geneid | 7490 |
---|---|
ensemblid | ENSG00000184937.16 |
hgncid | 12796 |
symbol | WT1 |
name | WT1 transcription factor |
refseq_nuc | NM_024426.6 |
refseq_prot | NP_077744.4 |
ensembl_nuc | ENST00000452863.10 |
ensembl_prot | ENSP00000415516.5 |
mane_status | MANE Select |
chr | chr11 |
start | 32387775 |
end | 32435539 |
strand | - |
ver | v1.2 |
region | chr11:32387775-32435539 |
region5000 | chr11:32382775-32440539 |
regionname0 | WT1_chr11_32387775_32435539 |
regionname5000 | WT1_chr11_32382775_32440539 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 449 | 328 | 86 | 62 | 126 | 4 | 48 | 102 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1569 | 94 | 1 | 15 | 61 | 2 | 15 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
c0002 | 1/1 | 1569 | 89 | 8 | 25 | 40 | 2 | 12 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
c0003 | 0/0 | 1569 | 47 | 28 | 8 | 4 | 0 | 7 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
c0004 | 0/0 | 1569 | 32 | 23 | 3 | 5 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
c0005 | 0/0 | 1569 | 15 | 3 | 0 | 5 | 0 | 7 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
c0006 | 0/0 | 1569 | 14 | 1 | 1 | 8 | 0 | 4 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
c0007 | 0/0 | 1569 | 9 | 1 | 5 | 2 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
c0008 | 0/0 | 1569 | 7 | 6 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
c0009 | 0/0 | 1569 | 6 | 6 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
c0010 | 0/0 | 1569 | 6 | 5 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
c0011 | 0/0 | 1569 | 3 | 0 | 3 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
c0012 | 0/0 | 1569 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
c0013 | 0/0 | 1569 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
c0014 | 0/0 | 1569 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
c0015 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
c0016 | 0/0 | 1569 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1463 | 101 | 5 | 27 | 48 | 1 | 18 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0002 | 0/0 | 1458 | 95 | 5 | 16 | 57 | 2 | 15 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0003 | 0/0 | 1459 | 28 | 16 | 6 | 0 | 0 | 6 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0004 | 0/0 | 1457 | 16 | 16 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0005 | 0/0 | 1457 | 14 | 0 | 0 | 8 | 0 | 6 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0006 | 0/0 | 1459 | 11 | 11 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0007 | 0/0 | 1465 | 10 | 1 | 4 | 5 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0008 | 0/0 | 1463 | 7 | 7 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0009 | 0/0 | 1461 | 6 | 3 | 0 | 3 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0010 | 0/0 | 1461 | 3 | 2 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0011 | 0/0 | 1457 | 3 | 3 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0012 | 0/0 | 1460 | 3 | 0 | 1 | 2 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0013 | 0/0 | 1458 | 3 | 0 | 1 | 0 | 0 | 2 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0014 | 0/0 | 1465 | 3 | 2 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0015 | 0/0 | 1461 | 3 | 0 | 2 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0016 | 0/0 | 1459 | 3 | 3 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0017 | 0/0 | 1459 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0018 | 0/0 | 1463 | 2 | 1 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0019 | 0/0 | 1458 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0020 | 0/0 | 1457 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0021 | 0/0 | 1453 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0022 | 0/0 | 1463 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0023 | 0/0 | 1461 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0024 | 0/0 | 1457 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0025 | 0/0 | 1453 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0026 | 0/0 | 1459 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0027 | 0/0 | 1457 | 1 | 0 | 0 | 0 | 1 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0028 | 0/0 | 1461 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0029 | 0/0 | 1461 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0030 | 0/0 | 1457 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0031 | 0/0 | 1465 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0032 | 0/0 | 1457 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
t0033 | 0/0 | 1461 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0003 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0088 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0104 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1569 | 94 | 1 | 15 | 61 | 2 | 15 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0002 | 1/1 | 1569 | 89 | 8 | 25 | 40 | 2 | 12 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0003 | 0/0 | 1569 | 47 | 28 | 8 | 4 | 0 | 7 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0004 | 0/0 | 1569 | 32 | 23 | 3 | 5 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0005 | 0/0 | 1569 | 15 | 3 | 0 | 5 | 0 | 7 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0006 | 0/0 | 1569 | 14 | 1 | 1 | 8 | 0 | 4 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0007 | 0/0 | 1569 | 9 | 1 | 5 | 2 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0008 | 0/0 | 1569 | 7 | 6 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0009 | 0/0 | 1569 | 6 | 6 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0010 | 0/0 | 1569 | 6 | 5 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0011 | 0/0 | 1569 | 3 | 0 | 3 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0012 | 0/0 | 1569 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0013 | 0/0 | 1569 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0014 | 0/0 | 1569 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0015 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0016 | 0/0 | 1569 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 3026 | 82 | 1 | 13 | 54 | 2 | 12 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0001t0005 | 0/0 | 3025 | 5 | 0 | 0 | 5 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0001t0012 | 0/0 | 3028 | 3 | 0 | 1 | 2 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0001t0013 | 0/0 | 3026 | 3 | 0 | 1 | 0 | 0 | 2 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0001t0019 | 0/0 | 3026 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0002t0001 | 1/1 | 3031 | 73 | 1 | 19 | 38 | 1 | 12 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0002t0003 | 0/0 | 3027 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0002t0004 | 0/0 | 3025 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0002t0007 | 0/0 | 3033 | 4 | 0 | 4 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0002t0011 | 0/0 | 3025 | 3 | 3 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0002t0015 | 0/0 | 3029 | 3 | 0 | 2 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0002t0026 | 0/0 | 3027 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0002t0027 | 0/0 | 3025 | 1 | 0 | 0 | 0 | 1 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0003t0001 | 0/0 | 3031 | 6 | 1 | 1 | 2 | 0 | 2 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0003t0002 | 0/0 | 3026 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0003t0003 | 0/0 | 3027 | 11 | 2 | 4 | 0 | 0 | 5 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0003t0004 | 0/0 | 3025 | 11 | 11 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0003t0006 | 0/0 | 3027 | 7 | 7 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0003t0009 | 0/0 | 3029 | 2 | 0 | 0 | 2 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0003t0010 | 0/0 | 3029 | 3 | 2 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0003t0016 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0003t0024 | 0/0 | 3025 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0003t0025 | 0/0 | 3021 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0003t0029 | 0/0 | 3029 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0003t0031 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0003t0032 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0004t0001 | 0/0 | 3031 | 5 | 2 | 2 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0004t0003 | 0/0 | 3027 | 7 | 6 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0004t0004 | 0/0 | 3025 | 3 | 3 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0004t0006 | 0/0 | 3027 | 3 | 3 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0004t0007 | 0/0 | 3033 | 6 | 1 | 0 | 5 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0004t0009 | 0/0 | 3029 | 3 | 3 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0004t0017 | 0/0 | 3027 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0004t0018 | 0/0 | 3031 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0004t0020 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0004t0030 | 0/0 | 3025 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0005t0002 | 0/0 | 3026 | 6 | 3 | 0 | 2 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0005t0005 | 0/0 | 3025 | 8 | 0 | 0 | 2 | 0 | 6 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0005t0022 | 0/0 | 3031 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0006t0001 | 0/0 | 3031 | 10 | 1 | 0 | 7 | 0 | 2 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0006t0002 | 0/0 | 3026 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0006t0003 | 0/0 | 3027 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0006t0009 | 0/0 | 3029 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0006t0018 | 0/0 | 3031 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0007t0001 | 0/0 | 3031 | 2 | 0 | 2 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0007t0002 | 0/0 | 3026 | 5 | 0 | 3 | 1 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0007t0005 | 0/0 | 3025 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0007t0028 | 0/0 | 3029 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0008t0003 | 0/0 | 3027 | 7 | 6 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0009t0008 | 0/0 | 3031 | 5 | 5 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0009t0033 | 0/0 | 3029 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0010t0006 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0010t0008 | 0/0 | 3031 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0010t0014 | 0/0 | 3033 | 2 | 1 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0010t0016 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0010t0021 | 0/0 | 3021 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0011t0001 | 0/0 | 3031 | 3 | 0 | 3 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0012t0014 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0012t0023 | 0/0 | 3029 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0013t0001 | 0/0 | 3031 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0014t0008 | 0/0 | 3031 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0015t0001 | 0/0 | 3031 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
a0001c0016t0016 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | copy fasta | chr11 | 32382775 | 32440539 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0005g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0012g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0012g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0012g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0013g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0013g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0013g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0001t0019g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0003 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0088 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0104 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0007g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0007g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0007g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0007g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0011g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0011g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0011g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0015g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0015g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0015g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0026g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0002t0027g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0004g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0004g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0004g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0006g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0006g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0006g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0009g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0009g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0010g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0010g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0010g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0016g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0024g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0025g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0029g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0031g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0003t0032g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0003g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0006g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0006g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0007g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0007g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0007g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0007g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0007g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0007g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0009g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0009g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0009g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0017g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0017g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0018g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0020g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0004t0030g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0005g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0005g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0005g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0005g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0005g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0005g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0005g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0005t0022g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0009g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0006t0018g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0007t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0007t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0007t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0007t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0007t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0007t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0007t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0007t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0007t0028g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0008t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0008t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0008t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0008t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0008t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0008t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0008t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0009t0008g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0009t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0009t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0009t0008g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0009t0033g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0010t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0010t0008g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0010t0014g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0010t0014g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0010t0016g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0010t0021g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0011t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0011t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0011t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0012t0014g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0012t0023g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0013t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0014t0008g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0015t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
a0001c0016t0016g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0174 | EUR | GBR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0099 | EUR | GBR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00408 | hp1 | a0001 | c0007 | t0002 | g0044 | EAS | CHS | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | CHS | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00438 | hp1 | a0001 | c0015 | t0001 | g0045 | EAS | CHS | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | CHS | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | CHS | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | CHS | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | CHS | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | CHS | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | CHS | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | CHS | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00642 | hp1 | a0001 | c0008 | t0003 | g0287 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00733 | hp2 | a0001 | c0003 | t0003 | g0247 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00735 | hp1 | a0001 | c0004 | t0003 | g0016 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00735 | hp2 | a0001 | c0002 | t0007 | g0070 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0069 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG00741 | hp2 | a0001 | c0004 | t0001 | g0280 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0089 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0095 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01074 | hp1 | a0001 | c0002 | t0007 | g0086 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01074 | hp2 | a0001 | c0006 | t0018 | g0126 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01099 | hp1 | a0001 | c0003 | t0025 | g0238 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0098 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0108 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0082 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01109 | hp2 | a0001 | c0010 | t0014 | g0270 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0101 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01169 | hp2 | a0001 | c0003 | t0001 | g0236 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01175 | hp1 | a0001 | c0003 | t0024 | g0237 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01175 | hp2 | a0001 | c0007 | t0001 | g0053 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0100 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01243 | hp1 | a0001 | c0007 | t0002 | g0032 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01256 | hp1 | a0001 | c0004 | t0001 | g0282 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01256 | hp2 | a0001 | c0007 | t0001 | g0071 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0106 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01261 | hp2 | a0001 | c0003 | t0003 | g0248 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01346 | hp1 | a0001 | c0001 | t0013 | g0175 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01358 | hp1 | a0001 | c0002 | t0015 | g0050 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01358 | hp2 | a0001 | c0002 | t0015 | g0055 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01361 | hp1 | a0001 | c0003 | t0003 | g0245 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01496 | hp1 | a0001 | c0003 | t0010 | g0019 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0060 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01884 | hp1 | a0001 | c0005 | t0002 | g0253 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01884 | hp2 | a0001 | c0004 | t0020 | g0302 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01891 | hp1 | a0001 | c0004 | t0003 | g0016 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01891 | hp2 | a0001 | c0004 | t0009 | g0296 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01928 | hp2 | a0001 | c0011 | t0001 | g0023 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01975 | hp1 | a0001 | c0001 | t0012 | g0152 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01975 | hp2 | a0001 | c0011 | t0001 | g0021 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01978 | hp2 | a0001 | c0011 | t0001 | g0022 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0103 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01981 | hp2 | a0001 | c0007 | t0002 | g0105 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01993 | hp1 | a0001 | c0002 | t0007 | g0043 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | KHV | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | KHV | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02055 | hp1 | a0001 | c0004 | t0017 | g0283 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02055 | hp2 | a0001 | c0004 | t0003 | g0293 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | KHV | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | KHV | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | KHV | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | KHV | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | KHV | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | KHV | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | KHV | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02129 | hp2 | a0001 | c0005 | t0005 | g0258 | EAS | KHV | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | KHV | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | KHV | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02145 | hp1 | a0001 | c0004 | t0003 | g0273 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02145 | hp2 | a0001 | c0003 | t0016 | g0224 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02148 | hp2 | a0001 | c0007 | t0002 | g0102 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | CDX | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | CDX | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02257 | hp1 | a0001 | c0006 | t0001 | g0212 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02257 | hp2 | a0001 | c0003 | t0004 | g0231 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02280 | hp1 | a0001 | c0009 | t0033 | g0306 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02280 | hp2 | a0001 | c0010 | t0021 | g0216 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02300 | hp1 | a0001 | c0003 | t0003 | g0246 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02300 | hp2 | a0001 | c0002 | t0007 | g0085 | AMR | PEL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02451 | hp1 | a0001 | c0010 | t0006 | g0217 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02451 | hp2 | a0001 | c0003 | t0010 | g0018 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02572 | hp1 | a0001 | c0002 | t0011 | g0029 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02572 | hp2 | a0001 | c0009 | t0008 | g0034 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0165 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02602 | hp2 | a0001 | c0006 | t0001 | g0151 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02622 | hp1 | a0001 | c0008 | t0003 | g0285 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02622 | hp2 | a0001 | c0003 | t0004 | g0242 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02630 | hp1 | a0001 | c0008 | t0003 | g0289 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02630 | hp2 | a0001 | c0014 | t0008 | g0035 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02647 | hp1 | a0001 | c0003 | t0004 | g0233 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02647 | hp2 | a0001 | c0004 | t0007 | g0286 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0091 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02683 | hp2 | a0001 | c0001 | t0019 | g0020 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0092 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02717 | hp1 | a0001 | c0004 | t0004 | g0275 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02717 | hp2 | a0001 | c0002 | t0011 | g0026 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02723 | hp1 | a0001 | c0003 | t0004 | g0012 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02723 | hp2 | a0001 | c0008 | t0003 | g0292 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0157 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02738 | hp1 | a0001 | c0003 | t0001 | g0235 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0054 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02818 | hp1 | a0001 | c0003 | t0010 | g0017 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02818 | hp2 | a0001 | c0004 | t0017 | g0279 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02886 | hp1 | a0001 | c0004 | t0006 | g0015 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02886 | hp2 | a0001 | c0004 | t0004 | g0274 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02895 | hp1 | a0001 | c0003 | t0004 | g0241 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02895 | hp2 | a0001 | c0003 | t0006 | g0226 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02896 | hp1 | a0001 | c0002 | t0004 | g0028 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02896 | hp2 | a0001 | c0012 | t0023 | g0210 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02897 | hp1 | a0001 | c0002 | t0004 | g0027 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02897 | hp2 | a0001 | c0003 | t0006 | g0227 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02965 | hp1 | a0001 | c0010 | t0014 | g0257 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02965 | hp2 | a0001 | c0004 | t0018 | g0295 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02970 | hp1 | a0001 | c0003 | t0004 | g0011 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02970 | hp2 | a0001 | c0007 | t0028 | g0033 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02976 | hp1 | a0001 | c0004 | t0030 | g0301 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02976 | hp2 | a0001 | c0004 | t0009 | g0294 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03017 | hp1 | a0001 | c0013 | t0001 | g0024 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03017 | hp2 | a0001 | c0003 | t0003 | g0230 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03098 | hp1 | a0001 | c0009 | t0008 | g0030 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03098 | hp2 | a0001 | c0009 | t0008 | g0004 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03130 | hp1 | a0001 | c0003 | t0004 | g0012 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03130 | hp2 | a0001 | c0002 | t0011 | g0025 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03139 | hp1 | a0001 | c0003 | t0003 | g0215 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03139 | hp2 | a0001 | c0003 | t0006 | g0225 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03195 | hp1 | a0001 | c0003 | t0006 | g0219 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03195 | hp2 | a0001 | c0004 | t0001 | g0014 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03209 | hp1 | a0001 | c0003 | t0004 | g0013 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03209 | hp2 | a0001 | c0004 | t0006 | g0015 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03225 | hp1 | a0001 | c0004 | t0009 | g0288 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03225 | hp2 | a0001 | c0003 | t0006 | g0220 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0163 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03239 | hp2 | a0001 | c0004 | t0001 | g0284 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03453 | hp1 | a0001 | c0008 | t0003 | g0297 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03453 | hp2 | a0001 | c0002 | t0003 | g0068 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03486 | hp1 | a0001 | c0009 | t0008 | g0031 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03486 | hp2 | a0001 | c0010 | t0008 | g0218 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03490 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03490 | hp2 | a0001 | c0005 | t0005 | g0268 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03491 | hp1 | a0001 | c0001 | t0013 | g0143 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03491 | hp2 | a0001 | c0003 | t0003 | g0252 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03492 | hp1 | a0001 | c0001 | t0013 | g0148 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03516 | hp1 | a0001 | c0003 | t0006 | g0228 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03516 | hp2 | a0001 | c0002 | t0003 | g0059 | AFR | ESN | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03540 | hp1 | a0001 | c0004 | t0006 | g0291 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03540 | hp2 | a0001 | c0009 | t0008 | g0004 | AFR | GWD | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03579 | hp1 | a0001 | c0003 | t0004 | g0011 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03579 | hp2 | a0001 | c0003 | t0004 | g0013 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03654 | hp1 | a0001 | c0005 | t0005 | g0261 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03654 | hp2 | a0001 | c0003 | t0003 | g0250 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0039 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0037 | SAS | STU | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03688 | hp2 | a0001 | c0003 | t0003 | g0249 | SAS | STU | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03704 | hp1 | a0001 | c0007 | t0002 | g0041 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03704 | hp2 | a0001 | c0005 | t0005 | g0260 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0036 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03710 | hp2 | a0001 | c0006 | t0002 | g0181 | SAS | PJL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | BEB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0122 | SAS | BEB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03927 | hp1 | a0001 | c0005 | t0005 | g0262 | SAS | BEB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0057 | SAS | BEB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0180 | SAS | BEB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03942 | hp2 | a0001 | c0005 | t0005 | g0255 | SAS | BEB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0109 | SAS | STU | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG04115 | hp2 | a0001 | c0005 | t0002 | g0267 | SAS | STU | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG04184 | hp1 | a0001 | c0006 | t0001 | g0112 | SAS | BEB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | BEB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG04199 | hp1 | a0001 | c0006 | t0003 | g0170 | SAS | STU | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG04199 | hp2 | a0001 | c0003 | t0001 | g0269 | SAS | STU | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG04204 | hp1 | a0001 | c0005 | t0005 | g0263 | SAS | STU | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0167 | SAS | STU | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | STU | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG04228 | hp2 | a0001 | c0003 | t0003 | g0244 | SAS | STU | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18522 | hp1 | a0001 | c0003 | t0032 | g0234 | AFR | YRI | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18522 | hp2 | a0001 | c0004 | t0001 | g0014 | AFR | YRI | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18940 | hp1 | a0001 | c0005 | t0002 | g0243 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18942 | hp1 | a0001 | c0005 | t0002 | g0265 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18942 | hp2 | a0001 | c0004 | t0007 | g0278 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18947 | hp1 | a0001 | c0004 | t0007 | g0304 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18950 | hp2 | a0001 | c0003 | t0001 | g0266 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18953 | hp2 | a0001 | c0002 | t0026 | g0093 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18956 | hp1 | a0001 | c0004 | t0007 | g0305 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18960 | hp2 | a0001 | c0002 | t0015 | g0052 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18961 | hp2 | a0001 | c0006 | t0009 | g0178 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18963 | hp2 | a0001 | c0006 | t0001 | g0168 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18964 | hp1 | a0001 | c0004 | t0007 | g0277 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18973 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18979 | hp2 | a0001 | c0004 | t0007 | g0276 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18982 | hp2 | a0001 | c0006 | t0001 | g0164 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18983 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18985 | hp2 | a0001 | c0001 | t0005 | g0115 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18987 | hp2 | a0001 | c0003 | t0009 | g0239 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18991 | hp1 | a0001 | c0005 | t0022 | g0256 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18992 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18992 | hp2 | a0001 | c0001 | t0012 | g0196 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18995 | hp1 | a0001 | c0006 | t0001 | g0146 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18997 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19003 | hp2 | a0001 | c0006 | t0001 | g0199 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19005 | hp2 | a0001 | c0006 | t0001 | g0198 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19010 | hp1 | a0001 | c0003 | t0009 | g0229 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19030 | hp1 | a0001 | c0012 | t0014 | g0211 | AFR | LWK | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19030 | hp2 | a0001 | c0003 | t0006 | g0223 | AFR | LWK | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19043 | hp1 | a0001 | c0003 | t0031 | g0251 | AFR | LWK | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19043 | hp2 | a0001 | c0008 | t0003 | g0281 | AFR | LWK | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19056 | hp2 | a0001 | c0005 | t0005 | g0264 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19063 | hp2 | a0001 | c0001 | t0012 | g0201 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19066 | hp1 | a0001 | c0003 | t0001 | g0259 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19083 | hp2 | a0001 | c0001 | t0005 | g0159 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19084 | hp1 | a0001 | c0006 | t0001 | g0154 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19091 | hp1 | a0001 | c0001 | t0005 | g0117 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19240 | hp1 | a0001 | c0004 | t0004 | g0298 | AFR | YRI | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA19240 | hp2 | a0001 | c0004 | t0003 | g0300 | AFR | YRI | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA20129 | hp1 | a0001 | c0005 | t0002 | g0213 | AFR | ASW | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA20129 | hp2 | a0001 | c0003 | t0002 | g0232 | AFR | ASW | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0141 | EUR | TSI | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA20752 | hp2 | a0001 | c0002 | t0027 | g0090 | EUR | TSI | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | GIH | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0081 | SAS | GIH | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | CLM | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02109 | hp1 | a0001 | c0004 | t0003 | g0272 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02109 | hp2 | a0001 | c0003 | t0001 | g0254 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02486 | hp1 | a0001 | c0010 | t0016 | g0271 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02486 | hp2 | a0001 | c0004 | t0003 | g0303 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02559 | hp1 | a0001 | c0003 | t0003 | g0214 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG02559 | hp2 | a0001 | c0003 | t0029 | g0221 | AFR | ACB | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03471 | hp1 | a0001 | c0016 | t0016 | g0299 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
HG03471 | hp2 | a0001 | c0008 | t0003 | g0290 | AFR | MSL | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18955 | hp1 | a0001 | c0007 | t0005 | g0042 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA18955 | hp2 | a0001 | c0006 | t0001 | g0114 | EAS | JPT | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA21309 | hp1 | a0001 | c0005 | t0002 | g0222 | AFR | LWK | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
NA21309 | hp2 | a0001 | c0003 | t0004 | g0240 | AFR | LWK | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0088 | REF | REF | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0104 | REF | REF | WT1_chr11_32382775_32440539 | WT1 | chr11 | 32382775 | 32440539 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:32392048
|
C | T | 1 | a0001c0014 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.1371G>A | p.Gln457Gln | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/10 | 1550/3031 | 1371/1569 | 457/522 | chr11 | 32392048 | ||
chr11:32396399
|
T | C | 4 | a0001c0001a0001c0005a0001c0007others(1): Show | 125 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(122): Show |
synonymous_variant | LOW | c.1122A>G | p.Arg374Arg | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/10 | 1301/3031 | 1122/1569 | 374/522 | chr11 | 32396399 | ||
chr11:32399987
|
T | C | 5 | a0001c0009a0001c0010a0001c0012others(2): Show | 16 | HG01109.hp2 HG02280.hp1 HG02280.hp2 others(13): Show |
synonymous_variant | LOW | c.1074A>G | p.Gln358Gln | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/10 | 1253/3031 | 1074/1569 | 358/522 | chr11 | 32399987 | ||
chr11:32428585
|
G | A | 1 | a0001c0015 | 1 | HG00438.hp1 | synonymous_variant | LOW | c.696C>T | p.Ser232Ser | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 2/10 | 875/3031 | 696/1569 | 232/522 | chr11 | 32428585 | ||
chr11:32434752
|
G | A | 3 | a0001c0004a0001c0008a0001c0016 | 40 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(37): Show |
synonymous_variant | LOW | c.609C>T | p.Asn203Asn | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/10 | 788/3031 | 609/1569 | 203/522 | chr11 | 32434752 | ||
chr11:32434848
|
G | T | 1 | a0001c0013 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.513C>A | p.Gly171Gly | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/10 | 692/3031 | 513/1569 | 171/522 | chr11 | 32434848 | ||
chr11:32435016
|
G | A | 3 | a0001c0001a0001c0006a0001c0012 | 110 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(107): Show |
synonymous_variant | LOW | c.345C>T | p.Pro115Pro | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/10 | 524/3031 | 345/1569 | 115/522 | chr11 | 32435016 | ||
chr11:32435148
|
C | A | 6 | a0001c0003a0001c0004a0001c0005others(3): Show | 108 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(105): Show |
synonymous_variant | LOW | c.213G>T | p.Pro71Pro | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/10 | 392/3031 | 213/1569 | 71/522 | chr11 | 32435148 | ||
chr11:32435180
|
G | T | 1 | a0001c0011 | 3 | HG01928.hp2 HG01975.hp2 HG01978.hp2 |
synonymous_variant | LOW | c.181C>A | p.Arg61Arg | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/10 | 360/3031 | 181/1569 | 61/522 | chr11 | 32435180 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:32387849
|
T | C | 2 | a0001c0002t0011a0001c0004t0020 | 4 | HG01884.hp2 HG02572.hp1 HG02717.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1209A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 1209 | chr11 | 32387849 | |||||
chr11:32387926
|
T | A | 1 | a0001c0001t0013 | 3 | HG01346.hp1 HG03491.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1132A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 1132 | chr11 | 32387926 | |||||
chr11:32387960
|
G | A | 4 | a0001c0003t0016a0001c0010t0016a0001c0010t0021others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1098C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 1098 | chr11 | 32387960 | |||||
chr11:32388003
|
A | AAC | 5 | a0001c0002t0007a0001c0003t0031a0001c0004t0007others(2): Show | 14 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1053_*1054dupGT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 1054 | chr11 | 32388003 | |||||
chr11:32388003
|
AAC | A | 9 | a0001c0002t0015a0001c0003t0009a0001c0003t0010others(6): Show | 16 | HG01358.hp1 HG01358.hp2 HG01496.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1053_*1054delGT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 1053 | chr11 | 32388003 | |||||
chr11:32388003
|
AACAC | A | 14 | a0001c0001t0012a0001c0002t0003a0001c0002t0026others(11): Show | 48 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1051_*1054delGTGT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 1051 | chr11 | 32388003 | |||||
chr11:32388003
|
AACACAC | A | 19 | a0001c0001t0002a0001c0001t0005a0001c0001t0013others(16): Show | 137 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*1049_*1054delGTGT others(2): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 1049 | chr11 | 32388003 | |||||
chr11:32388003
|
AACACACA others(3): Show |
A | 2 | a0001c0003t0025a0001c0010t0021 | 2 | HG01099.hp1 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1045_*1054delGTGT others(6): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 1045 | chr11 | 32388003 | |||||
chr11:32388079
|
A | AT | 8 | a0001c0001t0002a0001c0001t0012a0001c0001t0013others(5): Show | 102 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*978dupA | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 978 | chr11 | 32388079 | |||||
chr11:32388155
|
C | T | 1 | a0001c0007t0028 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*903G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 903 | chr11 | 32388155 | |||||
chr11:32388194
|
A | C | 4 | a0001c0003t0016a0001c0010t0016a0001c0010t0021others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*864T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 864 | chr11 | 32388194 | |||||
chr11:32388223
|
T | C | 2 | a0001c0003t0024a0001c0003t0025 | 2 | HG01099.hp1 HG01175.hp1 |
3_prime_UTR_variant | MODIFIER | c.*835A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 835 | chr11 | 32388223 | |||||
chr11:32388238
|
C | G | 3 | a0001c0002t0004a0001c0003t0004a0001c0004t0004 | 16 | HG02257.hp2 HG02622.hp2 HG02647.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*820G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 820 | chr11 | 32388238 | |||||
chr11:32388456
|
T | C | 47 | a0001c0001t0002a0001c0001t0005a0001c0001t0012others(44): Show | 205 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*602A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 602 | chr11 | 32388456 | |||||
chr11:32388516
|
C | T | 1 | a0001c0004t0030 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*542G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 542 | chr11 | 32388516 | |||||
chr11:32388713
|
C | T | 1 | a0001c0002t0011 | 3 | HG02572.hp1 HG02717.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*345G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 345 | chr11 | 32388713 | |||||
chr11:32388791
|
C | G | 49 | a0001c0001t0002a0001c0001t0005a0001c0001t0012others(46): Show | 210 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*267G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 267 | chr11 | 32388791 | |||||
chr11:32388834
|
T | C | 13 | a0001c0002t0003a0001c0003t0003a0001c0003t0009others(10): Show | 39 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*224A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 224 | chr11 | 32388834 | |||||
chr11:32388920
|
C | T | 1 | a0001c0004t0020 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*138G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 138 | chr11 | 32388920 | |||||
chr11:32388970
|
T | C | 16 | a0001c0002t0003a0001c0003t0003a0001c0003t0009others(13): Show | 44 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*88A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 88 | chr11 | 32388970 | |||||
chr11:32389042
|
C | A | 3 | a0001c0003t0016a0001c0010t0016a0001c0016t0016 | 3 | HG02145.hp2 HG02486.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*16G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 10/10 | 16 | chr11 | 32389042 | |||||
chr11:32435420
|
G | T | 1 | a0001c0001t0019 | 1 | HG02683.hp2 | 5_prime_UTR_variant | MODIFIER | c.-60C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/10 | 60 | chr11 | 32435420 | |||||
chr11:32435423
|
G | A | 1 | a0001c0009t0033 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-63C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/10 | 63 | chr11 | 32435423 | |||||
chr11:32435435
|
G | T | 1 | a0001c0003t0010 | 3 | HG01496.hp1 HG02451.hp2 HG02818.hp1 |
5_prime_UTR_variant | MODIFIER | c.-75C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/10 | 75 | chr11 | 32435435 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:32389189
|
C | T | 1 | a0001c0001t0002g0155 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1448-10G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32389189 | ||||||
chr11:32389228
|
A | G | 177 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(174): Show | 184 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.1448-49T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32389228 | ||||||
chr11:32389408
|
C | A | 2 | a0001c0005t0005g0255a0001c0005t0005g0268 | 2 | HG03490.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1448-229G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32389408 | ||||||
chr11:32389554
|
G | A | 48 | a0001c0002t0001g0048a0001c0002t0003g0059a0001c0002t0003g0068others(45): Show | 49 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1448-375C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32389554 | ||||||
chr11:32389694
|
T | A | 95 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(92): Show | 97 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1448-515A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32389694 | ||||||
chr11:32389795
|
G | C | 1 | a0001c0003t0004g0233 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1448-616C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32389795 | ||||||
chr11:32389826
|
C | G | 2 | a0001c0003t0024g0237a0001c0003t0025g0238 | 2 | HG01099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1448-647G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32389826 | ||||||
chr11:32389874
|
T | C | 2 | a0001c0003t0024g0237a0001c0003t0025g0238 | 2 | HG01099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1448-695A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32389874 | ||||||
chr11:32389902
|
A | G | 1 | a0001c0002t0001g0077 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1448-723T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32389902 | ||||||
chr11:32390089
|
G | T | 4 | a0001c0010t0014g0257a0001c0010t0014g0270a0001c0012t0014g0211others(1): Show | 4 | HG01109.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1448-910C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32390089 | ||||||
chr11:32390414
|
C | T | 4 | a0001c0003t0016g0224a0001c0010t0016g0271a0001c0010t0021g0216others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1448-1235G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32390414 | ||||||
chr11:32390458
|
C | G | 1 | a0001c0004t0001g0280 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1448-1279G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32390458 | ||||||
chr11:32390483
|
A | G | 4 | a0001c0009t0008g0004a0001c0009t0008g0034a0001c0010t0008g0218others(1): Show | 5 | HG02572.hp2 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1448-1304T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32390483 | ||||||
chr11:32390487
|
C | T | 3 | a0001c0004t0006g0015a0001c0004t0006g0291a0001c0010t0006g0217 | 4 | HG02451.hp1 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1448-1308G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32390487 | ||||||
chr11:32390494
|
T | C | 49 | a0001c0002t0003g0059a0001c0002t0003g0068a0001c0003t0003g0214others(46): Show | 50 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1448-1315A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32390494 | ||||||
chr11:32390520
|
G | A | 10 | a0001c0001t0002g0010a0001c0001t0002g0135a0001c0001t0002g0166others(7): Show | 11 | HG00642.hp2 HG01071.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1448-1341C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32390520 | ||||||
chr11:32390952
|
A | T | 1 | a0001c0002t0001g0076 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1447+1020T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32390952 | ||||||
chr11:32390971
|
TTGTTTG | T | 44 | a0001c0002t0003g0059a0001c0002t0003g0068a0001c0003t0003g0214others(41): Show | 45 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.1447+995_1447+1000 others(9): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32390971 | ||||||
chr11:32390973
|
GTTTGT | G | 134 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(131): Show | 140 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.1447+994_1447+998d others(7): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32390973 | ||||||
chr11:32390978
|
T | G | 44 | a0001c0002t0003g0059a0001c0002t0003g0068a0001c0003t0003g0214others(41): Show | 45 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.1447+994A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32390978 | ||||||
chr11:32391089
|
C | T | 1 | a0001c0009t0033g0306 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1447+883G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32391089 | ||||||
chr11:32391090
|
G | A | 4 | a0001c0003t0016g0224a0001c0010t0016g0271a0001c0010t0021g0216others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1447+882C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32391090 | ||||||
chr11:32391141
|
T | C | 1 | a0001c0001t0002g0128 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1447+831A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32391141 | ||||||
chr11:32391237
|
A | AACC | 44 | a0001c0002t0003g0059a0001c0002t0003g0068a0001c0003t0003g0214others(41): Show | 45 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.1447+734_1447+735i others(5): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32391237 | ||||||
chr11:32391262
|
A | G | 1 | a0001c0001t0002g0144 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1447+710T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32391262 | ||||||
chr11:32391277
|
C | T | 4 | a0001c0003t0016g0224a0001c0010t0016g0271a0001c0010t0021g0216others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1447+695G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32391277 | ||||||
chr11:32391337
|
T | C | 4 | a0001c0009t0008g0004a0001c0009t0008g0034a0001c0010t0008g0218others(1): Show | 5 | HG02572.hp2 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1447+635A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32391337 | ||||||
chr11:32391361
|
A | G | 3 | a0001c0011t0001g0021a0001c0011t0001g0022a0001c0011t0001g0023 | 3 | HG01928.hp2 HG01975.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1447+611T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32391361 | ||||||
chr11:32391523
|
C | T | 2 | a0001c0002t0003g0059a0001c0002t0003g0068 | 2 | HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1447+449G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32391523 | ||||||
chr11:32391572
|
A | G | 1 | a0001c0004t0003g0293 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1447+400T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 9/9 | chr11 | 32391572 | ||||||
chr11:32392096
|
C | T | 1 | a0001c0003t0003g0245 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1355-32G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 8/9 | chr11 | 32392096 | ||||||
chr11:32392151
|
C | T | 10 | a0001c0001t0002g0010a0001c0001t0002g0135a0001c0001t0002g0166others(7): Show | 11 | HG00642.hp2 HG01071.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1355-87G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 8/9 | chr11 | 32392151 | ||||||
chr11:32392787
|
G | T | 35 | a0001c0002t0003g0059a0001c0002t0003g0068a0001c0003t0003g0214others(32): Show | 36 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1265-32C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32392787 | ||||||
chr11:32392896
|
A | C | 4 | a0001c0010t0014g0257a0001c0010t0014g0270a0001c0012t0014g0211others(1): Show | 4 | HG01109.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1265-141T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32392896 | ||||||
chr11:32392928
|
G | A | 4 | a0001c0003t0010g0017a0001c0003t0010g0018a0001c0003t0010g0019others(1): Show | 4 | HG01496.hp1 HG02451.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1265-173C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32392928 | ||||||
chr11:32392936
|
G | C | 3 | a0001c0004t0009g0288a0001c0004t0009g0294a0001c0004t0009g0296 | 3 | HG01891.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1265-181C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32392936 | ||||||
chr11:32392972
|
T | TA | 44 | a0001c0001t0005g0008a0001c0001t0005g0115a0001c0001t0005g0117others(41): Show | 49 | HG00558.hp1 HG02129.hp2 HG02257.hp2 others(46): Show |
intron_variant | MODIFIER | c.1265-218dupT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32392972 | ||||||
chr11:32393004
|
G | A | 14 | a0001c0001t0005g0008a0001c0001t0005g0115a0001c0001t0005g0117others(11): Show | 15 | HG02129.hp2 HG03490.hp2 HG03654.hp1 others(12): Show |
intron_variant | MODIFIER | c.1265-249C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32393004 | ||||||
chr11:32393041
|
A | G | 1 | a0001c0007t0028g0033 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1265-286T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32393041 | ||||||
chr11:32393100
|
C | T | 7 | a0001c0003t0006g0219a0001c0003t0006g0220a0001c0003t0006g0223others(4): Show | 7 | HG02895.hp2 HG02897.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1265-345G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32393100 | ||||||
chr11:32393101
|
G | A | 10 | a0001c0001t0002g0123a0001c0001t0002g0131a0001c0001t0002g0132others(7): Show | 10 | HG00558.hp2 HG00621.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.1265-346C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32393101 | ||||||
chr11:32393330
|
G | T | 1 | a0001c0006t0001g0212 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1265-575C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32393330 | ||||||
chr11:32393406
|
C | T | 3 | a0001c0001t0002g0119a0001c0001t0002g0187a0001c0001t0002g0208 | 3 | NA18947.hp2 NA18950.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1265-651G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32393406 | ||||||
chr11:32393564
|
CA | C | 138 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(135): Show | 141 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.1265-810delT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32393564 | ||||||
chr11:32393763
|
A | G | 1 | a0001c0005t0005g0268 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1265-1008T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32393763 | ||||||
chr11:32393929
|
G | A | 2 | a0001c0005t0005g0261a0001c0005t0005g0263 | 2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1265-1174C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32393929 | ||||||
chr11:32393941
|
A | G | 110 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(107): Show | 112 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1265-1186T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32393941 | ||||||
chr11:32393983
|
C | T | 35 | a0001c0002t0003g0059a0001c0002t0003g0068a0001c0003t0003g0214others(32): Show | 36 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1265-1228G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32393983 | ||||||
chr11:32394140
|
G | A | 1 | a0001c0010t0021g0216 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1265-1385C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32394140 | ||||||
chr11:32394145
|
C | T | 4 | a0001c0003t0010g0017a0001c0003t0010g0018a0001c0003t0010g0019others(1): Show | 4 | HG01496.hp1 HG02451.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1265-1390G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32394145 | ||||||
chr11:32394146
|
G | A | 1 | a0001c0005t0002g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1265-1391C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32394146 | ||||||
chr11:32394276
|
T | C | 14 | a0001c0001t0005g0008a0001c0001t0005g0115a0001c0001t0005g0117others(11): Show | 15 | HG02129.hp2 HG03490.hp2 HG03654.hp1 others(12): Show |
intron_variant | MODIFIER | c.1265-1521A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32394276 | ||||||
chr11:32394339
|
C | T | 2 | a0001c0002t0001g0051a0001c0002t0001g0075 | 2 | NA18978.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1265-1584G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32394339 | ||||||
chr11:32394391
|
T | C | 4 | a0001c0003t0016g0224a0001c0010t0016g0271a0001c0010t0021g0216others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1265-1636A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32394391 | ||||||
chr11:32394539
|
C | T | 1 | a0001c0007t0028g0033 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1264+1718G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32394539 | ||||||
chr11:32395042
|
A | T | 4 | a0001c0003t0016g0224a0001c0010t0016g0271a0001c0010t0021g0216others(1): Show | 4 | HG02145.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1264+1215T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395042 | ||||||
chr11:32395329
|
G | A | 103 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(100): Show | 105 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1264+928C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395329 | ||||||
chr11:32395438
|
C | T | 2 | a0001c0003t0003g0244a0001c0007t0028g0033 | 2 | HG02970.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1264+819G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395438 | ||||||
chr11:32395477
|
C | CT | 6 | a0001c0001t0012g0196a0001c0002t0001g0089a0001c0002t0001g0091others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.1264+779dupA | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395477 | ||||||
chr11:32395514
|
C | T | 98 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(95): Show | 100 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1264+743G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395514 | ||||||
chr11:32395622
|
C | T | 1 | a0001c0007t0002g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1264+635G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395622 | ||||||
chr11:32395633
|
T | C | 1 | a0001c0002t0001g0060 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1264+624A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395633 | ||||||
chr11:32395687
|
C | T | 3 | a0001c0010t0014g0257a0001c0012t0014g0211a0001c0012t0023g0210 | 3 | HG02896.hp2 HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1264+570G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395687 | ||||||
chr11:32395708
|
C | T | 1 | a0001c0016t0016g0299 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1264+549G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395708 | ||||||
chr11:32395761
|
CT | C | 103 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(100): Show | 105 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1264+495delA | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395761 | ||||||
chr11:32395802
|
C | T | 1 | a0001c0005t0002g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1264+455G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395802 | ||||||
chr11:32395886
|
A | G | 103 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(100): Show | 105 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1264+371T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395886 | ||||||
chr11:32395901
|
G | A | 31 | a0001c0001t0005g0008a0001c0001t0005g0115a0001c0001t0005g0117others(28): Show | 35 | HG02129.hp2 HG02257.hp2 HG02572.hp1 others(32): Show |
intron_variant | MODIFIER | c.1264+356C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395901 | ||||||
chr11:32395980
|
A | C | 57 | a0001c0002t0003g0059a0001c0002t0003g0068a0001c0003t0003g0214others(54): Show | 60 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.1264+277T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32395980 | ||||||
chr11:32396122
|
A | G | 1 | a0001c0001t0002g0157 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1264+135T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32396122 | ||||||
chr11:32396123
|
A | T | 102 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(99): Show | 104 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.1264+134T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32396123 | ||||||
chr11:32396144
|
A | C | 2 | a0001c0003t0024g0237a0001c0003t0025g0238 | 2 | HG01099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1264+113T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 7/9 | chr11 | 32396144 | ||||||
chr11:32396567
|
C | T | 9 | a0001c0002t0004g0027a0001c0002t0004g0028a0001c0003t0002g0232others(6): Show | 11 | HG02647.hp1 HG02717.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1114-160G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32396567 | ||||||
chr11:32396688
|
A | G | 1 | a0001c0003t0010g0017 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1114-281T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32396688 | ||||||
chr11:32396880
|
A | G | 1 | a0001c0009t0033g0306 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1114-473T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32396880 | ||||||
chr11:32396931
|
G | A | 7 | a0001c0010t0014g0257a0001c0010t0014g0270a0001c0010t0016g0271others(4): Show | 7 | HG01109.hp2 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1114-524C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32396931 | ||||||
chr11:32397059
|
T | A | 101 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(98): Show | 103 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1114-652A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32397059 | ||||||
chr11:32397345
|
C | G | 7 | a0001c0009t0008g0004a0001c0009t0008g0030a0001c0009t0008g0031others(4): Show | 8 | HG02280.hp1 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1114-938G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32397345 | ||||||
chr11:32397413
|
T | C | 2 | a0001c0009t0008g0030a0001c0009t0008g0031 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1114-1006A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32397413 | ||||||
chr11:32397482
|
A | AT | 148 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(145): Show | 154 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(151): Show |
intron_variant | MODIFIER | c.1114-1076dupA | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32397482 | ||||||
chr11:32397482
|
A | ATT | 33 | a0001c0002t0004g0027a0001c0002t0004g0028a0001c0003t0001g0235others(30): Show | 36 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.1114-1077_1114-107 others(6): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32397482 | ||||||
chr11:32397493
|
T | G | 1 | a0001c0004t0007g0286 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1114-1086A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32397493 | ||||||
chr11:32397500
|
G | A | 4 | a0001c0001t0002g0134a0001c0001t0002g0165a0001c0001t0002g0169others(1): Show | 4 | HG02602.hp1 HG02683.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114-1093C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32397500 | ||||||
chr11:32397504
|
G | A | 3 | a0001c0001t0002g0139a0001c0001t0002g0141a0001c0001t0002g0163 | 3 | HG03239.hp1 HG03831.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1114-1097C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32397504 | ||||||
chr11:32397606
|
C | T | 1 | a0001c0001t0002g0189 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1114-1199G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32397606 | ||||||
chr11:32397806
|
A | T | 101 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(98): Show | 103 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1114-1399T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32397806 | ||||||
chr11:32398230
|
C | T | 3 | a0001c0003t0004g0231a0001c0003t0004g0240a0001c0003t0004g0242 | 3 | HG02257.hp2 HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1113+1718G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32398230 | ||||||
chr11:32398235
|
C | T | 4 | a0001c0004t0009g0288a0001c0004t0009g0294a0001c0004t0009g0296others(1): Show | 4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+1713G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32398235 | ||||||
chr11:32398349
|
G | A | 15 | a0001c0001t0005g0008a0001c0001t0005g0115a0001c0001t0005g0117others(12): Show | 16 | HG02129.hp2 HG03490.hp2 HG03654.hp1 others(13): Show |
intron_variant | MODIFIER | c.1113+1599C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32398349 | ||||||
chr11:32398505
|
T | C | 3 | a0001c0003t0009g0229a0001c0003t0009g0239a0001c0006t0009g0178 | 3 | NA18961.hp2 NA18987.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1113+1443A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32398505 | ||||||
chr11:32398669
|
A | T | 2 | a0001c0005t0002g0213a0001c0005t0002g0253 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1113+1279T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32398669 | ||||||
chr11:32398674
|
T | C | 1 | a0001c0001t0002g0163 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1113+1274A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32398674 | ||||||
chr11:32398773
|
A | T | 8 | a0001c0003t0006g0219a0001c0003t0006g0220a0001c0003t0006g0223others(5): Show | 8 | HG02145.hp2 HG02895.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1113+1175T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32398773 | ||||||
chr11:32398790
|
A | G | 1 | a0001c0002t0001g0061 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1113+1158T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32398790 | ||||||
chr11:32398946
|
G | A | 101 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(98): Show | 103 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1113+1002C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32398946 | ||||||
chr11:32398971
|
AC | A | 11 | a0001c0003t0006g0219a0001c0003t0006g0220a0001c0003t0006g0223others(8): Show | 12 | HG02145.hp2 HG02451.hp1 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1113+976delG | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32398971 | ||||||
chr11:32399016
|
C | T | 1 | a0001c0010t0006g0217 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1113+932G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32399016 | ||||||
chr11:32399024
|
T | C | 105 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(102): Show | 107 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1113+924A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32399024 | ||||||
chr11:32399025
|
G | A | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+923C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32399025 | ||||||
chr11:32399086
|
G | A | 3 | a0001c0004t0009g0288a0001c0004t0009g0294a0001c0004t0009g0296 | 3 | HG01891.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1113+862C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32399086 | ||||||
chr11:32399153
|
T | C | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+795A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32399153 | ||||||
chr11:32399348
|
C | T | 3 | a0001c0004t0009g0288a0001c0004t0009g0294a0001c0004t0009g0296 | 3 | HG01891.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1113+600G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32399348 | ||||||
chr11:32399354
|
T | C | 1 | a0001c0001t0002g0113 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1113+594A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32399354 | ||||||
chr11:32399429
|
A | G | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113+519T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32399429 | ||||||
chr11:32399444
|
T | C | 1 | a0001c0001t0002g0179 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1113+504A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32399444 | ||||||
chr11:32399727
|
C | G | 1 | a0001c0004t0020g0302 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1113+221G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32399727 | ||||||
chr11:32399727
|
C | T | 7 | a0001c0009t0008g0004a0001c0009t0008g0030a0001c0009t0008g0031others(4): Show | 8 | HG02280.hp1 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1113+221G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 6/9 | chr11 | 32399727 | ||||||
chr11:32400105
|
T | C | 1 | a0001c0004t0020g0302 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1017-61A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32400105 | ||||||
chr11:32400108
|
T | C | 7 | a0001c0002t0001g0046a0001c0002t0001g0062a0001c0002t0001g0067others(4): Show | 7 | HG00621.hp2 HG02015.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.1017-64A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32400108 | ||||||
chr11:32400291
|
C | T | 1 | a0001c0005t0002g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1017-247G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32400291 | ||||||
chr11:32400295
|
G | T | 1 | a0001c0002t0011g0025 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1017-251C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32400295 | ||||||
chr11:32400431
|
G | A | 97 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(94): Show | 99 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1017-387C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32400431 | ||||||
chr11:32400446
|
G | A | 15 | a0001c0001t0005g0008a0001c0001t0005g0115a0001c0001t0005g0117others(12): Show | 16 | HG02129.hp2 HG03490.hp2 HG03654.hp1 others(13): Show |
intron_variant | MODIFIER | c.1017-402C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32400446 | ||||||
chr11:32400526
|
G | A | 1 | a0001c0001t0002g0161 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1017-482C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32400526 | ||||||
chr11:32400646
|
C | T | 3 | a0001c0010t0014g0257a0001c0012t0014g0211a0001c0012t0023g0210 | 3 | HG02896.hp2 HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1017-602G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32400646 | ||||||
chr11:32400740
|
C | T | 3 | a0001c0004t0009g0288a0001c0004t0009g0294a0001c0004t0009g0296 | 3 | HG01891.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1017-696G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32400740 | ||||||
chr11:32400966
|
T | C | 1 | a0001c0002t0001g0040 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1017-922A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32400966 | ||||||
chr11:32401178
|
G | T | 34 | a0001c0002t0003g0059a0001c0002t0003g0068a0001c0003t0003g0214others(31): Show | 35 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1017-1134C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32401178 | ||||||
chr11:32401274
|
T | G | 1 | a0001c0001t0002g0157 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1017-1230A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32401274 | ||||||
chr11:32401472
|
G | A | 7 | a0001c0008t0003g0281a0001c0008t0003g0285a0001c0008t0003g0287others(4): Show | 7 | HG00642.hp1 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1017-1428C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32401472 | ||||||
chr11:32401505
|
CG | C | 149 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(146): Show | 153 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.1017-1462delC | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32401505 | ||||||
chr11:32401507
|
G | T | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017-1463C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32401507 | ||||||
chr11:32401523
|
G | T | 1 | a0001c0006t0001g0112 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1017-1479C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32401523 | ||||||
chr11:32401653
|
C | A | 11 | a0001c0003t0006g0219a0001c0003t0006g0220a0001c0003t0006g0223others(8): Show | 12 | HG02145.hp2 HG02451.hp1 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1017-1609G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32401653 | ||||||
chr11:32401654
|
C | T | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017-1610G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32401654 | ||||||
chr11:32401827
|
A | G | 32 | a0001c0001t0005g0008a0001c0001t0005g0115a0001c0001t0005g0117others(29): Show | 36 | HG02129.hp2 HG02257.hp2 HG02572.hp1 others(33): Show |
intron_variant | MODIFIER | c.1017-1783T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32401827 | ||||||
chr11:32401906
|
C | T | 1 | a0001c0003t0003g0249 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1017-1862G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32401906 | ||||||
chr11:32401962
|
G | A | 3 | a0001c0010t0014g0257a0001c0012t0014g0211a0001c0012t0023g0210 | 3 | HG02896.hp2 HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1017-1918C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32401962 | ||||||
chr11:32402045
|
G | C | 1 | a0001c0004t0020g0302 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1017-2001C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32402045 | ||||||
chr11:32402117
|
G | A | 1 | a0001c0005t0002g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1017-2073C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32402117 | ||||||
chr11:32402206
|
T | C | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017-2162A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32402206 | ||||||
chr11:32402302
|
C | A | 1 | a0001c0012t0014g0211 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1017-2258G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32402302 | ||||||
chr11:32402368
|
A | G | 1 | a0001c0005t0005g0258 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1017-2324T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32402368 | ||||||
chr11:32402580
|
C | G | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017-2536G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32402580 | ||||||
chr11:32402590
|
G | A | 1 | a0001c0001t0002g0145 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1017-2546C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32402590 | ||||||
chr11:32402750
|
A | C | 1 | a0001c0008t0003g0292 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1017-2706T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32402750 | ||||||
chr11:32402750
|
A | T | 142 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(139): Show | 145 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.1017-2706T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32402750 | ||||||
chr11:32402843
|
C | A | 57 | a0001c0001t0005g0008a0001c0001t0005g0115a0001c0001t0005g0117others(54): Show | 62 | HG01099.hp1 HG01109.hp2 HG01169.hp2 others(59): Show |
intron_variant | MODIFIER | c.1017-2799G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32402843 | ||||||
chr11:32402843
|
C | G | 133 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(130): Show | 136 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.1017-2799G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32402843 | ||||||
chr11:32402940
|
G | C | 1 | a0001c0004t0020g0302 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1017-2896C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32402940 | ||||||
chr11:32403058
|
T | C | 185 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(182): Show | 193 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(190): Show |
intron_variant | MODIFIER | c.1017-3014A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32403058 | ||||||
chr11:32403278
|
C | G | 5 | a0001c0002t0001g0089a0001c0002t0001g0091a0001c0002t0001g0095others(2): Show | 5 | HG00099.hp2 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1017-3234G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32403278 | ||||||
chr11:32403329
|
A | C | 1 | a0001c0002t0001g0048 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1017-3285T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32403329 | ||||||
chr11:32403555
|
C | A | 1 | a0001c0004t0018g0295 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1017-3511G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32403555 | ||||||
chr11:32403572
|
CT | C | 20 | a0001c0001t0002g0119a0001c0002t0001g0101a0001c0003t0010g0017others(17): Show | 21 | HG01109.hp2 HG01169.hp1 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.1017-3529delA | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32403572 | ||||||
chr11:32403572
|
CTT | C | 112 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(109): Show | 115 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.1017-3530_1017-352 others(6): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32403572 | ||||||
chr11:32403572
|
CTTT | C | 24 | a0001c0001t0002g0179a0001c0001t0002g0187a0001c0001t0012g0196others(21): Show | 24 | HG00733.hp2 HG01261.hp2 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.1017-3531_1017-352 others(7): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32403572 | ||||||
chr11:32403601
|
G | A | 1 | a0001c0002t0001g0084 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1017-3557C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32403601 | ||||||
chr11:32403614
|
G | A | 2 | a0001c0003t0002g0232a0001c0003t0004g0012 | 3 | HG02723.hp1 HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1017-3570C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32403614 | ||||||
chr11:32403736
|
G | A | 4 | a0001c0010t0014g0257a0001c0010t0021g0216a0001c0012t0014g0211others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017-3692C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32403736 | ||||||
chr11:32403762
|
A | C | 4 | a0001c0010t0014g0257a0001c0010t0021g0216a0001c0012t0014g0211others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017-3718T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32403762 | ||||||
chr11:32403951
|
ACTCT | A | 5 | a0001c0003t0003g0214a0001c0003t0003g0215a0001c0003t0031g0251others(2): Show | 5 | HG02109.hp1 HG02559.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017-3911_1017-390 others(8): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32403951 | ||||||
chr11:32404101
|
TC | T | 32 | a0001c0001t0005g0008a0001c0001t0005g0115a0001c0001t0005g0117others(29): Show | 36 | HG02129.hp2 HG02257.hp2 HG02572.hp1 others(33): Show |
intron_variant | MODIFIER | c.1017-4058delG | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32404101 | ||||||
chr11:32404195
|
G | A | 7 | a0001c0003t0003g0230a0001c0003t0003g0244a0001c0003t0003g0252others(4): Show | 7 | HG03017.hp2 HG03491.hp2 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.1017-4151C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32404195 | ||||||
chr11:32404252
|
G | C | 135 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(132): Show | 138 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1017-4208C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32404252 | ||||||
chr11:32404268
|
C | CA | 11 | a0001c0002t0001g0047a0001c0002t0001g0054a0001c0002t0001g0094others(8): Show | 12 | HG00558.hp1 HG01099.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1017-4225dupT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32404268 | ||||||
chr11:32404268
|
CA | C | 62 | a0001c0001t0002g0149a0001c0001t0002g0166a0001c0001t0002g0208others(59): Show | 66 | HG01109.hp2 HG01496.hp1 HG01884.hp2 others(63): Show |
intron_variant | MODIFIER | c.1017-4225delT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32404268 | ||||||
chr11:32404268
|
CAA | C | 125 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(122): Show | 128 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.1017-4226_1017-422 others(6): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32404268 | ||||||
chr11:32404316
|
T | C | 1 | a0001c0006t0002g0181 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1017-4272A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32404316 | ||||||
chr11:32404457
|
G | T | 2 | a0001c0007t0001g0053a0001c0007t0001g0071 | 2 | HG01175.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.1017-4413C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32404457 | ||||||
chr11:32404563
|
C | T | 4 | a0001c0010t0014g0257a0001c0010t0021g0216a0001c0012t0014g0211others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017-4519G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32404563 | ||||||
chr11:32404608
|
C | A | 32 | a0001c0001t0005g0008a0001c0001t0005g0115a0001c0001t0005g0117others(29): Show | 36 | HG02129.hp2 HG02257.hp2 HG02572.hp1 others(33): Show |
intron_variant | MODIFIER | c.1017-4564G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32404608 | ||||||
chr11:32404923
|
G | A | 1 | a0001c0004t0001g0280 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1017-4879C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32404923 | ||||||
chr11:32405023
|
A | G | 2 | a0001c0002t0001g0083a0001c0002t0001g0094 | 2 | HG00558.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1017-4979T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405023 | ||||||
chr11:32405077
|
T | A | 1 | a0001c0001t0002g0173 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1017-5033A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405077 | ||||||
chr11:32405130
|
A | T | 1 | a0001c0004t0004g0275 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1017-5086T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405130 | ||||||
chr11:32405158
|
C | T | 135 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(132): Show | 138 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1017-5114G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405158 | ||||||
chr11:32405323
|
G | A | 2 | a0001c0004t0004g0274a0001c0004t0004g0275 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1017-5279C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405323 | ||||||
chr11:32405376
|
G | A | 1 | a0001c0002t0007g0086 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1017-5332C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405376 | ||||||
chr11:32405407
|
C | G | 131 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(128): Show | 134 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.1017-5363G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405407 | ||||||
chr11:32405455
|
A | C | 5 | a0001c0009t0008g0004a0001c0009t0008g0034a0001c0009t0033g0306others(2): Show | 6 | HG02280.hp1 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1017-5411T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405455 | ||||||
chr11:32405490
|
A | G | 96 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(93): Show | 98 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1017-5446T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405490 | ||||||
chr11:32405510
|
T | A | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017-5466A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405510 | ||||||
chr11:32405634
|
C | CAT | 180 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(177): Show | 187 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(184): Show |
intron_variant | MODIFIER | c.1017-5591_1017-559 others(6): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405634 | ||||||
chr11:32405768
|
T | A | 1 | a0001c0001t0002g0179 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1017-5724A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405768 | ||||||
chr11:32405816
|
A | G | 1 | a0001c0002t0001g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1017-5772T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405816 | ||||||
chr11:32405821
|
G | A | 2 | a0001c0011t0001g0022a0001c0011t0001g0023 | 2 | HG01928.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1017-5777C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405821 | ||||||
chr11:32405875
|
C | T | 3 | a0001c0010t0014g0270a0001c0010t0016g0271a0001c0016t0016g0299 | 3 | HG01109.hp2 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1017-5831G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405875 | ||||||
chr11:32405882
|
T | G | 145 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(142): Show | 148 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.1017-5838A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405882 | ||||||
chr11:32405937
|
G | A | 1 | a0001c0005t0002g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1017-5893C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405937 | ||||||
chr11:32405966
|
G | A | 1 | a0001c0001t0002g0195 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1017-5922C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32405966 | ||||||
chr11:32406133
|
G | A | 1 | a0001c0001t0002g0179 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1017-6089C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406133 | ||||||
chr11:32406191
|
A | C | 1 | a0001c0002t0001g0056 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1017-6147T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406191 | ||||||
chr11:32406277
|
G | A | 145 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(142): Show | 148 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.1017-6233C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406277 | ||||||
chr11:32406283
|
C | T | 3 | a0001c0010t0014g0270a0001c0010t0016g0271a0001c0016t0016g0299 | 3 | HG01109.hp2 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1017-6239G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406283 | ||||||
chr11:32406319
|
A | T | 2 | a0001c0002t0001g0074a0001c0006t0001g0199 | 2 | HG00408.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1017-6275T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406319 | ||||||
chr11:32406459
|
G | A | 135 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(132): Show | 138 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1017-6415C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406459 | ||||||
chr11:32406486
|
A | C | 139 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(136): Show | 142 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.1017-6442T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406486 | ||||||
chr11:32406618
|
C | T | 135 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(132): Show | 138 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1017-6574G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406618 | ||||||
chr11:32406628
|
A | AT | 138 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(135): Show | 141 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.1017-6585_1017-658 others(5): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406628 | ||||||
chr11:32406630
|
A | AT | 3 | a0001c0002t0001g0036a0001c0002t0001g0094a0001c0004t0017g0279 | 3 | HG00558.hp1 HG02818.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1017-6587_1017-658 others(5): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406630 | ||||||
chr11:32406630
|
A | T | 183 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(180): Show | 190 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.1017-6586T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406630 | ||||||
chr11:32406632
|
T | A | 1 | a0001c0002t0001g0079 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1017-6588A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406632 | ||||||
chr11:32406642
|
T | C | 1 | a0001c0009t0008g0034 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1017-6598A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406642 | ||||||
chr11:32406771
|
C | T | 10 | a0001c0003t0006g0219a0001c0003t0006g0220a0001c0003t0006g0223others(7): Show | 11 | HG02145.hp2 HG02559.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.1017-6727G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406771 | ||||||
chr11:32406816
|
C | T | 2 | a0001c0005t0002g0213a0001c0005t0002g0253 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1017-6772G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406816 | ||||||
chr11:32406956
|
G | A | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017-6912C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406956 | ||||||
chr11:32406999
|
T | C | 135 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(132): Show | 138 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1017-6955A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32406999 | ||||||
chr11:32407170
|
G | A | 2 | a0001c0005t0002g0213a0001c0005t0002g0253 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1017-7126C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407170 | ||||||
chr11:32407238
|
GAAAAACA others(1): Show |
G | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017-7202_1017-719 others(12): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407238 | ||||||
chr11:32407252
|
CA | C | 5 | a0001c0002t0001g0002a0001c0002t0001g0047a0001c0002t0001g0049others(2): Show | 8 | NA18960.hp2 NA18961.hp1 NA18965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1017-7209delT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407252 | ||||||
chr11:32407405
|
CAGA | C | 7 | a0001c0003t0003g0230a0001c0003t0003g0244a0001c0003t0003g0252others(4): Show | 7 | HG03017.hp2 HG03491.hp2 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.1017-7364_1017-736 others(7): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407405 | ||||||
chr11:32407432
|
A | G | 135 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(132): Show | 138 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1017-7388T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407432 | ||||||
chr11:32407510
|
C | T | 4 | a0001c0010t0014g0257a0001c0010t0021g0216a0001c0012t0014g0211others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017-7466G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407510 | ||||||
chr11:32407549
|
C | T | 1 | a0001c0001t0002g0144 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1017-7505G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407549 | ||||||
chr11:32407550
|
C | T | 34 | a0001c0002t0003g0059a0001c0002t0003g0068a0001c0003t0003g0214others(31): Show | 35 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1017-7506G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407550 | ||||||
chr11:32407553
|
C | T | 177 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(174): Show | 184 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.1017-7509G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407553 | ||||||
chr11:32407558
|
T | C | 3 | a0001c0010t0014g0270a0001c0010t0016g0271a0001c0016t0016g0299 | 3 | HG01109.hp2 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1017-7514A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407558 | ||||||
chr11:32407713
|
T | C | 139 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(136): Show | 142 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.1017-7669A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407713 | ||||||
chr11:32407715
|
T | C | 3 | a0001c0010t0014g0270a0001c0010t0016g0271a0001c0016t0016g0299 | 3 | HG01109.hp2 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1017-7671A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407715 | ||||||
chr11:32407912
|
C | T | 12 | a0001c0003t0006g0219a0001c0003t0006g0220a0001c0003t0006g0223others(9): Show | 13 | HG02145.hp2 HG02451.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1017-7868G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407912 | ||||||
chr11:32407949
|
G | A | 2 | a0001c0001t0002g0194a0001c0001t0002g0203 | 2 | HG00597.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1017-7905C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407949 | ||||||
chr11:32407957
|
T | C | 135 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(132): Show | 138 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1017-7913A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407957 | ||||||
chr11:32407971
|
C | T | 12 | a0001c0003t0006g0219a0001c0003t0006g0220a0001c0003t0006g0223others(9): Show | 13 | HG02145.hp2 HG02451.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1017-7927G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32407971 | ||||||
chr11:32408116
|
G | C | 3 | a0001c0010t0014g0270a0001c0010t0016g0271a0001c0016t0016g0299 | 3 | HG01109.hp2 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1017-8072C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408116 | ||||||
chr11:32408120
|
G | A | 135 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(132): Show | 138 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1017-8076C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408120 | ||||||
chr11:32408121
|
G | T | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017-8077C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408121 | ||||||
chr11:32408127
|
G | A | 2 | a0001c0002t0001g0072a0001c0006t0001g0164 | 2 | NA18944.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1017-8083C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408127 | ||||||
chr11:32408161
|
T | C | 4 | a0001c0010t0014g0257a0001c0010t0021g0216a0001c0012t0014g0211others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017-8117A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408161 | ||||||
chr11:32408203
|
C | T | 3 | a0001c0004t0009g0288a0001c0004t0009g0294a0001c0004t0009g0296 | 3 | HG01891.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1017-8159G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408203 | ||||||
chr11:32408213
|
G | GA | 11 | a0001c0002t0001g0051a0001c0002t0001g0065a0001c0003t0029g0221others(8): Show | 11 | HG01884.hp1 HG02559.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1017-8170dupT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408213 | ||||||
chr11:32408213
|
G | GAA | 95 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0111others(92): Show | 97 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1017-8171_1017-817 others(6): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408213 | ||||||
chr11:32408213
|
G | GAAA | 33 | a0001c0001t0002g0110a0001c0001t0002g0138a0001c0001t0002g0149others(30): Show | 34 | HG00642.hp1 HG00735.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1017-8172_1017-817 others(7): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408213 | ||||||
chr11:32408213
|
G | GAAAA | 6 | a0001c0003t0003g0247a0001c0003t0003g0248a0001c0003t0003g0249others(3): Show | 6 | HG00733.hp2 HG01261.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1017-8173_1017-817 others(8): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408213 | ||||||
chr11:32408330
|
T | G | 1 | a0001c0002t0007g0043 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1016+8160A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408330 | ||||||
chr11:32408356
|
A | T | 2 | a0001c0005t0002g0213a0001c0005t0002g0253 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1016+8134T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408356 | ||||||
chr11:32408514
|
T | TA | 33 | a0001c0002t0001g0001a0001c0002t0001g0005a0001c0002t0001g0007others(30): Show | 41 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.1016+7975dupT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408514 | ||||||
chr11:32408514
|
TA | T | 8 | a0001c0002t0001g0060a0001c0002t0001g0073a0001c0002t0001g0091others(5): Show | 8 | HG00099.hp2 HG00735.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1016+7975delT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408514 | ||||||
chr11:32408514
|
TAAAA | T | 16 | a0001c0001t0005g0008a0001c0001t0005g0115a0001c0001t0005g0117others(13): Show | 17 | HG01496.hp1 HG02129.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1016+7972_1016+797 others(8): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408514 | ||||||
chr11:32408514
|
TAAAAA | T | 20 | a0001c0002t0004g0028a0001c0002t0011g0025a0001c0002t0011g0026others(17): Show | 23 | HG01099.hp1 HG01175.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1016+7971_1016+797 others(9): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408514 | ||||||
chr11:32408514
|
TAAAAAA | T | 20 | a0001c0002t0004g0027a0001c0003t0001g0235a0001c0003t0001g0236others(17): Show | 21 | HG00733.hp2 HG01109.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.1016+7970_1016+797 others(10): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408514 | ||||||
chr11:32408514
|
TAAAAAAA | T | 28 | a0001c0001t0002g0174a0001c0001t0002g0209a0001c0002t0001g0069others(25): Show | 29 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.1016+7969_1016+797 others(11): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408514 | ||||||
chr11:32408514
|
TAAAAAAA others(1): Show |
T | 97 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(94): Show | 99 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1016+7968_1016+797 others(12): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408514 | ||||||
chr11:32408514
|
TAAAAAAA others(3): Show |
T | 4 | a0001c0010t0014g0257a0001c0010t0021g0216a0001c0012t0014g0211others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+7966_1016+797 others(14): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408514 | ||||||
chr11:32408514
|
TAAAAAAA others(8): Show |
T | 2 | a0001c0002t0001g0063a0001c0006t0001g0114 | 2 | NA18955.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1016+7961_1016+797 others(19): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408514 | ||||||
chr11:32408536
|
A | G | 2 | a0001c0001t0013g0143a0001c0001t0013g0148 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1016+7954T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408536 | ||||||
chr11:32408540
|
A | G | 141 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(138): Show | 144 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.1016+7950T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408540 | ||||||
chr11:32408829
|
T | C | 4 | a0001c0010t0014g0257a0001c0010t0021g0216a0001c0012t0014g0211others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+7661A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408829 | ||||||
chr11:32408851
|
G | A | 2 | a0001c0005t0002g0213a0001c0005t0002g0253 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1016+7639C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408851 | ||||||
chr11:32408939
|
T | C | 139 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(136): Show | 142 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.1016+7551A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408939 | ||||||
chr11:32408955
|
T | C | 4 | a0001c0010t0014g0257a0001c0010t0021g0216a0001c0012t0014g0211others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+7535A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32408955 | ||||||
chr11:32409055
|
G | A | 202 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(199): Show | 211 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(208): Show |
intron_variant | MODIFIER | c.1016+7435C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32409055 | ||||||
chr11:32409083
|
T | C | 2 | a0001c0005t0002g0213a0001c0005t0002g0253 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1016+7407A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32409083 | ||||||
chr11:32409109
|
G | A | 3 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0015g0055 | 8 | HG00639.hp2 HG01243.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1016+7381C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32409109 | ||||||
chr11:32409192
|
T | A | 1 | a0001c0002t0001g0056 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1016+7298A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32409192 | ||||||
chr11:32409193
|
G | T | 1 | a0001c0002t0001g0056 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1016+7297C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32409193 | ||||||
chr11:32409194
|
T | G | 1 | a0001c0002t0001g0056 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1016+7296A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32409194 | ||||||
chr11:32409232
|
A | T | 98 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(95): Show | 100 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1016+7258T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32409232 | ||||||
chr11:32409240
|
C | T | 32 | a0001c0001t0005g0008a0001c0001t0005g0115a0001c0001t0005g0117others(29): Show | 36 | HG02129.hp2 HG02257.hp2 HG02572.hp1 others(33): Show |
intron_variant | MODIFIER | c.1016+7250G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32409240 | ||||||
chr11:32409301
|
G | T | 2 | a0001c0008t0003g0285a0001c0008t0003g0289 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1016+7189C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32409301 | ||||||
chr11:32409543
|
C | A | 4 | a0001c0010t0014g0257a0001c0010t0021g0216a0001c0012t0014g0211others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+6947G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32409543 | ||||||
chr11:32409731
|
C | T | 1 | a0001c0001t0002g0166 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1016+6759G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32409731 | ||||||
chr11:32409798
|
G | A | 141 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(138): Show | 144 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.1016+6692C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32409798 | ||||||
chr11:32409894
|
AT | A | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+6595delA | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32409894 | ||||||
chr11:32410028
|
G | A | 135 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(132): Show | 138 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1016+6462C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32410028 | ||||||
chr11:32410133
|
G | A | 9 | a0001c0003t0006g0219a0001c0003t0006g0220a0001c0003t0006g0223others(6): Show | 9 | HG02145.hp2 HG02559.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1016+6357C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32410133 | ||||||
chr11:32410183
|
G | A | 3 | a0001c0010t0014g0270a0001c0010t0016g0271a0001c0016t0016g0299 | 3 | HG01109.hp2 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1016+6307C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32410183 | ||||||
chr11:32410243
|
C | A | 5 | a0001c0009t0008g0004a0001c0009t0008g0034a0001c0009t0033g0306others(2): Show | 6 | HG02280.hp1 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1016+6247G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32410243 | ||||||
chr11:32410264
|
A | G | 1 | a0001c0005t0005g0260 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1016+6226T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32410264 | ||||||
chr11:32410338
|
C | T | 1 | a0001c0005t0005g0264 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1016+6152G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32410338 | ||||||
chr11:32410399
|
C | T | 135 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(132): Show | 138 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1016+6091G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32410399 | ||||||
chr11:32410463
|
C | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0147 | 2 | NA18995.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1016+6027G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32410463 | ||||||
chr11:32410477
|
G | A | 139 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(136): Show | 142 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.1016+6013C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32410477 | ||||||
chr11:32410513
|
T | C | 3 | a0001c0003t0010g0017a0001c0003t0010g0018a0001c0003t0010g0019 | 3 | HG01496.hp1 HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1016+5977A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32410513 | ||||||
chr11:32410598
|
C | T | 4 | a0001c0003t0010g0017a0001c0003t0010g0018a0001c0003t0010g0019others(1): Show | 4 | HG01496.hp1 HG02451.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+5892G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32410598 | ||||||
chr11:32410620
|
T | A | 1 | a0001c0010t0008g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1016+5870A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32410620 | ||||||
chr11:32410847
|
G | A | 4 | a0001c0010t0014g0257a0001c0010t0021g0216a0001c0012t0014g0211others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+5643C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32410847 | ||||||
chr11:32411068
|
T | TAC | 8 | a0001c0002t0001g0094a0001c0002t0001g0109a0001c0002t0011g0025others(5): Show | 8 | HG00558.hp1 HG02572.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1016+5420_1016+542 others(6): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | ||||||
chr11:32411068
|
T | TACACACA others(3): Show |
6 | a0001c0001t0002g0161a0001c0001t0002g0189a0001c0004t0009g0288others(3): Show | 6 | HG00438.hp2 HG01891.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1016+5412_1016+542 others(14): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | ||||||
chr11:32411068
|
T | TACACACA others(5): Show |
14 | a0001c0001t0002g0120a0001c0001t0002g0125a0001c0001t0002g0128others(11): Show | 14 | HG02074.hp2 HG03453.hp2 HG03516.hp2 others(11): Show |
intron_variant | MODIFIER | c.1016+5410_1016+542 others(16): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | ||||||
chr11:32411068
|
T | TACACACA others(7): Show |
76 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(73): Show | 78 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1016+5408_1016+542 others(18): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | ||||||
chr11:32411068
|
T | TACACACA others(9): Show |
8 | a0001c0001t0002g0119a0001c0001t0002g0123a0001c0001t0002g0179others(5): Show | 8 | HG01884.hp1 HG01934.hp2 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.1016+5406_1016+542 others(20): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | ||||||
chr11:32411068
|
T | TACACACA others(11): Show |
8 | a0001c0003t0032g0234a0001c0004t0003g0016a0001c0004t0003g0273others(5): Show | 9 | HG00735.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1016+5404_1016+542 others(22): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | ||||||
chr11:32411068
|
T | TACACACA others(13): Show |
9 | a0001c0003t0024g0237a0001c0008t0003g0285a0001c0008t0003g0287others(6): Show | 9 | HG00642.hp1 HG01175.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1016+5402_1016+542 others(24): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | ||||||
chr11:32411068
|
T | TACACACA others(15): Show |
5 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0025g0238others(2): Show | 5 | HG01099.hp1 HG01169.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1016+5400_1016+542 others(26): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | ||||||
chr11:32411068
|
T | TACACACA others(17): Show |
6 | a0001c0003t0003g0230a0001c0003t0003g0249a0001c0003t0003g0252others(3): Show | 6 | HG03017.hp2 HG03491.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.1016+5398_1016+542 others(28): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | ||||||
chr11:32411068
|
T | TACACACA others(19): Show |
6 | a0001c0003t0003g0245a0001c0003t0003g0246a0001c0003t0003g0247others(3): Show | 6 | HG00733.hp2 HG01361.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1016+5396_1016+542 others(30): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | ||||||
chr11:32411068
|
T | TACACACA others(21): Show |
1 | a0001c0003t0003g0248 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1016+5421_1016+542 others(32): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | ||||||
chr11:32411068
|
T | TACACACA others(23): Show |
1 | a0001c0003t0003g0244 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1016+5421_1016+542 others(34): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | ||||||
chr11:32411068
|
T | TACACACA others(27): Show |
1 | a0001c0003t0003g0250 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1016+5421_1016+542 others(38): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | ||||||
chr11:32411068
|
T | TACACAGA others(7): Show |
1 | a0001c0001t0002g0172 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1016+5421_1016+542 others(18): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | ||||||
chr11:32411068
|
TAC | T | 4 | a0001c0004t0007g0286a0001c0010t0014g0270a0001c0010t0016g0271others(1): Show | 4 | HG01109.hp2 HG02486.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1016+5420_1016+542 others(6): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411068 | ||||||
chr11:32411351
|
C | G | 2 | a0001c0002t0011g0025a0001c0002t0011g0026 | 2 | HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1016+5139G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411351 | ||||||
chr11:32411497
|
G | T | 97 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(94): Show | 99 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1016+4993C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411497 | ||||||
chr11:32411498
|
T | C | 1 | a0001c0004t0017g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1016+4992A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411498 | ||||||
chr11:32411616
|
C | A | 3 | a0001c0003t0003g0245a0001c0003t0003g0246a0001c0003t0003g0247 | 3 | HG00733.hp2 HG01361.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1016+4874G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411616 | ||||||
chr11:32411653
|
C | T | 2 | a0001c0005t0002g0213a0001c0005t0002g0253 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1016+4837G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411653 | ||||||
chr11:32411698
|
A | G | 1 | a0001c0002t0001g0005 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1016+4792T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411698 | ||||||
chr11:32411775
|
A | G | 1 | a0001c0007t0028g0033 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1016+4715T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411775 | ||||||
chr11:32411879
|
T | C | 4 | a0001c0010t0014g0257a0001c0010t0021g0216a0001c0012t0014g0211others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+4611A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411879 | ||||||
chr11:32411883
|
G | GA | 6 | a0001c0002t0001g0047a0001c0003t0001g0235a0001c0003t0001g0236others(3): Show | 6 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.1016+4606dupT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411883 | ||||||
chr11:32411901
|
T | C | 34 | a0001c0002t0003g0059a0001c0002t0003g0068a0001c0003t0003g0214others(31): Show | 35 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1016+4589A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411901 | ||||||
chr11:32411924
|
G | A | 1 | a0001c0009t0033g0306 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1016+4566C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411924 | ||||||
chr11:32411933
|
T | G | 4 | a0001c0010t0014g0257a0001c0010t0021g0216a0001c0012t0014g0211others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+4557A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411933 | ||||||
chr11:32411951
|
G | T | 1 | a0001c0001t0002g0145 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1016+4539C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411951 | ||||||
chr11:32411958
|
G | C | 1 | a0001c0007t0028g0033 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1016+4532C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411958 | ||||||
chr11:32411973
|
G | T | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+4517C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411973 | ||||||
chr11:32411983
|
T | C | 1 | a0001c0002t0001g0080 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1016+4507A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411983 | ||||||
chr11:32411998
|
G | C | 34 | a0001c0002t0003g0059a0001c0002t0003g0068a0001c0003t0003g0214others(31): Show | 35 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1016+4492C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32411998 | ||||||
chr11:32412032
|
G | T | 1 | a0001c0001t0002g0123 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1016+4458C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412032 | ||||||
chr11:32412326
|
T | C | 139 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(136): Show | 142 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.1016+4164A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412326 | ||||||
chr11:32412496
|
T | C | 1 | a0001c0003t0004g0240 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1016+3994A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412496 | ||||||
chr11:32412560
|
G | C | 2 | a0001c0003t0004g0240a0001c0003t0004g0242 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1016+3930C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412560 | ||||||
chr11:32412606
|
T | C | 31 | a0001c0001t0005g0008a0001c0001t0005g0115a0001c0001t0005g0117others(28): Show | 35 | HG02129.hp2 HG02257.hp2 HG02572.hp1 others(32): Show |
intron_variant | MODIFIER | c.1016+3884A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412606 | ||||||
chr11:32412634
|
G | A | 135 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(132): Show | 138 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.1016+3856C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412634 | ||||||
chr11:32412711
|
C | T | 4 | a0001c0010t0014g0257a0001c0010t0021g0216a0001c0012t0014g0211others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+3779G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412711 | ||||||
chr11:32412717
|
T | TAAAAATC others(303): Show |
2 | a0001c0001t0002g0135a0001c0007t0002g0041 | 2 | HG03704.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.1016+3772_1016+377 others(314): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412717 | ||||||
chr11:32412717
|
T | TAAAAATC others(304): Show |
88 | a0001c0001t0002g0010a0001c0001t0002g0110a0001c0001t0002g0111others(85): Show | 89 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1016+3772_1016+377 others(315): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412717 | ||||||
chr11:32412717
|
T | TAAAAATC others(305): Show |
7 | a0001c0001t0002g0009a0001c0001t0002g0113a0001c0001t0002g0142others(4): Show | 8 | HG01346.hp1 HG02258.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.1016+3772_1016+377 others(316): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412717 | ||||||
chr11:32412717
|
T | TAAAAATC others(313): Show |
1 | a0001c0004t0009g0294 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1016+3772_1016+377 others(324): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412717 | ||||||
chr11:32412717
|
T | TAAAAATC others(315): Show |
2 | a0001c0004t0009g0288a0001c0004t0009g0296 | 2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1016+3772_1016+377 others(326): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412717 | ||||||
chr11:32412717
|
T | TAAAAATC others(307): Show |
1 | a0001c0005t0002g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1016+3772_1016+377 others(318): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412717 | ||||||
chr11:32412720
|
A | AAATCTAA others(302): Show |
1 | a0001c0003t0032g0234 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1016+3769_1016+377 others(313): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412720 | ||||||
chr11:32412720
|
A | AAATCTAA others(303): Show |
4 | a0001c0003t0003g0230a0001c0003t0003g0244a0001c0003t0003g0248others(1): Show | 4 | HG01261.hp2 HG03017.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.1016+3769_1016+377 others(314): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412720 | ||||||
chr11:32412720
|
A | AAATCTAA others(302): Show |
29 | a0001c0002t0003g0059a0001c0002t0003g0068a0001c0003t0003g0214others(26): Show | 30 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.1016+3769_1016+377 others(313): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412720 | ||||||
chr11:32412768
|
G | A | 1 | a0001c0002t0001g0109 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1016+3722C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32412768 | ||||||
chr11:32413015
|
G | T | 3 | a0001c0004t0009g0288a0001c0004t0009g0294a0001c0004t0009g0296 | 3 | HG01891.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1016+3475C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413015 | ||||||
chr11:32413028
|
A | T | 2 | a0001c0005t0002g0213a0001c0005t0002g0253 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1016+3462T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413028 | ||||||
chr11:32413059
|
T | A | 4 | a0001c0009t0008g0004a0001c0009t0008g0034a0001c0010t0008g0218others(1): Show | 5 | HG02572.hp2 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1016+3431A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413059 | ||||||
chr11:32413080
|
G | A | 129 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(126): Show | 132 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.1016+3410C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413080 | ||||||
chr11:32413355
|
G | A | 34 | a0001c0002t0003g0059a0001c0002t0003g0068a0001c0003t0003g0214others(31): Show | 35 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1016+3135C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413355 | ||||||
chr11:32413446
|
C | T | 4 | a0001c0010t0014g0257a0001c0010t0021g0216a0001c0012t0014g0211others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+3044G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413446 | ||||||
chr11:32413501
|
AT | A | 4 | a0001c0010t0014g0257a0001c0010t0021g0216a0001c0012t0014g0211others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+2988delA | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413501 | ||||||
chr11:32413530
|
A | G | 1 | a0001c0002t0001g0048 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1016+2960T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413530 | ||||||
chr11:32413637
|
A | G | 1 | a0001c0001t0002g0160 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1016+2853T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413637 | ||||||
chr11:32413643
|
A | G | 4 | a0001c0002t0011g0025a0001c0004t0009g0288a0001c0004t0009g0294others(1): Show | 4 | HG01891.hp2 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1016+2847T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413643 | ||||||
chr11:32413939
|
C | T | 1 | a0001c0007t0028g0033 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1016+2551G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413939 | ||||||
chr11:32413978
|
G | A | 1 | a0001c0005t0002g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1016+2512C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413978 | ||||||
chr11:32413983
|
G | A | 30 | a0001c0001t0002g0140a0001c0001t0005g0008a0001c0001t0005g0115others(27): Show | 34 | HG02129.hp2 HG02257.hp2 HG02622.hp2 others(31): Show |
intron_variant | MODIFIER | c.1016+2507C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413983 | ||||||
chr11:32413998
|
A | G | 4 | a0001c0004t0009g0288a0001c0004t0009g0294a0001c0004t0009g0296others(1): Show | 4 | HG01891.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+2492T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32413998 | ||||||
chr11:32414011
|
T | C | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+2479A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414011 | ||||||
chr11:32414016
|
C | T | 1 | a0001c0002t0001g0109 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1016+2474G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414016 | ||||||
chr11:32414026
|
G | A | 4 | a0001c0010t0014g0257a0001c0010t0021g0216a0001c0012t0014g0211others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+2464C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414026 | ||||||
chr11:32414078
|
T | C | 1 | a0001c0012t0014g0211 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1016+2412A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414078 | ||||||
chr11:32414084
|
C | T | 4 | a0001c0009t0008g0004a0001c0009t0008g0034a0001c0010t0008g0218others(1): Show | 5 | HG02572.hp2 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1016+2406G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414084 | ||||||
chr11:32414085
|
G | A | 15 | a0001c0001t0002g0140a0001c0001t0005g0008a0001c0001t0005g0115others(12): Show | 16 | HG02129.hp2 HG03490.hp2 HG03654.hp1 others(13): Show |
intron_variant | MODIFIER | c.1016+2405C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414085 | ||||||
chr11:32414129
|
T | C | 1 | a0001c0006t0001g0198 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1016+2361A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414129 | ||||||
chr11:32414192
|
C | G | 3 | a0001c0001t0002g0128a0001c0001t0002g0130a0001c0001t0002g0160 | 3 | HG02074.hp2 NA18952.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1016+2298G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414192 | ||||||
chr11:32414307
|
C | T | 2 | a0001c0002t0001g0089a0001c0002t0001g0095 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1016+2183G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414307 | ||||||
chr11:32414325
|
T | C | 1 | a0001c0001t0019g0020 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1016+2165A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414325 | ||||||
chr11:32414454
|
T | C | 5 | a0001c0009t0008g0004a0001c0009t0008g0034a0001c0009t0033g0306others(2): Show | 6 | HG02280.hp1 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1016+2036A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414454 | ||||||
chr11:32414519
|
C | T | 2 | a0001c0003t0006g0219a0001c0003t0006g0223 | 2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1016+1971G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414519 | ||||||
chr11:32414599
|
G | A | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+1891C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414599 | ||||||
chr11:32414602
|
G | A | 4 | a0001c0010t0014g0257a0001c0010t0021g0216a0001c0012t0014g0211others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+1888C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414602 | ||||||
chr11:32414648
|
G | A | 2 | a0001c0001t0002g0113a0001c0005t0002g0222 | 2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1016+1842C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414648 | ||||||
chr11:32414868
|
A | G | 166 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(163): Show | 173 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.1016+1622T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414868 | ||||||
chr11:32414872
|
C | CA | 18 | a0001c0001t0002g0169a0001c0001t0019g0020a0001c0002t0001g0051others(15): Show | 19 | HG01109.hp2 HG01243.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.1016+1617dupT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414872 | ||||||
chr11:32414872
|
CA | C | 11 | a0001c0001t0002g0192a0001c0002t0001g0062a0001c0002t0001g0096others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.1016+1617delT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414872 | ||||||
chr11:32414873
|
A | C | 6 | a0001c0003t0003g0245a0001c0003t0003g0246a0001c0003t0003g0247others(3): Show | 6 | HG00733.hp2 HG01261.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1016+1617T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32414873 | ||||||
chr11:32415345
|
AC | A | 5 | a0001c0009t0008g0004a0001c0009t0008g0034a0001c0009t0033g0306others(2): Show | 6 | HG02280.hp1 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1016+1144delG | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32415345 | ||||||
chr11:32415386
|
C | T | 1 | a0001c0003t0006g0223 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1016+1104G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32415386 | ||||||
chr11:32415417
|
G | C | 1 | a0001c0004t0004g0275 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1016+1073C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32415417 | ||||||
chr11:32415439
|
G | A | 4 | a0001c0010t0014g0257a0001c0010t0021g0216a0001c0012t0014g0211others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+1051C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32415439 | ||||||
chr11:32415555
|
G | A | 2 | a0001c0003t0003g0214a0001c0003t0003g0215 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1016+935C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32415555 | ||||||
chr11:32415572
|
C | T | 4 | a0001c0010t0014g0257a0001c0010t0021g0216a0001c0012t0014g0211others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+918G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32415572 | ||||||
chr11:32415643
|
G | A | 32 | a0001c0003t0003g0214a0001c0003t0003g0215a0001c0003t0003g0230others(29): Show | 33 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.1016+847C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32415643 | ||||||
chr11:32415663
|
T | C | 169 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(166): Show | 176 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(173): Show |
intron_variant | MODIFIER | c.1016+827A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32415663 | ||||||
chr11:32415764
|
A | T | 6 | a0001c0003t0003g0245a0001c0003t0003g0246a0001c0003t0003g0247others(3): Show | 6 | HG00733.hp2 HG01261.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1016+726T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32415764 | ||||||
chr11:32415981
|
T | G | 4 | a0001c0010t0014g0257a0001c0010t0021g0216a0001c0012t0014g0211others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+509A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32415981 | ||||||
chr11:32416079
|
G | C | 1 | a0001c0002t0001g0083 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1016+411C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32416079 | ||||||
chr11:32416086
|
A | G | 5 | a0001c0003t0004g0013a0001c0003t0004g0231a0001c0003t0004g0240others(2): Show | 6 | HG02257.hp2 HG02622.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1016+404T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32416086 | ||||||
chr11:32416131
|
G | C | 167 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(164): Show | 174 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.1016+359C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32416131 | ||||||
chr11:32416153
|
T | C | 295 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(292): Show | 317 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(314): Show |
intron_variant | MODIFIER | c.1016+337A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32416153 | ||||||
chr11:32416270
|
T | A | 1 | a0001c0002t0001g0103 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1016+220A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32416270 | ||||||
chr11:32416295
|
A | C | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1016+195T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32416295 | ||||||
chr11:32416326
|
T | A | 27 | a0001c0001t0002g0187a0001c0002t0004g0027a0001c0002t0004g0028others(24): Show | 30 | HG02129.hp2 HG02257.hp2 HG02622.hp2 others(27): Show |
intron_variant | MODIFIER | c.1016+164A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32416326 | ||||||
chr11:32416327
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1016+163C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32416327 | ||||||
chr11:32416356
|
G | A | 32 | a0001c0003t0003g0214a0001c0003t0003g0215a0001c0003t0003g0230others(29): Show | 33 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.1016+134C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32416356 | ||||||
chr11:32416368
|
T | G | 163 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(160): Show | 170 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.1016+122A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32416368 | ||||||
chr11:32416409
|
G | A | 3 | a0001c0003t0010g0017a0001c0003t0010g0018a0001c0003t0010g0019 | 3 | HG01496.hp1 HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1016+81C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 5/9 | chr11 | 32416409 | ||||||
chr11:32416564
|
A | G | 1 | a0001c0005t0002g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.966-24T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32416564 | ||||||
chr11:32416708
|
G | A | 1 | a0001c0005t0005g0258 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.966-168C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32416708 | ||||||
chr11:32416784
|
T | G | 1 | a0001c0004t0004g0298 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.966-244A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32416784 | ||||||
chr11:32416931
|
T | C | 170 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(167): Show | 177 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.966-391A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32416931 | ||||||
chr11:32416973
|
A | C | 2 | a0001c0005t0002g0213a0001c0005t0002g0253 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.966-433T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32416973 | ||||||
chr11:32417032
|
T | C | 3 | a0001c0004t0009g0288a0001c0004t0009g0294a0001c0004t0009g0296 | 3 | HG01891.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.966-492A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32417032 | ||||||
chr11:32417138
|
C | T | 101 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(98): Show | 104 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.965+439G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32417138 | ||||||
chr11:32417148
|
T | C | 3 | a0001c0004t0009g0288a0001c0004t0009g0294a0001c0004t0009g0296 | 3 | HG01891.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.965+429A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32417148 | ||||||
chr11:32417153
|
G | A | 168 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(165): Show | 175 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.965+424C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32417153 | ||||||
chr11:32417207
|
C | T | 200 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(197): Show | 209 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(206): Show |
intron_variant | MODIFIER | c.965+370G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32417207 | ||||||
chr11:32417208
|
G | C | 1 | a0001c0004t0001g0014 | 2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.965+369C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32417208 | ||||||
chr11:32417242
|
T | C | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.965+335A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32417242 | ||||||
chr11:32417322
|
A | G | 1 | a0001c0002t0001g0007 | 2 | HG00639.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.965+255T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32417322 | ||||||
chr11:32417447
|
T | G | 1 | a0001c0010t0021g0216 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.965+130A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32417447 | ||||||
chr11:32417455
|
T | C | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.965+122A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32417455 | ||||||
chr11:32417492
|
T | C | 168 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(165): Show | 175 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.965+85A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 4/9 | chr11 | 32417492 | ||||||
chr11:32417752
|
C | T | 4 | a0001c0010t0014g0257a0001c0010t0021g0216a0001c0012t0014g0211others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.888-98G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32417752 | ||||||
chr11:32417946
|
G | A | 2 | a0001c0002t0001g0089a0001c0002t0001g0095 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.888-292C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32417946 | ||||||
chr11:32418242
|
A | ATG | 6 | a0001c0007t0002g0032a0001c0007t0028g0033a0001c0010t0014g0257others(3): Show | 6 | HG01243.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.888-589_888-588ins others(2): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418242 | ||||||
chr11:32418243
|
T | TG | 123 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(120): Show | 126 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.888-590_888-589ins others(1): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418243 | ||||||
chr11:32418244
|
T | A | 5 | a0001c0007t0028g0033a0001c0010t0014g0257a0001c0010t0021g0216others(2): Show | 5 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.888-590A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418244 | ||||||
chr11:32418244
|
T | G | 39 | a0001c0001t0002g0205a0001c0002t0004g0027a0001c0002t0004g0028others(36): Show | 43 | HG00642.hp1 HG00735.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.888-590A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418244 | ||||||
chr11:32418244
|
T | TA | 103 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(100): Show | 117 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.888-591dupT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418244 | ||||||
chr11:32418245
|
A | T | 39 | a0001c0001t0002g0205a0001c0002t0004g0027a0001c0002t0004g0028others(36): Show | 43 | HG00642.hp1 HG00735.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.888-591T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418245 | ||||||
chr11:32418253
|
A | G | 3 | a0001c0002t0011g0025a0001c0002t0011g0026a0001c0002t0011g0029 | 3 | HG02572.hp1 HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.888-599T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418253 | ||||||
chr11:32418278
|
C | T | 168 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(165): Show | 175 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.888-624G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418278 | ||||||
chr11:32418334
|
G | A | 32 | a0001c0003t0003g0214a0001c0003t0003g0215a0001c0003t0003g0230others(29): Show | 33 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.888-680C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418334 | ||||||
chr11:32418492
|
A | C | 46 | a0001c0002t0004g0027a0001c0002t0004g0028a0001c0003t0002g0232others(43): Show | 50 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.888-838T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418492 | ||||||
chr11:32418581
|
A | T | 97 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(94): Show | 100 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.888-927T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418581 | ||||||
chr11:32418692
|
C | A | 1 | a0001c0002t0001g0067 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.888-1038G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418692 | ||||||
chr11:32418727
|
A | G | 1 | a0001c0005t0005g0260 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.888-1073T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418727 | ||||||
chr11:32418801
|
C | T | 1 | a0001c0002t0001g0006 | 2 | HG02074.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.888-1147G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418801 | ||||||
chr11:32418803
|
G | A | 3 | a0001c0004t0009g0288a0001c0004t0009g0294a0001c0004t0009g0296 | 3 | HG01891.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.888-1149C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418803 | ||||||
chr11:32418810
|
G | A | 4 | a0001c0010t0014g0257a0001c0010t0021g0216a0001c0012t0014g0211others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.888-1156C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418810 | ||||||
chr11:32418830
|
C | A | 1 | a0001c0007t0002g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.888-1176G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32418830 | ||||||
chr11:32419095
|
T | C | 7 | a0001c0003t0003g0230a0001c0003t0003g0244a0001c0003t0003g0252others(4): Show | 7 | HG03017.hp2 HG03491.hp2 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.888-1441A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32419095 | ||||||
chr11:32419109
|
C | T | 3 | a0001c0003t0010g0017a0001c0003t0010g0018a0001c0003t0010g0019 | 3 | HG01496.hp1 HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.888-1455G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32419109 | ||||||
chr11:32419195
|
T | G | 1 | a0001c0003t0003g0248 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.888-1541A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32419195 | ||||||
chr11:32419479
|
A | T | 1 | a0001c0004t0003g0293 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.888-1825T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32419479 | ||||||
chr11:32419565
|
C | T | 58 | a0001c0001t0002g0187a0001c0002t0004g0027a0001c0002t0004g0028others(55): Show | 62 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.888-1911G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32419565 | ||||||
chr11:32419577
|
C | A | 1 | a0001c0002t0001g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.888-1923G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32419577 | ||||||
chr11:32419710
|
G | A | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.888-2056C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32419710 | ||||||
chr11:32419743
|
G | C | 3 | a0001c0001t0002g0194a0001c0001t0002g0203a0001c0005t0002g0243 | 3 | HG00597.hp2 NA18940.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.888-2089C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32419743 | ||||||
chr11:32419825
|
C | T | 1 | a0001c0001t0002g0169 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.888-2171G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32419825 | ||||||
chr11:32419831
|
C | T | 202 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(199): Show | 211 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(208): Show |
intron_variant | MODIFIER | c.888-2177G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32419831 | ||||||
chr11:32420166
|
G | A | 3 | a0001c0010t0014g0270a0001c0010t0016g0271a0001c0016t0016g0299 | 3 | HG01109.hp2 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.888-2512C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420166 | ||||||
chr11:32420364
|
T | C | 14 | a0001c0002t0004g0027a0001c0002t0004g0028a0001c0003t0002g0232others(11): Show | 17 | HG02257.hp2 HG02622.hp2 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.888-2710A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420364 | ||||||
chr11:32420453
|
C | T | 4 | a0001c0010t0014g0257a0001c0010t0021g0216a0001c0012t0014g0211others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.888-2799G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420453 | ||||||
chr11:32420456
|
T | C | 1 | a0001c0005t0022g0256 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.888-2802A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420456 | ||||||
chr11:32420504
|
A | G | 13 | a0001c0002t0004g0027a0001c0002t0004g0028a0001c0003t0004g0011others(10): Show | 16 | HG02257.hp2 HG02622.hp2 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.888-2850T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420504 | ||||||
chr11:32420551
|
G | C | 1 | a0001c0009t0033g0306 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.888-2897C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420551 | ||||||
chr11:32420555
|
C | T | 4 | a0001c0010t0014g0257a0001c0010t0021g0216a0001c0012t0014g0211others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.888-2901G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420555 | ||||||
chr11:32420588
|
A | G | 1 | a0001c0001t0002g0157 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.888-2934T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420588 | ||||||
chr11:32420618
|
C | T | 1 | a0001c0001t0002g0189 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.888-2964G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420618 | ||||||
chr11:32420641
|
A | G | 2 | a0001c0006t0001g0146a0001c0006t0001g0154 | 2 | NA18995.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.888-2987T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420641 | ||||||
chr11:32420729
|
A | G | 167 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(164): Show | 174 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.888-3075T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420729 | ||||||
chr11:32420922
|
G | T | 6 | a0001c0003t0003g0245a0001c0003t0003g0246a0001c0003t0003g0247others(3): Show | 6 | HG00733.hp2 HG01261.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.888-3268C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420922 | ||||||
chr11:32420992
|
A | C | 1 | a0001c0001t0005g0159 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.888-3338T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420992 | ||||||
chr11:32420994
|
A | C | 1 | a0001c0007t0028g0033 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.888-3340T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32420994 | ||||||
chr11:32421042
|
C | T | 1 | a0001c0003t0032g0234 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.888-3388G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32421042 | ||||||
chr11:32421090
|
A | G | 169 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(166): Show | 176 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(173): Show |
intron_variant | MODIFIER | c.888-3436T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32421090 | ||||||
chr11:32421109
|
C | T | 3 | a0001c0003t0001g0266a0001c0005t0005g0264a0001c0005t0022g0256 | 3 | NA18950.hp2 NA18991.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.888-3455G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32421109 | ||||||
chr11:32421187
|
T | C | 4 | a0001c0010t0014g0257a0001c0010t0021g0216a0001c0012t0014g0211others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.888-3533A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32421187 | ||||||
chr11:32421301
|
G | C | 4 | a0001c0010t0014g0257a0001c0010t0021g0216a0001c0012t0014g0211others(1): Show | 4 | HG02280.hp2 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.888-3647C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32421301 | ||||||
chr11:32421360
|
C | A | 1 | a0001c0004t0003g0303 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.888-3706G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32421360 | ||||||
chr11:32421498
|
T | A | 4 | a0001c0009t0008g0004a0001c0009t0008g0034a0001c0010t0008g0218others(1): Show | 5 | HG02572.hp2 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.888-3844A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32421498 | ||||||
chr11:32421775
|
G | C | 1 | a0001c0006t0001g0112 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.888-4121C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32421775 | ||||||
chr11:32422153
|
G | A | 2 | a0001c0003t0024g0237a0001c0003t0025g0238 | 2 | HG01099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.888-4499C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422153 | ||||||
chr11:32422244
|
C | T | 1 | a0001c0007t0028g0033 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.888-4590G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422244 | ||||||
chr11:32422474
|
A | G | 177 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(174): Show | 186 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.888-4820T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422474 | ||||||
chr11:32422489
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.888-4835C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422489 | ||||||
chr11:32422543
|
G | T | 1 | a0001c0009t0008g0034 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.888-4889C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422543 | ||||||
chr11:32422547
|
A | G | 3 | a0001c0003t0010g0017a0001c0003t0010g0018a0001c0003t0010g0019 | 3 | HG01496.hp1 HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.888-4893T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422547 | ||||||
chr11:32422600
|
C | T | 2 | a0001c0002t0003g0059a0001c0002t0003g0068 | 2 | HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.888-4946G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422600 | ||||||
chr11:32422601
|
G | A | 176 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(173): Show | 185 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.888-4947C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422601 | ||||||
chr11:32422656
|
G | A | 3 | a0001c0003t0001g0254a0001c0005t0002g0213a0001c0005t0002g0253 | 3 | HG01884.hp1 HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.888-5002C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422656 | ||||||
chr11:32422698
|
G | T | 2 | a0001c0010t0014g0270a0001c0010t0016g0271 | 2 | HG01109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.888-5044C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422698 | ||||||
chr11:32422757
|
T | C | 1 | a0001c0001t0002g0177 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.888-5103A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422757 | ||||||
chr11:32422811
|
C | G | 1 | a0001c0007t0028g0033 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.887+5145G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422811 | ||||||
chr11:32422829
|
T | C | 177 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(174): Show | 186 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.887+5127A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422829 | ||||||
chr11:32422861
|
G | A | 9 | a0001c0006t0001g0212a0001c0009t0008g0004a0001c0009t0008g0034others(6): Show | 10 | HG02257.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.887+5095C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422861 | ||||||
chr11:32422953
|
C | T | 7 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0054others(4): Show | 12 | HG00639.hp2 HG01243.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.887+5003G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32422953 | ||||||
chr11:32423134
|
C | A | 1 | a0001c0010t0008g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.887+4822G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32423134 | ||||||
chr11:32423219
|
G | A | 33 | a0001c0004t0001g0014a0001c0004t0001g0280a0001c0004t0001g0282others(30): Show | 35 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.887+4737C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32423219 | ||||||
chr11:32423240
|
C | T | 3 | a0001c0004t0009g0288a0001c0004t0009g0294a0001c0004t0009g0296 | 3 | HG01891.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.887+4716G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32423240 | ||||||
chr11:32423262
|
G | A | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.887+4694C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32423262 | ||||||
chr11:32423436
|
G | C | 4 | a0001c0009t0008g0004a0001c0009t0008g0034a0001c0010t0008g0218others(1): Show | 5 | HG02572.hp2 HG02630.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.887+4520C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32423436 | ||||||
chr11:32423649
|
T | C | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.887+4307A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32423649 | ||||||
chr11:32423679
|
T | C | 1 | a0001c0007t0002g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.887+4277A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32423679 | ||||||
chr11:32423701
|
C | A | 1 | a0001c0007t0028g0033 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.887+4255G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32423701 | ||||||
chr11:32423860
|
T | C | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.887+4096A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32423860 | ||||||
chr11:32424066
|
G | A | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.887+3890C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424066 | ||||||
chr11:32424086
|
C | T | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.887+3870G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424086 | ||||||
chr11:32424160
|
C | CA | 7 | a0001c0003t0006g0227a0001c0006t0001g0212a0001c0010t0014g0257others(4): Show | 7 | HG02257.hp1 HG02280.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.887+3795dupT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424160 | ||||||
chr11:32424160
|
C | CAA | 18 | a0001c0001t0002g0129a0001c0001t0002g0134a0001c0001t0002g0158others(15): Show | 19 | HG00438.hp1 HG00639.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.887+3794_887+3795d others(4): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424160 | ||||||
chr11:32424160
|
C | CAAA | 117 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(114): Show | 124 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.887+3793_887+3795d others(5): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424160 | ||||||
chr11:32424160
|
C | CAAAA | 39 | a0001c0001t0002g0122a0001c0001t0002g0138a0001c0001t0002g0139others(36): Show | 40 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.887+3792_887+3795d others(6): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424160 | ||||||
chr11:32424160
|
CA | C | 43 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(40): Show | 54 | HG00099.hp2 HG00408.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.887+3795delT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424160 | ||||||
chr11:32424160
|
CAA | C | 7 | a0001c0002t0001g0107a0001c0003t0001g0235a0001c0003t0001g0236others(4): Show | 7 | HG01099.hp1 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.887+3794_887+3795d others(4): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424160 | ||||||
chr11:32424160
|
CAAA | C | 17 | a0001c0003t0001g0259a0001c0003t0001g0266a0001c0005t0002g0253others(14): Show | 17 | HG01243.hp1 HG01884.hp1 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.887+3793_887+3795d others(5): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424160 | ||||||
chr11:32424165
|
A | T | 6 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(3): Show | 6 | HG01099.hp1 HG01109.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.887+3791T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424165 | ||||||
chr11:32424187
|
C | G | 1 | a0001c0003t0001g0269 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.887+3769G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424187 | ||||||
chr11:32424296
|
T | C | 1 | a0001c0005t0002g0253 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.887+3660A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424296 | ||||||
chr11:32424312
|
C | T | 3 | a0001c0004t0006g0015a0001c0004t0006g0291a0001c0010t0006g0217 | 4 | HG02451.hp1 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.887+3644G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424312 | ||||||
chr11:32424334
|
A | T | 1 | a0001c0001t0002g0188 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.887+3622T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424334 | ||||||
chr11:32424462
|
C | G | 1 | a0001c0012t0023g0210 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.887+3494G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424462 | ||||||
chr11:32424484
|
T | G | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.887+3472A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424484 | ||||||
chr11:32424527
|
G | A | 33 | a0001c0004t0001g0014a0001c0004t0001g0280a0001c0004t0001g0282others(30): Show | 35 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.887+3429C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424527 | ||||||
chr11:32424542
|
T | C | 5 | a0001c0006t0001g0212a0001c0010t0014g0257a0001c0010t0021g0216others(2): Show | 5 | HG02257.hp1 HG02280.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.887+3414A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424542 | ||||||
chr11:32424589
|
G | C | 78 | a0001c0002t0004g0027a0001c0002t0004g0028a0001c0002t0011g0025others(75): Show | 83 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.887+3367C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424589 | ||||||
chr11:32424594
|
T | C | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.887+3362A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424594 | ||||||
chr11:32424613
|
G | A | 33 | a0001c0004t0001g0014a0001c0004t0001g0280a0001c0004t0001g0282others(30): Show | 35 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.887+3343C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424613 | ||||||
chr11:32424790
|
G | A | 153 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(150): Show | 160 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.887+3166C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424790 | ||||||
chr11:32424868
|
G | A | 5 | a0001c0001t0002g0150a0001c0001t0002g0157a0001c0001t0002g0167others(2): Show | 5 | HG02698.hp1 HG02735.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.887+3088C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424868 | ||||||
chr11:32424938
|
G | C | 11 | a0001c0003t0002g0232a0001c0003t0004g0011a0001c0003t0004g0012others(8): Show | 14 | HG02257.hp2 HG02622.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.887+3018C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424938 | ||||||
chr11:32424998
|
T | C | 3 | a0001c0009t0008g0004a0001c0009t0008g0034a0001c0014t0008g0035 | 4 | HG02572.hp2 HG02630.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.887+2958A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32424998 | ||||||
chr11:32425155
|
C | A | 72 | a0001c0002t0001g0084a0001c0002t0004g0027a0001c0002t0004g0028others(69): Show | 77 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.887+2801G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32425155 | ||||||
chr11:32425155
|
C | T | 1 | a0001c0001t0002g0127 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.887+2801G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32425155 | ||||||
chr11:32425180
|
GA | G | 107 | a0001c0001t0002g0157a0001c0001t0012g0196a0001c0002t0001g0001others(104): Show | 120 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.887+2775delT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32425180 | ||||||
chr11:32425180
|
GAA | G | 60 | a0001c0002t0001g0089a0001c0002t0003g0059a0001c0002t0004g0027others(57): Show | 62 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.887+2774_887+2775d others(4): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32425180 | ||||||
chr11:32425297
|
G | T | 19 | a0001c0003t0003g0214a0001c0003t0003g0215a0001c0003t0006g0219others(16): Show | 20 | HG01496.hp1 HG02145.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.887+2659C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32425297 | ||||||
chr11:32425328
|
GA | G | 67 | a0001c0002t0001g0098a0001c0002t0011g0029a0001c0003t0001g0254others(64): Show | 72 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.887+2627delT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32425328 | ||||||
chr11:32425439
|
C | A | 24 | a0001c0002t0004g0027a0001c0002t0004g0028a0001c0002t0011g0025others(21): Show | 25 | HG01243.hp1 HG02129.hp2 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.887+2517G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32425439 | ||||||
chr11:32425465
|
A | G | 33 | a0001c0004t0001g0014a0001c0004t0001g0280a0001c0004t0001g0282others(30): Show | 35 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.887+2491T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32425465 | ||||||
chr11:32425497
|
G | A | 1 | a0001c0010t0016g0271 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.887+2459C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32425497 | ||||||
chr11:32425505
|
A | G | 4 | a0001c0004t0003g0016a0001c0004t0003g0273a0001c0004t0003g0300others(1): Show | 5 | HG00735.hp1 HG01891.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.887+2451T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32425505 | ||||||
chr11:32425590
|
A | C | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.887+2366T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32425590 | ||||||
chr11:32425729
|
A | G | 24 | a0001c0003t0002g0232a0001c0003t0003g0230a0001c0003t0003g0244others(21): Show | 27 | HG00733.hp2 HG01261.hp2 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.887+2227T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32425729 | ||||||
chr11:32425801
|
C | G | 222 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(219): Show | 232 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(229): Show |
intron_variant | MODIFIER | c.887+2155G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32425801 | ||||||
chr11:32426055
|
T | A | 2 | a0001c0004t0004g0274a0001c0004t0004g0275 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.887+1901A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426055 | ||||||
chr11:32426169
|
A | T | 1 | a0001c0002t0001g0072 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.887+1787T>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426169 | ||||||
chr11:32426234
|
G | A | 4 | a0001c0003t0001g0269a0001c0010t0014g0257a0001c0010t0014g0270others(1): Show | 4 | HG01109.hp2 HG02486.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.887+1722C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426234 | ||||||
chr11:32426296
|
G | C | 1 | a0001c0007t0002g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.887+1660C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426296 | ||||||
chr11:32426318
|
G | T | 67 | a0001c0003t0001g0254a0001c0003t0001g0269a0001c0003t0002g0232others(64): Show | 72 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.887+1638C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426318 | ||||||
chr11:32426659
|
A | G | 24 | a0001c0002t0004g0027a0001c0002t0004g0028a0001c0002t0011g0025others(21): Show | 25 | HG01243.hp1 HG02129.hp2 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.887+1297T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426659 | ||||||
chr11:32426660
|
A | ATT | 34 | a0001c0004t0001g0014a0001c0004t0001g0280a0001c0004t0001g0282others(31): Show | 36 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.887+1295_887+1296i others(4): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426660 | ||||||
chr11:32426672
|
G | T | 21 | a0001c0002t0004g0027a0001c0002t0004g0028a0001c0002t0011g0025others(18): Show | 21 | HG01243.hp1 HG02129.hp2 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.887+1284C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426672 | ||||||
chr11:32426693
|
G | A | 68 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0001g0254others(65): Show | 73 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.887+1263C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426693 | ||||||
chr11:32426693
|
G | GA | 24 | a0001c0001t0002g0111a0001c0002t0001g0087a0001c0002t0004g0027others(21): Show | 24 | HG01243.hp1 HG02129.hp2 HG02572.hp1 others(21): Show |
intron_variant | MODIFIER | c.887+1262dupT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426693 | ||||||
chr11:32426709
|
T | C | 219 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(216): Show | 229 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(226): Show |
intron_variant | MODIFIER | c.887+1247A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426709 | ||||||
chr11:32426754
|
C | T | 1 | a0001c0004t0020g0302 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.887+1202G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426754 | ||||||
chr11:32426773
|
C | A | 3 | a0001c0003t0001g0266a0001c0005t0002g0265a0001c0005t0022g0256 | 3 | NA18942.hp1 NA18950.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.887+1183G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426773 | ||||||
chr11:32426808
|
C | T | 1 | a0001c0003t0001g0259 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.887+1148G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426808 | ||||||
chr11:32426868
|
C | A | 1 | a0001c0002t0001g0088 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.887+1088G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32426868 | ||||||
chr11:32427023
|
A | C | 222 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(219): Show | 232 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(229): Show |
intron_variant | MODIFIER | c.887+933T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32427023 | ||||||
chr11:32427272
|
G | T | 1 | a0001c0001t0002g0144 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.887+684C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32427272 | ||||||
chr11:32427275
|
G | A | 1 | a0001c0010t0014g0257 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.887+681C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32427275 | ||||||
chr11:32427283
|
A | G | 1 | a0001c0003t0001g0254 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.887+673T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32427283 | ||||||
chr11:32427349
|
C | G | 222 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(219): Show | 232 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(229): Show |
intron_variant | MODIFIER | c.887+607G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32427349 | ||||||
chr11:32427413
|
G | A | 1 | a0001c0001t0002g0194 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.887+543C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32427413 | ||||||
chr11:32427552
|
G | A | 4 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0024g0237others(1): Show | 4 | HG01099.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.887+404C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32427552 | ||||||
chr11:32427727
|
C | T | 1 | a0001c0007t0002g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.887+229G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32427727 | ||||||
chr11:32427728
|
G | C | 90 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0001g0254others(87): Show | 96 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.887+228C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32427728 | ||||||
chr11:32427871
|
C | G | 132 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(129): Show | 136 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.887+85G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32427871 | ||||||
chr11:32427874
|
C | A | 132 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(129): Show | 136 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.887+82G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32427874 | ||||||
chr11:32427940
|
C | T | 86 | a0001c0003t0001g0254a0001c0003t0001g0269a0001c0003t0002g0232others(83): Show | 92 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.887+16G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 3/9 | chr11 | 32427940 | ||||||
chr11:32428078
|
C | A | 1 | a0001c0007t0028g0033 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.785-20G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 2/9 | chr11 | 32428078 | ||||||
chr11:32428115
|
G | A | 132 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(129): Show | 136 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.785-57C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 2/9 | chr11 | 32428115 | ||||||
chr11:32428218
|
A | G | 1 | a0001c0001t0002g0156 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.785-160T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 2/9 | chr11 | 32428218 | ||||||
chr11:32428230
|
T | G | 2 | a0001c0004t0006g0015a0001c0004t0006g0291 | 3 | HG02886.hp1 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.785-172A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 2/9 | chr11 | 32428230 | ||||||
chr11:32428253
|
G | T | 71 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0001g0254others(68): Show | 76 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.785-195C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 2/9 | chr11 | 32428253 | ||||||
chr11:32428329
|
G | A | 1 | a0001c0006t0001g0164 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.784+168C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 2/9 | chr11 | 32428329 | ||||||
chr11:32428330
|
G | A | 1 | a0001c0007t0002g0105 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.784+167C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 2/9 | chr11 | 32428330 | ||||||
chr11:32428695
|
G | A | 1 | a0001c0002t0001g0036 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.662-76C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32428695 | ||||||
chr11:32428698
|
C | CG | 80 | a0001c0001t0002g0113a0001c0001t0002g0200a0001c0003t0001g0254others(77): Show | 86 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.662-80dupC | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32428698 | ||||||
chr11:32428698
|
CG | C | 10 | a0001c0002t0001g0005a0001c0002t0001g0036a0001c0002t0001g0037others(7): Show | 11 | HG00408.hp1 HG00438.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.662-80delC | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32428698 | ||||||
chr11:32428703
|
G | A | 1 | a0001c0009t0033g0306 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.662-84C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32428703 | ||||||
chr11:32428704
|
G | T | 2 | a0001c0007t0001g0053a0001c0007t0001g0071 | 2 | HG01175.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.662-85C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32428704 | ||||||
chr11:32428830
|
C | G | 3 | a0001c0009t0008g0004a0001c0009t0008g0034a0001c0014t0008g0035 | 4 | HG02572.hp2 HG02630.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-211G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32428830 | ||||||
chr11:32428865
|
A | G | 1 | a0001c0016t0016g0299 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.662-246T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32428865 | ||||||
chr11:32429109
|
T | C | 3 | a0001c0003t0010g0017a0001c0003t0010g0018a0001c0003t0010g0019 | 3 | HG01496.hp1 HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.662-490A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429109 | ||||||
chr11:32429119
|
G | A | 5 | a0001c0002t0004g0027a0001c0002t0004g0028a0001c0002t0011g0025others(2): Show | 5 | HG02572.hp1 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.662-500C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429119 | ||||||
chr11:32429187
|
T | A | 3 | a0001c0009t0008g0004a0001c0009t0008g0034a0001c0014t0008g0035 | 4 | HG02572.hp2 HG02630.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-568A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429187 | ||||||
chr11:32429260
|
C | A | 35 | a0001c0004t0001g0014a0001c0004t0001g0280a0001c0004t0001g0282others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.662-641G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429260 | ||||||
chr11:32429279
|
C | T | 70 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0001g0254others(67): Show | 75 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.662-660G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429279 | ||||||
chr11:32429293
|
C | T | 1 | a0001c0004t0020g0302 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.662-674G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429293 | ||||||
chr11:32429304
|
G | A | 4 | a0001c0003t0002g0232a0001c0003t0004g0011a0001c0003t0004g0012others(1): Show | 6 | HG02647.hp1 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.662-685C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429304 | ||||||
chr11:32429330
|
G | C | 1 | a0001c0007t0028g0033 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.662-711C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429330 | ||||||
chr11:32429344
|
A | G | 222 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(219): Show | 232 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(229): Show |
intron_variant | MODIFIER | c.662-725T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429344 | ||||||
chr11:32429457
|
A | G | 222 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(219): Show | 232 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(229): Show |
intron_variant | MODIFIER | c.662-838T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429457 | ||||||
chr11:32429462
|
T | TC | 21 | a0001c0001t0002g0133a0001c0001t0002g0142a0001c0001t0002g0187others(18): Show | 22 | HG00558.hp1 HG00642.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.662-844dupG | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429462 | ||||||
chr11:32429462
|
TC | T | 126 | a0001c0001t0002g0009a0001c0001t0002g0110a0001c0001t0002g0111others(123): Show | 128 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.662-844delG | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429462 | ||||||
chr11:32429462
|
TCC | T | 51 | a0001c0001t0002g0121a0001c0001t0002g0125a0001c0001t0002g0129others(48): Show | 56 | HG01070.hp2 HG01243.hp1 HG02129.hp2 others(53): Show |
intron_variant | MODIFIER | c.662-845_662-844del others(2): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429462 | ||||||
chr11:32429462
|
TCCC | T | 23 | a0001c0002t0001g0005a0001c0002t0001g0036a0001c0002t0001g0037others(20): Show | 24 | HG00408.hp1 HG00438.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.662-846_662-844del others(3): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429462 | ||||||
chr11:32429472
|
C | G | 3 | a0001c0001t0002g0116a0001c0001t0005g0008a0001c0001t0005g0117 | 4 | HG02015.hp1 NA18973.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-853G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429472 | ||||||
chr11:32429547
|
T | G | 89 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0001g0254others(86): Show | 95 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(92): Show |
intron_variant | MODIFIER | c.662-928A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429547 | ||||||
chr11:32429553
|
T | A | 222 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(219): Show | 232 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(229): Show |
intron_variant | MODIFIER | c.662-934A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429553 | ||||||
chr11:32429558
|
C | T | 5 | a0001c0002t0004g0027a0001c0002t0004g0028a0001c0002t0011g0025others(2): Show | 5 | HG02572.hp1 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.662-939G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429558 | ||||||
chr11:32429608
|
C | T | 1 | a0001c0009t0033g0306 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.662-989G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429608 | ||||||
chr11:32429709
|
A | G | 1 | a0001c0005t0005g0258 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.662-1090T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429709 | ||||||
chr11:32429796
|
C | T | 1 | a0001c0002t0001g0037 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.662-1177G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429796 | ||||||
chr11:32429978
|
G | GA | 12 | a0001c0002t0004g0027a0001c0002t0004g0028a0001c0002t0011g0025others(9): Show | 13 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.662-1360dupT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429978 | ||||||
chr11:32429978
|
G | GAAA | 103 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(100): Show | 106 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.662-1362_662-1360d others(5): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429978 | ||||||
chr11:32429986
|
A | AG | 102 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0001g0254others(99): Show | 108 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.662-1368_662-1367i others(3): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429986 | ||||||
chr11:32429998
|
G | GA | 75 | a0001c0001t0002g0165a0001c0001t0019g0020a0001c0003t0002g0232others(72): Show | 81 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.662-1380dupT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429998 | ||||||
chr11:32429998
|
GA | G | 7 | a0001c0001t0002g0179a0001c0002t0001g0096a0001c0009t0008g0004others(4): Show | 8 | HG02280.hp2 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.662-1380delT | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32429998 | ||||||
chr11:32430004
|
A | G | 2 | a0001c0010t0014g0270a0001c0010t0016g0271 | 2 | HG01109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.662-1385T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430004 | ||||||
chr11:32430005
|
A | C | 1 | a0001c0009t0033g0306 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.662-1386T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430005 | ||||||
chr11:32430293
|
A | G | 1 | a0001c0002t0001g0058 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.662-1674T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430293 | ||||||
chr11:32430374
|
T | G | 222 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(219): Show | 232 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(229): Show |
intron_variant | MODIFIER | c.662-1755A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430374 | ||||||
chr11:32430375
|
G | C | 102 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0001g0254others(99): Show | 108 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.662-1756C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430375 | ||||||
chr11:32430404
|
A | C | 120 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(117): Show | 124 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.662-1785T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430404 | ||||||
chr11:32430432
|
C | CAGAGAGA others(19): Show |
1 | a0001c0006t0001g0199 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.662-1814_662-1813i others(28): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | ||||||
chr11:32430432
|
C | CAGAGAGA others(27): Show |
1 | a0001c0001t0002g0203 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.662-1814_662-1813i others(36): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | ||||||
chr11:32430432
|
C | CAGAGAGA others(29): Show |
1 | a0001c0001t0002g0202 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.662-1814_662-1813i others(38): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | ||||||
chr11:32430432
|
C | CAGAGAGA others(16): Show |
1 | a0001c0001t0002g0166 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.662-1814_662-1813i others(25): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | ||||||
chr11:32430432
|
C | CAGAGAGA others(18): Show |
1 | a0001c0001t0002g0177 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.662-1814_662-1813i others(27): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | ||||||
chr11:32430432
|
C | CAGAGAGA others(30): Show |
1 | a0001c0006t0001g0212 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.662-1814_662-1813i others(39): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | ||||||
chr11:32430432
|
C | CAGAGAGA others(17): Show |
12 | a0001c0001t0002g0009a0001c0001t0002g0116a0001c0001t0002g0156others(9): Show | 13 | HG00639.hp1 HG02015.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.662-1814_662-1813i others(26): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | ||||||
chr11:32430432
|
C | CAGAGAGA others(19): Show |
14 | a0001c0001t0002g0118a0001c0001t0002g0122a0001c0001t0002g0167others(11): Show | 14 | HG00099.hp1 HG01346.hp1 HG03831.hp2 others(11): Show |
intron_variant | MODIFIER | c.662-1814_662-1813i others(28): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | ||||||
chr11:32430432
|
C | CAGAGAGA others(21): Show |
11 | a0001c0001t0002g0010a0001c0001t0002g0179a0001c0001t0002g0180others(8): Show | 12 | HG01071.hp2 HG01106.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.662-1814_662-1813i others(30): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | ||||||
chr11:32430432
|
C | CAGAGAGA others(23): Show |
10 | a0001c0001t0002g0188a0001c0001t0002g0189a0001c0001t0002g0190others(7): Show | 10 | HG00438.hp2 HG00642.hp2 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.662-1814_662-1813i others(32): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | ||||||
chr11:32430432
|
C | CAGAGAGA others(25): Show |
4 | a0001c0001t0002g0119a0001c0001t0002g0197a0001c0001t0012g0196others(1): Show | 4 | HG01361.hp2 NA18947.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-1814_662-1813i others(34): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | ||||||
chr11:32430432
|
C | CAGAGAGA others(29): Show |
1 | a0001c0001t0012g0201 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.662-1814_662-1813i others(38): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | ||||||
chr11:32430432
|
C | CAGAGAGA others(18): Show |
1 | a0001c0001t0019g0020 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.662-1814_662-1813i others(27): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | ||||||
chr11:32430432
|
C | CAGAGAGA others(22): Show |
1 | a0001c0006t0009g0178 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.662-1814_662-1813i others(31): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | ||||||
chr11:32430432
|
C | CAGAGAGA others(28): Show |
1 | a0001c0001t0002g0200 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.662-1814_662-1813i others(37): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430432 | ||||||
chr11:32430433
|
A | AGAGAGAG others(14): Show |
1 | a0001c0001t0002g0155 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.662-1815_662-1814i others(23): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430433 | ||||||
chr11:32430433
|
A | AGAGAGAG others(15): Show |
17 | a0001c0001t0002g0121a0001c0001t0002g0144a0001c0001t0002g0145others(14): Show | 17 | HG01975.hp1 HG02071.hp1 HG02602.hp2 others(14): Show |
intron_variant | MODIFIER | c.662-1815_662-1814i others(24): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430433 | ||||||
chr11:32430435
|
A | AGAGAGAG others(13): Show |
14 | a0001c0001t0002g0120a0001c0001t0002g0134a0001c0001t0002g0135others(11): Show | 15 | HG00733.hp1 HG02896.hp2 HG03669.hp1 others(12): Show |
intron_variant | MODIFIER | c.662-1817_662-1816i others(22): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430435 | ||||||
chr11:32430437
|
A | AGAGAGAG others(10): Show |
1 | a0001c0001t0002g0133 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.662-1819_662-1818i others(19): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430437 | ||||||
chr11:32430437
|
A | AGAGAGAG others(11): Show |
3 | a0001c0001t0002g0113a0001c0001t0002g0132a0001c0009t0008g0030 | 3 | HG00558.hp2 HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.662-1819_662-1818i others(20): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430437 | ||||||
chr11:32430439
|
A | AGAGAGAG others(9): Show |
5 | a0001c0001t0002g0129a0001c0001t0002g0130a0001c0001t0002g0131others(2): Show | 5 | HG01070.hp2 HG01243.hp1 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.662-1821_662-1820i others(18): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430439 | ||||||
chr11:32430441
|
A | AGAGAGAG others(7): Show |
4 | a0001c0001t0002g0127a0001c0002t0004g0027a0001c0002t0004g0028others(1): Show | 4 | HG01943.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-1823_662-1822i others(16): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430441 | ||||||
chr11:32430443
|
A | AGAGAGGG others(5): Show |
2 | a0001c0001t0002g0125a0001c0006t0018g0126 | 2 | HG01074.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.662-1825_662-1824i others(14): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430443 | ||||||
chr11:32430445
|
A | AGAGGGAG others(3): Show |
2 | a0001c0001t0002g0123a0001c0001t0002g0124 | 2 | NA18983.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.662-1827_662-1826i others(12): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430445 | ||||||
chr11:32430445
|
A | AGAGGGAG others(4): Show |
2 | a0001c0002t0011g0025a0001c0002t0011g0026 | 2 | HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.662-1827_662-1826i others(13): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430445 | ||||||
chr11:32430448
|
G | GGGAGGGG others(1): Show |
3 | a0001c0009t0008g0004a0001c0009t0008g0034a0001c0014t0008g0035 | 4 | HG02572.hp2 HG02630.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-1830_662-1829i others(10): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430448 | ||||||
chr11:32430449
|
A | G | 2 | a0001c0001t0002g0110a0001c0001t0002g0111 | 2 | NA18965.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.662-1830T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430449 | ||||||
chr11:32430451
|
G | A | 119 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(116): Show | 123 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.662-1832C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430451 | ||||||
chr11:32430451
|
G | GAGGGAGA others(6): Show |
1 | a0001c0001t0002g0128 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.662-1833_662-1832i others(15): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430451 | ||||||
chr11:32430453
|
A | G | 2 | a0001c0001t0002g0110a0001c0001t0002g0111 | 2 | NA18965.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.662-1834T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430453 | ||||||
chr11:32430455
|
G | A | 118 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0113others(115): Show | 122 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.662-1836C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | ||||||
chr11:32430455
|
G | GAGAGAGA others(6): Show |
3 | a0001c0004t0009g0288a0001c0008t0003g0289a0001c0008t0003g0290 | 3 | HG02630.hp1 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.662-1837_662-1836i others(15): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | ||||||
chr11:32430455
|
G | GAGAGAGA others(8): Show |
2 | a0001c0003t0003g0248a0001c0004t0003g0293 | 2 | HG01261.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.662-1837_662-1836i others(17): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | ||||||
chr11:32430455
|
G | GAGAGAGA others(10): Show |
1 | a0001c0003t0006g0225 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.662-1837_662-1836i others(19): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | ||||||
chr11:32430455
|
G | GAGAGAGA others(12): Show |
1 | a0001c0010t0014g0270 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.662-1837_662-1836i others(21): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | ||||||
chr11:32430455
|
G | GAGAGAGA others(14): Show |
1 | a0001c0004t0003g0273 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.662-1837_662-1836i others(23): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | ||||||
chr11:32430455
|
G | GAGAGAGA others(22): Show |
1 | a0001c0004t0004g0298 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.662-1837_662-1836i others(31): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | ||||||
chr11:32430455
|
G | GGA | 3 | a0001c0002t0001g0007a0001c0003t0003g0214a0001c0003t0032g0234 | 4 | HG00639.hp2 HG01243.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-1838_662-1837d others(4): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | ||||||
chr11:32430455
|
G | GGAGA | 6 | a0001c0002t0015g0055a0001c0004t0001g0014a0001c0004t0001g0280others(3): Show | 7 | HG00741.hp2 HG01358.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.662-1840_662-1837d others(6): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | ||||||
chr11:32430455
|
G | GGAGAGA | 8 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0003g0215others(5): Show | 8 | HG01169.hp2 HG01256.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.662-1842_662-1837d others(8): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | ||||||
chr11:32430455
|
G | GGAGAGAG others(1): Show |
11 | a0001c0003t0009g0229a0001c0003t0009g0239a0001c0003t0010g0017others(8): Show | 11 | HG01099.hp1 HG01175.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.662-1844_662-1837d others(10): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | ||||||
chr11:32430455
|
G | GGAGAGAG others(3): Show |
2 | a0001c0003t0003g0230a0001c0003t0004g0240 | 2 | HG03017.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.662-1846_662-1837d others(12): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | ||||||
chr11:32430455
|
G | GGAGAGAG others(5): Show |
4 | a0001c0003t0004g0231a0001c0003t0004g0241a0001c0004t0007g0305others(1): Show | 4 | HG02257.hp2 HG02622.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-1848_662-1837d others(14): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | ||||||
chr11:32430455
|
G | GGAGAGAG others(7): Show |
9 | a0001c0003t0003g0244a0001c0003t0003g0245a0001c0003t0004g0242others(6): Show | 10 | HG00642.hp1 HG01361.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.662-1850_662-1837d others(16): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | ||||||
chr11:32430455
|
G | GGAGAGAG others(9): Show |
13 | a0001c0002t0001g0106a0001c0003t0001g0269a0001c0003t0003g0246others(10): Show | 14 | HG00733.hp2 HG01261.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.662-1852_662-1837d others(18): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | ||||||
chr11:32430455
|
G | GGAGAGAG others(11): Show |
6 | a0001c0003t0003g0249a0001c0003t0006g0223a0001c0003t0006g0228others(3): Show | 6 | HG02145.hp2 HG02976.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.662-1854_662-1837d others(20): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | ||||||
chr11:32430455
|
G | GGAGAGAG others(13): Show |
6 | a0001c0003t0003g0250a0001c0003t0006g0226a0001c0003t0006g0227others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.662-1856_662-1837d others(22): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | ||||||
chr11:32430455
|
G | GGAGAGAG others(15): Show |
4 | a0001c0003t0003g0252a0001c0003t0031g0251a0001c0010t0014g0257others(1): Show | 4 | HG02486.hp1 HG02965.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-1858_662-1837d others(24): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | ||||||
chr11:32430455
|
G | GGAGAGAG others(17): Show |
1 | a0001c0008t0003g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.662-1860_662-1837d others(26): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | ||||||
chr11:32430455
|
G | GGGGAGAG others(7): Show |
1 | a0001c0005t0002g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.662-1837_662-1836i others(16): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | ||||||
chr11:32430455
|
G | GGGGAGAG others(11): Show |
1 | a0001c0003t0001g0254 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.662-1837_662-1836i others(20): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | ||||||
chr11:32430455
|
G | GGGGAGAG others(15): Show |
1 | a0001c0005t0002g0253 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.662-1837_662-1836i others(24): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | ||||||
chr11:32430455
|
GGA | G | 14 | a0001c0002t0001g0054a0001c0002t0001g0096a0001c0002t0001g0097others(11): Show | 14 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(11): Show |
intron_variant | MODIFIER | c.662-1838_662-1837d others(4): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | ||||||
chr11:32430455
|
GGAGA | G | 69 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(66): Show | 76 | HG00408.hp2 HG00558.hp1 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.662-1840_662-1837d others(6): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | ||||||
chr11:32430455
|
GGAGAGAG others(1): Show |
G | 3 | a0001c0003t0002g0232a0001c0003t0004g0011a0001c0003t0004g0012 | 5 | HG02723.hp1 HG02970.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.662-1844_662-1837d others(10): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430455 | ||||||
chr11:32430459
|
A | G | 1 | a0001c0002t0001g0057 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.662-1840T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430459 | ||||||
chr11:32430463
|
A | G | 1 | a0001c0002t0001g0056 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.662-1844T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430463 | ||||||
chr11:32430477
|
A | G | 1 | a0001c0001t0002g0209 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.662-1858T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430477 | ||||||
chr11:32430486
|
G | C | 1 | a0001c0004t0003g0273 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.662-1867C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430486 | ||||||
chr11:32430486
|
G | GAGAGAGA others(7): Show |
1 | a0001c0016t0016g0299 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.662-1868_662-1867i others(16): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430486 | ||||||
chr11:32430486
|
G | GAGAGAGA others(11): Show |
1 | a0001c0004t0003g0303 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.662-1868_662-1867i others(20): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430486 | ||||||
chr11:32430486
|
G | GAGAGAGA others(13): Show |
2 | a0001c0004t0003g0016a0001c0004t0003g0300 | 3 | HG00735.hp1 HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.662-1868_662-1867i others(22): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430486 | ||||||
chr11:32430486
|
G | GAGAGAGA others(17): Show |
1 | a0001c0004t0030g0301 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.662-1868_662-1867i others(26): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430486 | ||||||
chr11:32430491
|
A | G | 3 | a0001c0003t0001g0254a0001c0005t0002g0213a0001c0005t0002g0253 | 3 | HG01884.hp1 HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.662-1872T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430491 | ||||||
chr11:32430492
|
C | T | 1 | a0001c0001t0002g0122 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.662-1873G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430492 | ||||||
chr11:32430545
|
AGC | A | 13 | a0001c0003t0003g0214a0001c0003t0003g0215a0001c0003t0006g0219others(10): Show | 13 | HG02145.hp2 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.662-1928_662-1927d others(4): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430545 | ||||||
chr11:32430694
|
GC | G | 108 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(105): Show | 111 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.662-2076delG | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430694 | ||||||
chr11:32430792
|
C | T | 12 | a0001c0002t0004g0027a0001c0002t0004g0028a0001c0002t0011g0025others(9): Show | 13 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.662-2173G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430792 | ||||||
chr11:32430929
|
G | A | 11 | a0001c0002t0001g0005a0001c0002t0001g0036a0001c0002t0001g0037others(8): Show | 12 | HG00408.hp1 HG00438.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.662-2310C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430929 | ||||||
chr11:32430978
|
G | C | 108 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(105): Show | 111 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.662-2359C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32430978 | ||||||
chr11:32431032
|
C | T | 1 | a0001c0013t0001g0024 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.662-2413G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431032 | ||||||
chr11:32431052
|
G | C | 1 | a0001c0005t0002g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.662-2433C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431052 | ||||||
chr11:32431143
|
C | A | 1 | a0001c0005t0002g0253 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.662-2524G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431143 | ||||||
chr11:32431288
|
G | T | 12 | a0001c0002t0004g0027a0001c0002t0004g0028a0001c0002t0011g0025others(9): Show | 13 | HG01243.hp1 HG02280.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.662-2669C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431288 | ||||||
chr11:32431342
|
C | T | 102 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0001g0254others(99): Show | 108 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.662-2723G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431342 | ||||||
chr11:32431379
|
C | G | 233 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(230): Show | 244 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(241): Show |
intron_variant | MODIFIER | c.662-2760G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431379 | ||||||
chr11:32431399
|
C | G | 102 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0001g0254others(99): Show | 108 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.662-2780G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431399 | ||||||
chr11:32431426
|
G | A | 4 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(1): Show | 4 | NA18964.hp2 NA18981.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-2807C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431426 | ||||||
chr11:32431434
|
C | CT | 21 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049others(18): Show | 21 | HG01175.hp2 HG01358.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.662-2816dupA | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431434 | ||||||
chr11:32431444
|
T | G | 1 | a0001c0004t0020g0302 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.662-2825A>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431444 | ||||||
chr11:32431450
|
TTTC | T | 36 | a0001c0002t0011g0026a0001c0004t0001g0014a0001c0004t0001g0280others(33): Show | 39 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.662-2834_662-2832d others(5): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431450 | ||||||
chr11:32431451
|
TTC | T | 52 | a0001c0002t0004g0027a0001c0002t0004g0028a0001c0002t0007g0043others(49): Show | 55 | HG00408.hp1 HG00438.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.662-2834_662-2833d others(4): Show |
WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431451 | ||||||
chr11:32431452
|
TC | T | 121 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(118): Show | 126 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.662-2834delG | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431452 | ||||||
chr11:32431453
|
C | T | 23 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0002t0001g0036others(20): Show | 23 | HG01496.hp1 HG02145.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.662-2834G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431453 | ||||||
chr11:32431476
|
G | T | 2 | a0001c0010t0006g0217a0001c0010t0021g0216 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.662-2857C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431476 | ||||||
chr11:32431485
|
G | T | 3 | a0001c0004t0007g0276a0001c0004t0007g0277a0001c0004t0007g0278 | 3 | NA18942.hp2 NA18964.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.662-2866C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431485 | ||||||
chr11:32431603
|
AT | A | 227 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(224): Show | 237 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.662-2985delA | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431603 | ||||||
chr11:32431643
|
G | A | 1 | a0001c0004t0003g0303 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.662-3024C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431643 | ||||||
chr11:32431808
|
C | A | 1 | a0001c0001t0002g0208 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.661+2892G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431808 | ||||||
chr11:32431867
|
C | T | 2 | a0001c0010t0006g0217a0001c0010t0021g0216 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.661+2833G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431867 | ||||||
chr11:32431990
|
C | T | 120 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(117): Show | 124 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.661+2710G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32431990 | ||||||
chr11:32432057
|
A | C | 1 | a0001c0001t0002g0119 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.661+2643T>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32432057 | ||||||
chr11:32432076
|
G | A | 102 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0001g0254others(99): Show | 108 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.661+2624C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32432076 | ||||||
chr11:32432221
|
T | C | 1 | a0001c0003t0001g0254 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.661+2479A>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32432221 | ||||||
chr11:32432276
|
C | T | 2 | a0001c0004t0004g0274a0001c0004t0004g0275 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.661+2424G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32432276 | ||||||
chr11:32432409
|
G | C | 2 | a0001c0004t0007g0304a0001c0004t0007g0305 | 2 | NA18947.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.661+2291C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32432409 | ||||||
chr11:32432442
|
C | T | 11 | a0001c0001t0002g0009a0001c0001t0002g0110a0001c0001t0002g0111others(8): Show | 13 | HG02015.hp1 HG02258.hp2 HG04184.hp1 others(10): Show |
intron_variant | MODIFIER | c.661+2258G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32432442 | ||||||
chr11:32432487
|
G | C | 3 | a0001c0009t0008g0004a0001c0009t0008g0034a0001c0014t0008g0035 | 4 | HG02572.hp2 HG02630.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.661+2213C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32432487 | ||||||
chr11:32432670
|
C | T | 2 | a0001c0003t0003g0214a0001c0003t0003g0215 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.661+2030G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32432670 | ||||||
chr11:32432716
|
G | A | 102 | a0001c0003t0001g0235a0001c0003t0001g0236a0001c0003t0001g0254others(99): Show | 108 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.661+1984C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32432716 | ||||||
chr11:32432753
|
G | A | 5 | a0001c0002t0001g0108a0001c0002t0001g0109a0001c0011t0001g0021others(2): Show | 5 | HG01106.hp2 HG01928.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.661+1947C>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32432753 | ||||||
chr11:32432803
|
A | G | 1 | a0001c0004t0003g0273 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.661+1897T>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32432803 | ||||||
chr11:32432996
|
C | G | 2 | a0001c0009t0008g0030a0001c0009t0008g0031 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.661+1704G>C | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32432996 | ||||||
chr11:32433056
|
T | A | 1 | a0001c0001t0002g0209 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.661+1644A>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32433056 | ||||||
chr11:32433136
|
C | T | 3 | a0001c0009t0008g0004a0001c0009t0008g0034a0001c0014t0008g0035 | 4 | HG02572.hp2 HG02630.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.661+1564G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32433136 | ||||||
chr11:32433366
|
C | T | 1 | a0001c0004t0003g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.661+1334G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32433366 | ||||||
chr11:32433371
|
G | T | 5 | a0001c0002t0004g0027a0001c0002t0004g0028a0001c0002t0011g0025others(2): Show | 5 | HG02572.hp1 HG02717.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+1329C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32433371 | ||||||
chr11:32433464
|
C | T | 1 | a0001c0002t0001g0046 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.661+1236G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32433464 | ||||||
chr11:32433519
|
C | T | 11 | a0001c0002t0001g0005a0001c0002t0001g0036a0001c0002t0001g0037others(8): Show | 12 | HG00408.hp1 HG00438.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.661+1181G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32433519 | ||||||
chr11:32433981
|
C | A | 222 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(219): Show | 232 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(229): Show |
intron_variant | MODIFIER | c.661+719G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32433981 | ||||||
chr11:32434015
|
C | A | 3 | a0001c0006t0001g0212a0001c0012t0014g0211a0001c0012t0023g0210 | 3 | HG02257.hp1 HG02896.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.661+685G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32434015 | ||||||
chr11:32434037
|
G | C | 3 | a0001c0009t0008g0004a0001c0009t0008g0034a0001c0014t0008g0035 | 4 | HG02572.hp2 HG02630.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.661+663C>G | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32434037 | ||||||
chr11:32434307
|
G | T | 120 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0110others(117): Show | 124 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.661+393C>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32434307 | ||||||
chr11:32434480
|
C | T | 1 | a0001c0005t0002g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.661+220G>A | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32434480 | ||||||
chr11:32434539
|
C | A | 17 | a0001c0003t0001g0259a0001c0003t0001g0266a0001c0003t0001g0269others(14): Show | 17 | HG01109.hp2 HG02129.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.661+161G>T | WT1 | ENSG00000184937.16 | transcript | ENST00000452863.10 | protein_coding | 1/9 | chr11 | 32434539 |