
|
T | A | 224 | a0001c0001t0001g0220a0001c0001t0002g0001a0001c0001t0002g0005others(221): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1382-566A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94440642 | ||||||
chr13:94440676
|
G | GT | 147 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0056others(144): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.1382-601dupA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94440676 | ||||||
chr13:94440676
|
G | GTT | 35 | a0001c0001t0001g0066a0001c0001t0001g0168a0001c0001t0002g0123others(32): Show | 35 | HG00140.hp2 HG01123.hp2 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.1382-602_1382-601d others(4): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94440676 | ||||||
chr13:94440676
|
G | GTTT | 46 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(43): Show | 48 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.1382-603_1382-601d others(5): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94440676 | ||||||
chr13:94440676
|
G | GTTTT | 9 | a0001c0001t0004g0075a0001c0001t0004g0081a0001c0001t0005g0309others(6): Show | 9 | HG00741.hp1 HG01358.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1382-604_1382-601d others(6): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94440676 | ||||||
chr13:94440676
|
G | T | 1 | a0001c0001t0029g0280 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1382-600C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94440676 | ||||||
chr13:94441050
|
T | C | 1 | a0001c0004t0006g0232 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1382-974A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94441050 | ||||||
chr13:94441065
|
C | T | 25 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(22): Show | 26 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.1382-989G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94441065 | ||||||
chr13:94441337
|
T | A | 22 | a0001c0001t0001g0263a0001c0001t0002g0005a0001c0001t0002g0109others(19): Show | 23 | HG00438.hp1 HG00544.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.1382-1261A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94441337 | ||||||
chr13:94441720
|
A | G | 1 | a0001c0001t0002g0270 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1382-1644T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94441720 | ||||||
chr13:94441872
|
G | T | 11 | a0001c0001t0008g0002a0001c0001t0008g0012a0001c0001t0008g0013others(8): Show | 12 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1381+1564C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94441872 | ||||||
chr13:94441920
|
T | C | 1 | a0001c0001t0009g0301 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1381+1516A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94441920 | ||||||
chr13:94441921
|
A | T | 1 | a0001c0001t0008g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1381+1515T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94441921 | ||||||
chr13:94442017
|
A | AT | 12 | a0001c0001t0008g0002a0001c0001t0008g0012a0001c0001t0008g0013others(9): Show | 13 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1381+1418dupA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94442017 | ||||||
chr13:94442018
|
T | C | 2 | a0001c0001t0001g0184a0001c0001t0022g0160 | 2 | HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1381+1418A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94442018 | ||||||
chr13:94442131
|
C | T | 204 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0001g0259others(201): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1381+1305G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94442131 | ||||||
chr13:94442153
|
G | T | 1 | a0001c0001t0011g0103 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1381+1283C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94442153 | ||||||
chr13:94442461
|
T | C | 1 | a0001c0001t0019g0300 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1381+975A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94442461 | ||||||
chr13:94442485
|
T | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0178 | 2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.1381+951A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94442485 | ||||||
chr13:94442498
|
A | G | 6 | a0001c0001t0007g0084a0001c0001t0007g0085a0001c0001t0007g0086others(3): Show | 6 | HG02622.hp2 HG02717.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1381+938T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94442498 | ||||||
chr13:94442732
|
G | A | 4 | a0001c0001t0006g0011a0001c0001t0006g0141a0001c0001t0006g0145others(1): Show | 4 | HG01891.hp1 HG03209.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1381+704C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94442732 | ||||||
chr13:94442742
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1381+694A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94442742 | ||||||
chr13:94442762
|
T | C | 24 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(21): Show | 25 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.1381+674A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94442762 | ||||||
chr13:94442814
|
C | T | 2 | a0001c0001t0001g0193a0001c0001t0017g0192 | 2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1381+622G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94442814 | ||||||
chr13:94442824
|
A | G | 216 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0001g0259others(213): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.1381+612T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94442824 | ||||||
chr13:94443022
|
C | A | 12 | a0001c0001t0008g0002a0001c0001t0008g0012a0001c0001t0008g0013others(9): Show | 13 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1381+414G>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94443022 | ||||||
chr13:94443077
|
T | C | 204 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0001g0259others(201): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1381+359A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94443077 | ||||||
chr13:94443137
|
A | T | 216 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0001g0259others(213): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.1381+299T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94443137 | ||||||
chr13:94443228
|
CA | C | 4 | a0001c0001t0006g0290a0001c0001t0006g0292a0001c0001t0006g0298others(1): Show | 4 | HG02615.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1381+207delT | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94443228 | ||||||
chr13:94443275
|
A | G | 215 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0001g0259others(212): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1381+161T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94443275 | ||||||
chr13:94443288
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1381+148G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 7/7 | chr13 | 94443288 | ||||||
chr13:94443674
|
A | C | 2 | a0001c0001t0006g0009a0001c0001t0006g0010 | 2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1180-37T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94443674 | ||||||
chr13:94443759
|
T | C | 204 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0001g0259others(201): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1180-122A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94443759 | ||||||
chr13:94443773
|
C | T | 12 | a0001c0001t0008g0002a0001c0001t0008g0012a0001c0001t0008g0013others(9): Show | 13 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1180-136G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94443773 | ||||||
chr13:94443857
|
A | G | 55 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(52): Show | 56 | HG00597.hp2 HG00621.hp2 HG01168.hp2 others(53): Show |
intron_variant | MODIFIER | c.1180-220T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94443857 | ||||||
chr13:94443868
|
T | C | 1 | a0001c0001t0003g0217 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1180-231A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94443868 | ||||||
chr13:94444021
|
C | T | 3 | a0001c0001t0015g0203a0001c0001t0015g0204a0001c0001t0028g0202 | 3 | HG01884.hp1 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1180-384G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444021 | ||||||
chr13:94444033
|
G | C | 12 | a0001c0001t0008g0002a0001c0001t0008g0012a0001c0001t0008g0013others(9): Show | 13 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1180-396C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444033 | ||||||
chr13:94444155
|
C | T | 216 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0001g0259others(213): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.1180-518G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444155 | ||||||
chr13:94444251
|
G | A | 216 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0001g0259others(213): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.1180-614C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444251 | ||||||
chr13:94444348
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1180-711C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444348 | ||||||
chr13:94444383
|
C | T | 12 | a0001c0001t0008g0002a0001c0001t0008g0012a0001c0001t0008g0013others(9): Show | 13 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1180-746G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444383 | ||||||
chr13:94444422
|
C | G | 5 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0182others(2): Show | 5 | NA18942.hp2 NA18965.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180-785G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444422 | ||||||
chr13:94444518
|
T | C | 1 | a0001c0001t0005g0314 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1180-881A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444518 | ||||||
chr13:94444549
|
A | T | 1 | a0001c0001t0005g0314 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1180-912T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444549 | ||||||
chr13:94444670
|
G | A | 1 | a0001c0001t0006g0240 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1180-1033C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444670 | ||||||
chr13:94444762
|
T | C | 2 | a0001c0001t0006g0011a0001c0001t0006g0141 | 2 | NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1180-1125A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444762 | ||||||
chr13:94444797
|
T | C | 213 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0001g0259others(210): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1180-1160A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444797 | ||||||
chr13:94444941
|
A | G | 216 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0001g0259others(213): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.1180-1304T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444941 | ||||||
chr13:94444945
|
T | C | 71 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0002g0001others(68): Show | 73 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.1180-1308A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444945 | ||||||
chr13:94444979
|
G | A | 1 | a0001c0001t0004g0241 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1180-1342C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94444979 | ||||||
chr13:94445087
|
T | C | 12 | a0001c0001t0008g0002a0001c0001t0008g0012a0001c0001t0008g0013others(9): Show | 13 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1180-1450A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94445087 | ||||||
chr13:94445210
|
T | C | 1 | a0001c0001t0003g0065 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1180-1573A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94445210 | ||||||
chr13:94445336
|
T | G | 1 | a0001c0001t0001g0187 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1180-1699A>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94445336 | ||||||
chr13:94445407
|
A | G | 213 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0001g0259others(210): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1180-1770T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94445407 | ||||||
chr13:94445479
|
C | T | 2 | a0001c0001t0002g0270a0001c0001t0003g0236 | 2 | HG04184.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1180-1842G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94445479 | ||||||
chr13:94445702
|
C | T | 201 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0001g0259others(198): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1180-2065G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94445702 | ||||||
chr13:94445750
|
G | A | 1 | a0001c0001t0002g0281 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1180-2113C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94445750 | ||||||
chr13:94445892
|
C | T | 4 | a0001c0001t0010g0283a0001c0001t0010g0284a0001c0001t0010g0285others(1): Show | 4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180-2255G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94445892 | ||||||
chr13:94445944
|
T | G | 3 | a0001c0001t0002g0130a0001c0001t0002g0138a0001c0001t0002g0260 | 3 | HG02559.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1180-2307A>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94445944 | ||||||
chr13:94446004
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1180-2367C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94446004 | ||||||
chr13:94446189
|
A | G | 1 | a0001c0001t0007g0213 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1180-2552T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94446189 | ||||||
chr13:94446352
|
G | T | 1 | a0001c0001t0030g0291 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1180-2715C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94446352 | ||||||
chr13:94446422
|
G | C | 1 | a0001c0001t0006g0088 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1180-2785C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94446422 | ||||||
chr13:94446449
|
T | A | 1 | a0001c0001t0002g0126 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1180-2812A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94446449 | ||||||
chr13:94446550
|
C | T | 1 | a0001c0001t0029g0280 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1180-2913G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94446550 | ||||||
chr13:94446584
|
T | C | 3 | a0001c0001t0015g0203a0001c0001t0015g0204a0001c0001t0028g0202 | 3 | HG01884.hp1 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1180-2947A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94446584 | ||||||
chr13:94446744
|
C | T | 47 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(44): Show | 48 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.1180-3107G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94446744 | ||||||
chr13:94446805
|
T | C | 23 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0073others(20): Show | 24 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.1180-3168A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94446805 | ||||||
chr13:94446853
|
A | C | 3 | a0001c0001t0002g0130a0001c0001t0002g0138a0001c0001t0002g0260 | 3 | HG02559.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1180-3216T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94446853 | ||||||
chr13:94447255
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1180-3618C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94447255 | ||||||
chr13:94447323
|
A | G | 33 | a0001c0001t0005g0007a0001c0001t0005g0308a0001c0001t0005g0309others(30): Show | 35 | HG01109.hp2 HG01346.hp2 HG01358.hp2 others(32): Show |
intron_variant | MODIFIER | c.1180-3686T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94447323 | ||||||
chr13:94447355
|
C | T | 55 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(52): Show | 56 | HG00597.hp2 HG00621.hp2 HG01168.hp2 others(53): Show |
intron_variant | MODIFIER | c.1180-3718G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94447355 | ||||||
chr13:94447653
|
C | T | 4 | a0001c0001t0003g0229a0001c0001t0006g0088a0001c0001t0014g0099others(1): Show | 4 | HG03490.hp1 HG03492.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180-4016G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94447653 | ||||||
chr13:94447657
|
T | C | 1 | a0001c0001t0008g0002 | 2 | HG02486.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1180-4020A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94447657 | ||||||
chr13:94447659
|
A | T | 1 | a0001c0001t0001g0167 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1180-4022T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94447659 | ||||||
chr13:94447676
|
G | T | 1 | a0001c0001t0004g0073 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1180-4039C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94447676 | ||||||
chr13:94447886
|
G | C | 80 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(77): Show | 83 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.1180-4249C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94447886 | ||||||
chr13:94448050
|
C | G | 1 | a0001c0001t0023g0215 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1180-4413G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94448050 | ||||||
chr13:94448114
|
G | T | 1 | a0001c0001t0003g0282 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1180-4477C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94448114 | ||||||
chr13:94448228
|
G | C | 11 | a0001c0001t0007g0068a0001c0001t0007g0084a0001c0001t0007g0085others(8): Show | 11 | HG01192.hp1 HG01243.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1180-4591C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94448228 | ||||||
chr13:94448243
|
T | TCAA | 11 | a0001c0001t0007g0068a0001c0001t0007g0084a0001c0001t0007g0085others(8): Show | 11 | HG01192.hp1 HG01243.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1180-4609_1180-460 others(7): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94448243 | ||||||
chr13:94448502
|
T | C | 1 | a0001c0001t0019g0300 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1180-4865A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94448502 | ||||||
chr13:94448587
|
A | G | 215 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0001g0259others(212): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1180-4950T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94448587 | ||||||
chr13:94448797
|
G | A | 4 | a0001c0001t0006g0011a0001c0001t0006g0141a0001c0001t0006g0145others(1): Show | 4 | HG01891.hp1 HG03209.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180-5160C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94448797 | ||||||
chr13:94448809
|
C | G | 7 | a0001c0001t0008g0002a0001c0001t0008g0012a0001c0001t0008g0013others(4): Show | 8 | HG01981.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1180-5172G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94448809 | ||||||
chr13:94448903
|
CA | C | 11 | a0001c0001t0008g0002a0001c0001t0008g0012a0001c0001t0008g0013others(8): Show | 12 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1180-5267delT | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94448903 | ||||||
chr13:94448914
|
T | A | 21 | a0001c0001t0005g0007a0001c0001t0005g0308a0001c0001t0005g0309others(18): Show | 22 | HG01109.hp2 HG01346.hp2 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.1180-5277A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94448914 | ||||||
chr13:94449021
|
C | T | 70 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0002g0001others(67): Show | 72 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.1180-5384G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94449021 | ||||||
chr13:94449084
|
G | GA | 7 | a0001c0001t0005g0315a0001c0001t0005g0316a0001c0001t0005g0317others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1180-5448dupT | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94449084 | ||||||
chr13:94449170
|
T | C | 1 | a0001c0001t0003g0217 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1180-5533A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94449170 | ||||||
chr13:94449318
|
T | A | 1 | a0001c0001t0006g0145 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1180-5681A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94449318 | ||||||
chr13:94449379
|
C | G | 1 | a0001c0001t0020g0279 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1180-5742G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94449379 | ||||||
chr13:94449395
|
C | T | 9 | a0001c0001t0009g0295a0001c0001t0009g0301a0001c0001t0009g0303others(6): Show | 9 | HG01243.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1180-5758G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94449395 | ||||||
chr13:94449535
|
C | G | 77 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0002g0001others(74): Show | 79 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.1180-5898G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94449535 | ||||||
chr13:94449776
|
A | G | 14 | a0001c0001t0006g0290a0001c0001t0006g0292a0001c0001t0006g0298others(11): Show | 14 | HG01243.hp2 HG02055.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1180-6139T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94449776 | ||||||
chr13:94449822
|
TATGTAAT others(4): Show |
T | 29 | a0001c0001t0005g0007a0001c0001t0005g0308a0001c0001t0005g0309others(26): Show | 30 | HG01109.hp2 HG01346.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.1180-6196_1180-618 others(15): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94449822 | ||||||
chr13:94450150
|
G | A | 11 | a0001c0001t0008g0002a0001c0001t0008g0012a0001c0001t0008g0013others(8): Show | 12 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1180-6513C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94450150 | ||||||
chr13:94450181
|
C | T | 2 | a0001c0001t0004g0074a0001c0001t0004g0209 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1180-6544G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94450181 | ||||||
chr13:94450182
|
G | T | 1 | a0005c0008t0001g0161 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1180-6545C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94450182 | ||||||
chr13:94450360
|
G | A | 1 | a0001c0001t0002g0123 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1180-6723C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94450360 | ||||||
chr13:94450361
|
C | T | 2 | a0001c0001t0005g0322a0001c0001t0005g0323 | 2 | HG01884.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1180-6724G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94450361 | ||||||
chr13:94450423
|
C | A | 5 | a0002c0002t0006g0287a0002c0002t0006g0288a0002c0002t0006g0296others(2): Show | 5 | HG02895.hp1 HG02897.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180-6786G>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94450423 | ||||||
chr13:94450443
|
G | A | 215 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0001g0259others(212): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1180-6806C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94450443 | ||||||
chr13:94450495
|
A | G | 1 | a0001c0001t0006g0009 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1180-6858T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94450495 | ||||||
chr13:94450496
|
T | C | 6 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0001t0005g0314others(3): Show | 6 | HG01346.hp2 HG01358.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180-6859A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94450496 | ||||||
chr13:94450592
|
C | T | 2 | a0002c0002t0006g0287a0002c0002t0006g0296 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1180-6955G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94450592 | ||||||
chr13:94450671
|
A | G | 1 | a0001c0001t0002g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1180-7034T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94450671 | ||||||
chr13:94450792
|
C | T | 212 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0001g0259others(209): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1180-7155G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94450792 | ||||||
chr13:94451020
|
A | T | 24 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(21): Show | 25 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.1180-7383T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94451020 | ||||||
chr13:94451030
|
T | C | 3 | a0001c0001t0002g0130a0001c0001t0002g0138a0001c0001t0002g0260 | 3 | HG02559.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1180-7393A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94451030 | ||||||
chr13:94451230
|
A | T | 4 | a0001c0001t0010g0283a0001c0001t0010g0284a0001c0001t0010g0285others(1): Show | 4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180-7593T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94451230 | ||||||
chr13:94451352
|
C | T | 73 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0002g0001others(70): Show | 75 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.1180-7715G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94451352 | ||||||
chr13:94451440
|
T | C | 72 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0002g0001others(69): Show | 74 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.1180-7803A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94451440 | ||||||
chr13:94451531
|
A | T | 1 | a0001c0001t0009g0301 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1180-7894T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94451531 | ||||||
chr13:94451637
|
G | T | 1 | a0001c0001t0001g0263 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1180-8000C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94451637 | ||||||
chr13:94451761
|
A | C | 5 | a0002c0002t0006g0287a0002c0002t0006g0288a0002c0002t0006g0296others(2): Show | 5 | HG02895.hp1 HG02897.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180-8124T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94451761 | ||||||
chr13:94451891
|
C | G | 4 | a0001c0001t0010g0283a0001c0001t0010g0284a0001c0001t0010g0285others(1): Show | 4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+8200G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94451891 | ||||||
chr13:94451919
|
G | GT | 58 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(55): Show | 59 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1179+8171dupA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94451919 | ||||||
chr13:94451952
|
C | T | 4 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0039others(1): Show | 4 | HG02080.hp1 NA18970.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+8139G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94451952 | ||||||
chr13:94451992
|
C | A | 9 | a0001c0001t0002g0110a0001c0001t0002g0119a0001c0001t0002g0121others(6): Show | 9 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.1179+8099G>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94451992 | ||||||
chr13:94452039
|
C | CT | 58 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(55): Show | 59 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1179+8051dupA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94452039 | ||||||
chr13:94452206
|
T | C | 3 | a0001c0001t0011g0103a0001c0001t0011g0238a0001c0001t0011g0239 | 3 | HG02572.hp1 HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1179+7885A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94452206 | ||||||
chr13:94452292
|
C | T | 2 | a0001c0001t0004g0080a0001c0001t0004g0081 | 2 | HG03239.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1179+7799G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94452292 | ||||||
chr13:94452885
|
A | G | 1 | a0001c0001t0001g0023 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1179+7206T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94452885 | ||||||
chr13:94452976
|
T | C | 4 | a0001c0001t0010g0283a0001c0001t0010g0284a0001c0001t0010g0285others(1): Show | 4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+7115A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94452976 | ||||||
chr13:94453145
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1179+6946A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94453145 | ||||||
chr13:94453172
|
A | T | 1 | a0001c0001t0002g0115 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1179+6919T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94453172 | ||||||
chr13:94453318
|
T | C | 325 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(322): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1179+6773A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94453318 | ||||||
chr13:94453547
|
T | C | 5 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(2): Show | 5 | HG02602.hp1 HG03669.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.1179+6544A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94453547 | ||||||
chr13:94453595
|
AC | A | 11 | a0001c0001t0008g0002a0001c0001t0008g0012a0001c0001t0008g0013others(8): Show | 12 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1179+6495delG | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94453595 | ||||||
chr13:94453654
|
A | T | 1 | a0001c0001t0023g0215 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1179+6437T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94453654 | ||||||
chr13:94454229
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1179+5862T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94454229 | ||||||
chr13:94454240
|
T | C | 3 | a0001c0001t0003g0070a0001c0001t0003g0102a0001c0001t0003g0236 | 3 | HG00438.hp2 HG02083.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1179+5851A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94454240 | ||||||
chr13:94454376
|
G | A | 11 | a0001c0001t0008g0002a0001c0001t0008g0012a0001c0001t0008g0013others(8): Show | 12 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1179+5715C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94454376 | ||||||
chr13:94454894
|
C | G | 215 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0001g0259others(212): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1179+5197G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94454894 | ||||||
chr13:94454993
|
G | C | 73 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0002g0001others(70): Show | 75 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.1179+5098C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94454993 | ||||||
chr13:94455051
|
A | G | 28 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(25): Show | 28 | HG00597.hp1 HG00609.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.1179+5040T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455051 | ||||||
chr13:94455324
|
G | A | 1 | a0001c0001t0004g0208 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1179+4767C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455324 | ||||||
chr13:94455336
|
T | C | 215 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0001g0259others(212): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1179+4755A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455336 | ||||||
chr13:94455381
|
T | TAG | 43 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0048others(40): Show | 44 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.1179+4708_1179+470 others(6): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455381 | ||||||
chr13:94455381
|
T | TAGAG | 64 | a0001c0001t0001g0259a0001c0001t0001g0263a0001c0001t0002g0001others(61): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.1179+4706_1179+470 others(8): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455381 | ||||||
chr13:94455381
|
T | TAGAGAG | 5 | a0001c0001t0002g0112a0001c0001t0002g0122a0001c0001t0003g0221others(2): Show | 5 | HG00597.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1179+4704_1179+470 others(10): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455381 | ||||||
chr13:94455381
|
T | TAGAGAGA others(1): Show |
11 | a0001c0001t0002g0108a0001c0001t0003g0102a0001c0001t0003g0217others(8): Show | 11 | HG01192.hp1 HG01243.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1179+4702_1179+470 others(12): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455381 | ||||||
chr13:94455381
|
T | TAGAGAGA others(3): Show |
38 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0002g0246others(35): Show | 39 | HG00438.hp2 HG00621.hp2 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.1179+4700_1179+470 others(14): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455381 | ||||||
chr13:94455381
|
T | TAGAGAGA others(5): Show |
16 | a0001c0001t0003g0095a0001c0001t0005g0007a0001c0001t0005g0308others(13): Show | 17 | HG01109.hp2 HG01346.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.1179+4698_1179+470 others(16): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455381 | ||||||
chr13:94455381
|
T | TAGAGAGA others(7): Show |
15 | a0001c0001t0005g0317a0001c0001t0005g0322a0001c0001t0006g0009others(12): Show | 15 | HG02486.hp1 HG02622.hp2 HG02895.hp1 others(12): Show |
intron_variant | MODIFIER | c.1179+4696_1179+470 others(18): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455381 | ||||||
chr13:94455381
|
T | TAGAGAGA others(9): Show |
3 | a0001c0001t0005g0327a0001c0001t0010g0283a0001c0001t0010g0285 | 3 | HG01123.hp2 HG04184.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1179+4694_1179+470 others(20): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455381 | ||||||
chr13:94455381
|
T | TAGAGAGA others(11): Show |
3 | a0001c0001t0005g0316a0001c0001t0010g0284a0001c0001t0010g0286 | 3 | HG01256.hp1 HG01257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1179+4692_1179+470 others(22): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455381 | ||||||
chr13:94455381
|
T | TAGAGAGA others(13): Show |
1 | a0001c0001t0015g0203 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1179+4690_1179+470 others(24): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455381 | ||||||
chr13:94455381
|
T | TAGAGAGA others(17): Show |
1 | a0001c0001t0015g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1179+4686_1179+470 others(28): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455381 | ||||||
chr13:94455381
|
T | TAGAGAGA others(21): Show |
1 | a0001c0001t0028g0202 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1179+4682_1179+470 others(32): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455381 | ||||||
chr13:94455381
|
TAGAGAG | T | 7 | a0001c0001t0003g0087a0001c0001t0003g0090a0001c0001t0003g0229others(4): Show | 7 | HG03490.hp1 HG03492.hp1 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.1179+4704_1179+470 others(10): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455381 | ||||||
chr13:94455561
|
A | G | 1 | a0001c0003t0004g0234 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1179+4530T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94455561 | ||||||
chr13:94456124
|
G | A | 4 | a0001c0001t0006g0011a0001c0001t0006g0141a0001c0001t0006g0145others(1): Show | 4 | HG01891.hp1 HG03209.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+3967C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94456124 | ||||||
chr13:94456247
|
C | T | 30 | a0001c0001t0005g0007a0001c0001t0005g0308a0001c0001t0005g0309others(27): Show | 31 | HG01109.hp2 HG01346.hp2 HG01358.hp2 others(28): Show |
intron_variant | MODIFIER | c.1179+3844G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94456247 | ||||||
chr13:94456291
|
A | G | 4 | a0001c0001t0010g0283a0001c0001t0010g0284a0001c0001t0010g0285others(1): Show | 4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+3800T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94456291 | ||||||
chr13:94456667
|
C | T | 2 | a0001c0001t0001g0223a0001c0001t0003g0096 | 2 | NA18939.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1179+3424G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94456667 | ||||||
chr13:94456723
|
G | A | 19 | a0001c0001t0001g0263a0001c0001t0002g0005a0001c0001t0002g0109others(16): Show | 20 | HG00438.hp1 HG00544.hp2 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.1179+3368C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94456723 | ||||||
chr13:94456862
|
G | T | 55 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(52): Show | 56 | HG00597.hp2 HG00621.hp2 HG01168.hp2 others(53): Show |
intron_variant | MODIFIER | c.1179+3229C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94456862 | ||||||
chr13:94456971
|
A | G | 2 | a0001c0001t0001g0193a0001c0001t0017g0192 | 2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1179+3120T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94456971 | ||||||
chr13:94456990
|
C | T | 1 | a0001c0001t0015g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1179+3101G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94456990 | ||||||
chr13:94457029
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1179+3062G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457029 | ||||||
chr13:94457061
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1179+3030G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457061 | ||||||
chr13:94457107
|
A | G | 64 | a0001c0001t0001g0020a0001c0001t0001g0178a0001c0001t0001g0184others(61): Show | 65 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.1179+2984T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457107 | ||||||
chr13:94457125
|
G | A | 1 | a0001c0001t0030g0291 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1179+2966C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457125 | ||||||
chr13:94457229
|
T | C | 215 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0001g0259others(212): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1179+2862A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457229 | ||||||
chr13:94457358
|
G | C | 14 | a0001c0001t0006g0290a0001c0001t0006g0292a0001c0001t0006g0298others(11): Show | 14 | HG01243.hp2 HG02055.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1179+2733C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457358 | ||||||
chr13:94457378
|
T | C | 2 | a0001c0001t0005g0322a0001c0001t0005g0323 | 2 | HG01884.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1179+2713A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457378 | ||||||
chr13:94457429
|
G | A | 27 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(24): Show | 28 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1179+2662C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457429 | ||||||
chr13:94457504
|
A | T | 5 | a0001c0001t0002g0126a0001c0001t0002g0264a0001c0001t0002g0265others(2): Show | 5 | HG01943.hp1 HG01952.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1179+2587T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457504 | ||||||
chr13:94457522
|
C | G | 1 | a0001c0001t0031g0144 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1179+2569G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457522 | ||||||
chr13:94457522
|
C | T | 1 | a0001c0004t0006g0232 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1179+2569G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457522 | ||||||
chr13:94457565
|
A | G | 5 | a0002c0002t0006g0287a0002c0002t0006g0288a0002c0002t0006g0296others(2): Show | 5 | HG02895.hp1 HG02897.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1179+2526T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457565 | ||||||
chr13:94457656
|
C | T | 3 | a0001c0001t0015g0203a0001c0001t0015g0204a0001c0001t0028g0202 | 3 | HG01884.hp1 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1179+2435G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457656 | ||||||
chr13:94457764
|
C | T | 2 | a0001c0001t0002g0139a0001c0001t0002g0261 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1179+2327G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457764 | ||||||
chr13:94457778
|
G | T | 1 | a0001c0001t0001g0035 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1179+2313C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457778 | ||||||
chr13:94457851
|
T | C | 140 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(137): Show | 144 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.1179+2240A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457851 | ||||||
chr13:94457952
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1179+2139G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457952 | ||||||
chr13:94457958
|
C | T | 27 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(24): Show | 28 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1179+2133G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94457958 | ||||||
chr13:94458000
|
C | A | 4 | a0001c0001t0010g0283a0001c0001t0010g0284a0001c0001t0010g0285others(1): Show | 4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+2091G>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458000 | ||||||
chr13:94458001
|
G | A | 3 | a0001c0001t0006g0011a0001c0001t0006g0145a0001c0001t0031g0144 | 3 | HG01891.hp1 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1179+2090C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458001 | ||||||
chr13:94458056
|
T | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0146 | 3 | NA18968.hp2 NA18974.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1179+2035A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458056 | ||||||
chr13:94458066
|
C | T | 4 | a0001c0001t0010g0283a0001c0001t0010g0284a0001c0001t0010g0285others(1): Show | 4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+2025G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458066 | ||||||
chr13:94458081
|
C | T | 1 | a0001c0001t0007g0196 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1179+2010G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458081 | ||||||
chr13:94458290
|
C | T | 59 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(56): Show | 60 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1179+1801G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458290 | ||||||
chr13:94458299
|
T | G | 2 | a0001c0001t0002g0123a0001c0001t0002g0125 | 2 | HG02602.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1179+1792A>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458299 | ||||||
chr13:94458313
|
A | G | 1 | a0001c0001t0002g0281 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1179+1778T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458313 | ||||||
chr13:94458397
|
C | G | 3 | a0001c0001t0015g0203a0001c0001t0015g0204a0001c0001t0028g0202 | 3 | HG01884.hp1 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1179+1694G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458397 | ||||||
chr13:94458457
|
G | A | 4 | a0001c0001t0010g0283a0001c0001t0010g0284a0001c0001t0010g0285others(1): Show | 4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+1634C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458457 | ||||||
chr13:94458518
|
T | G | 1 | a0001c0001t0031g0144 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1179+1573A>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458518 | ||||||
chr13:94458646
|
A | G | 3 | a0001c0001t0001g0029a0001c0001t0001g0173a0001c0001t0001g0176 | 3 | HG03654.hp1 HG03942.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1179+1445T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458646 | ||||||
chr13:94458685
|
C | T | 3 | a0001c0001t0006g0011a0001c0001t0006g0145a0001c0001t0031g0144 | 3 | HG01891.hp1 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1179+1406G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458685 | ||||||
chr13:94458695
|
G | A | 4 | a0001c0001t0010g0283a0001c0001t0010g0284a0001c0001t0010g0285others(1): Show | 4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+1396C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458695 | ||||||
chr13:94458790
|
A | G | 24 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(21): Show | 25 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.1179+1301T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458790 | ||||||
chr13:94458854
|
G | A | 8 | a0001c0001t0005g0007a0001c0001t0005g0310a0001c0001t0005g0311others(5): Show | 9 | HG01109.hp2 HG01884.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1179+1237C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458854 | ||||||
chr13:94458864
|
G | T | 2 | a0001c0001t0008g0014a0001c0001t0008g0140 | 2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1179+1227C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458864 | ||||||
chr13:94458918
|
A | C | 27 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(24): Show | 28 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1179+1173T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458918 | ||||||
chr13:94458968
|
C | G | 1 | a0001c0001t0002g0105 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1179+1123G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94458968 | ||||||
chr13:94459052
|
G | GT | 59 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(56): Show | 60 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1179+1038_1179+103 others(5): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94459052 | ||||||
chr13:94459053
|
G | T | 86 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(83): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1179+1038C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94459053 | ||||||
chr13:94459093
|
G | T | 4 | a0001c0001t0010g0283a0001c0001t0010g0284a0001c0001t0010g0285others(1): Show | 4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1179+998C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94459093 | ||||||
chr13:94459153
|
A | G | 2 | a0001c0001t0011g0238a0001c0001t0011g0239 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1179+938T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94459153 | ||||||
chr13:94459154
|
C | T | 11 | a0001c0001t0006g0141a0001c0001t0008g0002a0001c0001t0008g0012others(8): Show | 12 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1179+937G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94459154 | ||||||
chr13:94459255
|
T | C | 107 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(104): Show | 110 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.1179+836A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94459255 | ||||||
chr13:94459341
|
T | A | 1 | a0001c0001t0005g0314 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1179+750A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94459341 | ||||||
chr13:94459405
|
C | T | 59 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(56): Show | 60 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.1179+686G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94459405 | ||||||
chr13:94459414
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1179+677C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94459414 | ||||||
chr13:94459544
|
T | C | 62 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(59): Show | 64 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.1179+547A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94459544 | ||||||
chr13:94459578
|
G | A | 22 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0022others(19): Show | 23 | HG00558.hp1 HG00673.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.1179+513C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94459578 | ||||||
chr13:94459606
|
G | A | 1 | a0001c0001t0028g0202 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1179+485C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 6/7 | chr13 | 94459606 | ||||||
chr13:94460343
|
C | T | 9 | a0001c0001t0003g0004a0001c0001t0003g0098a0001c0001t0003g0201others(6): Show | 10 | NA18959.hp1 NA18962.hp2 NA18978.hp1 others(7): Show |
intron_variant | MODIFIER | c.1044-117G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 5/7 | chr13 | 94460343 | ||||||
chr13:94460726
|
C | T | 21 | a0001c0001t0005g0007a0001c0001t0005g0308a0001c0001t0005g0309others(18): Show | 22 | HG01109.hp2 HG01346.hp2 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.1044-500G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 5/7 | chr13 | 94460726 | ||||||
chr13:94460746
|
T | C | 145 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(142): Show | 149 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.1044-520A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 5/7 | chr13 | 94460746 | ||||||
chr13:94460916
|
C | T | 1 | a0001c0001t0003g0102 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1044-690G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 5/7 | chr13 | 94460916 | ||||||
chr13:94461074
|
G | A | 1 | a0001c0001t0006g0011 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1044-848C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 5/7 | chr13 | 94461074 | ||||||
chr13:94461292
|
C | T | 27 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(24): Show | 28 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1043+718G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 5/7 | chr13 | 94461292 | ||||||
chr13:94461505
|
C | A | 2 | a0001c0001t0002g0110a0001c0001t0002g0258 | 2 | HG01261.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1043+505G>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 5/7 | chr13 | 94461505 | ||||||
chr13:94461606
|
G | C | 14 | a0001c0001t0006g0290a0001c0001t0006g0292a0001c0001t0006g0298others(11): Show | 14 | HG01243.hp2 HG02055.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1043+404C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 5/7 | chr13 | 94461606 | ||||||
chr13:94461902
|
A | C | 1 | a0001c0003t0004g0100 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1043+108T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 5/7 | chr13 | 94461902 | ||||||
chr13:94461978
|
C | T | 1 | a0001c0001t0019g0300 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1043+32G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 5/7 | chr13 | 94461978 | ||||||
chr13:94462345
|
C | T | 56 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(53): Show | 57 | HG00597.hp2 HG00621.hp2 HG01168.hp2 others(54): Show |
intron_variant | MODIFIER | c.864-156G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94462345 | ||||||
chr13:94462380
|
G | T | 1 | a0001c0001t0001g0022 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.864-191C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94462380 | ||||||
chr13:94462502
|
GA | G | 14 | a0001c0001t0006g0011a0001c0001t0006g0141a0001c0001t0006g0145others(11): Show | 15 | HG01891.hp1 HG01981.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.864-314delT | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94462502 | ||||||
chr13:94462612
|
T | C | 27 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(24): Show | 28 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.864-423A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94462612 | ||||||
chr13:94462635
|
AC | A | 27 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(24): Show | 28 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.864-447delG | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94462635 | ||||||
chr13:94462742
|
A | T | 2 | a0001c0001t0003g0207a0001c0001t0025g0228 | 2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.864-553T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94462742 | ||||||
chr13:94462820
|
T | C | 1 | a0001c0001t0005g0326 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.864-631A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94462820 | ||||||
chr13:94462921
|
C | G | 27 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(24): Show | 28 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.864-732G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94462921 | ||||||
chr13:94463057
|
G | A | 4 | a0001c0001t0006g0290a0001c0001t0006g0292a0001c0001t0006g0298others(1): Show | 4 | HG02615.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.864-868C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463057 | ||||||
chr13:94463078
|
G | A | 27 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(24): Show | 28 | HG00438.hp1 HG00544.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.864-889C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463078 | ||||||
chr13:94463138
|
T | A | 4 | a0001c0001t0006g0290a0001c0001t0006g0292a0001c0001t0006g0298others(1): Show | 4 | HG02615.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.864-949A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463138 | ||||||
chr13:94463243
|
C | A | 11 | a0001c0001t0007g0068a0001c0001t0007g0084a0001c0001t0007g0085others(8): Show | 11 | HG01192.hp1 HG01243.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.864-1054G>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463243 | ||||||
chr13:94463273
|
A | C | 1 | a0001c0001t0001g0034 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.864-1084T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463273 | ||||||
chr13:94463285
|
C | CT | 8 | a0001c0001t0001g0034a0001c0001t0001g0167a0001c0001t0001g0178others(5): Show | 8 | HG00438.hp2 HG00597.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.864-1097dupA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463285 | ||||||
chr13:94463285
|
CT | C | 72 | a0001c0001t0001g0016a0001c0001t0002g0111a0001c0001t0002g0138others(69): Show | 74 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.864-1097delA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463285 | ||||||
chr13:94463378
|
C | T | 76 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(73): Show | 78 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.864-1189G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463378 | ||||||
chr13:94463470
|
TGTCAGGC others(18): Show |
T | 55 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(52): Show | 56 | HG00597.hp2 HG00621.hp2 HG01168.hp2 others(53): Show |
intron_variant | MODIFIER | c.864-1306_864-1282d others(27): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463470 | ||||||
chr13:94463514
|
T | C | 24 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(21): Show | 25 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.864-1325A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463514 | ||||||
chr13:94463526
|
G | C | 1 | a0001c0001t0003g0067 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.864-1337C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463526 | ||||||
chr13:94463570
|
G | A | 1 | a0001c0001t0004g0079 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.864-1381C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463570 | ||||||
chr13:94463574
|
G | A | 26 | a0001c0001t0005g0007a0001c0001t0005g0308a0001c0001t0005g0309others(23): Show | 27 | HG01109.hp2 HG01346.hp2 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.864-1385C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463574 | ||||||
chr13:94463579
|
C | T | 1 | a0001c0001t0002g0269 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.864-1390G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463579 | ||||||
chr13:94463602
|
C | T | 1 | a0001c0001t0002g0122 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.864-1413G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463602 | ||||||
chr13:94463651
|
G | A | 1 | a0001c0001t0029g0280 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.864-1462C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94463651 | ||||||
chr13:94464006
|
G | C | 60 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0002g0108others(57): Show | 61 | HG00280.hp1 HG00597.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.863+1627C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464006 | ||||||
chr13:94464024
|
T | C | 24 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(21): Show | 25 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.863+1609A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464024 | ||||||
chr13:94464099
|
T | C | 63 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0002g0108others(60): Show | 64 | HG00280.hp1 HG00438.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.863+1534A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464099 | ||||||
chr13:94464188
|
C | T | 55 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(52): Show | 56 | HG00597.hp2 HG00621.hp2 HG01168.hp2 others(53): Show |
intron_variant | MODIFIER | c.863+1445G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464188 | ||||||
chr13:94464243
|
A | G | 23 | a0001c0001t0006g0290a0001c0001t0006g0292a0001c0001t0006g0298others(20): Show | 23 | HG01192.hp1 HG01243.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.863+1390T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464243 | ||||||
chr13:94464244
|
G | A | 1 | a0001c0001t0019g0300 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.863+1389C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464244 | ||||||
chr13:94464270
|
C | T | 4 | a0001c0001t0006g0290a0001c0001t0006g0292a0001c0001t0006g0298others(1): Show | 4 | HG02615.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.863+1363G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464270 | ||||||
chr13:94464438
|
G | A | 38 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(35): Show | 40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.863+1195C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464438 | ||||||
chr13:94464468
|
T | G | 1 | a0001c0001t0001g0151 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.863+1165A>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464468 | ||||||
chr13:94464476
|
C | T | 11 | a0001c0001t0007g0068a0001c0001t0007g0084a0001c0001t0007g0085others(8): Show | 11 | HG01192.hp1 HG01243.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.863+1157G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464476 | ||||||
chr13:94464490
|
A | C | 22 | a0001c0001t0005g0007a0001c0001t0005g0308a0001c0001t0005g0309others(19): Show | 23 | HG01109.hp2 HG01346.hp2 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.863+1143T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464490 | ||||||
chr13:94464556
|
C | T | 24 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(21): Show | 25 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.863+1077G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464556 | ||||||
chr13:94464568
|
A | C | 1 | a0001c0001t0006g0298 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.863+1065T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464568 | ||||||
chr13:94464576
|
G | A | 1 | a0001c0001t0029g0280 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.863+1057C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464576 | ||||||
chr13:94464630
|
C | G | 38 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(35): Show | 40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.863+1003G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464630 | ||||||
chr13:94464661
|
C | A | 38 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(35): Show | 40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.863+972G>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464661 | ||||||
chr13:94464736
|
G | T | 38 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(35): Show | 40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.863+897C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464736 | ||||||
chr13:94464769
|
G | A | 1 | a0001c0001t0004g0071 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.863+864C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464769 | ||||||
chr13:94464871
|
C | T | 1 | a0001c0001t0007g0086 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.863+762G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94464871 | ||||||
chr13:94465131
|
C | A | 21 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0290others(18): Show | 21 | HG01243.hp2 HG02145.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.863+502G>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94465131 | ||||||
chr13:94465142
|
C | T | 38 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(35): Show | 40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.863+491G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94465142 | ||||||
chr13:94465171
|
G | A | 1 | a0001c0001t0004g0072 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.863+462C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94465171 | ||||||
chr13:94465417
|
CATAACCA | C | 53 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(50): Show | 54 | HG00597.hp2 HG00621.hp2 HG01168.hp2 others(51): Show |
intron_variant | MODIFIER | c.863+209_863+215del others(7): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94465417 | ||||||
chr13:94465418
|
A | C | 1 | a0001c0001t0002g0130 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.863+215T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94465418 | ||||||
chr13:94465422
|
C | T | 38 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(35): Show | 40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.863+211G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94465422 | ||||||
chr13:94465443
|
G | GAT | 37 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(34): Show | 39 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.863+188_863+189dup others(2): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94465443 | ||||||
chr13:94465446
|
A | AT | 72 | a0001c0001t0001g0032a0001c0001t0001g0133a0001c0001t0001g0134others(69): Show | 74 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.863+186dupA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94465446 | ||||||
chr13:94465447
|
T | TA | 101 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(98): Show | 103 | HG00597.hp2 HG00621.hp2 HG01109.hp2 others(100): Show |
intron_variant | MODIFIER | c.863+185_863+186ins others(1): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94465447 | ||||||
chr13:94465545
|
AACAGCAC others(3): Show |
A | 1 | a0001c0001t0002g0245 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.863+78_863+87delAT others(8): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94465545 | ||||||
chr13:94465609
|
C | T | 1 | a0003c0005t0016g0302 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.863+24G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 4/7 | chr13 | 94465609 | ||||||
chr13:94465966
|
TTTTATAT others(7): Show |
T | 1 | a0001c0001t0002g0266 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.697-181_697-168del others(14): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465966 | ||||||
chr13:94465967
|
TTTATATA others(6): Show |
T | 1 | a0001c0001t0001g0276 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.697-181_697-169del others(13): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465967 | ||||||
chr13:94465968
|
T | TATATATA others(4): Show |
2 | a0001c0001t0001g0023a0001c0001t0001g0053 | 2 | NA18980.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.697-170_697-169ins others(11): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
T | TATATATA others(6): Show |
1 | a0001c0001t0003g0225 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.697-170_697-169ins others(13): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
T | TATATATA others(10): Show |
1 | a0001c0001t0003g0159 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.697-170_697-169ins others(17): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
T | TTA | 25 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0031others(22): Show | 25 | HG00673.hp1 HG01099.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.697-171_697-170dup others(2): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
T | TTATA | 20 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0041others(17): Show | 20 | HG00673.hp2 HG01071.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.697-173_697-170dup others(4): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
T | TTATATA | 21 | a0001c0001t0001g0047a0001c0001t0001g0055a0001c0001t0001g0152others(18): Show | 21 | HG00597.hp1 HG00642.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.697-175_697-170dup others(6): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
T | TTATATAT others(1): Show |
6 | a0001c0001t0001g0020a0001c0001t0001g0134a0001c0001t0001g0169others(3): Show | 6 | HG00609.hp1 HG02523.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.697-177_697-170dup others(8): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
T | TTATATAT others(3): Show |
14 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0034others(11): Show | 15 | HG00558.hp1 HG01175.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.697-179_697-170dup others(10): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
T | TTATATAT others(5): Show |
5 | a0001c0001t0001g0146a0001c0001t0001g0184a0001c0001t0002g0120others(2): Show | 5 | HG02129.hp2 HG03834.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.697-181_697-170dup others(12): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
T | TTATATAT others(7): Show |
3 | a0001c0001t0001g0048a0001c0001t0003g0057a0001c0001t0003g0098 | 3 | HG01069.hp2 NA18983.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.697-183_697-170dup others(14): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
T | TTATATAT others(9): Show |
2 | a0001c0001t0015g0204a0001c0001t0037g0329 | 2 | HG01884.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.697-185_697-170dup others(16): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
T | TTATATAT others(11): Show |
1 | a0001c0001t0003g0226 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.697-187_697-170dup others(18): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
TTA | T | 23 | a0001c0001t0001g0024a0001c0001t0001g0038a0001c0001t0001g0045others(20): Show | 24 | HG01358.hp1 HG01515.hp2 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.697-171_697-170del others(2): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
TTATA | T | 20 | a0001c0001t0001g0017a0001c0001t0001g0052a0001c0001t0001g0170others(17): Show | 20 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.697-173_697-170del others(4): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
TTATATA | T | 12 | a0001c0001t0001g0029a0001c0001t0001g0149a0001c0001t0001g0277others(9): Show | 12 | HG01168.hp2 HG02145.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.697-175_697-170del others(6): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
TTATATAT others(1): Show |
T | 9 | a0001c0001t0001g0049a0001c0001t0001g0162a0001c0001t0001g0173others(6): Show | 9 | HG01074.hp2 HG02055.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.697-177_697-170del others(8): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
TTATATAT others(3): Show |
T | 18 | a0001c0001t0001g0039a0001c0001t0001g0133a0001c0001t0001g0135others(15): Show | 19 | HG01109.hp2 HG02080.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.697-179_697-170del others(10): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
TTATATAT others(5): Show |
T | 9 | a0001c0001t0001g0249a0001c0001t0002g0005a0001c0001t0002g0126others(6): Show | 10 | HG01516.hp2 HG01891.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.697-181_697-170del others(12): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
TTATATAT others(7): Show |
T | 11 | a0001c0001t0001g0050a0001c0001t0001g0185a0001c0001t0001g0263others(8): Show | 11 | HG00438.hp1 HG01261.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.697-183_697-170del others(14): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
TTATATAT others(9): Show |
T | 7 | a0001c0001t0001g0156a0001c0001t0002g0109a0001c0001t0002g0138others(4): Show | 7 | HG00544.hp2 HG00558.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.697-185_697-170del others(16): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
TTATATAT others(11): Show |
T | 4 | a0001c0001t0001g0181a0001c0001t0002g0130a0001c0001t0002g0260others(1): Show | 4 | HG02559.hp2 HG03516.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.697-187_697-170del others(18): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
TTATATAT others(13): Show |
T | 5 | a0001c0001t0001g0193a0001c0001t0002g0257a0001c0001t0005g0315others(2): Show | 5 | HG01255.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.697-189_697-170del others(20): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
TTATATAT others(15): Show |
T | 11 | a0001c0001t0002g0119a0001c0001t0002g0121a0001c0001t0002g0129others(8): Show | 12 | HG00099.hp1 HG00733.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.697-191_697-170del others(22): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
TTATATAT others(17): Show |
T | 18 | a0001c0001t0002g0001a0001c0001t0002g0110a0001c0001t0002g0118others(15): Show | 19 | HG00099.hp2 HG00323.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.697-193_697-170del others(24): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
TTATATAT others(21): Show |
T | 6 | a0001c0001t0001g0148a0001c0001t0002g0108a0001c0001t0002g0116others(3): Show | 6 | HG00280.hp1 HG03490.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.697-197_697-170del others(28): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
TTATATAT others(23): Show |
T | 1 | a0001c0001t0004g0081 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.697-199_697-170del others(30): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
TTATATAT others(25): Show |
T | 6 | a0001c0001t0001g0028a0001c0001t0003g0091a0001c0001t0004g0080others(3): Show | 6 | HG01256.hp2 HG01346.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.697-201_697-170del others(32): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
TTATATAT others(27): Show |
T | 21 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(18): Show | 22 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.697-203_697-170del others(34): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
TTATATAT others(29): Show |
T | 3 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0177 | 3 | NA18995.hp2 NA19012.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.697-205_697-170del others(36): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
TTATATAT others(31): Show |
T | 1 | a0001c0001t0001g0259 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.697-207_697-170del others(38): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
TTATATAT others(33): Show |
T | 2 | a0001c0004t0006g0231a0001c0004t0006g0232 | 2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.697-209_697-170del others(40): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94465968
|
TTATATAT others(35): Show |
T | 1 | a0009c0014t0001g0306 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.697-211_697-170del others(42): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94465968 | ||||||
chr13:94466012
|
ATAT | A | 3 | a0001c0001t0002g0105a0001c0001t0002g0106a0008c0009t0002g0271 | 3 | HG03669.hp1 HG03688.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.697-216_697-214del others(3): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94466012 | ||||||
chr13:94466016
|
A | C | 6 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(3): Show | 6 | HG02602.hp1 HG02683.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.697-217T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94466016 | ||||||
chr13:94466103
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.697-304A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94466103 | ||||||
chr13:94466352
|
G | C | 30 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(27): Show | 31 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.696+206C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94466352 | ||||||
chr13:94466481
|
T | C | 38 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(35): Show | 40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.696+77A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94466481 | ||||||
chr13:94466487
|
C | T | 38 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(35): Show | 40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.696+71G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 3/7 | chr13 | 94466487 | ||||||
chr13:94466753
|
A | G | 23 | a0001c0001t0005g0007a0001c0001t0005g0308a0001c0001t0005g0309others(20): Show | 24 | HG01109.hp2 HG01346.hp2 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.596-95T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94466753 | ||||||
chr13:94466755
|
G | T | 1 | a0001c0001t0003g0061 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.596-97C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94466755 | ||||||
chr13:94466839
|
A | G | 1 | a0001c0001t0002g0281 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.596-181T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94466839 | ||||||
chr13:94466938
|
A | C | 1 | a0001c0001t0031g0144 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.596-280T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94466938 | ||||||
chr13:94466959
|
A | C | 1 | a0001c0001t0002g0254 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.596-301T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94466959 | ||||||
chr13:94466964
|
T | C | 23 | a0001c0001t0005g0007a0001c0001t0005g0308a0001c0001t0005g0309others(20): Show | 24 | HG01109.hp2 HG01346.hp2 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.596-306A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94466964 | ||||||
chr13:94467000
|
T | A | 1 | a0001c0001t0001g0135 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.596-342A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94467000 | ||||||
chr13:94467015
|
G | T | 84 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(81): Show | 87 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.596-357C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94467015 | ||||||
chr13:94467173
|
A | G | 38 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(35): Show | 40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.596-515T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94467173 | ||||||
chr13:94467355
|
GT | G | 4 | a0001c0001t0010g0283a0001c0001t0010g0284a0001c0001t0010g0285others(1): Show | 4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.596-698delA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94467355 | ||||||
chr13:94467491
|
G | C | 4 | a0001c0001t0010g0283a0001c0001t0010g0284a0001c0001t0010g0285others(1): Show | 4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.596-833C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94467491 | ||||||
chr13:94467525
|
A | G | 1 | a0001c0001t0006g0088 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.596-867T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94467525 | ||||||
chr13:94467531
|
G | A | 22 | a0001c0001t0005g0007a0001c0001t0005g0308a0001c0001t0005g0309others(19): Show | 23 | HG01109.hp2 HG01346.hp2 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.596-873C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94467531 | ||||||
chr13:94467861
|
C | T | 4 | a0001c0001t0010g0283a0001c0001t0010g0284a0001c0001t0010g0285others(1): Show | 4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.595+885G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94467861 | ||||||
chr13:94467964
|
A | C | 61 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0002g0108others(58): Show | 62 | HG00280.hp1 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.595+782T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94467964 | ||||||
chr13:94467987
|
T | C | 6 | a0001c0001t0011g0103a0001c0001t0011g0238a0001c0001t0011g0239others(3): Show | 6 | HG01884.hp1 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.595+759A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94467987 | ||||||
chr13:94468070
|
A | G | 24 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(21): Show | 25 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.595+676T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94468070 | ||||||
chr13:94468190
|
G | A | 6 | a0001c0001t0011g0103a0001c0001t0011g0238a0001c0001t0011g0239others(3): Show | 6 | HG01884.hp1 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.595+556C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94468190 | ||||||
chr13:94468239
|
T | C | 20 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0290others(17): Show | 20 | HG01243.hp2 HG02145.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.595+507A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94468239 | ||||||
chr13:94468409
|
T | A | 61 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0002g0108others(58): Show | 62 | HG00280.hp1 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.595+337A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94468409 | ||||||
chr13:94468425
|
T | C | 4 | a0001c0001t0010g0283a0001c0001t0010g0284a0001c0001t0010g0285others(1): Show | 4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.595+321A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94468425 | ||||||
chr13:94468452
|
C | T | 4 | a0001c0001t0010g0283a0001c0001t0010g0284a0001c0001t0010g0285others(1): Show | 4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.595+294G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94468452 | ||||||
chr13:94468493
|
G | A | 1 | a0001c0001t0008g0143 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.595+253C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94468493 | ||||||
chr13:94468597
|
GTA | G | 6 | a0001c0001t0011g0103a0001c0001t0011g0238a0001c0001t0011g0239others(3): Show | 6 | HG01884.hp1 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.595+147_595+148del others(2): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 2/7 | chr13 | 94468597 | ||||||
chr13:94469180
|
C | T | 1 | a0001c0001t0004g0072 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.296-135G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94469180 | ||||||
chr13:94469234
|
G | A | 30 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(27): Show | 31 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.296-189C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94469234 | ||||||
chr13:94469369
|
A | G | 2 | a0001c0001t0001g0184a0001c0001t0022g0160 | 2 | HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.296-324T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94469369 | ||||||
chr13:94469388
|
T | C | 22 | a0001c0001t0005g0007a0001c0001t0005g0308a0001c0001t0005g0309others(19): Show | 23 | HG01109.hp2 HG01346.hp2 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.296-343A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94469388 | ||||||
chr13:94469544
|
T | A | 8 | a0001c0001t0009g0295a0001c0001t0009g0301a0001c0001t0009g0303others(5): Show | 8 | HG01243.hp2 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.296-499A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94469544 | ||||||
chr13:94469625
|
G | A | 8 | a0001c0001t0006g0141a0001c0001t0008g0002a0001c0001t0008g0012others(5): Show | 9 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.296-580C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94469625 | ||||||
chr13:94469692
|
C | T | 23 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0073others(20): Show | 24 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.296-647G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94469692 | ||||||
chr13:94469741
|
G | C | 1 | a0001c0001t0019g0300 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.296-696C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94469741 | ||||||
chr13:94469791
|
A | G | 1 | a0001c0001t0002g0122 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.296-746T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94469791 | ||||||
chr13:94469803
|
G | A | 3 | a0001c0001t0009g0295a0001c0001t0009g0304a0001c0001t0009g0305 | 3 | HG02280.hp2 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.296-758C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94469803 | ||||||
chr13:94470416
|
G | A | 1 | a0006c0013t0001g0021 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.296-1371C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94470416 | ||||||
chr13:94470662
|
T | G | 42 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(39): Show | 44 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.296-1617A>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94470662 | ||||||
chr13:94470677
|
C | T | 1 | a0009c0014t0001g0306 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.296-1632G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94470677 | ||||||
chr13:94470733
|
T | C | 1 | a0001c0001t0001g0053 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.296-1688A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94470733 | ||||||
chr13:94470911
|
G | T | 8 | a0001c0001t0006g0141a0001c0001t0008g0002a0001c0001t0008g0012others(5): Show | 9 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.296-1866C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94470911 | ||||||
chr13:94470936
|
C | T | 38 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(35): Show | 39 | HG00597.hp2 HG00621.hp2 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.296-1891G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94470936 | ||||||
chr13:94470972
|
A | G | 23 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(20): Show | 24 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.296-1927T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94470972 | ||||||
chr13:94471132
|
GAAAGGAA others(16): Show |
G | 1 | a0001c0001t0002g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.296-2110_296-2088d others(25): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94471132 | ||||||
chr13:94471227
|
T | C | 4 | a0001c0001t0010g0283a0001c0001t0010g0284a0001c0001t0010g0285others(1): Show | 4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-2182A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94471227 | ||||||
chr13:94471259
|
G | A | 1 | a0001c0001t0019g0300 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.296-2214C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94471259 | ||||||
chr13:94471296
|
T | C | 1 | a0001c0001t0013g0036 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.296-2251A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94471296 | ||||||
chr13:94471392
|
T | C | 18 | a0001c0001t0006g0141a0001c0001t0008g0002a0001c0001t0008g0012others(15): Show | 19 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.296-2347A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94471392 | ||||||
chr13:94471413
|
C | T | 23 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0073others(20): Show | 24 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.296-2368G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94471413 | ||||||
chr13:94471548
|
A | T | 4 | a0001c0001t0010g0283a0001c0001t0010g0284a0001c0001t0010g0285others(1): Show | 4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-2503T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94471548 | ||||||
chr13:94471663
|
C | T | 38 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(35): Show | 40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.296-2618G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94471663 | ||||||
chr13:94472259
|
A | G | 3 | a0001c0001t0003g0087a0001c0001t0003g0090a0001c0001t0023g0215 | 3 | NA18970.hp1 NA19064.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.296-3214T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472259 | ||||||
chr13:94472513
|
CATACATA others(7): Show |
C | 1 | a0001c0012t0002g0250 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.296-3482_296-3469d others(16): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472513 | ||||||
chr13:94472517
|
C | T | 42 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(39): Show | 44 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.296-3472G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472517 | ||||||
chr13:94472517
|
CATACATA others(1): Show |
C | 3 | a0001c0001t0005g0321a0001c0001t0005g0322a0001c0001t0005g0323 | 3 | HG01884.hp2 HG02145.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.296-3480_296-3473d others(10): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472517 | ||||||
chr13:94472517
|
CATACATA others(3): Show |
C | 3 | a0001c0001t0002g0112a0001c0001t0005g0007a0001c0001t0034g0312 | 4 | HG02055.hp2 HG02257.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-3482_296-3473d others(12): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472517 | ||||||
chr13:94472517
|
CATACATA others(5): Show |
C | 3 | a0001c0001t0005g0313a0001c0001t0005g0316a0001c0001t0027g0113 | 3 | HG00140.hp2 HG02647.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.296-3484_296-3473d others(14): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472517 | ||||||
chr13:94472517
|
CATACATA others(7): Show |
C | 1 | a0001c0001t0005g0318 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.296-3486_296-3473d others(16): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472517 | ||||||
chr13:94472517
|
CATACATA others(11): Show |
C | 1 | a0001c0001t0018g0114 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.296-3490_296-3473d others(20): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472517 | ||||||
chr13:94472517
|
CATACATA others(25): Show |
C | 1 | a0001c0001t0002g0252 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.296-3504_296-3473d others(34): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472517 | ||||||
chr13:94472521
|
C | T | 127 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(124): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.296-3476G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472521 | ||||||
chr13:94472521
|
CAT | C | 5 | a0001c0001t0001g0037a0001c0001t0001g0170a0001c0001t0001g0171others(2): Show | 5 | HG00621.hp1 HG01255.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.296-3478_296-3477d others(4): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472521 | ||||||
chr13:94472521
|
CATATAT | C | 4 | a0001c0001t0001g0038a0001c0001t0001g0156a0001c0001t0005g0319others(1): Show | 4 | HG00558.hp2 HG01358.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-3482_296-3477d others(8): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472521 | ||||||
chr13:94472521
|
CATATATA others(3): Show |
C | 3 | a0001c0001t0001g0023a0001c0001t0003g0057a0001c0001t0003g0172 | 3 | HG01069.hp2 HG03710.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.296-3486_296-3477d others(12): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472521 | ||||||
chr13:94472521
|
CATATATA others(5): Show |
C | 2 | a0001c0001t0001g0053a0001c0001t0001g0193 | 2 | NA19030.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.296-3488_296-3477d others(14): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472521 | ||||||
chr13:94472521
|
CATATATA others(15): Show |
C | 2 | a0001c0001t0006g0083a0001c0001t0007g0213 | 2 | HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.296-3498_296-3477d others(24): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472521 | ||||||
chr13:94472521
|
CATATATA others(17): Show |
C | 1 | a0001c0001t0007g0084 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.296-3500_296-3477d others(26): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472521 | ||||||
chr13:94472523
|
T | C | 1 | a0001c0004t0006g0232 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.296-3478A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472523 | ||||||
chr13:94472525
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.296-3480A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472525 | ||||||
chr13:94472532
|
ATATATAT others(36): Show |
A | 4 | a0001c0003t0004g0100a0001c0003t0004g0234a0001c0003t0004g0235others(1): Show | 4 | HG02559.hp1 HG02818.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.296-3530_296-3488d others(45): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472532 | ||||||
chr13:94472532
|
ATATATAT others(37): Show |
A | 1 | a0001c0001t0004g0073 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.296-3531_296-3488d others(46): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472532 | ||||||
chr13:94472533
|
TATATATA others(28): Show |
T | 1 | a0001c0001t0005g0324 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.296-3523_296-3489d others(37): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472533 | ||||||
chr13:94472534
|
ATATATAT others(28): Show |
A | 1 | a0001c0001t0005g0314 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.296-3524_296-3490d others(37): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472534 | ||||||
chr13:94472534
|
ATATATAT others(32): Show |
A | 1 | a0001c0001t0029g0280 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.296-3528_296-3490d others(41): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472534 | ||||||
chr13:94472534
|
ATATATAT others(34): Show |
A | 1 | a0001c0001t0004g0071 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.296-3530_296-3490d others(43): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472534 | ||||||
chr13:94472534
|
ATATATAT others(35): Show |
A | 1 | a0001c0001t0004g0072 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.296-3531_296-3490d others(44): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472534 | ||||||
chr13:94472534
|
ATATATAT others(36): Show |
A | 1 | a0001c0001t0004g0208 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.296-3532_296-3490d others(45): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472534 | ||||||
chr13:94472534
|
ATATATAT others(37): Show |
A | 15 | a0001c0001t0004g0006a0001c0001t0004g0074a0001c0001t0004g0075others(12): Show | 16 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(13): Show |
intron_variant | MODIFIER | c.296-3533_296-3490d others(46): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472534 | ||||||
chr13:94472536
|
ATATATAT others(27): Show |
A | 1 | a0001c0001t0019g0300 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.296-3525_296-3492d others(36): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472536 | ||||||
chr13:94472536
|
ATATATAT others(29): Show |
A | 1 | a0001c0001t0001g0249 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.296-3527_296-3492d others(38): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472536 | ||||||
chr13:94472536
|
ATATATAT others(30): Show |
A | 21 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(18): Show | 22 | HG00438.hp1 HG00544.hp2 HG01943.hp1 others(19): Show |
intron_variant | MODIFIER | c.296-3528_296-3492d others(39): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472536 | ||||||
chr13:94472536
|
ATATATAT others(33): Show |
A | 4 | a0001c0001t0006g0141a0001c0001t0008g0002a0001c0001t0008g0140others(1): Show | 5 | HG02486.hp2 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.296-3531_296-3492d others(42): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472536 | ||||||
chr13:94472536
|
ATATATAT others(34): Show |
A | 2 | a0001c0001t0008g0013a0001c0001t0008g0014 | 2 | HG01981.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.296-3532_296-3492d others(43): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472536 | ||||||
chr13:94472536
|
ATATATAT others(36): Show |
A | 5 | a0001c0001t0011g0103a0001c0001t0011g0238a0001c0001t0011g0239others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.296-3534_296-3492d others(45): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472536 | ||||||
chr13:94472536
|
ATATATAT others(37): Show |
A | 1 | a0001c0001t0004g0212 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.296-3535_296-3492d others(46): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472536 | ||||||
chr13:94472538
|
ATATATAT others(26): Show |
A | 1 | a0001c0001t0002g0254 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.296-3526_296-3494d others(35): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472538 | ||||||
chr13:94472538
|
ATATATAT others(29): Show |
A | 1 | a0001c0001t0001g0155 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.296-3529_296-3494d others(38): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472538 | ||||||
chr13:94472538
|
ATATATAT others(30): Show |
A | 1 | a0001c0001t0002g0132 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.296-3530_296-3494d others(39): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472538 | ||||||
chr13:94472538
|
ATATATAT others(32): Show |
A | 1 | a0001c0001t0008g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.296-3532_296-3494d others(41): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472538 | ||||||
chr13:94472538
|
ATATATAT others(36): Show |
A | 1 | a0001c0001t0015g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.296-3536_296-3494d others(45): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472538 | ||||||
chr13:94472540
|
ATATATAT others(24): Show |
A | 1 | a0001c0001t0003g0216 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.296-3526_296-3496d others(33): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472540 | ||||||
chr13:94472540
|
ATATATAT others(26): Show |
A | 1 | a0001c0001t0002g0128 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.296-3528_296-3496d others(35): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472540 | ||||||
chr13:94472542
|
ATATATAT others(23): Show |
A | 3 | a0001c0001t0003g0217a0001c0001t0006g0205a0001c0001t0012g0089 | 3 | HG02615.hp2 NA18978.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.296-3527_296-3498d others(32): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472542 | ||||||
chr13:94472542
|
ATATATAT others(24): Show |
A | 22 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(19): Show | 23 | HG00597.hp2 HG00621.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.296-3528_296-3498d others(33): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472542 | ||||||
chr13:94472542
|
ATATATAT others(25): Show |
A | 2 | a0001c0001t0003g0227a0001c0001t0003g0282 | 2 | HG01168.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.296-3529_296-3498d others(34): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472542 | ||||||
chr13:94472542
|
ATATATAT others(26): Show |
A | 1 | a0001c0001t0020g0279 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.296-3530_296-3498d others(35): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472542 | ||||||
chr13:94472542
|
ATATATAT others(30): Show |
A | 1 | a0001c0001t0008g0143 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.296-3534_296-3498d others(39): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472542 | ||||||
chr13:94472544
|
ATATATAT others(18): Show |
A | 1 | a0001c0001t0006g0011 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.296-3524_296-3500d others(27): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472544 | ||||||
chr13:94472544
|
ATATATAT others(22): Show |
A | 1 | a0001c0001t0003g0200 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.296-3528_296-3500d others(31): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472544 | ||||||
chr13:94472544
|
ATATATAT others(23): Show |
A | 2 | a0001c0001t0003g0201a0001c0001t0003g0207 | 2 | HG04199.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.296-3529_296-3500d others(32): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472544 | ||||||
chr13:94472544
|
ATATATAT others(24): Show |
A | 5 | a0001c0001t0003g0087a0001c0001t0006g0088a0001c0001t0014g0099others(2): Show | 5 | HG03490.hp1 HG03492.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.296-3530_296-3500d others(33): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472544 | ||||||
chr13:94472544
|
ATATATAT others(25): Show |
A | 1 | a0001c0001t0006g0145 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.296-3531_296-3500d others(34): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472544 | ||||||
chr13:94472546
|
ATATATAT others(16): Show |
A | 5 | a0001c0001t0007g0085a0001c0001t0007g0086a0001c0001t0007g0214others(2): Show | 5 | HG02622.hp2 HG02717.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.296-3524_296-3502d others(25): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472546 | ||||||
chr13:94472546
|
ATATATAT others(23): Show |
A | 1 | a0001c0001t0003g0229 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.296-3531_296-3502d others(32): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472546 | ||||||
chr13:94472546
|
ATATATAT others(24): Show |
A | 1 | a0001c0001t0023g0215 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.296-3532_296-3502d others(33): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472546 | ||||||
chr13:94472548
|
ATATATAT others(16): Show |
A | 1 | a0001c0004t0006g0231 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.296-3526_296-3504d others(25): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472548 | ||||||
chr13:94472548
|
ATATATAT others(19): Show |
A | 1 | a0001c0001t0006g0240 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.296-3529_296-3504d others(28): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472548 | ||||||
chr13:94472548
|
ATATATAT others(27): Show |
A | 2 | a0001c0001t0010g0284a0001c0001t0010g0286 | 2 | HG01256.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.296-3537_296-3504d others(36): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472548 | ||||||
chr13:94472550
|
ATATATAT others(13): Show |
A | 2 | a0001c0001t0001g0020a0001c0001t0001g0178 | 2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.296-3525_296-3506d others(22): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472550 | ||||||
chr13:94472550
|
ATATATAT others(14): Show |
A | 1 | a0001c0004t0006g0232 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.296-3526_296-3506d others(23): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472550 | ||||||
chr13:94472551
|
TATATATA others(8): Show |
T | 1 | a0001c0001t0005g0317 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.296-3521_296-3507d others(17): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472551 | ||||||
chr13:94472551
|
TATATATA others(10): Show |
T | 1 | a0001c0001t0002g0278 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.296-3523_296-3507d others(19): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472551 | ||||||
chr13:94472552
|
ATATATAT others(13): Show |
A | 1 | a0001c0001t0001g0048 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.296-3527_296-3508d others(22): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472552 | ||||||
chr13:94472552
|
ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0019 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.296-3528_296-3508d others(23): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472552 | ||||||
chr13:94472552
|
ATATATAT others(15): Show |
A | 1 | a0001c0001t0002g0245 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.296-3529_296-3508d others(24): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472552 | ||||||
chr13:94472553
|
TATATATA others(6): Show |
T | 1 | a0001c0001t0005g0310 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.296-3521_296-3509d others(15): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472553 | ||||||
chr13:94472553
|
TATATATA others(8): Show |
T | 1 | a0001c0001t0002g0111 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.296-3523_296-3509d others(17): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472553 | ||||||
chr13:94472554
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0002g0253 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.296-3526_296-3510d others(19): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472554 | ||||||
chr13:94472554
|
ATATATAT others(12): Show |
A | 1 | a0001c0001t0001g0050 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.296-3528_296-3510d others(21): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472554 | ||||||
chr13:94472554
|
ATATATAT others(13): Show |
A | 2 | a0001c0001t0001g0149a0001c0001t0001g0186 | 2 | HG01993.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.296-3529_296-3510d others(22): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472554 | ||||||
chr13:94472555
|
TATATATA others(4): Show |
T | 2 | a0001c0001t0035g0320a0003c0005t0016g0302 | 2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.296-3521_296-3511d others(13): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472555 | ||||||
chr13:94472556
|
ATATATAT others(6): Show |
A | 3 | a0001c0001t0002g0136a0001c0001t0002g0251a0001c0001t0005g0326 | 3 | HG00099.hp2 HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.296-3524_296-3512d others(15): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472556 | ||||||
chr13:94472556
|
ATATATAT others(7): Show |
A | 2 | a0001c0001t0006g0010a0001c0001t0017g0192 | 2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.296-3525_296-3512d others(16): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472556 | ||||||
chr13:94472556
|
ATATATAT others(10): Show |
A | 6 | a0001c0001t0001g0152a0001c0001t0001g0185a0001c0001t0002g0125others(3): Show | 6 | HG01261.hp1 HG03139.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.296-3528_296-3512d others(19): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472556 | ||||||
chr13:94472556
|
ATATATAT others(11): Show |
A | 3 | a0001c0001t0002g0130a0001c0001t0002g0139a0001c0001t0002g0281 | 3 | HG02559.hp2 HG02809.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.296-3529_296-3512d others(20): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472556 | ||||||
chr13:94472556
|
ATATATAT others(12): Show |
A | 3 | a0001c0001t0002g0104a0001c0001t0002g0243a0001c0001t0002g0274 | 3 | HG01109.hp1 HG02683.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.296-3530_296-3512d others(21): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472556 | ||||||
chr13:94472556
|
ATATATAT others(16): Show |
A | 1 | a0001c0001t0001g0052 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.296-3534_296-3512d others(25): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472556 | ||||||
chr13:94472556
|
ATATATAT others(22): Show |
A | 1 | a0001c0001t0010g0283 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.296-3540_296-3512d others(31): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472556 | ||||||
chr13:94472556
|
ATATATAT others(23): Show |
A | 1 | a0001c0001t0010g0285 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.296-3541_296-3512d others(32): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472556 | ||||||
chr13:94472557
|
TATATATA others(4): Show |
T | 3 | a0001c0001t0005g0315a0001c0001t0005g0325a0001c0001t0006g0009 | 3 | HG01891.hp2 HG02896.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.296-3523_296-3513d others(13): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472557 | ||||||
chr13:94472558
|
ATATATAT others(5): Show |
A | 2 | a0001c0001t0003g0070a0001c0001t0003g0102 | 2 | HG00438.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.296-3525_296-3514d others(14): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472558 | ||||||
chr13:94472558
|
ATATATAT others(6): Show |
A | 1 | a0001c0001t0003g0042 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.296-3526_296-3514d others(15): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472558 | ||||||
chr13:94472558
|
ATATATAT others(7): Show |
A | 1 | a0001c0001t0001g0184 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.296-3527_296-3514d others(16): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472558 | ||||||
chr13:94472558
|
ATATATAT others(8): Show |
A | 5 | a0001c0001t0001g0259a0001c0001t0002g0107a0001c0001t0002g0122others(2): Show | 5 | HG01123.hp1 HG02451.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.296-3528_296-3514d others(17): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472558 | ||||||
chr13:94472558
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0002g0273 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.296-3530_296-3514d others(19): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472558 | ||||||
chr13:94472558
|
ATATATAT others(12): Show |
A | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.296-3532_296-3514d others(21): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472558 | ||||||
chr13:94472559
|
TATATATA others(2): Show |
T | 7 | a0001c0001t0001g0017a0001c0001t0003g0026a0001c0001t0003g0159others(4): Show | 7 | HG01071.hp2 HG01099.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.296-3523_296-3515d others(11): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472559 | ||||||
chr13:94472560
|
ATATATAT others(3): Show |
A | 1 | a0001c0001t0001g0177 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.296-3525_296-3516d others(12): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472560 | ||||||
chr13:94472560
|
ATATATAT others(4): Show |
A | 2 | a0001c0001t0002g0115a0001c0001t0002g0116 | 2 | HG03490.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.296-3526_296-3516d others(13): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472560 | ||||||
chr13:94472560
|
ATATATAT others(5): Show |
A | 2 | a0001c0001t0001g0047a0001c0001t0002g0118 | 2 | HG01257.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.296-3527_296-3516d others(14): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472560 | ||||||
chr13:94472560
|
ATATATAT others(6): Show |
A | 1 | a0001c0001t0002g0258 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.296-3528_296-3516d others(15): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472560 | ||||||
chr13:94472560
|
ATATATAT others(7): Show |
A | 2 | a0001c0001t0002g0110a0008c0009t0002g0271 | 2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.296-3529_296-3516d others(16): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472560 | ||||||
chr13:94472561
|
TATATATA | T | 3 | a0001c0001t0001g0025a0001c0001t0005g0309a0001c0001t0005g0311 | 3 | HG01109.hp2 HG01358.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.296-3523_296-3517d others(9): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472561 | ||||||
chr13:94472562
|
A | T | 2 | a0001c0001t0007g0196a0001c0001t0007g0197 | 2 | HG01192.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.296-3517T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472562 | ||||||
chr13:94472562
|
ATATATAT others(3): Show |
A | 4 | a0001c0001t0002g0255a0001c0001t0003g0195a0001c0001t0013g0044others(1): Show | 4 | HG00280.hp1 NA18963.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-3527_296-3518d others(12): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472562 | ||||||
chr13:94472562
|
ATATATAT others(4): Show |
A | 5 | a0001c0001t0001g0016a0001c0001t0002g0108a0001c0001t0002g0121others(2): Show | 5 | HG00099.hp1 HG01255.hp2 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.296-3528_296-3518d others(13): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472562 | ||||||
chr13:94472562
|
ATATATAT others(5): Show |
A | 2 | a0001c0001t0002g0129a0001c0001t0002g0270 | 2 | HG02293.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.296-3529_296-3518d others(14): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472562 | ||||||
chr13:94472564
|
A | T | 3 | a0001c0001t0007g0196a0001c0001t0007g0197a0001c0001t0030g0291 | 3 | HG01192.hp1 HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.296-3519T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472564 | ||||||
chr13:94472564
|
ATATATTT others(2): Show |
A | 8 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0066others(5): Show | 8 | HG00673.hp1 HG00741.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.296-3528_296-3520d others(11): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472564 | ||||||
chr13:94472564
|
ATATATTT others(3): Show |
A | 2 | a0001c0001t0002g0001a0001c0001t0002g0269 | 3 | HG01516.hp1 HG01517.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.296-3529_296-3520d others(12): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472564 | ||||||
chr13:94472564
|
ATATATTT others(4): Show |
A | 3 | a0001c0001t0001g0187a0001c0001t0002g0131a0001c0001t0002g0272 | 3 | HG00733.hp2 HG03239.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.296-3530_296-3520d others(13): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472564 | ||||||
chr13:94472564
|
ATATATTT others(5): Show |
A | 1 | a0001c0001t0001g0188 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.296-3531_296-3520d others(14): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472564 | ||||||
chr13:94472566
|
A | T | 5 | a0001c0001t0007g0196a0001c0001t0007g0197a0001c0001t0007g0198others(2): Show | 5 | HG01192.hp1 HG01243.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.296-3521T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472566 | ||||||
chr13:94472566
|
ATATTTT | A | 7 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0147others(4): Show | 7 | HG03688.hp1 NA18747.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.296-3527_296-3522d others(8): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472566 | ||||||
chr13:94472566
|
ATATTTTT others(4): Show |
A | 1 | a0001c0001t0033g0153 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.296-3532_296-3522d others(13): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472566 | ||||||
chr13:94472566
|
ATATTTTT others(5): Show |
A | 1 | a0001c0001t0001g0154 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.296-3533_296-3522d others(14): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472566 | ||||||
chr13:94472567
|
TA | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0059a0001c0001t0006g0292others(1): Show | 4 | HG01928.hp2 HG01975.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.296-3523delT | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472567 | ||||||
chr13:94472568
|
A | T | 27 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0053others(24): Show | 28 | HG01192.hp1 HG01243.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.296-3523T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472568 | ||||||
chr13:94472568
|
ATT | A | 8 | a0001c0001t0001g0018a0001c0001t0001g0039a0001c0001t0001g0043others(5): Show | 8 | HG01496.hp1 HG03942.hp1 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.296-3525_296-3524d others(4): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472568 | ||||||
chr13:94472568
|
ATTT | A | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0179others(4): Show | 7 | HG00544.hp1 HG00609.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.296-3526_296-3524d others(5): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472568 | ||||||
chr13:94472568
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0189 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.296-3533_296-3524d others(12): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472568 | ||||||
chr13:94472570
|
T | A | 7 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0002g0112others(4): Show | 7 | HG00140.hp2 HG01175.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.296-3525A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472570 | ||||||
chr13:94472572
|
T | A | 4 | a0001c0001t0001g0043a0001c0001t0001g0148a0001c0001t0001g0151others(1): Show | 4 | HG01496.hp1 NA18959.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.296-3527A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472572 | ||||||
chr13:94472573
|
T | A | 2 | a0001c0001t0003g0065a0004c0006t0001g0008 | 2 | HG00544.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.296-3528A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472573 | ||||||
chr13:94472574
|
T | A | 1 | a0001c0001t0032g0051 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.296-3529A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472574 | ||||||
chr13:94472575
|
T | A | 1 | a0001c0001t0003g0065 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.296-3530A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472575 | ||||||
chr13:94472601
|
C | G | 1 | a0001c0001t0006g0088 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.296-3556G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472601 | ||||||
chr13:94472642
|
C | T | 2 | a0001c0001t0002g0246a0001c0001t0006g0083 | 2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.296-3597G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472642 | ||||||
chr13:94472660
|
C | T | 30 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(27): Show | 31 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.296-3615G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472660 | ||||||
chr13:94472676
|
G | A | 7 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(4): Show | 7 | HG02074.hp2 HG02080.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.296-3631C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472676 | ||||||
chr13:94472724
|
G | C | 2 | a0001c0001t0006g0009a0001c0001t0006g0010 | 2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.296-3679C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472724 | ||||||
chr13:94472725
|
G | A | 8 | a0001c0001t0006g0141a0001c0001t0008g0002a0001c0001t0008g0012others(5): Show | 9 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.296-3680C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472725 | ||||||
chr13:94472750
|
T | G | 51 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(48): Show | 52 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.296-3705A>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472750 | ||||||
chr13:94472835
|
G | A | 4 | a0001c0001t0010g0283a0001c0001t0010g0284a0001c0001t0010g0285others(1): Show | 4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-3790C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94472835 | ||||||
chr13:94473004
|
C | T | 4 | a0001c0001t0010g0283a0001c0001t0010g0284a0001c0001t0010g0285others(1): Show | 4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-3959G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473004 | ||||||
chr13:94473006
|
T | A | 1 | a0001c0001t0006g0240 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.296-3961A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473006 | ||||||
chr13:94473033
|
A | T | 1 | a0001c0001t0023g0215 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.296-3988T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473033 | ||||||
chr13:94473155
|
T | C | 2 | a0001c0001t0011g0238a0001c0001t0011g0239 | 2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.296-4110A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473155 | ||||||
chr13:94473223
|
G | A | 1 | a0001c0001t0029g0280 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.296-4178C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473223 | ||||||
chr13:94473265
|
A | G | 1 | a0001c0001t0002g0246 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.296-4220T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473265 | ||||||
chr13:94473520
|
G | A | 1 | a0001c0001t0011g0239 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.296-4475C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473520 | ||||||
chr13:94473627
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.296-4582G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473627 | ||||||
chr13:94473691
|
T | C | 1 | a0001c0001t0002g0278 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.296-4646A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473691 | ||||||
chr13:94473773
|
T | G | 42 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(39): Show | 44 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.296-4728A>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473773 | ||||||
chr13:94473777
|
G | C | 42 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(39): Show | 44 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.296-4732C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473777 | ||||||
chr13:94473781
|
T | G | 42 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(39): Show | 44 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.296-4736A>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473781 | ||||||
chr13:94473782
|
A | C | 1 | a0001c0001t0003g0087 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.296-4737T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473782 | ||||||
chr13:94473782
|
A | G | 42 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(39): Show | 44 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.296-4737T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94473782 | ||||||
chr13:94474016
|
T | C | 1 | a0001c0001t0010g0283 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.295+4945A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474016 | ||||||
chr13:94474099
|
T | C | 95 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(92): Show | 98 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.295+4862A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474099 | ||||||
chr13:94474115
|
G | A | 2 | a0001c0001t0014g0099a0001c0001t0014g0230 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.295+4846C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474115 | ||||||
chr13:94474258
|
GA | G | 120 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(117): Show | 123 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.295+4702delT | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474258 | ||||||
chr13:94474297
|
C | A | 38 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(35): Show | 39 | HG00597.hp2 HG00621.hp2 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.295+4664G>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474297 | ||||||
chr13:94474308
|
T | C | 3 | a0001c0001t0006g0011a0001c0001t0006g0145a0001c0001t0031g0144 | 3 | HG01891.hp1 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.295+4653A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474308 | ||||||
chr13:94474309
|
C | G | 1 | a0001c0001t0004g0233 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.295+4652G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474309 | ||||||
chr13:94474406
|
A | G | 1 | a0001c0001t0003g0082 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.295+4555T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474406 | ||||||
chr13:94474413
|
A | C | 3 | a0001c0001t0006g0011a0001c0001t0006g0145a0001c0001t0031g0144 | 3 | HG01891.hp1 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.295+4548T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474413 | ||||||
chr13:94474562
|
G | A | 7 | a0001c0001t0005g0315a0001c0001t0005g0316a0001c0001t0005g0317others(4): Show | 7 | HG01891.hp2 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.295+4399C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474562 | ||||||
chr13:94474588
|
C | T | 1 | a0001c0001t0011g0103 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.295+4373G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474588 | ||||||
chr13:94474594
|
T | C | 4 | a0001c0001t0010g0283a0001c0001t0010g0284a0001c0001t0010g0285others(1): Show | 4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.295+4367A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474594 | ||||||
chr13:94474693
|
G | A | 1 | a0001c0001t0029g0280 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.295+4268C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474693 | ||||||
chr13:94474702
|
C | T | 42 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0004g0072others(39): Show | 44 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.295+4259G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474702 | ||||||
chr13:94474848
|
G | A | 1 | a0001c0001t0020g0279 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.295+4113C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474848 | ||||||
chr13:94474892
|
G | A | 1 | a0001c0001t0019g0300 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.295+4069C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94474892 | ||||||
chr13:94475015
|
G | A | 3 | a0001c0001t0006g0011a0001c0001t0006g0145a0001c0001t0031g0144 | 3 | HG01891.hp1 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.295+3946C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475015 | ||||||
chr13:94475021
|
G | A | 1 | a0001c0001t0006g0145 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.295+3940C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475021 | ||||||
chr13:94475049
|
C | A | 2 | a0001c0004t0006g0231a0001c0004t0006g0232 | 2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.295+3912G>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475049 | ||||||
chr13:94475184
|
C | T | 1 | a0001c0001t0029g0280 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.295+3777G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475184 | ||||||
chr13:94475213
|
T | A | 6 | a0001c0001t0011g0103a0001c0001t0011g0238a0001c0001t0011g0239others(3): Show | 6 | HG01884.hp1 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.295+3748A>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475213 | ||||||
chr13:94475251
|
A | C | 1 | a0006c0013t0001g0021 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.295+3710T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475251 | ||||||
chr13:94475256
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.295+3705G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475256 | ||||||
chr13:94475282
|
C | T | 48 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(45): Show | 49 | HG00597.hp2 HG00621.hp2 HG01168.hp2 others(46): Show |
intron_variant | MODIFIER | c.295+3679G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475282 | ||||||
chr13:94475294
|
A | C | 1 | a0001c0001t0001g0156 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.295+3667T>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475294 | ||||||
chr13:94475375
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.295+3586C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475375 | ||||||
chr13:94475377
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.295+3584C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475377 | ||||||
chr13:94475503
|
G | A | 1 | a0001c0001t0008g0143 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.295+3458C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475503 | ||||||
chr13:94475978
|
G | T | 1 | a0001c0001t0001g0155 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.295+2983C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475978 | ||||||
chr13:94475981
|
G | T | 1 | a0001c0001t0002g0136 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.295+2980C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94475981 | ||||||
chr13:94476093
|
T | G | 3 | a0001c0001t0004g0101a0001c0001t0004g0211a0001c0001t0004g0212 | 3 | HG00140.hp1 HG01515.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.295+2868A>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476093 | ||||||
chr13:94476108
|
C | T | 89 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(86): Show | 92 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.295+2853G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476108 | ||||||
chr13:94476120
|
A | G | 5 | a0002c0002t0006g0287a0002c0002t0006g0288a0002c0002t0006g0296others(2): Show | 5 | HG02895.hp1 HG02897.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.295+2841T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476120 | ||||||
chr13:94476180
|
C | CT | 18 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(15): Show | 18 | HG01346.hp2 HG01884.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.295+2780dupA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476180 | ||||||
chr13:94476180
|
C | CTT | 6 | a0001c0001t0006g0141a0001c0001t0008g0002a0001c0001t0008g0012others(3): Show | 7 | HG01981.hp2 HG02486.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.295+2779_295+2780d others(4): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476180 | ||||||
chr13:94476180
|
CT | C | 71 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(68): Show | 72 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.295+2780delA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476180 | ||||||
chr13:94476180
|
CTT | C | 67 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(64): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.295+2779_295+2780d others(4): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476180 | ||||||
chr13:94476180
|
CTTT | C | 9 | a0001c0001t0002g0107a0001c0001t0002g0136a0001c0001t0002g0137others(6): Show | 9 | HG00099.hp2 HG01123.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.295+2778_295+2780d others(5): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476180 | ||||||
chr13:94476180
|
CTTTTTTT others(5): Show |
C | 4 | a0001c0001t0006g0290a0001c0001t0006g0292a0001c0001t0006g0298others(1): Show | 4 | HG02615.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.295+2769_295+2780d others(14): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476180 | ||||||
chr13:94476212
|
G | T | 4 | a0001c0001t0010g0283a0001c0001t0010g0284a0001c0001t0010g0285others(1): Show | 4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.295+2749C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476212 | ||||||
chr13:94476274
|
C | G | 119 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(116): Show | 122 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.295+2687G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476274 | ||||||
chr13:94476289
|
A | G | 1 | a0001c0001t0029g0280 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.295+2672T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476289 | ||||||
chr13:94476303
|
T | G | 3 | a0001c0001t0011g0103a0001c0001t0011g0238a0001c0001t0011g0239 | 3 | HG02572.hp1 HG02818.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.295+2658A>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476303 | ||||||
chr13:94476469
|
C | CT | 32 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0191others(29): Show | 32 | HG00438.hp2 HG01192.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.295+2491dupA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476469 | ||||||
chr13:94476469
|
CT | C | 79 | a0001c0001t0001g0059a0001c0001t0001g0133a0001c0001t0001g0134others(76): Show | 81 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.295+2491delA | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476469 | ||||||
chr13:94476514
|
T | C | 86 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(83): Show | 88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.295+2447A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476514 | ||||||
chr13:94476537
|
G | A | 1 | a0001c0001t0004g0241 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.295+2424C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476537 | ||||||
chr13:94476624
|
C | T | 1 | a0001c0001t0002g0107 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.295+2337G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476624 | ||||||
chr13:94476756
|
G | T | 23 | a0001c0001t0006g0290a0001c0001t0006g0292a0001c0001t0006g0298others(20): Show | 23 | HG01192.hp1 HG01243.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.295+2205C>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476756 | ||||||
chr13:94476831
|
G | A | 1 | a0001c0001t0029g0280 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.295+2130C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476831 | ||||||
chr13:94476880
|
G | A | 4 | a0001c0001t0010g0283a0001c0001t0010g0284a0001c0001t0010g0285others(1): Show | 4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.295+2081C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476880 | ||||||
chr13:94476899
|
C | A | 93 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(90): Show | 96 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.295+2062G>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94476899 | ||||||
chr13:94477084
|
C | G | 1 | a0001c0001t0003g0200 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.295+1877G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94477084 | ||||||
chr13:94477107
|
A | T | 4 | a0001c0001t0002g0104a0001c0001t0002g0105a0001c0001t0002g0106others(1): Show | 4 | HG02683.hp2 HG03669.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.295+1854T>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94477107 | ||||||
chr13:94477108
|
T | C | 3 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0019g0300 | 3 | HG02965.hp2 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.295+1853A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94477108 | ||||||
chr13:94477156
|
T | C | 235 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0133others(232): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.295+1805A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94477156 | ||||||
chr13:94477157
|
G | A | 5 | a0001c0001t0007g0068a0001c0001t0007g0196a0001c0001t0007g0197others(2): Show | 5 | HG01192.hp1 HG01243.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.295+1804C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94477157 | ||||||
chr13:94477181
|
T | C | 122 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(119): Show | 125 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.295+1780A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94477181 | ||||||
chr13:94477418
|
G | A | 8 | a0001c0001t0006g0141a0001c0001t0008g0002a0001c0001t0008g0012others(5): Show | 9 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.295+1543C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94477418 | ||||||
chr13:94477517
|
T | C | 1 | a0001c0003t0004g0242 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.295+1444A>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94477517 | ||||||
chr13:94477660
|
T | TA | 129 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(126): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.295+1300dupT | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94477660 | ||||||
chr13:94477660
|
T | TAA | 93 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0003g0004others(90): Show | 96 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.295+1299_295+1300d others(4): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94477660 | ||||||
chr13:94477785
|
TGAGAA | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0146a0001c0001t0001g0147others(2): Show | 5 | NA18968.hp2 NA18974.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.295+1171_295+1175d others(7): Show |
DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94477785 | ||||||
chr13:94477857
|
A | G | 3 | a0001c0001t0006g0011a0001c0001t0006g0145a0001c0001t0031g0144 | 3 | HG01891.hp1 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.295+1104T>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94477857 | ||||||
chr13:94477961
|
G | A | 8 | a0001c0001t0009g0295a0001c0001t0009g0301a0001c0001t0009g0303others(5): Show | 8 | HG01243.hp2 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.295+1000C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94477961 | ||||||
chr13:94478041
|
G | A | 78 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(75): Show | 80 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.295+920C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94478041 | ||||||
chr13:94478151
|
C | T | 8 | a0001c0001t0006g0141a0001c0001t0008g0002a0001c0001t0008g0012others(5): Show | 9 | HG01981.hp2 HG02257.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.295+810G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94478151 | ||||||
chr13:94478157
|
G | C | 1 | a0001c0001t0002g0281 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.295+804C>G | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94478157 | ||||||
chr13:94478157
|
G | GC | 168 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(165): Show | 169 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.295+803dupG | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94478157 | ||||||
chr13:94478165
|
C | G | 1 | a0001c0001t0002g0001 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.295+796G>C | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94478165 | ||||||
chr13:94478206
|
G | A | 1 | a0001c0001t0003g0282 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.295+755C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94478206 | ||||||
chr13:94478311
|
G | A | 4 | a0001c0001t0010g0283a0001c0001t0010g0284a0001c0001t0010g0285others(1): Show | 4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.295+650C>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94478311 | ||||||
chr13:94478638
|
C | T | 3 | a0001c0001t0005g0308a0001c0001t0005g0309a0001c0007t0005g0307 | 3 | HG01346.hp2 HG01358.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.295+323G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94478638 | ||||||
chr13:94478671
|
C | A | 21 | a0001c0001t0006g0009a0001c0001t0006g0010a0001c0001t0006g0290others(18): Show | 21 | HG01243.hp2 HG02145.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.295+290G>T | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94478671 | ||||||
chr13:94478743
|
C | T | 1 | a0001c0001t0006g0011 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.295+218G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94478743 | ||||||
chr13:94478828
|
C | T | 2 | a0001c0001t0006g0009a0001c0001t0006g0010 | 2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.295+133G>A | DCT | ENSG00000080166.16 | transcript | ENST00000377028.10 | protein_coding | 1/7 | chr13 | 94478828 |