geneid | 5172 |
---|---|
ensemblid | ENSG00000091137.14 |
hgncid | 8818 |
symbol | SLC26A4 |
name | solute carrier family 26 member 4 |
refseq_nuc | NM_000441.2 |
refseq_prot | NP_000432.1 |
ensembl_nuc | ENST00000644269.2 |
ensembl_prot | ENSP00000494017.1 |
mane_status | MANE Select |
chr | chr7 |
start | 107660828 |
end | 107717809 |
strand | + |
ver | v1.2 |
region | chr7:107660828-107717809 |
region5000 | chr7:107655828-107722809 |
regionname0 | SLC26A4_chr7_107660828_107717809 |
regionname5000 | SLC26A4_chr7_107655828_107722809 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 780 | 336 | 72 | 70 | 146 | 16 | 30 | 111 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0002 | 0/0 | 780 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0003 | 0/0 | 780 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0004 | 0/0 | 780 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0005 | 0/0 | 780 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0006 | 0/0 | 780 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0007 | 0/0 | 780 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0008 | 0/0 | 780 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0009 | 0/0 | 780 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0010 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0011 | 0/0 | 780 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0012 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0013 | 0/0 | 780 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0014 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0015 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0016 | 0/0 | 780 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2343 | 329 | 67 | 70 | 145 | 16 | 29 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
c0002 | 0/0 | 2343 | 4 | 4 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
c0003 | 0/0 | 2343 | 4 | 4 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
c0004 | 0/0 | 2343 | 3 | 3 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
c0005 | 0/0 | 2343 | 3 | 0 | 0 | 0 | 0 | 3 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
c0006 | 0/0 | 2343 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
c0007 | 0/0 | 2343 | 2 | 0 | 0 | 0 | 0 | 2 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
c0008 | 0/0 | 2343 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
c0009 | 0/0 | 2343 | 2 | 1 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
c0010 | 0/0 | 2343 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
c0011 | 0/0 | 2343 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
c0012 | 0/0 | 2343 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
c0013 | 0/0 | 2343 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
c0014 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
c0015 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
c0016 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
c0017 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
c0018 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
c0019 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
c0020 | 0/0 | 2343 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
c0021 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
c0022 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2393 | 155 | 31 | 27 | 77 | 6 | 14 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0002 | 0/0 | 2392 | 76 | 1 | 17 | 42 | 4 | 12 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0003 | 1/0 | 2395 | 39 | 17 | 11 | 1 | 2 | 7 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0004 | 0/0 | 2393 | 15 | 2 | 2 | 11 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0005 | 0/0 | 2394 | 13 | 2 | 4 | 4 | 2 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0006 | 0/0 | 2392 | 11 | 2 | 4 | 3 | 1 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0007 | 0/0 | 2392 | 7 | 7 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0008 | 0/0 | 2396 | 7 | 4 | 2 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0009 | 0/0 | 2391 | 5 | 5 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0010 | 0/0 | 2391 | 4 | 4 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0011 | 0/0 | 2392 | 4 | 0 | 0 | 4 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0012 | 0/0 | 2395 | 3 | 1 | 0 | 1 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0013 | 0/0 | 2393 | 3 | 3 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0014 | 0/0 | 2393 | 3 | 3 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0015 | 0/0 | 2393 | 2 | 0 | 0 | 2 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0016 | 0/0 | 2392 | 2 | 1 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0017 | 0/0 | 2395 | 2 | 0 | 2 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0018 | 0/0 | 2393 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0019 | 0/0 | 2395 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0020 | 0/0 | 2392 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0021 | 0/0 | 2395 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0022 | 0/0 | 2393 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0023 | 0/0 | 2393 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0024 | 0/0 | 2396 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0025 | 0/0 | 2395 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0026 | 0/0 | 2393 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0027 | 0/0 | 2395 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0028 | 0/0 | 2380 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0029 | 0/1 | 2395 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0030 | 0/0 | 2395 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
t0031 | 0/0 | 2393 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0081 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0335 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2343 | 329 | 67 | 70 | 145 | 16 | 29 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0006 | 0/0 | 2343 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0011 | 0/0 | 2343 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0012 | 0/0 | 2343 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0019 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0022 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0002c0002 | 0/0 | 2343 | 4 | 4 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0002c0009 | 0/0 | 2343 | 2 | 1 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0003c0003 | 0/0 | 2343 | 4 | 4 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0004c0004 | 0/0 | 2343 | 3 | 3 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0005c0005 | 0/0 | 2343 | 3 | 0 | 0 | 0 | 0 | 3 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0006c0008 | 0/0 | 2343 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0007c0010 | 0/0 | 2343 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0008c0007 | 0/0 | 2343 | 2 | 0 | 0 | 0 | 0 | 2 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0009c0020 | 0/0 | 2343 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0010c0016 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0011c0017 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0012c0018 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0013c0015 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0014c0021 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0015c0014 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0016c0013 | 0/0 | 2343 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4735 | 147 | 28 | 27 | 75 | 6 | 11 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0001t0002 | 0/0 | 4734 | 73 | 1 | 17 | 41 | 4 | 10 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0001t0003 | 1/0 | 4737 | 32 | 12 | 11 | 1 | 2 | 5 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0001t0004 | 0/0 | 4735 | 15 | 2 | 2 | 11 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0001t0005 | 0/0 | 4736 | 12 | 1 | 4 | 4 | 2 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0001t0006 | 0/0 | 4734 | 8 | 1 | 3 | 2 | 1 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0001t0007 | 0/0 | 4734 | 5 | 5 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0001t0008 | 0/0 | 4738 | 7 | 4 | 2 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0001t0009 | 0/0 | 4733 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0001t0010 | 0/0 | 4733 | 4 | 4 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0001t0011 | 0/0 | 4734 | 3 | 0 | 0 | 3 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0001t0012 | 0/0 | 4737 | 3 | 1 | 0 | 1 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0001t0013 | 0/0 | 4735 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0001t0015 | 0/0 | 4735 | 2 | 0 | 0 | 2 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0001t0016 | 0/0 | 4734 | 2 | 1 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0001t0017 | 0/0 | 4737 | 2 | 0 | 2 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0001t0019 | 0/0 | 4737 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0001t0020 | 0/0 | 4734 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0001t0021 | 0/0 | 4737 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0001t0022 | 0/0 | 4735 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0001t0023 | 0/0 | 4735 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0001t0026 | 0/0 | 4735 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0001t0027 | 0/0 | 4737 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0001t0028 | 0/0 | 4722 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0001t0029 | 0/1 | 4737 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0001t0031 | 0/0 | 4735 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0006t0001 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0006t0006 | 0/0 | 4734 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0011t0007 | 0/0 | 4734 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0012t0001 | 0/0 | 4735 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0019t0001 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0001c0022t0006 | 0/0 | 4734 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0002c0002t0013 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0002c0002t0014 | 0/0 | 4735 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0002c0002t0018 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0002c0009t0024 | 0/0 | 4738 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0002c0009t0025 | 0/0 | 4737 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0003c0003t0003 | 0/0 | 4737 | 4 | 4 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0004c0004t0009 | 0/0 | 4733 | 3 | 3 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0005c0005t0001 | 0/0 | 4735 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0005c0005t0002 | 0/0 | 4734 | 2 | 0 | 0 | 0 | 0 | 2 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0006c0008t0014 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0006c0008t0030 | 0/0 | 4737 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0007c0010t0003 | 0/0 | 4737 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0007c0010t0005 | 0/0 | 4736 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0008c0007t0003 | 0/0 | 4737 | 2 | 0 | 0 | 0 | 0 | 2 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0009c0020t0001 | 0/0 | 4735 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0010c0016t0011 | 0/0 | 4734 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0011c0017t0001 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0012c0018t0002 | 0/0 | 4734 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0013c0015t0018 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0014c0021t0001 | 0/0 | 4735 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0015c0014t0001 | 0/0 | 4735 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
a0016c0013t0006 | 0/0 | 4734 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | copy fasta | chr7 | 107655828 | 107722809 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0002g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0081 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0003g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0005g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0005g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0005g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0005g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0005g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0005g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0005g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0005g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0005g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0006g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0006g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0006g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0006g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0006g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0006g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0006g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0006g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0007g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0007g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0007g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0007g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0007g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0008g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0008g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0008g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0008g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0008g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0008g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0009g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0009g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0010g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0010g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0010g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0011g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0011g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0011g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0012g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0012g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0012g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0013g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0013g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0015g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0015g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0016g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0016g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0017g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0017g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0019g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0020g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0021g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0022g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0023g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0026g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0027g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0028g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0029g0335 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0001t0031g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0006t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0006t0006g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0011t0007g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0011t0007g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0012t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0019t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0001c0022t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0002c0002t0013g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0002c0002t0014g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0002c0002t0014g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0002c0002t0018g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0002c0009t0024g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0002c0009t0025g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0003c0003t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0003c0003t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0003c0003t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0003c0003t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0004c0004t0009g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0004c0004t0009g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0004c0004t0009g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0005c0005t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0005c0005t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0005c0005t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0006c0008t0014g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0006c0008t0030g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0007c0010t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0007c0010t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0008c0007t0003g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0008c0007t0003g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0009c0020t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0010c0016t0011g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0011c0017t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0012c0018t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0013c0015t0018g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0014c0021t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0015c0014t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
a0016c0013t0006g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0301 | EUR | GBR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | GBR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00140 | hp2 | a0001 | c0001 | t0005 | g0332 | EUR | GBR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0325 | EUR | FIN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0070 | EUR | FIN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00323 | hp2 | a0001 | c0001 | t0012 | g0276 | EUR | FIN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00408 | hp2 | a0001 | c0022 | t0006 | g0054 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00438 | hp2 | a0001 | c0001 | t0011 | g0273 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00544 | hp1 | a0014 | c0021 | t0001 | g0127 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00597 | hp1 | a0001 | c0001 | t0022 | g0084 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00639 | hp2 | a0001 | c0001 | t0017 | g0304 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00642 | hp2 | a0001 | c0001 | t0008 | g0294 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0261 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01069 | hp1 | a0001 | c0001 | t0005 | g0284 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0339 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0327 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0292 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01074 | hp1 | a0001 | c0001 | t0006 | g0039 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01074 | hp2 | a0002 | c0009 | t0024 | g0193 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0293 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0354 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01109 | hp1 | a0016 | c0013 | t0006 | g0104 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0322 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0256 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0071 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01169 | hp2 | a0001 | c0001 | t0005 | g0251 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0306 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01175 | hp2 | a0001 | c0001 | t0005 | g0333 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0040 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01243 | hp1 | a0001 | c0001 | t0006 | g0038 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01243 | hp2 | a0001 | c0001 | t0008 | g0138 | AMR | PUR | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0168 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0351 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0324 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0350 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0353 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01358 | hp1 | a0001 | c0001 | t0023 | g0317 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0087 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01433 | hp1 | a0001 | c0001 | t0005 | g0334 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01433 | hp2 | a0001 | c0001 | t0016 | g0095 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01515 | hp1 | a0001 | c0001 | t0005 | g0105 | EUR | IBS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0069 | EUR | IBS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01516 | hp1 | a0001 | c0001 | t0006 | g0211 | EUR | IBS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0216 | EUR | IBS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | IBS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0237 | EUR | IBS | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0271 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01891 | hp2 | a0002 | c0009 | t0025 | g0316 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01952 | hp2 | a0001 | c0001 | t0004 | g0093 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01978 | hp2 | a0001 | c0001 | t0006 | g0215 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0267 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0277 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02027 | hp1 | a0001 | c0001 | t0004 | g0161 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02055 | hp1 | a0006 | c0008 | t0030 | g0036 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02055 | hp2 | a0001 | c0001 | t0013 | g0341 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02129 | hp2 | a0001 | c0001 | t0006 | g0272 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | KHV | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02148 | hp1 | a0001 | c0001 | t0017 | g0094 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | CDX | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | CDX | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | CDX | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CDX | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02257 | hp1 | a0001 | c0011 | t0007 | g0329 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02258 | hp1 | a0001 | c0001 | t0008 | g0197 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02280 | hp1 | a0001 | c0011 | t0007 | g0328 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02280 | hp2 | a0001 | c0001 | t0006 | g0214 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02451 | hp1 | a0001 | c0001 | t0012 | g0288 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02451 | hp2 | a0001 | c0006 | t0006 | g0348 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02602 | hp1 | a0001 | c0001 | t0006 | g0037 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0257 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02615 | hp1 | a0001 | c0001 | t0016 | g0347 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0182 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02622 | hp2 | a0011 | c0017 | t0001 | g0133 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02698 | hp2 | a0008 | c0007 | t0003 | g0355 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0132 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02723 | hp1 | a0002 | c0002 | t0013 | g0078 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02723 | hp2 | a0007 | c0010 | t0003 | g0177 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02735 | hp1 | a0001 | c0001 | t0031 | g0172 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02738 | hp1 | a0001 | c0001 | t0005 | g0318 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02738 | hp2 | a0009 | c0020 | t0001 | g0295 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02809 | hp2 | a0001 | c0001 | t0008 | g0192 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02818 | hp2 | a0004 | c0004 | t0009 | g0018 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02886 | hp2 | a0001 | c0001 | t0009 | g0062 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02895 | hp1 | a0004 | c0004 | t0009 | g0029 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0190 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02896 | hp1 | a0004 | c0004 | t0009 | g0007 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02922 | hp2 | a0003 | c0003 | t0003 | g0173 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02965 | hp1 | a0003 | c0003 | t0003 | g0021 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02965 | hp2 | a0001 | c0001 | t0008 | g0030 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02970 | hp1 | a0001 | c0001 | t0027 | g0139 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02976 | hp1 | a0003 | c0003 | t0003 | g0174 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0253 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03098 | hp2 | a0002 | c0002 | t0014 | g0356 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03130 | hp1 | a0001 | c0001 | t0010 | g0002 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03139 | hp1 | a0013 | c0015 | t0018 | g0184 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03139 | hp2 | a0001 | c0001 | t0007 | g0196 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03195 | hp1 | a0001 | c0001 | t0007 | g0181 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03209 | hp1 | a0001 | c0001 | t0007 | g0342 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03209 | hp2 | a0003 | c0003 | t0003 | g0016 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0176 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03225 | hp2 | a0001 | c0006 | t0001 | g0349 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0281 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0022 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0360 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03486 | hp1 | a0001 | c0001 | t0010 | g0056 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0096 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0266 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03516 | hp1 | a0001 | c0001 | t0007 | g0344 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03540 | hp2 | a0001 | c0001 | t0007 | g0346 | AFR | GWD | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03579 | hp1 | a0006 | c0008 | t0014 | g0057 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03654 | hp1 | a0008 | c0007 | t0003 | g0308 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0336 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0352 | SAS | BEB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0270 | SAS | BEB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03834 | hp2 | a0005 | c0005 | t0002 | g0156 | SAS | BEB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03942 | hp1 | a0001 | c0012 | t0001 | g0058 | SAS | BEB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03942 | hp2 | a0005 | c0005 | t0002 | g0155 | SAS | BEB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | STU | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0313 | SAS | STU | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0280 | SAS | BEB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG04184 | hp2 | a0005 | c0005 | t0001 | g0151 | SAS | BEB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | STU | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0254 | SAS | STU | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0129 | AFR | YRI | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | YRI | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18906 | hp1 | a0001 | c0001 | t0005 | g0358 | AFR | YRI | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18906 | hp2 | a0001 | c0001 | t0021 | g0359 | AFR | YRI | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18939 | hp1 | a0001 | c0001 | t0004 | g0259 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18946 | hp1 | a0015 | c0014 | t0001 | g0048 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18963 | hp2 | a0001 | c0001 | t0005 | g0152 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18966 | hp2 | a0001 | c0001 | t0015 | g0042 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18977 | hp1 | a0001 | c0001 | t0005 | g0224 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18979 | hp2 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18980 | hp1 | a0001 | c0001 | t0004 | g0269 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18981 | hp1 | a0010 | c0016 | t0011 | g0112 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18983 | hp1 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18984 | hp1 | a0001 | c0001 | t0012 | g0245 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18987 | hp1 | a0001 | c0001 | t0004 | g0311 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18989 | hp2 | a0001 | c0001 | t0020 | g0074 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18992 | hp1 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18992 | hp2 | a0001 | c0001 | t0015 | g0118 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18998 | hp1 | a0012 | c0018 | t0002 | g0028 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA18999 | hp2 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19030 | hp1 | a0001 | c0019 | t0001 | g0171 | AFR | LWK | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0188 | AFR | LWK | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | LWK | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19043 | hp2 | a0001 | c0001 | t0013 | g0345 | AFR | LWK | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19067 | hp2 | a0001 | c0001 | t0026 | g0213 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19068 | hp2 | a0001 | c0001 | t0011 | g0108 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19072 | hp1 | a0001 | c0001 | t0028 | g0231 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19074 | hp2 | a0001 | c0001 | t0011 | g0066 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19076 | hp2 | a0001 | c0001 | t0006 | g0088 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19077 | hp2 | a0001 | c0001 | t0004 | g0310 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19078 | hp2 | a0001 | c0001 | t0005 | g0298 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19080 | hp1 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19082 | hp1 | a0001 | c0001 | t0008 | g0158 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19082 | hp2 | a0001 | c0001 | t0005 | g0141 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19083 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | YRI | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | YRI | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0343 | AFR | ASW | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA20129 | hp2 | a0001 | c0001 | t0010 | g0002 | AFR | ASW | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0320 | EUR | TSI | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | GIH | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0315 | SAS | GIH | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02109 | hp1 | a0002 | c0002 | t0018 | g0014 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02109 | hp2 | a0002 | c0002 | t0014 | g0357 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02486 | hp2 | a0001 | c0001 | t0019 | g0186 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG02559 | hp2 | a0007 | c0010 | t0005 | g0180 | AFR | ACB | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG03471 | hp2 | a0001 | c0001 | t0009 | g0187 | AFR | MSL | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | USA | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
HG06807 | hp2 | a0001 | c0001 | t0010 | g0049 | AFR | USA | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | USA | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0046 | AFR | USA | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0103 | AFR | LWK | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
NA21309 | hp2 | a0001 | c0001 | t0008 | g0178 | AFR | LWK | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0029 | g0335 | REF | REF | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0081 | REF | REF | SLC26A4_chr7_107655828_107722809 | SLC26A4 | chr7 | 107655828 | 107722809 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:107661658
|
G | T | 1 | a0005 | 3 | HG03834.hp2 HG03942.hp2 HG04184.hp2 |
missense_variant | MODERATE | c.17G>T | p.Gly6Val | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 2/21 | 48/4737 | 17/2343 | 6/780 | chr7 | 107661658 | ||
chr7:107683334
|
A | C | 1 | a0004 | 3 | HG02818.hp2 HG02895.hp1 HG02896.hp1 |
missense_variant | MODERATE | c.898A>C | p.Ile300Leu | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 7/21 | 929/4737 | 898/2343 | 300/780 | chr7 | 107683334 | ||
chr7:107683506
|
A | T | 1 | a0003 | 4 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(1): Show |
missense_variant | MODERATE | c.970A>T | p.Asn324Tyr | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/21 | 1001/4737 | 970/2343 | 324/780 | chr7 | 107683506 | ||
chr7:107689112
|
T | C | 1 | a0016 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.1061T>C | p.Phe354Ser | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 9/21 | 1092/4737 | 1061/2343 | 354/780 | chr7 | 107689112 | ||
chr7:107689120
|
G | A | 1 | a0015 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.1069G>A | p.Ala357Thr | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 9/21 | 1100/4737 | 1069/2343 | 357/780 | chr7 | 107689120 | ||
chr7:107690148
|
A | T | 1 | a0014 | 1 | HG00544.hp1 | missense_variant | MODERATE | c.1174A>T | p.Asn392Tyr | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/21 | 1205/4737 | 1174/2343 | 392/780 | chr7 | 107690148 | ||
chr7:107694642
|
A | T | 1 | a0009 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.1363A>T | p.Ile455Phe | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 12/21 | 1394/4737 | 1363/2343 | 455/780 | chr7 | 107694642 | ||
chr7:107700084
|
T | C | 1 | a0013 | 1 | HG03139.hp1 | missense_variant&splice_region_variant | MODERATE | c.1616T>C | p.Ile539Thr | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 15/21 | 1647/4737 | 1616/2343 | 539/780 | chr7 | 107700084 | ||
chr7:107701183
|
T | C | 1 | a0008 | 2 | HG02698.hp2 HG03654.hp1 |
missense_variant | MODERATE | c.1790T>C | p.Leu597Ser | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 16/21 | 1821/4737 | 1790/2343 | 597/780 | chr7 | 107701183 | ||
chr7:107701849
|
T | G | 4 | a0002a0006a0007others(1): Show | 11 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
missense_variant | MODERATE | c.1826T>G | p.Val609Gly | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/21 | 1857/4737 | 1826/2343 | 609/780 | chr7 | 107701849 | ||
chr7:107701998
|
G | C | 1 | a0010 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.1975G>C | p.Val659Leu | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/21 | 2006/4737 | 1975/2343 | 659/780 | chr7 | 107701998 | ||
chr7:107704355
|
G | T | 1 | a0007 | 2 | HG02559.hp2 HG02723.hp2 |
missense_variant | MODERATE | c.2059G>T | p.Asp687Tyr | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/21 | 2090/4737 | 2059/2343 | 687/780 | chr7 | 107704355 | ||
chr7:107710132
|
A | G | 1 | a0012 | 1 | NA18998.hp1 | missense_variant | MODERATE | c.2168A>G | p.His723Arg | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/21 | 2199/4737 | 2168/2343 | 723/780 | chr7 | 107710132 | ||
chr7:107710154
|
G | T | 1 | a0011 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.2190G>T | p.Gln730His | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/21 | 2221/4737 | 2190/2343 | 730/780 | chr7 | 107710154 | ||
chr7:107710182
|
G | A | 2 | a0006a0007 | 4 | HG02055.hp1 HG02559.hp2 HG02723.hp2 others(1): Show |
missense_variant | MODERATE | c.2218G>A | p.Gly740Ser | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/21 | 2249/4737 | 2218/2343 | 740/780 | chr7 | 107710182 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:107661656
|
C | A | 1 | a0001c0006 | 2 | HG02451.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.15C>A | p.Gly5Gly | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 2/21 | 46/4737 | 15/2343 | 5/780 | chr7 | 107661656 | ||
chr7:107661716
|
G | C | 1 | a0001c0012 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.75G>C | p.Pro25Pro | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 2/21 | 106/4737 | 75/2343 | 25/780 | chr7 | 107661716 | ||
chr7:107663356
|
C | G | 1 | a0001c0022 | 1 | HG00408.hp2 | synonymous_variant | LOW | c.225C>G | p.Leu75Leu | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/21 | 256/4737 | 225/2343 | 75/780 | chr7 | 107663356 | ||
chr7:107695983
|
C | T | 1 | a0001c0011 | 2 | HG02257.hp1 HG02280.hp1 |
synonymous_variant | LOW | c.1488C>T | p.Leu496Leu | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/21 | 1519/4737 | 1488/2343 | 496/780 | chr7 | 107695983 | ||
chr7:107698111
|
C | T | 1 | a0001c0019 | 1 | NA19030.hp1 | splice_region_variant&synonymous_variant | LOW | c.1614C>T | p.Asn538Asn | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/21 | 1645/4737 | 1614/2343 | 538/780 | chr7 | 107698111 | ||
chr7:107710094
|
C | T | 3 | a0002c0009a0006c0008a0007c0010 | 6 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
synonymous_variant | LOW | c.2130C>T | p.Asp710Asp | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/21 | 2161/4737 | 2130/2343 | 710/780 | chr7 | 107710094 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:107660847
|
C | T | 1 | a0001c0001t0031 | 1 | HG02735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-12C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 1/21 | 795 | chr7 | 107660847 | |||||
chr7:107715457
|
G | A | 1 | a0001c0001t0010 | 4 | HG03130.hp1 HG03486.hp1 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*11G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 11 | chr7 | 107715457 | |||||
chr7:107715515
|
C | A | 1 | a0001c0001t0015 | 2 | NA18966.hp2 NA18992.hp2 |
3_prime_UTR_variant | MODIFIER | c.*69C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 69 | chr7 | 107715515 | |||||
chr7:107715796
|
C | T | 1 | a0006c0008t0030 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*350C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 350 | chr7 | 107715796 | |||||
chr7:107715822
|
A | G | 2 | a0002c0002t0014a0006c0008t0014 | 3 | HG02109.hp2 HG03098.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*376A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 376 | chr7 | 107715822 | |||||
chr7:107715855
|
A | T | 1 | a0001c0001t0029 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*409A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 409 | chr7 | 107715855 | |||||
chr7:107716060
|
C | T | 2 | a0001c0001t0011a0010c0016t0011 | 4 | HG00438.hp2 NA18981.hp1 NA19068.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*614C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 614 | chr7 | 107716060 | |||||
chr7:107716138
|
C | A | 1 | a0001c0001t0016 | 2 | HG01433.hp2 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*692C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 692 | chr7 | 107716138 | |||||
chr7:107716145
|
G | A | 1 | a0001c0001t0019 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*699G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 699 | chr7 | 107716145 | |||||
chr7:107716174
|
GATCAAAA others(6): Show |
G | 1 | a0001c0001t0028 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*731_*743delCAAAAA others(7): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 731 | INFO_REALIGN_3_PRIME | chr7 | 107716174 | ||||
chr7:107716252
|
A | G | 2 | a0002c0002t0018a0013c0015t0018 | 2 | HG02109.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*806A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 806 | chr7 | 107716252 | |||||
chr7:107716314
|
G | A | 8 | a0001c0001t0002a0001c0001t0004a0001c0001t0011others(5): Show | 99 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*868G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 868 | chr7 | 107716314 | |||||
chr7:107716505
|
T | C | 1 | a0001c0001t0017 | 2 | HG00639.hp2 HG02148.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1059T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1059 | chr7 | 107716505 | |||||
chr7:107716535
|
T | C | 1 | a0001c0001t0021 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1089T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1089 | chr7 | 107716535 | |||||
chr7:107716748
|
T | G | 3 | a0001c0001t0009a0001c0001t0010a0004c0004t0009 | 9 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1302T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1302 | chr7 | 107716748 | |||||
chr7:107716890
|
T | C | 1 | a0001c0001t0022 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1444T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1444 | chr7 | 107716890 | |||||
chr7:107717056
|
C | T | 1 | a0001c0001t0020 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1610C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1610 | chr7 | 107717056 | |||||
chr7:107717128
|
C | T | 1 | a0001c0001t0027 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1682C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1682 | chr7 | 107717128 | |||||
chr7:107717235
|
G | A | 1 | a0001c0001t0023 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1789G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1789 | chr7 | 107717235 | |||||
chr7:107717243
|
G | C | 7 | a0001c0001t0007a0001c0001t0013a0001c0001t0016others(4): Show | 15 | HG01433.hp2 HG02055.hp2 HG02109.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1797G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1797 | chr7 | 107717243 | |||||
chr7:107717351
|
G | A | 2 | a0002c0009t0024a0002c0009t0025 | 2 | HG01074.hp2 HG01891.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1905G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1905 | chr7 | 107717351 | |||||
chr7:107717365
|
C | CA | 2 | a0001c0001t0008a0002c0009t0024 | 8 | HG00642.hp2 HG01074.hp2 HG01243.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1944dupA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1945 | INFO_REALIGN_3_PRIME | chr7 | 107717365 | ||||
chr7:107717365
|
CA | C | 2 | a0001c0001t0005a0007c0010t0005 | 13 | HG00140.hp2 HG01069.hp1 HG01169.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1944delA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1944 | INFO_REALIGN_3_PRIME | chr7 | 107717365 | ||||
chr7:107717365
|
CAA | C | 22 | a0001c0001t0001a0001c0001t0004a0001c0001t0013others(19): Show | 185 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*1943_*1944delAA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1943 | INFO_REALIGN_3_PRIME | chr7 | 107717365 | ||||
chr7:107717365
|
CAAA | C | 13 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(10): Show | 101 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1942_*1944delAAA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1942 | INFO_REALIGN_3_PRIME | chr7 | 107717365 | ||||
chr7:107717387
|
AAAAG | A | 3 | a0001c0001t0009a0001c0001t0010a0004c0004t0009 | 9 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1943_*1946delAAGA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1943 | INFO_REALIGN_3_PRIME | chr7 | 107717387 | ||||
chr7:107717428
|
C | A | 1 | a0001c0001t0026 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1982C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 21/21 | 1982 | chr7 | 107717428 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:107660893
|
G | A | 1 | a0004c0004t0009g0007 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-4+38G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 1/20 | chr7 | 107660893 | ||||||
chr7:107660945
|
T | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG00099.hp1 HG00280.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4+90T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 1/20 | chr7 | 107660945 | ||||||
chr7:107660963
|
G | A | 1 | a0004c0004t0009g0007 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-4+108G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 1/20 | chr7 | 107660963 | ||||||
chr7:107660984
|
C | T | 1 | a0001c0001t0001g0360 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-4+129C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 1/20 | chr7 | 107660984 | ||||||
chr7:107661086
|
T | C | 1 | a0001c0001t0001g0015 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-4+231T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 1/20 | chr7 | 107661086 | ||||||
chr7:107661121
|
C | G | 5 | a0001c0001t0005g0358a0001c0001t0021g0359a0002c0002t0014g0356others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-4+266C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 1/20 | chr7 | 107661121 | ||||||
chr7:107661268
|
G | C | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG00099.hp1 HG00280.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3-371G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 1/20 | chr7 | 107661268 | ||||||
chr7:107661378
|
C | T | 2 | a0001c0001t0002g0354a0008c0007t0003g0355 | 2 | HG01106.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.-3-261C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 1/20 | chr7 | 107661378 | ||||||
chr7:107661395
|
C | T | 2 | a0001c0001t0001g0353a0001c0001t0003g0352 | 2 | HG01261.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-3-244C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 1/20 | chr7 | 107661395 | ||||||
chr7:107661429
|
G | A | 1 | a0003c0003t0003g0016 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-3-210G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 1/20 | chr7 | 107661429 | ||||||
chr7:107661444
|
C | T | 2 | a0001c0001t0003g0350a0001c0001t0003g0351 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-3-195C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 1/20 | chr7 | 107661444 | ||||||
chr7:107661615
|
T | A | 1 | a0001c0001t0001g0017 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-3-24T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 1/20 | chr7 | 107661615 | ||||||
chr7:107661955
|
T | A | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0003c0003t0003g0021others(1): Show | 4 | HG02559.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.164+150T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 2/20 | chr7 | 107661955 | ||||||
chr7:107662005
|
G | A | 1 | a0001c0001t0003g0022 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.164+200G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 2/20 | chr7 | 107662005 | ||||||
chr7:107662463
|
C | A | 1 | a0001c0001t0001g0023 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.164+658C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 2/20 | chr7 | 107662463 | ||||||
chr7:107662489
|
A | G | 2 | a0001c0006t0001g0349a0001c0006t0006g0348 | 2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.164+684A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 2/20 | chr7 | 107662489 | ||||||
chr7:107662670
|
T | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG00099.hp1 HG00280.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.165-626T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 2/20 | chr7 | 107662670 | ||||||
chr7:107662924
|
A | G | 5 | a0001c0001t0005g0358a0001c0001t0021g0359a0002c0002t0014g0356others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.165-372A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 2/20 | chr7 | 107662924 | ||||||
chr7:107663177
|
A | T | 264 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(261): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.165-119A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 2/20 | chr7 | 107663177 | ||||||
chr7:107663183
|
C | T | 206 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(203): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.165-113C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 2/20 | chr7 | 107663183 | ||||||
chr7:107663751
|
C | T | 264 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(261): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.304+316C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107663751 | ||||||
chr7:107663791
|
C | T | 7 | a0001c0001t0001g0343a0001c0001t0007g0342a0001c0001t0007g0344others(4): Show | 7 | HG02055.hp2 HG02615.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.304+356C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107663791 | ||||||
chr7:107663828
|
C | A | 5 | a0001c0001t0005g0358a0001c0001t0021g0359a0002c0002t0014g0356others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.304+393C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107663828 | ||||||
chr7:107663832
|
C | T | 5 | a0001c0001t0005g0358a0001c0001t0021g0359a0002c0002t0014g0356others(2): Show | 5 | HG02109.hp2 HG02896.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.304+397C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107663832 | ||||||
chr7:107663926
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.304+491G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107663926 | ||||||
chr7:107663933
|
T | C | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | HG00642.hp1 HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.304+498T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107663933 | ||||||
chr7:107663943
|
A | C | 1 | a0001c0001t0002g0340 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.304+508A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107663943 | ||||||
chr7:107663992
|
A | G | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | HG00642.hp1 HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.304+557A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107663992 | ||||||
chr7:107664183
|
C | T | 153 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0199others(150): Show | 154 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.304+748C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664183 | ||||||
chr7:107664255
|
A | G | 1 | a0001c0019t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.304+820A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664255 | ||||||
chr7:107664265
|
T | C | 1 | a0001c0001t0002g0024 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.304+830T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664265 | ||||||
chr7:107664388
|
T | A | 12 | a0001c0001t0001g0017a0001c0001t0001g0120a0001c0001t0001g0121others(9): Show | 12 | HG00544.hp1 HG00621.hp2 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.304+953T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664388 | ||||||
chr7:107664395
|
C | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG00099.hp1 HG00280.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.304+960C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664395 | ||||||
chr7:107664422
|
G | A | 1 | a0001c0001t0002g0198 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.304+987G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664422 | ||||||
chr7:107664429
|
G | A | 1 | a0001c0001t0003g0129 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.304+994G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664429 | ||||||
chr7:107664521
|
C | T | 1 | a0004c0004t0009g0007 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.304+1086C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664521 | ||||||
chr7:107664670
|
G | A | 130 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0199others(127): Show | 131 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.304+1235G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664670 | ||||||
chr7:107664807
|
C | G | 15 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0110others(12): Show | 15 | HG00544.hp1 HG00621.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.304+1372C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664807 | ||||||
chr7:107664815
|
C | G | 1 | a0001c0001t0001g0339 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.304+1380C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664815 | ||||||
chr7:107664883
|
A | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG00099.hp1 HG00280.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.304+1448A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664883 | ||||||
chr7:107664886
|
G | A | 1 | a0002c0009t0025g0316 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.304+1451G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664886 | ||||||
chr7:107664968
|
C | T | 1 | a0001c0001t0002g0170 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.304+1533C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664968 | ||||||
chr7:107664985
|
A | G | 1 | a0001c0001t0008g0197 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.304+1550A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107664985 | ||||||
chr7:107665079
|
C | T | 2 | a0001c0001t0002g0315a0001c0001t0021g0359 | 2 | NA18906.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.304+1644C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107665079 | ||||||
chr7:107665145
|
A | G | 1 | a0001c0001t0007g0196 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.304+1710A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107665145 | ||||||
chr7:107665243
|
G | A | 6 | a0001c0001t0001g0175a0001c0001t0001g0360a0001c0001t0003g0176others(3): Show | 6 | HG02723.hp2 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.304+1808G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107665243 | ||||||
chr7:107665599
|
T | C | 1 | a0001c0001t0021g0359 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.304+2164T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107665599 | ||||||
chr7:107665657
|
CA | C | 4 | a0001c0001t0001g0169a0001c0001t0003g0168a0001c0006t0001g0349others(1): Show | 4 | HG00735.hp2 HG01255.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.304+2224delA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr7 | 107665657 | |||||
chr7:107665705
|
C | T | 1 | a0001c0001t0007g0196 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.304+2270C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107665705 | ||||||
chr7:107665822
|
C | T | 51 | a0001c0001t0001g0017a0001c0001t0001g0107a0001c0001t0001g0109others(48): Show | 51 | HG00544.hp1 HG00621.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.304+2387C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107665822 | ||||||
chr7:107665976
|
C | T | 45 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(42): Show | 46 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.304+2541C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107665976 | ||||||
chr7:107666019
|
C | T | 1 | a0004c0004t0009g0007 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.304+2584C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666019 | ||||||
chr7:107666020
|
T | C | 1 | a0004c0004t0009g0007 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.304+2585T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666020 | ||||||
chr7:107666046
|
A | C | 1 | a0007c0010t0003g0177 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.304+2611A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666046 | ||||||
chr7:107666053
|
G | A | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0003c0003t0003g0021others(1): Show | 4 | HG02559.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.304+2618G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666053 | ||||||
chr7:107666304
|
C | G | 2 | a0001c0001t0008g0178a0002c0009t0025g0316 | 2 | HG01891.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.304+2869C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666304 | ||||||
chr7:107666379
|
G | T | 24 | a0001c0001t0001g0183a0001c0001t0001g0185a0001c0001t0001g0189others(21): Show | 25 | HG01074.hp2 HG02055.hp2 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.304+2944G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666379 | ||||||
chr7:107666404
|
T | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0008g0197others(1): Show | 4 | HG02258.hp1 HG02559.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.304+2969T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666404 | ||||||
chr7:107666454
|
T | C | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(75): Show | 78 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.304+3019T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666454 | ||||||
chr7:107666465
|
G | T | 1 | a0001c0001t0001g0353 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.304+3030G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666465 | ||||||
chr7:107666622
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.304+3187A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666622 | ||||||
chr7:107666676
|
A | G | 1 | a0001c0001t0002g0106 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.304+3241A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666676 | ||||||
chr7:107666685
|
A | G | 3 | a0001c0001t0001g0179a0001c0006t0001g0349a0001c0006t0006g0348 | 3 | HG02451.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.304+3250A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666685 | ||||||
chr7:107666761
|
C | T | 88 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(85): Show | 89 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.304+3326C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666761 | ||||||
chr7:107666817
|
T | C | 2 | a0001c0001t0004g0206a0001c0001t0004g0207 | 2 | NA18983.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.304+3382T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666817 | ||||||
chr7:107666940
|
A | G | 2 | a0001c0001t0002g0083a0001c0001t0005g0333 | 2 | HG01175.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.304+3505A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107666940 | ||||||
chr7:107667013
|
A | C | 1 | a0001c0001t0001g0082 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.304+3578A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667013 | ||||||
chr7:107667092
|
G | C | 3 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0210 | 3 | NA18940.hp1 NA18953.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.304+3657G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667092 | ||||||
chr7:107667141
|
T | C | 3 | a0001c0001t0027g0139a0001c0019t0001g0171a0007c0010t0005g0180 | 3 | HG02559.hp2 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.304+3706T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667141 | ||||||
chr7:107667316
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.304+3881G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667316 | ||||||
chr7:107667458
|
GT | G | 50 | a0001c0001t0001g0025a0001c0001t0001g0079a0001c0001t0001g0080others(47): Show | 51 | HG00140.hp2 HG00642.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.304+4026delT | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr7 | 107667458 | |||||
chr7:107667460
|
T | TA | 14 | a0001c0001t0001g0012a0001c0001t0002g0026a0001c0001t0002g0027others(11): Show | 14 | HG00099.hp1 HG00741.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.304+4025_304+4026i others(3): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667460 | ||||||
chr7:107667460
|
T | TAA | 74 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0020others(71): Show | 75 | HG00408.hp2 HG00544.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.304+4025_304+4026i others(4): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667460 | ||||||
chr7:107667460
|
T | TAAA | 104 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(101): Show | 106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.304+4025_304+4026i others(5): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667460 | ||||||
chr7:107667460
|
T | TAAAA | 20 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(17): Show | 20 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.304+4025_304+4026i others(6): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667460 | ||||||
chr7:107667460
|
TTAAAAAA others(4): Show |
T | 1 | a0001c0001t0002g0102 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.304+4026_304+4036d others(13): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667460 | ||||||
chr7:107667461
|
T | A | 309 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(306): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.304+4026T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667461 | ||||||
chr7:107667487
|
C | T | 1 | a0003c0003t0003g0016 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.304+4052C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667487 | ||||||
chr7:107667733
|
G | A | 1 | a0001c0001t0007g0196 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.304+4298G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667733 | ||||||
chr7:107667896
|
C | G | 235 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(232): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.305-4242C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667896 | ||||||
chr7:107667934
|
A | C | 2 | a0001c0001t0003g0176a0003c0003t0003g0016 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.305-4204A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107667934 | ||||||
chr7:107668131
|
C | T | 1 | a0001c0001t0002g0077 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.305-4007C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107668131 | ||||||
chr7:107668532
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.305-3606G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107668532 | ||||||
chr7:107668611
|
A | G | 3 | a0002c0002t0013g0078a0002c0002t0014g0356a0002c0002t0014g0357 | 3 | HG02109.hp2 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.305-3527A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107668611 | ||||||
chr7:107668713
|
G | T | 21 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0160others(18): Show | 21 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.305-3425G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107668713 | ||||||
chr7:107668803
|
C | T | 1 | a0009c0020t0001g0295 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.305-3335C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107668803 | ||||||
chr7:107668804
|
G | A | 6 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0160others(3): Show | 6 | HG03225.hp2 HG03471.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.305-3334G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107668804 | ||||||
chr7:107668992
|
T | C | 11 | a0001c0001t0007g0196a0001c0001t0016g0347a0001c0011t0007g0328others(8): Show | 11 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.305-3146T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107668992 | ||||||
chr7:107669159
|
T | C | 1 | a0002c0002t0013g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.305-2979T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107669159 | ||||||
chr7:107669167
|
G | A | 6 | a0001c0001t0006g0037a0001c0001t0006g0038a0001c0001t0006g0039others(3): Show | 6 | HG00408.hp2 HG01074.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.305-2971G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107669167 | ||||||
chr7:107669217
|
G | A | 1 | a0002c0009t0025g0316 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.305-2921G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107669217 | ||||||
chr7:107669299
|
C | T | 4 | a0001c0019t0001g0171a0002c0009t0024g0193a0002c0009t0025g0316others(1): Show | 4 | HG01074.hp2 HG01891.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.305-2839C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107669299 | ||||||
chr7:107669302
|
G | A | 8 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0160others(5): Show | 8 | HG02922.hp2 HG02976.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.305-2836G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107669302 | ||||||
chr7:107669353
|
A | G | 5 | a0001c0001t0001g0097a0001c0001t0001g0137a0001c0001t0001g0179others(2): Show | 5 | HG02258.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.305-2785A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107669353 | ||||||
chr7:107669367
|
G | A | 236 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(233): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.305-2771G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107669367 | ||||||
chr7:107669419
|
C | T | 4 | a0001c0001t0002g0285a0001c0001t0002g0340a0001c0001t0003g0286others(1): Show | 4 | NA18977.hp2 NA19011.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.305-2719C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107669419 | ||||||
chr7:107669690
|
T | C | 2 | a0002c0002t0014g0356a0002c0002t0014g0357 | 2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.305-2448T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107669690 | ||||||
chr7:107669802
|
T | C | 2 | a0002c0002t0014g0356a0002c0002t0014g0357 | 2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.305-2336T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107669802 | ||||||
chr7:107670018
|
A | C | 2 | a0001c0001t0001g0236a0001c0001t0001g0247 | 2 | HG02735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.305-2120A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107670018 | ||||||
chr7:107670082
|
T | C | 1 | a0002c0002t0013g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.305-2056T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107670082 | ||||||
chr7:107670112
|
A | AT | 222 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(219): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.305-2011dupT | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr7 | 107670112 | |||||
chr7:107670112
|
AT | A | 9 | a0001c0001t0005g0251a0001c0001t0016g0347a0001c0019t0001g0171others(6): Show | 9 | HG01074.hp2 HG01169.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.305-2011delT | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr7 | 107670112 | |||||
chr7:107670177
|
T | A | 1 | a0001c0001t0001g0008 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.305-1961T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107670177 | ||||||
chr7:107670411
|
C | T | 4 | a0001c0019t0001g0171a0002c0009t0024g0193a0002c0009t0025g0316others(1): Show | 4 | HG01074.hp2 HG01891.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.305-1727C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107670411 | ||||||
chr7:107670427
|
G | A | 2 | a0002c0002t0014g0356a0002c0002t0014g0357 | 2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.305-1711G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107670427 | ||||||
chr7:107670743
|
A | G | 2 | a0001c0001t0003g0293a0001c0001t0005g0284 | 2 | HG01069.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.305-1395A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107670743 | ||||||
chr7:107670847
|
ATG | A | 3 | a0002c0002t0014g0356a0002c0002t0014g0357a0003c0003t0003g0021 | 3 | HG02109.hp2 HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.305-1289_305-1288d others(4): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr7 | 107670847 | |||||
chr7:107670957
|
A | G | 3 | a0001c0001t0007g0181a0004c0004t0009g0007a0004c0004t0009g0018 | 3 | HG02818.hp2 HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.305-1181A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107670957 | ||||||
chr7:107670973
|
GTTGTC | G | 3 | a0001c0001t0001g0082a0001c0001t0008g0197a0013c0015t0018g0184 | 3 | HG02258.hp1 HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.305-1158_305-1154d others(7): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr7 | 107670973 | |||||
chr7:107671085
|
C | T | 1 | a0001c0001t0002g0075 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.305-1053C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671085 | ||||||
chr7:107671102
|
C | A | 1 | a0003c0003t0003g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.305-1036C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671102 | ||||||
chr7:107671265
|
C | T | 1 | a0001c0001t0002g0313 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.305-873C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671265 | ||||||
chr7:107671308
|
G | A | 1 | a0001c0001t0001g0017 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.305-830G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671308 | ||||||
chr7:107671345
|
A | C | 8 | a0001c0001t0001g0009a0001c0001t0001g0234a0001c0001t0001g0235others(5): Show | 8 | HG01069.hp2 HG01261.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.305-793A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671345 | ||||||
chr7:107671375
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0003g0040a0001c0001t0003g0087others(1): Show | 4 | HG00280.hp1 HG01109.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.305-763G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671375 | ||||||
chr7:107671396
|
C | G | 7 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0136others(4): Show | 7 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.305-742C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671396 | ||||||
chr7:107671495
|
T | A | 1 | a0001c0001t0001g0080 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.305-643T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671495 | ||||||
chr7:107671594
|
T | A | 1 | a0001c0001t0001g0135 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.305-544T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671594 | ||||||
chr7:107671632
|
T | G | 194 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(191): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.305-506T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671632 | ||||||
chr7:107671660
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.305-478G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671660 | ||||||
chr7:107671681
|
A | C | 1 | a0001c0001t0003g0292 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.305-457A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671681 | ||||||
chr7:107671751
|
G | A | 3 | a0001c0001t0003g0253a0008c0007t0003g0308a0008c0007t0003g0355 | 3 | HG02698.hp2 HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.305-387G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671751 | ||||||
chr7:107671904
|
C | T | 1 | a0007c0010t0003g0177 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.305-234C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 3/20 | chr7 | 107671904 | ||||||
chr7:107672323
|
T | C | 1 | a0001c0001t0007g0196 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.415+75T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107672323 | ||||||
chr7:107672433
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.415+185G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107672433 | ||||||
chr7:107672488
|
T | G | 1 | a0001c0001t0001g0144 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.415+240T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107672488 | ||||||
chr7:107672668
|
A | T | 11 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0160others(8): Show | 11 | HG02818.hp2 HG02896.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.415+420A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107672668 | ||||||
chr7:107672879
|
C | T | 4 | a0001c0001t0001g0134a0001c0001t0003g0129a0001c0001t0003g0132others(1): Show | 4 | HG02622.hp1 HG02717.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.415+631C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107672879 | ||||||
chr7:107673268
|
C | T | 1 | a0007c0010t0003g0177 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.416-896C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107673268 | ||||||
chr7:107673282
|
A | G | 8 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0160others(5): Show | 8 | HG02922.hp2 HG02976.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.416-882A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107673282 | ||||||
chr7:107673407
|
A | G | 6 | a0001c0001t0001g0120a0001c0001t0002g0250a0001c0001t0002g0282others(3): Show | 6 | HG02015.hp1 HG02135.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.416-757A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107673407 | ||||||
chr7:107673481
|
T | C | 1 | a0001c0001t0001g0185 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.416-683T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107673481 | ||||||
chr7:107673502
|
G | A | 193 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(190): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.416-662G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107673502 | ||||||
chr7:107673709
|
C | T | 1 | a0001c0001t0003g0292 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.416-455C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107673709 | ||||||
chr7:107673968
|
C | T | 8 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0160others(5): Show | 8 | HG02922.hp2 HG02976.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.416-196C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107673968 | ||||||
chr7:107674041
|
C | A | 2 | a0001c0011t0007g0328a0001c0011t0007g0329 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.416-123C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107674041 | ||||||
chr7:107674148
|
G | T | 4 | a0001c0001t0016g0347a0002c0002t0014g0356a0002c0002t0014g0357others(1): Show | 4 | HG02109.hp2 HG02615.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-16G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107674148 | ||||||
chr7:107674151
|
T | C | 3 | a0001c0001t0003g0004a0001c0001t0009g0187a0001c0001t0019g0186 | 4 | HG02486.hp2 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-13T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107674151 | ||||||
chr7:107674157
|
T | C | 1 | a0001c0001t0008g0197 | 1 | HG02258.hp1 | splice_region_variant&intron_variant | LOW | c.416-7T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 4/20 | chr7 | 107674157 | ||||||
chr7:107674431
|
C | G | 1 | a0001c0001t0016g0347 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.600+83C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 5/20 | chr7 | 107674431 | ||||||
chr7:107674484
|
G | A | 2 | a0002c0002t0014g0356a0002c0002t0014g0357 | 2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.600+136G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 5/20 | chr7 | 107674484 | ||||||
chr7:107674651
|
G | A | 1 | a0001c0001t0003g0254 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.601-294G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 5/20 | chr7 | 107674651 | ||||||
chr7:107674679
|
T | G | 242 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(239): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.601-266T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 5/20 | chr7 | 107674679 | ||||||
chr7:107675191
|
C | T | 1 | a0001c0001t0004g0161 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.765+82C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107675191 | ||||||
chr7:107675285
|
T | TA | 6 | a0001c0001t0001g0142a0001c0001t0001g0153a0001c0001t0002g0167others(3): Show | 6 | HG02027.hp1 HG02922.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.765+197dupA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107675285 | |||||
chr7:107675285
|
TA | T | 190 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(187): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.765+197delA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107675285 | |||||
chr7:107675285
|
TAA | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0360a0001c0019t0001g0171others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.765+196_765+197del others(2): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107675285 | |||||
chr7:107675301
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.765+192A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107675301 | ||||||
chr7:107675303
|
A | AAAG | 8 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0136others(5): Show | 8 | HG00741.hp2 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.765+196_765+197ins others(3): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107675303 | |||||
chr7:107675303
|
A | G | 23 | a0001c0001t0001g0015a0001c0001t0001g0080a0001c0001t0001g0134others(20): Show | 23 | HG00642.hp2 HG01074.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.765+194A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107675303 | ||||||
chr7:107675358
|
T | C | 1 | a0001c0001t0007g0196 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.765+249T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107675358 | ||||||
chr7:107675426
|
G | C | 1 | a0001c0001t0001g0142 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.765+317G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107675426 | ||||||
chr7:107675462
|
G | A | 3 | a0001c0019t0001g0171a0002c0009t0024g0193a0002c0009t0025g0316 | 3 | HG01074.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.765+353G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107675462 | ||||||
chr7:107675500
|
C | T | 1 | a0001c0001t0004g0162 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.765+391C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107675500 | ||||||
chr7:107675545
|
TG | T | 360 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(357): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.765+439delG | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107675545 | |||||
chr7:107675574
|
C | CT | 20 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0136others(17): Show | 20 | HG01433.hp1 HG01433.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.765+482dupT | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107675574 | |||||
chr7:107675574
|
CT | C | 9 | a0001c0001t0001g0110a0001c0001t0001g0153a0001c0001t0002g0323others(6): Show | 9 | HG01891.hp2 HG02922.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.765+482delT | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107675574 | |||||
chr7:107675574
|
CTT | C | 51 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0017others(48): Show | 52 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.765+481_765+482del others(2): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107675574 | |||||
chr7:107675575
|
T | C | 1 | a0002c0009t0024g0193 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.765+466T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107675575 | ||||||
chr7:107675655
|
C | T | 7 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0136others(4): Show | 7 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.765+546C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107675655 | ||||||
chr7:107675719
|
G | A | 2 | a0001c0001t0002g0068a0001c0001t0012g0276 | 2 | HG00323.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.765+610G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107675719 | ||||||
chr7:107676207
|
A | G | 1 | a0001c0001t0002g0279 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.765+1098A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107676207 | ||||||
chr7:107676314
|
G | C | 2 | a0007c0010t0003g0177a0007c0010t0005g0180 | 2 | HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.765+1205G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107676314 | ||||||
chr7:107676392
|
G | A | 5 | a0001c0019t0001g0171a0002c0002t0014g0356a0002c0002t0014g0357others(2): Show | 5 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.765+1283G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107676392 | ||||||
chr7:107676418
|
A | G | 1 | a0001c0001t0008g0158 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.765+1309A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107676418 | ||||||
chr7:107676436
|
G | A | 3 | a0001c0001t0007g0196a0001c0011t0007g0328a0001c0011t0007g0329 | 3 | HG02257.hp1 HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.765+1327G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107676436 | ||||||
chr7:107676566
|
G | A | 2 | a0001c0001t0002g0285a0001c0001t0002g0340 | 2 | NA18977.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.765+1457G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107676566 | ||||||
chr7:107676650
|
T | G | 16 | a0001c0001t0001g0080a0001c0001t0001g0134a0001c0001t0002g0098others(13): Show | 16 | HG00558.hp1 HG00642.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.765+1541T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107676650 | ||||||
chr7:107676730
|
G | A | 179 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(176): Show | 182 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.765+1621G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107676730 | ||||||
chr7:107676798
|
C | T | 3 | a0001c0019t0001g0171a0002c0009t0024g0193a0002c0009t0025g0316 | 3 | HG01074.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.765+1689C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107676798 | ||||||
chr7:107677081
|
G | A | 4 | a0001c0001t0001g0169a0001c0001t0001g0330a0001c0001t0001g0331others(1): Show | 4 | HG00140.hp2 HG00735.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.765+1972G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107677081 | ||||||
chr7:107677099
|
C | T | 1 | a0002c0002t0013g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.765+1990C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107677099 | ||||||
chr7:107677210
|
C | A | 1 | a0001c0001t0001g0045 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.765+2101C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107677210 | ||||||
chr7:107677247
|
C | G | 1 | a0001c0001t0001g0091 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.765+2138C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107677247 | ||||||
chr7:107677265
|
A | G | 187 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(184): Show | 190 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.765+2156A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107677265 | ||||||
chr7:107677420
|
G | A | 2 | a0001c0011t0007g0328a0001c0011t0007g0329 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.765+2311G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107677420 | ||||||
chr7:107677471
|
C | T | 3 | a0004c0004t0009g0007a0004c0004t0009g0018a0004c0004t0009g0029 | 3 | HG02818.hp2 HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.765+2362C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107677471 | ||||||
chr7:107677608
|
A | AT | 8 | a0001c0001t0001g0205a0001c0001t0001g0223a0001c0001t0002g0113others(5): Show | 8 | HG01074.hp2 HG01928.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.765+2514dupT | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107677608 | |||||
chr7:107677608
|
AT | A | 11 | a0001c0001t0001g0069a0001c0001t0001g0232a0001c0001t0002g0208others(8): Show | 11 | HG01069.hp1 HG01169.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.765+2514delT | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107677608 | |||||
chr7:107677671
|
T | C | 14 | a0001c0001t0001g0059a0001c0001t0001g0092a0001c0001t0001g0109others(11): Show | 14 | HG00408.hp1 HG01123.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.765+2562T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107677671 | ||||||
chr7:107677792
|
A | G | 2 | a0007c0010t0003g0177a0007c0010t0005g0180 | 2 | HG02559.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.765+2683A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107677792 | ||||||
chr7:107677853
|
G | A | 3 | a0001c0001t0002g0070a0001c0001t0002g0216a0001c0001t0002g0237 | 3 | HG00323.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.765+2744G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107677853 | ||||||
chr7:107677970
|
G | T | 179 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(176): Show | 182 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.765+2861G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107677970 | ||||||
chr7:107678002
|
C | G | 1 | a0002c0002t0013g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.765+2893C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107678002 | ||||||
chr7:107678342
|
C | T | 8 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0124others(5): Show | 8 | HG00544.hp1 HG00621.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.765+3233C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107678342 | ||||||
chr7:107678598
|
C | T | 5 | a0001c0019t0001g0171a0002c0002t0014g0356a0002c0002t0014g0357others(2): Show | 5 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.765+3489C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107678598 | ||||||
chr7:107678633
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.765+3524A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107678633 | ||||||
chr7:107678737
|
G | GA | 12 | a0001c0001t0001g0097a0001c0001t0001g0130a0001c0001t0001g0135others(9): Show | 12 | HG01891.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.765+3642dupA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107678737 | |||||
chr7:107678737
|
GA | G | 150 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(147): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.765+3642delA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107678737 | |||||
chr7:107678737
|
GAA | G | 52 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0017others(49): Show | 53 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.765+3641_765+3642d others(4): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107678737 | |||||
chr7:107678840
|
T | A | 1 | a0002c0002t0013g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.765+3731T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107678840 | ||||||
chr7:107679047
|
A | G | 1 | a0001c0001t0004g0162 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.765+3938A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679047 | ||||||
chr7:107679526
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.766-3676G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679526 | ||||||
chr7:107679709
|
C | CTTTATAT others(34): Show |
2 | a0002c0002t0014g0356a0002c0002t0014g0357 | 2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.766-3492_766-3491i others(43): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107679709 | |||||
chr7:107679711
|
A | G | 2 | a0002c0002t0014g0356a0002c0002t0014g0357 | 2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.766-3491A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679711 | ||||||
chr7:107679781
|
A | G | 1 | a0001c0001t0005g0333 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.766-3421A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679781 | ||||||
chr7:107679796
|
A | AAATATAA others(16): Show |
1 | a0001c0001t0003g0168 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.766-3379_766-3357d others(25): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107679796 | |||||
chr7:107679800
|
A | G | 1 | a0013c0015t0018g0184 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.766-3402A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679800 | ||||||
chr7:107679834
|
T | TTATTATA others(31): Show |
1 | a0001c0001t0002g0309 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.766-3351_766-3314d others(40): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107679834 | |||||
chr7:107679858
|
T | C | 4 | a0001c0001t0001g0134a0001c0001t0003g0129a0001c0001t0003g0132others(1): Show | 4 | HG02622.hp1 HG02717.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.766-3344T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679858 | ||||||
chr7:107679859
|
A | C | 2 | a0001c0011t0007g0328a0001c0011t0007g0329 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.766-3343A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679859 | ||||||
chr7:107679861
|
T | A | 6 | a0001c0001t0002g0123a0001c0001t0007g0181a0002c0002t0013g0078others(3): Show | 6 | HG02723.hp1 HG02818.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.766-3341T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679861 | ||||||
chr7:107679869
|
C | CTTA | 185 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(182): Show | 188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.766-3331_766-3329d others(5): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107679869 | |||||
chr7:107679869
|
C | CTTATATT others(119): Show |
2 | a0004c0004t0009g0007a0004c0004t0009g0018 | 2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.766-3324_766-3323i others(128): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107679869 | |||||
chr7:107679869
|
C | CTTATATT others(78): Show |
2 | a0001c0001t0007g0181a0004c0004t0009g0029 | 2 | HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.766-3324_766-3323i others(87): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107679869 | |||||
chr7:107679869
|
C | CTTATATT others(37): Show |
2 | a0001c0001t0002g0123a0002c0002t0013g0078 | 2 | HG02723.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.766-3324_766-3323i others(46): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107679869 | |||||
chr7:107679869
|
C | CTTATTAT others(14): Show |
53 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0017others(50): Show | 54 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.766-3329_766-3328i others(23): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107679869 | |||||
chr7:107679881
|
A | G | 2 | a0001c0011t0007g0328a0001c0011t0007g0329 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.766-3321A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679881 | ||||||
chr7:107679882
|
A | C | 2 | a0001c0011t0007g0328a0001c0011t0007g0329 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.766-3320A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679882 | ||||||
chr7:107679891
|
T | A | 1 | a0001c0019t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.766-3311T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679891 | ||||||
chr7:107679894
|
A | C | 1 | a0001c0019t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.766-3308A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679894 | ||||||
chr7:107679896
|
A | T | 1 | a0001c0019t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.766-3306A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679896 | ||||||
chr7:107679899
|
C | A | 1 | a0001c0019t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.766-3303C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679899 | ||||||
chr7:107679902
|
A | ATAT | 190 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(187): Show | 193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.766-3296_766-3294d others(5): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107679902 | |||||
chr7:107679911
|
G | T | 5 | a0001c0001t0007g0181a0002c0002t0013g0078a0004c0004t0009g0007others(2): Show | 5 | HG02723.hp1 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-3291G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679911 | ||||||
chr7:107679944
|
T | TATCTTAT others(26): Show |
1 | a0001c0001t0012g0276 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.766-3250_766-3218d others(35): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107679944 | |||||
chr7:107679947
|
CTTATATA others(11): Show |
C | 7 | a0001c0011t0007g0328a0001c0011t0007g0329a0001c0019t0001g0171others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.766-3217_766-3200d others(20): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107679947 | |||||
chr7:107679949
|
T | C | 1 | a0001c0001t0007g0196 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.766-3253T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107679949 | ||||||
chr7:107679959
|
A | AATCTTAT others(16): Show |
7 | a0001c0001t0005g0333a0001c0001t0006g0211a0001c0001t0007g0181others(4): Show | 7 | HG01175.hp2 HG01358.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.766-3240_766-3218d others(25): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107679959 | |||||
chr7:107679995
|
AATCTT | A | 3 | a0001c0001t0001g0126a0001c0001t0003g0168a0014c0021t0001g0127 | 3 | HG00544.hp1 HG01255.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.766-3199_766-3195d others(7): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107679995 | |||||
chr7:107680015
|
T | C | 3 | a0001c0001t0003g0253a0008c0007t0003g0308a0008c0007t0003g0355 | 3 | HG02698.hp2 HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.766-3187T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680015 | ||||||
chr7:107680021
|
CTTA | C | 9 | a0001c0001t0001g0069a0001c0001t0001g0079a0001c0001t0001g0252others(6): Show | 9 | HG01167.hp1 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.766-3176_766-3174d others(5): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680021 | |||||
chr7:107680022
|
T | A | 1 | a0001c0001t0001g0010 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.766-3180T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680022 | ||||||
chr7:107680059
|
AATCTTAT others(16): Show |
A | 2 | a0001c0001t0003g0096a0001c0001t0003g0176 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-3127_766-3105d others(25): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680059 | |||||
chr7:107680063
|
TTATTA | T | 5 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0136others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-3135_766-3131d others(7): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680063 | |||||
chr7:107680063
|
TTATTATA others(108): Show |
T | 3 | a0003c0003t0003g0021a0003c0003t0003g0173a0003c0003t0003g0174 | 3 | HG02922.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.766-3135_766-3021d others(2): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680063 | |||||
chr7:107680078
|
T | A | 9 | a0001c0001t0001g0064a0001c0001t0001g0130a0001c0001t0001g0135others(6): Show | 9 | HG01255.hp1 HG01891.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.766-3124T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680078 | ||||||
chr7:107680084
|
T | A | 5 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0136others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-3118T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680084 | ||||||
chr7:107680085
|
C | T | 2 | a0002c0002t0014g0356a0002c0002t0014g0357 | 2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.766-3117C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680085 | ||||||
chr7:107680090
|
T | A | 2 | a0001c0001t0003g0096a0001c0001t0003g0176 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-3112T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680090 | ||||||
chr7:107680090
|
T | TATATAAT others(39): Show |
5 | a0001c0001t0001g0025a0001c0001t0001g0185a0001c0001t0001g0191others(2): Show | 5 | HG00438.hp2 HG02155.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.766-3030_766-2985d others(48): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680090 | |||||
chr7:107680090
|
TATATAAT others(16): Show |
T | 142 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(139): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.766-3007_766-2985d others(25): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680090 | |||||
chr7:107680090
|
TATATAAT others(39): Show |
T | 1 | a0001c0001t0004g0206 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.766-3030_766-2985d others(48): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680090 | |||||
chr7:107680098
|
C | A | 9 | a0001c0001t0001g0064a0001c0001t0001g0130a0001c0001t0001g0135others(6): Show | 9 | HG01255.hp1 HG01891.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.766-3104C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680098 | ||||||
chr7:107680100
|
T | A | 9 | a0001c0001t0001g0064a0001c0001t0001g0130a0001c0001t0001g0135others(6): Show | 9 | HG01255.hp1 HG01891.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.766-3102T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680100 | ||||||
chr7:107680102
|
T | A | 2 | a0001c0001t0003g0096a0001c0001t0003g0176 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-3100T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680102 | ||||||
chr7:107680108
|
TATATA | T | 5 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0136others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-3086_766-3082d others(7): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680108 | |||||
chr7:107680113
|
A | AATATATT others(11): Show |
2 | a0001c0001t0001g0064a0001c0001t0003g0168 | 2 | HG01255.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.766-3084_766-3083i others(20): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680113 | |||||
chr7:107680119
|
A | T | 2 | a0001c0001t0001g0160a0001c0001t0009g0062 | 2 | HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.766-3083A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680119 | ||||||
chr7:107680122
|
TTATCTTA others(3): Show |
T | 2 | a0001c0001t0003g0096a0001c0001t0003g0176 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-3076_766-3067d others(12): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680122 | |||||
chr7:107680132
|
A | G | 9 | a0001c0001t0001g0069a0001c0001t0001g0079a0001c0001t0001g0252others(6): Show | 9 | HG01167.hp1 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.766-3070A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680132 | ||||||
chr7:107680136
|
A | T | 2 | a0001c0001t0003g0096a0001c0001t0003g0176 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-3066A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680136 | ||||||
chr7:107680141
|
AATCTTAT others(21): Show |
A | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | HG00642.hp1 HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.766-3053_766-3026d others(30): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680141 | |||||
chr7:107680149
|
C | A | 5 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0136others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-3053C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680149 | ||||||
chr7:107680149
|
CTTATTAT others(19): Show |
C | 1 | a0001c0001t0001g0169 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.766-3048_766-3023d others(28): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680149 | |||||
chr7:107680154
|
TATATA | T | 5 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0136others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-3040_766-3036d others(7): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680154 | |||||
chr7:107680164
|
A | G | 2 | a0002c0002t0014g0356a0002c0002t0014g0357 | 2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.766-3038A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680164 | ||||||
chr7:107680165
|
A | G | 1 | a0001c0001t0003g0301 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.766-3037A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680165 | ||||||
chr7:107680168
|
TTATCTTA others(3): Show |
T | 5 | a0001c0019t0001g0171a0002c0002t0014g0356a0002c0002t0014g0357others(2): Show | 5 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.766-3030_766-3021d others(12): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680168 | |||||
chr7:107680172
|
C | A | 2 | a0001c0001t0003g0096a0001c0001t0003g0176 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-3030C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680172 | ||||||
chr7:107680177
|
T | A | 5 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0136others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-3025T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680177 | ||||||
chr7:107680178
|
A | ATATAATA others(6): Show |
1 | a0001c0001t0001g0339 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.766-3020_766-3008d others(15): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680178 | |||||
chr7:107680178
|
A | T | 5 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0136others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-3024A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680178 | ||||||
chr7:107680182
|
A | T | 5 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0136others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-3020A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680182 | ||||||
chr7:107680185
|
A | C | 2 | a0001c0001t0003g0096a0001c0001t0003g0176 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-3017A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680185 | ||||||
chr7:107680187
|
A | T | 2 | a0001c0001t0003g0096a0001c0001t0003g0176 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-3015A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680187 | ||||||
chr7:107680194
|
T | A | 8 | a0001c0019t0001g0171a0002c0002t0014g0356a0002c0002t0014g0357others(5): Show | 8 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.766-3008T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680194 | ||||||
chr7:107680194
|
T | TAATATAA others(6): Show |
71 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0017others(68): Show | 72 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.766-3008_766-3007i others(15): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680194 | ||||||
chr7:107680194
|
T | TCTTATTA others(75): Show |
1 | a0001c0001t0003g0190 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.766-2985_766-2984i others(84): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680194 | |||||
chr7:107680195
|
C | A | 2 | a0001c0001t0003g0096a0001c0001t0003g0176 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-3007C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680195 | ||||||
chr7:107680201
|
ATATAATA others(6): Show |
A | 1 | a0001c0001t0003g0320 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.766-2985_766-2973d others(15): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680201 | |||||
chr7:107680208
|
A | C | 2 | a0001c0001t0003g0096a0001c0001t0003g0176 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-2994A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680208 | ||||||
chr7:107680208
|
A | G | 5 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0136others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-2994A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680208 | ||||||
chr7:107680210
|
A | T | 7 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0136others(4): Show | 7 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.766-2992A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680210 | ||||||
chr7:107680213
|
C | A | 5 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0136others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-2989C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680213 | ||||||
chr7:107680218
|
A | T | 88 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0017others(85): Show | 89 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.766-2984A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680218 | ||||||
chr7:107680219
|
A | G | 1 | a0001c0001t0002g0099 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.766-2983A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680219 | ||||||
chr7:107680226
|
C | A | 2 | a0001c0001t0001g0160a0001c0001t0009g0062 | 2 | HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.766-2976C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680226 | ||||||
chr7:107680226
|
C | G | 2 | a0001c0001t0003g0096a0001c0001t0003g0176 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-2976C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680226 | ||||||
chr7:107680228
|
T | A | 2 | a0001c0001t0001g0160a0001c0001t0009g0062 | 2 | HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.766-2974T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680228 | ||||||
chr7:107680230
|
A | T | 88 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0017others(85): Show | 89 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.766-2972A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680230 | ||||||
chr7:107680231
|
C | A | 2 | a0001c0001t0003g0096a0001c0001t0003g0176 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-2971C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680231 | ||||||
chr7:107680236
|
T | A | 2 | a0001c0001t0001g0160a0001c0001t0009g0062 | 2 | HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.766-2966T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680236 | ||||||
chr7:107680236
|
TATATAAT others(57): Show |
T | 5 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0136others(2): Show | 5 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-2958_766-2895d others(66): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680236 | |||||
chr7:107680244
|
A | C | 4 | a0001c0001t0001g0160a0001c0001t0003g0096a0001c0001t0003g0176others(1): Show | 4 | HG02886.hp2 HG03225.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-2958A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680244 | ||||||
chr7:107680244
|
A | T | 1 | a0001c0001t0002g0283 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.766-2958A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680244 | ||||||
chr7:107680246
|
A | T | 4 | a0001c0001t0001g0160a0001c0001t0003g0096a0001c0001t0003g0176others(1): Show | 4 | HG02886.hp2 HG03225.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-2956A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680246 | ||||||
chr7:107680246
|
AATCTTAT others(11): Show |
A | 6 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0047others(3): Show | 6 | HG01496.hp1 HG01952.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.766-2940_766-2923d others(20): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680246 | |||||
chr7:107680248
|
T | A | 2 | a0001c0001t0001g0160a0001c0001t0009g0062 | 2 | HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.766-2954T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680248 | ||||||
chr7:107680249
|
C | CTTATA | 79 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0017others(76): Show | 80 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.766-2949_766-2948i others(7): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680249 | |||||
chr7:107680249
|
CTTATTAT others(93): Show |
C | 2 | a0001c0001t0016g0095a0001c0001t0016g0347 | 2 | HG01433.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.766-2922_766-2823d others(102): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680249 | |||||
chr7:107680262
|
C | A | 2 | a0001c0001t0001g0160a0001c0001t0009g0062 | 2 | HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.766-2940C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680262 | ||||||
chr7:107680262
|
C | G | 2 | a0001c0001t0003g0096a0001c0001t0003g0176 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-2940C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680262 | ||||||
chr7:107680264
|
T | A | 2 | a0001c0001t0001g0160a0001c0001t0009g0062 | 2 | HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.766-2938T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680264 | ||||||
chr7:107680267
|
C | A | 2 | a0001c0001t0003g0096a0001c0001t0003g0176 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.766-2935C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680267 | ||||||
chr7:107680272
|
T | A | 79 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0017others(76): Show | 80 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.766-2930T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680272 | ||||||
chr7:107680272
|
TATATA | T | 4 | a0001c0001t0001g0160a0001c0001t0003g0096a0001c0001t0003g0176others(1): Show | 4 | HG02886.hp2 HG03225.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-2922_766-2918d others(7): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680272 | |||||
chr7:107680273
|
A | T | 79 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0017others(76): Show | 80 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.766-2929A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680273 | ||||||
chr7:107680277
|
A | AATATAAT others(29): Show |
4 | a0001c0001t0001g0025a0001c0001t0001g0185a0001c0001t0001g0191others(1): Show | 4 | HG02615.hp2 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-2913_766-2912i others(38): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680277 | |||||
chr7:107680277
|
A | T | 79 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0017others(76): Show | 80 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.766-2925A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680277 | ||||||
chr7:107680277
|
AATATAAT others(34): Show |
A | 4 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0053others(1): Show | 4 | NA18941.hp1 NA18946.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-2899_766-2859d others(43): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680277 | |||||
chr7:107680287
|
T | TATTATAT others(6): Show |
6 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0047others(3): Show | 6 | HG01496.hp1 HG01952.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.766-2913_766-2912i others(15): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680287 | |||||
chr7:107680290
|
C | A | 142 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(139): Show | 145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.766-2912C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680290 | ||||||
chr7:107680295
|
T | A | 6 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0047others(3): Show | 6 | HG01496.hp1 HG01952.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.766-2907T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680295 | ||||||
chr7:107680295
|
TATATA | T | 202 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(199): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.766-2899_766-2895d others(7): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680295 | |||||
chr7:107680296
|
A | T | 6 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0047others(3): Show | 6 | HG01496.hp1 HG01952.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.766-2906A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680296 | ||||||
chr7:107680300
|
A | AATATAAT others(11): Show |
2 | a0001c0001t0001g0160a0001c0001t0009g0062 | 2 | HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.766-2889_766-2872d others(20): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680300 | |||||
chr7:107680300
|
A | AATCTTAT others(6): Show |
1 | a0006c0008t0030g0036 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.766-2900_766-2899i others(15): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680300 | |||||
chr7:107680300
|
A | AATCTTAT others(24): Show |
4 | a0001c0001t0003g0004a0001c0001t0003g0188a0001c0001t0009g0187others(1): Show | 5 | HG02486.hp2 HG02886.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-2900_766-2899i others(33): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680300 | |||||
chr7:107680300
|
A | AATCTTAT others(29): Show |
4 | a0001c0001t0007g0181a0004c0004t0009g0007a0004c0004t0009g0018others(1): Show | 4 | HG02818.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.766-2900_766-2899i others(38): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680300 | |||||
chr7:107680300
|
A | AATCTTAT others(65): Show |
1 | a0001c0001t0003g0168 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.766-2900_766-2899i others(74): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680300 | |||||
chr7:107680300
|
A | AATGTTAT others(21): Show |
1 | a0001c0001t0001g0080 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.766-2900_766-2899i others(30): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680300 | |||||
chr7:107680300
|
A | AATGTTAT others(24): Show |
13 | a0001c0001t0001g0134a0001c0001t0003g0031a0001c0001t0003g0129others(10): Show | 13 | HG00642.hp2 HG01243.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.766-2900_766-2899i others(33): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680300 | |||||
chr7:107680300
|
A | T | 6 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0047others(3): Show | 6 | HG01496.hp1 HG01952.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.766-2902A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680300 | ||||||
chr7:107680303
|
A | C | 1 | a0002c0002t0013g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.766-2899A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680303 | ||||||
chr7:107680305
|
A | T | 1 | a0002c0002t0013g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.766-2897A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680305 | ||||||
chr7:107680308
|
C | G | 99 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0017others(96): Show | 101 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.766-2894C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680308 | ||||||
chr7:107680313
|
A | C | 1 | a0006c0008t0030g0036 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.766-2889A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680313 | ||||||
chr7:107680313
|
A | T | 1 | a0001c0001t0031g0172 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.766-2889A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680313 | ||||||
chr7:107680326
|
C | G | 1 | a0006c0008t0030g0036 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.766-2876C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680326 | ||||||
chr7:107680328
|
T | TATATTAT others(6): Show |
1 | a0006c0008t0030g0036 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.766-2872_766-2871i others(15): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680328 | |||||
chr7:107680330
|
T | G | 1 | a0002c0002t0013g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.766-2872T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680330 | ||||||
chr7:107680331
|
C | A | 4 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0053others(1): Show | 4 | NA18941.hp1 NA18946.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-2871C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680331 | ||||||
chr7:107680344
|
G | C | 4 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0053others(1): Show | 4 | NA18941.hp1 NA18946.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-2858G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680344 | ||||||
chr7:107680361
|
T | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0017others(52): Show | 56 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.766-2841T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680361 | ||||||
chr7:107680380
|
G | C | 1 | a0001c0001t0007g0196 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.766-2822G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680380 | ||||||
chr7:107680380
|
G | GTTATATT others(29): Show |
1 | a0002c0002t0013g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.766-2805_766-2770d others(38): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107680380 | |||||
chr7:107680419
|
A | G | 1 | a0001c0001t0006g0272 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.766-2783A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680419 | ||||||
chr7:107680489
|
A | G | 1 | a0001c0001t0002g0075 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.766-2713A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680489 | ||||||
chr7:107680666
|
G | A | 14 | a0001c0001t0001g0080a0001c0001t0001g0134a0001c0001t0003g0031others(11): Show | 14 | HG00642.hp2 HG01243.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.766-2536G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680666 | ||||||
chr7:107680757
|
G | A | 246 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(243): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.766-2445G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107680757 | ||||||
chr7:107681081
|
T | C | 1 | a0001c0001t0001g0258 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.766-2121T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107681081 | ||||||
chr7:107681129
|
A | C | 275 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(272): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.766-2073A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107681129 | ||||||
chr7:107681130
|
A | C | 275 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(272): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.766-2072A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107681130 | ||||||
chr7:107681221
|
T | A | 56 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(53): Show | 58 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.766-1981T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107681221 | ||||||
chr7:107681270
|
A | G | 97 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(94): Show | 99 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.766-1932A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107681270 | ||||||
chr7:107681313
|
C | T | 12 | a0001c0001t0001g0343a0001c0001t0007g0342a0001c0001t0007g0344others(9): Show | 12 | HG01074.hp2 HG01433.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.766-1889C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107681313 | ||||||
chr7:107681316
|
T | C | 1 | a0002c0002t0013g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.766-1886T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107681316 | ||||||
chr7:107681567
|
TAAAGA | T | 61 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0013others(58): Show | 62 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.766-1630_766-1626d others(7): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107681567 | |||||
chr7:107681674
|
G | C | 34 | a0001c0001t0001g0134a0001c0001t0003g0022a0001c0001t0003g0031others(31): Show | 34 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.766-1528G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107681674 | ||||||
chr7:107681703
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.766-1499A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107681703 | ||||||
chr7:107681746
|
C | T | 1 | a0012c0018t0002g0028 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.766-1456C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107681746 | ||||||
chr7:107681779
|
T | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0337others(1): Show | 4 | HG02109.hp1 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.766-1423T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107681779 | ||||||
chr7:107681849
|
T | C | 10 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0136others(7): Show | 10 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.766-1353T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107681849 | ||||||
chr7:107681999
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.766-1203A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107681999 | ||||||
chr7:107682021
|
C | G | 1 | a0014c0021t0001g0127 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.766-1181C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682021 | ||||||
chr7:107682104
|
T | TA | 37 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0065others(34): Show | 37 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.766-1072dupA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107682104 | |||||
chr7:107682104
|
TA | T | 8 | a0001c0001t0002g0157a0001c0001t0003g0132a0001c0001t0003g0188others(5): Show | 8 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.766-1072delA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107682104 | |||||
chr7:107682105
|
A | T | 1 | a0001c0001t0005g0358 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.766-1097A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682105 | ||||||
chr7:107682130
|
A | T | 3 | a0001c0001t0003g0176a0002c0002t0014g0356a0002c0002t0014g0357 | 3 | HG02109.hp2 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.766-1072A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682130 | ||||||
chr7:107682130
|
AT | A | 28 | a0001c0001t0001g0025a0001c0001t0001g0134a0001c0001t0001g0140others(25): Show | 28 | HG01074.hp2 HG01243.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.766-1064delT | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107682130 | |||||
chr7:107682130
|
ATT | A | 18 | a0001c0001t0001g0125a0001c0001t0003g0244a0001c0001t0003g0254others(15): Show | 19 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.766-1065_766-1064d others(4): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107682130 | |||||
chr7:107682131
|
T | A | 186 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(183): Show | 188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.766-1071T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682131 | ||||||
chr7:107682132
|
T | A | 199 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(196): Show | 201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.766-1070T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682132 | ||||||
chr7:107682133
|
T | A | 6 | a0001c0001t0003g0301a0001c0001t0007g0196a0004c0004t0009g0007others(3): Show | 6 | HG00099.hp2 HG02818.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.766-1069T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682133 | ||||||
chr7:107682139
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.766-1063A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682139 | ||||||
chr7:107682235
|
G | A | 1 | a0001c0001t0006g0272 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.766-967G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682235 | ||||||
chr7:107682247
|
G | C | 1 | a0001c0012t0001g0058 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.766-955G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682247 | ||||||
chr7:107682661
|
A | AAC | 3 | a0001c0001t0003g0176a0002c0002t0014g0356a0002c0002t0014g0357 | 3 | HG02109.hp2 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.766-525_766-524dup others(2): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr7 | 107682661 | |||||
chr7:107682699
|
A | C | 12 | a0001c0001t0001g0003a0001c0001t0001g0033a0001c0001t0001g0034others(9): Show | 13 | HG00621.hp1 NA18940.hp2 NA18966.hp2 others(10): Show |
intron_variant | MODIFIER | c.766-503A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682699 | ||||||
chr7:107682744
|
C | A | 4 | a0003c0003t0003g0016a0003c0003t0003g0021a0003c0003t0003g0173others(1): Show | 4 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.766-458C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682744 | ||||||
chr7:107682746
|
T | G | 230 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(227): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.766-456T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682746 | ||||||
chr7:107682764
|
C | G | 242 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(239): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.766-438C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682764 | ||||||
chr7:107682804
|
C | G | 1 | a0001c0001t0001g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.766-398C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682804 | ||||||
chr7:107682830
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.766-372G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682830 | ||||||
chr7:107682847
|
A | G | 1 | a0001c0001t0001g0336 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.766-355A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682847 | ||||||
chr7:107682989
|
T | C | 1 | a0001c0001t0002g0102 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.766-213T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107682989 | ||||||
chr7:107683154
|
G | A | 3 | a0001c0019t0001g0171a0002c0009t0024g0193a0002c0009t0025g0316 | 3 | HG01074.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.766-48G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 6/20 | chr7 | 107683154 | ||||||
chr7:107683668
|
G | T | 242 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(239): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1001+131G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107683668 | ||||||
chr7:107683705
|
A | G | 3 | a0001c0019t0001g0171a0002c0009t0024g0193a0002c0009t0025g0316 | 3 | HG01074.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1001+168A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107683705 | ||||||
chr7:107683787
|
G | C | 1 | a0001c0001t0003g0176 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1001+250G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107683787 | ||||||
chr7:107683897
|
C | G | 1 | a0001c0001t0009g0062 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1001+360C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107683897 | ||||||
chr7:107683955
|
A | G | 1 | a0001c0001t0003g0244 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1001+418A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107683955 | ||||||
chr7:107684130
|
G | A | 1 | a0001c0006t0006g0348 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1001+593G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107684130 | ||||||
chr7:107684224
|
G | A | 1 | a0001c0001t0002g0309 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1001+687G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107684224 | ||||||
chr7:107684235
|
G | A | 6 | a0001c0001t0003g0004a0001c0001t0003g0132a0001c0001t0003g0188others(3): Show | 7 | HG02055.hp1 HG02486.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1001+698G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107684235 | ||||||
chr7:107684285
|
C | T | 3 | a0001c0001t0003g0176a0002c0002t0014g0356a0002c0002t0014g0357 | 3 | HG02109.hp2 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1001+748C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107684285 | ||||||
chr7:107684329
|
G | A | 249 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(246): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.1001+792G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107684329 | ||||||
chr7:107684345
|
G | A | 2 | a0001c0001t0015g0042a0001c0001t0015g0118 | 2 | NA18966.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1001+808G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107684345 | ||||||
chr7:107684384
|
G | T | 1 | a0001c0001t0003g0301 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1001+847G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107684384 | ||||||
chr7:107684397
|
G | C | 8 | a0001c0001t0003g0004a0001c0001t0003g0132a0001c0001t0003g0188others(5): Show | 9 | HG02055.hp1 HG02486.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1001+860G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107684397 | ||||||
chr7:107684520
|
A | C | 1 | a0001c0001t0001g0218 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1001+983A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107684520 | ||||||
chr7:107684708
|
A | C | 120 | a0001c0001t0001g0069a0001c0001t0001g0076a0001c0001t0001g0079others(117): Show | 122 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1001+1171A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107684708 | ||||||
chr7:107684799
|
A | G | 2 | a0001c0001t0001g0300a0001c0001t0001g0307 | 2 | NA18939.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1001+1262A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107684799 | ||||||
chr7:107684835
|
G | A | 3 | a0001c0019t0001g0171a0002c0009t0024g0193a0002c0009t0025g0316 | 3 | HG01074.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1001+1298G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107684835 | ||||||
chr7:107684936
|
GTTTAGGG others(6): Show |
G | 115 | a0001c0001t0001g0069a0001c0001t0001g0076a0001c0001t0001g0079others(112): Show | 116 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.1001+1403_1001+141 others(17): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107684936 | |||||
chr7:107685271
|
C | T | 3 | a0001c0019t0001g0171a0002c0009t0024g0193a0002c0009t0025g0316 | 3 | HG01074.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1001+1734C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107685271 | ||||||
chr7:107685598
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1001+2061A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107685598 | ||||||
chr7:107685610
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1001+2073T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107685610 | ||||||
chr7:107685692
|
C | G | 111 | a0001c0001t0001g0069a0001c0001t0001g0076a0001c0001t0001g0079others(108): Show | 112 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1001+2155C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107685692 | ||||||
chr7:107685771
|
C | G | 207 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(204): Show | 211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.1001+2234C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107685771 | ||||||
chr7:107685861
|
T | A | 6 | a0001c0001t0002g0086a0001c0001t0002g0102a0001c0001t0002g0167others(3): Show | 6 | HG00438.hp2 HG02155.hp1 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.1001+2324T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107685861 | ||||||
chr7:107685946
|
T | A | 2 | a0001c0011t0007g0328a0001c0011t0007g0329 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1001+2409T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107685946 | ||||||
chr7:107686053
|
A | C | 1 | a0001c0001t0001g0221 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1001+2516A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686053 | ||||||
chr7:107686108
|
G | GGT | 4 | a0001c0001t0001g0120a0001c0001t0001g0305a0001c0001t0005g0298others(1): Show | 4 | HG03017.hp2 HG03139.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001+2586_1001+258 others(6): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686108 | |||||
chr7:107686121
|
G | T | 1 | a0001c0001t0006g0215 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1001+2584G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686121 | ||||||
chr7:107686267
|
T | C | 3 | a0001c0001t0007g0181a0001c0011t0007g0328a0001c0011t0007g0329 | 3 | HG02257.hp1 HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1001+2730T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686267 | ||||||
chr7:107686267
|
T | TCCTTCCC others(20): Show |
4 | a0001c0001t0002g0280a0001c0001t0002g0281a0001c0001t0002g0324others(1): Show | 4 | HG00280.hp2 HG01258.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1001+2753_1002-273 others(31): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686267 | |||||
chr7:107686267
|
TCCTTCCC others(29): Show |
T | 2 | a0001c0001t0001g0217a0001c0001t0003g0182 | 2 | HG02622.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1002-2755_1002-272 others(40): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686267 | |||||
chr7:107686290
|
T | C | 3 | a0001c0001t0007g0181a0001c0011t0007g0328a0001c0011t0007g0329 | 3 | HG02257.hp1 HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1001+2753T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686290 | ||||||
chr7:107686290
|
TCCTACCT others(11): Show |
T | 1 | a0001c0001t0001g0183 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1001+2757_1002-274 others(22): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686290 | |||||
chr7:107686294
|
A | C | 3 | a0001c0001t0007g0181a0001c0011t0007g0328a0001c0011t0007g0329 | 3 | HG02257.hp1 HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1001+2757A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686294 | ||||||
chr7:107686294
|
ACCTTCCC others(2): Show |
A | 183 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(180): Show | 185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.1002-2736_1002-272 others(13): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686294 | |||||
chr7:107686298
|
T | G | 1 | a0002c0002t0013g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1002-2755T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686298 | ||||||
chr7:107686300
|
C | A | 1 | a0002c0002t0013g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1002-2753C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686300 | ||||||
chr7:107686303
|
C | CCCTTCCC others(38): Show |
2 | a0001c0001t0001g0065a0001c0001t0007g0181 | 2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1002-2737_1002-273 others(49): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686303 | |||||
chr7:107686303
|
C | CCCTTTCC others(74): Show |
1 | a0001c0011t0007g0328 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1002-2746_1002-274 others(85): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686303 | |||||
chr7:107686303
|
C | CCCTTTCC others(65): Show |
1 | a0001c0011t0007g0329 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1002-2746_1002-274 others(76): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686303 | |||||
chr7:107686309
|
C | CCTCCCTT others(11): Show |
1 | a0001c0006t0001g0349 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1002-2737_1002-273 others(22): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686309 | |||||
chr7:107686317
|
C | T | 2 | a0001c0001t0001g0065a0001c0006t0001g0349 | 2 | HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1002-2736C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686317 | ||||||
chr7:107686324
|
T | C | 2 | a0001c0001t0001g0065a0001c0006t0001g0349 | 2 | HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1002-2729T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686324 | ||||||
chr7:107686324
|
TTTCCTAC others(20): Show |
T | 3 | a0001c0001t0004g0238a0001c0001t0004g0259a0001c0001t0004g0310 | 3 | NA18939.hp1 NA18992.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1002-2719_1002-269 others(31): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686324 | |||||
chr7:107686334
|
G | T | 2 | a0001c0001t0001g0065a0001c0006t0001g0349 | 2 | HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1002-2719G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686334 | ||||||
chr7:107686336
|
A | ACTCCCTT others(20): Show |
1 | a0001c0001t0003g0168 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1002-2696_1002-267 others(31): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686336 | |||||
chr7:107686336
|
A | C | 2 | a0001c0001t0001g0065a0001c0006t0001g0349 | 2 | HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1002-2717A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686336 | ||||||
chr7:107686344
|
T | C | 2 | a0001c0011t0007g0328a0001c0011t0007g0329 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1002-2709T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686344 | ||||||
chr7:107686390
|
C | T | 1 | a0001c0001t0004g0103 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1002-2663C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686390 | ||||||
chr7:107686393
|
C | T | 1 | a0001c0001t0004g0103 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1002-2660C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686393 | ||||||
chr7:107686394
|
C | T | 1 | a0001c0001t0004g0103 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1002-2659C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686394 | ||||||
chr7:107686398
|
C | T | 1 | a0001c0001t0004g0103 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1002-2655C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686398 | ||||||
chr7:107686399
|
T | A | 1 | a0005c0005t0001g0151 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1002-2654T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686399 | ||||||
chr7:107686400
|
C | T | 1 | a0001c0001t0004g0161 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1002-2653C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686400 | ||||||
chr7:107686405
|
T | C | 1 | a0001c0001t0004g0103 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1002-2648T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686405 | ||||||
chr7:107686405
|
T | TC | 3 | a0001c0001t0001g0059a0001c0001t0001g0091a0001c0001t0004g0161 | 3 | HG02027.hp1 NA19003.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1002-2648_1002-264 others(5): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686405 | ||||||
chr7:107686405
|
T | TCTTTCTT others(26): Show |
1 | a0001c0001t0001g0229 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1002-2648_1002-264 others(37): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686405 | ||||||
chr7:107686405
|
T | TTCTTTCT others(7): Show |
1 | a0001c0001t0001g0120 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1002-2647_1002-264 others(18): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | |||||
chr7:107686405
|
T | TTCTTTCT others(15): Show |
1 | a0001c0001t0005g0141 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1002-2647_1002-264 others(26): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | |||||
chr7:107686405
|
T | TTTCTTCT others(11): Show |
1 | a0001c0001t0005g0152 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1002-2646_1002-264 others(22): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | |||||
chr7:107686405
|
T | TTTCTTTC others(20): Show |
1 | a0001c0001t0001g0246 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1002-2646_1002-264 others(31): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | |||||
chr7:107686405
|
T | TTTTC | 33 | a0001c0001t0001g0079a0001c0001t0002g0001a0001c0001t0002g0006others(30): Show | 35 | HG00558.hp2 HG01123.hp1 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.1002-2600_1002-259 others(8): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | |||||
chr7:107686405
|
T | TTTTCTTT others(1): Show |
22 | a0001c0001t0002g0055a0001c0001t0002g0067a0001c0001t0002g0157others(19): Show | 22 | HG00639.hp2 HG01070.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1002-2604_1002-259 others(12): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | |||||
chr7:107686405
|
T | TTTTCTTT others(5): Show |
16 | a0001c0001t0001g0252a0001c0001t0002g0005a0001c0001t0002g0077others(13): Show | 16 | HG00438.hp1 HG00438.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.1002-2608_1002-259 others(16): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | |||||
chr7:107686405
|
T | TTTTCTTT others(9): Show |
4 | a0001c0001t0002g0123a0001c0001t0002g0278a0001c0001t0002g0323others(1): Show | 4 | HG02148.hp1 HG02155.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.1002-2612_1002-259 others(20): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | |||||
chr7:107686405
|
T | TTTTCTTT others(13): Show |
2 | a0001c0001t0002g0279a0001c0001t0016g0347 | 2 | HG00544.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1002-2616_1002-259 others(24): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | |||||
chr7:107686405
|
T | TTTTCTTT others(36): Show |
1 | a0001c0001t0001g0150 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1002-2626_1002-262 others(47): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | |||||
chr7:107686405
|
T | TTTTTTCT others(15): Show |
1 | a0001c0001t0006g0037 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1002-2645_1002-264 others(26): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | |||||
chr7:107686405
|
TTTTC | T | 10 | a0001c0001t0002g0098a0001c0001t0002g0154a0001c0001t0002g0266others(7): Show | 10 | HG00558.hp1 HG00735.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1002-2600_1002-259 others(8): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | |||||
chr7:107686405
|
TTTTCTTT others(1): Show |
T | 16 | a0001c0001t0002g0198a0001c0001t0003g0022a0001c0001t0003g0040others(13): Show | 16 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1002-2604_1002-259 others(12): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | |||||
chr7:107686405
|
TTTTCTTT others(5): Show |
T | 15 | a0001c0001t0001g0134a0001c0001t0002g0068a0001c0001t0003g0031others(12): Show | 15 | HG00099.hp2 HG00642.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.1002-2608_1002-259 others(16): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686405 | |||||
chr7:107686441
|
C | CTGTTCTT others(14): Show |
1 | a0001c0001t0001g0143 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1002-2611_1002-261 others(25): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686441 | |||||
chr7:107686441
|
C | CTT | 5 | a0001c0001t0001g0120a0001c0001t0001g0246a0001c0001t0005g0141others(2): Show | 5 | HG01261.hp1 HG02602.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.1002-2610_1002-260 others(6): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686441 | |||||
chr7:107686441
|
C | CTTTCTTT others(3): Show |
9 | a0001c0001t0001g0064a0001c0001t0001g0082a0001c0001t0001g0135others(6): Show | 10 | HG01074.hp1 HG01891.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1002-2610_1002-260 others(14): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686441 | |||||
chr7:107686441
|
C | CTTTCTTT others(7): Show |
21 | a0001c0001t0001g0114a0001c0001t0001g0130a0001c0001t0001g0131others(18): Show | 21 | HG01074.hp2 HG01099.hp2 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.1002-2609_1002-259 others(18): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686441 | |||||
chr7:107686441
|
C | CTTTCTTT others(11): Show |
38 | a0001c0001t0001g0012a0001c0001t0001g0041a0001c0001t0001g0044others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(35): Show |
intron_variant | MODIFIER | c.1002-2597_1002-259 others(22): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686441 | |||||
chr7:107686441
|
C | CTTTCTTT others(15): Show |
43 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(40): Show | 44 | HG00280.hp1 HG00408.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.1002-2597_1002-259 others(26): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686441 | |||||
chr7:107686441
|
C | CTTTCTTT others(19): Show |
41 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0023others(38): Show | 41 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1002-2597_1002-259 others(30): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686441 | |||||
chr7:107686441
|
C | CTTTCTTT others(30): Show |
1 | a0001c0001t0001g0228 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1002-2597_1002-259 others(41): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686441 | |||||
chr7:107686441
|
C | CTTTCTTT others(23): Show |
16 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0050others(13): Show | 17 | HG00544.hp1 HG00642.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.1002-2597_1002-259 others(34): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686441 | |||||
chr7:107686441
|
C | CTTTCTTT others(27): Show |
11 | a0001c0001t0001g0115a0001c0001t0001g0142a0001c0001t0001g0146others(8): Show | 11 | HG00735.hp2 HG01099.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.1002-2597_1002-259 others(38): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686441 | |||||
chr7:107686441
|
C | CTTTCTTT others(31): Show |
5 | a0001c0001t0001g0145a0001c0001t0001g0236a0001c0001t0001g0296others(2): Show | 5 | HG00741.hp1 HG01109.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1002-2597_1002-259 others(42): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686441 | |||||
chr7:107686441
|
C | CTTTCTTT others(39): Show |
1 | a0001c0001t0001g0219 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1002-2597_1002-259 others(50): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686441 | |||||
chr7:107686442
|
T | TTTCTTTC others(12): Show |
1 | a0001c0001t0005g0334 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1002-2597_1002-259 others(23): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686442 | |||||
chr7:107686442
|
T | TTTCTTTC others(16): Show |
1 | a0001c0001t0001g0205 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1002-2597_1002-259 others(27): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686442 | |||||
chr7:107686442
|
T | TTTCTTTC others(24): Show |
2 | a0001c0001t0001g0080a0001c0001t0001g0117 | 2 | HG01081.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1002-2597_1002-259 others(35): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686442 | |||||
chr7:107686443
|
T | TTCTTTCT others(15): Show |
1 | a0001c0001t0001g0166 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1002-2597_1002-259 others(26): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686443 | |||||
chr7:107686443
|
T | TTCTTTCT others(19): Show |
3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0089 | 3 | NA19010.hp1 NA19063.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1002-2597_1002-259 others(30): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686443 | |||||
chr7:107686443
|
T | TTCTTTCT others(23): Show |
1 | a0001c0001t0001g0033 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1002-2597_1002-259 others(34): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686443 | |||||
chr7:107686443
|
T | TTCTTTCT others(27): Show |
1 | a0001c0001t0006g0088 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1002-2597_1002-259 others(38): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686443 | |||||
chr7:107686454
|
T | TTTCTTCT others(21): Show |
1 | a0001c0001t0005g0298 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1002-2597_1002-259 others(32): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107686454 | |||||
chr7:107686464
|
T | G | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | HG00642.hp1 HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1002-2589T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686464 | ||||||
chr7:107686557
|
G | A | 191 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(188): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1002-2496G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686557 | ||||||
chr7:107686599
|
T | C | 5 | a0002c0002t0013g0078a0006c0008t0014g0057a0006c0008t0030g0036others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1002-2454T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686599 | ||||||
chr7:107686600
|
G | A | 1 | a0002c0002t0013g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1002-2453G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686600 | ||||||
chr7:107686623
|
G | A | 1 | a0001c0001t0003g0176 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1002-2430G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686623 | ||||||
chr7:107686663
|
A | T | 2 | a0001c0011t0007g0328a0001c0011t0007g0329 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1002-2390A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686663 | ||||||
chr7:107686736
|
T | A | 203 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(200): Show | 205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.1002-2317T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686736 | ||||||
chr7:107686790
|
T | C | 1 | a0001c0001t0016g0347 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1002-2263T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686790 | ||||||
chr7:107686829
|
C | G | 1 | a0001c0001t0003g0176 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1002-2224C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686829 | ||||||
chr7:107686900
|
C | T | 1 | a0002c0002t0018g0014 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1002-2153C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686900 | ||||||
chr7:107686961
|
T | C | 1 | a0001c0001t0002g0277 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1002-2092T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107686961 | ||||||
chr7:107687296
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1002-1757G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107687296 | ||||||
chr7:107687386
|
C | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0107a0001c0001t0001g0164others(1): Show | 4 | HG00597.hp1 NA18970.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1002-1667C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107687386 | ||||||
chr7:107687407
|
C | T | 106 | a0001c0001t0001g0252a0001c0001t0001g0264a0001c0001t0001g0289others(103): Show | 108 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1002-1646C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107687407 | ||||||
chr7:107687504
|
A | G | 1 | a0001c0001t0001g0134 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1002-1549A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107687504 | ||||||
chr7:107687870
|
G | A | 193 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(190): Show | 195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.1002-1183G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107687870 | ||||||
chr7:107688038
|
TTAGG | T | 17 | a0001c0001t0001g0023a0001c0001t0001g0050a0001c0001t0001g0091others(14): Show | 17 | HG01106.hp1 HG02071.hp1 HG02155.hp2 others(14): Show |
intron_variant | MODIFIER | c.1002-1010_1002-100 others(8): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr7 | 107688038 | |||||
chr7:107688039
|
T | C | 1 | a0001c0001t0009g0062 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1002-1014T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107688039 | ||||||
chr7:107688051
|
C | A | 1 | a0001c0001t0003g0176 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1002-1002C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107688051 | ||||||
chr7:107688092
|
A | C | 318 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(315): Show | 322 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.1002-961A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107688092 | ||||||
chr7:107688213
|
C | G | 7 | a0001c0001t0009g0062a0001c0001t0009g0187a0001c0011t0007g0328others(4): Show | 7 | HG02257.hp1 HG02280.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1002-840C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107688213 | ||||||
chr7:107688252
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1002-801A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107688252 | ||||||
chr7:107688288
|
G | A | 2 | a0001c0001t0002g0067a0001c0001t0002g0268 | 2 | NA18963.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.1002-765G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107688288 | ||||||
chr7:107688369
|
T | G | 21 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0082others(18): Show | 21 | HG00140.hp2 HG00735.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.1002-684T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107688369 | ||||||
chr7:107688511
|
G | A | 2 | a0001c0001t0001g0339a0001c0001t0001g0353 | 2 | HG01069.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1002-542G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107688511 | ||||||
chr7:107688677
|
A | T | 1 | a0001c0001t0007g0196 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1002-376A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 8/20 | chr7 | 107688677 | ||||||
chr7:107689367
|
G | C | 1 | a0001c0001t0003g0176 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1149+167G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 9/20 | chr7 | 107689367 | ||||||
chr7:107689391
|
T | A | 3 | a0001c0001t0001g0025a0001c0001t0001g0185a0001c0001t0001g0189 | 3 | HG02896.hp2 HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1149+191T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 9/20 | chr7 | 107689391 | ||||||
chr7:107689484
|
G | T | 2 | a0001c0001t0001g0175a0001c0001t0003g0190 | 2 | HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1149+284G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 9/20 | chr7 | 107689484 | ||||||
chr7:107689536
|
T | A | 5 | a0001c0001t0007g0181a0003c0003t0003g0016a0003c0003t0003g0021others(2): Show | 5 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1149+336T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 9/20 | chr7 | 107689536 | ||||||
chr7:107689671
|
C | T | 3 | a0001c0019t0001g0171a0002c0009t0024g0193a0002c0009t0025g0316 | 3 | HG01074.hp2 HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1150-453C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 9/20 | chr7 | 107689671 | ||||||
chr7:107689989
|
C | T | 15 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0070others(12): Show | 15 | HG00280.hp2 HG00323.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1150-135C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 9/20 | chr7 | 107689989 | ||||||
chr7:107690556
|
T | C | 7 | a0001c0001t0009g0062a0001c0001t0009g0187a0001c0011t0007g0328others(4): Show | 7 | HG02257.hp1 HG02280.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1263+319T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107690556 | ||||||
chr7:107690646
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0044a0001c0001t0001g0212others(1): Show | 4 | HG00140.hp1 HG00639.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1263+409C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107690646 | ||||||
chr7:107691108
|
T | TAC | 28 | a0001c0001t0001g0023a0001c0001t0001g0065a0001c0001t0001g0191others(25): Show | 29 | HG00438.hp1 HG00438.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.1263+905_1263+906d others(4): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691108 | |||||
chr7:107691108
|
T | TACAC | 108 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(105): Show | 109 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.1263+903_1263+906d others(6): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691108 | |||||
chr7:107691108
|
T | TACACAC | 113 | a0001c0001t0001g0076a0001c0001t0001g0080a0001c0001t0001g0082others(110): Show | 115 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1263+901_1263+906d others(8): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691108 | |||||
chr7:107691108
|
T | TACACACA others(1): Show |
43 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.1263+899_1263+906d others(10): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691108 | |||||
chr7:107691108
|
T | TACACACA others(3): Show |
14 | a0001c0001t0001g0034a0001c0001t0001g0121a0001c0001t0001g0144others(11): Show | 14 | HG00621.hp1 HG01123.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.1263+897_1263+906d others(12): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691108 | |||||
chr7:107691108
|
T | TACACACA others(5): Show |
4 | a0001c0001t0001g0041a0001c0001t0001g0122a0001c0001t0001g0175others(1): Show | 4 | HG00621.hp2 HG01928.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.1263+895_1263+906d others(14): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691108 | |||||
chr7:107691108
|
TAC | T | 11 | a0001c0001t0001g0227a0001c0001t0001g0336a0001c0001t0003g0168others(8): Show | 11 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1263+905_1263+906d others(4): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691108 | |||||
chr7:107691144
|
T | C | 3 | a0001c0001t0001g0225a0001c0001t0001g0260a0001c0001t0005g0224 | 3 | NA18960.hp1 NA18977.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1263+907T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691144 | ||||||
chr7:107691167
|
C | T | 185 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(182): Show | 187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1263+930C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691167 | ||||||
chr7:107691218
|
T | C | 1 | a0001c0001t0003g0176 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1263+981T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691218 | ||||||
chr7:107691256
|
C | T | 6 | a0001c0001t0001g0343a0001c0001t0007g0342a0001c0001t0007g0344others(3): Show | 6 | HG02055.hp2 HG03209.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1263+1019C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691256 | ||||||
chr7:107691276
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0360 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1263+1039C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691276 | ||||||
chr7:107691307
|
A | G | 1 | a0001c0001t0004g0161 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1263+1070A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691307 | ||||||
chr7:107691426
|
T | C | 2 | a0001c0001t0003g0176a0001c0001t0007g0196 | 2 | HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1263+1189T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691426 | ||||||
chr7:107691481
|
G | A | 1 | a0001c0001t0006g0038 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1263+1244G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691481 | ||||||
chr7:107691504
|
A | AAT | 96 | a0001c0001t0001g0264a0001c0001t0001g0289a0001c0001t0002g0001others(93): Show | 98 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1263+1277_1263+127 others(6): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691504 | |||||
chr7:107691510
|
T | TACACACA others(3): Show |
1 | a0001c0001t0001g0050 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1263+1274_1263+127 others(14): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691510 | |||||
chr7:107691512
|
T | C | 19 | a0001c0001t0001g0017a0001c0001t0001g0050a0001c0001t0001g0051others(16): Show | 19 | HG00597.hp1 HG01891.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.1263+1275T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691512 | ||||||
chr7:107691512
|
T | TACACACA others(3): Show |
14 | a0001c0001t0001g0023a0001c0001t0001g0142a0001c0001t0001g0145others(11): Show | 14 | HG01106.hp1 HG02155.hp2 NA18953.hp2 others(11): Show |
intron_variant | MODIFIER | c.1263+1276_1263+127 others(14): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691512 | |||||
chr7:107691514
|
T | C | 151 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(148): Show | 153 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1263+1277T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691514 | ||||||
chr7:107691514
|
T | TAC | 3 | a0001c0001t0003g0031a0001c0001t0003g0176a0001c0001t0007g0196 | 3 | HG03139.hp2 HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1263+1307_1263+130 others(6): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691514 | |||||
chr7:107691514
|
T | TACAC | 4 | a0001c0001t0007g0181a0003c0003t0003g0016a0003c0003t0003g0173others(1): Show | 4 | HG02922.hp2 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1263+1305_1263+130 others(8): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691514 | |||||
chr7:107691514
|
T | TACACACA others(7): Show |
1 | a0003c0003t0003g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1263+1295_1263+130 others(18): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691514 | |||||
chr7:107691514
|
T | TATAC | 5 | a0001c0001t0002g0279a0001c0001t0004g0238a0001c0001t0004g0259others(2): Show | 5 | HG00544.hp2 HG02451.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.1263+1278_1263+127 others(8): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691514 | |||||
chr7:107691514
|
T | TATACAC | 5 | a0001c0001t0002g0055a0001c0001t0002g0083a0001c0001t0002g0106others(2): Show | 5 | HG01123.hp1 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1263+1278_1263+127 others(10): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691514 | |||||
chr7:107691514
|
T | TATACACA others(3): Show |
2 | a0001c0001t0001g0175a0001c0001t0003g0190 | 2 | HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1263+1278_1263+127 others(14): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691514 | |||||
chr7:107691516
|
C | T | 3 | a0001c0001t0004g0046a0001c0001t0029g0335a0002c0002t0013g0078 | 3 | HG02723.hp1 NA20300.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1263+1279C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691516 | ||||||
chr7:107691546
|
A | C | 266 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(263): Show | 270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.1263+1309A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691546 | ||||||
chr7:107691548
|
C | A | 101 | a0001c0001t0001g0175a0001c0001t0001g0264a0001c0001t0001g0289others(98): Show | 103 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1263+1311C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691548 | ||||||
chr7:107691548
|
C | CACAA | 9 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(6): Show | 9 | HG00597.hp1 HG00642.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.1263+1312_1263+131 others(8): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691548 | |||||
chr7:107691548
|
C | CACACAA | 19 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0033others(16): Show | 19 | HG01433.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1263+1312_1263+131 others(10): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691548 | |||||
chr7:107691548
|
C | CACACACA others(1): Show |
88 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(85): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.1263+1312_1263+131 others(12): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691548 | |||||
chr7:107691548
|
C | CACACACA others(3): Show |
32 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0025others(29): Show | 32 | HG01123.hp2 HG01175.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1263+1312_1263+131 others(14): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691548 | |||||
chr7:107691548
|
C | CACACACA others(4): Show |
1 | a0001c0001t0001g0179 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1263+1312_1263+131 others(15): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691548 | |||||
chr7:107691548
|
C | CACACACA others(5): Show |
8 | a0001c0001t0001g0010a0001c0001t0001g0032a0001c0001t0001g0052others(5): Show | 8 | HG03130.hp2 HG03491.hp2 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.1263+1312_1263+131 others(16): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691548 | |||||
chr7:107691548
|
C | CACACACA others(6): Show |
2 | a0001c0001t0007g0342a0001c0001t0013g0341 | 2 | HG02055.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1263+1312_1263+131 others(17): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691548 | |||||
chr7:107691548
|
C | CACACACA others(7): Show |
1 | a0001c0001t0007g0344 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1263+1312_1263+131 others(18): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691548 | |||||
chr7:107691548
|
C | CACACACA others(9): Show |
1 | a0001c0001t0001g0140 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1263+1312_1263+131 others(20): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691548 | |||||
chr7:107691548
|
CAT | C | 21 | a0001c0001t0001g0023a0001c0001t0001g0050a0001c0001t0001g0142others(18): Show | 21 | HG01106.hp1 HG01358.hp1 HG02071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1263+1328_1263+132 others(6): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691548 | |||||
chr7:107691550
|
T | C | 264 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(261): Show | 268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.1263+1313T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691550 | ||||||
chr7:107691552
|
T | TATATATA others(9): Show |
3 | a0001c0001t0004g0238a0001c0001t0004g0259a0001c0001t0004g0310 | 3 | NA18939.hp1 NA18992.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1263+1327_1263+132 others(20): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107691552 | |||||
chr7:107691565
|
A | T | 1 | a0001c0001t0012g0288 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1263+1328A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691565 | ||||||
chr7:107691566
|
T | C | 1 | a0001c0001t0012g0288 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1263+1329T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691566 | ||||||
chr7:107691569
|
T | A | 1 | a0001c0001t0012g0288 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1263+1332T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691569 | ||||||
chr7:107691570
|
C | T | 1 | a0001c0001t0012g0288 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1263+1333C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691570 | ||||||
chr7:107691776
|
T | A | 1 | a0001c0001t0028g0231 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1263+1539T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691776 | ||||||
chr7:107691777
|
A | T | 1 | a0001c0001t0028g0231 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1263+1540A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691777 | ||||||
chr7:107691778
|
T | A | 1 | a0001c0001t0028g0231 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1263+1541T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107691778 | ||||||
chr7:107692029
|
C | T | 2 | a0001c0001t0003g0256a0001c0001t0005g0251 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1263+1792C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107692029 | ||||||
chr7:107692058
|
G | A | 2 | a0001c0001t0003g0129a0001c0001t0008g0197 | 2 | HG02258.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1263+1821G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107692058 | ||||||
chr7:107692148
|
T | C | 1 | a0001c0019t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1263+1911T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107692148 | ||||||
chr7:107692151
|
C | T | 1 | a0001c0019t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1263+1914C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107692151 | ||||||
chr7:107692650
|
A | T | 2 | a0001c0001t0003g0004a0001c0001t0019g0186 | 3 | HG02486.hp2 HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1264-1753A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107692650 | ||||||
chr7:107692869
|
A | G | 193 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(190): Show | 195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.1264-1534A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107692869 | ||||||
chr7:107692944
|
A | T | 1 | a0001c0001t0028g0231 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1264-1459A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107692944 | ||||||
chr7:107693133
|
A | G | 2 | a0001c0001t0002g0098a0001c0001t0002g0123 | 2 | HG00558.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1264-1270A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107693133 | ||||||
chr7:107693176
|
C | T | 1 | a0001c0001t0001g0338 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1264-1227C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107693176 | ||||||
chr7:107693177
|
G | A | 2 | a0002c0002t0018g0014a0013c0015t0018g0184 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1264-1226G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107693177 | ||||||
chr7:107693256
|
T | A | 1 | a0001c0001t0028g0231 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1264-1147T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107693256 | ||||||
chr7:107693425
|
G | C | 3 | a0001c0001t0001g0148a0001c0001t0001g0201a0001c0001t0005g0141 | 3 | NA18983.hp2 NA19011.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1264-978G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107693425 | ||||||
chr7:107693553
|
GCTT | G | 8 | a0001c0001t0001g0134a0001c0001t0003g0004a0001c0001t0003g0129others(5): Show | 9 | HG02258.hp1 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1264-847_1264-845d others(5): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr7 | 107693553 | |||||
chr7:107693558
|
T | A | 1 | a0001c0001t0002g0323 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1264-845T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107693558 | ||||||
chr7:107693581
|
C | T | 105 | a0001c0001t0001g0264a0001c0001t0001g0289a0001c0001t0002g0001others(102): Show | 107 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1264-822C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107693581 | ||||||
chr7:107693738
|
C | T | 2 | a0001c0001t0002g0275a0001c0001t0002g0279 | 2 | HG00544.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.1264-665C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107693738 | ||||||
chr7:107694068
|
T | A | 105 | a0001c0001t0001g0264a0001c0001t0001g0289a0001c0001t0002g0001others(102): Show | 107 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1264-335T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107694068 | ||||||
chr7:107694216
|
C | T | 183 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(180): Show | 185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.1264-187C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 10/20 | chr7 | 107694216 | ||||||
chr7:107694527
|
T | C | 11 | a0001c0001t0001g0041a0001c0001t0001g0085a0001c0001t0001g0128others(8): Show | 11 | HG02083.hp2 HG02135.hp1 HG03834.hp1 others(8): Show |
intron_variant | MODIFIER | c.1341+47T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 11/20 | chr7 | 107694527 | ||||||
chr7:107694903
|
T | G | 4 | a0006c0008t0014g0057a0006c0008t0030g0036a0007c0010t0003g0177others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1437+187T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 12/20 | chr7 | 107694903 | ||||||
chr7:107694959
|
T | C | 5 | a0001c0001t0001g0010a0001c0001t0001g0044a0001c0001t0001g0212others(2): Show | 5 | HG00140.hp1 HG00639.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.1437+243T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 12/20 | chr7 | 107694959 | ||||||
chr7:107695180
|
T | C | 1 | a0001c0001t0031g0172 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1437+464T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 12/20 | chr7 | 107695180 | ||||||
chr7:107695613
|
C | A | 99 | a0001c0001t0001g0264a0001c0001t0001g0289a0001c0001t0002g0001others(96): Show | 101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.1438-320C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 12/20 | chr7 | 107695613 | ||||||
chr7:107695675
|
G | T | 4 | a0006c0008t0014g0057a0006c0008t0030g0036a0007c0010t0003g0177others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1438-258G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 12/20 | chr7 | 107695675 | ||||||
chr7:107695779
|
C | T | 5 | a0001c0001t0003g0031a0001c0001t0005g0358a0001c0001t0008g0030others(2): Show | 5 | HG00642.hp2 HG02809.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1438-154C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 12/20 | chr7 | 107695779 | ||||||
chr7:107695919
|
A | G | 2 | a0002c0002t0018g0014a0013c0015t0018g0184 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1438-14A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 12/20 | chr7 | 107695919 | ||||||
chr7:107696135
|
C | T | 4 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(1): Show | 4 | HG02015.hp2 NA18980.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1544+96C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107696135 | ||||||
chr7:107696248
|
G | T | 1 | a0001c0001t0007g0181 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1544+209G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107696248 | ||||||
chr7:107696308
|
G | A | 1 | a0001c0001t0002g0026 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1544+269G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107696308 | ||||||
chr7:107696333
|
T | C | 1 | a0001c0001t0001g0023 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1544+294T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107696333 | ||||||
chr7:107696431
|
T | A | 2 | a0002c0002t0018g0014a0013c0015t0018g0184 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1544+392T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107696431 | ||||||
chr7:107696437
|
T | G | 10 | a0001c0001t0001g0025a0001c0001t0001g0169a0001c0001t0001g0185others(7): Show | 10 | HG00140.hp2 HG00735.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.1544+398T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107696437 | ||||||
chr7:107696465
|
C | T | 1 | a0001c0001t0003g0168 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1544+426C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107696465 | ||||||
chr7:107696482
|
C | A | 1 | a0003c0003t0003g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1544+443C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107696482 | ||||||
chr7:107696701
|
A | G | 1 | a0001c0001t0005g0334 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1544+662A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107696701 | ||||||
chr7:107696813
|
G | T | 2 | a0002c0002t0014g0356a0002c0002t0014g0357 | 2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1544+774G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107696813 | ||||||
chr7:107696950
|
C | T | 2 | a0002c0009t0024g0193a0002c0009t0025g0316 | 2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1544+911C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107696950 | ||||||
chr7:107696951
|
G | A | 6 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0160others(3): Show | 6 | HG03225.hp2 HG03471.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1544+912G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107696951 | ||||||
chr7:107697012
|
A | G | 1 | a0001c0001t0002g0098 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1544+973A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107697012 | ||||||
chr7:107697123
|
C | T | 2 | a0001c0001t0001g0072a0001c0001t0001g0199 | 2 | HG00408.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1545-919C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107697123 | ||||||
chr7:107697865
|
A | T | 1 | a0001c0001t0001g0189 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1545-177A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107697865 | ||||||
chr7:107697894
|
A | G | 1 | a0001c0001t0028g0231 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1545-148A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107697894 | ||||||
chr7:107698037
|
T | G | 2 | a0002c0002t0018g0014a0013c0015t0018g0184 | 2 | HG02109.hp1 HG03139.hp1 |
splice_region_variant&intron_variant | LOW | c.1545-5T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 13/20 | chr7 | 107698037 | ||||||
chr7:107698316
|
G | A | 1 | a0001c0011t0007g0329 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1614+205G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107698316 | ||||||
chr7:107698539
|
A | G | 2 | a0001c0001t0016g0095a0001c0001t0016g0347 | 2 | HG01433.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1614+428A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107698539 | ||||||
chr7:107698554
|
T | A | 1 | a0001c0001t0002g0278 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1614+443T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107698554 | ||||||
chr7:107698563
|
C | T | 1 | a0002c0002t0013g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1614+452C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107698563 | ||||||
chr7:107698606
|
T | C | 1 | a0002c0002t0013g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1614+495T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107698606 | ||||||
chr7:107698651
|
G | A | 1 | a0001c0001t0001g0124 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1614+540G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107698651 | ||||||
chr7:107698702
|
T | G | 1 | a0001c0001t0027g0139 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1614+591T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107698702 | ||||||
chr7:107698733
|
G | A | 2 | a0001c0001t0002g0266a0001c0001t0002g0313 | 2 | HG03492.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1614+622G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107698733 | ||||||
chr7:107699017
|
G | A | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | HG00642.hp1 HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1614+906G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107699017 | ||||||
chr7:107699054
|
T | C | 2 | a0002c0002t0018g0014a0013c0015t0018g0184 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1614+943T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107699054 | ||||||
chr7:107699220
|
A | C | 2 | a0001c0001t0016g0095a0001c0001t0016g0347 | 2 | HG01433.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1615-863A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107699220 | ||||||
chr7:107699466
|
G | A | 305 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(302): Show | 309 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.1615-617G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107699466 | ||||||
chr7:107699562
|
C | G | 1 | a0001c0022t0006g0054 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1615-521C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107699562 | ||||||
chr7:107699574
|
G | A | 2 | a0006c0008t0014g0057a0006c0008t0030g0036 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1615-509G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107699574 | ||||||
chr7:107699597
|
T | TCCAAGAG others(45): Show |
1 | a0001c0001t0001g0137 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1615-484_1615-433d others(54): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr7 | 107699597 | |||||
chr7:107699656
|
C | T | 5 | a0001c0001t0002g0250a0001c0001t0002g0282a0001c0001t0002g0283others(2): Show | 5 | HG02015.hp1 HG02135.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.1615-427C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107699656 | ||||||
chr7:107699657
|
G | A | 1 | a0001c0001t0002g0255 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1615-426G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107699657 | ||||||
chr7:107699693
|
C | T | 1 | a0001c0001t0008g0178 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1615-390C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107699693 | ||||||
chr7:107699700
|
G | T | 1 | a0001c0001t0001g0159 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1615-383G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107699700 | ||||||
chr7:107699927
|
CA | C | 6 | a0002c0009t0024g0193a0002c0009t0025g0316a0006c0008t0014g0057others(3): Show | 6 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1615-140delA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr7 | 107699927 | |||||
chr7:107699927
|
CAA | C | 19 | a0001c0001t0001g0230a0001c0001t0002g0026a0001c0001t0002g0027others(16): Show | 19 | HG00280.hp2 HG00323.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1615-141_1615-140d others(4): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr7 | 107699927 | |||||
chr7:107699927
|
CAAA | C | 286 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(283): Show | 290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.1615-142_1615-140d others(5): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr7 | 107699927 | |||||
chr7:107699930
|
A | C | 1 | a0001c0001t0002g0165 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1615-153A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107699930 | ||||||
chr7:107699969
|
C | A | 1 | a0001c0001t0005g0318 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1615-114C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 14/20 | chr7 | 107699969 | ||||||
chr7:107700180
|
G | A | 1 | a0001c0001t0001g0023 | 1 | NA18954.hp2 | splice_region_variant&intron_variant | LOW | c.1707+5G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 15/20 | chr7 | 107700180 | ||||||
chr7:107700251
|
G | C | 9 | a0002c0002t0013g0078a0002c0002t0018g0014a0002c0009t0024g0193others(6): Show | 9 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1707+76G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 15/20 | chr7 | 107700251 | ||||||
chr7:107700386
|
T | C | 9 | a0002c0002t0013g0078a0002c0002t0018g0014a0002c0009t0024g0193others(6): Show | 9 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1707+211T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 15/20 | chr7 | 107700386 | ||||||
chr7:107701083
|
T | A | 3 | a0001c0001t0002g0070a0001c0001t0002g0216a0001c0001t0002g0237 | 3 | HG00323.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1708-18T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 15/20 | chr7 | 107701083 | ||||||
chr7:107701670
|
A | C | 1 | a0001c0001t0003g0254 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1804-157A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 16/20 | chr7 | 107701670 | ||||||
chr7:107701740
|
T | G | 2 | a0002c0002t0014g0356a0002c0002t0014g0357 | 2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1804-87T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 16/20 | chr7 | 107701740 | ||||||
chr7:107701821
|
G | A | 1 | a0001c0001t0002g0309 | 1 | HG02056.hp2 | splice_region_variant&intron_variant | LOW | c.1804-6G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 16/20 | chr7 | 107701821 | ||||||
chr7:107702110
|
T | C | 2 | a0002c0009t0024g0193a0002c0009t0025g0316 | 2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.2034+53T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107702110 | ||||||
chr7:107702189
|
G | A | 4 | a0003c0003t0003g0016a0003c0003t0003g0021a0003c0003t0003g0173others(1): Show | 4 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2034+132G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107702189 | ||||||
chr7:107702224
|
C | G | 2 | a0002c0002t0014g0356a0002c0002t0014g0357 | 2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2034+167C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107702224 | ||||||
chr7:107702430
|
G | A | 2 | a0002c0002t0018g0014a0013c0015t0018g0184 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2034+373G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107702430 | ||||||
chr7:107702445
|
A | G | 1 | a0003c0003t0003g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2034+388A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107702445 | ||||||
chr7:107702518
|
C | T | 1 | a0001c0001t0003g0190 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2034+461C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107702518 | ||||||
chr7:107702642
|
G | A | 2 | a0002c0002t0014g0356a0002c0002t0014g0357 | 2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2034+585G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107702642 | ||||||
chr7:107702684
|
C | CA | 183 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(180): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.2034+645dupA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr7 | 107702684 | |||||
chr7:107702807
|
C | A | 3 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316 | 3 | HG01074.hp2 HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2034+750C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107702807 | ||||||
chr7:107702871
|
G | T | 1 | a0004c0004t0009g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2034+814G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107702871 | ||||||
chr7:107702943
|
G | A | 5 | a0002c0002t0013g0078a0002c0002t0018g0014a0002c0009t0024g0193others(2): Show | 5 | HG01074.hp2 HG01891.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.2034+886G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107702943 | ||||||
chr7:107703095
|
T | A | 1 | a0001c0001t0027g0139 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2034+1038T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107703095 | ||||||
chr7:107703164
|
T | C | 3 | a0003c0003t0003g0016a0003c0003t0003g0173a0003c0003t0003g0174 | 3 | HG02922.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2034+1107T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107703164 | ||||||
chr7:107703317
|
C | G | 101 | a0001c0001t0001g0230a0001c0001t0001g0264a0001c0001t0001g0289others(98): Show | 103 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.2035-1014C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107703317 | ||||||
chr7:107703327
|
A | T | 1 | a0013c0015t0018g0184 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2035-1004A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107703327 | ||||||
chr7:107703410
|
G | A | 1 | a0001c0001t0002g0313 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2035-921G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107703410 | ||||||
chr7:107703469
|
C | G | 2 | a0002c0009t0024g0193a0002c0009t0025g0316 | 2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.2035-862C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107703469 | ||||||
chr7:107703490
|
G | T | 1 | a0001c0001t0002g0315 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2035-841G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107703490 | ||||||
chr7:107703509
|
T | A | 360 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(357): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.2035-822T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107703509 | ||||||
chr7:107703564
|
A | G | 4 | a0006c0008t0014g0057a0006c0008t0030g0036a0007c0010t0003g0177others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2035-767A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107703564 | ||||||
chr7:107703588
|
A | G | 180 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(177): Show | 181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.2035-743A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107703588 | ||||||
chr7:107703753
|
A | G | 1 | a0002c0002t0013g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2035-578A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107703753 | ||||||
chr7:107703771
|
C | T | 177 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(174): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.2035-560C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107703771 | ||||||
chr7:107703772
|
T | C | 314 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(311): Show | 318 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.2035-559T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107703772 | ||||||
chr7:107704109
|
T | C | 2 | a0002c0002t0018g0014a0013c0015t0018g0184 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2035-222T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107704109 | ||||||
chr7:107704121
|
C | T | 181 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(178): Show | 182 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.2035-210C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 17/20 | chr7 | 107704121 | ||||||
chr7:107704508
|
T | C | 2 | a0002c0002t0018g0014a0013c0015t0018g0184 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2089+123T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107704508 | ||||||
chr7:107704539
|
C | T | 1 | a0001c0001t0006g0272 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2089+154C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107704539 | ||||||
chr7:107704563
|
T | C | 1 | a0002c0002t0013g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2089+178T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107704563 | ||||||
chr7:107704720
|
A | T | 4 | a0001c0001t0009g0062a0004c0004t0009g0007a0004c0004t0009g0018others(1): Show | 4 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089+335A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107704720 | ||||||
chr7:107704739
|
C | A | 2 | a0001c0001t0001g0148a0001c0001t0005g0141 | 2 | NA18983.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2089+354C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107704739 | ||||||
chr7:107704806
|
T | C | 3 | a0001c0001t0003g0253a0008c0007t0003g0308a0008c0007t0003g0355 | 3 | HG02698.hp2 HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.2089+421T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107704806 | ||||||
chr7:107704946
|
C | T | 1 | a0001c0001t0002g0327 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2089+561C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107704946 | ||||||
chr7:107704947
|
G | A | 196 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(193): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.2089+562G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107704947 | ||||||
chr7:107705001
|
G | A | 1 | a0001c0001t0007g0181 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2089+616G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107705001 | ||||||
chr7:107705341
|
G | A | 2 | a0001c0001t0002g0001a0005c0005t0002g0156 | 3 | HG03491.hp1 HG03492.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.2089+956G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107705341 | ||||||
chr7:107705642
|
G | GT | 200 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(197): Show | 201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.2089+1259dupT | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr7 | 107705642 | |||||
chr7:107705765
|
C | A | 9 | a0002c0002t0013g0078a0002c0002t0018g0014a0002c0009t0024g0193others(6): Show | 9 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2089+1380C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107705765 | ||||||
chr7:107705825
|
C | T | 2 | a0002c0009t0024g0193a0002c0009t0025g0316 | 2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.2089+1440C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107705825 | ||||||
chr7:107705946
|
T | C | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2089+1561T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107705946 | ||||||
chr7:107705997
|
A | G | 1 | a0001c0001t0009g0187 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2089+1612A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107705997 | ||||||
chr7:107706086
|
T | C | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2089+1701T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706086 | ||||||
chr7:107706091
|
C | T | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2089+1706C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706091 | ||||||
chr7:107706180
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2089+1795C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706180 | ||||||
chr7:107706217
|
G | A | 3 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316 | 3 | HG01074.hp2 HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2089+1832G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706217 | ||||||
chr7:107706305
|
T | A | 11 | a0002c0002t0013g0078a0002c0002t0014g0356a0002c0002t0014g0357others(8): Show | 11 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2089+1920T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706305 | ||||||
chr7:107706314
|
A | G | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2089+1929A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706314 | ||||||
chr7:107706329
|
G | T | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2089+1944G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706329 | ||||||
chr7:107706477
|
A | C | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2089+2092A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706477 | ||||||
chr7:107706512
|
T | C | 1 | a0002c0002t0013g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2089+2127T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706512 | ||||||
chr7:107706597
|
C | T | 3 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316 | 3 | HG01074.hp2 HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2089+2212C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706597 | ||||||
chr7:107706608
|
G | C | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2089+2223G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706608 | ||||||
chr7:107706629
|
T | C | 2 | a0002c0002t0018g0014a0013c0015t0018g0184 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2089+2244T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706629 | ||||||
chr7:107706645
|
C | T | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2089+2260C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706645 | ||||||
chr7:107706669
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2089+2284C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706669 | ||||||
chr7:107706752
|
C | CT | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2089+2368dupT | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr7 | 107706752 | |||||
chr7:107706795
|
G | C | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2089+2410G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706795 | ||||||
chr7:107706804
|
C | T | 4 | a0006c0008t0014g0057a0006c0008t0030g0036a0007c0010t0003g0177others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2089+2419C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706804 | ||||||
chr7:107706805
|
A | G | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2089+2420A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706805 | ||||||
chr7:107706907
|
C | T | 5 | a0001c0001t0003g0176a0001c0001t0007g0196a0001c0001t0016g0095others(2): Show | 5 | HG01433.hp2 HG02615.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.2089+2522C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107706907 | ||||||
chr7:107707019
|
A | T | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0160others(1): Show | 4 | HG03225.hp2 HG03540.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2089+2634A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707019 | ||||||
chr7:107707154
|
T | C | 3 | a0005c0005t0002g0156a0007c0010t0003g0177a0007c0010t0005g0180 | 3 | HG02559.hp2 HG02723.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.2089+2769T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707154 | ||||||
chr7:107707158
|
C | G | 1 | a0002c0002t0013g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2089+2773C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707158 | ||||||
chr7:107707338
|
T | C | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-2716T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707338 | ||||||
chr7:107707349
|
C | A | 1 | a0001c0001t0001g0353 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2090-2705C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707349 | ||||||
chr7:107707351
|
A | T | 196 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(193): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.2090-2703A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707351 | ||||||
chr7:107707417
|
A | T | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-2637A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707417 | ||||||
chr7:107707456
|
C | T | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-2598C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707456 | ||||||
chr7:107707522
|
T | A | 6 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0136others(3): Show | 6 | HG01891.hp1 HG02451.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2090-2532T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707522 | ||||||
chr7:107707544
|
G | A | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-2510G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707544 | ||||||
chr7:107707605
|
A | G | 2 | a0002c0009t0024g0193a0002c0009t0025g0316 | 2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.2090-2449A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707605 | ||||||
chr7:107707617
|
A | G | 1 | a0001c0001t0002g0309 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2090-2437A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707617 | ||||||
chr7:107707659
|
G | A | 3 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316 | 3 | HG01074.hp2 HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2090-2395G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707659 | ||||||
chr7:107707789
|
C | T | 2 | a0002c0009t0024g0193a0002c0009t0025g0316 | 2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.2090-2265C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707789 | ||||||
chr7:107707793
|
T | C | 2 | a0001c0001t0002g0100a0001c0001t0002g0154 | 2 | HG00558.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.2090-2261T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707793 | ||||||
chr7:107707875
|
G | T | 2 | a0002c0002t0014g0356a0002c0002t0014g0357 | 2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2090-2179G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707875 | ||||||
chr7:107707927
|
C | A | 202 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(199): Show | 203 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.2090-2127C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707927 | ||||||
chr7:107707963
|
A | G | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-2091A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107707963 | ||||||
chr7:107708053
|
A | G | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-2001A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708053 | ||||||
chr7:107708233
|
A | G | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-1821A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708233 | ||||||
chr7:107708283
|
G | T | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-1771G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708283 | ||||||
chr7:107708310
|
G | A | 2 | a0002c0002t0014g0356a0002c0002t0014g0357 | 2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2090-1744G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708310 | ||||||
chr7:107708315
|
G | T | 2 | a0001c0001t0008g0138a0001c0001t0021g0359 | 2 | HG01243.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2090-1739G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708315 | ||||||
chr7:107708419
|
A | C | 4 | a0001c0001t0001g0059a0001c0001t0001g0225a0001c0001t0001g0260others(1): Show | 4 | NA18960.hp1 NA18977.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.2090-1635A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708419 | ||||||
chr7:107708445
|
T | C | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-1609T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708445 | ||||||
chr7:107708555
|
T | A | 11 | a0002c0002t0013g0078a0002c0002t0014g0356a0002c0002t0014g0357others(8): Show | 11 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2090-1499T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708555 | ||||||
chr7:107708682
|
C | T | 1 | a0001c0001t0002g0100 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2090-1372C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708682 | ||||||
chr7:107708685
|
C | G | 4 | a0001c0001t0003g0176a0001c0001t0007g0196a0001c0001t0016g0095others(1): Show | 4 | HG01433.hp2 HG02615.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2090-1369C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708685 | ||||||
chr7:107708702
|
T | A | 5 | a0001c0001t0001g0025a0001c0001t0001g0082a0001c0001t0001g0185others(2): Show | 5 | HG02896.hp2 HG03041.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2090-1352T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708702 | ||||||
chr7:107708702
|
TA | T | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-1346delA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr7 | 107708702 | |||||
chr7:107708703
|
A | T | 5 | a0001c0001t0003g0253a0001c0001t0003g0271a0001c0001t0003g0320others(2): Show | 5 | HG01884.hp1 HG02698.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.2090-1351A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708703 | ||||||
chr7:107708704
|
A | T | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-1350A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708704 | ||||||
chr7:107708827
|
A | G | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-1227A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708827 | ||||||
chr7:107708840
|
G | T | 183 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(180): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.2090-1214G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708840 | ||||||
chr7:107708847
|
G | A | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-1207G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708847 | ||||||
chr7:107708953
|
G | A | 2 | a0002c0002t0014g0356a0002c0002t0014g0357 | 2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2090-1101G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708953 | ||||||
chr7:107708958
|
T | G | 1 | a0001c0001t0001g0220 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2090-1096T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708958 | ||||||
chr7:107708974
|
G | T | 1 | a0001c0001t0001g0043 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2090-1080G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107708974 | ||||||
chr7:107709018
|
C | T | 4 | a0001c0001t0002g0005a0001c0001t0002g0275a0001c0001t0002g0279others(1): Show | 4 | HG00544.hp2 HG02071.hp2 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.2090-1036C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107709018 | ||||||
chr7:107709027
|
G | A | 4 | a0001c0001t0009g0062a0004c0004t0009g0007a0004c0004t0009g0018others(1): Show | 4 | HG02818.hp2 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2090-1027G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107709027 | ||||||
chr7:107709035
|
A | G | 1 | a0001c0001t0002g0106 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2090-1019A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107709035 | ||||||
chr7:107709147
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0114 | 2 | HG00597.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.2090-907C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107709147 | ||||||
chr7:107709282
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2090-772T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107709282 | ||||||
chr7:107709582
|
G | T | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-472G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107709582 | ||||||
chr7:107709661
|
G | A | 2 | a0001c0001t0002g0285a0001c0001t0002g0340 | 2 | NA18977.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.2090-393G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107709661 | ||||||
chr7:107709678
|
C | T | 1 | a0001c0001t0002g0327 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2090-376C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107709678 | ||||||
chr7:107709720
|
T | C | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-334T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107709720 | ||||||
chr7:107709858
|
G | T | 2 | a0002c0002t0014g0356a0002c0002t0014g0357 | 2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2090-196G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107709858 | ||||||
chr7:107709868
|
GC | G | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-183delC | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr7 | 107709868 | |||||
chr7:107709900
|
G | A | 2 | a0002c0002t0018g0014a0013c0015t0018g0184 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2090-154G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107709900 | ||||||
chr7:107709944
|
A | C | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2090-110A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107709944 | ||||||
chr7:107709994
|
A | AAAAC | 14 | a0001c0001t0027g0139a0002c0002t0013g0078a0002c0002t0014g0356others(11): Show | 14 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2090-52_2090-49dup others(4): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr7 | 107709994 | |||||
chr7:107710047
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG03540.hp1 | splice_region_variant&intron_variant | LOW | c.2090-7T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 18/20 | chr7 | 107710047 | ||||||
chr7:107710328
|
G | GT | 7 | a0002c0002t0013g0078a0002c0009t0024g0193a0002c0009t0025g0316others(4): Show | 7 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2235+135dupT | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr7 | 107710328 | |||||
chr7:107710353
|
A | G | 2 | a0002c0002t0014g0356a0002c0002t0014g0357 | 2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2235+154A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107710353 | ||||||
chr7:107710505
|
C | T | 2 | a0002c0002t0014g0356a0002c0002t0014g0357 | 2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2235+306C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107710505 | ||||||
chr7:107710587
|
G | A | 1 | a0004c0004t0009g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2235+388G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107710587 | ||||||
chr7:107710645
|
A | G | 1 | a0001c0001t0002g0325 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2235+446A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107710645 | ||||||
chr7:107710666
|
T | A | 1 | a0001c0001t0027g0139 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2235+467T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107710666 | ||||||
chr7:107710719
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0360 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2235+520A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107710719 | ||||||
chr7:107710890
|
A | G | 1 | a0001c0001t0001g0297 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2235+691A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107710890 | ||||||
chr7:107710978
|
G | A | 6 | a0002c0009t0024g0193a0002c0009t0025g0316a0006c0008t0014g0057others(3): Show | 6 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.2235+779G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107710978 | ||||||
chr7:107711073
|
GGA | G | 4 | a0001c0001t0003g0176a0001c0001t0007g0196a0001c0001t0016g0095others(1): Show | 4 | HG01433.hp2 HG02615.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2235+879_2235+880d others(4): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr7 | 107711073 | |||||
chr7:107711152
|
GA | G | 8 | a0001c0001t0001g0017a0001c0001t0001g0145a0001c0001t0001g0150others(5): Show | 8 | HG02055.hp1 HG02559.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2235+965delA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr7 | 107711152 | |||||
chr7:107711436
|
A | G | 1 | a0001c0001t0004g0162 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2236-1103A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107711436 | ||||||
chr7:107711503
|
G | A | 1 | a0001c0001t0002g0055 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2236-1036G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107711503 | ||||||
chr7:107711672
|
G | A | 98 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(95): Show | 100 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.2236-867G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107711672 | ||||||
chr7:107711766
|
G | T | 3 | a0001c0001t0001g0072a0001c0001t0001g0092a0001c0001t0001g0199 | 3 | HG00408.hp1 NA18957.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.2236-773G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107711766 | ||||||
chr7:107711784
|
C | G | 1 | a0001c0001t0016g0095 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2236-755C>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107711784 | ||||||
chr7:107711954
|
T | G | 1 | a0001c0001t0001g0120 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2236-585T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107711954 | ||||||
chr7:107712010
|
T | A | 1 | a0001c0001t0001g0336 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2236-529T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107712010 | ||||||
chr7:107712112
|
T | G | 1 | a0001c0001t0007g0196 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2236-427T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107712112 | ||||||
chr7:107712193
|
G | C | 1 | a0001c0001t0031g0172 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2236-346G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107712193 | ||||||
chr7:107712374
|
T | C | 2 | a0002c0009t0024g0193a0002c0009t0025g0316 | 2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.2236-165T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107712374 | ||||||
chr7:107712388
|
G | T | 6 | a0002c0009t0024g0193a0002c0009t0025g0316a0006c0008t0014g0057others(3): Show | 6 | HG01074.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.2236-151G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 19/20 | chr7 | 107712388 | ||||||
chr7:107712683
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2319+61C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107712683 | ||||||
chr7:107713159
|
G | A | 9 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(6): Show | 9 | HG00544.hp1 HG00621.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.2319+537G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107713159 | ||||||
chr7:107713367
|
T | A | 4 | a0003c0003t0003g0016a0003c0003t0003g0021a0003c0003t0003g0173others(1): Show | 4 | HG02922.hp2 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2319+745T>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107713367 | ||||||
chr7:107713569
|
G | A | 2 | a0002c0009t0024g0193a0002c0009t0025g0316 | 2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.2319+947G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107713569 | ||||||
chr7:107713588
|
C | T | 191 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(188): Show | 192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.2319+966C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107713588 | ||||||
chr7:107713638
|
C | T | 4 | a0006c0008t0014g0057a0006c0008t0030g0036a0007c0010t0003g0177others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2319+1016C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107713638 | ||||||
chr7:107713640
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2319+1018A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107713640 | ||||||
chr7:107713688
|
A | G | 2 | a0002c0009t0024g0193a0002c0009t0025g0316 | 2 | HG01074.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.2319+1066A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107713688 | ||||||
chr7:107713909
|
G | T | 1 | a0001c0001t0001g0195 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2319+1287G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107713909 | ||||||
chr7:107713909
|
GTAT | G | 202 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(199): Show | 203 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.2319+1307_2319+130 others(7): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107713909 | |||||
chr7:107714005
|
C | T | 1 | a0001c0001t0002g0327 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2319+1383C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107714005 | ||||||
chr7:107714085
|
AT | A | 328 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(325): Show | 333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.2320-1326delT | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107714085 | |||||
chr7:107714275
|
G | A | 4 | a0001c0001t0001g0252a0001c0001t0003g0256a0001c0001t0003g0257others(1): Show | 4 | HG01167.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.2320-1148G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107714275 | ||||||
chr7:107714430
|
G | C | 1 | a0001c0001t0001g0121 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2320-993G>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107714430 | ||||||
chr7:107714471
|
G | A | 1 | a0001c0001t0012g0288 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2320-952G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107714471 | ||||||
chr7:107714568
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2320-855C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107714568 | ||||||
chr7:107714626
|
G | A | 1 | a0001c0001t0001g0035 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2320-797G>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107714626 | ||||||
chr7:107714902
|
C | A | 1 | a0001c0001t0012g0276 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2320-521C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107714902 | ||||||
chr7:107715066
|
T | TA | 9 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0169others(6): Show | 9 | HG00140.hp2 HG00621.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.2320-338dupA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107715066 | |||||
chr7:107715066
|
T | TAAA | 8 | a0001c0001t0003g0096a0001c0001t0003g0176a0003c0003t0003g0016others(5): Show | 8 | HG02559.hp2 HG02723.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.2320-340_2320-338d others(5): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107715066 | |||||
chr7:107715066
|
T | TAAAAAAA others(6): Show |
5 | a0001c0001t0002g0291a0001c0001t0007g0181a0001c0001t0007g0342others(2): Show | 5 | HG02015.hp1 HG03195.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2320-350_2320-338d others(15): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107715066 | |||||
chr7:107715066
|
T | TAAAAAAA others(7): Show |
39 | a0001c0001t0002g0001a0001c0001t0002g0026a0001c0001t0002g0027others(36): Show | 40 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.2320-351_2320-338d others(16): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107715066 | |||||
chr7:107715066
|
T | TAAAAAAA others(8): Show |
26 | a0001c0001t0002g0077a0001c0001t0002g0086a0001c0001t0002g0098others(23): Show | 26 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.2320-352_2320-338d others(17): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107715066 | |||||
chr7:107715066
|
T | TAAAAAAA others(9): Show |
7 | a0001c0001t0002g0005a0001c0001t0002g0075a0001c0001t0002g0263others(4): Show | 7 | HG00544.hp2 HG04184.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.2320-353_2320-338d others(18): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107715066 | |||||
chr7:107715066
|
T | TAAAAAAA others(10): Show |
3 | a0001c0001t0002g0275a0001c0001t0004g0238a0001c0001t0004g0259 | 3 | HG02071.hp2 NA18939.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.2320-354_2320-338d others(19): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107715066 | |||||
chr7:107715066
|
T | TAAAAAAA others(11): Show |
8 | a0001c0001t0002g0024a0001c0001t0002g0119a0001c0001t0002g0165others(5): Show | 8 | HG01070.hp1 HG01993.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.2320-355_2320-338d others(20): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107715066 | |||||
chr7:107715066
|
T | TAAAAAAA others(12): Show |
10 | a0001c0001t0002g0006a0001c0001t0002g0067a0001c0001t0002g0170others(7): Show | 11 | HG01255.hp2 HG01978.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.2320-356_2320-338d others(21): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107715066 | |||||
chr7:107715066
|
T | TAAAAAAA others(13): Show |
3 | a0001c0001t0004g0269a0001c0001t0004g0311a0012c0018t0002g0028 | 3 | NA18980.hp1 NA18987.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.2320-338_2320-337i others(22): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107715066 | |||||
chr7:107715066
|
T | TAAAAAAA others(14): Show |
1 | a0001c0001t0002g0073 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2320-338_2320-337i others(23): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107715066 | |||||
chr7:107715066
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TA | T | 7 | a0001c0001t0001g0117a0001c0001t0001g0243a0001c0001t0006g0088others(4): Show | 8 | HG01081.hp2 HG01993.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.2320-338delA | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107715066 | |||||
chr7:107715237
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C | A | 1 | a0001c0001t0001g0035 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2320-186C>A | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715237 | ||||||
chr7:107715237
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C | CAA | 15 | a0001c0001t0009g0062a0001c0001t0009g0187a0001c0001t0010g0002others(12): Show | 16 | HG01074.hp2 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2320-173_2320-172d others(4): Show |
SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr7 | 107715237 | |||||
chr7:107715300
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T | C | 2 | a0002c0002t0018g0014a0013c0015t0018g0184 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2320-123T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715300 | ||||||
chr7:107715312
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A | T | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-111A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715312 | ||||||
chr7:107715314
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G | T | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-109G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715314 | ||||||
chr7:107715315
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A | T | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-108A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715315 | ||||||
chr7:107715316
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G | T | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-107G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715316 | ||||||
chr7:107715319
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G | T | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-104G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715319 | ||||||
chr7:107715321
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A | T | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-102A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715321 | ||||||
chr7:107715322
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G | T | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-101G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715322 | ||||||
chr7:107715324
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A | T | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-99A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715324 | ||||||
chr7:107715325
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A | T | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-98A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715325 | ||||||
chr7:107715326
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G | T | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-97G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715326 | ||||||
chr7:107715331
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C | T | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-92C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715331 | ||||||
chr7:107715332
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A | T | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-91A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715332 | ||||||
chr7:107715333
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A | T | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-90A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715333 | ||||||
chr7:107715335
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A | T | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-88A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715335 | ||||||
chr7:107715340
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A | T | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-83A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715340 | ||||||
chr7:107715341
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A | C | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-82A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715341 | ||||||
chr7:107715342
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A | T | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-81A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715342 | ||||||
chr7:107715344
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A | G | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-79A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715344 | ||||||
chr7:107715345
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C | T | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-78C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715345 | ||||||
chr7:107715346
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A | T | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-77A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715346 | ||||||
chr7:107715348
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A | T | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-75A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715348 | ||||||
chr7:107715351
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T | G | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-72T>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715351 | ||||||
chr7:107715352
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A | G | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-71A>G | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715352 | ||||||
chr7:107715354
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A | C | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-69A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715354 | ||||||
chr7:107715355
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A | T | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-68A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715355 | ||||||
chr7:107715356
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A | T | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-67A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715356 | ||||||
chr7:107715357
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A | C | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-66A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715357 | ||||||
chr7:107715358
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A | T | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-65A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715358 | ||||||
chr7:107715360
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G | T | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-63G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715360 | ||||||
chr7:107715361
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A | C | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-62A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715361 | ||||||
chr7:107715363
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A | T | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-60A>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715363 | ||||||
chr7:107715364
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A | C | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-59A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715364 | ||||||
chr7:107715366
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G | T | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-57G>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715366 | ||||||
chr7:107715367
|
C | T | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-56C>T | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715367 | ||||||
chr7:107715370
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A | C | 1 | a0001c0001t0002g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2320-53A>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715370 | ||||||
chr7:107715401
|
T | C | 3 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0005g0332 | 3 | HG00140.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2320-22T>C | SLC26A4 | ENSG00000091137.14 | transcript | ENST00000644269.2 | protein_coding | 20/20 | chr7 | 107715401 |