| geneid | 116369 |
|---|---|
| ensemblid | ENSG00000112053.14 |
| hgncid | 14468 |
| symbol | SLC26A8 |
| name | solute carrier family 26 member 8 |
| refseq_nuc | NM_052961.4 |
| refseq_prot | NP_443193.1 |
| ensembl_nuc | ENST00000490799.6 |
| ensembl_prot | ENSP00000417638.1 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 35943516 |
| end | 36024641 |
| strand | - |
| ver | v1.2 |
| region | chr6:35943516-36024641 |
| region5000 | chr6:35938516-36029641 |
| regionname0 | SLC26A8_chr6_35943516_36024641 |
| regionname5000 | SLC26A8_chr6_35938516_36029641 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 970 | 117 | 13 | 23 | 61 | 6 | 12 | 45 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0002 | 0/0 | 970 | 74 | 25 | 12 | 31 | 1 | 5 | 25 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0003 | 0/0 | 970 | 34 | 21 | 6 | 4 | 1 | 2 | 4 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0004 | 0/0 | 970 | 19 | 9 | 2 | 8 | 0 | 0 | 6 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0005 | 0/0 | 970 | 19 | 6 | 3 | 7 | 0 | 3 | 6 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0006 | 0/0 | 970 | 18 | 0 | 11 | 4 | 3 | 0 | 4 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0007 | 0/0 | 970 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0008 | 0/0 | 970 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0009 | 0/0 | 970 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0010 | 0/0 | 970 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0011 | 0/0 | 970 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0012 | 0/0 | 970 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0013 | 0/0 | 970 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0014 | 0/0 | 970 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0015 | 0/0 | 970 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0016 | 0/0 | 970 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0017 | 0/0 | 970 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0018 | 0/0 | 970 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0019 | 0/0 | 970 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0020 | 0/0 | 970 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0021 | 0/0 | 970 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2913 | 117 | 13 | 23 | 61 | 6 | 12 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0002 | 0/0 | 2913 | 66 | 17 | 12 | 31 | 1 | 5 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0003 | 0/0 | 2913 | 32 | 19 | 6 | 4 | 1 | 2 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0004 | 0/0 | 2913 | 19 | 9 | 2 | 8 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0005 | 0/0 | 2913 | 18 | 5 | 3 | 7 | 0 | 3 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0006 | 0/0 | 2913 | 17 | 0 | 10 | 4 | 3 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0007 | 0/0 | 2913 | 5 | 5 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0008 | 0/0 | 2913 | 4 | 4 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0009 | 0/0 | 2913 | 3 | 2 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0010 | 0/0 | 2913 | 3 | 3 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0011 | 0/0 | 2913 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0012 | 0/0 | 2913 | 2 | 0 | 2 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0013 | 0/0 | 2913 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0014 | 0/0 | 2913 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0015 | 0/0 | 2913 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0016 | 0/0 | 2913 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0017 | 0/0 | 2913 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0018 | 0/0 | 2913 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0019 | 0/0 | 2913 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0020 | 0/0 | 2913 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0021 | 0/0 | 2913 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0022 | 0/0 | 2913 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0023 | 0/0 | 2913 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0024 | 0/0 | 2913 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0025 | 0/0 | 2913 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0026 | 0/0 | 2913 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0027 | 0/0 | 2913 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0028 | 0/0 | 2913 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| c0029 | 0/0 | 2913 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 525 | 182 | 59 | 39 | 56 | 11 | 15 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| t0002 | 0/0 | 525 | 120 | 29 | 23 | 58 | 1 | 9 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| t0003 | 0/0 | 525 | 2 | 0 | 0 | 2 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| t0004 | 0/0 | 525 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| t0005 | 0/0 | 525 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0048 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2913 | 117 | 13 | 23 | 61 | 6 | 12 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0002c0002 | 0/0 | 2913 | 66 | 17 | 12 | 31 | 1 | 5 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0002c0010 | 0/0 | 2913 | 3 | 3 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0002c0011 | 0/0 | 2913 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0002c0013 | 0/0 | 2913 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0002c0025 | 0/0 | 2913 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0003c0003 | 0/0 | 2913 | 32 | 19 | 6 | 4 | 1 | 2 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0003c0015 | 0/0 | 2913 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0003c0016 | 0/0 | 2913 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0004c0004 | 0/0 | 2913 | 19 | 9 | 2 | 8 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0005c0005 | 0/0 | 2913 | 18 | 5 | 3 | 7 | 0 | 3 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0005c0020 | 0/0 | 2913 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0006c0006 | 0/0 | 2913 | 17 | 0 | 10 | 4 | 3 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0006c0018 | 0/0 | 2913 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0007c0007 | 0/0 | 2913 | 5 | 5 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0008c0008 | 0/0 | 2913 | 4 | 4 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0009c0009 | 0/0 | 2913 | 3 | 2 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0010c0012 | 0/0 | 2913 | 2 | 0 | 2 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0011c0014 | 0/0 | 2913 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0012c0017 | 0/0 | 2913 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0013c0019 | 0/0 | 2913 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0014c0021 | 0/0 | 2913 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0015c0028 | 0/0 | 2913 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0016c0024 | 0/0 | 2913 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0017c0023 | 0/0 | 2913 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0018c0026 | 0/0 | 2913 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0019c0027 | 0/0 | 2913 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0020c0029 | 0/0 | 2913 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0021c0022 | 0/0 | 2913 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3437 | 37 | 3 | 7 | 15 | 5 | 5 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0001c0001t0002 | 0/0 | 3437 | 80 | 10 | 16 | 46 | 1 | 7 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0002c0002t0001 | 0/0 | 3437 | 48 | 8 | 10 | 24 | 1 | 5 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0002c0002t0002 | 0/0 | 3437 | 17 | 8 | 2 | 7 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0002c0002t0004 | 0/0 | 3437 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0002c0010t0001 | 0/0 | 3437 | 3 | 3 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0002c0011t0001 | 0/0 | 3437 | 2 | 2 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0002c0013t0001 | 0/0 | 3437 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0002c0013t0002 | 0/0 | 3437 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0002c0025t0002 | 0/0 | 3437 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0003c0003t0001 | 0/0 | 3437 | 23 | 16 | 6 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0003c0003t0002 | 0/0 | 3437 | 9 | 3 | 0 | 4 | 0 | 2 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0003c0015t0001 | 0/0 | 3437 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0003c0016t0005 | 0/0 | 3437 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0004c0004t0001 | 0/0 | 3437 | 19 | 9 | 2 | 8 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0005c0005t0001 | 0/0 | 3437 | 15 | 5 | 2 | 5 | 0 | 3 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0005c0005t0002 | 0/0 | 3437 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0005c0005t0003 | 0/0 | 3437 | 2 | 0 | 0 | 2 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0005c0020t0002 | 0/0 | 3437 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0006c0006t0001 | 0/0 | 3437 | 14 | 0 | 7 | 4 | 3 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0006c0006t0002 | 0/0 | 3437 | 3 | 0 | 3 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0006c0018t0002 | 0/0 | 3437 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0007c0007t0002 | 0/0 | 3437 | 5 | 5 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0008c0008t0001 | 0/0 | 3437 | 4 | 4 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0009c0009t0001 | 0/0 | 3437 | 3 | 2 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0010c0012t0001 | 0/0 | 3437 | 2 | 0 | 2 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0011c0014t0001 | 0/0 | 3437 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0012c0017t0001 | 0/0 | 3437 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0013c0019t0001 | 0/0 | 3437 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0014c0021t0001 | 0/0 | 3437 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0015c0028t0002 | 0/0 | 3437 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0016c0024t0001 | 0/0 | 3437 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0017c0023t0001 | 0/0 | 3437 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0018c0026t0001 | 0/0 | 3437 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0019c0027t0001 | 0/0 | 3437 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0020c0029t0001 | 0/0 | 3437 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| a0021c0022t0001 | 0/0 | 3437 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | copy fasta | chr6 | 35938516 | 36029641 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0048 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0001c0001t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0002t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0010t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0010t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0010t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0011t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0011t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0013t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0013t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0002c0025t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0003t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0015t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0003c0016t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0004c0004t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0004c0004t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0004c0004t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0004c0004t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0004c0004t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0004c0004t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0004c0004t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0004c0004t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0004c0004t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0004c0004t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0004c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0004c0004t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0004c0004t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0004c0004t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0004c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0004c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0004c0004t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0004c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0004c0004t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0005c0005t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0005c0005t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0005c0005t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0005c0005t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0005c0005t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0005c0005t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0005c0005t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0005c0005t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0005c0005t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0005c0005t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0005c0005t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0005c0005t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0005c0005t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0005c0005t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0005c0005t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0005c0005t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0005c0005t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0005c0005t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0005c0020t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0006c0006t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0006c0006t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0006c0006t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0006c0006t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0006c0006t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0006c0006t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0006c0006t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0006c0006t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0006c0006t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0006c0006t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0006c0006t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0006c0006t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0006c0006t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0006c0006t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0006c0006t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0006c0006t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0006c0006t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0006c0018t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0007c0007t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0007c0007t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0007c0007t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0007c0007t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0007c0007t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0008c0008t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0008c0008t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0008c0008t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0008c0008t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0009c0009t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0009c0009t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0009c0009t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0010c0012t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0010c0012t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0011c0014t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0012c0017t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0013c0019t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0014c0021t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0015c0028t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0016c0024t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0017c0023t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0018c0026t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0019c0027t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0020c0029t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| a0021c0022t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0006 | c0006 | t0001 | g0180 | EUR | GBR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0138 | EUR | GBR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | FIN | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG00280 | hp2 | a0006 | c0006 | t0001 | g0181 | EUR | FIN | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | FIN | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0191 | EUR | FIN | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | CHS | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG00597 | hp2 | a0004 | c0004 | t0001 | g0151 | EAS | CHS | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | CHS | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG00621 | hp2 | a0004 | c0004 | t0001 | g0096 | EAS | CHS | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0111 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG00639 | hp2 | a0006 | c0006 | t0001 | g0175 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG00642 | hp1 | a0006 | c0006 | t0001 | g0157 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG00642 | hp2 | a0003 | c0003 | t0001 | g0052 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | CHS | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | CHS | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG00733 | hp1 | a0004 | c0004 | t0001 | g0016 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0120 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG00738 | hp2 | a0006 | c0006 | t0001 | g0174 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG00741 | hp1 | a0003 | c0003 | t0001 | g0031 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01070 | hp1 | a0006 | c0006 | t0001 | g0140 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01070 | hp2 | a0005 | c0005 | t0001 | g0182 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01081 | hp2 | a0005 | c0005 | t0001 | g0176 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01099 | hp1 | a0003 | c0003 | t0001 | g0028 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01099 | hp2 | a0006 | c0006 | t0001 | g0171 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0077 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0197 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0069 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01168 | hp1 | a0006 | c0006 | t0002 | g0255 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0073 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01169 | hp1 | a0006 | c0006 | t0002 | g0256 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0070 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0078 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01175 | hp2 | a0003 | c0003 | t0001 | g0027 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01255 | hp1 | a0006 | c0006 | t0001 | g0158 | AMR | CLM | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01255 | hp2 | a0017 | c0023 | t0001 | g0020 | AMR | CLM | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0071 | AMR | CLM | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01256 | hp2 | a0010 | c0012 | t0001 | g0049 | AMR | CLM | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0268 | AMR | CLM | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01258 | hp2 | a0010 | c0012 | t0001 | g0068 | AMR | CLM | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | CLM | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01358 | hp1 | a0006 | c0006 | t0001 | g0159 | AMR | CLM | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | CLM | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01361 | hp1 | a0009 | c0009 | t0001 | g0092 | AMR | CLM | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01361 | hp2 | a0003 | c0003 | t0001 | g0030 | AMR | CLM | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0266 | AMR | CLM | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01433 | hp2 | a0004 | c0004 | t0001 | g0026 | AMR | CLM | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0270 | AMR | CLM | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01496 | hp2 | a0021 | c0022 | t0001 | g0061 | AMR | CLM | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | IBS | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | IBS | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0132 | EUR | IBS | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01516 | hp2 | a0003 | c0003 | t0001 | g0009 | EUR | IBS | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01884 | hp1 | a0002 | c0013 | t0001 | g0019 | AFR | ACB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | ACB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01891 | hp1 | a0003 | c0003 | t0001 | g0018 | AFR | ACB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | ACB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0267 | AMR | PEL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01928 | hp2 | a0003 | c0003 | t0001 | g0029 | AMR | PEL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0130 | AMR | PEL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01981 | hp2 | a0006 | c0006 | t0002 | g0249 | AMR | PEL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0259 | AMR | PEL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02004 | hp1 | a0005 | c0005 | t0002 | g0247 | AMR | PEL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | PEL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | KHV | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | KHV | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | KHV | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0155 | AFR | ACB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0251 | AFR | ACB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | KHV | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0117 | EAS | KHV | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | KHV | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0116 | EAS | KHV | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | KHV | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0296 | EAS | KHV | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | KHV | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | KHV | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02132 | hp1 | a0005 | c0005 | t0001 | g0163 | EAS | KHV | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | KHV | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02135 | hp1 | a0015 | c0028 | t0002 | g0258 | EAS | KHV | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02145 | hp1 | a0004 | c0004 | t0001 | g0004 | AFR | ACB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02145 | hp2 | a0003 | c0003 | t0001 | g0036 | AFR | ACB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0257 | AMR | PEL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0250 | EAS | CDX | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | CDX | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0198 | AFR | ACB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02257 | hp2 | a0003 | c0003 | t0001 | g0095 | AFR | ACB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0195 | AFR | ACB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02258 | hp2 | a0004 | c0004 | t0001 | g0013 | AFR | ACB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02280 | hp1 | a0014 | c0021 | t0001 | g0094 | AFR | ACB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02280 | hp2 | a0003 | c0003 | t0001 | g0045 | AFR | ACB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02300 | hp1 | a0006 | c0018 | t0002 | g0248 | AMR | PEL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0271 | AMR | PEL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02451 | hp1 | a0002 | c0013 | t0002 | g0234 | AFR | ACB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02451 | hp2 | a0007 | c0007 | t0002 | g0298 | AFR | ACB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02572 | hp1 | a0002 | c0010 | t0001 | g0063 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0041 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02615 | hp1 | a0007 | c0007 | t0002 | g0244 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02615 | hp2 | a0003 | c0003 | t0001 | g0089 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02622 | hp1 | a0005 | c0005 | t0001 | g0022 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02622 | hp2 | a0008 | c0008 | t0001 | g0042 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02630 | hp1 | a0008 | c0008 | t0001 | g0043 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02630 | hp2 | a0003 | c0003 | t0001 | g0038 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02647 | hp1 | a0008 | c0008 | t0001 | g0044 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0214 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0129 | SAS | PJL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02683 | hp2 | a0018 | c0026 | t0001 | g0127 | SAS | PJL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0119 | SAS | PJL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0072 | SAS | PJL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0211 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02717 | hp2 | a0007 | c0007 | t0002 | g0233 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02723 | hp1 | a0004 | c0004 | t0001 | g0084 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02723 | hp2 | a0004 | c0004 | t0001 | g0003 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02809 | hp1 | a0003 | c0003 | t0001 | g0008 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02809 | hp2 | a0005 | c0005 | t0001 | g0023 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02818 | hp1 | a0003 | c0003 | t0002 | g0220 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0199 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0196 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02895 | hp1 | a0002 | c0010 | t0001 | g0062 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02895 | hp2 | a0003 | c0003 | t0001 | g0005 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02896 | hp1 | a0005 | c0005 | t0001 | g0024 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02896 | hp2 | a0002 | c0011 | t0001 | g0056 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02897 | hp1 | a0003 | c0003 | t0001 | g0014 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02897 | hp2 | a0002 | c0011 | t0001 | g0058 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | ESN | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02922 | hp2 | a0002 | c0025 | t0002 | g0202 | AFR | ESN | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0057 | AFR | ESN | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02965 | hp2 | a0003 | c0003 | t0001 | g0017 | AFR | ESN | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02976 | hp1 | a0002 | c0002 | t0004 | g0184 | AFR | ESN | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0059 | AFR | ESN | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0305 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03041 | hp2 | a0004 | c0004 | t0001 | g0015 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03098 | hp1 | a0004 | c0004 | t0001 | g0012 | AFR | MSL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0231 | AFR | MSL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0200 | AFR | ESN | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03130 | hp2 | a0003 | c0003 | t0001 | g0035 | AFR | ESN | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03139 | hp1 | a0004 | c0004 | t0001 | g0010 | AFR | ESN | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03139 | hp2 | a0008 | c0008 | t0001 | g0090 | AFR | ESN | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03195 | hp1 | a0002 | c0010 | t0001 | g0064 | AFR | ESN | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | ESN | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03209 | hp1 | a0009 | c0009 | t0001 | g0093 | AFR | MSL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03209 | hp2 | a0007 | c0007 | t0002 | g0232 | AFR | MSL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03225 | hp1 | a0003 | c0003 | t0001 | g0037 | AFR | MSL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03225 | hp2 | a0003 | c0003 | t0001 | g0091 | AFR | MSL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0218 | SAS | PJL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03453 | hp1 | a0012 | c0017 | t0001 | g0025 | AFR | MSL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | MSL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03486 | hp1 | a0011 | c0014 | t0001 | g0128 | AFR | MSL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03540 | hp1 | a0004 | c0004 | t0001 | g0011 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03540 | hp2 | a0003 | c0003 | t0001 | g0002 | AFR | GWD | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03579 | hp1 | a0004 | c0004 | t0001 | g0007 | AFR | MSL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03579 | hp2 | a0003 | c0003 | t0002 | g0299 | AFR | MSL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03688 | hp1 | a0005 | c0005 | t0001 | g0169 | SAS | STU | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0190 | SAS | STU | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0131 | SAS | PJL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0153 | SAS | PJL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03710 | hp2 | a0003 | c0003 | t0002 | g0239 | SAS | PJL | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03831 | hp1 | a0005 | c0005 | t0001 | g0179 | SAS | BEB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0235 | SAS | BEB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03834 | hp1 | a0003 | c0003 | t0002 | g0238 | SAS | BEB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | STU | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG04115 | hp2 | a0005 | c0005 | t0001 | g0164 | SAS | STU | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0290 | SAS | BEB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | STU | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | STU | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18522 | hp1 | a0005 | c0020 | t0002 | g0192 | AFR | YRI | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0146 | AFR | YRI | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | CHB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18906 | hp1 | a0013 | c0019 | t0001 | g0166 | AFR | YRI | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18906 | hp2 | a0003 | c0003 | t0001 | g0006 | AFR | YRI | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18939 | hp2 | a0006 | c0006 | t0001 | g0173 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18941 | hp2 | a0004 | c0004 | t0001 | g0033 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18942 | hp2 | a0006 | c0006 | t0001 | g0162 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18944 | hp1 | a0004 | c0004 | t0001 | g0088 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18944 | hp2 | a0003 | c0003 | t0002 | g0240 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18947 | hp1 | a0005 | c0005 | t0003 | g0160 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18948 | hp1 | a0006 | c0006 | t0001 | g0168 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0287 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18952 | hp1 | a0004 | c0004 | t0001 | g0087 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0272 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18973 | hp1 | a0004 | c0004 | t0001 | g0085 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18975 | hp1 | a0005 | c0005 | t0001 | g0177 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18978 | hp2 | a0003 | c0003 | t0002 | g0243 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18980 | hp1 | a0002 | c0002 | t0002 | g0279 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18981 | hp1 | a0005 | c0005 | t0001 | g0183 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18981 | hp2 | a0004 | c0004 | t0001 | g0034 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0291 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18986 | hp1 | a0004 | c0004 | t0001 | g0086 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18986 | hp2 | a0005 | c0005 | t0001 | g0178 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18989 | hp1 | a0005 | c0005 | t0003 | g0167 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19007 | hp2 | a0005 | c0005 | t0001 | g0170 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0150 | AFR | LWK | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19030 | hp2 | a0005 | c0005 | t0001 | g0021 | AFR | LWK | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19057 | hp1 | a0003 | c0003 | t0002 | g0242 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0212 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19063 | hp1 | a0006 | c0006 | t0001 | g0161 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19088 | hp2 | a0003 | c0003 | t0002 | g0241 | EAS | JPT | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0040 | AFR | YRI | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA19240 | hp2 | a0003 | c0003 | t0002 | g0193 | AFR | YRI | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA20129 | hp1 | a0019 | c0027 | t0001 | g0051 | AFR | ASW | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ASW | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA20805 | hp1 | a0016 | c0024 | t0001 | g0115 | EUR | TSI | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA20805 | hp2 | a0006 | c0006 | t0001 | g0172 | EUR | TSI | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA20905 | hp1 | a0020 | c0029 | t0001 | g0152 | SAS | GIH | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0194 | SAS | GIH | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | CLM | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0074 | AMR | CLM | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02109 | hp1 | a0003 | c0003 | t0001 | g0039 | AFR | ACB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02109 | hp2 | a0007 | c0007 | t0002 | g0245 | AFR | ACB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0207 | AFR | ACB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02486 | hp2 | a0009 | c0009 | t0001 | g0149 | AFR | ACB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02559 | hp1 | a0003 | c0015 | t0001 | g0112 | AFR | ACB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0133 | AFR | ACB | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG06807 | hp1 | a0005 | c0005 | t0001 | g0165 | AFR | USA | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| HG06807 | hp2 | a0003 | c0016 | t0005 | g0301 | AFR | USA | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | USA | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | USA | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0137 | REF | REF | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0048 | REF | REF | SLC26A8_chr6_35938516_36029641 | SLC26A8 | chr6 | 35938516 | 36029641 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:35944079
|
G | A | 1 | a0016 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.2734C>T | p.Pro912Ser | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 20/20 | 2874/3437 | 2734/2913 | 912/970 | chr6 | 35944079 | ||
| chr6:35944166
|
C | G | 1 | a0013 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.2647G>C | p.Glu883Gln | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 20/20 | 2787/3437 | 2647/2913 | 883/970 | chr6 | 35944166 | ||
| chr6:35951188
|
C | T | 1 | a0010 | 2 | HG01256.hp2 HG01258.hp2 |
missense_variant | MODERATE | c.2447G>A | p.Arg816Gln | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/20 | 2587/3437 | 2447/2913 | 816/970 | chr6 | 35951188 | ||
| chr6:35951210
|
C | T | 1 | a0017 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.2425G>A | p.Asp809Asn | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/20 | 2565/3437 | 2425/2913 | 809/970 | chr6 | 35951210 | ||
| chr6:35955184
|
C | T | 1 | a0008 | 4 | HG02622.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
missense_variant | MODERATE | c.2200G>A | p.Val734Met | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/20 | 2340/3437 | 2200/2913 | 734/970 | chr6 | 35955184 | ||
| chr6:35955469
|
T | C | 14 | a0002a0003a0005others(11): Show | 148 | HG00639.hp1 HG00642.hp2 HG00733.hp2 others(145): Show |
missense_variant | MODERATE | c.1915A>G | p.Ile639Val | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/20 | 2055/3437 | 1915/2913 | 639/970 | chr6 | 35955469 | ||
| chr6:35959497
|
C | A | 1 | a0018 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.1826G>T | p.Cys609Phe | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/20 | 1966/3437 | 1826/2913 | 609/970 | chr6 | 35959497 | ||
| chr6:35959582
|
C | A | 1 | a0014 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.1741G>T | p.Val581Leu | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/20 | 1881/3437 | 1741/2913 | 581/970 | chr6 | 35959582 | ||
| chr6:35959590
|
A | G | 2 | a0007a0011 | 6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
missense_variant&splice_region_variant | MODERATE | c.1733T>C | p.Val578Ala | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/20 | 1873/3437 | 1733/2913 | 578/970 | chr6 | 35959590 | ||
| chr6:35961069
|
T | C | 1 | a0019 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.1492A>G | p.Ile498Val | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 13/20 | 1632/3437 | 1492/2913 | 498/970 | chr6 | 35961069 | ||
| chr6:35968927
|
T | A | 1 | a0015 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.1315A>T | p.Met439Leu | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/20 | 1455/3437 | 1315/2913 | 439/970 | chr6 | 35968927 | ||
| chr6:35977242
|
T | C | 1 | a0020 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.1135A>G | p.Ile379Val | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/20 | 1275/3437 | 1135/2913 | 379/970 | chr6 | 35977242 | ||
| chr6:35992613
|
C | T | 3 | a0005a0006a0013 | 38 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(35): Show |
missense_variant | MODERATE | c.689G>A | p.Ser230Asn | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 6/20 | 829/3437 | 689/2913 | 230/970 | chr6 | 35992613 | ||
| chr6:35997919
|
C | A | 1 | a0012 | 1 | HG03453.hp1 | missense_variant&splice_region_variant | MODERATE | c.446G>T | p.Gly149Val | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/20 | 586/3437 | 446/2913 | 149/970 | chr6 | 35997919 | ||
| chr6:35999995
|
T | C | 5 | a0005a0006a0009others(2): Show | 42 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(39): Show |
missense_variant | MODERATE | c.442A>G | p.Ile148Val | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 4/20 | 582/3437 | 442/2913 | 148/970 | chr6 | 35999995 | ||
| chr6:36012311
|
A | G | 1 | a0021 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.250T>C | p.Cys84Arg | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/20 | 390/3437 | 250/2913 | 84/970 | chr6 | 36012311 | ||
| chr6:36012344
|
C | T | 11 | a0003a0004a0005others(8): Show | 106 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(103): Show |
missense_variant | MODERATE | c.217G>A | p.Val73Met | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/20 | 357/3437 | 217/2913 | 73/970 | chr6 | 36012344 | ||
| chr6:36019607
|
G | T | 1 | a0011 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.101C>A | p.Thr34Asn | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/20 | 241/3437 | 101/2913 | 34/970 | chr6 | 36019607 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:35955281
|
C | T | 1 | a0002c0011 | 2 | HG02896.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.2103G>A | p.Ala701Ala | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/20 | 2243/3437 | 2103/2913 | 701/970 | chr6 | 35955281 | ||
| chr6:35955482
|
G | A | 3 | a0002c0025a0003c0016a0005c0020 | 3 | HG02922.hp2 HG06807.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.1902C>T | p.Pro634Pro | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/20 | 2042/3437 | 1902/2913 | 634/970 | chr6 | 35955482 | ||
| chr6:35977266
|
G | A | 1 | a0002c0010 | 3 | HG02572.hp1 HG02895.hp1 HG03195.hp1 |
synonymous_variant | LOW | c.1111C>T | p.Leu371Leu | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/20 | 1251/3437 | 1111/2913 | 371/970 | chr6 | 35977266 | ||
| chr6:35982144
|
C | T | 1 | a0006c0018 | 1 | HG02300.hp1 | synonymous_variant | LOW | c.1002G>A | p.Thr334Thr | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/20 | 1142/3437 | 1002/2913 | 334/970 | chr6 | 35982144 | ||
| chr6:36000035
|
C | T | 1 | a0003c0015 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.402G>A | p.Ser134Ser | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 4/20 | 542/3437 | 402/2913 | 134/970 | chr6 | 36000035 | ||
| chr6:36019648
|
T | C | 1 | a0002c0013 | 2 | HG01884.hp1 HG02451.hp1 |
synonymous_variant | LOW | c.60A>G | p.Ser20Ser | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/20 | 200/3437 | 60/2913 | 20/970 | chr6 | 36019648 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:35943809
|
T | A | 1 | a0005c0005t0003 | 2 | NA18947.hp1 NA18989.hp1 |
3_prime_UTR_variant | MODIFIER | c.*91A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 20/20 | 91 | chr6 | 35943809 | |||||
| chr6:35943811
|
G | A | 1 | a0003c0016t0005 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*89C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 20/20 | 89 | chr6 | 35943811 | |||||
| chr6:36024507
|
G | A | 1 | a0002c0002t0004 | 1 | HG02976.hp1 | 5_prime_UTR_variant | MODIFIER | c.-6C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/20 | 4800 | chr6 | 36024507 | |||||
| chr6:36024555
|
T | C | 12 | a0001c0001t0002a0002c0002t0002a0002c0013t0002others(9): Show | 121 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(118): Show |
5_prime_UTR_variant | MODIFIER | c.-54A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/20 | 4848 | chr6 | 36024555 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:35944341
|
C | A | 1 | a0008c0008t0001g0090 | 1 | HG03139.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.2473-1G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35944341 | ||||||
| chr6:35944439
|
G | A | 1 | a0003c0003t0002g0220 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2473-99C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35944439 | ||||||
| chr6:35944460
|
C | G | 4 | a0005c0005t0001g0021a0005c0005t0001g0022a0005c0005t0001g0023others(1): Show | 4 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2473-120G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35944460 | ||||||
| chr6:35944492
|
A | G | 71 | a0001c0001t0002g0208a0001c0001t0002g0295a0002c0002t0001g0041others(68): Show | 71 | HG00639.hp2 HG00642.hp2 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.2473-152T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35944492 | ||||||
| chr6:35944509
|
AAATAAT | A | 61 | a0001c0001t0001g0110a0001c0001t0002g0219a0001c0001t0002g0278others(58): Show | 61 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.2473-175_2473-170d others(8): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35944509 | ||||||
| chr6:35944510
|
AATAATAA others(19): Show |
A | 1 | a0001c0001t0001g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2473-196_2473-171d others(28): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35944510 | ||||||
| chr6:35944548
|
A | T | 18 | a0001c0001t0002g0288a0001c0001t0002g0289a0001c0001t0002g0290others(15): Show | 18 | HG00642.hp2 HG01070.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.2473-208T>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35944548 | ||||||
| chr6:35944551
|
T | A | 7 | a0003c0003t0001g0006a0003c0003t0001g0008a0003c0003t0001g0009others(4): Show | 7 | HG01516.hp2 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2473-211A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35944551 | ||||||
| chr6:35944616
|
C | A | 5 | a0003c0003t0002g0239a0003c0003t0002g0240a0003c0003t0002g0241others(2): Show | 5 | HG03710.hp2 NA18944.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.2473-276G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35944616 | ||||||
| chr6:35944795
|
C | T | 2 | a0002c0002t0001g0041a0003c0003t0001g0052 | 2 | HG00642.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.2473-455G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35944795 | ||||||
| chr6:35945141
|
T | C | 71 | a0001c0001t0002g0208a0001c0001t0002g0295a0002c0002t0001g0041others(68): Show | 71 | HG00639.hp2 HG00642.hp2 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.2473-801A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35945141 | ||||||
| chr6:35945319
|
C | A | 27 | a0001c0001t0001g0046a0001c0001t0001g0105a0001c0001t0002g0206others(24): Show | 27 | HG00673.hp1 HG01255.hp1 HG01515.hp1 others(24): Show |
intron_variant | MODIFIER | c.2473-979G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35945319 | ||||||
| chr6:35945320
|
G | A | 1 | a0006c0006t0001g0168 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2473-980C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35945320 | ||||||
| chr6:35945347
|
G | A | 5 | a0001c0001t0002g0213a0001c0001t0002g0227a0001c0001t0002g0293others(2): Show | 5 | NA18950.hp2 NA18987.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.2473-1007C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35945347 | ||||||
| chr6:35945348
|
C | A | 5 | a0001c0001t0002g0213a0001c0001t0002g0227a0001c0001t0002g0293others(2): Show | 5 | NA18950.hp2 NA18987.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.2473-1008G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35945348 | ||||||
| chr6:35945360
|
C | A | 2 | a0003c0003t0001g0045a0003c0003t0002g0193 | 2 | HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2473-1020G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35945360 | ||||||
| chr6:35945447
|
T | C | 3 | a0007c0007t0002g0232a0007c0007t0002g0233a0007c0007t0002g0245 | 3 | HG02109.hp2 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2473-1107A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35945447 | ||||||
| chr6:35945664
|
G | A | 1 | a0003c0003t0001g0030 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2473-1324C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35945664 | ||||||
| chr6:35946037
|
G | T | 4 | a0008c0008t0001g0042a0008c0008t0001g0043a0008c0008t0001g0044others(1): Show | 4 | HG02622.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.2473-1697C>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35946037 | ||||||
| chr6:35946068
|
C | T | 1 | a0020c0029t0001g0152 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2473-1728G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35946068 | ||||||
| chr6:35946157
|
C | G | 1 | a0001c0001t0001g0138 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2473-1817G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35946157 | ||||||
| chr6:35946196
|
A | T | 1 | a0001c0001t0002g0304 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2473-1856T>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35946196 | ||||||
| chr6:35947120
|
C | G | 1 | a0004c0004t0001g0003 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2473-2780G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35947120 | ||||||
| chr6:35947452
|
A | G | 4 | a0005c0005t0001g0021a0005c0005t0001g0022a0005c0005t0001g0023others(1): Show | 4 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2473-3112T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35947452 | ||||||
| chr6:35947593
|
A | C | 1 | a0001c0001t0001g0138 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2473-3253T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35947593 | ||||||
| chr6:35947811
|
C | A | 1 | a0002c0002t0002g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2472+3352G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35947811 | ||||||
| chr6:35948104
|
A | T | 1 | a0001c0001t0002g0251 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2472+3059T>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35948104 | ||||||
| chr6:35948213
|
T | C | 1 | a0001c0001t0002g0226 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2472+2950A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35948213 | ||||||
| chr6:35948243
|
C | A | 18 | a0001c0001t0002g0295a0002c0002t0001g0119a0002c0002t0002g0272others(15): Show | 18 | HG00639.hp2 HG01070.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.2472+2920G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35948243 | ||||||
| chr6:35948275
|
T | C | 2 | a0001c0001t0001g0110a0001c0001t0002g0278 | 2 | HG00280.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.2472+2888A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35948275 | ||||||
| chr6:35948306
|
T | C | 30 | a0002c0002t0001g0146a0002c0002t0001g0155a0002c0002t0002g0195others(27): Show | 30 | HG01109.hp1 HG01255.hp2 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.2472+2857A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35948306 | ||||||
| chr6:35948387
|
G | A | 1 | a0002c0025t0002g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2472+2776C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35948387 | ||||||
| chr6:35948512
|
C | T | 2 | a0002c0002t0001g0116a0002c0002t0002g0250 | 2 | HG02080.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.2472+2651G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35948512 | ||||||
| chr6:35948603
|
AAAAC | A | 23 | a0001c0001t0002g0208a0001c0001t0002g0295a0002c0002t0001g0041others(20): Show | 23 | HG00639.hp2 HG00642.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.2472+2556_2472+255 others(8): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35948603 | ||||||
| chr6:35948655
|
C | T | 1 | a0001c0001t0002g0208 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2472+2508G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35948655 | ||||||
| chr6:35948698
|
T | G | 1 | a0002c0002t0001g0150 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2472+2465A>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35948698 | ||||||
| chr6:35948765
|
T | A | 1 | a0001c0001t0002g0217 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2472+2398A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35948765 | ||||||
| chr6:35948772
|
A | T | 5 | a0003c0003t0002g0239a0003c0003t0002g0240a0003c0003t0002g0241others(2): Show | 5 | HG03710.hp2 NA18944.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.2472+2391T>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35948772 | ||||||
| chr6:35948788
|
C | T | 5 | a0003c0003t0002g0239a0003c0003t0002g0240a0003c0003t0002g0241others(2): Show | 5 | HG03710.hp2 NA18944.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.2472+2375G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35948788 | ||||||
| chr6:35948796
|
T | C | 1 | a0001c0001t0002g0194 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2472+2367A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35948796 | ||||||
| chr6:35948932
|
T | C | 31 | a0002c0002t0001g0146a0002c0002t0001g0155a0002c0002t0002g0195others(28): Show | 31 | HG01109.hp1 HG01255.hp2 HG01361.hp1 others(28): Show |
intron_variant | MODIFIER | c.2472+2231A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35948932 | ||||||
| chr6:35949135
|
T | TA | 18 | a0001c0001t0002g0295a0002c0002t0001g0119a0002c0002t0002g0272others(15): Show | 18 | HG00639.hp2 HG01070.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.2472+2027dupT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35949135 | ||||||
| chr6:35949176
|
G | A | 4 | a0008c0008t0001g0042a0008c0008t0001g0043a0008c0008t0001g0044others(1): Show | 4 | HG02622.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.2472+1987C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35949176 | ||||||
| chr6:35949202
|
G | A | 1 | a0003c0003t0001g0037 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2472+1961C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35949202 | ||||||
| chr6:35949204
|
C | T | 3 | a0007c0007t0002g0232a0007c0007t0002g0233a0007c0007t0002g0245 | 3 | HG02109.hp2 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2472+1959G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35949204 | ||||||
| chr6:35949215
|
T | C | 63 | a0001c0001t0002g0208a0001c0001t0002g0295a0002c0002t0001g0041others(60): Show | 63 | HG00639.hp2 HG00642.hp2 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.2472+1948A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35949215 | ||||||
| chr6:35949381
|
G | A | 1 | a0003c0016t0005g0301 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2472+1782C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35949381 | ||||||
| chr6:35949436
|
A | G | 1 | a0002c0002t0001g0143 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2472+1727T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35949436 | ||||||
| chr6:35949670
|
A | T | 2 | a0001c0001t0002g0277a0001c0001t0002g0300 | 2 | NA18948.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.2472+1493T>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35949670 | ||||||
| chr6:35949677
|
A | G | 31 | a0002c0002t0001g0146a0002c0002t0001g0155a0002c0002t0002g0195others(28): Show | 31 | HG01109.hp1 HG01255.hp2 HG01361.hp1 others(28): Show |
intron_variant | MODIFIER | c.2472+1486T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35949677 | ||||||
| chr6:35949698
|
A | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG00735.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2472+1465T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35949698 | ||||||
| chr6:35949739
|
C | T | 3 | a0002c0002t0001g0081a0002c0002t0002g0257a0005c0005t0002g0247 | 3 | HG02004.hp1 HG02027.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.2472+1424G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35949739 | ||||||
| chr6:35949795
|
T | TTG | 5 | a0003c0003t0002g0239a0003c0003t0002g0240a0003c0003t0002g0241others(2): Show | 5 | HG03710.hp2 NA18944.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.2472+1366_2472+136 others(6): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35949795 | ||||||
| chr6:35949817
|
G | GT | 11 | a0001c0001t0002g0269a0002c0002t0001g0069a0002c0002t0001g0070others(8): Show | 11 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.2472+1345dupA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35949817 | ||||||
| chr6:35949832
|
G | A | 1 | a0006c0006t0002g0249 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2472+1331C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35949832 | ||||||
| chr6:35949841
|
C | T | 63 | a0001c0001t0002g0208a0001c0001t0002g0295a0002c0002t0001g0041others(60): Show | 63 | HG00639.hp2 HG00642.hp2 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.2472+1322G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35949841 | ||||||
| chr6:35949908
|
C | G | 25 | a0002c0002t0002g0195a0002c0002t0002g0196a0002c0002t0002g0197others(22): Show | 25 | HG01109.hp1 HG01255.hp2 HG01516.hp2 others(22): Show |
intron_variant | MODIFIER | c.2472+1255G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35949908 | ||||||
| chr6:35949938
|
T | G | 1 | a0002c0002t0001g0041 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2472+1225A>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35949938 | ||||||
| chr6:35949951
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0083a0001c0001t0001g0101others(52): Show | 56 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.2472+1212C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35949951 | ||||||
| chr6:35949956
|
C | A | 3 | a0007c0007t0002g0232a0007c0007t0002g0233a0007c0007t0002g0245 | 3 | HG02109.hp2 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2472+1207G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35949956 | ||||||
| chr6:35949967
|
G | A | 3 | a0002c0002t0001g0119a0005c0005t0001g0165a0013c0019t0001g0166 | 3 | HG02698.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2472+1196C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35949967 | ||||||
| chr6:35950065
|
G | A | 5 | a0003c0003t0002g0239a0003c0003t0002g0240a0003c0003t0002g0241others(2): Show | 5 | HG03710.hp2 NA18944.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.2472+1098C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35950065 | ||||||
| chr6:35950088
|
C | T | 5 | a0003c0003t0002g0239a0003c0003t0002g0240a0003c0003t0002g0241others(2): Show | 5 | HG03710.hp2 NA18944.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.2472+1075G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35950088 | ||||||
| chr6:35950103
|
C | T | 1 | a0017c0023t0001g0020 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2472+1060G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35950103 | ||||||
| chr6:35950197
|
T | C | 1 | a0001c0001t0001g0101 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2472+966A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35950197 | ||||||
| chr6:35950321
|
A | C | 1 | a0001c0001t0002g0290 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2472+842T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35950321 | ||||||
| chr6:35950351
|
G | A | 5 | a0002c0002t0004g0184a0003c0003t0001g0002a0007c0007t0002g0244others(2): Show | 5 | HG02451.hp2 HG02615.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2472+812C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35950351 | ||||||
| chr6:35950418
|
C | A | 1 | a0001c0001t0001g0100 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2472+745G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35950418 | ||||||
| chr6:35950435
|
C | T | 1 | a0001c0001t0002g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2472+728G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35950435 | ||||||
| chr6:35950518
|
C | A | 1 | a0002c0002t0001g0041 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2472+645G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35950518 | ||||||
| chr6:35950562
|
G | A | 3 | a0007c0007t0002g0232a0007c0007t0002g0233a0007c0007t0002g0245 | 3 | HG02109.hp2 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2472+601C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35950562 | ||||||
| chr6:35950743
|
T | A | 1 | a0002c0002t0001g0041 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2472+420A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35950743 | ||||||
| chr6:35950879
|
T | C | 1 | a0001c0001t0002g0187 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2472+284A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35950879 | ||||||
| chr6:35951096
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2472+67G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 19/19 | chr6 | 35951096 | ||||||
| chr6:35951424
|
C | T | 5 | a0003c0003t0002g0239a0003c0003t0002g0240a0003c0003t0002g0241others(2): Show | 5 | HG03710.hp2 NA18944.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.2287+21G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 18/19 | chr6 | 35951424 | ||||||
| chr6:35951426
|
T | C | 1 | a0002c0002t0001g0041 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2287+19A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 18/19 | chr6 | 35951426 | ||||||
| chr6:35951503
|
T | G | 1 | a0004c0004t0001g0086 | 1 | NA18986.hp1 | splice_region_variant&intron_variant | LOW | c.2233-4A>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35951503 | ||||||
| chr6:35951504
|
G | T | 1 | a0004c0004t0001g0086 | 1 | NA18986.hp1 | splice_region_variant&intron_variant | LOW | c.2233-5C>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35951504 | ||||||
| chr6:35951591
|
G | T | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2233-92C>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35951591 | ||||||
| chr6:35951661
|
C | T | 1 | a0002c0002t0002g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2233-162G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35951661 | ||||||
| chr6:35951665
|
G | A | 1 | a0006c0006t0001g0175 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2233-166C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35951665 | ||||||
| chr6:35951720
|
A | G | 2 | a0001c0001t0002g0208a0003c0003t0002g0299 | 2 | HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2233-221T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35951720 | ||||||
| chr6:35951855
|
C | T | 2 | a0001c0001t0002g0208a0003c0003t0002g0299 | 2 | HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2233-356G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35951855 | ||||||
| chr6:35952044
|
G | A | 5 | a0003c0003t0002g0239a0003c0003t0002g0240a0003c0003t0002g0241others(2): Show | 5 | HG03710.hp2 NA18944.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.2233-545C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35952044 | ||||||
| chr6:35952107
|
G | A | 3 | a0003c0003t0001g0017a0003c0003t0001g0018a0003c0003t0001g0095 | 3 | HG01891.hp1 HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2233-608C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35952107 | ||||||
| chr6:35952133
|
G | C | 3 | a0001c0001t0002g0203a0001c0001t0002g0225a0002c0013t0001g0019 | 3 | HG00741.hp2 HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2233-634C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35952133 | ||||||
| chr6:35952225
|
A | C | 291 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(288): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.2233-726T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35952225 | ||||||
| chr6:35952298
|
C | T | 1 | a0003c0003t0001g0002 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2233-799G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35952298 | ||||||
| chr6:35952797
|
C | T | 1 | a0003c0003t0002g0239 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2233-1298G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35952797 | ||||||
| chr6:35952824
|
G | A | 2 | a0007c0007t0002g0232a0007c0007t0002g0233 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2233-1325C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35952824 | ||||||
| chr6:35952862
|
A | T | 3 | a0001c0001t0002g0288a0001c0001t0002g0289a0001c0001t0002g0302 | 3 | NA18975.hp2 NA18977.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.2233-1363T>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35952862 | ||||||
| chr6:35952875
|
G | T | 4 | a0003c0003t0002g0240a0003c0003t0002g0241a0003c0003t0002g0242others(1): Show | 4 | NA18944.hp2 NA18978.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.2233-1376C>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35952875 | ||||||
| chr6:35952963
|
G | T | 2 | a0002c0025t0002g0202a0003c0016t0005g0301 | 2 | HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2233-1464C>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35952963 | ||||||
| chr6:35953010
|
T | A | 1 | a0004c0004t0001g0085 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2233-1511A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35953010 | ||||||
| chr6:35953013
|
C | CA | 76 | a0001c0001t0001g0047a0001c0001t0001g0054a0001c0001t0001g0125others(73): Show | 76 | HG00639.hp1 HG00673.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.2233-1515dupT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35953013 | ||||||
| chr6:35953013
|
C | CAA | 7 | a0001c0001t0002g0186a0002c0002t0001g0078a0002c0002t0001g0130others(4): Show | 7 | HG00642.hp2 HG00735.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.2233-1516_2233-151 others(6): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35953013 | ||||||
| chr6:35953013
|
CA | C | 45 | a0001c0001t0001g0154a0001c0001t0002g0227a0001c0001t0002g0289others(42): Show | 45 | HG00733.hp2 HG00741.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.2233-1515delT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35953013 | ||||||
| chr6:35953045
|
A | C | 2 | a0005c0005t0001g0165a0013c0019t0001g0166 | 2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2233-1546T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35953045 | ||||||
| chr6:35953091
|
T | C | 3 | a0002c0002t0001g0074a0002c0002t0001g0130a0002c0002t0001g0132 | 3 | HG01123.hp2 HG01516.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.2233-1592A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35953091 | ||||||
| chr6:35953101
|
C | T | 4 | a0008c0008t0001g0042a0008c0008t0001g0043a0008c0008t0001g0044others(1): Show | 4 | HG02622.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.2233-1602G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35953101 | ||||||
| chr6:35953380
|
CTTAA | C | 39 | a0002c0002t0001g0119a0002c0002t0002g0198a0002c0002t0002g0207others(36): Show | 39 | HG01070.hp2 HG01081.hp2 HG02109.hp2 others(36): Show |
intron_variant | MODIFIER | c.2232+1768_2232+177 others(8): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35953380 | ||||||
| chr6:35953679
|
A | G | 2 | a0004c0004t0001g0096a0004c0004t0001g0151 | 2 | HG00597.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.2232+1473T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35953679 | ||||||
| chr6:35953721
|
C | A | 1 | a0003c0003t0002g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2232+1431G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35953721 | ||||||
| chr6:35953776
|
C | T | 1 | a0003c0003t0002g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2232+1376G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35953776 | ||||||
| chr6:35953882
|
G | A | 1 | a0001c0001t0002g0228 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2232+1270C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35953882 | ||||||
| chr6:35954124
|
G | T | 1 | a0001c0001t0002g0281 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2232+1028C>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35954124 | ||||||
| chr6:35954211
|
A | C | 2 | a0003c0003t0001g0045a0003c0003t0002g0193 | 2 | HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2232+941T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35954211 | ||||||
| chr6:35954515
|
C | G | 9 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0120others(6): Show | 9 | HG00733.hp2 HG00741.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.2232+637G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35954515 | ||||||
| chr6:35954642
|
C | G | 3 | a0006c0006t0001g0140a0006c0006t0001g0157a0006c0006t0001g0172 | 3 | HG00642.hp1 HG01070.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2232+510G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35954642 | ||||||
| chr6:35954668
|
G | A | 4 | a0005c0005t0001g0021a0005c0005t0001g0022a0005c0005t0001g0023others(1): Show | 4 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2232+484C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35954668 | ||||||
| chr6:35954683
|
G | A | 1 | a0001c0001t0002g0285 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2232+469C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35954683 | ||||||
| chr6:35954892
|
C | T | 1 | a0002c0002t0002g0214 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2232+260G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35954892 | ||||||
| chr6:35955061
|
C | A | 1 | a0001c0001t0002g0229 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2232+91G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 17/19 | chr6 | 35955061 | ||||||
| chr6:35955653
|
G | A | 1 | a0001c0001t0002g0228 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1864-133C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35955653 | ||||||
| chr6:35955759
|
T | C | 6 | a0007c0007t0002g0232a0007c0007t0002g0233a0007c0007t0002g0244others(3): Show | 6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1864-239A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35955759 | ||||||
| chr6:35955831
|
A | G | 3 | a0002c0025t0002g0202a0003c0016t0005g0301a0005c0020t0002g0192 | 3 | HG02922.hp2 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1864-311T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35955831 | ||||||
| chr6:35955872
|
T | A | 1 | a0001c0001t0001g0154 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1864-352A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35955872 | ||||||
| chr6:35955873
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1864-353G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35955873 | ||||||
| chr6:35956166
|
G | A | 1 | a0003c0003t0002g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1864-646C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35956166 | ||||||
| chr6:35956349
|
A | G | 28 | a0002c0002t0002g0198a0002c0002t0002g0207a0002c0002t0002g0214others(25): Show | 28 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.1864-829T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35956349 | ||||||
| chr6:35956361
|
G | A | 1 | a0020c0029t0001g0152 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1864-841C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35956361 | ||||||
| chr6:35956428
|
C | CA | 14 | a0001c0001t0002g0235a0002c0002t0001g0146a0002c0002t0001g0155others(11): Show | 14 | HG00642.hp2 HG01175.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.1864-909dupT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35956428 | ||||||
| chr6:35956428
|
CA | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0047a0001c0001t0001g0050others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1864-909delT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35956428 | ||||||
| chr6:35956428
|
CAA | C | 68 | a0001c0001t0002g0194a0001c0001t0002g0213a0001c0001t0002g0227others(65): Show | 68 | HG00639.hp1 HG01106.hp1 HG01123.hp2 others(65): Show |
intron_variant | MODIFIER | c.1864-910_1864-909d others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35956428 | ||||||
| chr6:35956649
|
G | T | 4 | a0008c0008t0001g0042a0008c0008t0001g0043a0008c0008t0001g0044others(1): Show | 4 | HG02622.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1864-1129C>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35956649 | ||||||
| chr6:35956924
|
GA | G | 145 | a0002c0002t0001g0032a0002c0002t0001g0040a0002c0002t0001g0041others(142): Show | 145 | HG00639.hp1 HG00642.hp2 HG00733.hp2 others(142): Show |
intron_variant | MODIFIER | c.1864-1405delT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35956924 | ||||||
| chr6:35956947
|
G | A | 3 | a0002c0025t0002g0202a0003c0016t0005g0301a0005c0020t0002g0192 | 3 | HG02922.hp2 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1864-1427C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35956947 | ||||||
| chr6:35956982
|
G | A | 1 | a0006c0006t0001g0175 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1864-1462C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35956982 | ||||||
| chr6:35957015
|
G | A | 1 | a0003c0003t0002g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1864-1495C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35957015 | ||||||
| chr6:35957175
|
T | A | 3 | a0002c0025t0002g0202a0003c0016t0005g0301a0005c0020t0002g0192 | 3 | HG02922.hp2 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1864-1655A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35957175 | ||||||
| chr6:35957217
|
C | T | 1 | a0003c0003t0001g0002 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1864-1697G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35957217 | ||||||
| chr6:35957265
|
T | C | 1 | a0011c0014t0001g0128 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1864-1745A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35957265 | ||||||
| chr6:35957330
|
AT | A | 90 | a0001c0001t0001g0053a0001c0001t0001g0154a0001c0001t0002g0289others(87): Show | 90 | HG00639.hp1 HG01070.hp2 HG01081.hp2 others(87): Show |
intron_variant | MODIFIER | c.1864-1811delA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35957330 | ||||||
| chr6:35957343
|
A | G | 1 | a0002c0002t0004g0184 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1864-1823T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35957343 | ||||||
| chr6:35957380
|
A | C | 41 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0120others(38): Show | 41 | HG00642.hp2 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1864-1860T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35957380 | ||||||
| chr6:35957407
|
G | A | 6 | a0002c0002t0002g0198a0002c0002t0002g0207a0002c0013t0002g0234others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1864-1887C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35957407 | ||||||
| chr6:35957606
|
CT | C | 121 | a0002c0002t0001g0032a0002c0002t0001g0057a0002c0002t0001g0059others(118): Show | 121 | HG00642.hp2 HG01070.hp2 HG01081.hp2 others(118): Show |
intron_variant | MODIFIER | c.1863+1853delA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35957606 | ||||||
| chr6:35957606
|
CTT | C | 12 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0065others(9): Show | 12 | HG00733.hp2 HG00741.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.1863+1852_1863+185 others(6): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35957606 | ||||||
| chr6:35957624
|
G | T | 6 | a0002c0002t0002g0198a0002c0002t0002g0207a0002c0013t0002g0234others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1863+1836C>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35957624 | ||||||
| chr6:35957710
|
G | C | 1 | a0003c0003t0002g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1863+1750C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35957710 | ||||||
| chr6:35957732
|
G | T | 1 | a0002c0002t0001g0041 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1863+1728C>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35957732 | ||||||
| chr6:35957825
|
C | T | 1 | a0001c0001t0002g0216 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1863+1635G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35957825 | ||||||
| chr6:35957881
|
C | T | 1 | a0003c0003t0002g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1863+1579G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35957881 | ||||||
| chr6:35958021
|
C | T | 59 | a0002c0002t0001g0032a0002c0002t0001g0057a0002c0002t0001g0059others(56): Show | 59 | HG00639.hp1 HG01106.hp1 HG01123.hp2 others(56): Show |
intron_variant | MODIFIER | c.1863+1439G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35958021 | ||||||
| chr6:35958177
|
C | T | 1 | a0001c0001t0002g0300 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1863+1283G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35958177 | ||||||
| chr6:35958214
|
A | C | 1 | a0003c0003t0001g0035 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1863+1246T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35958214 | ||||||
| chr6:35958329
|
G | A | 7 | a0002c0002t0002g0198a0002c0002t0002g0207a0002c0002t0004g0184others(4): Show | 7 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1863+1131C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35958329 | ||||||
| chr6:35958586
|
C | T | 1 | a0002c0002t0004g0184 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1863+874G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35958586 | ||||||
| chr6:35958978
|
C | G | 1 | a0003c0003t0002g0239 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1863+482G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35958978 | ||||||
| chr6:35959013
|
T | C | 8 | a0002c0002t0002g0214a0003c0003t0001g0002a0003c0003t0002g0239others(5): Show | 8 | HG02647.hp2 HG03540.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1863+447A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35959013 | ||||||
| chr6:35959057
|
C | G | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1863+403G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35959057 | ||||||
| chr6:35959284
|
T | C | 3 | a0002c0002t0002g0195a0002c0002t0002g0197a0002c0002t0002g0200 | 3 | HG01109.hp1 HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1863+176A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35959284 | ||||||
| chr6:35959316
|
C | A | 4 | a0002c0002t0002g0195a0002c0002t0002g0197a0002c0002t0002g0200others(1): Show | 4 | HG01109.hp1 HG02258.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1863+144G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35959316 | ||||||
| chr6:35959317
|
C | T | 2 | a0001c0001t0002g0210a0001c0001t0002g0211 | 2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1863+143G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35959317 | ||||||
| chr6:35959381
|
A | AT | 9 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0120others(6): Show | 9 | HG00733.hp2 HG00741.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1863+78dupA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35959381 | ||||||
| chr6:35959391
|
T | TTAAGAAA others(325): Show |
1 | a0003c0003t0001g0002 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1863+68_1863+69ins others(332): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35959391 | ||||||
| chr6:35959391
|
T | TTAAGAAA others(330): Show |
1 | a0002c0002t0002g0214 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1863+68_1863+69ins others(337): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 16/19 | chr6 | 35959391 | ||||||
| chr6:35959649
|
G | C | 1 | a0014c0021t0001g0094 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1732-58C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 15/19 | chr6 | 35959649 | ||||||
| chr6:35959706
|
G | C | 6 | a0007c0007t0002g0232a0007c0007t0002g0233a0007c0007t0002g0244others(3): Show | 6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1731+8C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 15/19 | chr6 | 35959706 | ||||||
| chr6:35959909
|
T | A | 1 | a0002c0002t0002g0214 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1639-103A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 14/19 | chr6 | 35959909 | ||||||
| chr6:35960001
|
C | T | 59 | a0002c0002t0001g0032a0002c0002t0001g0057a0002c0002t0001g0059others(56): Show | 59 | HG00639.hp1 HG01106.hp1 HG01123.hp2 others(56): Show |
intron_variant | MODIFIER | c.1639-195G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 14/19 | chr6 | 35960001 | ||||||
| chr6:35960065
|
C | T | 1 | a0005c0005t0001g0183 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1639-259G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 14/19 | chr6 | 35960065 | ||||||
| chr6:35960094
|
A | G | 1 | a0001c0001t0002g0277 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1639-288T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 14/19 | chr6 | 35960094 | ||||||
| chr6:35960120
|
G | A | 1 | a0005c0020t0002g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1639-314C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 14/19 | chr6 | 35960120 | ||||||
| chr6:35960222
|
A | G | 6 | a0002c0002t0001g0146a0002c0002t0001g0155a0003c0003t0001g0052others(3): Show | 6 | HG00642.hp2 HG01361.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1639-416T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 14/19 | chr6 | 35960222 | ||||||
| chr6:35960411
|
T | C | 1 | a0002c0002t0001g0119 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1638+432A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 14/19 | chr6 | 35960411 | ||||||
| chr6:35960513
|
A | G | 26 | a0002c0002t0002g0198a0002c0002t0002g0207a0002c0002t0002g0214others(23): Show | 26 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(23): Show |
intron_variant | MODIFIER | c.1638+330T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 14/19 | chr6 | 35960513 | ||||||
| chr6:35960627
|
C | G | 1 | a0005c0020t0002g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1638+216G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 14/19 | chr6 | 35960627 | ||||||
| chr6:35960675
|
T | A | 16 | a0002c0002t0001g0150a0002c0013t0001g0019a0003c0003t0001g0005others(13): Show | 16 | HG01516.hp2 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1638+168A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 14/19 | chr6 | 35960675 | ||||||
| chr6:35960717
|
C | T | 2 | a0002c0025t0002g0202a0003c0016t0005g0301 | 2 | HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1638+126G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 14/19 | chr6 | 35960717 | ||||||
| chr6:35960768
|
T | A | 1 | a0017c0023t0001g0020 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1638+75A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 14/19 | chr6 | 35960768 | ||||||
| chr6:35961321
|
C | T | 6 | a0001c0001t0001g0053a0001c0001t0001g0103a0001c0001t0001g0108others(3): Show | 6 | HG00099.hp1 HG00280.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1462-222G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 12/19 | chr6 | 35961321 | ||||||
| chr6:35961383
|
G | C | 1 | a0014c0021t0001g0094 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1462-284C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 12/19 | chr6 | 35961383 | ||||||
| chr6:35961414
|
A | G | 2 | a0002c0002t0002g0214a0003c0003t0001g0002 | 2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1462-315T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 12/19 | chr6 | 35961414 | ||||||
| chr6:35961434
|
G | A | 5 | a0002c0002t0001g0146a0002c0002t0001g0155a0009c0009t0001g0092others(2): Show | 5 | HG01361.hp1 HG02055.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1462-335C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 12/19 | chr6 | 35961434 | ||||||
| chr6:35961455
|
A | G | 2 | a0002c0002t0002g0196a0002c0002t0002g0199 | 2 | HG02818.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1462-356T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 12/19 | chr6 | 35961455 | ||||||
| chr6:35961925
|
A | G | 5 | a0003c0003t0002g0239a0003c0003t0002g0240a0003c0003t0002g0241others(2): Show | 5 | HG03710.hp2 NA18944.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1461+601T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 12/19 | chr6 | 35961925 | ||||||
| chr6:35961958
|
T | C | 2 | a0001c0001t0002g0213a0001c0001t0002g0227 | 2 | NA18987.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1461+568A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 12/19 | chr6 | 35961958 | ||||||
| chr6:35962044
|
A | G | 286 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(283): Show | 287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.1461+482T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 12/19 | chr6 | 35962044 | ||||||
| chr6:35962157
|
C | T | 1 | a0006c0006t0001g0159 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1461+369G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 12/19 | chr6 | 35962157 | ||||||
| chr6:35962225
|
CA | C | 119 | a0001c0001t0001g0154a0001c0001t0002g0280a0002c0002t0001g0032others(116): Show | 119 | HG00639.hp1 HG00642.hp2 HG00733.hp2 others(116): Show |
intron_variant | MODIFIER | c.1461+300delT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 12/19 | chr6 | 35962225 | ||||||
| chr6:35962225
|
CAA | C | 30 | a0002c0002t0002g0198a0002c0002t0002g0207a0002c0002t0002g0214others(27): Show | 30 | HG01516.hp2 HG02109.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.1461+299_1461+300d others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 12/19 | chr6 | 35962225 | ||||||
| chr6:35962295
|
A | G | 26 | a0002c0002t0002g0198a0002c0002t0002g0207a0002c0002t0002g0214others(23): Show | 26 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(23): Show |
intron_variant | MODIFIER | c.1461+231T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 12/19 | chr6 | 35962295 | ||||||
| chr6:35962305
|
C | G | 2 | a0002c0002t0001g0113a0002c0002t0002g0212 | 2 | NA18967.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1461+221G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 12/19 | chr6 | 35962305 | ||||||
| chr6:35962349
|
C | T | 9 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0120others(6): Show | 9 | HG00733.hp2 HG00741.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1461+177G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 12/19 | chr6 | 35962349 | ||||||
| chr6:35962735
|
A | G | 1 | a0001c0001t0002g0206 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1366-114T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35962735 | ||||||
| chr6:35962931
|
G | A | 1 | a0005c0005t0001g0170 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1366-310C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35962931 | ||||||
| chr6:35962996
|
C | T | 1 | a0017c0023t0001g0020 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1366-375G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35962996 | ||||||
| chr6:35963293
|
C | T | 1 | a0001c0001t0002g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1366-672G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35963293 | ||||||
| chr6:35963388
|
G | A | 7 | a0002c0002t0002g0214a0003c0003t0001g0002a0003c0003t0002g0239others(4): Show | 7 | HG02647.hp2 HG03540.hp2 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.1366-767C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35963388 | ||||||
| chr6:35963408
|
C | T | 2 | a0002c0002t0001g0142a0003c0003t0002g0299 | 2 | HG02165.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1366-787G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35963408 | ||||||
| chr6:35963493
|
G | A | 1 | a0001c0001t0002g0252 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1366-872C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35963493 | ||||||
| chr6:35963556
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1366-935A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35963556 | ||||||
| chr6:35964026
|
A | G | 6 | a0002c0002t0002g0198a0002c0002t0002g0207a0002c0013t0002g0234others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1366-1405T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35964026 | ||||||
| chr6:35964037
|
C | T | 1 | a0005c0020t0002g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1366-1416G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35964037 | ||||||
| chr6:35964122
|
C | T | 25 | a0002c0002t0002g0198a0002c0002t0002g0207a0002c0002t0002g0214others(22): Show | 25 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(22): Show |
intron_variant | MODIFIER | c.1366-1501G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35964122 | ||||||
| chr6:35964258
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1366-1637T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35964258 | ||||||
| chr6:35964289
|
G | A | 20 | a0002c0002t0001g0119a0002c0002t0002g0272a0005c0005t0001g0021others(17): Show | 20 | HG01070.hp2 HG01081.hp2 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.1366-1668C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35964289 | ||||||
| chr6:35964408
|
A | G | 1 | a0002c0002t0002g0200 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1366-1787T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35964408 | ||||||
| chr6:35964511
|
G | A | 7 | a0002c0002t0002g0214a0003c0003t0001g0002a0003c0003t0002g0239others(4): Show | 7 | HG02647.hp2 HG03540.hp2 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.1366-1890C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35964511 | ||||||
| chr6:35964646
|
C | CA | 13 | a0002c0002t0001g0065a0002c0002t0001g0066a0002c0002t0001g0067others(10): Show | 13 | HG01169.hp2 HG01175.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.1366-2026dupT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35964646 | ||||||
| chr6:35964764
|
A | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(299): Show | 303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.1366-2143T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35964764 | ||||||
| chr6:35964898
|
C | A | 1 | a0001c0001t0001g0156 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1366-2277G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35964898 | ||||||
| chr6:35964916
|
G | A | 5 | a0003c0003t0002g0239a0003c0003t0002g0240a0003c0003t0002g0241others(2): Show | 5 | HG03710.hp2 NA18944.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1366-2295C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35964916 | ||||||
| chr6:35964958
|
C | A | 20 | a0002c0002t0001g0119a0002c0002t0002g0272a0005c0005t0001g0021others(17): Show | 20 | HG01070.hp2 HG01081.hp2 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.1366-2337G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35964958 | ||||||
| chr6:35964960
|
A | C | 148 | a0002c0002t0001g0032a0002c0002t0001g0040a0002c0002t0001g0041others(145): Show | 148 | HG00639.hp1 HG00642.hp2 HG00733.hp2 others(145): Show |
intron_variant | MODIFIER | c.1366-2339T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35964960 | ||||||
| chr6:35964966
|
C | CA | 133 | a0002c0002t0001g0032a0002c0002t0001g0040a0002c0002t0001g0041others(130): Show | 133 | HG00639.hp1 HG00642.hp2 HG00733.hp2 others(130): Show |
intron_variant | MODIFIER | c.1366-2346dupT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35964966 | ||||||
| chr6:35964966
|
C | CAA | 6 | a0002c0002t0002g0198a0002c0013t0002g0234a0003c0003t0001g0018others(3): Show | 6 | HG01891.hp1 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1366-2347_1366-234 others(6): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35964966 | ||||||
| chr6:35964990
|
A | G | 7 | a0002c0002t0002g0214a0003c0003t0001g0002a0003c0003t0002g0239others(4): Show | 7 | HG02647.hp2 HG03540.hp2 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.1366-2369T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35964990 | ||||||
| chr6:35965134
|
CA | C | 7 | a0002c0002t0002g0214a0003c0003t0001g0002a0003c0003t0002g0239others(4): Show | 7 | HG02647.hp2 HG03540.hp2 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.1366-2514delT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35965134 | ||||||
| chr6:35965251
|
G | C | 5 | a0002c0002t0001g0146a0002c0002t0001g0155a0009c0009t0001g0092others(2): Show | 5 | HG01361.hp1 HG02055.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1366-2630C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35965251 | ||||||
| chr6:35965379
|
G | A | 4 | a0008c0008t0001g0042a0008c0008t0001g0043a0008c0008t0001g0044others(1): Show | 4 | HG02622.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1366-2758C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35965379 | ||||||
| chr6:35965476
|
T | G | 9 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0120others(6): Show | 9 | HG00733.hp2 HG00741.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1366-2855A>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35965476 | ||||||
| chr6:35965508
|
C | T | 4 | a0008c0008t0001g0042a0008c0008t0001g0043a0008c0008t0001g0044others(1): Show | 4 | HG02622.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1366-2887G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35965508 | ||||||
| chr6:35965516
|
C | T | 3 | a0005c0005t0001g0164a0005c0005t0001g0176a0005c0005t0001g0182 | 3 | HG01070.hp2 HG01081.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1366-2895G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35965516 | ||||||
| chr6:35965550
|
C | T | 61 | a0002c0002t0001g0032a0002c0002t0001g0057a0002c0002t0001g0059others(58): Show | 61 | HG00639.hp1 HG01106.hp1 HG01123.hp2 others(58): Show |
intron_variant | MODIFIER | c.1366-2929G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35965550 | ||||||
| chr6:35965553
|
A | G | 6 | a0007c0007t0002g0232a0007c0007t0002g0233a0007c0007t0002g0244others(3): Show | 6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1366-2932T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35965553 | ||||||
| chr6:35965597
|
G | C | 5 | a0003c0003t0002g0239a0003c0003t0002g0240a0003c0003t0002g0241others(2): Show | 5 | HG03710.hp2 NA18944.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1366-2976C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35965597 | ||||||
| chr6:35965642
|
A | T | 1 | a0003c0003t0001g0002 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1366-3021T>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35965642 | ||||||
| chr6:35965669
|
C | T | 1 | a0003c0003t0002g0238 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1366-3048G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35965669 | ||||||
| chr6:35965682
|
CA | C | 8 | a0001c0001t0001g0118a0001c0001t0001g0122a0001c0001t0002g0282others(5): Show | 8 | HG01516.hp2 HG02647.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1366-3062delT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35965682 | ||||||
| chr6:35965696
|
A | G | 3 | a0005c0005t0001g0164a0005c0005t0001g0176a0005c0005t0001g0182 | 3 | HG01070.hp2 HG01081.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1366-3075T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35965696 | ||||||
| chr6:35965730
|
C | T | 1 | a0001c0001t0002g0194 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1366-3109G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35965730 | ||||||
| chr6:35965906
|
G | T | 8 | a0002c0002t0002g0195a0002c0002t0002g0196a0002c0002t0002g0197others(5): Show | 8 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1365+2971C>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35965906 | ||||||
| chr6:35966001
|
CA | C | 110 | a0002c0002t0001g0032a0002c0002t0001g0040a0002c0002t0001g0041others(107): Show | 110 | HG00639.hp1 HG00733.hp2 HG00741.hp1 others(107): Show |
intron_variant | MODIFIER | c.1365+2875delT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35966001 | ||||||
| chr6:35966130
|
G | A | 1 | a0003c0003t0002g0220 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1365+2747C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35966130 | ||||||
| chr6:35966427
|
GCAA | G | 20 | a0002c0002t0001g0119a0002c0002t0002g0272a0005c0005t0001g0021others(17): Show | 20 | HG01070.hp2 HG01081.hp2 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.1365+2447_1365+244 others(7): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35966427 | ||||||
| chr6:35966820
|
C | T | 4 | a0003c0003t0002g0240a0003c0003t0002g0241a0003c0003t0002g0242others(1): Show | 4 | NA18944.hp2 NA18978.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1365+2057G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35966820 | ||||||
| chr6:35966850
|
G | A | 1 | a0002c0002t0002g0214 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1365+2027C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35966850 | ||||||
| chr6:35966918
|
C | T | 1 | a0002c0002t0002g0231 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1365+1959G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35966918 | ||||||
| chr6:35967143
|
C | T | 4 | a0002c0002t0001g0059a0002c0010t0001g0062a0002c0010t0001g0063others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1365+1734G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35967143 | ||||||
| chr6:35967174
|
G | A | 7 | a0002c0002t0002g0198a0002c0002t0002g0207a0002c0002t0004g0184others(4): Show | 7 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1365+1703C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35967174 | ||||||
| chr6:35967253
|
G | A | 1 | a0003c0003t0002g0220 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1365+1624C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35967253 | ||||||
| chr6:35967324
|
G | A | 4 | a0003c0003t0002g0240a0003c0003t0002g0241a0003c0003t0002g0242others(1): Show | 4 | NA18944.hp2 NA18978.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1365+1553C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35967324 | ||||||
| chr6:35967378
|
G | A | 1 | a0005c0020t0002g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1365+1499C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35967378 | ||||||
| chr6:35967523
|
C | A | 1 | a0001c0001t0002g0304 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1365+1354G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35967523 | ||||||
| chr6:35967695
|
G | T | 1 | a0002c0002t0002g0291 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1365+1182C>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35967695 | ||||||
| chr6:35967932
|
C | T | 1 | a0003c0003t0002g0220 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1365+945G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35967932 | ||||||
| chr6:35968102
|
C | A | 3 | a0002c0002t0001g0119a0005c0005t0001g0165a0013c0019t0001g0166 | 3 | HG02698.hp1 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1365+775G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968102 | ||||||
| chr6:35968167
|
C | T | 8 | a0002c0002t0002g0214a0003c0003t0001g0002a0003c0003t0002g0239others(5): Show | 8 | HG02647.hp2 HG03540.hp2 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.1365+710G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968167 | ||||||
| chr6:35968225
|
A | G | 2 | a0002c0025t0002g0202a0003c0016t0005g0301 | 2 | HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1365+652T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968225 | ||||||
| chr6:35968297
|
A | G | 4 | a0003c0003t0002g0240a0003c0003t0002g0241a0003c0003t0002g0242others(1): Show | 4 | NA18944.hp2 NA18978.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1365+580T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968297 | ||||||
| chr6:35968339
|
T | C | 1 | a0003c0003t0002g0238 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1365+538A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968339 | ||||||
| chr6:35968358
|
G | A | 1 | a0002c0002t0004g0184 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1365+519C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968358 | ||||||
| chr6:35968447
|
C | T | 1 | a0005c0020t0002g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1365+430G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968447 | ||||||
| chr6:35968491
|
A | G | 3 | a0003c0003t0001g0005a0003c0003t0001g0014a0003c0003t0001g0018 | 3 | HG01891.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1365+386T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968491 | ||||||
| chr6:35968570
|
T | TAAATATA others(20): Show |
5 | a0002c0002t0002g0195a0002c0002t0002g0200a0002c0002t0002g0231others(2): Show | 5 | HG02257.hp2 HG02258.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1365+280_1365+306d others(29): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968570 | ||||||
| chr6:35968585
|
GTGTA | G | 3 | a0006c0006t0001g0140a0006c0006t0001g0157a0006c0006t0001g0172 | 3 | HG00642.hp1 HG01070.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1365+288_1365+291d others(6): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968585 | ||||||
| chr6:35968589
|
A | ATG | 9 | a0001c0001t0001g0001a0001c0001t0001g0122a0001c0001t0001g0123others(6): Show | 10 | HG00621.hp2 NA18941.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.1365+286_1365+287d others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968589 | ||||||
| chr6:35968589
|
A | ATGTGTGT others(22): Show |
1 | a0002c0002t0002g0197 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1365+287_1365+288i others(31): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968589 | ||||||
| chr6:35968589
|
ATG | A | 19 | a0001c0001t0001g0055a0001c0001t0001g0118a0001c0001t0002g0235others(16): Show | 19 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.1365+286_1365+287d others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968589 | ||||||
| chr6:35968589
|
ATGTG | A | 4 | a0002c0011t0001g0056a0002c0011t0001g0058a0005c0005t0001g0164others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1365+284_1365+287d others(6): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968589 | ||||||
| chr6:35968591
|
G | GTGTGTGA others(10): Show |
1 | a0003c0003t0001g0028 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1365+285_1365+286i others(19): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968591 | ||||||
| chr6:35968591
|
G | GTGTGTGA others(18): Show |
3 | a0002c0002t0002g0196a0003c0003t0001g0052a0017c0023t0001g0020 | 3 | HG00642.hp2 HG01255.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1365+285_1365+286i others(27): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968591 | ||||||
| chr6:35968593
|
G | GTGTGAAA others(16): Show |
3 | a0002c0002t0002g0199a0003c0003t0001g0029a0003c0003t0001g0031 | 3 | HG00741.hp1 HG01928.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1365+283_1365+284i others(25): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968593 | ||||||
| chr6:35968597
|
G | GAAA | 23 | a0002c0002t0001g0146a0002c0002t0001g0150a0002c0002t0001g0155others(20): Show | 23 | HG01361.hp1 HG01516.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1365+279_1365+280i others(5): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968597 | ||||||
| chr6:35968597
|
G | GAAATATA others(12): Show |
5 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0120others(2): Show | 5 | HG00733.hp2 HG01175.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1365+279_1365+280i others(21): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968597 | ||||||
| chr6:35968599
|
G | A | 24 | a0002c0002t0001g0146a0002c0002t0001g0150a0002c0002t0001g0155others(21): Show | 24 | HG01099.hp1 HG01361.hp1 HG01516.hp2 others(21): Show |
intron_variant | MODIFIER | c.1365+278C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968599 | ||||||
| chr6:35968601
|
G | A | 23 | a0002c0002t0001g0146a0002c0002t0001g0150a0002c0002t0001g0155others(20): Show | 23 | HG01361.hp1 HG01516.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1365+276C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968601 | ||||||
| chr6:35968602
|
T | C | 23 | a0002c0002t0001g0146a0002c0002t0001g0150a0002c0002t0001g0155others(20): Show | 23 | HG01361.hp1 HG01516.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1365+275A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968602 | ||||||
| chr6:35968603
|
G | A | 23 | a0002c0002t0001g0146a0002c0002t0001g0150a0002c0002t0001g0155others(20): Show | 23 | HG01361.hp1 HG01516.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1365+274C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968603 | ||||||
| chr6:35968605
|
G | A | 23 | a0002c0002t0001g0146a0002c0002t0001g0150a0002c0002t0001g0155others(20): Show | 23 | HG01361.hp1 HG01516.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1365+272C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968605 | ||||||
| chr6:35968605
|
G | GAA | 6 | a0002c0002t0001g0073a0002c0002t0001g0078a0002c0002t0001g0116others(3): Show | 6 | HG01168.hp2 HG01175.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1365+271_1365+272i others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968605 | ||||||
| chr6:35968605
|
G | GAATA | 6 | a0002c0002t0001g0098a0002c0002t0001g0102a0002c0002t0001g0144others(3): Show | 6 | HG02572.hp1 HG03710.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1365+271_1365+272i others(6): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968605 | ||||||
| chr6:35968605
|
G | GAATATA | 5 | a0002c0002t0001g0060a0002c0002t0001g0081a0002c0002t0001g0099others(2): Show | 5 | HG02027.hp1 HG02165.hp1 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.1365+271_1365+272i others(8): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968605 | ||||||
| chr6:35968605
|
G | GAATATAT others(1): Show |
3 | a0002c0002t0001g0082a0002c0002t0001g0143a0002c0002t0002g0212 | 3 | NA18994.hp1 NA18998.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1365+271_1365+272i others(10): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968605 | ||||||
| chr6:35968605
|
G | GAATATAT others(3): Show |
1 | a0002c0002t0001g0077 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1365+271_1365+272i others(12): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968605 | ||||||
| chr6:35968605
|
G | GAATATAT others(5): Show |
2 | a0002c0002t0001g0113a0002c0002t0001g0141 | 2 | NA18967.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1365+271_1365+272i others(14): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968605 | ||||||
| chr6:35968605
|
G | GAATATAT others(9): Show |
1 | a0002c0010t0001g0062 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1365+271_1365+272i others(18): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968605 | ||||||
| chr6:35968605
|
GTGTGTA | G | 5 | a0002c0002t0001g0074a0002c0002t0001g0111a0002c0002t0001g0114others(2): Show | 5 | HG00639.hp1 HG01123.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1365+266_1365+271d others(8): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968605 | ||||||
| chr6:35968605
|
GTGTGTAT others(1): Show |
G | 4 | a0002c0002t0001g0129a0003c0003t0002g0238a0005c0005t0001g0176others(1): Show | 4 | HG01070.hp2 HG01081.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1365+264_1365+271d others(10): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968605 | ||||||
| chr6:35968605
|
GTGTGTAT others(3): Show |
G | 7 | a0002c0002t0001g0057a0002c0002t0001g0119a0005c0005t0001g0021others(4): Show | 7 | HG02698.hp1 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1365+262_1365+271d others(12): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968605 | ||||||
| chr6:35968605
|
GTGTGTAT others(4): Show |
G | 1 | a0005c0005t0001g0022 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1365+261_1365+271d others(13): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968605 | ||||||
| chr6:35968605
|
GTGTGTAT others(5): Show |
G | 2 | a0005c0005t0001g0177a0005c0005t0001g0178 | 2 | NA18975.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1365+260_1365+271d others(14): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968605 | ||||||
| chr6:35968605
|
GTGTGTAT others(7): Show |
G | 5 | a0002c0002t0002g0272a0005c0005t0001g0163a0005c0005t0001g0170others(2): Show | 5 | HG02132.hp1 NA18947.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.1365+258_1365+271d others(16): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968605 | ||||||
| chr6:35968605
|
GTGTGTAT others(9): Show |
G | 1 | a0002c0002t0004g0184 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1365+256_1365+271d others(18): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968605 | ||||||
| chr6:35968605
|
GTGTGTAT others(15): Show |
G | 6 | a0002c0002t0001g0059a0002c0002t0002g0198a0002c0002t0002g0207others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1365+250_1365+271d others(24): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968605 | ||||||
| chr6:35968605
|
GTGTGTAT others(17): Show |
G | 1 | a0003c0003t0001g0035 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1365+248_1365+271d others(26): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968605 | ||||||
| chr6:35968606
|
T | A | 14 | a0002c0002t0001g0065a0002c0002t0001g0066a0002c0002t0001g0067others(11): Show | 14 | HG01256.hp1 HG01256.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1365+271A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968606 | ||||||
| chr6:35968607
|
G | A | 42 | a0002c0002t0001g0060a0002c0002t0001g0065a0002c0002t0001g0066others(39): Show | 42 | HG00642.hp1 HG01070.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1365+270C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968607 | ||||||
| chr6:35968607
|
G | GTA | 6 | a0001c0001t0001g0054a0001c0001t0001g0097a0001c0001t0001g0148others(3): Show | 6 | HG00735.hp1 HG02129.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.1365+269_1365+270i others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968607 | ||||||
| chr6:35968607
|
G | GTATATAT others(5): Show |
2 | a0006c0006t0002g0255a0006c0006t0002g0256 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1365+269_1365+270i others(14): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968607 | ||||||
| chr6:35968607
|
G | GTATATAT others(19): Show |
1 | a0001c0001t0002g0190 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1365+269_1365+270i others(28): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968607 | ||||||
| chr6:35968607
|
GTGTA | G | 12 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0053others(9): Show | 12 | HG00280.hp1 HG01099.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.1365+266_1365+269d others(6): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968607 | ||||||
| chr6:35968607
|
GTGTATA | G | 6 | a0001c0001t0002g0194a0001c0001t0002g0230a0001c0001t0002g0288others(3): Show | 6 | HG00639.hp2 HG02723.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.1365+264_1365+269d others(8): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968607 | ||||||
| chr6:35968607
|
GTGTATAT others(1): Show |
G | 8 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0109others(5): Show | 8 | HG01515.hp1 HG01515.hp2 HG04204.hp2 others(5): Show |
intron_variant | MODIFIER | c.1365+262_1365+269d others(10): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968607 | ||||||
| chr6:35968607
|
GTGTATAT others(5): Show |
G | 1 | a0005c0005t0001g0179 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1365+258_1365+269d others(14): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968607 | ||||||
| chr6:35968607
|
GTGTATAT others(9): Show |
G | 1 | a0020c0029t0001g0152 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1365+254_1365+269d others(18): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968607 | ||||||
| chr6:35968607
|
GTGTATAT others(23): Show |
G | 1 | a0001c0001t0002g0251 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1365+240_1365+269d others(32): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968607 | ||||||
| chr6:35968608
|
T | A | 9 | a0002c0002t0001g0032a0002c0002t0001g0069a0002c0002t0001g0070others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.1365+269A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968608 | ||||||
| chr6:35968609
|
G | A | 75 | a0001c0001t0001g0054a0001c0001t0001g0097a0001c0001t0001g0100others(72): Show | 75 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.1365+268C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968609 | ||||||
| chr6:35968609
|
G | GTA | 6 | a0001c0001t0002g0208a0001c0001t0002g0281a0001c0001t0002g0286others(3): Show | 6 | HG00597.hp1 HG01884.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1365+266_1365+267d others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968609 | ||||||
| chr6:35968609
|
G | GTATA | 6 | a0001c0001t0002g0282a0001c0001t0002g0304a0004c0004t0001g0010others(3): Show | 6 | HG03041.hp2 HG03139.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.1365+264_1365+267d others(6): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968609 | ||||||
| chr6:35968609
|
G | GTATATA | 4 | a0001c0001t0001g0050a0001c0001t0002g0284a0004c0004t0001g0012others(1): Show | 4 | HG00673.hp1 HG01255.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1365+262_1365+267d others(8): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968609 | ||||||
| chr6:35968609
|
G | GTGTA | 4 | a0001c0001t0001g0134a0001c0001t0002g0228a0004c0004t0001g0033others(1): Show | 4 | HG00621.hp1 HG02148.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.1365+267_1365+268i others(6): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968609 | ||||||
| chr6:35968609
|
G | GTGTATA | 3 | a0001c0001t0002g0203a0001c0001t0002g0219a0004c0004t0001g0007 | 3 | HG02922.hp1 HG03579.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1365+267_1365+268i others(8): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968609 | ||||||
| chr6:35968609
|
G | GTGTGTGT others(5): Show |
4 | a0008c0008t0001g0042a0008c0008t0001g0043a0008c0008t0001g0044others(1): Show | 4 | HG02622.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1365+267_1365+268i others(14): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968609 | ||||||
| chr6:35968609
|
G | GTGTGTGT others(7): Show |
2 | a0003c0003t0002g0240a0003c0003t0002g0241 | 2 | NA18944.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1365+267_1365+268i others(16): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968609 | ||||||
| chr6:35968609
|
G | GTGTGTGT others(15): Show |
2 | a0003c0003t0002g0242a0003c0003t0002g0243 | 2 | NA18978.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1365+267_1365+268i others(24): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968609 | ||||||
| chr6:35968609
|
GTA | G | 12 | a0001c0001t0001g0135a0001c0001t0002g0206a0001c0001t0002g0210others(9): Show | 12 | HG00099.hp1 HG00733.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1365+266_1365+267d others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968609 | ||||||
| chr6:35968609
|
GTATA | G | 48 | a0001c0001t0001g0083a0001c0001t0001g0136a0001c0001t0001g0137others(45): Show | 48 | HG00280.hp2 HG00323.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.1365+264_1365+267d others(6): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968609 | ||||||
| chr6:35968609
|
GTATATA | G | 5 | a0001c0001t0002g0201a0001c0001t0002g0236a0001c0001t0002g0303others(2): Show | 5 | HG01167.hp2 HG01891.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1365+262_1365+267d others(8): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968609 | ||||||
| chr6:35968609
|
GTATATAT others(3): Show |
G | 4 | a0001c0001t0002g0187a0001c0001t0002g0189a0001c0001t0002g0209others(1): Show | 4 | HG01081.hp1 HG03195.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1365+258_1365+267d others(12): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968609 | ||||||
| chr6:35968609
|
GTATATAT others(5): Show |
G | 2 | a0001c0001t0002g0188a0001c0001t0002g0285 | 2 | HG01123.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1365+256_1365+267d others(14): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968609 | ||||||
| chr6:35968609
|
GTATATAT others(9): Show |
G | 4 | a0001c0001t0002g0259a0001c0001t0002g0262a0001c0001t0002g0266others(1): Show | 4 | HG01346.hp1 HG01433.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1365+252_1365+267d others(18): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968609 | ||||||
| chr6:35968609
|
GTATATAT others(17): Show |
G | 3 | a0002c0025t0002g0202a0003c0016t0005g0301a0004c0004t0001g0085 | 3 | HG02922.hp2 HG06807.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1365+244_1365+267d others(26): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968609 | ||||||
| chr6:35968609
|
GTATATAT others(19): Show |
G | 6 | a0007c0007t0002g0232a0007c0007t0002g0233a0007c0007t0002g0244others(3): Show | 6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1365+242_1365+267d others(28): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968609 | ||||||
| chr6:35968609
|
GTATATAT others(21): Show |
G | 1 | a0002c0002t0002g0214 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1365+240_1365+267d others(30): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968609 | ||||||
| chr6:35968610
|
T | A | 2 | a0002c0011t0001g0056a0002c0011t0001g0058 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1365+267A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968610 | ||||||
| chr6:35968611
|
A | G | 18 | a0001c0001t0001g0101a0001c0001t0002g0204a0001c0001t0002g0211others(15): Show | 18 | HG00597.hp2 HG00642.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.1365+266T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968611 | ||||||
| chr6:35968612
|
T | A | 5 | a0002c0002t0001g0074a0002c0002t0001g0111a0002c0002t0001g0114others(2): Show | 5 | HG00639.hp1 HG01123.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1365+265A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968612 | ||||||
| chr6:35968613
|
A | G | 19 | a0001c0001t0001g0135a0001c0001t0002g0210a0001c0001t0002g0223others(16): Show | 19 | HG00733.hp1 HG00733.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1365+264T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968613 | ||||||
| chr6:35968614
|
T | A | 2 | a0002c0002t0001g0129a0003c0003t0002g0238 | 2 | HG02683.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1365+263A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968614 | ||||||
| chr6:35968615
|
A | G | 56 | a0001c0001t0001g0083a0001c0001t0001g0136a0001c0001t0001g0137others(53): Show | 56 | HG00323.hp2 HG00673.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.1365+262T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968615 | ||||||
| chr6:35968616
|
T | A | 1 | a0002c0002t0001g0057 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1365+261A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968616 | ||||||
| chr6:35968617
|
A | G | 10 | a0001c0001t0002g0217a0001c0001t0002g0236a0002c0002t0001g0040others(7): Show | 10 | HG00733.hp2 HG00741.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1365+260T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968617 | ||||||
| chr6:35968619
|
A | G | 30 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0120others(27): Show | 30 | HG00733.hp2 HG01099.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.1365+258T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968619 | ||||||
| chr6:35968621
|
A | G | 28 | a0001c0001t0002g0187a0001c0001t0002g0189a0001c0001t0002g0209others(25): Show | 28 | HG01081.hp1 HG01361.hp1 HG01516.hp2 others(25): Show |
intron_variant | MODIFIER | c.1365+256T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968621 | ||||||
| chr6:35968623
|
A | G | 25 | a0001c0001t0002g0188a0002c0002t0001g0146a0002c0002t0001g0150others(22): Show | 25 | HG01123.hp1 HG01361.hp1 HG01516.hp2 others(22): Show |
intron_variant | MODIFIER | c.1365+254T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968623 | ||||||
| chr6:35968625
|
A | G | 24 | a0002c0002t0001g0146a0002c0002t0001g0150a0002c0002t0001g0155others(21): Show | 24 | HG01361.hp1 HG01516.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.1365+252T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968625 | ||||||
| chr6:35968627
|
A | G | 28 | a0001c0001t0002g0259a0001c0001t0002g0262a0001c0001t0002g0266others(25): Show | 28 | HG01346.hp1 HG01361.hp1 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.1365+250T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968627 | ||||||
| chr6:35968628
|
T | A | 1 | a0002c0002t0001g0059 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1365+249A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968628 | ||||||
| chr6:35968629
|
A | G | 23 | a0002c0002t0001g0146a0002c0002t0001g0150a0002c0002t0001g0155others(20): Show | 23 | HG01361.hp1 HG01516.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1365+248T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968629 | ||||||
| chr6:35968631
|
A | G | 23 | a0002c0002t0001g0146a0002c0002t0001g0150a0002c0002t0001g0155others(20): Show | 23 | HG01361.hp1 HG01516.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1365+246T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968631 | ||||||
| chr6:35968633
|
A | G | 23 | a0002c0002t0001g0146a0002c0002t0001g0150a0002c0002t0001g0155others(20): Show | 23 | HG01361.hp1 HG01516.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1365+244T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968633 | ||||||
| chr6:35968635
|
A | G | 23 | a0002c0002t0001g0146a0002c0002t0001g0150a0002c0002t0001g0155others(20): Show | 23 | HG01361.hp1 HG01516.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1365+242T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968635 | ||||||
| chr6:35968637
|
A | G | 31 | a0002c0002t0001g0146a0002c0002t0001g0150a0002c0002t0001g0155others(28): Show | 31 | HG01361.hp1 HG01516.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.1365+240T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968637 | ||||||
| chr6:35968655
|
C | A | 2 | a0002c0002t0001g0116a0002c0002t0002g0250 | 2 | HG02080.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1365+222G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968655 | ||||||
| chr6:35968714
|
C | G | 1 | a0006c0006t0001g0157 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1365+163G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968714 | ||||||
| chr6:35968737
|
T | C | 5 | a0003c0003t0002g0239a0003c0003t0002g0240a0003c0003t0002g0241others(2): Show | 5 | HG03710.hp2 NA18944.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1365+140A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968737 | ||||||
| chr6:35968760
|
C | A | 1 | a0005c0020t0002g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1365+117G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968760 | ||||||
| chr6:35968776
|
G | GC | 38 | a0001c0001t0001g0100a0001c0001t0001g0108a0001c0001t0001g0148others(35): Show | 38 | HG00741.hp1 HG00741.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.1365+100dupG | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968776 | ||||||
| chr6:35968782
|
C | G | 1 | a0001c0001t0002g0194 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1365+95G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968782 | ||||||
| chr6:35968842
|
G | A | 1 | a0017c0023t0001g0020 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1365+35C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 11/19 | chr6 | 35968842 | ||||||
| chr6:35968969
|
C | A | 1 | a0003c0003t0002g0239 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1288-15G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35968969 | ||||||
| chr6:35968971
|
A | C | 1 | a0002c0002t0002g0198 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1288-17T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35968971 | ||||||
| chr6:35969029
|
T | G | 1 | a0001c0001t0002g0223 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1288-75A>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35969029 | ||||||
| chr6:35969079
|
G | A | 1 | a0003c0003t0002g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1288-125C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35969079 | ||||||
| chr6:35969238
|
A | G | 32 | a0002c0002t0001g0146a0002c0002t0001g0150a0002c0002t0001g0155others(29): Show | 32 | HG00642.hp2 HG01109.hp1 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.1288-284T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35969238 | ||||||
| chr6:35969371
|
C | G | 1 | a0001c0001t0002g0224 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1288-417G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35969371 | ||||||
| chr6:35969475
|
G | A | 3 | a0006c0006t0001g0140a0006c0006t0001g0157a0006c0006t0001g0172 | 3 | HG00642.hp1 HG01070.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1288-521C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35969475 | ||||||
| chr6:35969553
|
A | G | 148 | a0002c0002t0001g0032a0002c0002t0001g0040a0002c0002t0001g0041others(145): Show | 148 | HG00639.hp1 HG00642.hp2 HG00733.hp2 others(145): Show |
intron_variant | MODIFIER | c.1288-599T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35969553 | ||||||
| chr6:35969596
|
C | CA | 73 | a0002c0002t0001g0032a0002c0002t0001g0057a0002c0002t0001g0059others(70): Show | 73 | HG00639.hp1 HG01070.hp2 HG01081.hp2 others(70): Show |
intron_variant | MODIFIER | c.1288-643dupT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35969596 | ||||||
| chr6:35969649
|
G | GCCCTAAA others(10): Show |
148 | a0002c0002t0001g0032a0002c0002t0001g0040a0002c0002t0001g0041others(145): Show | 148 | HG00639.hp1 HG00642.hp2 HG00733.hp2 others(145): Show |
intron_variant | MODIFIER | c.1288-696_1288-695i others(19): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35969649 | ||||||
| chr6:35969952
|
A | C | 1 | a0003c0003t0002g0243 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1288-998T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35969952 | ||||||
| chr6:35969959
|
A | C | 1 | a0001c0001t0002g0227 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1288-1005T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35969959 | ||||||
| chr6:35970090
|
C | A | 4 | a0003c0003t0002g0240a0003c0003t0002g0241a0003c0003t0002g0242others(1): Show | 4 | NA18944.hp2 NA18978.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1288-1136G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35970090 | ||||||
| chr6:35970238
|
G | C | 1 | a0002c0002t0001g0129 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1288-1284C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35970238 | ||||||
| chr6:35970268
|
C | T | 1 | a0005c0020t0002g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1288-1314G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35970268 | ||||||
| chr6:35970274
|
G | C | 1 | a0002c0002t0004g0184 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1288-1320C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35970274 | ||||||
| chr6:35970351
|
C | T | 1 | a0002c0002t0001g0077 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1288-1397G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35970351 | ||||||
| chr6:35970506
|
A | G | 1 | a0003c0003t0001g0038 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1288-1552T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35970506 | ||||||
| chr6:35970854
|
C | T | 41 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0120others(38): Show | 41 | HG00642.hp2 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1288-1900G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35970854 | ||||||
| chr6:35970888
|
C | T | 1 | a0003c0003t0002g0239 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1288-1934G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35970888 | ||||||
| chr6:35970943
|
G | A | 3 | a0003c0003t0001g0027a0003c0003t0001g0029a0003c0003t0001g0030 | 3 | HG01175.hp2 HG01361.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1288-1989C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35970943 | ||||||
| chr6:35971028
|
A | AAAC | 7 | a0001c0001t0002g0218a0002c0002t0001g0146a0002c0002t0001g0155others(4): Show | 7 | HG00642.hp2 HG01361.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1288-2077_1288-207 others(7): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35971028 | ||||||
| chr6:35971028
|
AAAC | A | 5 | a0002c0002t0002g0214a0003c0003t0001g0002a0005c0005t0001g0169others(2): Show | 5 | HG00639.hp2 HG01255.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1288-2077_1288-207 others(7): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35971028 | ||||||
| chr6:35971133
|
T | C | 5 | a0003c0003t0002g0239a0003c0003t0002g0240a0003c0003t0002g0241others(2): Show | 5 | HG03710.hp2 NA18944.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1288-2179A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35971133 | ||||||
| chr6:35971369
|
C | CT | 58 | a0002c0002t0001g0032a0002c0002t0001g0057a0002c0002t0001g0059others(55): Show | 58 | HG00639.hp1 HG01106.hp1 HG01123.hp2 others(55): Show |
intron_variant | MODIFIER | c.1288-2416dupA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35971369 | ||||||
| chr6:35971547
|
T | C | 1 | a0003c0003t0002g0220 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1288-2593A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35971547 | ||||||
| chr6:35971627
|
A | G | 16 | a0002c0002t0001g0119a0002c0002t0002g0272a0005c0005t0001g0163others(13): Show | 16 | HG01070.hp2 HG01081.hp2 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.1288-2673T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35971627 | ||||||
| chr6:35971641
|
A | G | 46 | a0002c0002t0001g0119a0002c0002t0002g0198a0002c0002t0002g0207others(43): Show | 46 | HG01070.hp2 HG01081.hp2 HG02109.hp2 others(43): Show |
intron_variant | MODIFIER | c.1288-2687T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35971641 | ||||||
| chr6:35971768
|
A | G | 2 | a0002c0002t0002g0214a0003c0003t0001g0002 | 2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1288-2814T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35971768 | ||||||
| chr6:35971781
|
T | C | 52 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0119others(49): Show | 52 | HG00733.hp2 HG00741.hp1 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.1288-2827A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35971781 | ||||||
| chr6:35971872
|
C | A | 43 | a0002c0002t0001g0119a0002c0002t0002g0198a0002c0002t0002g0207others(40): Show | 43 | HG01070.hp2 HG01081.hp2 HG02109.hp2 others(40): Show |
intron_variant | MODIFIER | c.1288-2918G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35971872 | ||||||
| chr6:35971911
|
C | T | 58 | a0002c0002t0001g0032a0002c0002t0001g0057a0002c0002t0001g0059others(55): Show | 58 | HG00639.hp1 HG01106.hp1 HG01123.hp2 others(55): Show |
intron_variant | MODIFIER | c.1288-2957G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35971911 | ||||||
| chr6:35971955
|
G | A | 44 | a0002c0002t0001g0119a0002c0002t0002g0198a0002c0002t0002g0207others(41): Show | 44 | HG01070.hp2 HG01081.hp2 HG02109.hp2 others(41): Show |
intron_variant | MODIFIER | c.1288-3001C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35971955 | ||||||
| chr6:35972028
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG00735.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1288-3074C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35972028 | ||||||
| chr6:35972218
|
C | A | 5 | a0003c0003t0002g0239a0003c0003t0002g0240a0003c0003t0002g0241others(2): Show | 5 | HG03710.hp2 NA18944.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1287+3157G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35972218 | ||||||
| chr6:35972283
|
G | A | 24 | a0002c0002t0002g0198a0002c0002t0002g0207a0002c0002t0002g0214others(21): Show | 24 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.1287+3092C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35972283 | ||||||
| chr6:35972291
|
G | A | 1 | a0003c0016t0005g0301 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1287+3084C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35972291 | ||||||
| chr6:35972393
|
G | GA | 51 | a0001c0001t0002g0302a0002c0002t0001g0059a0002c0002t0001g0073others(48): Show | 51 | HG00642.hp2 HG01070.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.1287+2981dupT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35972393 | ||||||
| chr6:35972506
|
G | A | 6 | a0007c0007t0002g0232a0007c0007t0002g0233a0007c0007t0002g0244others(3): Show | 6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1287+2869C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35972506 | ||||||
| chr6:35972610
|
G | C | 1 | a0003c0003t0001g0052 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1287+2765C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35972610 | ||||||
| chr6:35972756
|
C | T | 1 | a0003c0003t0002g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1287+2619G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35972756 | ||||||
| chr6:35972759
|
A | G | 5 | a0003c0003t0002g0239a0003c0003t0002g0240a0003c0003t0002g0241others(2): Show | 5 | HG03710.hp2 NA18944.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1287+2616T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35972759 | ||||||
| chr6:35972768
|
T | C | 1 | a0003c0003t0002g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1287+2607A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35972768 | ||||||
| chr6:35972933
|
G | T | 1 | a0002c0025t0002g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1287+2442C>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35972933 | ||||||
| chr6:35972979
|
A | G | 4 | a0008c0008t0001g0042a0008c0008t0001g0043a0008c0008t0001g0044others(1): Show | 4 | HG02622.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1287+2396T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35972979 | ||||||
| chr6:35973128
|
C | T | 1 | a0002c0002t0004g0184 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1287+2247G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35973128 | ||||||
| chr6:35973154
|
C | T | 1 | a0004c0004t0001g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1287+2221G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35973154 | ||||||
| chr6:35973199
|
A | G | 16 | a0002c0002t0001g0119a0002c0002t0002g0272a0005c0005t0001g0163others(13): Show | 16 | HG01070.hp2 HG01081.hp2 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.1287+2176T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35973199 | ||||||
| chr6:35973221
|
T | G | 147 | a0002c0002t0001g0032a0002c0002t0001g0040a0002c0002t0001g0041others(144): Show | 147 | HG00639.hp1 HG00642.hp2 HG00733.hp2 others(144): Show |
intron_variant | MODIFIER | c.1287+2154A>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35973221 | ||||||
| chr6:35973268
|
T | C | 1 | a0001c0001t0002g0283 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1287+2107A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35973268 | ||||||
| chr6:35973322
|
A | G | 6 | a0002c0002t0001g0120a0003c0003t0001g0027a0003c0003t0001g0028others(3): Show | 6 | HG00733.hp2 HG00741.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.1287+2053T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35973322 | ||||||
| chr6:35973465
|
G | A | 1 | a0009c0009t0001g0092 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1287+1910C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35973465 | ||||||
| chr6:35973835
|
C | T | 2 | a0001c0001t0002g0293a0001c0001t0002g0295 | 2 | NA18946.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1287+1540G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35973835 | ||||||
| chr6:35973910
|
C | T | 2 | a0001c0001t0002g0251a0001c0001t0002g0305 | 2 | HG02055.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1287+1465G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35973910 | ||||||
| chr6:35974033
|
T | C | 9 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0120others(6): Show | 9 | HG00733.hp2 HG00741.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1287+1342A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35974033 | ||||||
| chr6:35974054
|
A | T | 20 | a0002c0002t0001g0119a0002c0002t0002g0272a0005c0005t0001g0021others(17): Show | 20 | HG01070.hp2 HG01081.hp2 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.1287+1321T>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35974054 | ||||||
| chr6:35974305
|
A | G | 1 | a0002c0002t0002g0214 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1287+1070T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35974305 | ||||||
| chr6:35974536
|
C | T | 20 | a0002c0002t0001g0119a0002c0002t0002g0272a0005c0005t0001g0021others(17): Show | 20 | HG01070.hp2 HG01081.hp2 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.1287+839G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35974536 | ||||||
| chr6:35974575
|
G | A | 1 | a0003c0003t0002g0220 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1287+800C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35974575 | ||||||
| chr6:35974703
|
T | C | 2 | a0002c0025t0002g0202a0003c0016t0005g0301 | 2 | HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1287+672A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35974703 | ||||||
| chr6:35974886
|
G | A | 5 | a0003c0003t0002g0239a0003c0003t0002g0240a0003c0003t0002g0241others(2): Show | 5 | HG03710.hp2 NA18944.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1287+489C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35974886 | ||||||
| chr6:35974906
|
G | GT | 8 | a0001c0001t0002g0210a0001c0001t0002g0211a0001c0001t0002g0217others(5): Show | 8 | HG02129.hp1 HG02129.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1287+468dupA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35974906 | ||||||
| chr6:35974906
|
GT | G | 14 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0120others(11): Show | 14 | HG00733.hp2 HG00741.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1287+468delA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35974906 | ||||||
| chr6:35974972
|
G | A | 10 | a0007c0007t0002g0232a0007c0007t0002g0233a0007c0007t0002g0244others(7): Show | 10 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1287+403C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35974972 | ||||||
| chr6:35975037
|
C | T | 1 | a0003c0003t0001g0095 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1287+338G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35975037 | ||||||
| chr6:35975127
|
G | A | 2 | a0002c0002t0002g0214a0003c0003t0001g0002 | 2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1287+248C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35975127 | ||||||
| chr6:35975194
|
C | A | 1 | a0002c0002t0002g0291 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1287+181G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35975194 | ||||||
| chr6:35975348
|
T | C | 1 | a0005c0020t0002g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1287+27A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 10/19 | chr6 | 35975348 | ||||||
| chr6:35975492
|
T | C | 4 | a0003c0003t0001g0052a0009c0009t0001g0092a0009c0009t0001g0093others(1): Show | 4 | HG00642.hp2 HG01361.hp1 HG02486.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1174-4A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35975492 | ||||||
| chr6:35975521
|
G | A | 3 | a0007c0007t0002g0244a0007c0007t0002g0298a0011c0014t0001g0128 | 3 | HG02451.hp2 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1174-33C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35975521 | ||||||
| chr6:35975535
|
A | G | 19 | a0002c0002t0001g0059a0002c0002t0001g0150a0002c0013t0001g0019others(16): Show | 19 | HG01255.hp2 HG01516.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.1174-47T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35975535 | ||||||
| chr6:35975562
|
G | GTT | 32 | a0002c0002t0001g0059a0002c0002t0001g0150a0002c0002t0002g0195others(29): Show | 32 | HG00642.hp2 HG01109.hp1 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.1174-76_1174-75dup others(2): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35975562 | ||||||
| chr6:35975569
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1174-81A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35975569 | ||||||
| chr6:35975574
|
T | A | 1 | a0003c0003t0001g0002 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1174-86A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35975574 | ||||||
| chr6:35975577
|
A | G | 1 | a0001c0001t0002g0285 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1174-89T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35975577 | ||||||
| chr6:35975649
|
C | A | 1 | a0003c0003t0002g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1174-161G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35975649 | ||||||
| chr6:35975881
|
C | G | 4 | a0003c0003t0001g0052a0009c0009t0001g0092a0009c0009t0001g0093others(1): Show | 4 | HG00642.hp2 HG01361.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-393G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35975881 | ||||||
| chr6:35975913
|
C | CA | 80 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0097others(77): Show | 80 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.1174-426dupT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35975913 | ||||||
| chr6:35975913
|
C | CAA | 14 | a0001c0001t0002g0302a0002c0002t0002g0198a0002c0002t0002g0207others(11): Show | 14 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.1174-427_1174-426d others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35975913 | ||||||
| chr6:35975913
|
CA | C | 37 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0100others(34): Show | 37 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.1174-426delT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35975913 | ||||||
| chr6:35975927
|
A | G | 1 | a0002c0002t0001g0080 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1174-439T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35975927 | ||||||
| chr6:35975970
|
A | G | 2 | a0002c0002t0002g0214a0003c0003t0001g0002 | 2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1174-482T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35975970 | ||||||
| chr6:35976112
|
C | G | 6 | a0007c0007t0002g0232a0007c0007t0002g0233a0007c0007t0002g0244others(3): Show | 6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1174-624G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35976112 | ||||||
| chr6:35976240
|
G | A | 1 | a0003c0003t0002g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1174-752C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35976240 | ||||||
| chr6:35976338
|
C | T | 2 | a0007c0007t0002g0232a0007c0007t0002g0233 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1174-850G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35976338 | ||||||
| chr6:35976424
|
C | CA | 14 | a0001c0001t0001g0148a0002c0002t0001g0119a0005c0005t0001g0164others(11): Show | 14 | HG01070.hp2 HG01081.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1173+779dupT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35976424 | ||||||
| chr6:35976550
|
C | CT | 12 | a0001c0001t0002g0187a0001c0001t0002g0190a0001c0001t0002g0253others(9): Show | 12 | HG01081.hp1 HG01169.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.1173+653dupA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35976550 | ||||||
| chr6:35976550
|
C | CTTTTTTT others(3): Show |
6 | a0002c0002t0004g0184a0003c0003t0001g0002a0005c0005t0001g0022others(3): Show | 6 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1173+644_1173+653d others(12): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35976550 | ||||||
| chr6:35976550
|
C | CTTTTTTT others(4): Show |
8 | a0002c0002t0002g0214a0002c0013t0002g0234a0003c0003t0001g0037others(5): Show | 8 | HG02451.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1173+643_1173+653d others(13): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35976550 | ||||||
| chr6:35976550
|
C | CTTTTTTT others(5): Show |
8 | a0002c0002t0002g0198a0002c0002t0002g0207a0003c0003t0001g0035others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1173+642_1173+653d others(14): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35976550 | ||||||
| chr6:35976550
|
C | CTTTTTTT others(6): Show |
3 | a0003c0003t0002g0240a0003c0003t0002g0241a0003c0003t0002g0242 | 3 | NA18944.hp2 NA19057.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1173+641_1173+653d others(15): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35976550 | ||||||
| chr6:35976550
|
C | CTTTTTTT others(7): Show |
2 | a0003c0003t0002g0239a0003c0003t0002g0243 | 2 | HG03710.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.1173+640_1173+653d others(16): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35976550 | ||||||
| chr6:35976550
|
CTTTTT | C | 15 | a0002c0002t0001g0119a0002c0002t0002g0272a0005c0005t0001g0163others(12): Show | 15 | HG01070.hp2 HG01081.hp2 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.1173+649_1173+653d others(7): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35976550 | ||||||
| chr6:35976604
|
G | A | 1 | a0001c0001t0002g0271 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1173+600C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35976604 | ||||||
| chr6:35976619
|
C | G | 4 | a0003c0003t0002g0240a0003c0003t0002g0241a0003c0003t0002g0242others(1): Show | 4 | NA18944.hp2 NA18978.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1173+585G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35976619 | ||||||
| chr6:35976659
|
G | A | 6 | a0007c0007t0002g0232a0007c0007t0002g0233a0007c0007t0002g0244others(3): Show | 6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1173+545C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35976659 | ||||||
| chr6:35976842
|
C | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0122a0001c0001t0001g0123others(5): Show | 9 | HG01106.hp2 HG02040.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.1173+362G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35976842 | ||||||
| chr6:35977164
|
A | G | 2 | a0001c0001t0002g0209a0001c0001t0002g0226 | 2 | HG03195.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1173+40T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 9/19 | chr6 | 35977164 | ||||||
| chr6:35977442
|
C | CT | 19 | a0002c0002t0001g0119a0002c0002t0002g0272a0003c0003t0002g0240others(16): Show | 19 | HG01081.hp2 HG02132.hp1 HG02698.hp1 others(16): Show |
intron_variant | MODIFIER | c.1026-92dupA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35977442 | ||||||
| chr6:35977442
|
CT | C | 9 | a0001c0001t0001g0122a0001c0001t0002g0209a0002c0002t0001g0060others(6): Show | 9 | HG01169.hp1 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1026-92delA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35977442 | ||||||
| chr6:35977443
|
T | C | 1 | a0001c0001t0002g0281 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1026-92A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35977443 | ||||||
| chr6:35977468
|
A | G | 3 | a0002c0010t0001g0062a0002c0010t0001g0063a0002c0010t0001g0064 | 3 | HG02572.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1026-117T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35977468 | ||||||
| chr6:35977477
|
C | T | 24 | a0002c0002t0002g0198a0002c0002t0002g0207a0002c0002t0002g0214others(21): Show | 24 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.1026-126G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35977477 | ||||||
| chr6:35977504
|
A | G | 9 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0120others(6): Show | 9 | HG00733.hp2 HG00741.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1026-153T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35977504 | ||||||
| chr6:35977566
|
C | T | 147 | a0002c0002t0001g0032a0002c0002t0001g0040a0002c0002t0001g0041others(144): Show | 147 | HG00639.hp1 HG00642.hp2 HG00733.hp2 others(144): Show |
intron_variant | MODIFIER | c.1026-215G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35977566 | ||||||
| chr6:35977633
|
A | G | 2 | a0002c0002t0002g0214a0003c0003t0001g0002 | 2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1026-282T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35977633 | ||||||
| chr6:35977782
|
C | T | 13 | a0002c0002t0001g0065a0002c0002t0001g0066a0002c0002t0001g0067others(10): Show | 13 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.1026-431G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35977782 | ||||||
| chr6:35977856
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1026-505C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35977856 | ||||||
| chr6:35977872
|
G | A | 1 | a0002c0002t0002g0257 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1026-521C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35977872 | ||||||
| chr6:35977903
|
G | A | 7 | a0002c0002t0002g0198a0002c0002t0002g0207a0002c0002t0004g0184others(4): Show | 7 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1026-552C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35977903 | ||||||
| chr6:35977954
|
C | T | 2 | a0007c0007t0002g0244a0007c0007t0002g0298 | 2 | HG02451.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1026-603G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35977954 | ||||||
| chr6:35977989
|
G | A | 1 | a0002c0002t0002g0214 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1026-638C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35977989 | ||||||
| chr6:35978085
|
C | CA | 143 | a0002c0002t0001g0032a0002c0002t0001g0040a0002c0002t0001g0041others(140): Show | 143 | HG00639.hp1 HG00642.hp2 HG00733.hp2 others(140): Show |
intron_variant | MODIFIER | c.1026-735dupT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35978085 | ||||||
| chr6:35978146
|
G | GA | 6 | a0001c0001t0002g0206a0001c0001t0002g0209a0001c0001t0002g0226others(3): Show | 6 | HG02886.hp2 HG02922.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1026-796dupT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35978146 | ||||||
| chr6:35978146
|
GA | G | 33 | a0001c0001t0002g0236a0001c0001t0002g0300a0002c0002t0001g0119others(30): Show | 33 | HG01081.hp2 HG01109.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.1026-796delT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35978146 | ||||||
| chr6:35978146
|
GAA | G | 20 | a0002c0002t0002g0198a0002c0002t0002g0207a0002c0002t0002g0214others(17): Show | 20 | HG01070.hp2 HG02109.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1026-797_1026-796d others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35978146 | ||||||
| chr6:35978241
|
A | AT | 9 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0120others(6): Show | 9 | HG00733.hp2 HG00741.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1026-891_1026-890i others(3): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35978241 | ||||||
| chr6:35978244
|
A | T | 9 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0120others(6): Show | 9 | HG00733.hp2 HG00741.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1026-893T>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35978244 | ||||||
| chr6:35978245
|
C | G | 9 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0120others(6): Show | 9 | HG00733.hp2 HG00741.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1026-894G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35978245 | ||||||
| chr6:35978246
|
A | T | 9 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0120others(6): Show | 9 | HG00733.hp2 HG00741.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1026-895T>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35978246 | ||||||
| chr6:35978248
|
T | A | 9 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0120others(6): Show | 9 | HG00733.hp2 HG00741.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1026-897A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35978248 | ||||||
| chr6:35978249
|
A | AG | 9 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0120others(6): Show | 9 | HG00733.hp2 HG00741.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1026-899_1026-898i others(3): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35978249 | ||||||
| chr6:35978439
|
C | T | 6 | a0007c0007t0002g0232a0007c0007t0002g0233a0007c0007t0002g0244others(3): Show | 6 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1026-1088G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35978439 | ||||||
| chr6:35978564
|
C | T | 1 | a0015c0028t0002g0258 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1026-1213G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35978564 | ||||||
| chr6:35978689
|
A | G | 1 | a0005c0005t0001g0169 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1026-1338T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35978689 | ||||||
| chr6:35978810
|
G | GTCT | 4 | a0003c0003t0002g0240a0003c0003t0002g0241a0003c0003t0002g0242others(1): Show | 4 | NA18944.hp2 NA18978.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-1462_1026-146 others(7): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35978810 | ||||||
| chr6:35978810
|
GTCT | G | 17 | a0002c0002t0002g0198a0002c0002t0002g0207a0002c0002t0004g0184others(14): Show | 17 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1026-1462_1026-146 others(7): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35978810 | ||||||
| chr6:35978844
|
C | CT | 43 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0053others(40): Show | 43 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.1026-1494dupA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35978844 | ||||||
| chr6:35979007
|
A | AT | 36 | a0001c0001t0001g0001a0001c0001t0001g0100a0001c0001t0001g0122others(33): Show | 37 | HG00738.hp1 HG01106.hp2 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.1026-1657dupA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35979007 | ||||||
| chr6:35979007
|
A | ATTTT | 11 | a0004c0004t0001g0034a0004c0004t0001g0086a0004c0004t0001g0087others(8): Show | 11 | HG01070.hp2 HG02132.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1026-1660_1026-165 others(8): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35979007 | ||||||
| chr6:35979007
|
A | ATTTTT | 9 | a0002c0002t0002g0272a0005c0005t0001g0164a0005c0005t0001g0169others(6): Show | 9 | HG01081.hp2 HG03688.hp1 HG03831.hp1 others(6): Show |
intron_variant | MODIFIER | c.1026-1661_1026-165 others(9): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35979007 | ||||||
| chr6:35979007
|
AT | A | 38 | a0001c0001t0001g0101a0001c0001t0001g0156a0001c0001t0002g0191others(35): Show | 38 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1026-1657delA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35979007 | ||||||
| chr6:35979101
|
C | A | 1 | a0003c0003t0002g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1026-1750G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35979101 | ||||||
| chr6:35979130
|
G | A | 2 | a0001c0001t0002g0209a0001c0001t0002g0226 | 2 | HG03195.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1026-1779C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35979130 | ||||||
| chr6:35979231
|
A | G | 1 | a0003c0003t0002g0193 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1026-1880T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35979231 | ||||||
| chr6:35979294
|
G | A | 1 | a0005c0005t0001g0179 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1026-1943C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35979294 | ||||||
| chr6:35979308
|
G | A | 1 | a0002c0002t0002g0291 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1026-1957C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35979308 | ||||||
| chr6:35979400
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1026-2049G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35979400 | ||||||
| chr6:35979425
|
A | G | 1 | a0003c0003t0001g0052 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1026-2074T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35979425 | ||||||
| chr6:35979495
|
T | A | 1 | a0003c0003t0001g0009 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1026-2144A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35979495 | ||||||
| chr6:35979508
|
A | C | 3 | a0003c0003t0002g0241a0003c0003t0002g0242a0003c0003t0002g0243 | 3 | NA18978.hp2 NA19057.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1026-2157T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35979508 | ||||||
| chr6:35979578
|
C | G | 26 | a0002c0002t0002g0198a0002c0002t0002g0207a0002c0002t0002g0214others(23): Show | 26 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(23): Show |
intron_variant | MODIFIER | c.1026-2227G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35979578 | ||||||
| chr6:35979650
|
C | T | 9 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0120others(6): Show | 9 | HG00733.hp2 HG00741.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1026-2299G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35979650 | ||||||
| chr6:35979711
|
C | T | 20 | a0002c0002t0001g0119a0002c0002t0002g0272a0005c0005t0001g0021others(17): Show | 20 | HG01070.hp2 HG01081.hp2 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.1026-2360G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35979711 | ||||||
| chr6:35979901
|
A | G | 5 | a0003c0003t0002g0239a0003c0003t0002g0240a0003c0003t0002g0241others(2): Show | 5 | HG03710.hp2 NA18944.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1025+2220T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35979901 | ||||||
| chr6:35980230
|
C | A | 1 | a0002c0002t0004g0184 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1025+1891G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35980230 | ||||||
| chr6:35980233
|
A | G | 1 | a0002c0002t0002g0291 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1025+1888T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35980233 | ||||||
| chr6:35980690
|
G | A | 1 | a0006c0006t0001g0168 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1025+1431C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35980690 | ||||||
| chr6:35980719
|
T | C | 5 | a0003c0003t0002g0239a0003c0003t0002g0240a0003c0003t0002g0241others(2): Show | 5 | HG03710.hp2 NA18944.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1025+1402A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35980719 | ||||||
| chr6:35980884
|
G | A | 1 | a0003c0003t0002g0220 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1025+1237C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35980884 | ||||||
| chr6:35981226
|
A | G | 9 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0120others(6): Show | 9 | HG00733.hp2 HG00741.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1025+895T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35981226 | ||||||
| chr6:35981502
|
C | T | 4 | a0003c0003t0001g0005a0003c0003t0001g0014a0003c0003t0001g0045others(1): Show | 4 | HG02280.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025+619G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35981502 | ||||||
| chr6:35981720
|
A | G | 46 | a0002c0002t0001g0119a0002c0002t0002g0198a0002c0002t0002g0207others(43): Show | 46 | HG01070.hp2 HG01081.hp2 HG02109.hp2 others(43): Show |
intron_variant | MODIFIER | c.1025+401T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35981720 | ||||||
| chr6:35981728
|
G | A | 1 | a0003c0003t0002g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1025+393C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35981728 | ||||||
| chr6:35981906
|
G | A | 1 | a0005c0005t0001g0176 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1025+215C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35981906 | ||||||
| chr6:35981923
|
G | A | 8 | a0002c0002t0002g0195a0002c0002t0002g0196a0002c0002t0002g0197others(5): Show | 8 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1025+198C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35981923 | ||||||
| chr6:35981967
|
C | A | 1 | a0003c0003t0002g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1025+154G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35981967 | ||||||
| chr6:35981995
|
T | A | 20 | a0002c0002t0001g0119a0002c0002t0002g0272a0005c0005t0001g0021others(17): Show | 20 | HG01070.hp2 HG01081.hp2 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.1025+126A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35981995 | ||||||
| chr6:35982022
|
A | G | 8 | a0002c0002t0001g0074a0002c0002t0001g0111a0002c0002t0001g0114others(5): Show | 8 | HG00639.hp1 HG01123.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.1025+99T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35982022 | ||||||
| chr6:35982026
|
A | G | 1 | a0003c0003t0002g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1025+95T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35982026 | ||||||
| chr6:35982092
|
A | G | 1 | a0001c0001t0002g0300 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1025+29T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35982092 | ||||||
| chr6:35982097
|
A | G | 3 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0002g0230 | 3 | NA18943.hp1 NA18966.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.1025+24T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 8/19 | chr6 | 35982097 | ||||||
| chr6:35982298
|
G | C | 60 | a0002c0002t0001g0032a0002c0002t0001g0057a0002c0002t0001g0059others(57): Show | 60 | HG00639.hp1 HG01106.hp1 HG01123.hp2 others(57): Show |
intron_variant | MODIFIER | c.943-95C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35982298 | ||||||
| chr6:35982347
|
G | C | 1 | a0001c0001t0002g0277 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.943-144C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35982347 | ||||||
| chr6:35982380
|
A | C | 1 | a0008c0008t0001g0090 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.943-177T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35982380 | ||||||
| chr6:35982433
|
T | C | 62 | a0002c0002t0001g0032a0002c0002t0001g0057a0002c0002t0001g0059others(59): Show | 62 | HG00639.hp1 HG01106.hp1 HG01123.hp2 others(59): Show |
intron_variant | MODIFIER | c.943-230A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35982433 | ||||||
| chr6:35982464
|
C | T | 1 | a0003c0003t0001g0095 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.943-261G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35982464 | ||||||
| chr6:35982594
|
T | C | 7 | a0002c0002t0002g0198a0002c0002t0002g0207a0002c0002t0004g0184others(4): Show | 7 | HG02257.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.943-391A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35982594 | ||||||
| chr6:35982641
|
G | A | 4 | a0003c0003t0001g0052a0009c0009t0001g0092a0009c0009t0001g0093others(1): Show | 4 | HG00642.hp2 HG01361.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.943-438C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35982641 | ||||||
| chr6:35982670
|
G | C | 1 | a0002c0002t0001g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.943-467C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35982670 | ||||||
| chr6:35982780
|
G | C | 1 | a0006c0006t0001g0175 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.943-577C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35982780 | ||||||
| chr6:35982803
|
G | A | 3 | a0002c0002t0001g0040a0002c0002t0001g0041a0003c0003t0001g0095 | 3 | HG02257.hp2 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.943-600C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35982803 | ||||||
| chr6:35983575
|
A | G | 147 | a0002c0002t0001g0032a0002c0002t0001g0040a0002c0002t0001g0041others(144): Show | 147 | HG00639.hp1 HG00642.hp2 HG00733.hp2 others(144): Show |
intron_variant | MODIFIER | c.943-1372T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35983575 | ||||||
| chr6:35983765
|
G | A | 1 | a0003c0003t0002g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.943-1562C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35983765 | ||||||
| chr6:35983855
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.943-1652C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35983855 | ||||||
| chr6:35983875
|
A | G | 5 | a0002c0002t0004g0184a0008c0008t0001g0042a0008c0008t0001g0043others(2): Show | 5 | HG02622.hp2 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.943-1672T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35983875 | ||||||
| chr6:35984028
|
T | C | 1 | a0003c0003t0001g0002 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.943-1825A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35984028 | ||||||
| chr6:35984254
|
T | G | 3 | a0001c0001t0002g0251a0001c0001t0002g0305a0003c0003t0001g0002 | 3 | HG02055.hp2 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.943-2051A>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35984254 | ||||||
| chr6:35984319
|
A | AT | 23 | a0001c0001t0001g0050a0001c0001t0002g0191a0001c0001t0002g0194others(20): Show | 23 | HG00280.hp2 HG00323.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.943-2117dupA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35984319 | ||||||
| chr6:35984319
|
A | ATT | 79 | a0001c0001t0001g0083a0001c0001t0002g0185a0001c0001t0002g0186others(76): Show | 79 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.943-2118_943-2117d others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35984319 | ||||||
| chr6:35984319
|
A | ATTT | 20 | a0001c0001t0002g0201a0001c0001t0002g0215a0001c0001t0002g0216others(17): Show | 20 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.943-2119_943-2117d others(5): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35984319 | ||||||
| chr6:35984319
|
AT | A | 40 | a0002c0002t0001g0040a0002c0002t0001g0041a0002c0002t0001g0069others(37): Show | 40 | HG00733.hp2 HG00741.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.943-2117delA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35984319 | ||||||
| chr6:35984319
|
ATTTT | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(99): Show | 103 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.943-2120_943-2117d others(6): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35984319 | ||||||
| chr6:35984323
|
T | A | 1 | a0002c0002t0004g0184 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.943-2120A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35984323 | ||||||
| chr6:35984326
|
T | A | 1 | a0005c0020t0002g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.943-2123A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35984326 | ||||||
| chr6:35984330
|
T | TC | 4 | a0008c0008t0001g0042a0008c0008t0001g0043a0008c0008t0001g0044others(1): Show | 4 | HG02622.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.943-2128_943-2127i others(3): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35984330 | ||||||
| chr6:35984630
|
G | C | 1 | a0002c0002t0002g0279 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.943-2427C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35984630 | ||||||
| chr6:35984748
|
G | A | 1 | a0003c0003t0001g0052 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.943-2545C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35984748 | ||||||
| chr6:35984885
|
T | G | 7 | a0003c0003t0002g0299a0007c0007t0002g0232a0007c0007t0002g0233others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.943-2682A>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35984885 | ||||||
| chr6:35984892
|
C | G | 1 | a0005c0020t0002g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.943-2689G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35984892 | ||||||
| chr6:35985049
|
G | A | 2 | a0002c0002t0001g0040a0002c0002t0001g0041 | 2 | HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.943-2846C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35985049 | ||||||
| chr6:35985416
|
T | C | 5 | a0002c0002t0004g0184a0008c0008t0001g0042a0008c0008t0001g0043others(2): Show | 5 | HG01255.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.943-3213A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35985416 | ||||||
| chr6:35985505
|
C | T | 3 | a0007c0007t0002g0244a0007c0007t0002g0298a0011c0014t0001g0128 | 3 | HG02451.hp2 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.943-3302G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35985505 | ||||||
| chr6:35985521
|
C | T | 4 | a0001c0001t0002g0209a0002c0002t0004g0184a0002c0013t0002g0234others(1): Show | 4 | HG01255.hp2 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.943-3318G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35985521 | ||||||
| chr6:35985538
|
A | C | 48 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0100others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.943-3335T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35985538 | ||||||
| chr6:35985633
|
C | T | 1 | a0002c0002t0002g0250 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.943-3430G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35985633 | ||||||
| chr6:35985687
|
C | T | 7 | a0003c0003t0001g0002a0003c0003t0002g0299a0007c0007t0002g0232others(4): Show | 7 | HG02109.hp2 HG02615.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.943-3484G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35985687 | ||||||
| chr6:35985688
|
G | A | 1 | a0001c0001t0002g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.943-3485C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35985688 | ||||||
| chr6:35985692
|
C | CA | 48 | a0001c0001t0001g0050a0001c0001t0001g0053a0001c0001t0001g0054others(45): Show | 48 | HG00735.hp1 HG00741.hp1 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.943-3490dupT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35985692 | ||||||
| chr6:35985692
|
CA | C | 53 | a0001c0001t0001g0103a0001c0001t0002g0190a0001c0001t0002g0209others(50): Show | 53 | HG00597.hp1 HG00621.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.943-3490delT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35985692 | ||||||
| chr6:35985692
|
CAA | C | 15 | a0001c0001t0002g0236a0002c0002t0002g0231a0003c0003t0001g0052others(12): Show | 15 | HG00597.hp2 HG00642.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.943-3491_943-3490d others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35985692 | ||||||
| chr6:35985692
|
CAAA | C | 37 | a0005c0005t0001g0021a0005c0005t0001g0022a0005c0005t0001g0023others(34): Show | 37 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.943-3492_943-3490d others(5): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35985692 | ||||||
| chr6:35985711
|
A | G | 33 | a0005c0005t0001g0163a0005c0005t0001g0164a0005c0005t0001g0165others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.943-3508T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35985711 | ||||||
| chr6:35985712
|
A | G | 4 | a0009c0009t0001g0092a0009c0009t0001g0093a0009c0009t0001g0149others(1): Show | 4 | HG01361.hp1 HG02280.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.943-3509T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35985712 | ||||||
| chr6:35985717
|
A | G | 41 | a0005c0005t0001g0021a0005c0005t0001g0022a0005c0005t0001g0023others(38): Show | 41 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.943-3514T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35985717 | ||||||
| chr6:35985722
|
G | A | 3 | a0002c0002t0001g0057a0002c0011t0001g0056a0002c0011t0001g0058 | 3 | HG02896.hp2 HG02897.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.943-3519C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35985722 | ||||||
| chr6:35985919
|
A | G | 1 | a0012c0017t0001g0025 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.943-3716T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35985919 | ||||||
| chr6:35985953
|
A | AAT | 41 | a0005c0005t0001g0021a0005c0005t0001g0022a0005c0005t0001g0023others(38): Show | 41 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.943-3752_943-3751d others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35985953 | ||||||
| chr6:35986024
|
C | CT | 138 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0050others(135): Show | 139 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.943-3822dupA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35986024 | ||||||
| chr6:35986024
|
C | CTT | 33 | a0001c0001t0001g0047a0001c0001t0001g0053a0001c0001t0001g0054others(30): Show | 33 | HG00735.hp1 HG01123.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.943-3823_943-3822d others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35986024 | ||||||
| chr6:35986024
|
CT | C | 6 | a0001c0001t0002g0269a0001c0001t0002g0302a0003c0003t0001g0045others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.943-3822delA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35986024 | ||||||
| chr6:35986103
|
C | T | 6 | a0001c0001t0001g0001a0001c0001t0001g0122a0001c0001t0001g0123others(3): Show | 7 | NA18941.hp1 NA18950.hp1 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.943-3900G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35986103 | ||||||
| chr6:35986254
|
G | C | 1 | a0001c0001t0001g0108 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.943-4051C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35986254 | ||||||
| chr6:35986281
|
G | A | 1 | a0005c0020t0002g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.943-4078C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35986281 | ||||||
| chr6:35986285
|
C | T | 3 | a0002c0002t0001g0057a0002c0011t0001g0056a0002c0011t0001g0058 | 3 | HG02896.hp2 HG02897.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.943-4082G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35986285 | ||||||
| chr6:35986495
|
C | G | 12 | a0003c0003t0001g0052a0003c0003t0001g0095a0003c0003t0002g0193others(9): Show | 12 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.943-4292G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35986495 | ||||||
| chr6:35986502
|
A | C | 1 | a0005c0020t0002g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.943-4299T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35986502 | ||||||
| chr6:35986517
|
T | C | 1 | a0003c0003t0002g0220 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.943-4314A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35986517 | ||||||
| chr6:35986557
|
G | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(93): Show | 97 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.943-4354C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35986557 | ||||||
| chr6:35986758
|
T | A | 1 | a0012c0017t0001g0025 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.943-4555A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35986758 | ||||||
| chr6:35986953
|
C | T | 2 | a0001c0001t0002g0205a0001c0001t0002g0224 | 2 | HG02071.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.942+4706G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35986953 | ||||||
| chr6:35986957
|
T | C | 280 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(277): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.942+4702A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35986957 | ||||||
| chr6:35987022
|
T | A | 280 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(277): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.942+4637A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35987022 | ||||||
| chr6:35987164
|
G | A | 1 | a0012c0017t0001g0025 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.942+4495C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35987164 | ||||||
| chr6:35987214
|
G | C | 1 | a0003c0003t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.942+4445C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35987214 | ||||||
| chr6:35987265
|
G | A | 2 | a0005c0005t0001g0165a0013c0019t0001g0166 | 2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.942+4394C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35987265 | ||||||
| chr6:35987426
|
C | T | 6 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(3): Show | 6 | HG03710.hp2 HG03834.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.942+4233G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35987426 | ||||||
| chr6:35987658
|
A | G | 37 | a0005c0005t0001g0021a0005c0005t0001g0022a0005c0005t0001g0023others(34): Show | 37 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.942+4001T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35987658 | ||||||
| chr6:35987872
|
A | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG00738.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.942+3787T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35987872 | ||||||
| chr6:35987911
|
C | CT | 44 | a0003c0003t0002g0240a0003c0003t0002g0241a0003c0003t0002g0242others(41): Show | 44 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.942+3747dupA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35987911 | ||||||
| chr6:35987911
|
CT | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(219): Show | 223 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.942+3747delA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35987911 | ||||||
| chr6:35987911
|
CTT | C | 6 | a0001c0001t0002g0300a0002c0002t0001g0059a0002c0002t0004g0184others(3): Show | 6 | HG02280.hp2 HG02976.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.942+3746_942+3747d others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35987911 | ||||||
| chr6:35987990
|
C | T | 1 | a0004c0004t0001g0016 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.942+3669G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35987990 | ||||||
| chr6:35988021
|
C | T | 1 | a0003c0003t0002g0220 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.942+3638G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35988021 | ||||||
| chr6:35988025
|
C | G | 4 | a0009c0009t0001g0092a0009c0009t0001g0093a0009c0009t0001g0149others(1): Show | 4 | HG01361.hp1 HG02280.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.942+3634G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35988025 | ||||||
| chr6:35988055
|
C | T | 1 | a0005c0005t0001g0183 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.942+3604G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35988055 | ||||||
| chr6:35988056
|
A | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(167): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.942+3603T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35988056 | ||||||
| chr6:35988188
|
G | A | 1 | a0003c0003t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.942+3471C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35988188 | ||||||
| chr6:35988269
|
T | C | 3 | a0002c0002t0004g0184a0002c0013t0001g0019a0017c0023t0001g0020 | 3 | HG01255.hp2 HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.942+3390A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35988269 | ||||||
| chr6:35988389
|
G | T | 170 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(167): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.942+3270C>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35988389 | ||||||
| chr6:35988577
|
G | A | 1 | a0003c0003t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.942+3082C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35988577 | ||||||
| chr6:35988579
|
G | C | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG00735.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.942+3080C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35988579 | ||||||
| chr6:35988640
|
AAAAAG | A | 47 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.942+3014_942+3018d others(7): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35988640 | ||||||
| chr6:35988763
|
G | A | 1 | a0002c0002t0002g0214 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.942+2896C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35988763 | ||||||
| chr6:35988841
|
G | GT | 31 | a0001c0001t0001g0047a0001c0001t0001g0050a0001c0001t0002g0293others(28): Show | 31 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.942+2817dupA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35988841 | ||||||
| chr6:35988841
|
G | T | 2 | a0003c0003t0002g0239a0005c0020t0002g0192 | 2 | HG03710.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.942+2818C>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35988841 | ||||||
| chr6:35988841
|
GT | G | 85 | a0001c0001t0001g0083a0001c0001t0002g0186a0001c0001t0002g0187others(82): Show | 85 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.942+2817delA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35988841 | ||||||
| chr6:35989070
|
A | G | 1 | a0003c0003t0001g0002 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.942+2589T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35989070 | ||||||
| chr6:35989171
|
A | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(165): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.942+2488T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35989171 | ||||||
| chr6:35989641
|
T | C | 15 | a0002c0002t0001g0120a0003c0003t0001g0027a0003c0003t0001g0028others(12): Show | 15 | HG00733.hp2 HG00741.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.942+2018A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35989641 | ||||||
| chr6:35989754
|
A | G | 1 | a0003c0003t0001g0052 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.942+1905T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35989754 | ||||||
| chr6:35989894
|
GT | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(114): Show | 118 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.942+1764delA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35989894 | ||||||
| chr6:35989900
|
TTTTTG | T | 47 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.942+1754_942+1758d others(7): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35989900 | ||||||
| chr6:35989901
|
T | G | 110 | a0001c0001t0001g0083a0001c0001t0002g0185a0001c0001t0002g0186others(107): Show | 110 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.942+1758A>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35989901 | ||||||
| chr6:35989927
|
C | CT | 7 | a0001c0001t0001g0050a0001c0001t0002g0191a0001c0001t0002g0294others(4): Show | 7 | HG00323.hp2 HG00733.hp2 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.942+1731dupA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35989927 | ||||||
| chr6:35989927
|
C | CTT | 74 | a0001c0001t0001g0083a0001c0001t0002g0185a0001c0001t0002g0186others(71): Show | 74 | HG00621.hp1 HG00673.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.942+1730_942+1731d others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35989927 | ||||||
| chr6:35989927
|
C | CTTT | 22 | a0001c0001t0002g0201a0001c0001t0002g0203a0001c0001t0002g0206others(19): Show | 22 | HG00597.hp1 HG00673.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.942+1729_942+1731d others(5): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35989927 | ||||||
| chr6:35989927
|
CTT | C | 16 | a0002c0002t0001g0145a0003c0003t0001g0045a0003c0003t0001g0052others(13): Show | 16 | HG00642.hp2 HG01361.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.942+1730_942+1731d others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35989927 | ||||||
| chr6:35989927
|
CTTT | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(102): Show | 106 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.942+1729_942+1731d others(5): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35989927 | ||||||
| chr6:35989927
|
CTTTT | C | 44 | a0002c0002t0001g0071a0002c0002t0001g0080a0002c0002t0004g0184others(41): Show | 44 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.942+1728_942+1731d others(6): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35989927 | ||||||
| chr6:35989933
|
T | C | 1 | a0003c0003t0002g0220 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.942+1726A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35989933 | ||||||
| chr6:35989934
|
T | C | 1 | a0002c0002t0001g0145 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.942+1725A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35989934 | ||||||
| chr6:35989935
|
T | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(99): Show | 103 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.942+1724A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35989935 | ||||||
| chr6:35989936
|
T | C | 5 | a0002c0002t0001g0071a0002c0002t0001g0080a0002c0002t0004g0184others(2): Show | 5 | HG01256.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.942+1723A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35989936 | ||||||
| chr6:35989952
|
T | G | 1 | a0005c0020t0002g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.942+1707A>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35989952 | ||||||
| chr6:35989964
|
G | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(118): Show | 122 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.942+1695C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35989964 | ||||||
| chr6:35990036
|
C | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(93): Show | 97 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.942+1623G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35990036 | ||||||
| chr6:35990047
|
C | T | 1 | a0019c0027t0001g0051 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.942+1612G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35990047 | ||||||
| chr6:35990197
|
A | G | 2 | a0001c0001t0002g0210a0001c0001t0002g0211 | 2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.942+1462T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35990197 | ||||||
| chr6:35990235
|
C | A | 1 | a0001c0001t0001g0110 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.942+1424G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35990235 | ||||||
| chr6:35990344
|
G | T | 4 | a0002c0002t0004g0184a0002c0013t0001g0019a0002c0013t0002g0234others(1): Show | 4 | HG01255.hp2 HG01884.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.942+1315C>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35990344 | ||||||
| chr6:35990378
|
A | G | 1 | a0005c0020t0002g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.942+1281T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35990378 | ||||||
| chr6:35990563
|
G | C | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.942+1096C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35990563 | ||||||
| chr6:35990609
|
T | C | 1 | a0012c0017t0001g0025 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.942+1050A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35990609 | ||||||
| chr6:35990901
|
A | G | 7 | a0002c0002t0001g0065a0002c0002t0001g0066a0002c0002t0001g0067others(4): Show | 7 | HG02698.hp2 NA18959.hp1 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.942+758T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35990901 | ||||||
| chr6:35990917
|
C | T | 168 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(165): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.942+742G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35990917 | ||||||
| chr6:35991094
|
C | T | 48 | a0002c0002t0001g0116a0003c0003t0002g0238a0003c0003t0002g0239others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.942+565G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35991094 | ||||||
| chr6:35991127
|
G | A | 284 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(281): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.942+532C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35991127 | ||||||
| chr6:35991205
|
G | A | 47 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.942+454C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35991205 | ||||||
| chr6:35991236
|
A | G | 2 | a0002c0002t0001g0146a0002c0002t0001g0155 | 2 | HG02055.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.942+423T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35991236 | ||||||
| chr6:35991238
|
TA | T | 164 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.942+420delT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35991238 | ||||||
| chr6:35991384
|
G | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(167): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.942+275C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35991384 | ||||||
| chr6:35991401
|
C | CA | 13 | a0001c0001t0001g0050a0001c0001t0002g0221a0001c0001t0002g0223others(10): Show | 13 | HG00597.hp1 HG01361.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.942+257dupT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35991401 | ||||||
| chr6:35991401
|
CA | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(149): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.942+257delT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35991401 | ||||||
| chr6:35991401
|
CAA | C | 9 | a0002c0002t0001g0072a0002c0002t0004g0184a0002c0013t0001g0019others(6): Show | 9 | HG01255.hp2 HG01884.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.942+256_942+257del others(2): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35991401 | ||||||
| chr6:35991413
|
A | C | 5 | a0004c0004t0001g0026a0009c0009t0001g0092a0009c0009t0001g0093others(2): Show | 5 | HG01361.hp1 HG01433.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.942+246T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35991413 | ||||||
| chr6:35991426
|
A | T | 4 | a0005c0005t0001g0021a0005c0005t0001g0022a0005c0005t0001g0023others(1): Show | 4 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.942+233T>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35991426 | ||||||
| chr6:35991441
|
T | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(167): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.942+218A>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35991441 | ||||||
| chr6:35991570
|
G | A | 1 | a0001c0001t0002g0282 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.942+89C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35991570 | ||||||
| chr6:35991573
|
T | C | 12 | a0003c0003t0001g0052a0003c0003t0001g0095a0003c0003t0002g0193others(9): Show | 12 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.942+86A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 7/19 | chr6 | 35991573 | ||||||
| chr6:35991930
|
C | T | 5 | a0001c0001t0002g0204a0001c0001t0002g0215a0001c0001t0002g0216others(2): Show | 5 | HG00621.hp1 NA18939.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.793-122G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 6/19 | chr6 | 35991930 | ||||||
| chr6:35992168
|
C | T | 1 | a0003c0003t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.792+342G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 6/19 | chr6 | 35992168 | ||||||
| chr6:35992418
|
A | C | 1 | a0003c0003t0002g0239 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.792+92T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 6/19 | chr6 | 35992418 | ||||||
| chr6:35992477
|
T | C | 1 | a0002c0010t0001g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.792+33A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 6/19 | chr6 | 35992477 | ||||||
| chr6:35992496
|
T | C | 12 | a0003c0003t0001g0052a0003c0003t0001g0095a0003c0003t0002g0193others(9): Show | 12 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.792+14A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 6/19 | chr6 | 35992496 | ||||||
| chr6:35992837
|
C | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(166): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.628-163G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35992837 | ||||||
| chr6:35993155
|
C | A | 2 | a0002c0002t0001g0098a0002c0002t0001g0099 | 2 | NA18952.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.628-481G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35993155 | ||||||
| chr6:35993156
|
AT | A | 23 | a0001c0001t0001g0050a0002c0002t0001g0040a0002c0002t0001g0041others(20): Show | 23 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.628-483delA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35993156 | ||||||
| chr6:35993156
|
ATT | A | 22 | a0001c0001t0001g0083a0001c0001t0002g0210a0001c0001t0002g0211others(19): Show | 22 | HG01255.hp2 HG01884.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.628-484_628-483del others(2): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35993156 | ||||||
| chr6:35993156
|
ATTT | A | 88 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0002g0185others(85): Show | 88 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.628-485_628-483del others(3): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35993156 | ||||||
| chr6:35993156
|
ATTTT | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0053a0001c0001t0001g0054others(105): Show | 109 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.628-486_628-483del others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35993156 | ||||||
| chr6:35993156
|
ATTTTT | A | 9 | a0002c0002t0001g0130a0003c0003t0001g0027a0003c0003t0001g0036others(6): Show | 9 | HG01175.hp2 HG01981.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.628-487_628-483del others(5): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35993156 | ||||||
| chr6:35993157
|
T | A | 32 | a0005c0005t0001g0021a0005c0005t0001g0022a0005c0005t0001g0023others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.628-483A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35993157 | ||||||
| chr6:35993158
|
T | A | 14 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(11): Show | 14 | HG01361.hp1 HG01981.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.628-484A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35993158 | ||||||
| chr6:35993185
|
T | G | 3 | a0008c0008t0001g0042a0008c0008t0001g0043a0008c0008t0001g0044 | 3 | HG02622.hp2 HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.628-511A>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35993185 | ||||||
| chr6:35993185
|
T | TTGGG | 71 | a0001c0001t0001g0001a0001c0001t0001g0047a0001c0001t0001g0053others(68): Show | 72 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.628-512_628-511ins others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35993185 | ||||||
| chr6:35993186
|
T | TG | 19 | a0002c0002t0001g0120a0002c0013t0001g0019a0003c0003t0001g0002others(16): Show | 19 | HG00597.hp2 HG00642.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.628-513dupC | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35993186 | ||||||
| chr6:35993186
|
T | TGG | 17 | a0002c0002t0004g0184a0002c0013t0002g0234a0003c0003t0001g0030others(14): Show | 17 | HG00621.hp2 HG00741.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.628-514_628-513dup others(2): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35993186 | ||||||
| chr6:35993186
|
T | TGGGTG | 23 | a0001c0001t0001g0046a0001c0001t0001g0100a0001c0001t0001g0106others(20): Show | 23 | HG00280.hp1 HG01106.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.628-513_628-512ins others(5): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35993186 | ||||||
| chr6:35993188
|
GA | G | 80 | a0001c0001t0001g0083a0001c0001t0002g0185a0001c0001t0002g0186others(77): Show | 80 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.628-515delT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35993188 | ||||||
| chr6:35993189
|
A | G | 148 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(145): Show | 149 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.628-515T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35993189 | ||||||
| chr6:35993189
|
A | T | 3 | a0001c0001t0002g0221a0001c0001t0002g0230a0003c0003t0002g0220 | 3 | HG02818.hp1 NA18943.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.628-515T>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35993189 | ||||||
| chr6:35993191
|
G | C | 1 | a0012c0017t0001g0025 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.628-517C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35993191 | ||||||
| chr6:35993392
|
T | C | 1 | a0003c0016t0005g0301 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.628-718A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35993392 | ||||||
| chr6:35993521
|
G | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(166): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.628-847C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35993521 | ||||||
| chr6:35993579
|
T | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(93): Show | 97 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.628-905A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35993579 | ||||||
| chr6:35993646
|
T | C | 7 | a0002c0002t0001g0120a0003c0003t0001g0027a0003c0003t0001g0028others(4): Show | 7 | HG00733.hp2 HG00741.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.628-972A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35993646 | ||||||
| chr6:35993778
|
C | A | 1 | a0006c0006t0001g0172 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.628-1104G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35993778 | ||||||
| chr6:35993896
|
T | C | 1 | a0002c0010t0001g0064 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.628-1222A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35993896 | ||||||
| chr6:35993912
|
A | T | 48 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.628-1238T>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35993912 | ||||||
| chr6:35993917
|
A | G | 1 | a0003c0003t0001g0037 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.628-1243T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35993917 | ||||||
| chr6:35993946
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.628-1272T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35993946 | ||||||
| chr6:35994019
|
C | G | 48 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.628-1345G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994019 | ||||||
| chr6:35994102
|
T | C | 2 | a0005c0005t0001g0164a0005c0005t0001g0182 | 2 | HG01070.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.628-1428A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994102 | ||||||
| chr6:35994111
|
C | T | 2 | a0002c0002t0001g0117a0003c0003t0001g0045 | 2 | HG02071.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.628-1437G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994111 | ||||||
| chr6:35994111
|
CT | C | 11 | a0003c0003t0001g0052a0003c0003t0001g0095a0003c0003t0002g0193others(8): Show | 11 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.628-1438delA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994111 | ||||||
| chr6:35994112
|
T | C | 1 | a0002c0002t0001g0117 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.628-1438A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994112 | ||||||
| chr6:35994115
|
T | C | 1 | a0003c0003t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.628-1441A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994115 | ||||||
| chr6:35994115
|
T | G | 1 | a0004c0004t0001g0085 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.628-1441A>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994115 | ||||||
| chr6:35994115
|
TC | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(99): Show | 103 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.628-1442delG | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994115 | ||||||
| chr6:35994116
|
C | CT | 48 | a0003c0003t0001g0005a0003c0003t0001g0014a0003c0003t0001g0018others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.628-1443dupA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994116 | ||||||
| chr6:35994116
|
C | G | 11 | a0003c0003t0001g0052a0003c0003t0001g0095a0003c0003t0002g0193others(8): Show | 11 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.628-1442G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994116 | ||||||
| chr6:35994116
|
C | T | 10 | a0001c0001t0001g0054a0001c0001t0001g0100a0001c0001t0001g0118others(7): Show | 10 | HG00735.hp1 HG01255.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.628-1442G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994116 | ||||||
| chr6:35994197
|
C | G | 37 | a0005c0005t0001g0021a0005c0005t0001g0022a0005c0005t0001g0023others(34): Show | 37 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.628-1523G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994197 | ||||||
| chr6:35994200
|
C | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(48): Show | 52 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.628-1526G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994200 | ||||||
| chr6:35994266
|
C | T | 33 | a0005c0005t0001g0163a0005c0005t0001g0164a0005c0005t0001g0165others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.628-1592G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994266 | ||||||
| chr6:35994316
|
G | A | 3 | a0002c0002t0002g0195a0002c0002t0002g0197a0002c0002t0002g0200 | 3 | HG01109.hp1 HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.628-1642C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994316 | ||||||
| chr6:35994336
|
G | A | 4 | a0001c0001t0001g0050a0002c0002t0001g0040a0002c0002t0001g0041others(1): Show | 4 | HG02572.hp2 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-1662C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994336 | ||||||
| chr6:35994381
|
T | G | 4 | a0003c0003t0002g0240a0003c0003t0002g0241a0003c0003t0002g0242others(1): Show | 4 | NA18944.hp2 NA18978.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-1707A>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994381 | ||||||
| chr6:35994406
|
G | A | 8 | a0003c0003t0001g0002a0003c0003t0002g0299a0007c0007t0002g0232others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.628-1732C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994406 | ||||||
| chr6:35994414
|
A | G | 171 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(168): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.628-1740T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994414 | ||||||
| chr6:35994474
|
G | A | 1 | a0001c0001t0002g0190 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.628-1800C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994474 | ||||||
| chr6:35994498
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.628-1824C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994498 | ||||||
| chr6:35994500
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(107): Show | 111 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.628-1826C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994500 | ||||||
| chr6:35994520
|
T | C | 1 | a0003c0003t0001g0002 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.628-1846A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994520 | ||||||
| chr6:35994577
|
C | CT | 120 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(117): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.628-1904dupA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994577 | ||||||
| chr6:35994599
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(107): Show | 111 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.628-1925C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994599 | ||||||
| chr6:35994614
|
C | T | 1 | a0003c0003t0001g0030 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.628-1940G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994614 | ||||||
| chr6:35994658
|
C | G | 12 | a0003c0003t0001g0052a0003c0003t0001g0095a0003c0003t0002g0193others(9): Show | 12 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.628-1984G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994658 | ||||||
| chr6:35994701
|
G | A | 11 | a0003c0003t0001g0027a0003c0003t0001g0028a0003c0003t0001g0029others(8): Show | 11 | HG00741.hp1 HG01099.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.628-2027C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994701 | ||||||
| chr6:35994732
|
C | T | 1 | a0002c0002t0001g0150 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.628-2058G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994732 | ||||||
| chr6:35994733
|
G | A | 4 | a0001c0001t0002g0283a0001c0001t0002g0284a0001c0001t0002g0285others(1): Show | 4 | HG00673.hp1 HG02132.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-2059C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994733 | ||||||
| chr6:35994844
|
C | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(107): Show | 111 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.628-2170G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994844 | ||||||
| chr6:35994845
|
G | A | 38 | a0005c0005t0001g0021a0005c0005t0001g0022a0005c0005t0001g0023others(35): Show | 38 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.628-2171C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994845 | ||||||
| chr6:35994927
|
G | A | 48 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.628-2253C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35994927 | ||||||
| chr6:35995154
|
A | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(106): Show | 110 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.628-2480T>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35995154 | ||||||
| chr6:35995180
|
T | A | 1 | a0001c0001t0002g0270 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.628-2506A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35995180 | ||||||
| chr6:35995201
|
T | C | 110 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(107): Show | 111 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.628-2527A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35995201 | ||||||
| chr6:35995230
|
A | G | 4 | a0002c0002t0004g0184a0002c0013t0001g0019a0002c0013t0002g0234others(1): Show | 4 | HG01255.hp2 HG01884.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+2508T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35995230 | ||||||
| chr6:35995309
|
C | G | 3 | a0008c0008t0001g0042a0008c0008t0001g0043a0008c0008t0001g0044 | 3 | HG02622.hp2 HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.627+2429G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35995309 | ||||||
| chr6:35995314
|
T | C | 3 | a0008c0008t0001g0042a0008c0008t0001g0043a0008c0008t0001g0044 | 3 | HG02622.hp2 HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.627+2424A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35995314 | ||||||
| chr6:35995374
|
T | C | 4 | a0002c0002t0004g0184a0002c0013t0001g0019a0002c0013t0002g0234others(1): Show | 4 | HG01255.hp2 HG01884.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+2364A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35995374 | ||||||
| chr6:35995495
|
T | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(168): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.627+2243A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35995495 | ||||||
| chr6:35995496
|
G | C | 1 | a0001c0001t0002g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.627+2242C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35995496 | ||||||
| chr6:35995568
|
C | T | 3 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0002g0230 | 3 | NA18943.hp1 NA18966.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.627+2170G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35995568 | ||||||
| chr6:35995669
|
A | AT | 10 | a0001c0001t0002g0206a0002c0002t0002g0195a0002c0002t0002g0196others(7): Show | 10 | HG01109.hp1 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.627+2068dupA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35995669 | ||||||
| chr6:35995669
|
ATT | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(167): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.627+2067_627+2068d others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35995669 | ||||||
| chr6:35995767
|
T | C | 3 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0002g0230 | 3 | NA18943.hp1 NA18966.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.627+1971A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35995767 | ||||||
| chr6:35995865
|
C | T | 6 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(3): Show | 6 | HG03710.hp2 HG03834.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.627+1873G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35995865 | ||||||
| chr6:35996020
|
T | C | 1 | a0006c0006t0001g0162 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.627+1718A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35996020 | ||||||
| chr6:35996034
|
A | G | 2 | a0001c0001t0002g0209a0001c0001t0002g0226 | 2 | HG03195.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.627+1704T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35996034 | ||||||
| chr6:35996067
|
C | T | 1 | a0003c0003t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.627+1671G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35996067 | ||||||
| chr6:35996125
|
T | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(208): Show | 212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.627+1613A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35996125 | ||||||
| chr6:35996195
|
C | A | 1 | a0001c0001t0002g0294 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.627+1543G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35996195 | ||||||
| chr6:35996476
|
A | G | 4 | a0003c0003t0002g0240a0003c0003t0002g0241a0003c0003t0002g0242others(1): Show | 4 | NA18944.hp2 NA18978.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+1262T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35996476 | ||||||
| chr6:35996497
|
C | T | 1 | a0003c0003t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.627+1241G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35996497 | ||||||
| chr6:35996579
|
C | T | 1 | a0002c0002t0001g0150 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.627+1159G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35996579 | ||||||
| chr6:35996716
|
G | A | 11 | a0003c0003t0001g0027a0003c0003t0001g0028a0003c0003t0001g0029others(8): Show | 11 | HG00741.hp1 HG01099.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.627+1022C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35996716 | ||||||
| chr6:35996783
|
C | G | 4 | a0001c0001t0001g0050a0002c0002t0001g0040a0002c0002t0001g0041others(1): Show | 4 | HG02572.hp2 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+955G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35996783 | ||||||
| chr6:35996944
|
A | G | 3 | a0007c0007t0002g0244a0007c0007t0002g0298a0011c0014t0001g0128 | 3 | HG02451.hp2 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.627+794T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35996944 | ||||||
| chr6:35997111
|
A | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(208): Show | 212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.627+627T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35997111 | ||||||
| chr6:35997297
|
A | G | 171 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(168): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.627+441T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35997297 | ||||||
| chr6:35997388
|
G | A | 20 | a0002c0002t0001g0059a0002c0002t0001g0073a0002c0002t0001g0074others(17): Show | 20 | HG00639.hp1 HG01123.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.627+350C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35997388 | ||||||
| chr6:35997409
|
T | C | 1 | a0001c0001t0002g0260 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.627+329A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35997409 | ||||||
| chr6:35997433
|
C | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(168): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.627+305G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35997433 | ||||||
| chr6:35997504
|
G | A | 2 | a0003c0003t0002g0193a0004c0004t0001g0084 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.627+234C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35997504 | ||||||
| chr6:35997588
|
C | T | 38 | a0005c0005t0001g0021a0005c0005t0001g0022a0005c0005t0001g0023others(35): Show | 38 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.627+150G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35997588 | ||||||
| chr6:35997624
|
A | G | 5 | a0003c0003t0001g0035a0003c0003t0001g0036a0003c0003t0001g0037others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.627+114T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35997624 | ||||||
| chr6:35997625
|
T | A | 1 | a0002c0013t0002g0234 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.627+113A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 5/19 | chr6 | 35997625 | ||||||
| chr6:35998011
|
C | T | 2 | a0005c0005t0001g0164a0005c0005t0001g0182 | 2 | HG01070.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.446-92G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 4/19 | chr6 | 35998011 | ||||||
| chr6:35998033
|
C | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(119): Show | 123 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.446-114G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 4/19 | chr6 | 35998033 | ||||||
| chr6:35998092
|
T | A | 48 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.446-173A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 4/19 | chr6 | 35998092 | ||||||
| chr6:35998239
|
G | A | 4 | a0004c0004t0001g0011a0004c0004t0001g0012a0004c0004t0001g0013others(1): Show | 4 | HG00733.hp1 HG02258.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.446-320C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 4/19 | chr6 | 35998239 | ||||||
| chr6:35998555
|
CA | C | 130 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0126others(127): Show | 130 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(127): Show |
intron_variant | MODIFIER | c.446-637delT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 4/19 | chr6 | 35998555 | ||||||
| chr6:35998606
|
A | T | 48 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.446-687T>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 4/19 | chr6 | 35998606 | ||||||
| chr6:35998657
|
A | AT | 48 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.446-739dupA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 4/19 | chr6 | 35998657 | ||||||
| chr6:35998660
|
G | T | 48 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.446-741C>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 4/19 | chr6 | 35998660 | ||||||
| chr6:35998810
|
G | C | 1 | a0005c0020t0002g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.446-891C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 4/19 | chr6 | 35998810 | ||||||
| chr6:35998955
|
T | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(167): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.446-1036A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 4/19 | chr6 | 35998955 | ||||||
| chr6:35998971
|
T | G | 7 | a0003c0003t0001g0095a0003c0003t0002g0238a0003c0003t0002g0239others(4): Show | 7 | HG02257.hp2 HG03710.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.445+1021A>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 4/19 | chr6 | 35998971 | ||||||
| chr6:35999024
|
A | AC | 24 | a0001c0001t0001g0050a0002c0002t0001g0040a0002c0002t0001g0041others(21): Show | 24 | HG00733.hp1 HG01516.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.445+967_445+968ins others(1): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 4/19 | chr6 | 35999024 | ||||||
| chr6:35999027
|
T | A | 11 | a0003c0003t0001g0027a0003c0003t0001g0028a0003c0003t0001g0029others(8): Show | 11 | HG00741.hp1 HG01099.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.445+965A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 4/19 | chr6 | 35999027 | ||||||
| chr6:35999057
|
A | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(218): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.445+935T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 4/19 | chr6 | 35999057 | ||||||
| chr6:35999094
|
C | T | 1 | a0005c0020t0002g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.445+898G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 4/19 | chr6 | 35999094 | ||||||
| chr6:35999217
|
G | A | 1 | a0002c0002t0002g0291 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.445+775C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 4/19 | chr6 | 35999217 | ||||||
| chr6:35999272
|
A | G | 1 | a0002c0002t0001g0080 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.445+720T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 4/19 | chr6 | 35999272 | ||||||
| chr6:35999281
|
A | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(94): Show | 98 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.445+711T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 4/19 | chr6 | 35999281 | ||||||
| chr6:35999306
|
TGGTGGAT others(24): Show |
T | 4 | a0009c0009t0001g0092a0009c0009t0001g0093a0009c0009t0001g0149others(1): Show | 4 | HG01361.hp1 HG02280.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+655_445+685del others(31): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 4/19 | chr6 | 35999306 | ||||||
| chr6:35999413
|
A | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(119): Show | 123 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.445+579T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 4/19 | chr6 | 35999413 | ||||||
| chr6:35999510
|
G | A | 1 | a0003c0003t0002g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.445+482C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 4/19 | chr6 | 35999510 | ||||||
| chr6:35999540
|
T | G | 1 | a0003c0003t0001g0052 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.445+452A>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 4/19 | chr6 | 35999540 | ||||||
| chr6:35999554
|
G | C | 1 | a0002c0025t0002g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.445+438C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 4/19 | chr6 | 35999554 | ||||||
| chr6:35999973
|
A | G | 1 | a0005c0005t0001g0163 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.445+19T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 4/19 | chr6 | 35999973 | ||||||
| chr6:36000323
|
T | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(168): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.329-215A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36000323 | ||||||
| chr6:36000542
|
T | G | 6 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(3): Show | 6 | HG03710.hp2 HG03834.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.329-434A>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36000542 | ||||||
| chr6:36000549
|
G | A | 1 | a0003c0003t0001g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.329-441C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36000549 | ||||||
| chr6:36000671
|
A | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(94): Show | 98 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.329-563T>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36000671 | ||||||
| chr6:36000823
|
T | C | 3 | a0002c0002t0001g0074a0002c0002t0001g0130a0002c0002t0001g0132 | 3 | HG01123.hp2 HG01516.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.329-715A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36000823 | ||||||
| chr6:36001151
|
C | T | 1 | a0003c0003t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.329-1043G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36001151 | ||||||
| chr6:36001152
|
G | A | 12 | a0003c0003t0001g0052a0003c0003t0001g0095a0003c0003t0002g0193others(9): Show | 12 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.329-1044C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36001152 | ||||||
| chr6:36001159
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.329-1051A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36001159 | ||||||
| chr6:36001177
|
GGAGTGCA others(2): Show |
G | 11 | a0003c0003t0001g0095a0003c0003t0002g0193a0004c0004t0001g0033others(8): Show | 11 | HG00597.hp2 HG00621.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.329-1078_329-1070d others(11): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36001177 | ||||||
| chr6:36001205
|
C | T | 4 | a0009c0009t0001g0092a0009c0009t0001g0093a0009c0009t0001g0149others(1): Show | 4 | HG01361.hp1 HG02280.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.329-1097G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36001205 | ||||||
| chr6:36001241
|
G | C | 8 | a0004c0004t0001g0033a0004c0004t0001g0034a0004c0004t0001g0085others(5): Show | 8 | HG00597.hp2 HG00621.hp2 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.329-1133C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36001241 | ||||||
| chr6:36001303
|
T | C | 1 | a0012c0017t0001g0025 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.329-1195A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36001303 | ||||||
| chr6:36001363
|
C | T | 48 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.329-1255G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36001363 | ||||||
| chr6:36001364
|
G | A | 11 | a0003c0003t0001g0027a0003c0003t0001g0028a0003c0003t0001g0029others(8): Show | 11 | HG00741.hp1 HG01099.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.329-1256C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36001364 | ||||||
| chr6:36001417
|
C | T | 1 | a0003c0003t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.329-1309G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36001417 | ||||||
| chr6:36001418
|
G | A | 24 | a0001c0001t0001g0050a0002c0002t0001g0040a0002c0002t0001g0041others(21): Show | 24 | HG00733.hp1 HG01516.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.329-1310C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36001418 | ||||||
| chr6:36001439
|
C | T | 211 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(208): Show | 212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.329-1331G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36001439 | ||||||
| chr6:36001493
|
T | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(168): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.329-1385A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36001493 | ||||||
| chr6:36001533
|
G | A | 4 | a0001c0001t0001g0050a0002c0002t0001g0040a0002c0002t0001g0041others(1): Show | 4 | HG02572.hp2 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.329-1425C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36001533 | ||||||
| chr6:36001571
|
C | T | 4 | a0003c0003t0002g0299a0007c0007t0002g0232a0007c0007t0002g0233others(1): Show | 4 | HG02109.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.329-1463G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36001571 | ||||||
| chr6:36001991
|
C | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(168): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.329-1883G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36001991 | ||||||
| chr6:36002055
|
T | G | 1 | a0003c0003t0002g0220 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.329-1947A>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36002055 | ||||||
| chr6:36002116
|
T | C | 37 | a0005c0005t0001g0021a0005c0005t0001g0022a0005c0005t0001g0023others(34): Show | 37 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.329-2008A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36002116 | ||||||
| chr6:36002637
|
A | T | 3 | a0007c0007t0002g0244a0007c0007t0002g0298a0011c0014t0001g0128 | 3 | HG02451.hp2 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.329-2529T>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36002637 | ||||||
| chr6:36002665
|
C | T | 1 | a0003c0003t0001g0052 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.329-2557G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36002665 | ||||||
| chr6:36002711
|
C | CT | 170 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(167): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.329-2604dupA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36002711 | ||||||
| chr6:36002732
|
C | T | 1 | a0005c0020t0002g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.329-2624G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36002732 | ||||||
| chr6:36002849
|
G | A | 3 | a0007c0007t0002g0244a0007c0007t0002g0298a0011c0014t0001g0128 | 3 | HG02451.hp2 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.329-2741C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36002849 | ||||||
| chr6:36002888
|
G | C | 1 | a0002c0002t0001g0077 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.329-2780C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36002888 | ||||||
| chr6:36002934
|
C | T | 4 | a0002c0002t0001g0059a0002c0010t0001g0062a0002c0010t0001g0063others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.329-2826G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36002934 | ||||||
| chr6:36003004
|
G | A | 1 | a0003c0003t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.329-2896C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36003004 | ||||||
| chr6:36003071
|
C | T | 1 | a0001c0001t0002g0261 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.329-2963G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36003071 | ||||||
| chr6:36003261
|
T | G | 2 | a0001c0001t0002g0293a0001c0001t0002g0295 | 2 | NA18946.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.329-3153A>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36003261 | ||||||
| chr6:36003348
|
T | C | 6 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(3): Show | 6 | HG03710.hp2 HG03834.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.329-3240A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36003348 | ||||||
| chr6:36003356
|
C | T | 1 | a0018c0026t0001g0127 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.329-3248G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36003356 | ||||||
| chr6:36003667
|
C | CT | 120 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(117): Show | 121 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.329-3560dupA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36003667 | ||||||
| chr6:36003667
|
C | CTT | 49 | a0002c0002t0001g0153a0003c0003t0002g0238a0003c0003t0002g0239others(46): Show | 49 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.329-3561_329-3560d others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36003667 | ||||||
| chr6:36003671
|
T | C | 1 | a0003c0003t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.329-3563A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36003671 | ||||||
| chr6:36003684
|
CAG | C | 12 | a0003c0003t0001g0052a0003c0003t0001g0095a0003c0003t0002g0193others(9): Show | 12 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.329-3578_329-3577d others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36003684 | ||||||
| chr6:36003754
|
C | T | 4 | a0002c0002t0004g0184a0002c0013t0001g0019a0002c0013t0002g0234others(1): Show | 4 | HG01255.hp2 HG01884.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.329-3646G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36003754 | ||||||
| chr6:36003791
|
A | T | 1 | a0004c0004t0001g0016 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.329-3683T>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36003791 | ||||||
| chr6:36003818
|
C | T | 6 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(3): Show | 6 | HG03710.hp2 HG03834.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.329-3710G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36003818 | ||||||
| chr6:36003883
|
G | A | 110 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(107): Show | 111 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.329-3775C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36003883 | ||||||
| chr6:36003930
|
G | C | 1 | a0005c0020t0002g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.329-3822C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36003930 | ||||||
| chr6:36003955
|
C | T | 1 | a0003c0003t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.329-3847G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36003955 | ||||||
| chr6:36004074
|
C | CT | 28 | a0001c0001t0001g0055a0001c0001t0001g0138a0001c0001t0002g0221others(25): Show | 28 | HG00099.hp2 HG00639.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.329-3967dupA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36004074 | ||||||
| chr6:36004074
|
CT | C | 71 | a0001c0001t0001g0121a0001c0001t0002g0297a0001c0001t0002g0300others(68): Show | 71 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.329-3967delA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36004074 | ||||||
| chr6:36004190
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(206): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.329-4082A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36004190 | ||||||
| chr6:36004326
|
A | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(168): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.329-4218T>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36004326 | ||||||
| chr6:36004350
|
A | G | 1 | a0003c0003t0001g0052 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.329-4242T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36004350 | ||||||
| chr6:36004364
|
T | C | 1 | a0001c0001t0002g0300 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.329-4256A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36004364 | ||||||
| chr6:36004436
|
CTTTG | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(119): Show | 123 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.329-4332_329-4329d others(6): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36004436 | ||||||
| chr6:36004451
|
T | C | 8 | a0004c0004t0001g0033a0004c0004t0001g0034a0004c0004t0001g0085others(5): Show | 8 | HG00597.hp2 HG00621.hp2 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.329-4343A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36004451 | ||||||
| chr6:36004470
|
T | G | 4 | a0009c0009t0001g0092a0009c0009t0001g0093a0009c0009t0001g0149others(1): Show | 4 | HG01361.hp1 HG02280.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.329-4362A>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36004470 | ||||||
| chr6:36004494
|
T | C | 1 | a0006c0006t0001g0174 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.329-4386A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36004494 | ||||||
| chr6:36004610
|
T | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(168): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.329-4502A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36004610 | ||||||
| chr6:36004672
|
T | G | 1 | a0001c0001t0001g0109 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.329-4564A>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36004672 | ||||||
| chr6:36004682
|
C | CAG | 211 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(208): Show | 212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.329-4575_329-4574i others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36004682 | ||||||
| chr6:36004766
|
C | T | 3 | a0002c0002t0001g0098a0002c0002t0001g0099a0002c0002t0002g0296 | 3 | HG02083.hp2 NA18952.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.329-4658G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36004766 | ||||||
| chr6:36004820
|
A | AT | 19 | a0001c0001t0001g0050a0001c0001t0001g0054a0001c0001t0001g0136others(16): Show | 19 | HG00597.hp2 HG00735.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.329-4713dupA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36004820 | ||||||
| chr6:36004820
|
AT | A | 27 | a0001c0001t0001g0001a0001c0001t0001g0122a0001c0001t0001g0123others(24): Show | 28 | HG00642.hp2 HG01099.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.329-4713delA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36004820 | ||||||
| chr6:36004820
|
ATTT | A | 41 | a0003c0003t0002g0238a0003c0003t0002g0240a0003c0003t0002g0241others(38): Show | 41 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.329-4715_329-4713d others(5): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36004820 | ||||||
| chr6:36004854
|
A | G | 1 | a0003c0003t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.329-4746T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36004854 | ||||||
| chr6:36004903
|
C | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(119): Show | 123 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.329-4795G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36004903 | ||||||
| chr6:36004989
|
G | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(119): Show | 123 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.329-4881C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36004989 | ||||||
| chr6:36005056
|
T | A | 1 | a0006c0006t0001g0175 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.329-4948A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36005056 | ||||||
| chr6:36005262
|
A | G | 1 | a0003c0003t0001g0002 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.329-5154T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36005262 | ||||||
| chr6:36005424
|
T | A | 3 | a0002c0002t0001g0144a0002c0002t0001g0145a0002c0002t0001g0147 | 3 | NA18945.hp1 NA18977.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.329-5316A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36005424 | ||||||
| chr6:36005508
|
C | G | 2 | a0004c0004t0001g0096a0004c0004t0001g0151 | 2 | HG00597.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.329-5400G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36005508 | ||||||
| chr6:36005513
|
C | A | 1 | a0001c0001t0002g0235 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.329-5405G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36005513 | ||||||
| chr6:36005680
|
C | A | 2 | a0003c0003t0002g0238a0003c0003t0002g0239 | 2 | HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.329-5572G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36005680 | ||||||
| chr6:36005800
|
T | C | 6 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(3): Show | 6 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.329-5692A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36005800 | ||||||
| chr6:36005889
|
A | T | 1 | a0003c0003t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.329-5781T>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36005889 | ||||||
| chr6:36006054
|
T | C | 1 | a0003c0016t0005g0301 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.329-5946A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36006054 | ||||||
| chr6:36006064
|
G | A | 171 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(168): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.329-5956C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36006064 | ||||||
| chr6:36006122
|
G | A | 4 | a0003c0003t0002g0240a0003c0003t0002g0241a0003c0003t0002g0242others(1): Show | 4 | NA18944.hp2 NA18978.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.329-6014C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36006122 | ||||||
| chr6:36006149
|
T | C | 1 | a0018c0026t0001g0127 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.329-6041A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36006149 | ||||||
| chr6:36006174
|
C | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG00738.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.328+6059G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36006174 | ||||||
| chr6:36006340
|
G | A | 48 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.328+5893C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36006340 | ||||||
| chr6:36006395
|
C | T | 1 | a0005c0020t0002g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.328+5838G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36006395 | ||||||
| chr6:36006440
|
C | T | 24 | a0001c0001t0001g0050a0002c0002t0001g0040a0002c0002t0001g0041others(21): Show | 24 | HG00733.hp1 HG01516.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.328+5793G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36006440 | ||||||
| chr6:36006676
|
G | A | 1 | a0003c0003t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.328+5557C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36006676 | ||||||
| chr6:36006735
|
A | T | 1 | a0001c0001t0001g0137 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.328+5498T>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36006735 | ||||||
| chr6:36006782
|
T | C | 9 | a0001c0001t0002g0206a0002c0002t0002g0195a0002c0002t0002g0196others(6): Show | 9 | HG01109.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.328+5451A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36006782 | ||||||
| chr6:36006809
|
C | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(119): Show | 123 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.328+5424G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36006809 | ||||||
| chr6:36006872
|
A | C | 1 | a0002c0010t0001g0062 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.328+5361T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36006872 | ||||||
| chr6:36006897
|
C | A | 171 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(168): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.328+5336G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36006897 | ||||||
| chr6:36007032
|
C | T | 48 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.328+5201G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36007032 | ||||||
| chr6:36007159
|
T | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(208): Show | 212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.328+5074A>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36007159 | ||||||
| chr6:36007180
|
G | GAA | 171 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(168): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.328+5052_328+5053i others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36007180 | ||||||
| chr6:36007212
|
A | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(119): Show | 123 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.328+5021T>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36007212 | ||||||
| chr6:36007401
|
G | A | 5 | a0003c0003t0001g0045a0009c0009t0001g0092a0009c0009t0001g0093others(2): Show | 5 | HG01361.hp1 HG02280.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.328+4832C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36007401 | ||||||
| chr6:36007403
|
A | G | 14 | a0001c0001t0002g0236a0001c0001t0002g0259a0001c0001t0002g0260others(11): Show | 14 | HG01109.hp2 HG01167.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.328+4830T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36007403 | ||||||
| chr6:36007567
|
A | C | 1 | a0003c0016t0005g0301 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.328+4666T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36007567 | ||||||
| chr6:36007800
|
A | G | 1 | a0003c0003t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.328+4433T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36007800 | ||||||
| chr6:36007842
|
T | C | 2 | a0003c0003t0001g0029a0005c0005t0001g0177 | 2 | HG01928.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.328+4391A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36007842 | ||||||
| chr6:36007864
|
T | C | 1 | a0005c0005t0001g0176 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.328+4369A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36007864 | ||||||
| chr6:36007891
|
C | G | 1 | a0002c0002t0001g0080 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.328+4342G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36007891 | ||||||
| chr6:36007966
|
A | C | 3 | a0002c0002t0002g0195a0002c0002t0002g0197a0002c0002t0002g0200 | 3 | HG01109.hp1 HG02258.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.328+4267T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36007966 | ||||||
| chr6:36007992
|
C | A | 5 | a0001c0001t0002g0288a0001c0001t0002g0289a0001c0001t0002g0302others(2): Show | 5 | NA18945.hp2 NA18950.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.328+4241G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36007992 | ||||||
| chr6:36008021
|
A | G | 1 | a0003c0003t0001g0002 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.328+4212T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36008021 | ||||||
| chr6:36008044
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.328+4189G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36008044 | ||||||
| chr6:36008052
|
G | A | 1 | a0003c0003t0002g0220 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.328+4181C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36008052 | ||||||
| chr6:36008106
|
C | T | 48 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(45): Show | 48 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.328+4127G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36008106 | ||||||
| chr6:36008119
|
C | CA | 21 | a0001c0001t0001g0046a0001c0001t0001g0126a0001c0001t0001g0154others(18): Show | 21 | HG01106.hp1 HG01175.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.328+4113dupT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36008119 | ||||||
| chr6:36008119
|
CA | C | 60 | a0001c0001t0002g0259a0003c0003t0001g0002a0003c0003t0001g0045others(57): Show | 60 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.328+4113delT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36008119 | ||||||
| chr6:36008160
|
T | C | 4 | a0009c0009t0001g0092a0009c0009t0001g0093a0009c0009t0001g0149others(1): Show | 4 | HG01361.hp1 HG02280.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.328+4073A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36008160 | ||||||
| chr6:36008233
|
G | A | 4 | a0009c0009t0001g0092a0009c0009t0001g0093a0009c0009t0001g0149others(1): Show | 4 | HG01361.hp1 HG02280.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.328+4000C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36008233 | ||||||
| chr6:36008244
|
T | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(168): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.328+3989A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36008244 | ||||||
| chr6:36008295
|
A | AAAAAC | 11 | a0003c0003t0001g0052a0003c0003t0002g0193a0004c0004t0001g0033others(8): Show | 11 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.328+3933_328+3937d others(7): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36008295 | ||||||
| chr6:36008295
|
A | AAAAACAA others(3): Show |
1 | a0003c0003t0001g0095 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.328+3928_328+3937d others(12): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36008295 | ||||||
| chr6:36008295
|
AAAAAC | A | 5 | a0002c0002t0004g0184a0002c0013t0001g0019a0003c0003t0002g0238others(2): Show | 5 | HG01255.hp2 HG01884.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.328+3933_328+3937d others(7): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36008295 | ||||||
| chr6:36008406
|
T | C | 1 | a0003c0016t0005g0301 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.328+3827A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36008406 | ||||||
| chr6:36008536
|
C | T | 1 | a0002c0002t0002g0197 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.328+3697G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36008536 | ||||||
| chr6:36008963
|
A | G | 1 | a0015c0028t0002g0258 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.328+3270T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36008963 | ||||||
| chr6:36008987
|
T | C | 2 | a0001c0001t0002g0293a0001c0001t0002g0295 | 2 | NA18946.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.328+3246A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36008987 | ||||||
| chr6:36008994
|
C | T | 21 | a0001c0001t0001g0083a0001c0001t0002g0185a0001c0001t0002g0186others(18): Show | 21 | HG00323.hp2 HG00621.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.328+3239G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36008994 | ||||||
| chr6:36009001
|
G | A | 84 | a0003c0003t0001g0005a0003c0003t0001g0006a0003c0003t0001g0008others(81): Show | 84 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.328+3232C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36009001 | ||||||
| chr6:36009040
|
C | T | 1 | a0003c0016t0005g0301 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.328+3193G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36009040 | ||||||
| chr6:36009191
|
A | G | 4 | a0009c0009t0001g0092a0009c0009t0001g0093a0009c0009t0001g0149others(1): Show | 4 | HG01361.hp1 HG02280.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.328+3042T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36009191 | ||||||
| chr6:36009211
|
T | C | 146 | a0001c0001t0001g0050a0001c0001t0001g0083a0001c0001t0002g0185others(143): Show | 146 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.328+3022A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36009211 | ||||||
| chr6:36009353
|
A | C | 2 | a0003c0003t0002g0193a0004c0004t0001g0084 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.328+2880T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36009353 | ||||||
| chr6:36009353
|
AAAC | A | 34 | a0005c0005t0001g0163a0005c0005t0001g0164a0005c0005t0001g0165others(31): Show | 34 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.328+2877_328+2879d others(5): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36009353 | ||||||
| chr6:36009353
|
AAACAAC | A | 20 | a0003c0003t0001g0005a0003c0003t0001g0006a0003c0003t0001g0008others(17): Show | 20 | HG00733.hp1 HG01516.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.328+2874_328+2879d others(8): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36009353 | ||||||
| chr6:36009383
|
C | A | 60 | a0001c0001t0001g0050a0001c0001t0001g0083a0001c0001t0002g0185others(57): Show | 60 | HG00323.hp2 HG00621.hp1 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.328+2850G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36009383 | ||||||
| chr6:36009383
|
C | CAACAACA others(5): Show |
2 | a0003c0003t0002g0193a0004c0004t0001g0084 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.328+2849_328+2850i others(14): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36009383 | ||||||
| chr6:36009383
|
C | CAACAACA others(8): Show |
2 | a0003c0003t0001g0052a0003c0003t0001g0095 | 2 | HG00642.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.328+2849_328+2850i others(17): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36009383 | ||||||
| chr6:36009383
|
C | CAACAACA others(14): Show |
6 | a0004c0004t0001g0034a0004c0004t0001g0085a0004c0004t0001g0086others(3): Show | 6 | HG00597.hp2 NA18944.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.328+2849_328+2850i others(23): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36009383 | ||||||
| chr6:36009383
|
C | CAACAACA others(17): Show |
2 | a0004c0004t0001g0033a0004c0004t0001g0096 | 2 | HG00621.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.328+2849_328+2850i others(26): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36009383 | ||||||
| chr6:36009409
|
G | A | 55 | a0001c0001t0001g0050a0001c0001t0001g0083a0001c0001t0002g0185others(52): Show | 55 | HG00323.hp2 HG00621.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.328+2824C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36009409 | ||||||
| chr6:36009654
|
A | C | 6 | a0003c0003t0002g0238a0003c0003t0002g0239a0003c0003t0002g0240others(3): Show | 6 | HG03710.hp2 HG03834.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.328+2579T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36009654 | ||||||
| chr6:36009667
|
T | C | 20 | a0003c0003t0001g0005a0003c0003t0001g0006a0003c0003t0001g0008others(17): Show | 20 | HG00733.hp1 HG01516.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.328+2566A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36009667 | ||||||
| chr6:36009930
|
T | C | 4 | a0002c0002t0004g0184a0002c0013t0001g0019a0002c0013t0002g0234others(1): Show | 4 | HG01255.hp2 HG01884.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.328+2303A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36009930 | ||||||
| chr6:36009948
|
A | G | 1 | a0003c0003t0001g0052 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.328+2285T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36009948 | ||||||
| chr6:36009964
|
G | A | 1 | a0003c0016t0005g0301 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.328+2269C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36009964 | ||||||
| chr6:36010085
|
T | C | 150 | a0001c0001t0001g0050a0001c0001t0001g0083a0001c0001t0002g0185others(147): Show | 150 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.328+2148A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36010085 | ||||||
| chr6:36010137
|
C | T | 1 | a0001c0001t0002g0219 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.328+2096G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36010137 | ||||||
| chr6:36010223
|
G | A | 1 | a0001c0001t0002g0294 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.328+2010C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36010223 | ||||||
| chr6:36010411
|
T | C | 9 | a0003c0003t0001g0002a0003c0003t0001g0045a0003c0003t0002g0299others(6): Show | 9 | HG02109.hp2 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.328+1822A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36010411 | ||||||
| chr6:36010536
|
C | CT | 14 | a0001c0001t0001g0050a0001c0001t0002g0191a0001c0001t0002g0235others(11): Show | 14 | HG00323.hp2 HG00642.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.328+1696dupA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36010536 | ||||||
| chr6:36010536
|
C | CTT | 40 | a0001c0001t0001g0083a0001c0001t0002g0185a0001c0001t0002g0186others(37): Show | 40 | HG00621.hp1 HG00673.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.328+1695_328+1696d others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36010536 | ||||||
| chr6:36010536
|
CT | C | 6 | a0001c0001t0001g0136a0001c0001t0002g0295a0001c0001t0002g0297others(3): Show | 6 | HG00738.hp1 HG03225.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.328+1696delA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36010536 | ||||||
| chr6:36010601
|
C | T | 89 | a0003c0003t0001g0005a0003c0003t0001g0006a0003c0003t0001g0008others(86): Show | 89 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.328+1632G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36010601 | ||||||
| chr6:36010727
|
T | C | 1 | a0003c0003t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.328+1506A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36010727 | ||||||
| chr6:36010741
|
G | A | 37 | a0005c0005t0001g0021a0005c0005t0001g0022a0005c0005t0001g0023others(34): Show | 37 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.328+1492C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36010741 | ||||||
| chr6:36010886
|
C | T | 1 | a0003c0016t0005g0301 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.328+1347G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36010886 | ||||||
| chr6:36011233
|
G | A | 1 | a0005c0020t0002g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.328+1000C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36011233 | ||||||
| chr6:36011515
|
C | T | 1 | a0003c0003t0001g0095 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.328+718G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36011515 | ||||||
| chr6:36011630
|
C | T | 1 | a0003c0003t0002g0220 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.328+603G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36011630 | ||||||
| chr6:36011735
|
GTAAC | G | 3 | a0007c0007t0002g0244a0007c0007t0002g0298a0011c0014t0001g0128 | 3 | HG02451.hp2 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.328+494_328+497del others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36011735 | ||||||
| chr6:36011742
|
A | G | 1 | a0007c0007t0002g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.328+491T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36011742 | ||||||
| chr6:36011904
|
C | T | 89 | a0003c0003t0001g0005a0003c0003t0001g0006a0003c0003t0001g0008others(86): Show | 89 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.328+329G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36011904 | ||||||
| chr6:36011905
|
A | G | 303 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(300): Show | 304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.328+328T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36011905 | ||||||
| chr6:36011978
|
G | A | 1 | a0003c0003t0001g0031 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.328+255C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36011978 | ||||||
| chr6:36012081
|
A | G | 20 | a0003c0003t0001g0005a0003c0003t0001g0006a0003c0003t0001g0008others(17): Show | 20 | HG00733.hp1 HG01516.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.328+152T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36012081 | ||||||
| chr6:36012115
|
G | A | 1 | a0002c0002t0001g0081 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.328+118C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 3/19 | chr6 | 36012115 | ||||||
| chr6:36012429
|
G | A | 1 | a0012c0017t0001g0025 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.189-57C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36012429 | ||||||
| chr6:36012756
|
G | A | 2 | a0002c0002t0001g0060a0002c0002t0001g0082 | 2 | NA18949.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.189-384C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36012756 | ||||||
| chr6:36012935
|
T | C | 105 | a0003c0003t0001g0002a0003c0003t0001g0005a0003c0003t0001g0006others(102): Show | 105 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.189-563A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36012935 | ||||||
| chr6:36013158
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.189-786C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36013158 | ||||||
| chr6:36013173
|
T | C | 1 | a0003c0003t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.189-801A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36013173 | ||||||
| chr6:36013215
|
T | G | 148 | a0001c0001t0001g0050a0001c0001t0001g0083a0001c0001t0002g0185others(145): Show | 148 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.189-843A>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36013215 | ||||||
| chr6:36013346
|
G | A | 105 | a0003c0003t0001g0002a0003c0003t0001g0005a0003c0003t0001g0006others(102): Show | 105 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.189-974C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36013346 | ||||||
| chr6:36013515
|
G | A | 11 | a0003c0003t0001g0027a0003c0003t0001g0028a0003c0003t0001g0029others(8): Show | 11 | HG00741.hp1 HG01099.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.189-1143C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36013515 | ||||||
| chr6:36013741
|
C | T | 1 | a0002c0002t0002g0257 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.189-1369G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36013741 | ||||||
| chr6:36013777
|
A | G | 3 | a0008c0008t0001g0042a0008c0008t0001g0043a0008c0008t0001g0044 | 3 | HG02622.hp2 HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.189-1405T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36013777 | ||||||
| chr6:36013860
|
C | T | 106 | a0003c0003t0001g0002a0003c0003t0001g0005a0003c0003t0001g0006others(103): Show | 106 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.189-1488G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36013860 | ||||||
| chr6:36014073
|
C | T | 1 | a0003c0003t0001g0052 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.189-1701G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36014073 | ||||||
| chr6:36014228
|
A | G | 1 | a0011c0014t0001g0128 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.189-1856T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36014228 | ||||||
| chr6:36014372
|
C | T | 25 | a0001c0001t0002g0206a0002c0002t0002g0195a0002c0002t0002g0196others(22): Show | 25 | HG01109.hp1 HG02109.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.189-2000G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36014372 | ||||||
| chr6:36014583
|
T | TA | 28 | a0001c0001t0001g0050a0001c0001t0001g0083a0001c0001t0001g0110others(25): Show | 28 | HG00280.hp1 HG00323.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.189-2212dupT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36014583 | ||||||
| chr6:36014652
|
C | A | 18 | a0001c0001t0001g0083a0001c0001t0002g0185a0001c0001t0002g0186others(15): Show | 18 | HG00323.hp2 HG00621.hp1 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.189-2280G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36014652 | ||||||
| chr6:36014696
|
A | G | 20 | a0001c0001t0002g0201a0001c0001t0002g0203a0001c0001t0002g0208others(17): Show | 20 | HG00597.hp2 HG00621.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.189-2324T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36014696 | ||||||
| chr6:36014701
|
G | A | 21 | a0001c0001t0002g0201a0001c0001t0002g0203a0001c0001t0002g0208others(18): Show | 21 | HG00597.hp2 HG00621.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.189-2329C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36014701 | ||||||
| chr6:36014790
|
C | T | 1 | a0002c0002t0002g0250 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.189-2418G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36014790 | ||||||
| chr6:36014791
|
G | A | 5 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0211others(2): Show | 5 | HG02717.hp1 HG02922.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-2419C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36014791 | ||||||
| chr6:36014927
|
G | A | 2 | a0003c0003t0002g0238a0003c0003t0002g0239 | 2 | HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.189-2555C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36014927 | ||||||
| chr6:36015106
|
C | CT | 26 | a0001c0001t0001g0053a0001c0001t0001g0097a0001c0001t0002g0190others(23): Show | 26 | HG00597.hp2 HG01433.hp2 HG02004.hp2 others(23): Show |
intron_variant | MODIFIER | c.189-2735dupA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36015106 | ||||||
| chr6:36015106
|
CT | C | 7 | a0001c0001t0001g0047a0001c0001t0001g0134a0001c0001t0001g0148others(4): Show | 7 | HG01255.hp2 HG02148.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-2735delA | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36015106 | ||||||
| chr6:36015259
|
C | T | 11 | a0003c0003t0001g0027a0003c0003t0001g0028a0003c0003t0001g0029others(8): Show | 11 | HG00741.hp1 HG01099.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.189-2887G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36015259 | ||||||
| chr6:36015346
|
C | T | 37 | a0002c0002t0004g0184a0005c0005t0001g0021a0005c0005t0001g0022others(34): Show | 37 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.189-2974G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36015346 | ||||||
| chr6:36015387
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.189-3015T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36015387 | ||||||
| chr6:36015834
|
A | AG | 213 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(210): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.189-3463dupC | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36015834 | ||||||
| chr6:36015898
|
C | A | 1 | a0002c0013t0001g0019 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.189-3526G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36015898 | ||||||
| chr6:36015967
|
A | C | 1 | a0006c0006t0001g0159 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.188+3553T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36015967 | ||||||
| chr6:36016047
|
G | A | 2 | a0002c0002t0004g0184a0017c0023t0001g0020 | 2 | HG01255.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.188+3473C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36016047 | ||||||
| chr6:36016077
|
T | G | 1 | a0002c0002t0001g0150 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.188+3443A>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36016077 | ||||||
| chr6:36016096
|
C | T | 6 | a0004c0004t0001g0033a0004c0004t0001g0034a0004c0004t0001g0085others(3): Show | 6 | NA18941.hp2 NA18944.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.188+3424G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36016096 | ||||||
| chr6:36016097
|
G | A | 37 | a0002c0002t0004g0184a0005c0005t0001g0021a0005c0005t0001g0022others(34): Show | 37 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.188+3423C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36016097 | ||||||
| chr6:36016241
|
C | T | 1 | a0004c0004t0001g0003 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.188+3279G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36016241 | ||||||
| chr6:36016428
|
G | C | 1 | a0002c0002t0004g0184 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.188+3092C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36016428 | ||||||
| chr6:36016696
|
G | A | 4 | a0005c0005t0001g0021a0005c0005t0001g0022a0005c0005t0001g0023others(1): Show | 4 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+2824C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36016696 | ||||||
| chr6:36016873
|
A | G | 4 | a0003c0003t0002g0240a0003c0003t0002g0241a0003c0003t0002g0242others(1): Show | 4 | NA18944.hp2 NA18978.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+2647T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36016873 | ||||||
| chr6:36016930
|
G | T | 11 | a0003c0003t0001g0027a0003c0003t0001g0028a0003c0003t0001g0029others(8): Show | 11 | HG00741.hp1 HG01099.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.188+2590C>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36016930 | ||||||
| chr6:36017041
|
G | A | 1 | a0002c0002t0002g0231 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.188+2479C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36017041 | ||||||
| chr6:36017064
|
C | T | 2 | a0002c0002t0004g0184a0017c0023t0001g0020 | 2 | HG01255.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.188+2456G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36017064 | ||||||
| chr6:36017160
|
C | A | 37 | a0002c0002t0004g0184a0005c0005t0001g0021a0005c0005t0001g0022others(34): Show | 37 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.188+2360G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36017160 | ||||||
| chr6:36017196
|
T | TGGAAGGA others(1): Show |
24 | a0001c0001t0002g0201a0001c0001t0002g0203a0001c0001t0002g0204others(21): Show | 24 | HG00621.hp1 HG00673.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.188+2316_188+2323d others(10): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36017196 | ||||||
| chr6:36017210
|
G | GAAGGAGA others(2): Show |
178 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(175): Show | 179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.188+2309_188+2310i others(11): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36017210 | ||||||
| chr6:36017211
|
AG | A | 25 | a0001c0001t0002g0206a0002c0002t0002g0195a0002c0002t0002g0196others(22): Show | 25 | HG01109.hp1 HG02109.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.188+2308delC | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36017211 | ||||||
| chr6:36017214
|
A | G | 25 | a0001c0001t0002g0206a0002c0002t0002g0195a0002c0002t0002g0196others(22): Show | 25 | HG01109.hp1 HG02109.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.188+2306T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36017214 | ||||||
| chr6:36017215
|
A | G | 25 | a0001c0001t0002g0206a0002c0002t0002g0195a0002c0002t0002g0196others(22): Show | 25 | HG01109.hp1 HG02109.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.188+2305T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36017215 | ||||||
| chr6:36017220
|
A | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(176): Show | 180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.188+2300T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36017220 | ||||||
| chr6:36017246
|
T | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(238): Show | 242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.188+2274A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36017246 | ||||||
| chr6:36017344
|
C | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(201): Show | 205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.188+2176G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36017344 | ||||||
| chr6:36017359
|
C | T | 1 | a0002c0025t0002g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.188+2161G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36017359 | ||||||
| chr6:36017406
|
T | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(201): Show | 205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.188+2114A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36017406 | ||||||
| chr6:36017493
|
G | A | 30 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(27): Show | 30 | HG00323.hp2 HG00621.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.188+2027C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36017493 | ||||||
| chr6:36017562
|
G | T | 3 | a0005c0005t0001g0177a0005c0005t0001g0178a0005c0005t0001g0183 | 3 | NA18975.hp1 NA18981.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.188+1958C>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36017562 | ||||||
| chr6:36017594
|
C | T | 4 | a0002c0002t0001g0141a0002c0002t0001g0144a0002c0002t0001g0145others(1): Show | 4 | NA18945.hp1 NA18971.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.188+1926G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36017594 | ||||||
| chr6:36017627
|
C | A | 1 | a0012c0017t0001g0025 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.188+1893G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36017627 | ||||||
| chr6:36017632
|
CAACAA | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(201): Show | 205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.188+1883_188+1887d others(7): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36017632 | ||||||
| chr6:36017670
|
C | T | 1 | a0001c0001t0002g0303 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.188+1850G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36017670 | ||||||
| chr6:36017682
|
A | G | 14 | a0003c0003t0001g0027a0003c0003t0001g0028a0003c0003t0001g0029others(11): Show | 14 | HG00741.hp1 HG01099.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.188+1838T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36017682 | ||||||
| chr6:36017766
|
C | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(201): Show | 205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.188+1754G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36017766 | ||||||
| chr6:36017871
|
C | T | 2 | a0002c0002t0004g0184a0017c0023t0001g0020 | 2 | HG01255.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.188+1649G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36017871 | ||||||
| chr6:36018025
|
T | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(201): Show | 205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.188+1495A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36018025 | ||||||
| chr6:36018026
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG00735.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.188+1494C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36018026 | ||||||
| chr6:36018238
|
G | A | 1 | a0002c0002t0002g0296 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.188+1282C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36018238 | ||||||
| chr6:36018244
|
T | C | 1 | a0003c0003t0002g0220 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.188+1276A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36018244 | ||||||
| chr6:36018264
|
A | T | 1 | a0004c0004t0001g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.188+1256T>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36018264 | ||||||
| chr6:36018275
|
C | CCCCACCC others(83): Show |
1 | a0001c0001t0001g0135 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.188+1244_188+1245i others(92): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36018275 | ||||||
| chr6:36018277
|
A | C | 1 | a0001c0001t0001g0135 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.188+1243T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36018277 | ||||||
| chr6:36018278
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.188+1242T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36018278 | ||||||
| chr6:36018280
|
G | C | 1 | a0001c0001t0001g0135 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.188+1240C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36018280 | ||||||
| chr6:36018282
|
ATAAACAA others(83): Show |
A | 1 | a0001c0001t0001g0135 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.188+1148_188+1237d others(92): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36018282 | ||||||
| chr6:36018303
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.188+1217T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36018303 | ||||||
| chr6:36018372
|
T | C | 240 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(237): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.188+1148A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36018372 | ||||||
| chr6:36018373
|
C | G | 1 | a0001c0001t0001g0135 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.188+1147G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36018373 | ||||||
| chr6:36018492
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.188+1028C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36018492 | ||||||
| chr6:36018579
|
G | A | 11 | a0003c0003t0001g0027a0003c0003t0001g0028a0003c0003t0001g0029others(8): Show | 11 | HG00741.hp1 HG01099.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.188+941C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36018579 | ||||||
| chr6:36018594
|
A | G | 1 | a0002c0002t0001g0150 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.188+926T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36018594 | ||||||
| chr6:36018664
|
T | C | 17 | a0001c0001t0002g0206a0002c0002t0002g0195a0002c0002t0002g0196others(14): Show | 17 | HG01109.hp1 HG02109.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.188+856A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36018664 | ||||||
| chr6:36018675
|
C | A | 179 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(176): Show | 180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.188+845G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36018675 | ||||||
| chr6:36018733
|
T | G | 31 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(28): Show | 31 | HG00323.hp2 HG00621.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.188+787A>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36018733 | ||||||
| chr6:36018811
|
G | A | 3 | a0002c0002t0001g0057a0002c0011t0001g0056a0002c0011t0001g0058 | 3 | HG02896.hp2 HG02897.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.188+709C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36018811 | ||||||
| chr6:36018925
|
C | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(87): Show | 91 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.188+595G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36018925 | ||||||
| chr6:36018996
|
G | A | 1 | a0003c0003t0001g0052 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.188+524C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36018996 | ||||||
| chr6:36019083
|
G | A | 4 | a0003c0003t0002g0299a0007c0007t0002g0232a0007c0007t0002g0233others(1): Show | 4 | HG02109.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.188+437C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36019083 | ||||||
| chr6:36019195
|
G | A | 1 | a0001c0001t0002g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.188+325C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36019195 | ||||||
| chr6:36019207
|
T | C | 4 | a0003c0003t0002g0240a0003c0003t0002g0241a0003c0003t0002g0242others(1): Show | 4 | NA18944.hp2 NA18978.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+313A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36019207 | ||||||
| chr6:36019348
|
G | A | 3 | a0008c0008t0001g0042a0008c0008t0001g0043a0008c0008t0001g0044 | 3 | HG02622.hp2 HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.188+172C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36019348 | ||||||
| chr6:36019395
|
C | G | 3 | a0002c0002t0001g0057a0002c0011t0001g0056a0002c0011t0001g0058 | 3 | HG02896.hp2 HG02897.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.188+125G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36019395 | ||||||
| chr6:36019445
|
A | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(201): Show | 205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.188+75T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36019445 | ||||||
| chr6:36019489
|
C | T | 1 | a0003c0016t0005g0301 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.188+31G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36019489 | ||||||
| chr6:36019495
|
C | G | 4 | a0003c0003t0002g0240a0003c0003t0002g0241a0003c0003t0002g0242others(1): Show | 4 | NA18944.hp2 NA18978.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+25G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 2/19 | chr6 | 36019495 | ||||||
| chr6:36019730
|
C | A | 17 | a0003c0003t0001g0005a0003c0003t0001g0006a0003c0003t0001g0008others(14): Show | 17 | HG00733.hp1 HG01516.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.-2-21G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36019730 | ||||||
| chr6:36019868
|
T | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(176): Show | 180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.-2-159A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36019868 | ||||||
| chr6:36019890
|
T | C | 1 | a0001c0001t0002g0189 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-2-181A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36019890 | ||||||
| chr6:36020057
|
C | G | 1 | a0003c0003t0001g0045 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-2-348G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36020057 | ||||||
| chr6:36020099
|
A | T | 17 | a0003c0003t0001g0005a0003c0003t0001g0006a0003c0003t0001g0008others(14): Show | 17 | HG00733.hp1 HG01516.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.-2-390T>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36020099 | ||||||
| chr6:36020184
|
C | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(178): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.-2-475G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36020184 | ||||||
| chr6:36020269
|
T | C | 1 | a0003c0003t0002g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-2-560A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36020269 | ||||||
| chr6:36020426
|
A | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(178): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.-2-717T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36020426 | ||||||
| chr6:36020805
|
A | C | 17 | a0002c0002t0001g0040a0002c0002t0001g0041a0003c0003t0001g0027others(14): Show | 17 | HG00741.hp1 HG01099.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.-2-1096T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36020805 | ||||||
| chr6:36020985
|
C | T | 1 | a0006c0006t0001g0158 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-2-1276G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36020985 | ||||||
| chr6:36021181
|
A | G | 1 | a0002c0002t0001g0111 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-2-1472T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36021181 | ||||||
| chr6:36021235
|
T | C | 180 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(177): Show | 181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.-2-1526A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36021235 | ||||||
| chr6:36021242
|
A | G | 180 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(177): Show | 181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.-2-1533T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36021242 | ||||||
| chr6:36021344
|
C | T | 4 | a0003c0003t0002g0240a0003c0003t0002g0241a0003c0003t0002g0242others(1): Show | 4 | NA18944.hp2 NA18978.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-1635G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36021344 | ||||||
| chr6:36021385
|
G | A | 1 | a0003c0003t0002g0239 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-2-1676C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36021385 | ||||||
| chr6:36021653
|
C | T | 1 | a0001c0001t0002g0246 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-2-1944G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36021653 | ||||||
| chr6:36021707
|
T | C | 180 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(177): Show | 181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.-2-1998A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36021707 | ||||||
| chr6:36021751
|
T | C | 4 | a0005c0005t0001g0177a0005c0005t0001g0178a0005c0005t0001g0179others(1): Show | 4 | HG03831.hp1 NA18975.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-2042A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36021751 | ||||||
| chr6:36021946
|
C | T | 11 | a0002c0002t0002g0195a0002c0002t0002g0196a0002c0002t0002g0197others(8): Show | 11 | HG01109.hp1 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2-2237G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36021946 | ||||||
| chr6:36021960
|
C | T | 16 | a0003c0003t0001g0005a0003c0003t0001g0006a0003c0003t0001g0008others(13): Show | 16 | HG00733.hp1 HG01516.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.-2-2251G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36021960 | ||||||
| chr6:36021986
|
G | A | 2 | a0006c0006t0001g0180a0006c0006t0001g0181 | 2 | HG00099.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.-2-2277C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36021986 | ||||||
| chr6:36022010
|
C | T | 1 | a0002c0002t0002g0195 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-2-2301G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36022010 | ||||||
| chr6:36022031
|
G | A | 34 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(31): Show | 34 | HG00323.hp2 HG00621.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.-2-2322C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36022031 | ||||||
| chr6:36022209
|
C | T | 2 | a0002c0002t0004g0184a0017c0023t0001g0020 | 2 | HG01255.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-3+2295G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36022209 | ||||||
| chr6:36022212
|
C | G | 34 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(31): Show | 34 | HG00323.hp2 HG00621.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.-3+2292G>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36022212 | ||||||
| chr6:36022247
|
G | A | 1 | a0001c0001t0002g0297 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-3+2257C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36022247 | ||||||
| chr6:36022287
|
A | C | 9 | a0002c0002t0002g0195a0002c0002t0002g0196a0002c0002t0002g0197others(6): Show | 9 | HG01109.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3+2217T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36022287 | ||||||
| chr6:36022376
|
T | G | 37 | a0001c0001t0001g0001a0001c0001t0001g0053a0001c0001t0001g0054others(34): Show | 38 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.-3+2128A>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36022376 | ||||||
| chr6:36022385
|
G | A | 11 | a0002c0002t0002g0195a0002c0002t0002g0196a0002c0002t0002g0197others(8): Show | 11 | HG01109.hp1 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-3+2119C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36022385 | ||||||
| chr6:36022488
|
GTGCAGAT others(1): Show |
G | 199 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(196): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.-3+2008_-3+2015del others(8): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36022488 | ||||||
| chr6:36022545
|
A | G | 4 | a0003c0003t0002g0240a0003c0003t0002g0241a0003c0003t0002g0242others(1): Show | 4 | NA18944.hp2 NA18978.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+1959T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36022545 | ||||||
| chr6:36022627
|
C | T | 4 | a0003c0003t0002g0240a0003c0003t0002g0241a0003c0003t0002g0242others(1): Show | 4 | NA18944.hp2 NA18978.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+1877G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36022627 | ||||||
| chr6:36022640
|
G | A | 3 | a0002c0002t0001g0144a0002c0002t0001g0145a0002c0002t0001g0147 | 3 | NA18945.hp1 NA18977.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-3+1864C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36022640 | ||||||
| chr6:36022718
|
G | A | 6 | a0002c0002t0001g0141a0002c0002t0001g0142a0002c0002t0001g0143others(3): Show | 6 | HG02165.hp2 NA18945.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+1786C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36022718 | ||||||
| chr6:36022807
|
T | C | 1 | a0001c0001t0002g0223 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-3+1697A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36022807 | ||||||
| chr6:36022953
|
G | A | 1 | a0005c0020t0002g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-3+1551C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36022953 | ||||||
| chr6:36022996
|
G | GA | 42 | a0003c0003t0001g0027a0003c0003t0001g0028a0003c0003t0001g0029others(39): Show | 42 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.-3+1507dupT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36022996 | ||||||
| chr6:36023098
|
A | G | 199 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0047others(196): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.-3+1406T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36023098 | ||||||
| chr6:36023150
|
C | T | 2 | a0001c0001t0002g0205a0001c0001t0002g0224 | 2 | HG02071.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.-3+1354G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36023150 | ||||||
| chr6:36023162
|
T | TATCC | 47 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(44): Show | 47 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.-3+1338_-3+1341dup others(4): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36023162 | ||||||
| chr6:36023162
|
T | TATCCATC others(1): Show |
97 | a0001c0001t0001g0083a0001c0001t0001g0097a0001c0001t0001g0100others(94): Show | 97 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.-3+1334_-3+1341dup others(8): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36023162 | ||||||
| chr6:36023162
|
T | TATCCATC others(5): Show |
23 | a0001c0001t0001g0001a0001c0001t0001g0118a0001c0001t0001g0121others(20): Show | 24 | HG00639.hp1 HG00733.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.-3+1330_-3+1341dup others(12): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36023162 | ||||||
| chr6:36023162
|
T | TATCCATC others(9): Show |
20 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(17): Show | 20 | HG00099.hp2 HG00738.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.-3+1326_-3+1341dup others(16): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36023162 | ||||||
| chr6:36023162
|
T | TATCCATC others(13): Show |
2 | a0002c0002t0001g0146a0002c0002t0001g0147 | 2 | NA18522.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.-3+1322_-3+1341dup others(20): Show |
SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36023162 | ||||||
| chr6:36023255
|
A | T | 16 | a0003c0003t0001g0005a0003c0003t0001g0006a0003c0003t0001g0008others(13): Show | 16 | HG00733.hp1 HG01516.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.-3+1249T>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36023255 | ||||||
| chr6:36023278
|
G | C | 4 | a0003c0003t0002g0240a0003c0003t0002g0241a0003c0003t0002g0242others(1): Show | 4 | NA18944.hp2 NA18978.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+1226C>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36023278 | ||||||
| chr6:36023406
|
G | A | 3 | a0002c0013t0002g0234a0007c0007t0002g0232a0007c0007t0002g0233 | 3 | HG02451.hp1 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-3+1098C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36023406 | ||||||
| chr6:36023461
|
C | T | 37 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(34): Show | 37 | HG00323.hp2 HG00621.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.-3+1043G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36023461 | ||||||
| chr6:36023520
|
C | A | 6 | a0002c0002t0001g0040a0002c0002t0001g0041a0003c0003t0001g0045others(3): Show | 6 | HG02280.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+984G>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36023520 | ||||||
| chr6:36023546
|
C | CA | 13 | a0001c0001t0001g0148a0001c0001t0001g0154a0001c0001t0002g0227others(10): Show | 13 | HG00597.hp2 HG00621.hp1 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.-3+957dupT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36023546 | ||||||
| chr6:36023546
|
CA | C | 76 | a0001c0001t0002g0235a0001c0001t0002g0236a0001c0001t0002g0237others(73): Show | 76 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.-3+957delT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36023546 | ||||||
| chr6:36023546
|
CAA | C | 8 | a0002c0002t0004g0184a0002c0013t0001g0019a0002c0013t0002g0234others(5): Show | 8 | HG00642.hp1 HG01255.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-3+956_-3+957delTT | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36023546 | ||||||
| chr6:36023697
|
A | G | 38 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(35): Show | 38 | HG00323.hp2 HG00621.hp1 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.-3+807T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36023697 | ||||||
| chr6:36023735
|
A | G | 2 | a0002c0002t0004g0184a0017c0023t0001g0020 | 2 | HG01255.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-3+769T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36023735 | ||||||
| chr6:36023741
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-3+763C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36023741 | ||||||
| chr6:36023772
|
A | G | 2 | a0002c0002t0004g0184a0017c0023t0001g0020 | 2 | HG01255.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-3+732T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36023772 | ||||||
| chr6:36023773
|
C | T | 6 | a0002c0002t0002g0195a0002c0002t0002g0196a0002c0002t0002g0197others(3): Show | 6 | HG01109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3+731G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36023773 | ||||||
| chr6:36023917
|
T | C | 1 | a0001c0001t0002g0302 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-3+587A>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36023917 | ||||||
| chr6:36023924
|
C | T | 1 | a0001c0001t0002g0194 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-3+580G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36023924 | ||||||
| chr6:36024045
|
C | T | 119 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(116): Show | 119 | HG00323.hp2 HG00597.hp1 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.-3+459G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36024045 | ||||||
| chr6:36024114
|
A | G | 16 | a0003c0003t0001g0005a0003c0003t0001g0006a0003c0003t0001g0008others(13): Show | 16 | HG00733.hp1 HG01516.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.-3+390T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36024114 | ||||||
| chr6:36024135
|
A | C | 2 | a0003c0003t0002g0193a0005c0020t0002g0192 | 2 | NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-3+369T>G | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36024135 | ||||||
| chr6:36024163
|
C | T | 1 | a0003c0003t0001g0002 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-3+341G>A | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36024163 | ||||||
| chr6:36024258
|
A | G | 7 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(4): Show | 7 | HG00323.hp2 HG00735.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+246T>C | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36024258 | ||||||
| chr6:36024349
|
G | A | 27 | a0005c0005t0001g0163a0005c0005t0001g0164a0005c0005t0001g0165others(24): Show | 27 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.-3+155C>T | SLC26A8 | ENSG00000112053.14 | transcript | ENST00000490799.6 | protein_coding | 1/19 | chr6 | 36024349 |