geneid | 81567 |
---|---|
ensemblid | ENSG00000239264.9 |
hgncid | 21073 |
symbol | TXNDC5 |
name | thioredoxin domain containing 5 |
refseq_nuc | NM_030810.5 |
refseq_prot | NP_110437.2 |
ensembl_nuc | ENST00000379757.9 |
ensembl_prot | ENSP00000369081.4 |
mane_status | MANE Select |
chr | chr6 |
start | 7881517 |
end | 7910788 |
strand | - |
ver | v1.2 |
region | chr6:7881517-7910788 |
region5000 | chr6:7876517-7915788 |
regionname0 | TXNDC5_chr6_7881517_7910788 |
regionname5000 | TXNDC5_chr6_7876517_7915788 |
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 | 432 | 388 | 94 | 65 | 170 | 16 | 41 | 128 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0002 | 0/0 | 433 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0003 | 0/0 | 432 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0004 | 0/0 | 432 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0005 | 0/0 | 432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0006 | 0/0 | 432 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0007 | 0/0 | 432 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0008 | 0/0 | 432 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0009 | 0/0 | 432 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0010 | 0/0 | 432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
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 | 1299 | 329 | 68 | 55 | 150 | 14 | 40 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
c0002 | 0/0 | 1299 | 27 | 22 | 2 | 0 | 2 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
c0003 | 0/0 | 1299 | 24 | 0 | 7 | 17 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
c0004 | 0/0 | 1299 | 5 | 4 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
c0005 | 0/0 | 1302 | 4 | 0 | 4 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
c0006 | 0/0 | 1299 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
c0007 | 0/0 | 1299 | 2 | 0 | 1 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
c0008 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
c0009 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
c0010 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
c0011 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
c0012 | 0/0 | 1299 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
c0013 | 0/0 | 1299 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
c0014 | 0/0 | 1299 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
c0015 | 0/0 | 1299 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
c0016 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
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 | 1/1 | 1640 | 293 | 43 | 60 | 143 | 12 | 33 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
t0002 | 0/0 | 1625 | 37 | 30 | 4 | 0 | 2 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
t0003 | 0/0 | 1625 | 32 | 4 | 5 | 14 | 2 | 7 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
t0004 | 0/0 | 1625 | 7 | 7 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
t0005 | 0/0 | 1641 | 6 | 0 | 0 | 6 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
t0006 | 0/0 | 1640 | 4 | 1 | 1 | 0 | 0 | 2 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
t0007 | 0/0 | 1640 | 4 | 4 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
t0008 | 0/0 | 1640 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
t0009 | 0/0 | 1635 | 2 | 1 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
t0010 | 0/0 | 1640 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
t0011 | 0/0 | 1625 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
t0012 | 0/0 | 1625 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
t0013 | 0/0 | 1640 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
t0014 | 0/0 | 1640 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
t0015 | 0/0 | 1663 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
t0016 | 0/0 | 1640 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
t0017 | 0/0 | 1640 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
t0018 | 0/0 | 1640 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
t0019 | 0/0 | 1640 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
t0020 | 0/0 | 1620 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
t0021 | 0/0 | 1640 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
t0022 | 0/0 | 1640 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
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 | 22 | 1 | 8 | 10 | 2 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0002 | 0/0 | 12 | 0 | 0 | 11 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0003 | 0/0 | 8 | 0 | 4 | 0 | 1 | 3 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0004 | 0/0 | 7 | 0 | 0 | 3 | 2 | 2 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0005 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0007 | 0/0 | 6 | 0 | 2 | 2 | 1 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0008 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0009 | 0/0 | 6 | 1 | 1 | 4 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0010 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0014 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0017 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0021 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0028 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0043 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0050 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0052 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0054 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
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 | 1299 | 329 | 68 | 55 | 150 | 14 | 40 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0002 | 0/0 | 1299 | 27 | 22 | 2 | 0 | 2 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0003 | 0/0 | 1299 | 24 | 0 | 7 | 17 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0004 | 0/0 | 1299 | 5 | 4 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0009 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0010 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0016 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0002c0005 | 0/0 | 1302 | 4 | 0 | 4 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0003c0006 | 0/0 | 1299 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0004c0007 | 0/0 | 1299 | 2 | 0 | 1 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0005c0011 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0006c0013 | 0/0 | 1299 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0007c0014 | 0/0 | 1299 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0008c0015 | 0/0 | 1299 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0009c0012 | 0/0 | 1299 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0010c0008 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2938 | 251 | 36 | 46 | 124 | 12 | 31 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0001t0002 | 0/0 | 2923 | 15 | 14 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0001t0003 | 0/0 | 2923 | 31 | 4 | 5 | 13 | 2 | 7 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0001t0004 | 0/0 | 2923 | 7 | 7 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0001t0005 | 0/0 | 2939 | 6 | 0 | 0 | 6 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0001t0006 | 0/0 | 2938 | 4 | 1 | 1 | 0 | 0 | 2 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0001t0008 | 0/0 | 2938 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0001t0009 | 0/0 | 2933 | 2 | 1 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0001t0011 | 0/0 | 2923 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0001t0012 | 0/0 | 2923 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0001t0013 | 0/0 | 2938 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0001t0014 | 0/0 | 2938 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0001t0015 | 0/0 | 2961 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0001t0016 | 0/0 | 2938 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0001t0018 | 0/0 | 2938 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0001t0019 | 0/0 | 2938 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0001t0020 | 0/0 | 2918 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0001t0022 | 0/0 | 2938 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0002t0001 | 0/0 | 2938 | 5 | 5 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0002t0002 | 0/0 | 2923 | 15 | 10 | 2 | 0 | 2 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0002t0007 | 0/0 | 2938 | 4 | 4 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0002t0010 | 0/0 | 2938 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0002t0021 | 0/0 | 2938 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0003t0001 | 0/0 | 2938 | 24 | 0 | 7 | 17 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0004t0002 | 0/0 | 2923 | 5 | 4 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0009t0001 | 0/0 | 2938 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0010t0001 | 0/0 | 2938 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0001c0016t0003 | 0/0 | 2923 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0002c0005t0001 | 0/0 | 2941 | 4 | 0 | 4 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0003c0006t0001 | 0/0 | 2938 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0004c0007t0001 | 0/0 | 2938 | 2 | 0 | 1 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0005c0011t0002 | 0/0 | 2923 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0006c0013t0001 | 0/0 | 2938 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0007c0014t0001 | 0/0 | 2938 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0008c0015t0017 | 0/0 | 2938 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0009c0012t0001 | 0/0 | 2938 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
a0010c0008t0002 | 0/0 | 2923 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | copy fasta | chr6 | 7876517 | 7915788 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 22 | 1 | 8 | 10 | 2 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0002 | 0/0 | 12 | 0 | 0 | 11 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0003 | 0/0 | 8 | 0 | 4 | 0 | 1 | 3 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 3 | 2 | 2 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0007 | 0/0 | 6 | 0 | 2 | 2 | 1 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0008 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0009 | 0/0 | 6 | 1 | 1 | 4 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0010 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0028 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0043 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0052 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0002g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0003g0017 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0003g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0003g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0003g0054 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0004g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0005g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0005g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0006g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0006g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0006g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0008g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0009g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0009g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0011g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0011g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0012g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0013g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0014g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0015g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0016g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0018g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0019g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0020g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0001t0022g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0002t0002g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0002t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0002t0007g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0002t0007g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0002t0010g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0002t0010g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0002t0021g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0003t0001g0005 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0003t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0003t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0003t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0003t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0003t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0004t0002g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0004t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0009t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0010t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0001c0016t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0002c0005t0001g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0002c0005t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0003c0006t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0004c0007t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0004c0007t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0005c0011t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0006c0013t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0007c0014t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0008c0015t0017g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0009c0012t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
a0010c0008t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0069 | EUR | GBR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | GBR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0243 | EUR | FIN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00609 | hp2 | a0001 | c0001 | t0005 | g0044 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00621 | hp2 | a0001 | c0016 | t0003 | g0236 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00639 | hp1 | a0001 | c0002 | t0002 | g0116 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00639 | hp2 | a0001 | c0003 | t0001 | g0032 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00733 | hp2 | a0001 | c0001 | t0014 | g0212 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00735 | hp1 | a0002 | c0005 | t0001 | g0022 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00741 | hp1 | a0001 | c0001 | t0016 | g0106 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG00741 | hp2 | a0009 | c0012 | t0001 | g0074 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01074 | hp1 | a0001 | c0001 | t0006 | g0081 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01074 | hp2 | a0002 | c0005 | t0001 | g0022 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0127 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0150 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0032 | AMR | PUR | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0225 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01261 | hp1 | a0002 | c0005 | t0001 | g0022 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01361 | hp1 | a0001 | c0004 | t0002 | g0125 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01361 | hp2 | a0001 | c0003 | t0001 | g0042 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01433 | hp2 | a0002 | c0005 | t0001 | g0254 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0244 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | IBS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0031 | EUR | IBS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01517 | hp2 | a0001 | c0002 | t0002 | g0031 | EUR | IBS | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01884 | hp1 | a0001 | c0002 | t0002 | g0230 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01943 | hp1 | a0004 | c0007 | t0001 | g0252 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0214 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01993 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0120 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02080 | hp1 | a0001 | c0001 | t0005 | g0185 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02080 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02129 | hp1 | a0001 | c0003 | t0001 | g0161 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0170 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CDX | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CDX | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02165 | hp1 | a0001 | c0001 | t0020 | g0215 | EAS | CDX | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02257 | hp1 | a0001 | c0002 | t0010 | g0118 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02258 | hp1 | a0005 | c0011 | t0002 | g0058 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02273 | hp1 | a0001 | c0003 | t0001 | g0042 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02273 | hp2 | a0006 | c0013 | t0001 | g0156 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02280 | hp2 | a0001 | c0002 | t0010 | g0184 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02300 | hp2 | a0001 | c0003 | t0001 | g0177 | AMR | PEL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02451 | hp1 | a0001 | c0004 | t0002 | g0015 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02523 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02572 | hp2 | a0001 | c0001 | t0011 | g0261 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02622 | hp2 | a0001 | c0002 | t0002 | g0123 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02630 | hp1 | a0001 | c0001 | t0011 | g0259 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02647 | hp1 | a0001 | c0002 | t0007 | g0119 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02723 | hp2 | a0001 | c0001 | t0015 | g0194 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0247 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02809 | hp2 | a0001 | c0001 | t0013 | g0148 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02818 | hp1 | a0001 | c0002 | t0002 | g0124 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02818 | hp2 | a0010 | c0008 | t0002 | g0055 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02886 | hp1 | a0001 | c0002 | t0002 | g0126 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02895 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02896 | hp1 | a0003 | c0006 | t0001 | g0039 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02897 | hp1 | a0003 | c0006 | t0001 | g0039 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02897 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0103 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0258 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0037 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03041 | hp1 | a0001 | c0002 | t0007 | g0019 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0175 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0260 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03139 | hp2 | a0001 | c0002 | t0007 | g0019 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03195 | hp2 | a0001 | c0002 | t0007 | g0019 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0128 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03225 | hp1 | a0001 | c0002 | t0021 | g0255 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03453 | hp1 | a0001 | c0001 | t0019 | g0133 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03453 | hp2 | a0001 | c0001 | t0009 | g0073 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03486 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03490 | hp1 | a0001 | c0001 | t0006 | g0216 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | ESN | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0257 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03654 | hp1 | a0008 | c0015 | t0017 | g0079 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0117 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | STU | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0054 | SAS | STU | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | BEB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03831 | hp2 | a0004 | c0007 | t0001 | g0253 | SAS | BEB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03834 | hp1 | a0001 | c0001 | t0006 | g0217 | SAS | BEB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03942 | hp2 | a0007 | c0014 | t0001 | g0071 | SAS | BEB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | STU | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | STU | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0235 | SAS | BEB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0233 | SAS | STU | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0037 | SAS | STU | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | STU | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0017 | SAS | STU | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | YRI | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18522 | hp2 | a0001 | c0004 | t0002 | g0015 | AFR | YRI | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18747 | hp1 | a0001 | c0003 | t0001 | g0181 | EAS | CHB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18747 | hp2 | a0001 | c0003 | t0001 | g0020 | EAS | CHB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0176 | AFR | YRI | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18906 | hp2 | a0001 | c0002 | t0002 | g0129 | AFR | YRI | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18941 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18949 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18952 | hp2 | a0001 | c0001 | t0008 | g0027 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18954 | hp1 | a0001 | c0001 | t0005 | g0179 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18954 | hp2 | a0001 | c0001 | t0005 | g0174 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18957 | hp1 | a0001 | c0003 | t0001 | g0138 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18963 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18965 | hp2 | a0001 | c0001 | t0005 | g0044 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18970 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18972 | hp1 | a0001 | c0003 | t0001 | g0183 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18972 | hp2 | a0001 | c0009 | t0001 | g0056 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18977 | hp2 | a0001 | c0003 | t0001 | g0211 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18981 | hp1 | a0001 | c0010 | t0001 | g0057 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18985 | hp2 | a0001 | c0003 | t0001 | g0157 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18986 | hp2 | a0001 | c0003 | t0001 | g0020 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18988 | hp2 | a0001 | c0001 | t0005 | g0191 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0136 | AFR | LWK | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | LWK | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | LWK | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0256 | AFR | LWK | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19074 | hp1 | a0001 | c0001 | t0018 | g0146 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19076 | hp1 | a0001 | c0001 | t0022 | g0262 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19080 | hp1 | a0001 | c0003 | t0001 | g0210 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19083 | hp1 | a0001 | c0001 | t0008 | g0027 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19083 | hp2 | a0001 | c0001 | t0012 | g0231 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19088 | hp1 | a0001 | c0003 | t0001 | g0182 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19090 | hp2 | a0001 | c0003 | t0001 | g0020 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19091 | hp1 | a0001 | c0001 | t0009 | g0076 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | YRI | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA19240 | hp2 | a0001 | c0004 | t0002 | g0015 | AFR | YRI | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | ASW | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0054 | EUR | TSI | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | TSI | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | GIH | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | GIH | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG01123 | hp2 | a0001 | c0003 | t0001 | g0158 | AMR | CLM | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02486 | hp1 | a0001 | c0004 | t0002 | g0015 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0154 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | USA | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | USA | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA20300 | hp1 | a0001 | c0001 | t0006 | g0218 | AFR | USA | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | USA | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | LWK | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | LWK | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0043 | REF | REF | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0108 | REF | REF | TXNDC5_chr6_7876517_7915788 | TXNDC5 | chr6 | 7876517 | 7915788 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:7883187
|
G | A | 1 | a0006 | 1 | HG02273.hp2 | missense_variant | MODERATE | c.1256C>T | p.Ser419Leu | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1268/2938 | 1256/1299 | 419/432 | chr6 | 7883187 | ||
chr6:7884463
|
G | A | 1 | a0007 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.1072C>T | p.Pro358Ser | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/10 | 1084/2938 | 1072/1299 | 358/432 | chr6 | 7884463 | ||
chr6:7885974
|
A | G | 1 | a0003 | 2 | HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.1033T>C | p.Phe345Leu | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 8/10 | 1045/2938 | 1033/1299 | 345/432 | chr6 | 7885974 | ||
chr6:7889521
|
G | C | 1 | a0008 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.793C>G | p.Leu265Val | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 6/10 | 805/2938 | 793/1299 | 265/432 | chr6 | 7889521 | ||
chr6:7891641
|
C | T | 1 | a0009 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.712G>A | p.Glu238Lys | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/10 | 724/2938 | 712/1299 | 238/432 | chr6 | 7891641 | ||
chr6:7895115
|
C | T | 1 | a0005 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.607G>A | p.Val203Ile | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/10 | 619/2938 | 607/1299 | 203/432 | chr6 | 7895115 | ||
chr6:7910598
|
G | A | 1 | a0010 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.179C>T | p.Pro60Leu | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/10 | 191/2938 | 179/1299 | 60/432 | chr6 | 7910598 | ||
chr6:7910632
|
G | A | 1 | a0004 | 2 | HG01943.hp1 HG03831.hp2 |
missense_variant | MODERATE | c.145C>T | p.Pro49Ser | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/10 | 157/2938 | 145/1299 | 49/432 | chr6 | 7910632 | ||
chr6:7910637
|
T | TCCG | 1 | a0002 | 4 | HG00735.hp1 HG01074.hp2 HG01261.hp1 others(1): Show |
conservative_inframe_insertion | MODERATE | c.137_139dupCGG | p.Ala46dup | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/10 | 151/2938 | 139/1299 | 47/432 | chr6 | 7910637 | ||
chr6:7910745
|
A | G | 1 | a0010 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.32T>C | p.Leu11Pro | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/10 | 44/2938 | 32/1299 | 11/432 | chr6 | 7910745 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:7883153
|
G | A | 3 | a0001c0002a0001c0004a0005c0011 | 33 | HG00639.hp1 HG01081.hp1 HG01361.hp1 others(30): Show |
synonymous_variant | LOW | c.1290C>T | p.Asp430Asp | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1302/2938 | 1290/1299 | 430/432 | chr6 | 7883153 | ||
chr6:7884419
|
C | T | 1 | a0001c0003 | 24 | HG00639.hp2 HG01123.hp2 HG01243.hp2 others(21): Show |
synonymous_variant | LOW | c.1116G>A | p.Ala372Ala | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/10 | 1128/2938 | 1116/1299 | 372/432 | chr6 | 7884419 | ||
chr6:7891714
|
G | A | 1 | a0001c0004 | 5 | HG01361.hp1 HG02451.hp1 HG02486.hp1 others(2): Show |
synonymous_variant | LOW | c.639C>T | p.Phe213Phe | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/10 | 651/2938 | 639/1299 | 213/432 | chr6 | 7891714 | ||
chr6:7904600
|
G | A | 1 | a0001c0016 | 1 | HG00621.hp2 | synonymous_variant | LOW | c.387C>T | p.Ser129Ser | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/10 | 399/2938 | 387/1299 | 129/432 | chr6 | 7904600 | ||
chr6:7910681
|
C | T | 1 | a0001c0010 | 1 | NA18981.hp1 | synonymous_variant | LOW | c.96G>A | p.Gly32Gly | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/10 | 108/2938 | 96/1299 | 32/432 | chr6 | 7910681 | ||
chr6:7910729
|
C | T | 1 | a0001c0009 | 1 | NA18972.hp2 | synonymous_variant | LOW | c.48G>A | p.Ala16Ala | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/10 | 60/2938 | 48/1299 | 16/432 | chr6 | 7910729 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:7881520
|
T | A | 1 | a0001c0001t0016 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1624A>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1624 | chr6 | 7881520 | |||||
chr6:7881520
|
T | TA | 1 | a0001c0001t0005 | 6 | HG00609.hp2 HG02080.hp1 NA18954.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1623dupT | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1623 | chr6 | 7881520 | |||||
chr6:7881521
|
A | T | 1 | a0001c0001t0006 | 4 | HG01074.hp1 HG03490.hp1 HG03834.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1623T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1623 | chr6 | 7881521 | |||||
chr6:7881563
|
A | C | 1 | a0001c0001t0012 | 1 | NA19083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1581T>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1581 | chr6 | 7881563 | |||||
chr6:7881619
|
GTTGTGTG others(4): Show |
G | 11 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(8): Show | 80 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1514_*1524delTGTA others(7): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1514 | chr6 | 7881619 | |||||
chr6:7881631
|
A | C | 11 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(8): Show | 80 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1513T>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1513 | chr6 | 7881631 | |||||
chr6:7881632
|
G | C | 11 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(8): Show | 80 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1512C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1512 | chr6 | 7881632 | |||||
chr6:7881698
|
T | C | 11 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(8): Show | 80 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1446A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1446 | chr6 | 7881698 | |||||
chr6:7881788
|
G | C | 2 | a0001c0002t0007a0001c0002t0021 | 5 | HG02647.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1356C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1356 | chr6 | 7881788 | |||||
chr6:7881843
|
G | A | 1 | a0008c0015t0017 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1301C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1301 | chr6 | 7881843 | |||||
chr6:7881919
|
CCTAT | C | 11 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(8): Show | 80 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1221_*1224delATAG | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1221 | chr6 | 7881919 | |||||
chr6:7881972
|
G | A | 11 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(8): Show | 80 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1172C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1172 | chr6 | 7881972 | |||||
chr6:7882046
|
C | CCAGAGCA others(16): Show |
1 | a0001c0001t0015 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1075_*1097dupACAG others(19): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1097 | chr6 | 7882046 | |||||
chr6:7882100
|
C | T | 1 | a0001c0001t0014 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1044G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 1044 | chr6 | 7882100 | |||||
chr6:7882213
|
C | T | 1 | a0001c0001t0013 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*931G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 931 | chr6 | 7882213 | |||||
chr6:7882276
|
G | C | 1 | a0001c0001t0011 | 2 | HG02572.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*868C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 868 | chr6 | 7882276 | |||||
chr6:7882412
|
G | A | 1 | a0001c0001t0018 | 1 | NA19074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*732C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 732 | chr6 | 7882412 | |||||
chr6:7882749
|
G | A | 1 | a0001c0001t0019 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*395C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 395 | chr6 | 7882749 | |||||
chr6:7882840
|
C | T | 4 | a0001c0001t0003a0001c0001t0012a0001c0001t0020others(1): Show | 34 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*304G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 304 | chr6 | 7882840 | |||||
chr6:7882954
|
AAACTT | A | 2 | a0001c0001t0009a0001c0001t0020 | 3 | HG02165.hp1 HG03453.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*185_*189delAAGTT | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 185 | chr6 | 7882954 | |||||
chr6:7882962
|
C | T | 1 | a0001c0001t0008 | 2 | NA18952.hp2 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*182G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 182 | chr6 | 7882962 | |||||
chr6:7883082
|
G | C | 1 | a0001c0002t0010 | 2 | HG02257.hp1 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*62C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 10/10 | 62 | chr6 | 7883082 | |||||
chr6:7910778
|
G | A | 1 | a0001c0001t0022 | 1 | NA19076.hp1 | 5_prime_UTR_variant | MODIFIER | c.-2C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/10 | 2 | chr6 | 7910778 | |||||
chr6:7910778
|
G | C | 3 | a0001c0001t0004a0001c0001t0011a0001c0002t0021 | 10 | HG02451.hp2 HG02572.hp2 HG02630.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-2C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/10 | 2 | chr6 | 7910778 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:7883286
|
A | G | 4 | a0001c0001t0002g0013a0001c0001t0002g0101a0001c0001t0002g0102others(1): Show | 7 | HG01109.hp2 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1177-20T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7883286 | ||||||
chr6:7883400
|
T | C | 1 | a0001c0001t0001g0204 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1177-134A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7883400 | ||||||
chr6:7883442
|
G | A | 1 | a0001c0001t0001g0038 | 2 | NA18953.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1177-176C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7883442 | ||||||
chr6:7883614
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1177-348T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7883614 | ||||||
chr6:7883632
|
C | T | 1 | a0001c0001t0001g0010 | 5 | HG00323.hp1 HG00642.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1177-366G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7883632 | ||||||
chr6:7883683
|
A | G | 3 | a0001c0001t0001g0011a0001c0001t0001g0143a0001c0001t0001g0197 | 6 | HG00558.hp2 HG00609.hp1 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.1177-417T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7883683 | ||||||
chr6:7883872
|
T | G | 1 | a0001c0001t0001g0047 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1176+487A>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7883872 | ||||||
chr6:7883902
|
C | T | 1 | a0002c0005t0001g0022 | 3 | HG00735.hp1 HG01074.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1176+457G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7883902 | ||||||
chr6:7884003
|
C | T | 1 | a0001c0001t0006g0218 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1176+356G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7884003 | ||||||
chr6:7884009
|
G | A | 26 | a0001c0001t0003g0017a0001c0001t0003g0037a0001c0001t0003g0040others(23): Show | 33 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.1176+350C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7884009 | ||||||
chr6:7884058
|
C | T | 3 | a0001c0002t0002g0031a0001c0002t0002g0116a0001c0002t0002g0117 | 4 | HG00639.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.1176+301G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7884058 | ||||||
chr6:7884089
|
G | T | 1 | a0001c0001t0001g0087 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1176+270C>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7884089 | ||||||
chr6:7884174
|
G | A | 1 | a0001c0001t0003g0149 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1176+185C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7884174 | ||||||
chr6:7884184
|
G | A | 1 | a0001c0002t0002g0127 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1176+175C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7884184 | ||||||
chr6:7884218
|
CCAAA | C | 6 | a0001c0002t0001g0120a0001c0002t0001g0136a0001c0002t0007g0019others(3): Show | 8 | HG02055.hp2 HG02257.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1176+137_1176+140d others(6): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7884218 | ||||||
chr6:7884272
|
AGAGTGAG others(11): Show |
A | 1 | a0001c0001t0003g0233 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1176+69_1176+86del others(18): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 9/9 | chr6 | 7884272 | ||||||
chr6:7884495
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG02083.hp2 | splice_region_variant&intron_variant | LOW | c.1047-7G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 8/9 | chr6 | 7884495 | ||||||
chr6:7884951
|
C | A | 5 | a0001c0001t0001g0137a0001c0001t0001g0166a0001c0001t0001g0213others(2): Show | 5 | HG00733.hp2 HG01256.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047-463G>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 8/9 | chr6 | 7884951 | ||||||
chr6:7885021
|
C | T | 1 | a0001c0002t0001g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1047-533G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 8/9 | chr6 | 7885021 | ||||||
chr6:7885069
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(179): Show | 280 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.1047-581G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 8/9 | chr6 | 7885069 | ||||||
chr6:7885082
|
G | C | 1 | a0001c0001t0002g0122 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1047-594C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 8/9 | chr6 | 7885082 | ||||||
chr6:7885131
|
T | C | 9 | a0001c0002t0002g0016a0001c0002t0002g0123a0001c0002t0002g0124others(6): Show | 15 | HG01081.hp1 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1047-643A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 8/9 | chr6 | 7885131 | ||||||
chr6:7885285
|
T | C | 1 | a0005c0011t0002g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1046+676A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 8/9 | chr6 | 7885285 | ||||||
chr6:7885395
|
A | G | 7 | a0001c0002t0001g0120a0001c0002t0001g0136a0001c0002t0007g0019others(4): Show | 9 | HG02055.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1046+566T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 8/9 | chr6 | 7885395 | ||||||
chr6:7885428
|
C | G | 13 | a0001c0001t0001g0006a0001c0001t0001g0046a0001c0001t0001g0139others(10): Show | 20 | HG00423.hp1 HG00544.hp1 HG02155.hp1 others(17): Show |
intron_variant | MODIFIER | c.1046+533G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 8/9 | chr6 | 7885428 | ||||||
chr6:7885514
|
C | G | 1 | a0001c0001t0001g0162 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1046+447G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 8/9 | chr6 | 7885514 | ||||||
chr6:7885564
|
C | A | 1 | a0001c0001t0001g0077 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1046+397G>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 8/9 | chr6 | 7885564 | ||||||
chr6:7886139
|
A | T | 3 | a0001c0001t0002g0033a0001c0001t0002g0121a0001c0001t0002g0122 | 4 | HG01891.hp2 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.964-96T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886139 | ||||||
chr6:7886221
|
T | G | 1 | a0001c0003t0001g0183 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.964-178A>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886221 | ||||||
chr6:7886301
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(124): Show | 209 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.964-258G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886301 | ||||||
chr6:7886384
|
G | T | 1 | a0001c0001t0001g0025 | 2 | NA18962.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.964-341C>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886384 | ||||||
chr6:7886406
|
T | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(183): Show | 284 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.964-363A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886406 | ||||||
chr6:7886500
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.964-457G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886500 | ||||||
chr6:7886509
|
T | G | 1 | a0001c0001t0001g0239 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.964-466A>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886509 | ||||||
chr6:7886570
|
C | G | 1 | a0005c0011t0002g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.964-527G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886570 | ||||||
chr6:7886600
|
C | T | 1 | a0005c0011t0002g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.964-557G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886600 | ||||||
chr6:7886672
|
A | G | 57 | a0001c0001t0001g0203a0001c0001t0001g0206a0001c0001t0001g0224others(54): Show | 75 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.964-629T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886672 | ||||||
chr6:7886726
|
CTA | C | 2 | a0001c0002t0002g0016a0001c0002t0002g0128 | 5 | HG02895.hp2 HG02897.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.964-685_964-684del others(2): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886726 | ||||||
chr6:7886898
|
A | G | 59 | a0001c0001t0001g0075a0001c0001t0001g0167a0001c0001t0001g0198others(56): Show | 75 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.964-855T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886898 | ||||||
chr6:7886913
|
C | T | 1 | a0001c0003t0001g0181 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.964-870G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886913 | ||||||
chr6:7886990
|
A | G | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(129): Show | 211 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.964-947T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7886990 | ||||||
chr6:7887104
|
G | A | 54 | a0001c0001t0001g0035a0001c0001t0001g0143a0001c0001t0001g0180others(51): Show | 69 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.964-1061C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887104 | ||||||
chr6:7887106
|
C | CAACT | 54 | a0001c0001t0001g0035a0001c0001t0001g0143a0001c0001t0001g0180others(51): Show | 69 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.964-1067_964-1064d others(6): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887106 | ||||||
chr6:7887184
|
T | C | 1 | a0005c0011t0002g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.964-1141A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887184 | ||||||
chr6:7887187
|
TGTGGCCC others(19): Show |
T | 1 | a0009c0012t0001g0074 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.964-1170_964-1145d others(28): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887187 | ||||||
chr6:7887371
|
G | A | 6 | a0001c0002t0001g0120a0001c0002t0001g0136a0001c0002t0007g0019others(3): Show | 8 | HG02055.hp2 HG02257.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-1328C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887371 | ||||||
chr6:7887419
|
C | T | 2 | a0001c0004t0002g0015a0001c0004t0002g0125 | 5 | HG01361.hp1 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.963+1286G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887419 | ||||||
chr6:7887437
|
CT | C | 31 | a0001c0001t0001g0224a0001c0001t0001g0232a0001c0001t0003g0017others(28): Show | 39 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+1267delA | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887437 | ||||||
chr6:7887482
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.963+1223C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887482 | ||||||
chr6:7887501
|
T | TCTC | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(183): Show | 284 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.963+1201_963+1203d others(5): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887501 | ||||||
chr6:7887586
|
G | T | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(185): Show | 289 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(286): Show |
intron_variant | MODIFIER | c.963+1119C>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887586 | ||||||
chr6:7887600
|
G | A | 3 | a0001c0001t0002g0033a0001c0001t0002g0121a0001c0001t0002g0122 | 4 | HG01891.hp2 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+1105C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887600 | ||||||
chr6:7887633
|
C | T | 1 | a0001c0002t0001g0120 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.963+1072G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887633 | ||||||
chr6:7887681
|
A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(137): Show | 224 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.963+1024T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887681 | ||||||
chr6:7887712
|
C | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(183): Show | 284 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.963+993G>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887712 | ||||||
chr6:7887716
|
T | C | 8 | a0001c0001t0002g0013a0001c0001t0002g0101a0001c0001t0002g0102others(5): Show | 12 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.963+989A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887716 | ||||||
chr6:7887739
|
T | A | 1 | a0001c0001t0003g0150 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.963+966A>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887739 | ||||||
chr6:7887833
|
A | G | 8 | a0001c0001t0002g0013a0001c0001t0002g0101a0001c0001t0002g0102others(5): Show | 12 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.963+872T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887833 | ||||||
chr6:7887901
|
C | T | 7 | a0001c0001t0002g0013a0001c0001t0002g0101a0001c0001t0002g0102others(4): Show | 11 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.963+804G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887901 | ||||||
chr6:7887935
|
C | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(128): Show | 211 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.963+770G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887935 | ||||||
chr6:7887967
|
T | A | 1 | a0001c0002t0001g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.963+738A>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7887967 | ||||||
chr6:7888018
|
T | C | 8 | a0001c0001t0002g0013a0001c0001t0002g0101a0001c0001t0002g0102others(5): Show | 12 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.963+687A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7888018 | ||||||
chr6:7888032
|
T | C | 7 | a0001c0002t0001g0120a0001c0002t0001g0136a0001c0002t0007g0019others(4): Show | 9 | HG02055.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.963+673A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7888032 | ||||||
chr6:7888095
|
C | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(183): Show | 284 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.963+610G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7888095 | ||||||
chr6:7888312
|
C | G | 1 | a0001c0001t0008g0027 | 2 | NA18952.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.963+393G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7888312 | ||||||
chr6:7888378
|
A | T | 1 | a0001c0001t0001g0141 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.963+327T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7888378 | ||||||
chr6:7888450
|
A | T | 7 | a0001c0001t0001g0227a0001c0001t0001g0239a0001c0001t0002g0226others(4): Show | 7 | HG01884.hp1 HG02818.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.963+255T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7888450 | ||||||
chr6:7888500
|
G | A | 2 | a0004c0007t0001g0252a0004c0007t0001g0253 | 2 | HG01943.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.963+205C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7888500 | ||||||
chr6:7888516
|
G | A | 7 | a0001c0002t0001g0120a0001c0002t0001g0136a0001c0002t0007g0019others(4): Show | 9 | HG02055.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.963+189C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7888516 | ||||||
chr6:7888666
|
G | A | 1 | a0005c0011t0002g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.963+39C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7888666 | ||||||
chr6:7888676
|
T | C | 1 | a0005c0011t0002g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.963+29A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 7/9 | chr6 | 7888676 | ||||||
chr6:7888855
|
A | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(185): Show | 286 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(283): Show |
splice_region_variant&intron_variant | LOW | c.820-7T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 6/9 | chr6 | 7888855 | ||||||
chr6:7888868
|
G | A | 1 | a0001c0003t0001g0177 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.820-20C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 6/9 | chr6 | 7888868 | ||||||
chr6:7888959
|
G | A | 1 | a0007c0014t0001g0071 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.820-111C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 6/9 | chr6 | 7888959 | ||||||
chr6:7889021
|
C | T | 7 | a0001c0001t0002g0013a0001c0001t0002g0101a0001c0001t0002g0102others(4): Show | 11 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.820-173G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 6/9 | chr6 | 7889021 | ||||||
chr6:7889077
|
C | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(125): Show | 208 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.820-229G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 6/9 | chr6 | 7889077 | ||||||
chr6:7889125
|
A | C | 1 | a0001c0001t0001g0160 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.820-277T>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 6/9 | chr6 | 7889125 | ||||||
chr6:7889232
|
A | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(136): Show | 223 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.819+263T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 6/9 | chr6 | 7889232 | ||||||
chr6:7889233
|
A | G | 7 | a0001c0001t0002g0013a0001c0001t0002g0101a0001c0001t0002g0102others(4): Show | 11 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.819+262T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 6/9 | chr6 | 7889233 | ||||||
chr6:7889646
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.733-65T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7889646 | ||||||
chr6:7889661
|
C | T | 7 | a0001c0001t0002g0013a0001c0001t0002g0101a0001c0001t0002g0102others(4): Show | 11 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.733-80G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7889661 | ||||||
chr6:7889705
|
GC | G | 7 | a0001c0001t0001g0227a0001c0001t0001g0239a0001c0001t0002g0226others(4): Show | 7 | HG01884.hp1 HG02818.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.733-125delG | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7889705 | ||||||
chr6:7889839
|
T | C | 1 | a0001c0003t0001g0138 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.733-258A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7889839 | ||||||
chr6:7889888
|
T | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(136): Show | 223 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.733-307A>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7889888 | ||||||
chr6:7889934
|
T | C | 2 | a0001c0001t0001g0141a0001c0001t0015g0194 | 2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.733-353A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7889934 | ||||||
chr6:7889983
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.733-402T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7889983 | ||||||
chr6:7890039
|
G | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(115): Show | 195 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.733-458C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7890039 | ||||||
chr6:7890355
|
C | CGG | 3 | a0001c0001t0002g0033a0001c0001t0002g0121a0001c0001t0002g0122 | 4 | HG01891.hp2 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-776_733-775dup others(2): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7890355 | ||||||
chr6:7890543
|
A | T | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(134): Show | 223 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.733-962T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7890543 | ||||||
chr6:7890619
|
C | T | 8 | a0001c0001t0002g0013a0001c0001t0002g0101a0001c0001t0002g0102others(5): Show | 12 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.732+1002G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7890619 | ||||||
chr6:7890721
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.732+900T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7890721 | ||||||
chr6:7890754
|
A | T | 1 | a0001c0001t0001g0107 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.732+867T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7890754 | ||||||
chr6:7890758
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.732+863A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7890758 | ||||||
chr6:7890773
|
G | C | 1 | a0003c0006t0001g0039 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.732+848C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7890773 | ||||||
chr6:7890846
|
G | A | 7 | a0001c0001t0002g0013a0001c0001t0002g0101a0001c0001t0002g0102others(4): Show | 11 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.732+775C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7890846 | ||||||
chr6:7890927
|
G | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(118): Show | 198 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.732+694C>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7890927 | ||||||
chr6:7890935
|
T | A | 1 | a0005c0011t0002g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.732+686A>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7890935 | ||||||
chr6:7890997
|
T | C | 9 | a0001c0002t0002g0016a0001c0002t0002g0123a0001c0002t0002g0124others(6): Show | 15 | HG01081.hp1 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.732+624A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7890997 | ||||||
chr6:7891039
|
G | A | 1 | a0001c0001t0003g0248 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.732+582C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891039 | ||||||
chr6:7891050
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.732+571C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891050 | ||||||
chr6:7891151
|
T | C | 7 | a0001c0001t0002g0013a0001c0001t0002g0101a0001c0001t0002g0102others(4): Show | 11 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.732+470A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891151 | ||||||
chr6:7891170
|
T | C | 17 | a0001c0001t0001g0011a0001c0001t0001g0078a0001c0001t0001g0082others(14): Show | 23 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.732+451A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891170 | ||||||
chr6:7891281
|
C | T | 1 | a0001c0001t0001g0010 | 5 | HG00323.hp1 HG00642.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.732+340G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891281 | ||||||
chr6:7891292
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.732+329C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891292 | ||||||
chr6:7891317
|
T | G | 2 | a0001c0002t0010g0118a0001c0002t0010g0184 | 2 | HG02257.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.732+304A>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891317 | ||||||
chr6:7891356
|
C | T | 1 | a0001c0001t0019g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.732+265G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891356 | ||||||
chr6:7891440
|
G | T | 5 | a0001c0001t0001g0137a0001c0001t0001g0166a0001c0001t0001g0213others(2): Show | 5 | HG00733.hp2 HG01256.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.732+181C>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891440 | ||||||
chr6:7891449
|
A | C | 15 | a0001c0002t0001g0120a0001c0002t0001g0136a0001c0002t0002g0016others(12): Show | 23 | HG01081.hp1 HG01361.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.732+172T>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891449 | ||||||
chr6:7891541
|
C | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | NA18951.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.732+80G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891541 | ||||||
chr6:7891542
|
G | A | 39 | a0001c0001t0001g0224a0001c0001t0001g0227a0001c0001t0001g0232others(36): Show | 47 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.732+79C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891542 | ||||||
chr6:7891543
|
G | T | 1 | a0010c0008t0002g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.732+78C>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891543 | ||||||
chr6:7891570
|
T | C | 1 | a0001c0001t0001g0080 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.732+51A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 5/9 | chr6 | 7891570 | ||||||
chr6:7891910
|
C | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(179): Show | 280 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.617-174G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7891910 | ||||||
chr6:7891918
|
C | T | 2 | a0001c0001t0002g0169a0001c0001t0003g0149 | 2 | HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.617-182G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7891918 | ||||||
chr6:7892000
|
A | C | 1 | a0001c0001t0001g0114 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.617-264T>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7892000 | ||||||
chr6:7892014
|
C | T | 1 | a0001c0001t0005g0179 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.617-278G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7892014 | ||||||
chr6:7892090
|
G | C | 1 | a0001c0001t0001g0099 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.617-354C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7892090 | ||||||
chr6:7892092
|
A | G | 1 | a0001c0001t0001g0047 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.617-356T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7892092 | ||||||
chr6:7892220
|
GTCT | G | 3 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0199 | 5 | HG01081.hp2 HG01891.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.617-487_617-485del others(3): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7892220 | ||||||
chr6:7892342
|
G | A | 39 | a0001c0001t0001g0224a0001c0001t0001g0227a0001c0001t0001g0232others(36): Show | 47 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.617-606C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7892342 | ||||||
chr6:7892589
|
G | A | 4 | a0001c0003t0001g0032a0001c0003t0001g0042a0001c0003t0001g0158others(1): Show | 6 | HG00639.hp2 HG01123.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.617-853C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7892589 | ||||||
chr6:7892718
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.617-982A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7892718 | ||||||
chr6:7892789
|
A | T | 15 | a0001c0002t0001g0120a0001c0002t0001g0136a0001c0002t0002g0016others(12): Show | 23 | HG01081.hp1 HG01361.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.617-1053T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7892789 | ||||||
chr6:7892832
|
G | A | 7 | a0001c0001t0001g0221a0001c0002t0001g0120a0001c0002t0001g0136others(4): Show | 9 | HG02055.hp2 HG02257.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.617-1096C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7892832 | ||||||
chr6:7892854
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.617-1118T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7892854 | ||||||
chr6:7892930
|
T | C | 1 | a0001c0002t0001g0120 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.617-1194A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7892930 | ||||||
chr6:7892942
|
G | A | 7 | a0001c0001t0002g0013a0001c0001t0002g0101a0001c0001t0002g0102others(4): Show | 11 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.617-1206C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7892942 | ||||||
chr6:7893054
|
A | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(118): Show | 198 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.617-1318T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893054 | ||||||
chr6:7893094
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.617-1358G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893094 | ||||||
chr6:7893169
|
T | C | 1 | a0001c0001t0006g0081 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.617-1433A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893169 | ||||||
chr6:7893240
|
C | G | 6 | a0001c0002t0001g0120a0001c0002t0001g0136a0001c0002t0007g0019others(3): Show | 8 | HG02055.hp2 HG02257.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.617-1504G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893240 | ||||||
chr6:7893385
|
G | A | 5 | a0001c0001t0002g0169a0001c0001t0003g0040a0001c0001t0003g0149others(2): Show | 6 | HG01243.hp1 HG02145.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.617-1649C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893385 | ||||||
chr6:7893489
|
C | T | 2 | a0001c0001t0001g0093a0001c0001t0001g0095 | 2 | HG03239.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.616+1617G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893489 | ||||||
chr6:7893490
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.616+1616C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893490 | ||||||
chr6:7893497
|
C | T | 1 | a0001c0001t0002g0102 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.616+1609G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893497 | ||||||
chr6:7893535
|
G | GCCTGCCG others(12): Show |
2 | a0001c0001t0001g0239a0001c0001t0002g0033 | 3 | HG01891.hp2 HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.616+1552_616+1570d others(21): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893535 | ||||||
chr6:7893550
|
T | C | 1 | a0001c0002t0001g0120 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.616+1556A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893550 | ||||||
chr6:7893651
|
C | T | 1 | a0001c0001t0001g0047 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.616+1455G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893651 | ||||||
chr6:7893664
|
T | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0143a0001c0001t0001g0171others(1): Show | 7 | HG00558.hp2 HG00609.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.616+1442A>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893664 | ||||||
chr6:7893668
|
G | A | 1 | a0001c0010t0001g0057 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.616+1438C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893668 | ||||||
chr6:7893676
|
G | A | 9 | a0001c0002t0002g0016a0001c0002t0002g0123a0001c0002t0002g0124others(6): Show | 15 | HG01081.hp1 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.616+1430C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893676 | ||||||
chr6:7893695
|
CTT | C | 2 | a0001c0001t0003g0054a0001c0001t0003g0243 | 3 | HG00280.hp1 HG03688.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.616+1409_616+1410d others(4): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893695 | ||||||
chr6:7893732
|
A | G | 1 | a0001c0001t0013g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.616+1374T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893732 | ||||||
chr6:7893781
|
A | C | 7 | a0001c0001t0004g0023a0001c0001t0004g0256a0001c0001t0004g0257others(4): Show | 9 | HG02451.hp2 HG02572.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.616+1325T>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893781 | ||||||
chr6:7893837
|
C | G | 1 | a0001c0001t0001g0141 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.616+1269G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893837 | ||||||
chr6:7893849
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.616+1257C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893849 | ||||||
chr6:7893920
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.616+1186G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7893920 | ||||||
chr6:7894089
|
A | G | 1 | a0001c0001t0008g0027 | 2 | NA18952.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.616+1017T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7894089 | ||||||
chr6:7894249
|
C | T | 1 | a0001c0003t0001g0158 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.616+857G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7894249 | ||||||
chr6:7894453
|
A | C | 1 | a0001c0001t0001g0034 | 2 | NA19000.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.616+653T>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7894453 | ||||||
chr6:7894462
|
T | C | 18 | a0001c0001t0002g0013a0001c0001t0002g0101a0001c0001t0002g0102others(15): Show | 28 | HG00639.hp1 HG01081.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.616+644A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7894462 | ||||||
chr6:7894561
|
G | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(131): Show | 220 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.616+545C>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7894561 | ||||||
chr6:7894947
|
G | A | 1 | a0001c0001t0005g0191 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.616+159C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7894947 | ||||||
chr6:7895087
|
A | T | 1 | a0001c0001t0001g0135 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.616+19T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 4/9 | chr6 | 7895087 | ||||||
chr6:7895342
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.520-140C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7895342 | ||||||
chr6:7895655
|
C | T | 5 | a0001c0001t0001g0021a0001c0001t0001g0045a0001c0001t0001g0049others(2): Show | 9 | HG00423.hp2 HG00558.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.520-453G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7895655 | ||||||
chr6:7895673
|
A | G | 5 | a0001c0001t0001g0041a0001c0001t0001g0178a0001c0002t0001g0154others(2): Show | 6 | HG01884.hp2 HG02622.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-471T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7895673 | ||||||
chr6:7895680
|
G | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0034others(55): Show | 101 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.520-478C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7895680 | ||||||
chr6:7895747
|
T | C | 2 | a0001c0001t0001g0155a0001c0001t0001g0165 | 2 | HG02083.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.520-545A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7895747 | ||||||
chr6:7895837
|
A | C | 1 | a0005c0011t0002g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.520-635T>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7895837 | ||||||
chr6:7895837
|
A | T | 4 | a0001c0001t0001g0227a0001c0001t0002g0226a0001c0001t0002g0228others(1): Show | 4 | HG02922.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-635T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7895837 | ||||||
chr6:7895862
|
G | A | 1 | a0001c0002t0010g0118 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.520-660C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7895862 | ||||||
chr6:7895908
|
A | G | 4 | a0001c0001t0005g0044a0001c0001t0005g0174a0001c0001t0005g0185others(1): Show | 5 | HG00609.hp2 HG02080.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.520-706T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7895908 | ||||||
chr6:7896258
|
A | G | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(196): Show | 314 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.520-1056T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7896258 | ||||||
chr6:7896557
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.520-1355C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7896557 | ||||||
chr6:7896710
|
G | A | 1 | a0001c0001t0001g0047 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.520-1508C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7896710 | ||||||
chr6:7896779
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.520-1577G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7896779 | ||||||
chr6:7896826
|
G | A | 7 | a0001c0001t0002g0013a0001c0001t0002g0101a0001c0001t0002g0102others(4): Show | 11 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.520-1624C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7896826 | ||||||
chr6:7896830
|
T | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(240): Show | 368 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(365): Show |
intron_variant | MODIFIER | c.520-1628A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7896830 | ||||||
chr6:7897167
|
C | T | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(237): Show | 364 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.520-1965G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7897167 | ||||||
chr6:7897554
|
C | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0190 | 3 | HG01109.hp1 HG01168.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.519+2022G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7897554 | ||||||
chr6:7897634
|
T | A | 7 | a0001c0001t0002g0013a0001c0001t0002g0101a0001c0001t0002g0102others(4): Show | 11 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.519+1942A>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7897634 | ||||||
chr6:7897658
|
C | T | 1 | a0001c0001t0003g0054 | 2 | HG03688.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.519+1918G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7897658 | ||||||
chr6:7897777
|
T | C | 2 | a0001c0001t0001g0173a0001c0001t0001g0188 | 2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.519+1799A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7897777 | ||||||
chr6:7897853
|
A | T | 1 | a0001c0002t0007g0019 | 3 | HG03041.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.519+1723T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7897853 | ||||||
chr6:7897914
|
A | G | 42 | a0001c0001t0001g0224a0001c0001t0001g0227a0001c0001t0001g0232others(39): Show | 51 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.519+1662T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7897914 | ||||||
chr6:7898018
|
G | A | 3 | a0001c0001t0015g0194a0001c0002t0007g0019a0001c0002t0007g0119 | 5 | HG02647.hp1 HG02723.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+1558C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7898018 | ||||||
chr6:7898063
|
G | GT | 8 | a0001c0001t0001g0201a0001c0001t0002g0102a0001c0001t0003g0247others(5): Show | 8 | HG02080.hp1 HG02300.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.519+1512dupA | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7898063 | ||||||
chr6:7898414
|
T | C | 3 | a0001c0002t0007g0019a0001c0002t0007g0119a0001c0002t0021g0255 | 5 | HG02647.hp1 HG03041.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.519+1162A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7898414 | ||||||
chr6:7898530
|
G | C | 7 | a0001c0001t0002g0013a0001c0001t0002g0101a0001c0001t0002g0102others(4): Show | 11 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.519+1046C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7898530 | ||||||
chr6:7898642
|
A | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(179): Show | 280 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.519+934T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7898642 | ||||||
chr6:7898681
|
C | T | 1 | a0006c0013t0001g0156 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.519+895G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7898681 | ||||||
chr6:7898694
|
C | T | 1 | a0007c0014t0001g0071 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.519+882G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7898694 | ||||||
chr6:7898739
|
C | G | 1 | a0001c0001t0003g0243 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.519+837G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7898739 | ||||||
chr6:7898773
|
CATG | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(114): Show | 194 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.519+800_519+802del others(3): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7898773 | ||||||
chr6:7898900
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.519+676C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7898900 | ||||||
chr6:7899161
|
G | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(114): Show | 194 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.519+415C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899161 | ||||||
chr6:7899215
|
C | A | 1 | a0001c0001t0001g0083 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.519+361G>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899215 | ||||||
chr6:7899295
|
T | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(180): Show | 281 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(278): Show |
intron_variant | MODIFIER | c.519+281A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899295 | ||||||
chr6:7899315
|
A | G | 15 | a0001c0002t0001g0120a0001c0002t0001g0136a0001c0002t0002g0016others(12): Show | 23 | HG01081.hp1 HG01361.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.519+261T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899315 | ||||||
chr6:7899336
|
C | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(114): Show | 194 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.519+240G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899336 | ||||||
chr6:7899340
|
G | T | 8 | a0001c0001t0002g0013a0001c0001t0002g0101a0001c0001t0002g0102others(5): Show | 12 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.519+236C>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899340 | ||||||
chr6:7899352
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.519+224G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899352 | ||||||
chr6:7899380
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.519+196G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899380 | ||||||
chr6:7899418
|
G | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(171): Show | 268 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.519+158C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899418 | ||||||
chr6:7899424
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(179): Show | 280 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.519+152G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899424 | ||||||
chr6:7899532
|
A | AGAGGGAG others(1): Show |
46 | a0001c0001t0001g0224a0001c0001t0001g0227a0001c0001t0001g0232others(43): Show | 57 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.519+36_519+43dupCC others(6): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899532 | ||||||
chr6:7899532
|
A | AGAGGGAG others(5): Show |
7 | a0001c0001t0002g0226a0001c0001t0004g0257a0001c0002t0002g0016others(4): Show | 10 | HG02622.hp2 HG02818.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.519+32_519+43dupCC others(10): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899532 | ||||||
chr6:7899532
|
A | AGAGGGAG others(9): Show |
3 | a0001c0001t0004g0258a0001c0001t0004g0260a0001c0004t0002g0015 | 6 | HG02451.hp1 HG02486.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.519+28_519+43dupCC others(14): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899532 | ||||||
chr6:7899532
|
A | AGAGGGAG others(13): Show |
1 | a0001c0004t0002g0125 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.519+24_519+43dupCC others(18): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899532 | ||||||
chr6:7899532
|
AGAGGGAG others(1): Show |
A | 8 | a0001c0001t0002g0013a0001c0001t0002g0101a0001c0001t0002g0102others(5): Show | 12 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.519+36_519+43delCC others(6): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 3/9 | chr6 | 7899532 | ||||||
chr6:7899691
|
T | A | 1 | a0001c0001t0006g0217 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.414-10A>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7899691 | ||||||
chr6:7899757
|
A | G | 1 | a0001c0001t0003g0237 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.414-76T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7899757 | ||||||
chr6:7899795
|
T | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(131): Show | 219 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.414-114A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7899795 | ||||||
chr6:7899958
|
A | T | 1 | a0001c0001t0001g0195 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.414-277T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7899958 | ||||||
chr6:7900035
|
T | TTG | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.414-356_414-355dup others(2): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7900035 | ||||||
chr6:7900067
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.414-386T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7900067 | ||||||
chr6:7900069
|
G | A | 1 | a0001c0001t0002g0122 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.414-388C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7900069 | ||||||
chr6:7900212
|
C | G | 2 | a0001c0002t0002g0116a0001c0002t0002g0117 | 2 | HG00639.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.414-531G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7900212 | ||||||
chr6:7900252
|
T | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(114): Show | 194 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.414-571A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7900252 | ||||||
chr6:7900476
|
A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(137): Show | 229 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.414-795T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7900476 | ||||||
chr6:7900554
|
G | A | 1 | a0001c0001t0005g0174 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.414-873C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7900554 | ||||||
chr6:7900623
|
C | T | 7 | a0001c0001t0004g0023a0001c0001t0004g0256a0001c0001t0004g0257others(4): Show | 9 | HG02451.hp2 HG02572.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.414-942G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7900623 | ||||||
chr6:7900716
|
C | T | 6 | a0001c0002t0001g0120a0001c0002t0001g0136a0001c0002t0007g0019others(3): Show | 8 | HG02055.hp2 HG02257.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.414-1035G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7900716 | ||||||
chr6:7900726
|
C | T | 6 | a0001c0002t0001g0120a0001c0002t0001g0136a0001c0002t0007g0019others(3): Show | 8 | HG02055.hp2 HG02257.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.414-1045G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7900726 | ||||||
chr6:7900954
|
C | CA | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(113): Show | 193 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.414-1274dupT | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7900954 | ||||||
chr6:7900954
|
CA | C | 3 | a0001c0001t0001g0094a0001c0002t0007g0019a0001c0002t0007g0119 | 5 | HG02258.hp2 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-1274delT | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7900954 | ||||||
chr6:7900971
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.414-1290A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7900971 | ||||||
chr6:7901085
|
G | T | 1 | a0001c0001t0001g0025 | 2 | NA18962.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.414-1404C>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7901085 | ||||||
chr6:7901219
|
A | G | 3 | a0001c0002t0001g0154a0001c0002t0001g0175a0001c0002t0001g0176 | 3 | HG03098.hp1 HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.414-1538T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7901219 | ||||||
chr6:7901227
|
G | A | 8 | a0001c0001t0002g0013a0001c0001t0002g0101a0001c0001t0002g0102others(5): Show | 12 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.414-1546C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7901227 | ||||||
chr6:7901290
|
C | T | 2 | a0001c0002t0007g0019a0001c0002t0007g0119 | 4 | HG02647.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.414-1609G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7901290 | ||||||
chr6:7901422
|
A | G | 9 | a0001c0002t0002g0016a0001c0002t0002g0123a0001c0002t0002g0124others(6): Show | 15 | HG01081.hp1 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.414-1741T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7901422 | ||||||
chr6:7901430
|
G | GTA | 8 | a0001c0001t0002g0013a0001c0001t0002g0101a0001c0001t0002g0102others(5): Show | 12 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.414-1751_414-1750d others(4): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7901430 | ||||||
chr6:7901476
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.414-1795T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7901476 | ||||||
chr6:7901561
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.414-1880C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7901561 | ||||||
chr6:7901651
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.414-1970C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7901651 | ||||||
chr6:7901714
|
C | T | 24 | a0001c0001t0001g0224a0001c0001t0001g0232a0001c0001t0003g0017others(21): Show | 29 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.414-2033G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7901714 | ||||||
chr6:7901839
|
G | T | 1 | a0001c0001t0005g0185 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.414-2158C>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7901839 | ||||||
chr6:7901943
|
G | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(112): Show | 192 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.414-2262C>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7901943 | ||||||
chr6:7902042
|
G | C | 6 | a0001c0001t0002g0013a0001c0001t0002g0101a0001c0001t0002g0102others(3): Show | 9 | HG01109.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.414-2361C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7902042 | ||||||
chr6:7902133
|
G | A | 9 | a0001c0002t0002g0016a0001c0002t0002g0123a0001c0002t0002g0124others(6): Show | 15 | HG01081.hp1 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.413+2441C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7902133 | ||||||
chr6:7902234
|
T | C | 2 | a0001c0001t0001g0141a0001c0001t0015g0194 | 2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.413+2340A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7902234 | ||||||
chr6:7902298
|
G | A | 9 | a0001c0001t0001g0135a0001c0001t0002g0013a0001c0001t0002g0101others(6): Show | 13 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.413+2276C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7902298 | ||||||
chr6:7902409
|
GCC | G | 9 | a0001c0001t0001g0135a0001c0001t0002g0013a0001c0001t0002g0101others(6): Show | 13 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.413+2163_413+2164d others(4): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7902409 | ||||||
chr6:7902469
|
G | A | 1 | a0001c0002t0002g0230 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.413+2105C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7902469 | ||||||
chr6:7902706
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.413+1868C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7902706 | ||||||
chr6:7902724
|
G | A | 1 | a0001c0001t0003g0235 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.413+1850C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7902724 | ||||||
chr6:7902813
|
A | C | 7 | a0001c0001t0002g0013a0001c0001t0002g0101a0001c0001t0002g0102others(4): Show | 11 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.413+1761T>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7902813 | ||||||
chr6:7902872
|
C | T | 7 | a0001c0001t0002g0013a0001c0001t0002g0101a0001c0001t0002g0102others(4): Show | 11 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.413+1702G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7902872 | ||||||
chr6:7902882
|
T | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(113): Show | 193 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.413+1692A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7902882 | ||||||
chr6:7902959
|
G | A | 9 | a0001c0002t0002g0016a0001c0002t0002g0123a0001c0002t0002g0124others(6): Show | 15 | HG01081.hp1 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.413+1615C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7902959 | ||||||
chr6:7903151
|
T | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(257): Show | 400 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(397): Show |
intron_variant | MODIFIER | c.413+1423A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7903151 | ||||||
chr6:7903233
|
C | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0034others(49): Show | 93 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.413+1341G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7903233 | ||||||
chr6:7903274
|
G | A | 21 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0018others(18): Show | 33 | HG00099.hp1 HG00597.hp2 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.413+1300C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7903274 | ||||||
chr6:7903284
|
ATAG | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(127): Show | 215 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.413+1287_413+1289d others(5): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7903284 | ||||||
chr6:7903396
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(106): Show | 186 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.413+1178C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7903396 | ||||||
chr6:7903774
|
T | G | 6 | a0001c0001t0001g0132a0001c0001t0001g0134a0001c0001t0001g0141others(3): Show | 6 | HG02615.hp1 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.413+800A>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7903774 | ||||||
chr6:7903893
|
T | C | 3 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100 | 3 | HG02145.hp2 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.413+681A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7903893 | ||||||
chr6:7903932
|
T | G | 1 | a0001c0002t0001g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.413+642A>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7903932 | ||||||
chr6:7904075
|
T | C | 1 | a0001c0002t0001g0120 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.413+499A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7904075 | ||||||
chr6:7904213
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0029 | 6 | NA18939.hp2 NA18942.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.413+361C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7904213 | ||||||
chr6:7904241
|
G | A | 1 | a0001c0001t0001g0048 | 2 | NA18612.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.413+333C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7904241 | ||||||
chr6:7904443
|
A | T | 1 | a0001c0001t0001g0153 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.413+131T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7904443 | ||||||
chr6:7904556
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.413+18G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 2/9 | chr6 | 7904556 | ||||||
chr6:7904836
|
T | C | 2 | a0001c0001t0001g0249a0001c0001t0011g0261 | 2 | HG02572.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.264-113A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7904836 | ||||||
chr6:7904951
|
T | G | 1 | a0001c0001t0001g0092 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.264-228A>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7904951 | ||||||
chr6:7905036
|
C | T | 6 | a0001c0001t0001g0132a0001c0001t0001g0134a0001c0001t0001g0141others(3): Show | 6 | HG02615.hp1 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.264-313G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7905036 | ||||||
chr6:7905091
|
T | C | 1 | a0001c0001t0001g0068 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.264-368A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7905091 | ||||||
chr6:7905292
|
A | T | 2 | a0001c0004t0002g0015a0001c0004t0002g0125 | 5 | HG01361.hp1 HG02451.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.264-569T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7905292 | ||||||
chr6:7905300
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.264-577G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7905300 | ||||||
chr6:7905467
|
C | G | 1 | a0010c0008t0002g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.264-744G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7905467 | ||||||
chr6:7905786
|
G | T | 1 | a0010c0008t0002g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.264-1063C>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7905786 | ||||||
chr6:7905809
|
G | A | 1 | a0001c0001t0001g0052 | 2 | HG01081.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.264-1086C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7905809 | ||||||
chr6:7905919
|
T | C | 24 | a0001c0001t0001g0224a0001c0001t0001g0232a0001c0001t0003g0017others(21): Show | 29 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.264-1196A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7905919 | ||||||
chr6:7906086
|
AAAAAATT others(49): Show |
A | 3 | a0001c0001t0002g0033a0001c0001t0002g0121a0001c0001t0002g0122 | 4 | HG01891.hp2 HG02809.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.264-1419_264-1364d others(58): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906086 | ||||||
chr6:7906139
|
G | C | 1 | a0001c0001t0001g0195 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.264-1416C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906139 | ||||||
chr6:7906235
|
T | A | 1 | a0001c0001t0001g0195 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.264-1512A>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906235 | ||||||
chr6:7906267
|
G | A | 1 | a0005c0011t0002g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.264-1544C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906267 | ||||||
chr6:7906333
|
C | T | 1 | a0005c0011t0002g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.264-1610G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906333 | ||||||
chr6:7906424
|
T | C | 41 | a0001c0001t0001g0224a0001c0001t0001g0227a0001c0001t0001g0232others(38): Show | 51 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.264-1701A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906424 | ||||||
chr6:7906425
|
A | G | 41 | a0001c0001t0001g0224a0001c0001t0001g0227a0001c0001t0001g0232others(38): Show | 51 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.264-1702T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906425 | ||||||
chr6:7906458
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.264-1735G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906458 | ||||||
chr6:7906511
|
G | A | 1 | a0001c0001t0004g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.264-1788C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906511 | ||||||
chr6:7906515
|
G | A | 35 | a0001c0001t0001g0093a0001c0001t0001g0224a0001c0001t0001g0227others(32): Show | 41 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.264-1792C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906515 | ||||||
chr6:7906535
|
C | CA | 30 | a0001c0001t0001g0018a0001c0001t0001g0038a0001c0001t0001g0059others(27): Show | 37 | HG00544.hp2 HG01123.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.264-1813dupT | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906535 | ||||||
chr6:7906535
|
C | CAA | 67 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(64): Show | 126 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.264-1814_264-1813d others(4): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906535 | ||||||
chr6:7906535
|
C | CAAA | 26 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0049others(23): Show | 37 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.264-1815_264-1813d others(5): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906535 | ||||||
chr6:7906535
|
C | CAAAA | 7 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0192others(4): Show | 7 | HG01109.hp1 HG02129.hp2 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.264-1816_264-1813d others(6): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906535 | ||||||
chr6:7906553
|
A | G | 1 | a0001c0001t0001g0068 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.264-1830T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906553 | ||||||
chr6:7906556
|
AAG | A | 6 | a0001c0001t0002g0013a0001c0001t0002g0101a0001c0002t0002g0016others(3): Show | 13 | HG01109.hp2 HG01516.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.264-1835_264-1834d others(4): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906556 | ||||||
chr6:7906557
|
A | AAAC | 7 | a0001c0001t0004g0023a0001c0001t0004g0256a0001c0001t0004g0257others(4): Show | 9 | HG02451.hp2 HG02572.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.264-1835_264-1834i others(5): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906557 | ||||||
chr6:7906557
|
AG | A | 12 | a0001c0001t0002g0102a0001c0001t0002g0103a0001c0001t0003g0241others(9): Show | 17 | HG00639.hp1 HG01081.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.264-1835delC | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906557 | ||||||
chr6:7906558
|
G | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(157): Show | 245 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.264-1835C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906558 | ||||||
chr6:7906604
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.264-1881T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906604 | ||||||
chr6:7906673
|
C | CAA | 14 | a0001c0002t0001g0136a0001c0002t0002g0016a0001c0002t0002g0123others(11): Show | 22 | HG01081.hp1 HG01361.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.264-1952_264-1951d others(4): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906673 | ||||||
chr6:7906764
|
G | GA | 9 | a0001c0002t0002g0016a0001c0002t0002g0123a0001c0002t0002g0124others(6): Show | 15 | HG01081.hp1 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.264-2042dupT | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906764 | ||||||
chr6:7906906
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(109): Show | 190 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.264-2183G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7906906 | ||||||
chr6:7907021
|
G | A | 2 | a0001c0001t0001g0219a0001c0001t0001g0222 | 2 | HG02523.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.264-2298C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7907021 | ||||||
chr6:7907165
|
C | CTTTTTTT | 4 | a0001c0001t0002g0013a0001c0001t0002g0103a0001c0001t0003g0241others(1): Show | 7 | HG00438.hp1 HG01109.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.264-2449_264-2443d others(9): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7907165 | ||||||
chr6:7907165
|
C | CTTTTTTT others(1): Show |
29 | a0001c0001t0001g0227a0001c0001t0001g0232a0001c0001t0001g0239others(26): Show | 34 | HG00408.hp1 HG00597.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.264-2450_264-2443d others(10): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7907165 | ||||||
chr6:7907165
|
C | CTTTTTTT others(2): Show |
5 | a0001c0001t0001g0224a0001c0001t0002g0033a0001c0001t0002g0121others(2): Show | 6 | HG01891.hp2 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.264-2451_264-2443d others(11): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7907165 | ||||||
chr6:7907458
|
C | T | 1 | a0001c0001t0006g0216 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.264-2735G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7907458 | ||||||
chr6:7907552
|
T | C | 42 | a0001c0001t0001g0029a0001c0001t0001g0224a0001c0001t0001g0227others(39): Show | 53 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.264-2829A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7907552 | ||||||
chr6:7907651
|
G | C | 41 | a0001c0001t0001g0224a0001c0001t0001g0227a0001c0001t0001g0232others(38): Show | 51 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.263+2863C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7907651 | ||||||
chr6:7907727
|
A | T | 14 | a0001c0002t0001g0136a0001c0002t0002g0016a0001c0002t0002g0123others(11): Show | 22 | HG01081.hp1 HG01361.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.263+2787T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7907727 | ||||||
chr6:7907787
|
G | C | 1 | a0001c0001t0001g0107 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.263+2727C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7907787 | ||||||
chr6:7907874
|
G | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(179): Show | 280 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.263+2640C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7907874 | ||||||
chr6:7908070
|
G | C | 21 | a0001c0001t0002g0013a0001c0001t0002g0101a0001c0001t0002g0102others(18): Show | 33 | HG00639.hp1 HG01081.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.263+2444C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908070 | ||||||
chr6:7908112
|
A | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02615.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.263+2402T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908112 | ||||||
chr6:7908196
|
T | C | 1 | a0001c0001t0001g0196 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.263+2318A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908196 | ||||||
chr6:7908228
|
A | T | 2 | a0001c0002t0002g0116a0001c0002t0002g0117 | 2 | HG00639.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.263+2286T>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908228 | ||||||
chr6:7908237
|
T | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(118): Show | 199 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.263+2277A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908237 | ||||||
chr6:7908281
|
C | CA | 8 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0113others(5): Show | 8 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.263+2232dupT | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908281 | ||||||
chr6:7908281
|
CA | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(115): Show | 195 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.263+2232delT | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908281 | ||||||
chr6:7908281
|
CAA | C | 17 | a0001c0001t0001g0137a0001c0001t0001g0139a0001c0001t0001g0140others(14): Show | 22 | HG01081.hp1 HG01257.hp2 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.263+2231_263+2232d others(4): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908281 | ||||||
chr6:7908281
|
CAAA | C | 7 | a0001c0001t0002g0013a0001c0001t0002g0101a0001c0001t0002g0102others(4): Show | 11 | HG00639.hp1 HG01109.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.263+2230_263+2232d others(5): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908281 | ||||||
chr6:7908518
|
T | TA | 37 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(34): Show | 43 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.263+1995dupT | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908518 | ||||||
chr6:7908518
|
T | TAA | 7 | a0001c0001t0004g0023a0001c0001t0004g0256a0001c0001t0004g0257others(4): Show | 9 | HG02451.hp2 HG02572.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.263+1994_263+1995d others(4): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908518 | ||||||
chr6:7908518
|
TA | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(115): Show | 196 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.263+1995delT | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908518 | ||||||
chr6:7908522
|
A | C | 1 | a0001c0001t0001g0025 | 2 | NA18962.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.263+1992T>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908522 | ||||||
chr6:7908620
|
G | A | 1 | a0001c0001t0001g0206 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.263+1894C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908620 | ||||||
chr6:7908829
|
T | G | 1 | a0001c0003t0001g0211 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.263+1685A>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908829 | ||||||
chr6:7908963
|
G | A | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | NA18942.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.263+1551C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7908963 | ||||||
chr6:7909101
|
G | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(115): Show | 196 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.263+1413C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909101 | ||||||
chr6:7909108
|
T | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 300 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.263+1406A>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909108 | ||||||
chr6:7909226
|
G | A | 42 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0110others(39): Show | 55 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.263+1288C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909226 | ||||||
chr6:7909273
|
T | C | 7 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0104others(4): Show | 14 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.263+1241A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909273 | ||||||
chr6:7909373
|
TCTGG | T | 9 | a0001c0002t0002g0016a0001c0002t0002g0123a0001c0002t0002g0124others(6): Show | 15 | HG01081.hp1 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.263+1137_263+1140d others(6): Show |
TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909373 | ||||||
chr6:7909475
|
G | A | 2 | a0001c0003t0001g0210a0001c0003t0001g0211 | 2 | NA18977.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.263+1039C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909475 | ||||||
chr6:7909523
|
C | T | 3 | a0001c0001t0001g0132a0001c0001t0001g0134a0001c0001t0019g0133 | 3 | HG02615.hp1 HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.263+991G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909523 | ||||||
chr6:7909587
|
T | A | 2 | a0001c0001t0001g0213a0001c0001t0014g0212 | 2 | HG00733.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.263+927A>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909587 | ||||||
chr6:7909690
|
A | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | NA18951.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.263+824T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909690 | ||||||
chr6:7909734
|
C | T | 69 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0010others(66): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.263+780G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909734 | ||||||
chr6:7909811
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.263+703T>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909811 | ||||||
chr6:7909890
|
C | A | 1 | a0001c0001t0001g0112 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.263+624G>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909890 | ||||||
chr6:7909928
|
C | A | 1 | a0001c0001t0001g0113 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.263+586G>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909928 | ||||||
chr6:7909941
|
C | T | 1 | a0001c0001t0003g0214 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.263+573G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909941 | ||||||
chr6:7909999
|
T | C | 13 | a0001c0001t0002g0033a0001c0001t0002g0121a0001c0001t0002g0122others(10): Show | 16 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.263+515A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7909999 | ||||||
chr6:7910064
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.263+450C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910064 | ||||||
chr6:7910080
|
G | A | 9 | a0001c0002t0002g0016a0001c0002t0002g0123a0001c0002t0002g0124others(6): Show | 15 | HG01081.hp1 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.263+434C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910080 | ||||||
chr6:7910093
|
G | C | 1 | a0001c0001t0001g0115 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.263+421C>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910093 | ||||||
chr6:7910119
|
A | C | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 288 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.263+395T>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910119 | ||||||
chr6:7910144
|
C | G | 1 | a0001c0001t0001g0059 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.263+370G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910144 | ||||||
chr6:7910165
|
C | G | 1 | a0001c0001t0001g0034 | 2 | NA19000.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.263+349G>C | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910165 | ||||||
chr6:7910202
|
T | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(184): Show | 289 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.263+312A>G | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910202 | ||||||
chr6:7910266
|
C | A | 1 | a0001c0001t0001g0130 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.263+248G>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910266 | ||||||
chr6:7910273
|
GC | G | 8 | a0001c0001t0004g0023a0001c0001t0004g0256a0001c0001t0004g0257others(5): Show | 10 | HG02451.hp2 HG02572.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.263+240delG | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910273 | ||||||
chr6:7910275
|
C | T | 8 | a0001c0001t0004g0023a0001c0001t0004g0256a0001c0001t0004g0257others(5): Show | 10 | HG02451.hp2 HG02572.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.263+239G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910275 | ||||||
chr6:7910284
|
C | T | 1 | a0005c0011t0002g0058 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.263+230G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910284 | ||||||
chr6:7910312
|
G | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(113): Show | 193 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.263+202C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910312 | ||||||
chr6:7910329
|
C | A | 42 | a0001c0001t0001g0003a0001c0001t0001g0219a0001c0001t0001g0220others(39): Show | 54 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.263+185G>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910329 | ||||||
chr6:7910366
|
C | T | 1 | a0001c0001t0001g0024 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.263+148G>A | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910366 | ||||||
chr6:7910431
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.263+83C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910431 | ||||||
chr6:7910497
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.263+17C>T | TXNDC5 | ENSG00000239264.9 | transcript | ENST00000379757.9 | protein_coding | 1/9 | chr6 | 7910497 |