| geneid | 3694 |
|---|---|
| ensemblid | ENSG00000115221.12 |
| hgncid | 6161 |
| symbol | ITGB6 |
| name | integrin subunit beta 6 |
| refseq_nuc | NM_000888.5 |
| refseq_prot | NP_000879.2 |
| ensembl_nuc | ENST00000283249.7 |
| ensembl_prot | ENSP00000283249.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 160099671 |
| end | 160200272 |
| strand | - |
| ver | v1.2 |
| region | chr2:160099671-160200272 |
| region5000 | chr2:160094671-160205272 |
| regionname0 | ITGB6_chr2_160099671_160200272 |
| regionname5000 | ITGB6_chr2_160094671_160205272 |
| 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 | 788 | 347 | 81 | 59 | 155 | 14 | 36 | 121 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0002 | 0/0 | 788 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0003 | 0/0 | 788 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0004 | 0/0 | 788 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0005 | 0/0 | 373 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0006 | 0/0 | 788 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0007 | 0/0 | 788 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0008 | 0/0 | 788 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0009 | 0/0 | 788 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0010 | 0/0 | 788 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0011 | 0/0 | 788 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| 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 | 1/0 | 2367 | 134 | 58 | 18 | 36 | 6 | 15 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| c0002 | 0/0 | 2367 | 78 | 1 | 15 | 55 | 2 | 5 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| c0003 | 0/0 | 2367 | 69 | 16 | 15 | 29 | 2 | 7 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| c0004 | 0/0 | 2367 | 38 | 0 | 0 | 30 | 0 | 8 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| c0005 | 0/1 | 2367 | 18 | 1 | 10 | 1 | 4 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| c0006 | 0/0 | 2367 | 5 | 5 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| c0007 | 0/0 | 2367 | 2 | 0 | 0 | 2 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| c0008 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| c0009 | 0/0 | 2367 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| c0010 | 0/0 | 2367 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| c0011 | 0/0 | 2367 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| c0012 | 0/0 | 2367 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| c0013 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| c0014 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| c0015 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| c0016 | 0/0 | 2367 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| c0017 | 0/0 | 2367 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| c0018 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| c0019 | 0/0 | 2367 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| c0020 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| c0021 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2275 | 108 | 43 | 5 | 46 | 0 | 14 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| t0002 | 0/0 | 2274 | 71 | 1 | 10 | 53 | 2 | 5 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| t0003 | 0/0 | 2275 | 70 | 16 | 17 | 30 | 2 | 5 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| t0004 | 1/0 | 2275 | 64 | 6 | 15 | 23 | 6 | 13 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| t0005 | 0/1 | 2274 | 14 | 1 | 8 | 0 | 4 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| t0006 | 0/0 | 2274 | 5 | 0 | 5 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| t0007 | 0/0 | 2273 | 5 | 3 | 2 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| t0008 | 0/0 | 2275 | 5 | 5 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| t0009 | 0/0 | 2274 | 3 | 0 | 0 | 3 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| t0010 | 0/0 | 2275 | 2 | 2 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| t0011 | 0/0 | 2274 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| t0012 | 0/0 | 2275 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| t0013 | 0/0 | 2275 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| t0014 | 0/0 | 2275 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| t0015 | 0/0 | 2275 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| t0016 | 0/0 | 2275 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| t0017 | 0/0 | 2275 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| t0018 | 0/0 | 2275 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| t0019 | 0/0 | 2275 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| t0020 | 0/0 | 2275 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| t0021 | 0/0 | 2275 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| 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 | 6 | 0 | 0 | 6 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0009 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0205 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0327 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| 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 | 1/0 | 2367 | 134 | 58 | 18 | 36 | 6 | 15 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0002 | 0/0 | 2367 | 78 | 1 | 15 | 55 | 2 | 5 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0003 | 0/0 | 2367 | 69 | 16 | 15 | 29 | 2 | 7 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0004 | 0/0 | 2367 | 38 | 0 | 0 | 30 | 0 | 8 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0005 | 0/1 | 2367 | 18 | 1 | 10 | 1 | 4 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0006 | 0/0 | 2367 | 5 | 5 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0013 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0015 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0018 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0019 | 0/0 | 2367 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0021 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0002c0007 | 0/0 | 2367 | 2 | 0 | 0 | 2 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0003c0008 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0004c0020 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0005c0016 | 0/0 | 2367 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0006c0009 | 0/0 | 2367 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0007c0010 | 0/0 | 2367 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0008c0014 | 0/0 | 2367 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0009c0012 | 0/0 | 2367 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0010c0011 | 0/0 | 2367 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0011c0017 | 0/0 | 2367 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4641 | 63 | 42 | 4 | 14 | 0 | 3 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0001t0004 | 1/0 | 4641 | 58 | 6 | 12 | 22 | 6 | 11 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0001t0007 | 0/0 | 4639 | 5 | 3 | 2 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0001t0010 | 0/0 | 4641 | 2 | 2 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0001t0012 | 0/0 | 4641 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0001t0013 | 0/0 | 4641 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0001t0014 | 0/0 | 4641 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0001t0016 | 0/0 | 4641 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0001t0017 | 0/0 | 4641 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0001t0020 | 0/0 | 4641 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0002t0002 | 0/0 | 4640 | 69 | 1 | 10 | 51 | 2 | 5 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0002t0006 | 0/0 | 4640 | 5 | 0 | 5 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0002t0009 | 0/0 | 4640 | 3 | 0 | 0 | 3 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0002t0011 | 0/0 | 4640 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0003t0001 | 0/0 | 4641 | 2 | 0 | 0 | 0 | 0 | 2 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0003t0003 | 0/0 | 4641 | 65 | 16 | 15 | 27 | 2 | 5 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0003t0015 | 0/0 | 4641 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0003t0021 | 0/0 | 4641 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0004t0001 | 0/0 | 4641 | 37 | 0 | 0 | 29 | 0 | 8 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0004t0018 | 0/0 | 4641 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0005t0004 | 0/0 | 4641 | 4 | 0 | 2 | 1 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0005t0005 | 0/1 | 4640 | 14 | 1 | 8 | 0 | 4 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0006t0008 | 0/0 | 4641 | 5 | 5 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0013t0002 | 0/0 | 4640 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0015t0001 | 0/0 | 4641 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0018t0003 | 0/0 | 4641 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0019t0003 | 0/0 | 4641 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0001c0021t0003 | 0/0 | 4641 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0002c0007t0001 | 0/0 | 4641 | 2 | 0 | 0 | 2 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0003c0008t0019 | 0/0 | 4641 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0004c0020t0002 | 0/0 | 4640 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0005c0016t0001 | 0/0 | 4641 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0006c0009t0001 | 0/0 | 4641 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0007c0010t0004 | 0/0 | 4641 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0008c0014t0003 | 0/0 | 4641 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0009c0012t0003 | 0/0 | 4641 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0010c0011t0004 | 0/0 | 4641 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| a0011c0017t0001 | 0/0 | 4641 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | copy fasta | chr2 | 160094671 | 160205272 |
| 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 | 6 | 0 | 0 | 6 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0009 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0205 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0007g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0007g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0007g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0007g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0007g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0010g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0010g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0012g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0013g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0014g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0016g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0017g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0001t0020g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0006g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0006g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0006g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0009g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0009g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0009g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0002t0011g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0015g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0003t0021g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0004t0018g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0005t0004g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0005t0004g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0005t0004g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0005t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0005t0005g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0005t0005g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0005t0005g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0005t0005g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0005t0005g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0005t0005g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0005t0005g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0005t0005g0327 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0005t0005g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0005t0005g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0005t0005g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0005t0005g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0005t0005g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0005t0005g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0006t0008g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0006t0008g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0006t0008g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0006t0008g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0006t0008g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0013t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0015t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0018t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0019t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0001c0021t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0002c0007t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0002c0007t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0003c0008t0019g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0004c0020t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0005c0016t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0006c0009t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0007c0010t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0008c0014t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0009c0012t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0010c0011t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| a0011c0017t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0005 | t0005 | g0328 | EUR | GBR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0124 | EUR | GBR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00140 | hp1 | a0001 | c0005 | t0005 | g0015 | EUR | GBR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0087 | EUR | GBR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00280 | hp1 | a0001 | c0005 | t0005 | g0326 | EUR | FIN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0131 | EUR | FIN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00323 | hp1 | a0001 | c0003 | t0003 | g0195 | EUR | FIN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0140 | EUR | FIN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00408 | hp1 | a0001 | c0003 | t0003 | g0184 | EAS | CHS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00408 | hp2 | a0001 | c0002 | t0011 | g0041 | EAS | CHS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00423 | hp1 | a0001 | c0004 | t0001 | g0283 | EAS | CHS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | CHS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00597 | hp1 | a0001 | c0003 | t0003 | g0169 | EAS | CHS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0285 | EAS | CHS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00609 | hp1 | a0003 | c0008 | t0019 | g0014 | EAS | CHS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00609 | hp2 | a0001 | c0004 | t0001 | g0208 | EAS | CHS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00621 | hp1 | a0001 | c0004 | t0001 | g0275 | EAS | CHS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | CHS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00639 | hp2 | a0001 | c0005 | t0004 | g0020 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00642 | hp1 | a0001 | c0003 | t0003 | g0181 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00642 | hp2 | a0001 | c0005 | t0004 | g0019 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00673 | hp1 | a0001 | c0003 | t0003 | g0200 | EAS | CHS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00673 | hp2 | a0001 | c0004 | t0001 | g0281 | EAS | CHS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00733 | hp1 | a0001 | c0005 | t0005 | g0331 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00735 | hp1 | a0001 | c0002 | t0006 | g0003 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00735 | hp2 | a0001 | c0003 | t0003 | g0171 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00741 | hp1 | a0001 | c0003 | t0003 | g0188 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG00741 | hp2 | a0001 | c0005 | t0005 | g0325 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01069 | hp1 | a0001 | c0002 | t0006 | g0003 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01069 | hp2 | a0001 | c0019 | t0003 | g0083 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0187 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0129 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01071 | hp1 | a0001 | c0002 | t0006 | g0003 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0130 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01081 | hp1 | a0001 | c0003 | t0003 | g0226 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0141 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01099 | hp2 | a0001 | c0005 | t0005 | g0333 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01167 | hp1 | a0001 | c0005 | t0005 | g0332 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01167 | hp2 | a0001 | c0003 | t0003 | g0170 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0113 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01168 | hp2 | a0001 | c0001 | t0007 | g0314 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0313 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01169 | hp2 | a0001 | c0005 | t0005 | g0330 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01175 | hp1 | a0001 | c0003 | t0003 | g0004 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01175 | hp2 | a0010 | c0011 | t0004 | g0121 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0125 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0082 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0112 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01243 | hp2 | a0001 | c0003 | t0003 | g0189 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01255 | hp1 | a0001 | c0003 | t0003 | g0180 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0107 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01256 | hp2 | a0001 | c0003 | t0003 | g0173 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0035 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0090 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0089 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0106 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01261 | hp2 | a0005 | c0016 | t0001 | g0303 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01346 | hp1 | a0001 | c0003 | t0003 | g0004 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0105 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01358 | hp1 | a0001 | c0002 | t0006 | g0088 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01358 | hp2 | a0001 | c0005 | t0005 | g0324 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01496 | hp1 | a0001 | c0005 | t0005 | g0323 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01515 | hp1 | a0001 | c0003 | t0003 | g0190 | EUR | IBS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0210 | EUR | IBS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0009 | EUR | IBS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0044 | EUR | IBS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0224 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0036 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01891 | hp1 | a0001 | c0003 | t0003 | g0160 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01891 | hp2 | a0001 | c0001 | t0017 | g0291 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01934 | hp1 | a0001 | c0003 | t0003 | g0004 | AMR | PEL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0026 | AMR | PEL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0081 | AMR | PEL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01943 | hp2 | a0001 | c0003 | t0003 | g0179 | AMR | PEL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01993 | hp1 | a0001 | c0003 | t0003 | g0146 | AMR | PEL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0033 | AMR | PEL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02004 | hp1 | a0001 | c0003 | t0003 | g0182 | AMR | PEL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0142 | AMR | PEL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02027 | hp1 | a0001 | c0018 | t0003 | g0145 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02027 | hp2 | a0001 | c0004 | t0001 | g0260 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0076 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02040 | hp2 | a0001 | c0004 | t0001 | g0269 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02055 | hp1 | a0001 | c0003 | t0003 | g0157 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02055 | hp2 | a0011 | c0017 | t0001 | g0222 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02056 | hp1 | a0001 | c0003 | t0003 | g0152 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02056 | hp2 | a0001 | c0013 | t0002 | g0255 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02071 | hp2 | a0001 | c0004 | t0001 | g0270 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02074 | hp1 | a0001 | c0004 | t0001 | g0011 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0061 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02080 | hp1 | a0001 | c0004 | t0001 | g0293 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02129 | hp1 | a0001 | c0004 | t0001 | g0277 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0052 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0046 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0257 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02135 | hp1 | a0001 | c0003 | t0003 | g0178 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02135 | hp2 | a0001 | c0005 | t0004 | g0084 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0118 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02155 | hp1 | a0004 | c0020 | t0002 | g0037 | EAS | CDX | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02155 | hp2 | a0001 | c0003 | t0003 | g0175 | EAS | CDX | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0059 | EAS | CDX | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02165 | hp2 | a0001 | c0003 | t0003 | g0166 | EAS | CDX | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02257 | hp2 | a0001 | c0001 | t0010 | g0290 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02273 | hp2 | a0009 | c0012 | t0003 | g0193 | AMR | PEL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02280 | hp2 | a0001 | c0001 | t0014 | g0302 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02293 | hp1 | a0001 | c0005 | t0005 | g0016 | AMR | PEL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02293 | hp2 | a0001 | c0003 | t0003 | g0183 | AMR | PEL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02451 | hp1 | a0001 | c0001 | t0013 | g0234 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02451 | hp2 | a0001 | c0003 | t0003 | g0161 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02572 | hp2 | a0001 | c0006 | t0008 | g0305 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02615 | hp2 | a0001 | c0003 | t0003 | g0143 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0116 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02647 | hp2 | a0001 | c0006 | t0008 | g0092 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0127 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02683 | hp2 | a0001 | c0004 | t0001 | g0259 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02698 | hp1 | a0001 | c0003 | t0003 | g0225 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02698 | hp2 | a0001 | c0004 | t0001 | g0276 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02717 | hp1 | a0001 | c0001 | t0010 | g0289 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02717 | hp2 | a0001 | c0003 | t0003 | g0156 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02723 | hp2 | a0001 | c0003 | t0003 | g0304 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02735 | hp1 | a0001 | c0004 | t0001 | g0278 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02735 | hp2 | a0001 | c0003 | t0003 | g0168 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0022 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0322 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02818 | hp1 | a0001 | c0003 | t0003 | g0198 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0311 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02886 | hp1 | a0001 | c0001 | t0020 | g0336 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02895 | hp1 | a0001 | c0003 | t0003 | g0012 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02897 | hp1 | a0001 | c0003 | t0003 | g0012 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02965 | hp1 | a0001 | c0001 | t0016 | g0299 | AFR | ESN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02965 | hp2 | a0001 | c0005 | t0005 | g0329 | AFR | ESN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ESN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0120 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0115 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03130 | hp2 | a0001 | c0006 | t0008 | g0306 | AFR | ESN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03139 | hp2 | a0001 | c0003 | t0003 | g0202 | AFR | ESN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03209 | hp2 | a0001 | c0003 | t0003 | g0158 | AFR | MSL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | MSL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0117 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0108 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03491 | hp1 | a0001 | c0003 | t0003 | g0132 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03491 | hp2 | a0001 | c0005 | t0004 | g0021 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | ESN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03540 | hp2 | a0001 | c0006 | t0008 | g0093 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03579 | hp1 | a0001 | c0003 | t0003 | g0155 | AFR | MSL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03654 | hp1 | a0001 | c0004 | t0001 | g0298 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0045 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0133 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03669 | hp2 | a0001 | c0003 | t0001 | g0139 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03688 | hp1 | a0007 | c0010 | t0004 | g0136 | SAS | STU | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0320 | SAS | STU | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0085 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0109 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03710 | hp1 | a0006 | c0009 | t0001 | g0318 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0039 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0321 | SAS | BEB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03834 | hp2 | a0001 | c0004 | t0001 | g0297 | SAS | BEB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03942 | hp1 | a0001 | c0004 | t0001 | g0279 | SAS | BEB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0114 | SAS | BEB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG04115 | hp1 | a0001 | c0003 | t0003 | g0204 | SAS | STU | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0128 | SAS | STU | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG04184 | hp1 | a0001 | c0004 | t0001 | g0261 | SAS | BEB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0051 | SAS | BEB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0209 | SAS | STU | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG04199 | hp2 | a0001 | c0004 | t0001 | g0250 | SAS | STU | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0009 | SAS | STU | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0111 | SAS | STU | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG04228 | hp1 | a0001 | c0003 | t0003 | g0201 | SAS | STU | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG04228 | hp2 | a0001 | c0001 | t0012 | g0262 | SAS | STU | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18522 | hp2 | a0001 | c0003 | t0003 | g0159 | AFR | YRI | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0048 | EAS | CHB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18747 | hp2 | a0001 | c0004 | t0001 | g0292 | EAS | CHB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0135 | AFR | YRI | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0119 | AFR | YRI | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18940 | hp1 | a0001 | c0003 | t0003 | g0149 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18943 | hp2 | a0001 | c0003 | t0003 | g0191 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18946 | hp1 | a0001 | c0004 | t0001 | g0294 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0134 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0308 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18950 | hp2 | a0001 | c0003 | t0003 | g0207 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18951 | hp2 | a0001 | c0004 | t0001 | g0232 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18953 | hp1 | a0002 | c0007 | t0001 | g0273 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18953 | hp2 | a0001 | c0003 | t0003 | g0154 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18956 | hp1 | a0001 | c0003 | t0003 | g0144 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18957 | hp1 | a0001 | c0003 | t0003 | g0177 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18959 | hp2 | a0001 | c0021 | t0003 | g0334 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18960 | hp2 | a0001 | c0003 | t0003 | g0174 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18961 | hp1 | a0001 | c0004 | t0001 | g0227 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18961 | hp2 | a0001 | c0003 | t0003 | g0185 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18962 | hp2 | a0001 | c0003 | t0003 | g0186 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18963 | hp1 | a0001 | c0004 | t0001 | g0301 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18965 | hp1 | a0001 | c0002 | t0009 | g0050 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18965 | hp2 | a0001 | c0004 | t0001 | g0253 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18966 | hp2 | a0001 | c0003 | t0003 | g0164 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18967 | hp1 | a0001 | c0003 | t0003 | g0151 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18968 | hp2 | a0001 | c0004 | t0001 | g0263 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18969 | hp2 | a0001 | c0004 | t0001 | g0300 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18970 | hp1 | a0008 | c0014 | t0003 | g0153 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18974 | hp1 | a0001 | c0003 | t0003 | g0172 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18974 | hp2 | a0001 | c0001 | t0004 | g0268 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0287 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0056 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0242 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18982 | hp1 | a0001 | c0004 | t0001 | g0231 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18985 | hp1 | a0001 | c0004 | t0001 | g0286 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18986 | hp1 | a0001 | c0003 | t0003 | g0148 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18989 | hp1 | a0001 | c0003 | t0003 | g0197 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18994 | hp1 | a0001 | c0004 | t0001 | g0274 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18994 | hp2 | a0001 | c0003 | t0015 | g0147 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18995 | hp2 | a0001 | c0004 | t0001 | g0230 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18997 | hp1 | a0001 | c0004 | t0001 | g0280 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18997 | hp2 | a0001 | c0002 | t0009 | g0057 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18998 | hp1 | a0001 | c0004 | t0001 | g0192 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0284 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19006 | hp1 | a0001 | c0002 | t0009 | g0029 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19006 | hp2 | a0001 | c0001 | t0004 | g0296 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19009 | hp2 | a0001 | c0004 | t0001 | g0295 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19011 | hp2 | a0001 | c0003 | t0003 | g0150 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | LWK | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0315 | AFR | LWK | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | LWK | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19043 | hp2 | a0001 | c0003 | t0003 | g0203 | AFR | LWK | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19054 | hp1 | a0001 | c0003 | t0003 | g0167 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19055 | hp1 | a0001 | c0004 | t0018 | g0017 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19055 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0251 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19058 | hp2 | a0001 | c0015 | t0001 | g0229 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19068 | hp1 | a0001 | c0004 | t0001 | g0272 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19070 | hp2 | a0001 | c0004 | t0001 | g0011 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19072 | hp1 | a0001 | c0003 | t0021 | g0337 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19072 | hp2 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19075 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19078 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19079 | hp1 | a0001 | c0003 | t0003 | g0176 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19079 | hp2 | a0002 | c0007 | t0001 | g0271 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19081 | hp1 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19082 | hp1 | a0001 | c0004 | t0001 | g0194 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19086 | hp1 | a0001 | c0003 | t0003 | g0165 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19086 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19089 | hp1 | a0001 | c0001 | t0004 | g0258 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19089 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19090 | hp2 | a0001 | c0003 | t0003 | g0316 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19091 | hp1 | a0001 | c0004 | t0001 | g0228 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19091 | hp2 | a0001 | c0003 | t0003 | g0196 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0312 | AFR | YRI | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ASW | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA20805 | hp1 | a0001 | c0005 | t0005 | g0223 | EUR | TSI | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0123 | EUR | TSI | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01123 | hp1 | a0001 | c0002 | t0006 | g0086 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0122 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02109 | hp2 | a0001 | c0003 | t0003 | g0206 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02486 | hp1 | a0001 | c0006 | t0008 | g0307 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0137 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG03471 | hp2 | a0001 | c0003 | t0003 | g0162 | AFR | MSL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | USA | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | USA | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | USA | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | USA | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0005 | t0005 | g0327 | REF | REF | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0205 | REF | REF | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:160112088
|
T | C | 1 | a0009 | 1 | HG02273.hp2 | missense_variant | MODERATE | c.2093A>G | p.Asn698Ser | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/15 | 2302/4641 | 2093/2367 | 698/788 | chr2 | 160112088 | ||
| chr2:160126485
|
C | T | 1 | a0002 | 2 | NA18953.hp1 NA19079.hp2 |
missense_variant | MODERATE | c.1777G>A | p.Gly593Arg | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/15 | 1986/4641 | 1777/2367 | 593/788 | chr2 | 160126485 | ||
| chr2:160137443
|
G | A | 1 | a0008 | 1 | NA18970.hp1 | missense_variant | MODERATE | c.1651C>T | p.Leu551Phe | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/15 | 1860/4641 | 1651/2367 | 551/788 | chr2 | 160137443 | ||
| chr2:160137517
|
A | G | 1 | a0010 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.1577T>C | p.Leu526Ser | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/15 | 1786/4641 | 1577/2367 | 526/788 | chr2 | 160137517 | ||
| chr2:160137664
|
C | G | 1 | a0007 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.1430G>C | p.Gly477Ala | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/15 | 1639/4641 | 1430/2367 | 477/788 | chr2 | 160137664 | ||
| chr2:160137782
|
C | T | 1 | a0006 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.1312G>A | p.Val438Met | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/15 | 1521/4641 | 1312/2367 | 438/788 | chr2 | 160137782 | ||
| chr2:160138187
|
C | A | 1 | a0005 | 1 | HG01261.hp2 | stop_gained | HIGH | c.1120G>T | p.Glu374* | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 9/15 | 1329/4641 | 1120/2367 | 374/788 | chr2 | 160138187 | ||
| chr2:160142070
|
T | G | 1 | a0011 | 1 | HG02055.hp2 | missense_variant&splice_region_variant | MODERATE | c.1019A>C | p.Asn340Thr | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/15 | 1228/4641 | 1019/2367 | 340/788 | chr2 | 160142070 | ||
| chr2:160172625
|
T | G | 1 | a0004 | 1 | HG02155.hp1 | missense_variant | MODERATE | c.865A>C | p.Asn289His | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/15 | 1074/4641 | 865/2367 | 289/788 | chr2 | 160172625 | ||
| chr2:160200020
|
C | T | 1 | a0003 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.44G>A | p.Arg15Lys | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 1/15 | 253/4641 | 44/2367 | 15/788 | chr2 | 160200020 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:160112117
|
A | G | 7 | a0001c0003a0001c0018a0001c0019others(4): Show | 75 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(72): Show |
synonymous_variant | LOW | c.2064T>C | p.Asn688Asn | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/15 | 2273/4641 | 2064/2367 | 688/788 | chr2 | 160112117 | ||
| chr2:160126549
|
G | C | 3 | a0001c0002a0001c0013a0004c0020 | 80 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
synonymous_variant | LOW | c.1713C>G | p.Gly571Gly | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/15 | 1922/4641 | 1713/2367 | 571/788 | chr2 | 160126549 | ||
| chr2:160137837
|
C | T | 3 | a0001c0004a0001c0015a0002c0007 | 41 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(38): Show |
synonymous_variant | LOW | c.1257G>A | p.Val419Val | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/15 | 1466/4641 | 1257/2367 | 419/788 | chr2 | 160137837 | ||
| chr2:160138119
|
G | A | 1 | a0001c0015 | 1 | NA19058.hp2 | synonymous_variant | LOW | c.1188C>T | p.Asn396Asn | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 9/15 | 1397/4641 | 1188/2367 | 396/788 | chr2 | 160138119 | ||
| chr2:160169287
|
T | C | 1 | a0001c0018 | 1 | HG02027.hp1 | synonymous_variant | LOW | c.942A>G | p.Gln314Gln | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/15 | 1151/4641 | 942/2367 | 314/788 | chr2 | 160169287 | ||
| chr2:160172707
|
G | A | 4 | a0001c0002a0001c0005a0001c0019others(1): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
synonymous_variant | LOW | c.783C>T | p.Asp261Asp | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/15 | 992/4641 | 783/2367 | 261/788 | chr2 | 160172707 | ||
| chr2:160173998
|
T | C | 1 | a0001c0021 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.735A>G | p.Ala245Ala | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 5/15 | 944/4641 | 735/2367 | 245/788 | chr2 | 160173998 | ||
| chr2:160174016
|
G | C | 1 | a0001c0006 | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
synonymous_variant | LOW | c.717C>G | p.Pro239Pro | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 5/15 | 926/4641 | 717/2367 | 239/788 | chr2 | 160174016 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:160100052
|
C | T | 1 | a0001c0001t0017 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1684G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 1684 | chr2 | 160100052 | |||||
| chr2:160100165
|
A | G | 1 | a0001c0002t0011 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1571T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 1571 | chr2 | 160100165 | |||||
| chr2:160100219
|
C | A | 1 | a0001c0004t0018 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1517G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 1517 | chr2 | 160100219 | |||||
| chr2:160100227
|
T | C | 1 | a0003c0008t0019 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1509A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 1509 | chr2 | 160100227 | |||||
| chr2:160100536
|
T | C | 1 | a0001c0001t0012 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1200A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 1200 | chr2 | 160100536 | |||||
| chr2:160100573
|
A | C | 1 | a0001c0001t0016 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1163T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 1163 | chr2 | 160100573 | |||||
| chr2:160100629
|
TC | T | 7 | a0001c0002t0002a0001c0002t0006a0001c0002t0009others(4): Show | 94 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*1106delG | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 1106 | chr2 | 160100629 | |||||
| chr2:160100796
|
T | C | 1 | a0001c0002t0006 | 5 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*940A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 940 | chr2 | 160100796 | |||||
| chr2:160100892
|
T | A | 3 | a0001c0001t0010a0001c0001t0013a0001c0001t0020 | 4 | HG02257.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*844A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 844 | chr2 | 160100892 | |||||
| chr2:160100950
|
A | G | 1 | a0001c0001t0007 | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*786T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 786 | chr2 | 160100950 | |||||
| chr2:160100987
|
ACT | A | 1 | a0001c0001t0007 | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*747_*748delAG | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 747 | chr2 | 160100987 | |||||
| chr2:160100994
|
G | C | 9 | a0001c0003t0003a0001c0003t0015a0001c0003t0021others(6): Show | 73 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*742C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 742 | chr2 | 160100994 | |||||
| chr2:160101105
|
C | T | 1 | a0001c0003t0015 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*631G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 631 | chr2 | 160101105 | |||||
| chr2:160101115
|
A | T | 26 | a0001c0001t0001a0001c0001t0007a0001c0001t0010others(23): Show | 199 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*621T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 621 | chr2 | 160101115 | |||||
| chr2:160101123
|
A | G | 1 | a0001c0001t0014 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*613T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 613 | chr2 | 160101123 | |||||
| chr2:160101150
|
G | A | 1 | a0001c0006t0008 | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*586C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 586 | chr2 | 160101150 | |||||
| chr2:160101222
|
A | C | 1 | a0001c0001t0013 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*514T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 514 | chr2 | 160101222 | |||||
| chr2:160101313
|
C | G | 26 | a0001c0001t0001a0001c0001t0007a0001c0001t0010others(23): Show | 199 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*423G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 423 | chr2 | 160101313 | |||||
| chr2:160101335
|
G | A | 26 | a0001c0001t0001a0001c0001t0007a0001c0001t0010others(23): Show | 199 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*401C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 401 | chr2 | 160101335 | |||||
| chr2:160101377
|
C | T | 1 | a0001c0002t0009 | 3 | NA18965.hp1 NA18997.hp2 NA19006.hp1 |
3_prime_UTR_variant | MODIFIER | c.*359G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 359 | chr2 | 160101377 | |||||
| chr2:160101634
|
T | C | 1 | a0001c0005t0005 | 14 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*102A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 102 | chr2 | 160101634 | |||||
| chr2:160200073
|
T | C | 1 | a0001c0001t0020 | 1 | HG02886.hp1 | 5_prime_UTR_variant | MODIFIER | c.-10A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 1/15 | 10 | chr2 | 160200073 | |||||
| chr2:160200169
|
T | C | 1 | a0001c0003t0021 | 1 | NA19072.hp1 | 5_prime_UTR_variant | MODIFIER | c.-106A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 1/15 | 106 | chr2 | 160200169 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:160101838
|
GA | G | 152 | a0001c0001t0004g0009a0001c0001t0004g0105a0001c0001t0004g0106others(149): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
splice_region_variant&intron_variant | LOW | c.2269-5delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160101838 | ||||||
| chr2:160101838
|
GAA | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(181): Show | 198 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(195): Show |
splice_region_variant&intron_variant | LOW | c.2269-6_2269-5delTT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160101838 | ||||||
| chr2:160101840
|
A | G | 2 | a0001c0002t0002g0049a0001c0002t0002g0053 | 2 | NA18966.hp1 NA19054.hp2 |
splice_region_variant&intron_variant | LOW | c.2269-6T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160101840 | ||||||
| chr2:160101948
|
A | T | 70 | a0001c0003t0003g0004a0001c0003t0003g0012a0001c0003t0003g0132others(67): Show | 73 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.2269-114T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160101948 | ||||||
| chr2:160101949
|
A | T | 70 | a0001c0003t0003g0004a0001c0003t0003g0012a0001c0003t0003g0132others(67): Show | 73 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.2269-115T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160101949 | ||||||
| chr2:160101974
|
A | G | 16 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(13): Show | 17 | HG00639.hp1 HG01261.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2269-140T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160101974 | ||||||
| chr2:160102038
|
T | C | 1 | a0001c0002t0002g0039 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2269-204A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160102038 | ||||||
| chr2:160102196
|
G | A | 1 | a0001c0003t0003g0179 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2269-362C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160102196 | ||||||
| chr2:160102356
|
C | A | 3 | a0001c0003t0003g0202a0001c0003t0003g0203a0001c0003t0003g0206 | 3 | HG02109.hp2 HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2269-522G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160102356 | ||||||
| chr2:160102775
|
C | T | 283 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(280): Show | 303 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.2269-941G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160102775 | ||||||
| chr2:160102797
|
C | T | 1 | a0001c0004t0001g0269 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2269-963G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160102797 | ||||||
| chr2:160102797
|
CA | C | 98 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(95): Show | 104 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.2269-964delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160102797 | ||||||
| chr2:160102890
|
G | C | 1 | a0001c0002t0002g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2269-1056C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160102890 | ||||||
| chr2:160103053
|
A | C | 1 | a0001c0003t0003g0175 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2269-1219T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160103053 | ||||||
| chr2:160103292
|
T | C | 5 | a0001c0001t0007g0311a0001c0001t0007g0312a0001c0001t0007g0313others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2269-1458A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160103292 | ||||||
| chr2:160103547
|
T | C | 98 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(95): Show | 104 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.2269-1713A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160103547 | ||||||
| chr2:160103752
|
G | A | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2269-1918C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160103752 | ||||||
| chr2:160103858
|
T | C | 11 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(8): Show | 11 | HG00733.hp2 HG01099.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2269-2024A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160103858 | ||||||
| chr2:160103893
|
G | A | 5 | a0001c0001t0007g0311a0001c0001t0007g0312a0001c0001t0007g0313others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2269-2059C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160103893 | ||||||
| chr2:160104060
|
C | T | 89 | a0001c0001t0004g0117a0001c0002t0002g0002a0001c0002t0002g0006others(86): Show | 95 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.2269-2226G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160104060 | ||||||
| chr2:160104079
|
A | C | 1 | a0001c0001t0004g0187 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2269-2245T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160104079 | ||||||
| chr2:160104211
|
C | T | 1 | a0001c0003t0001g0139 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2269-2377G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160104211 | ||||||
| chr2:160104277
|
G | T | 98 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(95): Show | 104 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.2269-2443C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160104277 | ||||||
| chr2:160104421
|
G | A | 88 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(85): Show | 94 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.2269-2587C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160104421 | ||||||
| chr2:160104741
|
C | A | 16 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(13): Show | 17 | HG00639.hp1 HG01261.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2269-2907G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160104741 | ||||||
| chr2:160104950
|
T | TC | 14 | a0001c0005t0005g0015a0001c0005t0005g0016a0001c0005t0005g0223others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(11): Show |
intron_variant | MODIFIER | c.2268+2728dupG | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160104950 | ||||||
| chr2:160105093
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2268+2586C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160105093 | ||||||
| chr2:160105243
|
CT | C | 5 | a0001c0001t0007g0311a0001c0001t0007g0312a0001c0001t0007g0313others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2268+2435delA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160105243 | ||||||
| chr2:160105407
|
T | G | 10 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(7): Show | 10 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.2268+2272A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160105407 | ||||||
| chr2:160105415
|
A | G | 21 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(18): Show | 22 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.2268+2264T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160105415 | ||||||
| chr2:160105778
|
G | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0309a0001c0001t0001g0335 | 4 | HG01261.hp1 HG03516.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2268+1901C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160105778 | ||||||
| chr2:160105938
|
G | A | 7 | a0001c0001t0007g0313a0001c0001t0007g0314a0001c0006t0008g0092others(4): Show | 7 | HG01168.hp2 HG01169.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2268+1741C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160105938 | ||||||
| chr2:160105942
|
A | C | 5 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2268+1737T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160105942 | ||||||
| chr2:160106140
|
C | G | 10 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(7): Show | 10 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.2268+1539G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160106140 | ||||||
| chr2:160106147
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2268+1532G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160106147 | ||||||
| chr2:160106835
|
G | A | 6 | a0001c0002t0002g0061a0001c0006t0008g0092a0001c0006t0008g0093others(3): Show | 6 | HG02074.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2268+844C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160106835 | ||||||
| chr2:160106861
|
T | C | 65 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(62): Show | 74 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.2268+818A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160106861 | ||||||
| chr2:160107092
|
G | A | 98 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(95): Show | 104 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.2268+587C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160107092 | ||||||
| chr2:160107266
|
G | A | 1 | a0001c0002t0002g0087 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2268+413C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160107266 | ||||||
| chr2:160107546
|
G | T | 98 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(95): Show | 104 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.2268+133C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160107546 | ||||||
| chr2:160107547
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2268+132C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160107547 | ||||||
| chr2:160107548
|
A | G | 98 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(95): Show | 104 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.2268+131T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160107548 | ||||||
| chr2:160107569
|
G | T | 1 | a0001c0002t0009g0029 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2268+110C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160107569 | ||||||
| chr2:160107589
|
C | A | 16 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(13): Show | 17 | HG00639.hp1 HG01261.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2268+90G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160107589 | ||||||
| chr2:160107651
|
C | T | 5 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2268+28G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160107651 | ||||||
| chr2:160107946
|
G | A | 10 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(7): Show | 10 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.2102-101C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160107946 | ||||||
| chr2:160108154
|
A | G | 1 | a0001c0003t0001g0139 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2102-309T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108154 | ||||||
| chr2:160108189
|
T | G | 71 | a0001c0003t0001g0139a0001c0003t0003g0004a0001c0003t0003g0012others(68): Show | 74 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.2102-344A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108189 | ||||||
| chr2:160108214
|
A | AGT | 33 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0235others(30): Show | 37 | HG00280.hp2 HG00673.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.2102-371_2102-370d others(4): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108214 | ||||||
| chr2:160108214
|
A | AGTGT | 46 | a0001c0001t0001g0110a0001c0001t0001g0211a0001c0001t0001g0214others(43): Show | 47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.2102-373_2102-370d others(6): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108214 | ||||||
| chr2:160108214
|
A | AGTGTGT | 16 | a0001c0001t0001g0213a0001c0001t0001g0264a0001c0001t0007g0315others(13): Show | 16 | HG00280.hp1 HG00673.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.2102-375_2102-370d others(8): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108214 | ||||||
| chr2:160108214
|
A | AGTGTGTG others(1): Show |
40 | a0001c0001t0001g0101a0001c0001t0001g0212a0001c0001t0001g0215others(37): Show | 42 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.2102-377_2102-370d others(10): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108214 | ||||||
| chr2:160108214
|
A | AGTGTGTG others(3): Show |
27 | a0001c0001t0001g0008a0001c0001t0001g0095a0001c0001t0001g0102others(24): Show | 28 | HG00140.hp1 HG00733.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.2102-379_2102-370d others(12): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108214 | ||||||
| chr2:160108214
|
A | AGTGTGTG others(5): Show |
15 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(12): Show | 15 | HG00099.hp1 HG00639.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.2102-381_2102-370d others(14): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108214 | ||||||
| chr2:160108214
|
A | AGTGTGTG others(7): Show |
5 | a0001c0001t0001g0103a0001c0003t0001g0139a0001c0003t0003g0148others(2): Show | 5 | HG02280.hp1 HG03669.hp2 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.2102-383_2102-370d others(16): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108214 | ||||||
| chr2:160108214
|
A | AGTGTGTG others(9): Show |
2 | a0001c0003t0003g0151a0001c0003t0003g0152 | 2 | HG02056.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.2102-385_2102-370d others(18): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108214 | ||||||
| chr2:160108214
|
AGT | A | 20 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0243others(17): Show | 26 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.2102-371_2102-370d others(4): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108214 | ||||||
| chr2:160108214
|
AGTGT | A | 4 | a0001c0001t0004g0128a0001c0001t0004g0287a0001c0001t0010g0289others(1): Show | 4 | HG02257.hp2 HG02717.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.2102-373_2102-370d others(6): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108214 | ||||||
| chr2:160108214
|
AGTGTGTG others(3): Show |
A | 4 | a0001c0002t0002g0043a0001c0002t0002g0089a0001c0002t0002g0090others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.2102-379_2102-370d others(12): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108214 | ||||||
| chr2:160108214
|
AGTGTGTG others(5): Show |
A | 81 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(78): Show | 87 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.2102-381_2102-370d others(14): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108214 | ||||||
| chr2:160108254
|
T | C | 5 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321others(2): Show | 5 | HG00733.hp2 HG02738.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.2102-409A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108254 | ||||||
| chr2:160108612
|
C | A | 1 | a0001c0001t0010g0290 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2102-767G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108612 | ||||||
| chr2:160108635
|
G | A | 283 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(280): Show | 303 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.2102-790C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108635 | ||||||
| chr2:160108755
|
G | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(111): Show | 125 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(122): Show |
intron_variant | MODIFIER | c.2102-910C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108755 | ||||||
| chr2:160108824
|
A | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(111): Show | 125 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(122): Show |
intron_variant | MODIFIER | c.2102-979T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108824 | ||||||
| chr2:160108836
|
G | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(280): Show | 303 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.2102-991C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108836 | ||||||
| chr2:160108887
|
G | T | 5 | a0001c0001t0007g0311a0001c0001t0007g0312a0001c0001t0007g0313others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2102-1042C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108887 | ||||||
| chr2:160108900
|
T | A | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.2102-1055A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108900 | ||||||
| chr2:160108910
|
A | T | 1 | a0001c0004t0001g0275 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2102-1065T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108910 | ||||||
| chr2:160108911
|
T | G | 1 | a0001c0001t0004g0126 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2102-1066A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108911 | ||||||
| chr2:160108941
|
G | GA | 5 | a0001c0001t0007g0311a0001c0001t0007g0312a0001c0001t0007g0313others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2102-1097dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108941 | ||||||
| chr2:160108972
|
A | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(67): Show | 80 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.2102-1127T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108972 | ||||||
| chr2:160109154
|
C | T | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.2102-1309G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160109154 | ||||||
| chr2:160109270
|
T | C | 65 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(62): Show | 74 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.2102-1425A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160109270 | ||||||
| chr2:160109306
|
A | G | 1 | a0005c0016t0001g0303 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2102-1461T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160109306 | ||||||
| chr2:160109501
|
G | A | 1 | a0001c0002t0002g0069 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2102-1656C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160109501 | ||||||
| chr2:160109536
|
A | T | 1 | a0001c0001t0013g0234 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2102-1691T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160109536 | ||||||
| chr2:160109648
|
T | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(280): Show | 303 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.2102-1803A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160109648 | ||||||
| chr2:160109728
|
T | C | 1 | a0001c0003t0001g0139 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2102-1883A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160109728 | ||||||
| chr2:160109803
|
C | A | 1 | a0001c0005t0005g0327 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2102-1958G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160109803 | ||||||
| chr2:160109972
|
A | G | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.2101+2108T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160109972 | ||||||
| chr2:160109979
|
A | G | 1 | a0001c0005t0005g0333 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2101+2101T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160109979 | ||||||
| chr2:160110044
|
A | G | 1 | a0001c0004t0001g0261 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2101+2036T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110044 | ||||||
| chr2:160110070
|
C | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0101a0001c0001t0001g0102others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2101+2010G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110070 | ||||||
| chr2:160110107
|
T | C | 2 | a0001c0001t0001g0211a0001c0001t0001g0214 | 2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2101+1973A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110107 | ||||||
| chr2:160110257
|
A | G | 1 | a0001c0003t0003g0183 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2101+1823T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110257 | ||||||
| chr2:160110303
|
T | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0309 | 3 | HG03516.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2101+1777A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110303 | ||||||
| chr2:160110454
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2101+1626T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110454 | ||||||
| chr2:160110467
|
C | T | 1 | a0006c0009t0001g0318 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2101+1613G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110467 | ||||||
| chr2:160110532
|
G | A | 1 | a0001c0001t0010g0290 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2101+1548C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110532 | ||||||
| chr2:160110559
|
C | T | 1 | a0001c0003t0001g0139 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2101+1521G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110559 | ||||||
| chr2:160110622
|
A | G | 1 | a0001c0001t0007g0312 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2101+1458T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110622 | ||||||
| chr2:160110758
|
C | T | 71 | a0001c0003t0001g0209a0001c0003t0003g0004a0001c0003t0003g0012others(68): Show | 74 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.2101+1322G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110758 | ||||||
| chr2:160110782
|
T | C | 1 | a0001c0001t0017g0291 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2101+1298A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110782 | ||||||
| chr2:160110822
|
C | T | 95 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(92): Show | 101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.2101+1258G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110822 | ||||||
| chr2:160110931
|
T | G | 1 | a0001c0001t0004g0120 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2101+1149A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110931 | ||||||
| chr2:160110955
|
C | G | 1 | a0001c0001t0013g0234 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2101+1125G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110955 | ||||||
| chr2:160111093
|
C | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0244a0001c0001t0001g0245others(5): Show | 13 | HG02080.hp2 NA18941.hp2 NA18948.hp2 others(10): Show |
intron_variant | MODIFIER | c.2101+987G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111093 | ||||||
| chr2:160111104
|
TGAG | T | 88 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(85): Show | 94 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.2101+973_2101+975d others(5): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111104 | ||||||
| chr2:160111118
|
G | GC | 336 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(333): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.2101+961dupG | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111118 | ||||||
| chr2:160111136
|
GA | G | 170 | a0001c0001t0001g0247a0001c0001t0004g0111a0001c0001t0004g0112others(167): Show | 179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.2101+943delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111136 | ||||||
| chr2:160111497
|
A | T | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.2101+583T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111497 | ||||||
| chr2:160111544
|
T | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0245a0001c0001t0001g0246others(3): Show | 11 | NA18941.hp2 NA18948.hp2 NA18977.hp1 others(8): Show |
intron_variant | MODIFIER | c.2101+536A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111544 | ||||||
| chr2:160111599
|
G | GT | 19 | a0001c0001t0001g0010a0001c0001t0001g0235a0001c0001t0001g0237others(16): Show | 20 | HG01346.hp2 HG02027.hp2 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.2101+480dupA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111599 | ||||||
| chr2:160111599
|
G | GTT | 109 | a0001c0001t0001g0094a0001c0001t0001g0099a0001c0001t0001g0317others(106): Show | 115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.2101+479_2101+480d others(4): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111599 | ||||||
| chr2:160111599
|
G | GTTT | 20 | a0001c0001t0001g0008a0001c0001t0001g0095a0001c0001t0001g0096others(17): Show | 21 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.2101+478_2101+480d others(5): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111599 | ||||||
| chr2:160111599
|
G | GTTTT | 78 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(75): Show | 81 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.2101+477_2101+480d others(6): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111599 | ||||||
| chr2:160111656
|
C | T | 1 | a0001c0002t0002g0039 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2101+424G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111656 | ||||||
| chr2:160111767
|
A | G | 10 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(7): Show | 10 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.2101+313T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111767 | ||||||
| chr2:160111876
|
G | A | 72 | a0001c0003t0001g0139a0001c0003t0001g0209a0001c0003t0003g0004others(69): Show | 75 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.2101+204C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111876 | ||||||
| chr2:160111934
|
C | T | 19 | a0001c0002t0002g0006a0001c0002t0002g0038a0001c0002t0002g0042others(16): Show | 20 | HG00408.hp2 HG00621.hp2 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.2101+146G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111934 | ||||||
| chr2:160111944
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2101+136A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111944 | ||||||
| chr2:160112052
|
C | T | 1 | a0001c0002t0002g0030 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2101+28G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160112052 | ||||||
| chr2:160112232
|
CA | C | 181 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(178): Show | 190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.1982-34delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160112232 | ||||||
| chr2:160112314
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1982-115C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160112314 | ||||||
| chr2:160112327
|
G | T | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1982-128C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160112327 | ||||||
| chr2:160112634
|
A | G | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1982-435T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160112634 | ||||||
| chr2:160113045
|
T | C | 3 | a0001c0005t0004g0019a0001c0005t0004g0020a0001c0005t0004g0021 | 3 | HG00639.hp2 HG00642.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1982-846A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113045 | ||||||
| chr2:160113195
|
C | T | 1 | a0001c0004t0001g0274 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1982-996G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113195 | ||||||
| chr2:160113214
|
T | A | 1 | a0001c0002t0002g0064 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1982-1015A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113214 | ||||||
| chr2:160113234
|
C | T | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1982-1035G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113234 | ||||||
| chr2:160113258
|
C | T | 1 | a0001c0001t0004g0122 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1982-1059G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113258 | ||||||
| chr2:160113384
|
T | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(61): Show | 73 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.1982-1185A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113384 | ||||||
| chr2:160113389
|
G | A | 1 | a0001c0001t0014g0302 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1982-1190C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113389 | ||||||
| chr2:160113510
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1982-1311A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113510 | ||||||
| chr2:160113515
|
T | C | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1982-1316A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113515 | ||||||
| chr2:160113689
|
G | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(280): Show | 303 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.1982-1490C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113689 | ||||||
| chr2:160113694
|
G | A | 1 | a0001c0003t0003g0178 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1982-1495C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113694 | ||||||
| chr2:160113708
|
T | C | 1 | a0005c0016t0001g0303 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1982-1509A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113708 | ||||||
| chr2:160113768
|
G | A | 2 | a0001c0002t0002g0077a0001c0002t0002g0080 | 2 | NA18959.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1982-1569C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113768 | ||||||
| chr2:160113782
|
A | G | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1982-1583T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113782 | ||||||
| chr2:160113791
|
C | T | 1 | a0001c0003t0003g0198 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1982-1592G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113791 | ||||||
| chr2:160113879
|
G | A | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1982-1680C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113879 | ||||||
| chr2:160113905
|
C | A | 3 | a0001c0006t0008g0305a0001c0006t0008g0306a0001c0006t0008g0307 | 3 | HG02486.hp1 HG02572.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1982-1706G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113905 | ||||||
| chr2:160113914
|
C | A | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1982-1715G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113914 | ||||||
| chr2:160113942
|
C | T | 1 | a0001c0003t0003g0165 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1982-1743G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113942 | ||||||
| chr2:160114138
|
G | C | 1 | a0001c0001t0004g0308 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1982-1939C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114138 | ||||||
| chr2:160114224
|
C | T | 76 | a0001c0003t0001g0209a0001c0003t0003g0004a0001c0003t0003g0012others(73): Show | 79 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.1982-2025G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114224 | ||||||
| chr2:160114423
|
G | A | 16 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(13): Show | 17 | HG00639.hp1 HG01261.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1982-2224C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114423 | ||||||
| chr2:160114537
|
C | T | 1 | a0001c0003t0003g0155 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1982-2338G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114537 | ||||||
| chr2:160114607
|
C | T | 1 | a0001c0002t0002g0078 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1982-2408G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114607 | ||||||
| chr2:160114654
|
T | C | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1982-2455A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114654 | ||||||
| chr2:160114670
|
C | T | 1 | a0001c0002t0002g0085 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1982-2471G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114670 | ||||||
| chr2:160114676
|
C | T | 175 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(172): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.1982-2477G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114676 | ||||||
| chr2:160114683
|
C | T | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1982-2484G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114683 | ||||||
| chr2:160114699
|
G | A | 1 | a0001c0004t0001g0295 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1982-2500C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114699 | ||||||
| chr2:160114772
|
C | T | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1982-2573G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114772 | ||||||
| chr2:160114926
|
T | A | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1982-2727A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114926 | ||||||
| chr2:160114943
|
G | A | 208 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(205): Show | 218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1982-2744C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114943 | ||||||
| chr2:160114989
|
G | A | 1 | a0001c0001t0017g0291 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1982-2790C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114989 | ||||||
| chr2:160115000
|
G | A | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1982-2801C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115000 | ||||||
| chr2:160115022
|
C | T | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1982-2823G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115022 | ||||||
| chr2:160115068
|
G | C | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1982-2869C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115068 | ||||||
| chr2:160115087
|
A | G | 71 | a0001c0003t0001g0209a0001c0003t0003g0004a0001c0003t0003g0012others(68): Show | 74 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1982-2888T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115087 | ||||||
| chr2:160115164
|
A | G | 72 | a0001c0003t0001g0139a0001c0003t0001g0209a0001c0003t0003g0004others(69): Show | 75 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1982-2965T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115164 | ||||||
| chr2:160115170
|
G | A | 2 | a0001c0003t0003g0151a0001c0003t0003g0152 | 2 | HG02056.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1982-2971C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115170 | ||||||
| chr2:160115219
|
C | T | 16 | a0001c0003t0003g0144a0001c0003t0003g0150a0001c0003t0003g0154others(13): Show | 16 | HG00408.hp1 HG00597.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.1982-3020G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115219 | ||||||
| chr2:160115228
|
T | C | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1982-3029A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115228 | ||||||
| chr2:160115273
|
A | G | 283 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(280): Show | 303 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.1982-3074T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115273 | ||||||
| chr2:160115282
|
C | T | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1982-3083G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115282 | ||||||
| chr2:160115283
|
T | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(66): Show | 79 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1982-3084A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115283 | ||||||
| chr2:160115292
|
G | A | 209 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(206): Show | 219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1982-3093C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115292 | ||||||
| chr2:160115500
|
A | G | 1 | a0001c0004t0001g0277 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1982-3301T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115500 | ||||||
| chr2:160115513
|
C | T | 16 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(13): Show | 17 | HG00639.hp1 HG01261.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1982-3314G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115513 | ||||||
| chr2:160115732
|
C | A | 1 | a0001c0003t0001g0139 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1982-3533G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115732 | ||||||
| chr2:160115800
|
C | T | 1 | a0001c0002t0002g0027 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1982-3601G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115800 | ||||||
| chr2:160115887
|
C | A | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1982-3688G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115887 | ||||||
| chr2:160115907
|
C | T | 283 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(280): Show | 303 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.1982-3708G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115907 | ||||||
| chr2:160115941
|
G | T | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1982-3742C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115941 | ||||||
| chr2:160115942
|
T | C | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1982-3743A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115942 | ||||||
| chr2:160115967
|
G | C | 1 | a0001c0003t0003g0181 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1982-3768C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115967 | ||||||
| chr2:160116011
|
G | A | 1 | a0001c0003t0003g0173 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1982-3812C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116011 | ||||||
| chr2:160116030
|
T | G | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1982-3831A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116030 | ||||||
| chr2:160116137
|
G | A | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1982-3938C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116137 | ||||||
| chr2:160116162
|
C | T | 6 | a0001c0001t0001g0211a0001c0001t0001g0214a0001c0004t0001g0300others(3): Show | 6 | HG02258.hp1 NA18953.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.1982-3963G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116162 | ||||||
| chr2:160116163
|
G | A | 1 | a0001c0003t0003g0173 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1982-3964C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116163 | ||||||
| chr2:160116232
|
T | G | 10 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(7): Show | 10 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1982-4033A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116232 | ||||||
| chr2:160116315
|
T | C | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1982-4116A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116315 | ||||||
| chr2:160116358
|
G | C | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1982-4159C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116358 | ||||||
| chr2:160116451
|
C | T | 1 | a0001c0001t0007g0315 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1982-4252G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116451 | ||||||
| chr2:160116491
|
C | T | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1982-4292G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116491 | ||||||
| chr2:160116513
|
G | A | 1 | a0001c0002t0002g0085 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1982-4314C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116513 | ||||||
| chr2:160116575
|
A | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0235 | 3 | HG02572.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1982-4376T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116575 | ||||||
| chr2:160116578
|
A | T | 1 | a0001c0001t0014g0302 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1982-4379T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116578 | ||||||
| chr2:160116776
|
G | A | 7 | a0001c0004t0001g0259a0001c0004t0001g0279a0001c0006t0008g0092others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1982-4577C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116776 | ||||||
| chr2:160116854
|
G | A | 6 | a0001c0004t0001g0227a0001c0004t0001g0228a0001c0004t0001g0230others(3): Show | 6 | NA18951.hp2 NA18961.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.1982-4655C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116854 | ||||||
| chr2:160117025
|
T | A | 21 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(18): Show | 22 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1982-4826A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117025 | ||||||
| chr2:160117030
|
C | T | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1982-4831G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117030 | ||||||
| chr2:160117105
|
C | T | 1 | a0001c0002t0002g0046 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1982-4906G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117105 | ||||||
| chr2:160117211
|
A | AT | 5 | a0001c0001t0007g0311a0001c0001t0007g0312a0001c0001t0007g0313others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1982-5013dupA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117211 | ||||||
| chr2:160117259
|
T | G | 6 | a0001c0001t0001g0001a0001c0001t0001g0245a0001c0001t0001g0246others(3): Show | 11 | NA18941.hp2 NA18948.hp2 NA18977.hp1 others(8): Show |
intron_variant | MODIFIER | c.1982-5060A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117259 | ||||||
| chr2:160117271
|
A | T | 1 | a0001c0004t0001g0283 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1982-5072T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117271 | ||||||
| chr2:160117291
|
G | T | 1 | a0001c0002t0009g0057 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1982-5092C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117291 | ||||||
| chr2:160117342
|
G | A | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1982-5143C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117342 | ||||||
| chr2:160117402
|
T | A | 1 | a0001c0001t0004g0267 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1982-5203A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117402 | ||||||
| chr2:160117403
|
C | A | 1 | a0001c0001t0004g0267 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1982-5204G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117403 | ||||||
| chr2:160117418
|
G | C | 1 | a0001c0001t0004g0267 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1982-5219C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117418 | ||||||
| chr2:160117427
|
C | T | 5 | a0001c0002t0002g0038a0001c0002t0002g0046a0001c0002t0002g0076others(2): Show | 5 | HG02040.hp1 HG02056.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.1982-5228G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117427 | ||||||
| chr2:160117478
|
A | C | 1 | a0001c0001t0004g0187 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1982-5279T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117478 | ||||||
| chr2:160117754
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1982-5555G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117754 | ||||||
| chr2:160117755
|
A | C | 8 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(5): Show | 8 | HG00741.hp2 HG01261.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1982-5556T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117755 | ||||||
| chr2:160117755
|
A | G | 206 | a0001c0001t0001g0008a0001c0001t0001g0095a0001c0001t0001g0100others(203): Show | 216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1982-5556T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117755 | ||||||
| chr2:160117763
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1982-5564C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117763 | ||||||
| chr2:160117821
|
G | A | 1 | a0001c0002t0002g0031 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1982-5622C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117821 | ||||||
| chr2:160118041
|
A | G | 1 | a0001c0001t0001g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1981+5750T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118041 | ||||||
| chr2:160118223
|
T | C | 41 | a0001c0001t0001g0110a0001c0004t0001g0011a0001c0004t0001g0192others(38): Show | 42 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.1981+5568A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118223 | ||||||
| chr2:160118229
|
A | C | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1981+5562T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118229 | ||||||
| chr2:160118253
|
G | C | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1981+5538C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118253 | ||||||
| chr2:160118395
|
C | T | 2 | a0001c0001t0004g0108a0001c0001t0004g0109 | 2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1981+5396G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118395 | ||||||
| chr2:160118446
|
C | T | 16 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(13): Show | 17 | HG00639.hp1 HG01261.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1981+5345G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118446 | ||||||
| chr2:160118508
|
C | T | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1981+5283G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118508 | ||||||
| chr2:160118544
|
A | C | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1981+5247T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118544 | ||||||
| chr2:160118599
|
A | T | 1 | a0001c0003t0003g0173 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1981+5192T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118599 | ||||||
| chr2:160118638
|
A | C | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1981+5153T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118638 | ||||||
| chr2:160118671
|
T | C | 16 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(13): Show | 17 | HG00639.hp1 HG01261.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1981+5120A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118671 | ||||||
| chr2:160118671
|
T | G | 72 | a0001c0003t0001g0139a0001c0003t0001g0209a0001c0003t0003g0004others(69): Show | 75 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1981+5120A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118671 | ||||||
| chr2:160118701
|
A | C | 1 | a0001c0004t0001g0231 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1981+5090T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118701 | ||||||
| chr2:160118714
|
G | A | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1981+5077C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118714 | ||||||
| chr2:160118743
|
T | C | 76 | a0001c0001t0004g0141a0001c0001t0004g0142a0001c0002t0002g0002others(73): Show | 82 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.1981+5048A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118743 | ||||||
| chr2:160118744
|
G | A | 74 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(71): Show | 80 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.1981+5047C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118744 | ||||||
| chr2:160118771
|
A | G | 74 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(71): Show | 80 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.1981+5020T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118771 | ||||||
| chr2:160118926
|
G | C | 1 | a0001c0001t0004g0113 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1981+4865C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118926 | ||||||
| chr2:160118937
|
A | G | 5 | a0001c0002t0002g0038a0001c0002t0002g0046a0001c0002t0002g0076others(2): Show | 5 | HG02040.hp1 HG02056.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.1981+4854T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118937 | ||||||
| chr2:160118939
|
C | G | 1 | a0001c0001t0001g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1981+4852G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118939 | ||||||
| chr2:160118940
|
T | G | 1 | a0001c0001t0001g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1981+4851A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118940 | ||||||
| chr2:160118994
|
C | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0309 | 3 | HG03516.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1981+4797G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118994 | ||||||
| chr2:160119046
|
C | T | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1981+4745G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119046 | ||||||
| chr2:160119088
|
G | A | 103 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(100): Show | 109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.1981+4703C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119088 | ||||||
| chr2:160119137
|
A | G | 71 | a0001c0003t0001g0209a0001c0003t0003g0004a0001c0003t0003g0012others(68): Show | 74 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1981+4654T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119137 | ||||||
| chr2:160119198
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0309a0001c0001t0001g0335 | 4 | HG01261.hp1 HG03516.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1981+4593C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119198 | ||||||
| chr2:160119199
|
C | G | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1981+4592G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119199 | ||||||
| chr2:160119236
|
A | G | 1 | a0001c0001t0004g0131 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1981+4555T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119236 | ||||||
| chr2:160119260
|
A | G | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1981+4531T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119260 | ||||||
| chr2:160119273
|
A | C | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1981+4518T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119273 | ||||||
| chr2:160119285
|
C | T | 88 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(85): Show | 94 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.1981+4506G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119285 | ||||||
| chr2:160119361
|
G | A | 1 | a0001c0003t0003g0185 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1981+4430C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119361 | ||||||
| chr2:160119427
|
G | A | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1981+4364C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119427 | ||||||
| chr2:160119442
|
A | C | 1 | a0001c0003t0003g0152 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1981+4349T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119442 | ||||||
| chr2:160119562
|
C | T | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1981+4229G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119562 | ||||||
| chr2:160119609
|
A | G | 1 | a0001c0001t0001g0317 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1981+4182T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119609 | ||||||
| chr2:160119659
|
A | G | 5 | a0001c0001t0007g0311a0001c0001t0007g0312a0001c0001t0007g0313others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1981+4132T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119659 | ||||||
| chr2:160119670
|
T | C | 74 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(71): Show | 80 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.1981+4121A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119670 | ||||||
| chr2:160119686
|
G | A | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1981+4105C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119686 | ||||||
| chr2:160119737
|
G | A | 5 | a0001c0001t0007g0311a0001c0001t0007g0312a0001c0001t0007g0313others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1981+4054C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119737 | ||||||
| chr2:160119738
|
A | C | 5 | a0001c0001t0007g0311a0001c0001t0007g0312a0001c0001t0007g0313others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1981+4053T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119738 | ||||||
| chr2:160119755
|
G | A | 1 | a0001c0001t0004g0131 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1981+4036C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119755 | ||||||
| chr2:160119762
|
A | G | 1 | a0001c0004t0001g0261 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1981+4029T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119762 | ||||||
| chr2:160119925
|
A | C | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1981+3866T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119925 | ||||||
| chr2:160119930
|
G | A | 2 | a0001c0001t0004g0129a0001c0001t0004g0130 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1981+3861C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119930 | ||||||
| chr2:160119980
|
C | G | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1981+3811G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119980 | ||||||
| chr2:160119993
|
C | T | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1981+3798G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119993 | ||||||
| chr2:160120052
|
C | A | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1981+3739G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120052 | ||||||
| chr2:160120054
|
T | G | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1981+3737A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120054 | ||||||
| chr2:160120098
|
A | T | 1 | a0001c0003t0001g0139 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1981+3693T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120098 | ||||||
| chr2:160120109
|
C | T | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1981+3682G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120109 | ||||||
| chr2:160120218
|
G | A | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1981+3573C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120218 | ||||||
| chr2:160120247
|
G | T | 1 | a0001c0001t0001g0317 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1981+3544C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120247 | ||||||
| chr2:160120277
|
A | G | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1981+3514T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120277 | ||||||
| chr2:160120281
|
T | C | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1981+3510A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120281 | ||||||
| chr2:160120294
|
TAAGAAAA others(387): Show |
T | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1981+3103_1981+349 others(4): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120294 | ||||||
| chr2:160120345
|
T | G | 2 | a0001c0004t0001g0297a0001c0004t0001g0298 | 2 | HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1981+3446A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120345 | ||||||
| chr2:160120410
|
C | T | 1 | a0001c0001t0016g0299 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1981+3381G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120410 | ||||||
| chr2:160120433
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(63): Show | 75 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.1981+3358G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120433 | ||||||
| chr2:160120668
|
TA | T | 9 | a0001c0001t0001g0010a0001c0001t0001g0235a0001c0001t0004g0123others(6): Show | 10 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.1981+3122delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120668 | ||||||
| chr2:160120668
|
TAA | T | 57 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0110others(54): Show | 61 | HG00423.hp1 HG00621.hp1 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.1981+3121_1981+312 others(6): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120668 | ||||||
| chr2:160120668
|
TAAA | T | 9 | a0001c0001t0001g0001a0001c0001t0001g0245a0001c0001t0001g0246others(6): Show | 14 | HG00609.hp2 HG02895.hp2 NA18948.hp2 others(11): Show |
intron_variant | MODIFIER | c.1981+3120_1981+312 others(7): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120668 | ||||||
| chr2:160120668
|
TAAAAAAA others(6): Show |
T | 4 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0285others(1): Show | 4 | HG00597.hp2 HG02132.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.1981+3110_1981+312 others(17): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120668 | ||||||
| chr2:160120686
|
A | G | 1 | a0001c0004t0001g0259 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1981+3105T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120686 | ||||||
| chr2:160120731
|
G | A | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1981+3060C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120731 | ||||||
| chr2:160120768
|
G | A | 1 | a0001c0004t0001g0278 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1981+3023C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120768 | ||||||
| chr2:160120870
|
A | T | 15 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(12): Show | 15 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1981+2921T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120870 | ||||||
| chr2:160120877
|
C | A | 1 | a0001c0004t0001g0298 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1981+2914G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120877 | ||||||
| chr2:160120907
|
G | A | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1981+2884C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120907 | ||||||
| chr2:160120966
|
C | T | 1 | a0001c0001t0020g0336 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1981+2825G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120966 | ||||||
| chr2:160121040
|
C | A | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1981+2751G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121040 | ||||||
| chr2:160121068
|
A | C | 73 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(70): Show | 79 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.1981+2723T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121068 | ||||||
| chr2:160121183
|
C | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(61): Show | 73 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.1981+2608G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121183 | ||||||
| chr2:160121247
|
G | C | 1 | a0001c0004t0001g0277 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1981+2544C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121247 | ||||||
| chr2:160121258
|
A | G | 88 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(85): Show | 94 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.1981+2533T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121258 | ||||||
| chr2:160121396
|
C | T | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1981+2395G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121396 | ||||||
| chr2:160121430
|
T | C | 1 | a0001c0001t0004g0224 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1981+2361A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121430 | ||||||
| chr2:160121432
|
A | G | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1981+2359T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121432 | ||||||
| chr2:160121521
|
A | G | 9 | a0001c0002t0002g0018a0001c0002t0002g0023a0001c0002t0002g0024others(6): Show | 9 | HG00423.hp2 NA18956.hp2 NA18957.hp2 others(6): Show |
intron_variant | MODIFIER | c.1981+2270T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121521 | ||||||
| chr2:160121608
|
A | G | 1 | a0001c0003t0003g0316 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1981+2183T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121608 | ||||||
| chr2:160121648
|
G | T | 283 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(280): Show | 303 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.1981+2143C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121648 | ||||||
| chr2:160121654
|
C | T | 1 | a0001c0004t0001g0261 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1981+2137G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121654 | ||||||
| chr2:160121742
|
G | A | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1981+2049C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121742 | ||||||
| chr2:160121760
|
C | T | 1 | a0001c0004t0001g0292 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1981+2031G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121760 | ||||||
| chr2:160121776
|
A | AAG | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1981+2014_1981+201 others(6): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121776 | ||||||
| chr2:160121777
|
G | A | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1981+2014C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121777 | ||||||
| chr2:160121777
|
G | GA | 202 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(199): Show | 212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.1981+2013dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121777 | ||||||
| chr2:160121777
|
GA | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(66): Show | 79 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1981+2013delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121777 | ||||||
| chr2:160121824
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1981+1967G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121824 | ||||||
| chr2:160121824
|
CAT | C | 59 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0018others(56): Show | 62 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.1981+1965_1981+196 others(6): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121824 | ||||||
| chr2:160121855
|
C | T | 213 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(210): Show | 223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1981+1936G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121855 | ||||||
| chr2:160121889
|
C | CT | 12 | a0001c0002t0002g0058a0001c0003t0001g0139a0001c0005t0005g0015others(9): Show | 12 | HG00140.hp1 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1981+1901dupA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121889 | ||||||
| chr2:160121954
|
G | A | 1 | a0001c0004t0001g0253 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1981+1837C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121954 | ||||||
| chr2:160121988
|
C | T | 20 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0096others(17): Show | 21 | HG00639.hp1 HG01261.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1981+1803G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121988 | ||||||
| chr2:160122056
|
G | T | 1 | a0001c0013t0002g0255 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1981+1735C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160122056 | ||||||
| chr2:160122204
|
T | C | 1 | a0001c0003t0003g0172 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1981+1587A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160122204 | ||||||
| chr2:160122259
|
T | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0309 | 3 | HG03516.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1981+1532A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160122259 | ||||||
| chr2:160122331
|
T | C | 1 | a0001c0001t0001g0317 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1981+1460A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160122331 | ||||||
| chr2:160122375
|
G | A | 2 | a0001c0001t0004g0115a0001c0001t0004g0117 | 2 | HG03017.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1981+1416C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160122375 | ||||||
| chr2:160122401
|
A | G | 3 | a0001c0002t0002g0024a0001c0002t0002g0047a0001c0002t0002g0062 | 3 | NA18956.hp2 NA18985.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1981+1390T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160122401 | ||||||
| chr2:160122469
|
G | A | 211 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(208): Show | 221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.1981+1322C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160122469 | ||||||
| chr2:160122513
|
GA | G | 5 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1981+1277delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160122513 | ||||||
| chr2:160122581
|
T | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(280): Show | 303 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.1981+1210A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160122581 | ||||||
| chr2:160122607
|
C | T | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1981+1184G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160122607 | ||||||
| chr2:160122628
|
G | A | 1 | a0001c0001t0004g0251 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1981+1163C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160122628 | ||||||
| chr2:160122815
|
T | C | 72 | a0001c0003t0001g0139a0001c0003t0001g0209a0001c0003t0003g0004others(69): Show | 75 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1981+976A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160122815 | ||||||
| chr2:160123239
|
T | G | 1 | a0001c0002t0002g0039 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1981+552A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160123239 | ||||||
| chr2:160123348
|
C | T | 1 | a0001c0004t0001g0192 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1981+443G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160123348 | ||||||
| chr2:160123395
|
C | T | 1 | a0001c0002t0002g0034 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1981+396G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160123395 | ||||||
| chr2:160123671
|
C | A | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1981+120G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160123671 | ||||||
| chr2:160123677
|
C | A | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1981+114G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160123677 | ||||||
| chr2:160123734
|
A | G | 1 | a0001c0001t0001g0321 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1981+57T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160123734 | ||||||
| chr2:160123996
|
C | T | 1 | a0001c0004t0001g0230 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1884-108G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160123996 | ||||||
| chr2:160124285
|
A | T | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1884-397T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160124285 | ||||||
| chr2:160124451
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1884-563C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160124451 | ||||||
| chr2:160124521
|
A | G | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1884-633T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160124521 | ||||||
| chr2:160124929
|
A | T | 209 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(206): Show | 219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1884-1041T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160124929 | ||||||
| chr2:160124991
|
T | C | 1 | a0001c0015t0001g0229 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1884-1103A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160124991 | ||||||
| chr2:160125002
|
C | T | 5 | a0001c0001t0007g0311a0001c0001t0007g0312a0001c0001t0007g0313others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1884-1114G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160125002 | ||||||
| chr2:160125144
|
T | TC | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1883+1234dupG | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160125144 | ||||||
| chr2:160125151
|
C | G | 1 | a0001c0001t0001g0244 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1883+1228G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160125151 | ||||||
| chr2:160125223
|
A | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(66): Show | 79 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1883+1156T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160125223 | ||||||
| chr2:160125262
|
G | A | 16 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(13): Show | 17 | HG00639.hp1 HG01261.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1883+1117C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160125262 | ||||||
| chr2:160125285
|
C | G | 10 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(7): Show | 10 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1883+1094G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160125285 | ||||||
| chr2:160125436
|
C | T | 1 | a0001c0001t0004g0240 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1883+943G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160125436 | ||||||
| chr2:160125629
|
C | G | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1883+750G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160125629 | ||||||
| chr2:160125809
|
T | TAAAAG | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1883+569_1883+570i others(7): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160125809 | ||||||
| chr2:160125885
|
G | A | 1 | a0001c0005t0005g0331 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1883+494C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160125885 | ||||||
| chr2:160125920
|
T | C | 214 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(211): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1883+459A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160125920 | ||||||
| chr2:160126027
|
T | C | 2 | a0001c0001t0001g0252a0001c0001t0001g0264 | 2 | HG02895.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1883+352A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160126027 | ||||||
| chr2:160126040
|
C | T | 4 | a0001c0003t0003g0165a0001c0003t0003g0186a0001c0003t0003g0196others(1): Show | 4 | NA18962.hp2 NA18994.hp2 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.1883+339G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160126040 | ||||||
| chr2:160126148
|
A | G | 2 | a0001c0003t0003g0201a0001c0003t0003g0204 | 2 | HG04115.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1883+231T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160126148 | ||||||
| chr2:160126154
|
G | A | 1 | a0001c0001t0004g0187 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1883+225C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160126154 | ||||||
| chr2:160126248
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0235a0001c0001t0013g0234 | 4 | HG02451.hp1 HG02572.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1883+131C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160126248 | ||||||
| chr2:160126647
|
G | A | 3 | a0001c0005t0004g0019a0001c0005t0004g0020a0001c0005t0004g0021 | 3 | HG00639.hp2 HG00642.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1661-46C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160126647 | ||||||
| chr2:160126652
|
T | C | 1 | a0001c0001t0010g0289 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1661-51A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160126652 | ||||||
| chr2:160126656
|
A | G | 44 | a0001c0001t0001g0110a0001c0001t0001g0252a0001c0001t0001g0264others(41): Show | 45 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.1661-55T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160126656 | ||||||
| chr2:160126664
|
A | C | 1 | a0001c0003t0001g0139 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1661-63T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160126664 | ||||||
| chr2:160126805
|
T | C | 3 | a0001c0001t0004g0105a0001c0001t0004g0106a0001c0001t0004g0107 | 3 | HG01256.hp1 HG01258.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1661-204A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160126805 | ||||||
| chr2:160126834
|
T | G | 204 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(201): Show | 214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.1661-233A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160126834 | ||||||
| chr2:160126861
|
A | C | 1 | a0001c0001t0001g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1661-260T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160126861 | ||||||
| chr2:160127291
|
T | C | 213 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(210): Show | 223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1661-690A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160127291 | ||||||
| chr2:160127339
|
A | G | 14 | a0001c0005t0005g0015a0001c0005t0005g0016a0001c0005t0005g0223others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1661-738T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160127339 | ||||||
| chr2:160127378
|
A | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(279): Show | 302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.1661-777T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160127378 | ||||||
| chr2:160127494
|
A | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(63): Show | 75 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.1661-893T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160127494 | ||||||
| chr2:160127578
|
T | C | 213 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(210): Show | 223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1661-977A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160127578 | ||||||
| chr2:160127603
|
G | A | 71 | a0001c0003t0001g0209a0001c0003t0003g0004a0001c0003t0003g0012others(68): Show | 74 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1661-1002C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160127603 | ||||||
| chr2:160128038
|
A | G | 213 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(210): Show | 223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1661-1437T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160128038 | ||||||
| chr2:160128248
|
A | C | 21 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(18): Show | 22 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1661-1647T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160128248 | ||||||
| chr2:160128261
|
C | T | 1 | a0001c0001t0004g0140 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1661-1660G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160128261 | ||||||
| chr2:160128267
|
G | A | 1 | a0001c0003t0003g0186 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1661-1666C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160128267 | ||||||
| chr2:160128274
|
C | CA | 216 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(213): Show | 226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.1661-1674dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160128274 | ||||||
| chr2:160128326
|
A | G | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1661-1725T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160128326 | ||||||
| chr2:160128572
|
G | A | 1 | a0001c0002t0002g0052 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1661-1971C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160128572 | ||||||
| chr2:160128614
|
A | C | 213 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(210): Show | 223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1661-2013T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160128614 | ||||||
| chr2:160128618
|
G | A | 2 | a0001c0004t0001g0259a0001c0004t0001g0279 | 2 | HG02683.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1661-2017C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160128618 | ||||||
| chr2:160128676
|
G | A | 2 | a0001c0001t0004g0118a0001c0001t0004g0119 | 2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1661-2075C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160128676 | ||||||
| chr2:160128678
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1661-2077C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160128678 | ||||||
| chr2:160128951
|
A | G | 213 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(210): Show | 223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1661-2350T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160128951 | ||||||
| chr2:160129038
|
G | A | 14 | a0001c0005t0005g0015a0001c0005t0005g0016a0001c0005t0005g0223others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1661-2437C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129038 | ||||||
| chr2:160129075
|
A | C | 14 | a0001c0005t0005g0015a0001c0005t0005g0016a0001c0005t0005g0223others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1661-2474T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129075 | ||||||
| chr2:160129087
|
G | A | 5 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1661-2486C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129087 | ||||||
| chr2:160129104
|
G | A | 3 | a0001c0004t0001g0227a0001c0004t0001g0228a0001c0004t0001g0231 | 3 | NA18961.hp1 NA18982.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1661-2503C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129104 | ||||||
| chr2:160129265
|
A | T | 1 | a0001c0001t0004g0238 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1661-2664T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129265 | ||||||
| chr2:160129313
|
C | A | 33 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(30): Show | 34 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.1661-2712G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129313 | ||||||
| chr2:160129313
|
C | T | 1 | a0001c0003t0003g0173 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1661-2712G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129313 | ||||||
| chr2:160129392
|
C | CA | 103 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0013others(100): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.1661-2792dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129392 | ||||||
| chr2:160129392
|
C | CAA | 134 | a0001c0001t0001g0005a0001c0001t0001g0254a0001c0001t0016g0299others(131): Show | 143 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.1661-2793_1661-279 others(6): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129392 | ||||||
| chr2:160129392
|
C | CAAAAA | 24 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(21): Show | 25 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1661-2796_1661-279 others(9): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129392 | ||||||
| chr2:160129392
|
CAA | C | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1661-2793_1661-279 others(6): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129392 | ||||||
| chr2:160129513
|
A | G | 1 | a0001c0003t0003g0148 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1661-2912T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129513 | ||||||
| chr2:160129664
|
C | T | 1 | a0001c0004t0001g0281 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1661-3063G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129664 | ||||||
| chr2:160129668
|
A | T | 72 | a0001c0003t0001g0139a0001c0003t0001g0209a0001c0003t0003g0004others(69): Show | 75 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1661-3067T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129668 | ||||||
| chr2:160129746
|
T | C | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1661-3145A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129746 | ||||||
| chr2:160129885
|
T | C | 213 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(210): Show | 223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1661-3284A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129885 | ||||||
| chr2:160129911
|
T | C | 1 | a0001c0003t0001g0139 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1661-3310A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129911 | ||||||
| chr2:160129916
|
A | ATG | 4 | a0001c0003t0003g0183a0001c0003t0003g0188a0001c0003t0003g0189others(1): Show | 4 | HG00741.hp1 HG01243.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.1661-3317_1661-331 others(6): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129916 | ||||||
| chr2:160129916
|
A | G | 21 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(18): Show | 22 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1661-3315T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129916 | ||||||
| chr2:160129998
|
A | G | 213 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(210): Show | 223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1661-3397T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129998 | ||||||
| chr2:160130031
|
G | A | 169 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(166): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1661-3430C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160130031 | ||||||
| chr2:160130050
|
T | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(279): Show | 302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.1661-3449A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160130050 | ||||||
| chr2:160130326
|
C | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(204): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1661-3725G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160130326 | ||||||
| chr2:160130350
|
A | C | 1 | a0001c0001t0004g0137 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1661-3749T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160130350 | ||||||
| chr2:160130375
|
T | C | 1 | a0001c0004t0001g0192 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1661-3774A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160130375 | ||||||
| chr2:160130410
|
G | T | 213 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(210): Show | 223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1661-3809C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160130410 | ||||||
| chr2:160130609
|
C | A | 5 | a0001c0001t0007g0311a0001c0001t0007g0312a0001c0001t0007g0313others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1661-4008G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160130609 | ||||||
| chr2:160130625
|
T | A | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1661-4024A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160130625 | ||||||
| chr2:160130645
|
C | A | 208 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(205): Show | 218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1661-4044G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160130645 | ||||||
| chr2:160131097
|
G | T | 175 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(172): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.1661-4496C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160131097 | ||||||
| chr2:160131203
|
GT | G | 213 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(210): Show | 223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1661-4603delA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160131203 | ||||||
| chr2:160131220
|
A | G | 16 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(13): Show | 17 | HG00639.hp1 HG01261.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1661-4619T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160131220 | ||||||
| chr2:160131250
|
A | T | 39 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(36): Show | 40 | HG00639.hp1 HG00733.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.1661-4649T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160131250 | ||||||
| chr2:160131670
|
A | C | 10 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(7): Show | 10 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1661-5069T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160131670 | ||||||
| chr2:160131913
|
A | G | 2 | a0001c0002t0002g0066a0001c0002t0002g0067 | 2 | NA18968.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1661-5312T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160131913 | ||||||
| chr2:160132112
|
A | C | 33 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(30): Show | 34 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.1660+5322T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132112 | ||||||
| chr2:160132156
|
G | A | 1 | a0001c0001t0014g0302 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1660+5278C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132156 | ||||||
| chr2:160132369
|
C | T | 1 | a0001c0004t0001g0263 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1660+5065G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132369 | ||||||
| chr2:160132444
|
C | T | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1660+4990G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132444 | ||||||
| chr2:160132482
|
A | G | 1 | a0001c0002t0002g0072 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1660+4952T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132482 | ||||||
| chr2:160132501
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1660+4933A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132501 | ||||||
| chr2:160132511
|
G | A | 281 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(278): Show | 301 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.1660+4923C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132511 | ||||||
| chr2:160132514
|
G | A | 56 | a0001c0003t0003g0004a0001c0003t0003g0132a0001c0003t0003g0144others(53): Show | 58 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1660+4920C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132514 | ||||||
| chr2:160132553
|
T | C | 2 | a0001c0003t0003g0156a0001c0003t0003g0157 | 2 | HG02055.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1660+4881A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132553 | ||||||
| chr2:160132672
|
G | A | 1 | a0001c0002t0002g0045 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1660+4762C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132672 | ||||||
| chr2:160132690
|
A | C | 33 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(30): Show | 34 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.1660+4744T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132690 | ||||||
| chr2:160132748
|
G | T | 1 | a0001c0002t0002g0048 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1660+4686C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132748 | ||||||
| chr2:160132764
|
T | G | 4 | a0001c0003t0003g0012a0001c0003t0003g0161a0001c0003t0003g0162others(1): Show | 5 | HG02451.hp2 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1660+4670A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132764 | ||||||
| chr2:160132776
|
C | T | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1660+4658G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132776 | ||||||
| chr2:160132785
|
A | G | 208 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(205): Show | 218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1660+4649T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132785 | ||||||
| chr2:160132789
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0235 | 3 | HG02572.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1660+4645G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132789 | ||||||
| chr2:160132975
|
T | C | 87 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(84): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.1660+4459A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132975 | ||||||
| chr2:160133291
|
A | C | 208 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(205): Show | 218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1660+4143T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160133291 | ||||||
| chr2:160133384
|
T | C | 1 | a0001c0001t0004g0137 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1660+4050A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160133384 | ||||||
| chr2:160133482
|
C | G | 208 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(205): Show | 218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1660+3952G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160133482 | ||||||
| chr2:160133580
|
A | G | 1 | a0001c0002t0002g0085 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1660+3854T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160133580 | ||||||
| chr2:160133605
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1660+3829G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160133605 | ||||||
| chr2:160133632
|
CA | C | 14 | a0001c0005t0005g0015a0001c0005t0005g0016a0001c0005t0005g0223others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1660+3801delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160133632 | ||||||
| chr2:160133693
|
A | G | 1 | a0001c0002t0002g0061 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1660+3741T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160133693 | ||||||
| chr2:160133702
|
T | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0235a0001c0001t0013g0234 | 4 | HG02451.hp1 HG02572.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1660+3732A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160133702 | ||||||
| chr2:160133937
|
A | C | 213 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(210): Show | 223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1660+3497T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160133937 | ||||||
| chr2:160133998
|
A | G | 1 | a0001c0001t0004g0210 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1660+3436T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160133998 | ||||||
| chr2:160134153
|
A | G | 32 | a0001c0001t0004g0120a0001c0001t0004g0122a0001c0001t0004g0123others(29): Show | 32 | HG00099.hp2 HG00597.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.1660+3281T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134153 | ||||||
| chr2:160134217
|
C | T | 72 | a0001c0003t0001g0139a0001c0003t0001g0209a0001c0003t0003g0004others(69): Show | 75 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1660+3217G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134217 | ||||||
| chr2:160134486
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1660+2948C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134486 | ||||||
| chr2:160134496
|
T | C | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1660+2938A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134496 | ||||||
| chr2:160134530
|
G | A | 69 | a0001c0003t0001g0209a0001c0003t0003g0004a0001c0003t0003g0012others(66): Show | 72 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1660+2904C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134530 | ||||||
| chr2:160134598
|
A | C | 208 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(205): Show | 218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1660+2836T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134598 | ||||||
| chr2:160134600
|
T | C | 10 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0097others(7): Show | 10 | HG00639.hp1 HG01261.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1660+2834A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134600 | ||||||
| chr2:160134618
|
A | G | 2 | a0001c0004t0001g0300a0001c0004t0001g0301 | 2 | NA18963.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1660+2816T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134618 | ||||||
| chr2:160134656
|
A | G | 1 | a0001c0001t0001g0100 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1660+2778T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134656 | ||||||
| chr2:160134794
|
A | G | 3 | a0001c0002t0002g0024a0001c0002t0002g0047a0001c0002t0002g0062 | 3 | NA18956.hp2 NA18985.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1660+2640T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134794 | ||||||
| chr2:160134853
|
A | T | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1660+2581T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134853 | ||||||
| chr2:160134861
|
C | G | 208 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(205): Show | 218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1660+2573G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134861 | ||||||
| chr2:160134898
|
C | T | 1 | a0001c0001t0004g0116 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1660+2536G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134898 | ||||||
| chr2:160134957
|
G | A | 1 | a0003c0008t0019g0014 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1660+2477C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134957 | ||||||
| chr2:160134989
|
T | A | 5 | a0001c0002t0002g0069a0001c0002t0002g0070a0001c0002t0002g0071others(2): Show | 5 | NA18975.hp1 NA19002.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.1660+2445A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134989 | ||||||
| chr2:160135002
|
G | A | 5 | a0001c0001t0007g0311a0001c0001t0007g0312a0001c0001t0007g0313others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1660+2432C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135002 | ||||||
| chr2:160135145
|
T | C | 1 | a0001c0004t0001g0192 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1660+2289A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135145 | ||||||
| chr2:160135159
|
C | T | 213 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(210): Show | 223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1660+2275G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135159 | ||||||
| chr2:160135160
|
T | C | 206 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(203): Show | 216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1660+2274A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135160 | ||||||
| chr2:160135163
|
C | G | 5 | a0001c0001t0007g0311a0001c0001t0007g0312a0001c0001t0007g0313others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1660+2271G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135163 | ||||||
| chr2:160135217
|
C | G | 212 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(209): Show | 222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1660+2217G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135217 | ||||||
| chr2:160135236
|
T | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(63): Show | 75 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.1660+2198A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135236 | ||||||
| chr2:160135325
|
G | A | 2 | a0001c0001t0007g0313a0001c0001t0007g0314 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1660+2109C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135325 | ||||||
| chr2:160135392
|
T | G | 33 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(30): Show | 34 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.1660+2042A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135392 | ||||||
| chr2:160135413
|
C | G | 213 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(210): Show | 223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1660+2021G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135413 | ||||||
| chr2:160135558
|
T | A | 2 | a0001c0001t0001g0252a0001c0001t0001g0264 | 2 | HG02895.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1660+1876A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135558 | ||||||
| chr2:160135586
|
A | G | 208 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(205): Show | 218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1660+1848T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135586 | ||||||
| chr2:160135624
|
G | A | 70 | a0001c0003t0001g0209a0001c0003t0003g0004a0001c0003t0003g0012others(67): Show | 73 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.1660+1810C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135624 | ||||||
| chr2:160135644
|
C | G | 14 | a0001c0005t0005g0015a0001c0005t0005g0016a0001c0005t0005g0223others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1660+1790G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135644 | ||||||
| chr2:160135745
|
T | A | 1 | a0001c0001t0004g0115 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1660+1689A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135745 | ||||||
| chr2:160135911
|
G | T | 5 | a0001c0001t0007g0311a0001c0001t0007g0312a0001c0001t0007g0313others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1660+1523C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135911 | ||||||
| chr2:160135927
|
A | G | 213 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(210): Show | 223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1660+1507T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135927 | ||||||
| chr2:160135941
|
A | C | 213 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(210): Show | 223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1660+1493T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135941 | ||||||
| chr2:160135968
|
C | T | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1660+1466G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135968 | ||||||
| chr2:160136039
|
C | A | 21 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(18): Show | 22 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1660+1395G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136039 | ||||||
| chr2:160136087
|
T | C | 1 | a0001c0001t0004g0187 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1660+1347A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136087 | ||||||
| chr2:160136115
|
G | A | 2 | a0001c0001t0004g0251a0001c0001t0004g0296 | 2 | NA19006.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1660+1319C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136115 | ||||||
| chr2:160136132
|
A | G | 2 | a0001c0003t0003g0202a0001c0003t0003g0203 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1660+1302T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136132 | ||||||
| chr2:160136137
|
A | G | 4 | a0001c0003t0003g0165a0001c0003t0003g0186a0001c0003t0003g0196others(1): Show | 4 | NA18962.hp2 NA18994.hp2 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.1660+1297T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136137 | ||||||
| chr2:160136205
|
C | A | 1 | a0001c0001t0004g0140 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1660+1229G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136205 | ||||||
| chr2:160136258
|
C | G | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1660+1176G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136258 | ||||||
| chr2:160136279
|
A | T | 88 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(85): Show | 94 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.1660+1155T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136279 | ||||||
| chr2:160136284
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1660+1150T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136284 | ||||||
| chr2:160136285
|
A | C | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1660+1149T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136285 | ||||||
| chr2:160136360
|
T | C | 11 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(8): Show | 11 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1660+1074A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136360 | ||||||
| chr2:160136378
|
G | A | 71 | a0001c0003t0001g0139a0001c0003t0001g0209a0001c0003t0003g0004others(68): Show | 74 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1660+1056C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136378 | ||||||
| chr2:160136410
|
G | A | 213 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(210): Show | 223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1660+1024C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136410 | ||||||
| chr2:160136446
|
G | A | 1 | a0001c0001t0004g0115 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1660+988C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136446 | ||||||
| chr2:160136579
|
C | T | 14 | a0001c0005t0005g0015a0001c0005t0005g0016a0001c0005t0005g0223others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1660+855G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136579 | ||||||
| chr2:160136700
|
G | A | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1660+734C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136700 | ||||||
| chr2:160136742
|
T | G | 1 | a0001c0002t0002g0034 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1660+692A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136742 | ||||||
| chr2:160136838
|
T | G | 1 | a0001c0001t0001g0216 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1660+596A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136838 | ||||||
| chr2:160136888
|
C | A | 4 | a0001c0002t0002g0051a0001c0002t0002g0054a0001c0002t0002g0068others(1): Show | 4 | HG04184.hp2 NA18969.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1660+546G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136888 | ||||||
| chr2:160136907
|
G | C | 1 | a0001c0002t0002g0061 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1660+527C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136907 | ||||||
| chr2:160136915
|
G | T | 1 | a0001c0003t0001g0139 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1660+519C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136915 | ||||||
| chr2:160136948
|
G | A | 33 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(30): Show | 34 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.1660+486C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136948 | ||||||
| chr2:160136957
|
T | C | 213 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(210): Show | 223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1660+477A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136957 | ||||||
| chr2:160136960
|
G | A | 1 | a0001c0001t0004g0117 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1660+474C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136960 | ||||||
| chr2:160137017
|
A | G | 208 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(205): Show | 218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1660+417T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160137017 | ||||||
| chr2:160137052
|
T | TA | 69 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(66): Show | 79 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1660+381dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160137052 | ||||||
| chr2:160137052
|
TAAAAAAA others(5): Show |
T | 1 | a0001c0005t0005g0326 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1660+370_1660+381d others(14): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160137052 | ||||||
| chr2:160137053
|
A | T | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1660+381T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160137053 | ||||||
| chr2:160137054
|
A | T | 1 | a0001c0001t0001g0213 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1660+380T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160137054 | ||||||
| chr2:160137064
|
G | A | 1 | a0001c0002t0002g0062 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1660+370C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160137064 | ||||||
| chr2:160137064
|
GA | G | 201 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(198): Show | 211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.1660+369delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160137064 | ||||||
| chr2:160137065
|
A | G | 1 | a0001c0002t0002g0062 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1660+369T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160137065 | ||||||
| chr2:160137289
|
A | T | 208 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(205): Show | 218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1660+145T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160137289 | ||||||
| chr2:160137898
|
C | T | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1243-47G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 9/14 | chr2 | 160137898 | ||||||
| chr2:160137918
|
C | T | 1 | a0001c0003t0003g0132 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1243-67G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 9/14 | chr2 | 160137918 | ||||||
| chr2:160138253
|
A | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(66): Show | 79 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1108-54T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160138253 | ||||||
| chr2:160138257
|
G | C | 21 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(18): Show | 22 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1108-58C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160138257 | ||||||
| chr2:160138266
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0309 | 3 | HG03516.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1108-67C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160138266 | ||||||
| chr2:160138334
|
A | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(66): Show | 79 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1108-135T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160138334 | ||||||
| chr2:160138713
|
C | A | 1 | a0001c0004t0001g0272 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1108-514G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160138713 | ||||||
| chr2:160138723
|
T | G | 2 | a0001c0006t0008g0092a0001c0006t0008g0093 | 2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1108-524A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160138723 | ||||||
| chr2:160138738
|
A | G | 1 | a0001c0004t0001g0272 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1108-539T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160138738 | ||||||
| chr2:160138786
|
A | G | 6 | a0001c0004t0001g0253a0001c0004t0001g0283a0001c0004t0001g0292others(3): Show | 6 | HG00423.hp1 HG02080.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.1108-587T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160138786 | ||||||
| chr2:160138960
|
A | T | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1108-761T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160138960 | ||||||
| chr2:160139041
|
A | G | 6 | a0001c0001t0001g0001a0001c0001t0001g0245a0001c0001t0001g0246others(3): Show | 11 | NA18941.hp2 NA18948.hp2 NA18977.hp1 others(8): Show |
intron_variant | MODIFIER | c.1108-842T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160139041 | ||||||
| chr2:160139182
|
A | G | 5 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1108-983T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160139182 | ||||||
| chr2:160139373
|
T | TA | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1108-1175dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160139373 | ||||||
| chr2:160139425
|
G | A | 7 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1108-1226C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160139425 | ||||||
| chr2:160139437
|
A | G | 4 | a0001c0004t0001g0292a0001c0004t0001g0293a0001c0004t0001g0294others(1): Show | 4 | HG02080.hp1 NA18747.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.1108-1238T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160139437 | ||||||
| chr2:160139450
|
A | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(66): Show | 79 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1108-1251T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160139450 | ||||||
| chr2:160139548
|
G | A | 1 | a0001c0001t0004g0133 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1108-1349C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160139548 | ||||||
| chr2:160139586
|
C | T | 1 | a0001c0005t0005g0223 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1108-1387G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160139586 | ||||||
| chr2:160139707
|
A | G | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1108-1508T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160139707 | ||||||
| chr2:160139723
|
C | A | 1 | a0001c0001t0017g0291 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1108-1524G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160139723 | ||||||
| chr2:160139821
|
G | C | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1108-1622C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160139821 | ||||||
| chr2:160139880
|
A | G | 3 | a0001c0001t0001g0005a0001c0001t0001g0254a0001c0001t0016g0299 | 5 | HG02723.hp1 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1108-1681T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160139880 | ||||||
| chr2:160140215
|
A | G | 56 | a0001c0003t0003g0004a0001c0003t0003g0132a0001c0003t0003g0144others(53): Show | 58 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1107+1767T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160140215 | ||||||
| chr2:160140458
|
T | C | 281 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(278): Show | 301 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.1107+1524A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160140458 | ||||||
| chr2:160140570
|
G | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(66): Show | 79 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1107+1412C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160140570 | ||||||
| chr2:160140598
|
TTTAA | T | 10 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(7): Show | 10 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1107+1380_1107+138 others(8): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160140598 | ||||||
| chr2:160140636
|
G | A | 33 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(30): Show | 34 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.1107+1346C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160140636 | ||||||
| chr2:160140679
|
A | G | 1 | a0001c0002t0002g0036 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1107+1303T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160140679 | ||||||
| chr2:160140794
|
G | C | 2 | a0001c0001t0001g0211a0001c0001t0001g0214 | 2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1107+1188C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160140794 | ||||||
| chr2:160140807
|
T | C | 2 | a0001c0004t0001g0297a0001c0004t0001g0298 | 2 | HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1107+1175A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160140807 | ||||||
| chr2:160140899
|
A | AT | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1107+1082dupA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160140899 | ||||||
| chr2:160141008
|
G | A | 72 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(69): Show | 78 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.1107+974C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160141008 | ||||||
| chr2:160141011
|
G | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(279): Show | 302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.1107+971C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160141011 | ||||||
| chr2:160141047
|
A | G | 1 | a0001c0003t0003g0132 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1107+935T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160141047 | ||||||
| chr2:160141055
|
G | A | 33 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(30): Show | 34 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.1107+927C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160141055 | ||||||
| chr2:160141195
|
A | T | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1107+787T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160141195 | ||||||
| chr2:160141235
|
G | A | 212 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(209): Show | 222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1107+747C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160141235 | ||||||
| chr2:160141250
|
T | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0101a0001c0001t0001g0102others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1107+732A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160141250 | ||||||
| chr2:160141269
|
A | AG | 19 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0096others(16): Show | 20 | HG00639.hp1 HG00741.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.1107+712dupC | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160141269 | ||||||
| chr2:160141422
|
G | A | 21 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(18): Show | 22 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1107+560C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160141422 | ||||||
| chr2:160141616
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1107+366T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160141616 | ||||||
| chr2:160141618
|
A | G | 1 | a0002c0007t0001g0271 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1107+364T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160141618 | ||||||
| chr2:160141899
|
C | CTGCCTAA others(15): Show |
2 | a0001c0001t0001g0013a0001c0001t0001g0309 | 3 | HG03516.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1107+82_1107+83ins others(22): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160141899 | ||||||
| chr2:160142281
|
A | C | 66 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(63): Show | 75 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.1018-210T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160142281 | ||||||
| chr2:160142315
|
C | G | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1018-244G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160142315 | ||||||
| chr2:160142472
|
G | T | 1 | a0001c0001t0001g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1018-401C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160142472 | ||||||
| chr2:160142642
|
T | G | 1 | a0001c0021t0003g0334 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1018-571A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160142642 | ||||||
| chr2:160142732
|
A | G | 1 | a0001c0004t0001g0261 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1018-661T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160142732 | ||||||
| chr2:160142747
|
G | C | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-676C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160142747 | ||||||
| chr2:160142839
|
C | A | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-768G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160142839 | ||||||
| chr2:160143026
|
A | G | 88 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(85): Show | 94 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.1018-955T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160143026 | ||||||
| chr2:160143033
|
A | C | 21 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(18): Show | 22 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1018-962T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160143033 | ||||||
| chr2:160143085
|
C | A | 7 | a0001c0002t0002g0085a0001c0002t0002g0087a0001c0002t0002g0089others(4): Show | 9 | HG00140.hp2 HG00735.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.1018-1014G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160143085 | ||||||
| chr2:160143086
|
G | A | 1 | a0001c0001t0004g0187 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1018-1015C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160143086 | ||||||
| chr2:160143153
|
T | C | 2 | a0001c0001t0004g0268a0001c0001t0004g0284 | 2 | NA18974.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1018-1082A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160143153 | ||||||
| chr2:160143276
|
C | A | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-1205G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160143276 | ||||||
| chr2:160143284
|
A | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(279): Show | 302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.1018-1213T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160143284 | ||||||
| chr2:160143510
|
C | A | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-1439G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160143510 | ||||||
| chr2:160143602
|
C | T | 10 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(7): Show | 10 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1018-1531G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160143602 | ||||||
| chr2:160143832
|
T | C | 281 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(278): Show | 301 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.1018-1761A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160143832 | ||||||
| chr2:160143864
|
G | T | 1 | a0001c0003t0003g0132 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1018-1793C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160143864 | ||||||
| chr2:160143871
|
C | T | 10 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(7): Show | 10 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1018-1800G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160143871 | ||||||
| chr2:160143872
|
G | A | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-1801C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160143872 | ||||||
| chr2:160144103
|
A | C | 1 | a0001c0001t0014g0302 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1018-2032T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144103 | ||||||
| chr2:160144144
|
A | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(279): Show | 302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.1018-2073T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144144 | ||||||
| chr2:160144234
|
C | T | 1 | a0001c0001t0004g0256 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1018-2163G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144234 | ||||||
| chr2:160144271
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1018-2200C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144271 | ||||||
| chr2:160144317
|
T | C | 16 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(13): Show | 16 | HG00733.hp2 HG01070.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.1018-2246A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144317 | ||||||
| chr2:160144399
|
G | A | 7 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(4): Show | 7 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1018-2328C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144399 | ||||||
| chr2:160144403
|
T | G | 6 | a0001c0002t0002g0007a0001c0002t0002g0027a0001c0002t0002g0028others(3): Show | 7 | NA18954.hp2 NA18960.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.1018-2332A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144403 | ||||||
| chr2:160144561
|
C | T | 1 | a0001c0001t0004g0127 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1018-2490G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144561 | ||||||
| chr2:160144597
|
G | C | 1 | a0001c0003t0003g0181 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1018-2526C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144597 | ||||||
| chr2:160144658
|
C | T | 71 | a0001c0003t0001g0209a0001c0003t0003g0004a0001c0003t0003g0012others(68): Show | 74 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1018-2587G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144658 | ||||||
| chr2:160144666
|
A | G | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1018-2595T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144666 | ||||||
| chr2:160144732
|
C | T | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-2661G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144732 | ||||||
| chr2:160144865
|
C | T | 72 | a0001c0003t0001g0139a0001c0003t0001g0209a0001c0003t0003g0004others(69): Show | 75 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1018-2794G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144865 | ||||||
| chr2:160144929
|
T | A | 2 | a0001c0001t0004g0141a0001c0001t0004g0142 | 2 | HG01081.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1018-2858A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144929 | ||||||
| chr2:160144983
|
T | C | 3 | a0001c0002t0006g0003a0001c0002t0006g0086a0001c0002t0006g0088 | 5 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1018-2912A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144983 | ||||||
| chr2:160145099
|
C | T | 2 | a0001c0001t0001g0211a0001c0001t0001g0214 | 2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1018-3028G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160145099 | ||||||
| chr2:160145319
|
G | T | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-3248C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160145319 | ||||||
| chr2:160145435
|
T | G | 1 | a0001c0001t0012g0262 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1018-3364A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160145435 | ||||||
| chr2:160145468
|
A | T | 1 | a0001c0001t0001g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1018-3397T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160145468 | ||||||
| chr2:160145533
|
A | G | 1 | a0001c0002t0002g0039 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1018-3462T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160145533 | ||||||
| chr2:160145547
|
G | C | 2 | a0001c0003t0003g0012a0001c0003t0003g0304 | 3 | HG02723.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1018-3476C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160145547 | ||||||
| chr2:160145825
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1018-3754G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160145825 | ||||||
| chr2:160145828
|
G | A | 1 | a0001c0005t0005g0223 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1018-3757C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160145828 | ||||||
| chr2:160145881
|
C | T | 1 | a0001c0003t0003g0172 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1018-3810G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160145881 | ||||||
| chr2:160145891
|
T | C | 1 | a0001c0001t0001g0320 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1018-3820A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160145891 | ||||||
| chr2:160145905
|
C | T | 4 | a0001c0002t0002g0069a0001c0002t0002g0070a0001c0002t0002g0072others(1): Show | 4 | NA18975.hp1 NA19002.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.1018-3834G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160145905 | ||||||
| chr2:160146081
|
C | A | 12 | a0001c0002t0002g0006a0001c0002t0002g0042a0001c0002t0002g0043others(9): Show | 13 | HG00408.hp2 HG00621.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.1018-4010G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160146081 | ||||||
| chr2:160146098
|
GTGAGGCA others(11): Show |
G | 9 | a0001c0001t0004g0009a0001c0001t0004g0105a0001c0001t0004g0106others(6): Show | 10 | HG00280.hp2 HG01256.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1018-4045_1018-402 others(22): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160146098 | ||||||
| chr2:160146212
|
T | G | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-4141A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160146212 | ||||||
| chr2:160146249
|
G | C | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-4178C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160146249 | ||||||
| chr2:160146289
|
A | C | 1 | a0001c0003t0003g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1018-4218T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160146289 | ||||||
| chr2:160146340
|
C | T | 6 | a0001c0004t0001g0253a0001c0004t0001g0283a0001c0004t0001g0292others(3): Show | 6 | HG00423.hp1 HG02080.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.1018-4269G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160146340 | ||||||
| chr2:160146423
|
T | G | 2 | a0001c0003t0003g0159a0001c0003t0003g0160 | 2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1018-4352A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160146423 | ||||||
| chr2:160146595
|
T | C | 1 | a0001c0003t0003g0132 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1018-4524A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160146595 | ||||||
| chr2:160146932
|
C | T | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-4861G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160146932 | ||||||
| chr2:160147107
|
A | AAAAGG | 3 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0215 | 3 | HG02145.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1018-5041_1018-503 others(9): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160147107 | ||||||
| chr2:160147153
|
A | T | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1018-5082T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160147153 | ||||||
| chr2:160147425
|
T | G | 2 | a0001c0001t0001g0212a0001c0001t0001g0215 | 2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1018-5354A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160147425 | ||||||
| chr2:160147479
|
T | C | 5 | a0001c0003t0003g0156a0001c0003t0003g0157a0001c0003t0003g0158others(2): Show | 5 | HG01891.hp1 HG02055.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-5408A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160147479 | ||||||
| chr2:160147503
|
G | A | 1 | a0001c0002t0002g0073 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1018-5432C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160147503 | ||||||
| chr2:160147583
|
T | C | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-5512A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160147583 | ||||||
| chr2:160147687
|
C | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(125): Show | 139 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1018-5616G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160147687 | ||||||
| chr2:160147747
|
C | A | 1 | a0001c0003t0003g0207 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1018-5676G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160147747 | ||||||
| chr2:160147951
|
A | G | 9 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(6): Show | 9 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1018-5880T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160147951 | ||||||
| chr2:160147997
|
C | T | 321 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(318): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1018-5926G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160147997 | ||||||
| chr2:160148063
|
C | A | 1 | a0001c0003t0003g0182 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1018-5992G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148063 | ||||||
| chr2:160148340
|
C | T | 1 | a0001c0004t0001g0260 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1018-6269G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148340 | ||||||
| chr2:160148375
|
G | A | 1 | a0001c0005t0005g0331 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1018-6304C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148375 | ||||||
| chr2:160148453
|
T | C | 1 | a0001c0001t0004g0126 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1018-6382A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148453 | ||||||
| chr2:160148470
|
A | G | 1 | a0001c0001t0001g0100 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1018-6399T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148470 | ||||||
| chr2:160148472
|
T | G | 88 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(85): Show | 94 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.1018-6401A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148472 | ||||||
| chr2:160148576
|
G | A | 304 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(301): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.1018-6505C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148576 | ||||||
| chr2:160148650
|
C | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0245a0001c0001t0001g0246others(57): Show | 66 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.1018-6579G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148650 | ||||||
| chr2:160148651
|
C | G | 60 | a0001c0001t0001g0001a0001c0001t0001g0245a0001c0001t0001g0246others(57): Show | 66 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.1018-6580G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148651 | ||||||
| chr2:160148708
|
G | A | 1 | a0001c0003t0003g0183 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1018-6637C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148708 | ||||||
| chr2:160148779
|
G | T | 1 | a0001c0003t0003g0155 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1018-6708C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148779 | ||||||
| chr2:160148780
|
C | T | 1 | a0001c0003t0003g0155 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1018-6709G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148780 | ||||||
| chr2:160148824
|
A | G | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-6753T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148824 | ||||||
| chr2:160148835
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1018-6764G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148835 | ||||||
| chr2:160148849
|
A | G | 322 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(319): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1018-6778T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148849 | ||||||
| chr2:160149189
|
C | A | 1 | a0001c0003t0003g0184 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1018-7118G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160149189 | ||||||
| chr2:160149205
|
A | G | 1 | a0001c0001t0010g0289 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1018-7134T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160149205 | ||||||
| chr2:160149228
|
C | T | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1018-7157G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160149228 | ||||||
| chr2:160149256
|
G | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0101a0001c0001t0001g0102others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1018-7185C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160149256 | ||||||
| chr2:160149267
|
G | A | 316 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(313): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1018-7196C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160149267 | ||||||
| chr2:160149312
|
A | T | 65 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(62): Show | 69 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.1018-7241T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160149312 | ||||||
| chr2:160149345
|
A | G | 2 | a0001c0004t0001g0297a0001c0004t0001g0298 | 2 | HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1018-7274T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160149345 | ||||||
| chr2:160149416
|
A | G | 1 | a0001c0001t0004g0265 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1018-7345T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160149416 | ||||||
| chr2:160149492
|
TG | T | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-7422delC | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160149492 | ||||||
| chr2:160149602
|
C | T | 1 | a0001c0001t0004g0112 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1018-7531G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160149602 | ||||||
| chr2:160149827
|
A | C | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-7756T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160149827 | ||||||
| chr2:160150180
|
T | C | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-8109A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160150180 | ||||||
| chr2:160150260
|
C | T | 1 | a0001c0002t0002g0024 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1018-8189G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160150260 | ||||||
| chr2:160150261
|
G | T | 5 | a0001c0001t0007g0311a0001c0001t0007g0312a0001c0001t0007g0313others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-8190C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160150261 | ||||||
| chr2:160150289
|
TG | T | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-8219delC | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160150289 | ||||||
| chr2:160150299
|
T | C | 1 | a0001c0004t0001g0260 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1018-8228A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160150299 | ||||||
| chr2:160150335
|
A | T | 1 | a0001c0004t0018g0017 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1018-8264T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160150335 | ||||||
| chr2:160150553
|
C | T | 2 | a0001c0005t0004g0019a0001c0005t0004g0020 | 2 | HG00639.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.1018-8482G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160150553 | ||||||
| chr2:160150685
|
C | A | 1 | a0001c0001t0004g0126 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1018-8614G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160150685 | ||||||
| chr2:160150717
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1018-8646C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160150717 | ||||||
| chr2:160150828
|
T | TA | 5 | a0001c0001t0007g0311a0001c0001t0007g0312a0001c0001t0007g0313others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-8758dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160150828 | ||||||
| chr2:160151103
|
T | G | 1 | a0001c0004t0001g0230 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1018-9032A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160151103 | ||||||
| chr2:160151183
|
A | G | 74 | a0001c0001t0004g0187a0001c0003t0001g0139a0001c0003t0001g0209others(71): Show | 77 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.1018-9112T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160151183 | ||||||
| chr2:160151184
|
C | T | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1018-9113G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160151184 | ||||||
| chr2:160151190
|
T | A | 1 | a0001c0001t0004g0134 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1018-9119A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160151190 | ||||||
| chr2:160151201
|
C | T | 1 | a0001c0001t0001g0335 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1018-9130G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160151201 | ||||||
| chr2:160151354
|
A | G | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-9283T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160151354 | ||||||
| chr2:160151439
|
C | T | 321 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(318): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1018-9368G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160151439 | ||||||
| chr2:160151645
|
G | A | 4 | a0001c0003t0003g0170a0001c0003t0003g0171a0001c0003t0003g0195others(1): Show | 4 | HG00323.hp1 HG00735.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.1018-9574C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160151645 | ||||||
| chr2:160151678
|
A | T | 1 | a0001c0003t0003g0225 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1018-9607T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160151678 | ||||||
| chr2:160151732
|
A | C | 6 | a0001c0004t0001g0270a0001c0006t0008g0092a0001c0006t0008g0093others(3): Show | 6 | HG02071.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1018-9661T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160151732 | ||||||
| chr2:160152015
|
G | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(61): Show | 73 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.1018-9944C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152015 | ||||||
| chr2:160152022
|
G | A | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-9951C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152022 | ||||||
| chr2:160152038
|
C | T | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-9967G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152038 | ||||||
| chr2:160152112
|
C | G | 1 | a0001c0001t0001g0214 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1018-10041G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152112 | ||||||
| chr2:160152215
|
C | T | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-10144G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152215 | ||||||
| chr2:160152216
|
A | G | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-10145T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152216 | ||||||
| chr2:160152225
|
A | T | 4 | a0001c0003t0003g0170a0001c0003t0003g0171a0001c0003t0003g0195others(1): Show | 4 | HG00323.hp1 HG00735.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.1018-10154T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152225 | ||||||
| chr2:160152379
|
C | T | 175 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(172): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.1018-10308G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152379 | ||||||
| chr2:160152438
|
G | C | 1 | a0001c0004t0001g0208 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1018-10367C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152438 | ||||||
| chr2:160152441
|
C | T | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-10370G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152441 | ||||||
| chr2:160152475
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1018-10404T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152475 | ||||||
| chr2:160152484
|
C | A | 53 | a0001c0001t0004g0009a0001c0001t0004g0105a0001c0001t0004g0106others(50): Show | 54 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.1018-10413G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152484 | ||||||
| chr2:160152538
|
A | C | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-10467T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152538 | ||||||
| chr2:160152656
|
T | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(121): Show | 135 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.1018-10585A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152656 | ||||||
| chr2:160152658
|
T | G | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-10587A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152658 | ||||||
| chr2:160152668
|
G | T | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-10597C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152668 | ||||||
| chr2:160152689
|
C | T | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1018-10618G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152689 | ||||||
| chr2:160152979
|
G | T | 1 | a0001c0003t0003g0195 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1018-10908C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152979 | ||||||
| chr2:160152990
|
A | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0235 | 3 | HG02572.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1018-10919T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152990 | ||||||
| chr2:160153006
|
T | A | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-10935A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153006 | ||||||
| chr2:160153011
|
C | T | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1018-10940G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153011 | ||||||
| chr2:160153119
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(63): Show | 75 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.1018-11048G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153119 | ||||||
| chr2:160153384
|
T | A | 1 | a0001c0001t0004g0133 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1018-11313A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153384 | ||||||
| chr2:160153386
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1018-11315A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153386 | ||||||
| chr2:160153487
|
A | C | 1 | a0001c0004t0001g0269 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1018-11416T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153487 | ||||||
| chr2:160153586
|
A | G | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-11515T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153586 | ||||||
| chr2:160153610
|
C | T | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-11539G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153610 | ||||||
| chr2:160153646
|
C | T | 55 | a0001c0001t0004g0009a0001c0001t0004g0105a0001c0001t0004g0106others(52): Show | 56 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1018-11575G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153646 | ||||||
| chr2:160153742
|
G | GA | 6 | a0001c0004t0001g0280a0001c0006t0008g0092a0001c0006t0008g0093others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1018-11672dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153742 | ||||||
| chr2:160153760
|
C | A | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-11689G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153760 | ||||||
| chr2:160153834
|
G | A | 1 | a0001c0002t0002g0069 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1018-11763C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153834 | ||||||
| chr2:160153977
|
C | A | 1 | a0001c0001t0001g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1018-11906G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153977 | ||||||
| chr2:160153978
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1018-11907C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153978 | ||||||
| chr2:160153998
|
G | A | 1 | a0001c0002t0002g0053 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1018-11927C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153998 | ||||||
| chr2:160154043
|
G | A | 72 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(69): Show | 78 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.1018-11972C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154043 | ||||||
| chr2:160154054
|
G | A | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-11983C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154054 | ||||||
| chr2:160154118
|
A | G | 1 | a0001c0003t0001g0139 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1018-12047T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154118 | ||||||
| chr2:160154231
|
C | T | 71 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(68): Show | 77 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.1018-12160G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154231 | ||||||
| chr2:160154246
|
T | C | 209 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(206): Show | 219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1018-12175A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154246 | ||||||
| chr2:160154289
|
T | C | 1 | a0001c0004t0001g0228 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1018-12218A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154289 | ||||||
| chr2:160154304
|
C | A | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-12233G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154304 | ||||||
| chr2:160154393
|
T | C | 9 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(6): Show | 9 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1018-12322A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154393 | ||||||
| chr2:160154461
|
A | G | 1 | a0001c0002t0002g0059 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1018-12390T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154461 | ||||||
| chr2:160154530
|
T | A | 1 | a0001c0001t0004g0241 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1018-12459A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154530 | ||||||
| chr2:160154617
|
C | T | 14 | a0001c0005t0005g0015a0001c0005t0005g0016a0001c0005t0005g0223others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1018-12546G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154617 | ||||||
| chr2:160154623
|
C | G | 1 | a0001c0001t0004g0109 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1018-12552G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154623 | ||||||
| chr2:160154645
|
A | T | 1 | a0001c0001t0001g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1018-12574T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154645 | ||||||
| chr2:160154723
|
A | G | 1 | a0001c0001t0001g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1018-12652T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154723 | ||||||
| chr2:160154749
|
G | A | 1 | a0001c0003t0003g0185 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1018-12678C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154749 | ||||||
| chr2:160154786
|
C | T | 1 | a0001c0001t0007g0312 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1018-12715G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154786 | ||||||
| chr2:160154921
|
G | T | 10 | a0001c0002t0002g0002a0001c0002t0002g0026a0001c0002t0002g0032others(7): Show | 12 | HG01255.hp2 HG01257.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1018-12850C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154921 | ||||||
| chr2:160154945
|
A | G | 70 | a0001c0001t0001g0110a0001c0001t0004g0187a0001c0003t0001g0209others(67): Show | 73 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.1018-12874T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154945 | ||||||
| chr2:160155054
|
C | T | 3 | a0001c0001t0004g0138a0001c0001t0012g0262a0001c0003t0001g0139 | 3 | HG03669.hp2 HG04228.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1018-12983G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160155054 | ||||||
| chr2:160155068
|
T | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0235 | 3 | HG02572.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1018-12997A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160155068 | ||||||
| chr2:160155265
|
A | C | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-13194T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160155265 | ||||||
| chr2:160155384
|
A | G | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-13313T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160155384 | ||||||
| chr2:160155388
|
A | G | 2 | a0001c0002t0002g0076a0004c0020t0002g0037 | 2 | HG02040.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.1018-13317T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160155388 | ||||||
| chr2:160155599
|
G | A | 1 | a0001c0001t0004g0128 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1018-13528C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160155599 | ||||||
| chr2:160155661
|
G | A | 1 | a0001c0001t0001g0335 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1017+13551C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160155661 | ||||||
| chr2:160155905
|
A | G | 2 | a0001c0003t0003g0151a0001c0003t0003g0152 | 2 | HG02056.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1017+13307T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160155905 | ||||||
| chr2:160155950
|
T | C | 1 | a0001c0001t0004g0187 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1017+13262A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160155950 | ||||||
| chr2:160156170
|
G | A | 1 | a0001c0003t0003g0188 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1017+13042C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160156170 | ||||||
| chr2:160156217
|
A | C | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017+12995T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160156217 | ||||||
| chr2:160156556
|
C | T | 322 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(319): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1017+12656G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160156556 | ||||||
| chr2:160156590
|
TA | T | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1017+12621delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160156590 | ||||||
| chr2:160156685
|
C | G | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017+12527G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160156685 | ||||||
| chr2:160156872
|
G | A | 7 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1017+12340C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160156872 | ||||||
| chr2:160156951
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1017+12261C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160156951 | ||||||
| chr2:160157097
|
C | T | 1 | a0001c0003t0003g0195 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1017+12115G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157097 | ||||||
| chr2:160157415
|
G | A | 1 | a0001c0001t0004g0114 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1017+11797C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157415 | ||||||
| chr2:160157471
|
C | T | 1 | a0001c0002t0002g0064 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1017+11741G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157471 | ||||||
| chr2:160157491
|
T | A | 1 | a0001c0002t0002g0056 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1017+11721A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157491 | ||||||
| chr2:160157522
|
G | A | 1 | a0001c0003t0003g0165 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1017+11690C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157522 | ||||||
| chr2:160157673
|
G | A | 32 | a0001c0001t0004g0009a0001c0001t0004g0105a0001c0001t0004g0106others(29): Show | 33 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.1017+11539C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157673 | ||||||
| chr2:160157697
|
G | C | 334 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(331): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.1017+11515C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157697 | ||||||
| chr2:160157742
|
C | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(84): Show | 97 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.1017+11470G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157742 | ||||||
| chr2:160157748
|
C | CA | 36 | a0001c0001t0001g0094a0001c0001t0001g0163a0001c0001t0001g0211others(33): Show | 36 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.1017+11463dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157748 | ||||||
| chr2:160157748
|
C | CAA | 71 | a0001c0001t0001g0214a0001c0001t0004g0187a0001c0001t0012g0262others(68): Show | 74 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.1017+11462_1017+11 others(8): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157748 | ||||||
| chr2:160157748
|
C | CAAA | 17 | a0001c0001t0001g0100a0001c0001t0001g0110a0001c0003t0003g0151others(14): Show | 17 | HG00597.hp1 HG01099.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.1017+11461_1017+11 others(9): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157748 | ||||||
| chr2:160157748
|
CA | C | 32 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(29): Show | 32 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.1017+11463delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157748 | ||||||
| chr2:160157748
|
CAA | C | 8 | a0001c0001t0001g0322a0001c0001t0004g0111a0001c0001t0004g0112others(5): Show | 8 | HG01168.hp1 HG01243.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1017+11462_1017+11 others(8): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157748 | ||||||
| chr2:160157972
|
A | G | 14 | a0001c0005t0005g0015a0001c0005t0005g0016a0001c0005t0005g0223others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1017+11240T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157972 | ||||||
| chr2:160158119
|
T | TA | 88 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(85): Show | 98 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.1017+11092dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158119 | ||||||
| chr2:160158143
|
G | A | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1017+11069C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158143 | ||||||
| chr2:160158160
|
A | G | 1 | a0003c0008t0019g0014 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1017+11052T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158160 | ||||||
| chr2:160158195
|
A | G | 1 | a0001c0001t0004g0135 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1017+11017T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158195 | ||||||
| chr2:160158241
|
C | T | 1 | a0001c0001t0007g0311 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1017+10971G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158241 | ||||||
| chr2:160158343
|
C | T | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017+10869G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158343 | ||||||
| chr2:160158344
|
G | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(84): Show | 97 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.1017+10868C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158344 | ||||||
| chr2:160158402
|
G | A | 3 | a0001c0006t0008g0305a0001c0006t0008g0306a0001c0006t0008g0307 | 3 | HG02486.hp1 HG02572.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1017+10810C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158402 | ||||||
| chr2:160158541
|
C | T | 91 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(88): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.1017+10671G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158541 | ||||||
| chr2:160158555
|
T | G | 14 | a0001c0005t0005g0015a0001c0005t0005g0016a0001c0005t0005g0223others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1017+10657A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158555 | ||||||
| chr2:160158596
|
T | C | 322 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(319): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1017+10616A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158596 | ||||||
| chr2:160158683
|
G | A | 1 | a0001c0003t0003g0191 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1017+10529C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158683 | ||||||
| chr2:160158829
|
G | A | 1 | a0001c0005t0005g0329 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1017+10383C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158829 | ||||||
| chr2:160158870
|
G | C | 78 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(75): Show | 84 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.1017+10342C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158870 | ||||||
| chr2:160159053
|
C | T | 1 | a0001c0001t0007g0311 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1017+10159G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159053 | ||||||
| chr2:160159098
|
CA | C | 26 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0317others(23): Show | 26 | HG00597.hp1 HG00733.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.1017+10113delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159098 | ||||||
| chr2:160159295
|
C | T | 5 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1017+9917G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159295 | ||||||
| chr2:160159369
|
C | G | 1 | a0001c0002t0002g0063 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1017+9843G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159369 | ||||||
| chr2:160159449
|
G | A | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1017+9763C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159449 | ||||||
| chr2:160159604
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1017+9608T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159604 | ||||||
| chr2:160159813
|
G | T | 1 | a0001c0001t0001g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1017+9399C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159813 | ||||||
| chr2:160159836
|
T | TTTCCATT others(2): Show |
5 | a0001c0001t0007g0311a0001c0001t0007g0312a0001c0001t0007g0313others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017+9367_1017+937 others(13): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159836 | ||||||
| chr2:160159922
|
A | G | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1017+9290T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159922 | ||||||
| chr2:160159943
|
A | G | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1017+9269T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159943 | ||||||
| chr2:160159951
|
T | C | 1 | a0001c0003t0003g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1017+9261A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159951 | ||||||
| chr2:160159956
|
A | T | 1 | a0001c0003t0003g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1017+9256T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159956 | ||||||
| chr2:160159966
|
A | G | 2 | a0001c0001t0004g0108a0001c0001t0004g0109 | 2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1017+9246T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159966 | ||||||
| chr2:160159995
|
C | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(84): Show | 97 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.1017+9217G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159995 | ||||||
| chr2:160160060
|
G | A | 1 | a0001c0001t0013g0234 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1017+9152C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160160060 | ||||||
| chr2:160160220
|
G | A | 3 | a0001c0005t0005g0323a0001c0005t0005g0325a0001c0005t0005g0326 | 3 | HG00280.hp1 HG00741.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1017+8992C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160160220 | ||||||
| chr2:160160265
|
A | C | 32 | a0001c0001t0004g0009a0001c0001t0004g0105a0001c0001t0004g0106others(29): Show | 33 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.1017+8947T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160160265 | ||||||
| chr2:160160353
|
C | A | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1017+8859G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160160353 | ||||||
| chr2:160160354
|
G | A | 9 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(6): Show | 9 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1017+8858C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160160354 | ||||||
| chr2:160160470
|
A | C | 92 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(89): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.1017+8742T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160160470 | ||||||
| chr2:160160572
|
T | C | 1 | a0001c0002t0002g0022 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1017+8640A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160160572 | ||||||
| chr2:160161288
|
T | G | 9 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(6): Show | 9 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1017+7924A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160161288 | ||||||
| chr2:160161356
|
C | T | 2 | a0001c0002t0002g0038a0001c0002t0002g0046 | 2 | HG02132.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1017+7856G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160161356 | ||||||
| chr2:160161384
|
A | G | 1 | a0001c0005t0005g0323 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1017+7828T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160161384 | ||||||
| chr2:160161436
|
A | G | 9 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(6): Show | 9 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1017+7776T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160161436 | ||||||
| chr2:160161509
|
T | G | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017+7703A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160161509 | ||||||
| chr2:160161580
|
C | G | 10 | a0001c0002t0002g0002a0001c0002t0002g0026a0001c0002t0002g0032others(7): Show | 12 | HG01255.hp2 HG01257.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1017+7632G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160161580 | ||||||
| chr2:160161692
|
ACTTTT | A | 77 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(74): Show | 83 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1017+7515_1017+751 others(9): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160161692 | ||||||
| chr2:160161711
|
G | A | 1 | a0001c0001t0001g0252 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1017+7501C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160161711 | ||||||
| chr2:160161962
|
A | G | 1 | a0001c0002t0002g0042 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1017+7250T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160161962 | ||||||
| chr2:160162117
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1017+7095T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160162117 | ||||||
| chr2:160162254
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1017+6958G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160162254 | ||||||
| chr2:160162513
|
T | C | 1 | a0001c0002t0002g0056 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1017+6699A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160162513 | ||||||
| chr2:160162681
|
C | T | 3 | a0001c0006t0008g0305a0001c0006t0008g0306a0001c0006t0008g0307 | 3 | HG02486.hp1 HG02572.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1017+6531G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160162681 | ||||||
| chr2:160162721
|
C | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(84): Show | 97 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.1017+6491G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160162721 | ||||||
| chr2:160162775
|
C | T | 77 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(74): Show | 83 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1017+6437G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160162775 | ||||||
| chr2:160162817
|
G | A | 1 | a0001c0005t0004g0021 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1017+6395C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160162817 | ||||||
| chr2:160162919
|
G | A | 2 | a0001c0002t0002g0066a0001c0002t0002g0067 | 2 | NA18968.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1017+6293C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160162919 | ||||||
| chr2:160163118
|
C | T | 1 | a0001c0005t0004g0084 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1017+6094G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160163118 | ||||||
| chr2:160163153
|
G | A | 14 | a0001c0005t0005g0015a0001c0005t0005g0016a0001c0005t0005g0223others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1017+6059C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160163153 | ||||||
| chr2:160163358
|
G | A | 212 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(209): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.1017+5854C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160163358 | ||||||
| chr2:160163461
|
G | A | 73 | a0001c0001t0004g0187a0001c0003t0001g0209a0001c0003t0003g0004others(70): Show | 76 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.1017+5751C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160163461 | ||||||
| chr2:160163475
|
C | A | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1017+5737G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160163475 | ||||||
| chr2:160163571
|
G | A | 2 | a0001c0003t0003g0156a0001c0003t0003g0157 | 2 | HG02055.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1017+5641C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160163571 | ||||||
| chr2:160163631
|
C | CA | 6 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(3): Show | 6 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1017+5580dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160163631 | ||||||
| chr2:160163631
|
CA | C | 213 | a0001c0001t0001g0246a0001c0001t0001g0317a0001c0001t0001g0319others(210): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.1017+5580delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160163631 | ||||||
| chr2:160164169
|
T | G | 1 | a0001c0006t0008g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1017+5043A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160164169 | ||||||
| chr2:160164170
|
T | C | 1 | a0001c0001t0004g0137 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1017+5042A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160164170 | ||||||
| chr2:160164192
|
G | C | 101 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(98): Show | 107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.1017+5020C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160164192 | ||||||
| chr2:160164236
|
C | G | 2 | a0001c0001t0004g0122a0001c0001t0004g0123 | 2 | HG01123.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1017+4976G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160164236 | ||||||
| chr2:160164361
|
C | T | 1 | a0001c0001t0004g0140 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1017+4851G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160164361 | ||||||
| chr2:160164420
|
A | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(82): Show | 94 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.1017+4792T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160164420 | ||||||
| chr2:160164434
|
G | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(85): Show | 98 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.1017+4778C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160164434 | ||||||
| chr2:160164507
|
C | T | 73 | a0001c0001t0004g0187a0001c0003t0001g0209a0001c0003t0003g0004others(70): Show | 76 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.1017+4705G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160164507 | ||||||
| chr2:160164637
|
A | G | 1 | a0001c0004t0001g0250 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1017+4575T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160164637 | ||||||
| chr2:160164871
|
T | A | 1 | a0001c0001t0004g0111 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1017+4341A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160164871 | ||||||
| chr2:160164886
|
A | C | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017+4326T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160164886 | ||||||
| chr2:160165014
|
G | A | 1 | a0001c0005t0004g0019 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1017+4198C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160165014 | ||||||
| chr2:160165027
|
A | G | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1017+4185T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160165027 | ||||||
| chr2:160165528
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1017+3684G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160165528 | ||||||
| chr2:160165684
|
T | C | 2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1017+3528A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160165684 | ||||||
| chr2:160165874
|
G | T | 3 | a0001c0002t0002g0006a0001c0002t0002g0042a0001c0002t0002g0043 | 4 | HG00621.hp2 NA18941.hp1 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.1017+3338C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160165874 | ||||||
| chr2:160166039
|
T | C | 322 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(319): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1017+3173A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160166039 | ||||||
| chr2:160166048
|
T | C | 2 | a0001c0002t0002g0081a0001c0002t0002g0082 | 2 | HG01192.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1017+3164A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160166048 | ||||||
| chr2:160166077
|
A | G | 14 | a0001c0005t0005g0015a0001c0005t0005g0016a0001c0005t0005g0223others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1017+3135T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160166077 | ||||||
| chr2:160166134
|
T | C | 1 | a0001c0003t0003g0166 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1017+3078A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160166134 | ||||||
| chr2:160166283
|
C | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(84): Show | 97 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.1017+2929G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160166283 | ||||||
| chr2:160167144
|
G | A | 1 | a0001c0003t0003g0195 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1017+2068C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160167144 | ||||||
| chr2:160167193
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1017+2019T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160167193 | ||||||
| chr2:160167433
|
G | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(84): Show | 97 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.1017+1779C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160167433 | ||||||
| chr2:160167497
|
G | T | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017+1715C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160167497 | ||||||
| chr2:160167591
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0235 | 3 | HG02572.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1017+1621T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160167591 | ||||||
| chr2:160167821
|
C | T | 1 | a0001c0005t0005g0328 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1017+1391G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160167821 | ||||||
| chr2:160167941
|
A | T | 5 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321others(2): Show | 5 | HG00733.hp2 HG02738.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017+1271T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160167941 | ||||||
| chr2:160167985
|
T | TA | 199 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(196): Show | 213 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.1017+1226_1017+122 others(5): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160167985 | ||||||
| chr2:160167986
|
T | A | 322 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(319): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1017+1226A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160167986 | ||||||
| chr2:160167994
|
T | A | 1 | a0001c0005t0005g0331 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1017+1218A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160167994 | ||||||
| chr2:160167995
|
C | T | 32 | a0001c0001t0004g0009a0001c0001t0004g0105a0001c0001t0004g0106others(29): Show | 33 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.1017+1217G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160167995 | ||||||
| chr2:160168070
|
A | G | 5 | a0001c0001t0007g0311a0001c0001t0007g0312a0001c0001t0007g0313others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017+1142T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160168070 | ||||||
| chr2:160168137
|
C | T | 1 | a0001c0004t0001g0263 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1017+1075G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160168137 | ||||||
| chr2:160168266
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0254a0001c0001t0016g0299 | 5 | HG02723.hp1 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1017+946C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160168266 | ||||||
| chr2:160168638
|
C | T | 1 | a0001c0001t0004g0128 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1017+574G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160168638 | ||||||
| chr2:160168747
|
A | G | 5 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1017+465T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160168747 | ||||||
| chr2:160168775
|
C | CTG | 4 | a0001c0002t0002g0002a0001c0002t0002g0026a0001c0002t0002g0035others(1): Show | 6 | HG01255.hp2 HG01257.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.1017+435_1017+436d others(4): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160168775 | ||||||
| chr2:160168905
|
A | G | 8 | a0001c0002t0002g0002a0001c0002t0002g0026a0001c0002t0002g0032others(5): Show | 10 | HG01255.hp2 HG01257.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.1017+307T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160168905 | ||||||
| chr2:160169086
|
C | T | 1 | a0001c0002t0002g0069 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1017+126G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160169086 | ||||||
| chr2:160169174
|
A | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(81): Show | 93 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.1017+38T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160169174 | ||||||
| chr2:160169707
|
A | G | 1 | a0001c0003t0003g0168 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.922-400T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160169707 | ||||||
| chr2:160169708
|
T | C | 5 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.922-401A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160169708 | ||||||
| chr2:160169825
|
G | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(83): Show | 96 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.922-518C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160169825 | ||||||
| chr2:160169885
|
G | A | 1 | a0001c0004t0001g0281 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.922-578C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160169885 | ||||||
| chr2:160170114
|
A | AATATGTT others(18): Show |
2 | a0001c0001t0004g0116a0001c0001t0014g0302 | 2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.922-832_922-808dup others(25): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160170114 | ||||||
| chr2:160170228
|
A | C | 1 | a0001c0013t0002g0255 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.922-921T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160170228 | ||||||
| chr2:160170232
|
T | G | 1 | a0001c0004t0001g0261 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.922-925A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160170232 | ||||||
| chr2:160170297
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.922-990A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160170297 | ||||||
| chr2:160170346
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0309 | 3 | HG03516.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.922-1039G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160170346 | ||||||
| chr2:160170440
|
C | T | 5 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321others(2): Show | 5 | HG00733.hp2 HG02738.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.922-1133G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160170440 | ||||||
| chr2:160170457
|
C | T | 4 | a0001c0001t0010g0289a0001c0001t0010g0290a0001c0001t0017g0291others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.922-1150G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160170457 | ||||||
| chr2:160170648
|
A | C | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.922-1341T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160170648 | ||||||
| chr2:160170683
|
T | C | 259 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(256): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.922-1376A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160170683 | ||||||
| chr2:160171082
|
G | A | 5 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.921+1487C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171082 | ||||||
| chr2:160171220
|
T | A | 30 | a0001c0001t0004g0009a0001c0001t0004g0105a0001c0001t0004g0106others(27): Show | 31 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.921+1349A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171220 | ||||||
| chr2:160171327
|
T | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(255): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.921+1242A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171327 | ||||||
| chr2:160171329
|
A | AT | 35 | a0001c0001t0001g0213a0001c0001t0001g0245a0001c0001t0001g0322others(32): Show | 35 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.921+1239dupA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171329 | ||||||
| chr2:160171329
|
A | ATT | 8 | a0001c0001t0004g0009a0001c0001t0004g0129a0001c0001t0004g0130others(5): Show | 9 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.921+1238_921+1239d others(4): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171329 | ||||||
| chr2:160171329
|
A | T | 1 | a0001c0001t0004g0128 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.921+1240T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171329 | ||||||
| chr2:160171336
|
TA | T | 14 | a0001c0001t0001g0288a0001c0001t0007g0314a0001c0002t0002g0028others(11): Show | 14 | HG00099.hp1 HG00140.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.921+1232delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171336 | ||||||
| chr2:160171337
|
A | T | 245 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(242): Show | 263 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.921+1232T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171337 | ||||||
| chr2:160171373
|
C | T | 91 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(88): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.921+1196G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171373 | ||||||
| chr2:160171381
|
C | T | 1 | a0001c0004t0001g0208 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.921+1188G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171381 | ||||||
| chr2:160171397
|
C | T | 12 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(9): Show | 13 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.921+1172G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171397 | ||||||
| chr2:160171466
|
T | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(85): Show | 98 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.921+1103A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171466 | ||||||
| chr2:160171496
|
G | A | 2 | a0001c0003t0003g0225a0001c0003t0003g0226 | 2 | HG01081.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.921+1073C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171496 | ||||||
| chr2:160171581
|
G | A | 1 | a0009c0012t0003g0193 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.921+988C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171581 | ||||||
| chr2:160171623
|
C | T | 2 | a0001c0005t0005g0330a0001c0005t0005g0332 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.921+946G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171623 | ||||||
| chr2:160171676
|
T | C | 36 | a0001c0001t0001g0243a0001c0001t0004g0009a0001c0001t0004g0105others(33): Show | 37 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.921+893A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171676 | ||||||
| chr2:160171713
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0309a0001c0001t0001g0335 | 4 | HG01261.hp1 HG03516.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.921+856C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171713 | ||||||
| chr2:160171791
|
C | T | 29 | a0001c0001t0004g0009a0001c0001t0004g0105a0001c0001t0004g0106others(26): Show | 30 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.921+778G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171791 | ||||||
| chr2:160171897
|
G | A | 1 | a0001c0002t0009g0057 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.921+672C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171897 | ||||||
| chr2:160172150
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.921+419G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160172150 | ||||||
| chr2:160172173
|
A | C | 5 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.921+396T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160172173 | ||||||
| chr2:160172233
|
T | C | 1 | a0001c0004t0001g0250 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.921+336A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160172233 | ||||||
| chr2:160172409
|
T | C | 1 | a0001c0002t0002g0039 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.921+160A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160172409 | ||||||
| chr2:160172481
|
T | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(225): Show | 245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.921+88A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160172481 | ||||||
| chr2:160173081
|
A | G | 78 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(75): Show | 84 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.760-351T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 5/14 | chr2 | 160173081 | ||||||
| chr2:160173143
|
C | A | 1 | a0001c0001t0004g0134 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.760-413G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 5/14 | chr2 | 160173143 | ||||||
| chr2:160173198
|
C | T | 5 | a0001c0001t0007g0311a0001c0001t0007g0312a0001c0001t0007g0313others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.760-468G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 5/14 | chr2 | 160173198 | ||||||
| chr2:160173251
|
G | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(9): Show | 13 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.760-521C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 5/14 | chr2 | 160173251 | ||||||
| chr2:160173442
|
T | C | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.759+532A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 5/14 | chr2 | 160173442 | ||||||
| chr2:160173500
|
C | T | 3 | a0001c0002t0002g0023a0001c0002t0002g0030a0001c0002t0002g0031 | 3 | NA18957.hp2 NA19075.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.759+474G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 5/14 | chr2 | 160173500 | ||||||
| chr2:160173963
|
C | T | 1 | a0001c0021t0003g0334 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.759+11G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 5/14 | chr2 | 160173963 | ||||||
| chr2:160174218
|
A | G | 1 | a0001c0003t0003g0167 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.594-79T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160174218 | ||||||
| chr2:160174224
|
C | T | 1 | a0001c0002t0002g0068 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.594-85G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160174224 | ||||||
| chr2:160174412
|
AGT | A | 6 | a0001c0004t0001g0253a0001c0004t0001g0283a0001c0004t0001g0292others(3): Show | 6 | HG00423.hp1 HG02080.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.594-275_594-274del others(2): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160174412 | ||||||
| chr2:160174565
|
C | CT | 78 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(75): Show | 84 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.594-427dupA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160174565 | ||||||
| chr2:160174858
|
C | T | 77 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(74): Show | 83 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.594-719G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160174858 | ||||||
| chr2:160174875
|
G | A | 1 | a0001c0002t0002g0071 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.594-736C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160174875 | ||||||
| chr2:160175079
|
G | A | 14 | a0001c0005t0005g0015a0001c0005t0005g0016a0001c0005t0005g0223others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(11): Show |
intron_variant | MODIFIER | c.594-940C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160175079 | ||||||
| chr2:160175585
|
G | A | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.594-1446C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160175585 | ||||||
| chr2:160175637
|
C | T | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.594-1498G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160175637 | ||||||
| chr2:160175774
|
A | G | 92 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(89): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.594-1635T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160175774 | ||||||
| chr2:160175967
|
T | C | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.594-1828A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160175967 | ||||||
| chr2:160176001
|
C | T | 11 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0096others(8): Show | 12 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.594-1862G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160176001 | ||||||
| chr2:160176122
|
C | T | 1 | a0001c0003t0001g0209 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.594-1983G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160176122 | ||||||
| chr2:160176123
|
C | T | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.594-1984G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160176123 | ||||||
| chr2:160176289
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0235a0001c0001t0013g0234 | 4 | HG02451.hp1 HG02572.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.594-2150C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160176289 | ||||||
| chr2:160176324
|
T | G | 1 | a0001c0003t0003g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.594-2185A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160176324 | ||||||
| chr2:160176377
|
C | A | 1 | a0001c0001t0001g0248 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.594-2238G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160176377 | ||||||
| chr2:160176692
|
T | C | 6 | a0001c0001t0004g0105a0001c0001t0004g0106a0001c0001t0004g0107others(3): Show | 6 | HG01256.hp1 HG01258.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.594-2553A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160176692 | ||||||
| chr2:160176694
|
G | A | 1 | a0001c0002t0002g0058 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.594-2555C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160176694 | ||||||
| chr2:160176701
|
C | T | 5 | a0001c0003t0003g0012a0001c0003t0003g0161a0001c0003t0003g0162others(2): Show | 6 | HG01261.hp2 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.594-2562G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160176701 | ||||||
| chr2:160176707
|
T | C | 1 | a0001c0001t0004g0117 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.594-2568A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160176707 | ||||||
| chr2:160176766
|
A | C | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.594-2627T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160176766 | ||||||
| chr2:160176854
|
T | C | 1 | a0011c0017t0001g0222 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.594-2715A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160176854 | ||||||
| chr2:160177101
|
T | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0235a0001c0001t0013g0234 | 4 | HG02451.hp1 HG02572.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.594-2962A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160177101 | ||||||
| chr2:160177102
|
A | T | 11 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(8): Show | 13 | HG00140.hp2 HG00735.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.594-2963T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160177102 | ||||||
| chr2:160177206
|
T | C | 9 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(6): Show | 9 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.594-3067A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160177206 | ||||||
| chr2:160177272
|
T | C | 1 | a0001c0001t0004g0240 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.594-3133A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160177272 | ||||||
| chr2:160177644
|
G | A | 259 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(256): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.594-3505C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160177644 | ||||||
| chr2:160177868
|
G | C | 12 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(9): Show | 13 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.594-3729C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160177868 | ||||||
| chr2:160177885
|
A | AT | 92 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(89): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.594-3747dupA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160177885 | ||||||
| chr2:160178174
|
C | T | 1 | a0001c0002t0002g0040 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.594-4035G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178174 | ||||||
| chr2:160178277
|
G | A | 1 | a0001c0002t0002g0059 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.594-4138C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178277 | ||||||
| chr2:160178346
|
G | T | 1 | a0001c0003t0003g0166 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.594-4207C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178346 | ||||||
| chr2:160178406
|
G | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(81): Show | 93 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.594-4267C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178406 | ||||||
| chr2:160178426
|
G | A | 335 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(332): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.594-4287C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178426 | ||||||
| chr2:160178480
|
C | T | 227 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(224): Show | 244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.594-4341G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178480 | ||||||
| chr2:160178526
|
A | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(118): Show | 132 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(129): Show |
intron_variant | MODIFIER | c.594-4387T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178526 | ||||||
| chr2:160178538
|
T | A | 5 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.594-4399A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178538 | ||||||
| chr2:160178559
|
G | A | 1 | a0001c0002t0002g0036 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.594-4420C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178559 | ||||||
| chr2:160178670
|
T | TTC | 5 | a0001c0001t0001g0237a0001c0001t0004g0127a0001c0001t0004g0210others(2): Show | 5 | HG01515.hp2 HG02056.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.594-4533_594-4532d others(4): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178670 | ||||||
| chr2:160178688
|
C | CT | 28 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0013others(25): Show | 35 | HG01261.hp1 HG01891.hp2 HG02080.hp2 others(32): Show |
intron_variant | MODIFIER | c.594-4550dupA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178688 | ||||||
| chr2:160178688
|
CT | C | 94 | a0001c0001t0001g0095a0001c0001t0001g0220a0001c0001t0004g0116others(91): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.594-4550delA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178688 | ||||||
| chr2:160178688
|
CTT | C | 15 | a0001c0001t0001g0008a0001c0001t0001g0101a0001c0001t0001g0102others(12): Show | 16 | HG01167.hp1 HG01168.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.594-4551_594-4550d others(4): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178688 | ||||||
| chr2:160178689
|
T | TC | 78 | a0001c0001t0001g0110a0001c0001t0004g0009a0001c0001t0004g0105others(75): Show | 81 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.594-4551_594-4550i others(3): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178689 | ||||||
| chr2:160178690
|
T | C | 6 | a0001c0001t0004g0107a0001c0003t0003g0149a0001c0003t0003g0152others(3): Show | 6 | HG00323.hp1 HG00609.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.594-4551A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178690 | ||||||
| chr2:160178691
|
T | C | 1 | a0001c0001t0004g0116 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.594-4552A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178691 | ||||||
| chr2:160178747
|
G | T | 1 | a0004c0020t0002g0037 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.594-4608C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178747 | ||||||
| chr2:160178779
|
C | A | 1 | a0001c0002t0002g0060 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.594-4640G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178779 | ||||||
| chr2:160178784
|
G | A | 1 | a0001c0003t0021g0337 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.594-4645C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178784 | ||||||
| chr2:160179171
|
A | T | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.594-5032T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179171 | ||||||
| chr2:160179314
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.594-5175G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179314 | ||||||
| chr2:160179366
|
C | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0101a0001c0001t0001g0102others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.594-5227G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179366 | ||||||
| chr2:160179390
|
C | CT | 26 | a0001c0001t0001g0252a0001c0001t0004g0009a0001c0001t0004g0105others(23): Show | 27 | HG00280.hp2 HG00323.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.594-5252dupA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179390 | ||||||
| chr2:160179390
|
CT | C | 8 | a0001c0001t0001g0220a0001c0001t0004g0296a0001c0002t0002g0071others(5): Show | 8 | HG01257.hp2 HG02258.hp2 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.594-5252delA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179390 | ||||||
| chr2:160179462
|
C | T | 1 | a0001c0005t0005g0324 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.594-5323G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179462 | ||||||
| chr2:160179670
|
G | A | 1 | a0001c0001t0013g0234 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.594-5531C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179670 | ||||||
| chr2:160179688
|
G | A | 2 | a0001c0001t0001g0321a0001c0001t0004g0296 | 2 | HG03834.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.594-5549C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179688 | ||||||
| chr2:160179747
|
G | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(118): Show | 132 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(129): Show |
intron_variant | MODIFIER | c.594-5608C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179747 | ||||||
| chr2:160179765
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.594-5626G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179765 | ||||||
| chr2:160179854
|
T | C | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.594-5715A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179854 | ||||||
| chr2:160179874
|
G | T | 1 | a0001c0001t0001g0254 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.594-5735C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179874 | ||||||
| chr2:160179943
|
C | CA | 11 | a0001c0001t0004g0137a0001c0001t0020g0336a0001c0002t0002g0022others(8): Show | 11 | HG02074.hp2 HG02135.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.594-5805dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179943 | ||||||
| chr2:160179943
|
CA | C | 115 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0110others(112): Show | 122 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.594-5805delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179943 | ||||||
| chr2:160179943
|
CAA | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(101): Show | 113 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.594-5806_594-5805d others(4): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179943 | ||||||
| chr2:160179943
|
CAAA | C | 6 | a0001c0001t0001g0095a0001c0001t0004g0256a0001c0001t0004g0257others(3): Show | 6 | HG02056.hp2 HG02132.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.594-5807_594-5805d others(5): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179943 | ||||||
| chr2:160180028
|
G | A | 1 | a0001c0003t0003g0198 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.594-5889C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180028 | ||||||
| chr2:160180113
|
C | CA | 23 | a0001c0001t0001g0199a0001c0001t0001g0211a0001c0001t0001g0212others(20): Show | 23 | HG01168.hp1 HG01192.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.594-5975dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180113 | ||||||
| chr2:160180129
|
C | A | 4 | a0001c0001t0004g0287a0001c0004t0001g0231a0001c0004t0001g0253others(1): Show | 4 | NA18965.hp2 NA18975.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.594-5990G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180129 | ||||||
| chr2:160180129
|
CA | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0235a0001c0001t0013g0234 | 4 | HG02451.hp1 HG02572.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.594-5991delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180129 | ||||||
| chr2:160180130
|
A | C | 4 | a0001c0001t0004g0287a0001c0004t0001g0231a0001c0004t0001g0253others(1): Show | 4 | NA18965.hp2 NA18975.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.594-5991T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180130 | ||||||
| chr2:160180132
|
AC | A | 55 | a0001c0001t0001g0252a0001c0001t0001g0264a0001c0001t0001g0282others(52): Show | 56 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.594-5994delG | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180132 | ||||||
| chr2:160180133
|
C | A | 34 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(31): Show | 42 | HG01261.hp1 HG01891.hp2 HG02080.hp2 others(39): Show |
intron_variant | MODIFIER | c.594-5994G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180133 | ||||||
| chr2:160180197
|
A | G | 1 | a0010c0011t0004g0121 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.594-6058T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180197 | ||||||
| chr2:160180370
|
C | T | 5 | a0001c0001t0007g0311a0001c0001t0007g0312a0001c0001t0007g0313others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.594-6231G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180370 | ||||||
| chr2:160180425
|
C | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(118): Show | 132 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(129): Show |
intron_variant | MODIFIER | c.594-6286G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180425 | ||||||
| chr2:160180434
|
G | C | 77 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(74): Show | 83 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.594-6295C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180434 | ||||||
| chr2:160180451
|
A | G | 1 | a0001c0001t0013g0234 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.594-6312T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180451 | ||||||
| chr2:160180600
|
G | T | 2 | a0001c0003t0003g0159a0001c0003t0003g0160 | 2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.594-6461C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180600 | ||||||
| chr2:160180717
|
A | T | 1 | a0001c0003t0003g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.594-6578T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180717 | ||||||
| chr2:160180751
|
A | T | 12 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(9): Show | 13 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.594-6612T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180751 | ||||||
| chr2:160180810
|
G | A | 9 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(6): Show | 9 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.594-6671C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180810 | ||||||
| chr2:160181055
|
G | C | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.594-6916C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160181055 | ||||||
| chr2:160181078
|
G | A | 1 | a0001c0004t0001g0232 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.594-6939C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160181078 | ||||||
| chr2:160181207
|
C | T | 1 | a0001c0001t0013g0234 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.594-7068G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160181207 | ||||||
| chr2:160181210
|
A | G | 15 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(12): Show | 15 | HG00733.hp2 HG01099.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.594-7071T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160181210 | ||||||
| chr2:160181318
|
A | G | 15 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(12): Show | 15 | HG00733.hp2 HG01099.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.594-7179T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160181318 | ||||||
| chr2:160181402
|
C | T | 5 | a0001c0001t0007g0311a0001c0001t0007g0312a0001c0001t0007g0313others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.594-7263G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160181402 | ||||||
| chr2:160181492
|
G | C | 1 | a0001c0003t0003g0200 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.594-7353C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160181492 | ||||||
| chr2:160181496
|
T | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.594-7357A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160181496 | ||||||
| chr2:160181532
|
C | T | 2 | a0001c0003t0003g0156a0001c0003t0003g0157 | 2 | HG02055.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.594-7393G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160181532 | ||||||
| chr2:160181678
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0254a0001c0001t0016g0299 | 5 | HG02723.hp1 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.594-7539G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160181678 | ||||||
| chr2:160181769
|
G | A | 4 | a0001c0004t0001g0292a0001c0004t0001g0293a0001c0004t0001g0294others(1): Show | 4 | HG02080.hp1 NA18747.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.594-7630C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160181769 | ||||||
| chr2:160181898
|
C | T | 9 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(6): Show | 9 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.594-7759G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160181898 | ||||||
| chr2:160181982
|
C | T | 1 | a0001c0003t0003g0155 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.594-7843G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160181982 | ||||||
| chr2:160182071
|
A | G | 1 | a0003c0008t0019g0014 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.594-7932T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160182071 | ||||||
| chr2:160182147
|
C | T | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.594-8008G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160182147 | ||||||
| chr2:160182226
|
A | G | 1 | a0001c0004t0001g0253 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.594-8087T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160182226 | ||||||
| chr2:160182335
|
T | C | 1 | a0001c0003t0001g0209 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.594-8196A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160182335 | ||||||
| chr2:160182406
|
C | T | 77 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(74): Show | 83 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.594-8267G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160182406 | ||||||
| chr2:160182483
|
T | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(108): Show | 122 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(119): Show |
intron_variant | MODIFIER | c.594-8344A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160182483 | ||||||
| chr2:160182486
|
G | A | 1 | a0001c0003t0003g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.594-8347C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160182486 | ||||||
| chr2:160182520
|
G | A | 1 | a0001c0001t0004g0117 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.594-8381C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160182520 | ||||||
| chr2:160182760
|
C | T | 3 | a0001c0001t0004g0210a0001c0003t0003g0154a0008c0014t0003g0153 | 3 | HG01515.hp2 NA18953.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.594-8621G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160182760 | ||||||
| chr2:160182908
|
G | A | 1 | a0001c0001t0007g0315 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.594-8769C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160182908 | ||||||
| chr2:160183017
|
G | T | 2 | a0001c0003t0003g0151a0001c0003t0003g0152 | 2 | HG02056.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.594-8878C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160183017 | ||||||
| chr2:160183041
|
C | G | 3 | a0001c0002t0002g0023a0001c0002t0002g0030a0001c0002t0002g0031 | 3 | NA18957.hp2 NA19075.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.594-8902G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160183041 | ||||||
| chr2:160183179
|
T | C | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.594-9040A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160183179 | ||||||
| chr2:160183206
|
G | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(118): Show | 132 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(129): Show |
intron_variant | MODIFIER | c.594-9067C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160183206 | ||||||
| chr2:160183274
|
A | C | 31 | a0001c0001t0004g0009a0001c0001t0004g0105a0001c0001t0004g0106others(28): Show | 32 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.594-9135T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160183274 | ||||||
| chr2:160183444
|
C | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0235a0001c0001t0013g0234 | 4 | HG02451.hp1 HG02572.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.594-9305G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160183444 | ||||||
| chr2:160183652
|
T | C | 4 | a0001c0003t0003g0143a0001c0003t0003g0202a0001c0003t0003g0203others(1): Show | 4 | HG02109.hp2 HG02615.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.594-9513A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160183652 | ||||||
| chr2:160183675
|
G | A | 1 | a0001c0004t0018g0017 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.594-9536C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160183675 | ||||||
| chr2:160183840
|
T | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(82): Show | 94 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.594-9701A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160183840 | ||||||
| chr2:160183892
|
C | T | 1 | a0001c0002t0009g0029 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.594-9753G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160183892 | ||||||
| chr2:160183987
|
G | C | 17 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(14): Show | 18 | HG01168.hp2 HG01169.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.594-9848C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160183987 | ||||||
| chr2:160184056
|
C | T | 3 | a0001c0001t0004g0105a0001c0001t0004g0106a0001c0001t0004g0107 | 3 | HG01256.hp1 HG01258.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.594-9917G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160184056 | ||||||
| chr2:160184223
|
G | T | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.594-10084C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160184223 | ||||||
| chr2:160184291
|
C | T | 66 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(63): Show | 70 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.594-10152G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160184291 | ||||||
| chr2:160184343
|
A | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(257): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.594-10204T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160184343 | ||||||
| chr2:160184640
|
T | G | 2 | a0001c0006t0008g0306a0001c0006t0008g0307 | 2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.594-10501A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160184640 | ||||||
| chr2:160184752
|
C | A | 73 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(70): Show | 79 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.594-10613G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160184752 | ||||||
| chr2:160184846
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.593+10523T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160184846 | ||||||
| chr2:160184884
|
G | A | 92 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(89): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.593+10485C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160184884 | ||||||
| chr2:160184996
|
G | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(225): Show | 245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.593+10373C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160184996 | ||||||
| chr2:160185251
|
C | T | 1 | a0001c0001t0001g0244 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.593+10118G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160185251 | ||||||
| chr2:160185742
|
C | A | 9 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(6): Show | 9 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.593+9627G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160185742 | ||||||
| chr2:160186092
|
C | A | 5 | a0001c0001t0007g0311a0001c0001t0007g0312a0001c0001t0007g0313others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.593+9277G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160186092 | ||||||
| chr2:160186272
|
C | CA | 215 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(212): Show | 232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.593+9096dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160186272 | ||||||
| chr2:160186272
|
C | CAA | 15 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(12): Show | 15 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.593+9095_593+9096d others(4): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160186272 | ||||||
| chr2:160186368
|
C | T | 1 | a0001c0005t0004g0019 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.593+9001G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160186368 | ||||||
| chr2:160186606
|
C | T | 78 | a0001c0001t0004g0120a0001c0002t0002g0002a0001c0002t0002g0006others(75): Show | 84 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.593+8763G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160186606 | ||||||
| chr2:160186965
|
G | C | 5 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.593+8404C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160186965 | ||||||
| chr2:160187092
|
G | A | 14 | a0001c0005t0005g0015a0001c0005t0005g0016a0001c0005t0005g0223others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(11): Show |
intron_variant | MODIFIER | c.593+8277C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160187092 | ||||||
| chr2:160187119
|
A | G | 1 | a0001c0003t0003g0143 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.593+8250T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160187119 | ||||||
| chr2:160187305
|
A | C | 1 | a0001c0003t0003g0150 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.593+8064T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160187305 | ||||||
| chr2:160187504
|
C | G | 1 | a0001c0002t0002g0027 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.593+7865G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160187504 | ||||||
| chr2:160187644
|
T | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(102): Show | 115 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(112): Show |
intron_variant | MODIFIER | c.593+7725A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160187644 | ||||||
| chr2:160187646
|
C | T | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.593+7723G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160187646 | ||||||
| chr2:160187671
|
A | G | 17 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(14): Show | 18 | HG01168.hp2 HG01169.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.593+7698T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160187671 | ||||||
| chr2:160188151
|
C | T | 2 | a0001c0003t0003g0148a0001c0003t0003g0149 | 2 | NA18940.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.593+7218G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160188151 | ||||||
| chr2:160188156
|
T | C | 9 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(6): Show | 9 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.593+7213A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160188156 | ||||||
| chr2:160188212
|
G | T | 1 | a0001c0001t0001g0094 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.593+7157C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160188212 | ||||||
| chr2:160188330
|
G | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(118): Show | 132 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(129): Show |
intron_variant | MODIFIER | c.593+7039C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160188330 | ||||||
| chr2:160188444
|
A | G | 1 | a0001c0001t0001g0252 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.593+6925T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160188444 | ||||||
| chr2:160188606
|
C | CT | 10 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(7): Show | 10 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.593+6762dupA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160188606 | ||||||
| chr2:160188617
|
T | G | 3 | a0001c0002t0002g0065a0001c0002t0002g0073a0001c0002t0002g0074 | 3 | NA18973.hp1 NA19056.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.593+6752A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160188617 | ||||||
| chr2:160188689
|
C | T | 1 | a0001c0001t0004g0251 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.593+6680G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160188689 | ||||||
| chr2:160188690
|
G | A | 92 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(89): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.593+6679C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160188690 | ||||||
| chr2:160188770
|
A | T | 1 | a0001c0004t0001g0250 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.593+6599T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160188770 | ||||||
| chr2:160188869
|
G | A | 2 | a0001c0004t0001g0297a0001c0004t0001g0298 | 2 | HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.593+6500C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160188869 | ||||||
| chr2:160188940
|
G | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(84): Show | 97 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.593+6429C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160188940 | ||||||
| chr2:160189042
|
G | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(225): Show | 245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.593+6327C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189042 | ||||||
| chr2:160189142
|
C | T | 17 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(14): Show | 18 | HG01168.hp2 HG01169.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.593+6227G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189142 | ||||||
| chr2:160189155
|
A | G | 1 | a0001c0002t0002g0026 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.593+6214T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189155 | ||||||
| chr2:160189403
|
G | A | 14 | a0001c0005t0005g0015a0001c0005t0005g0016a0001c0005t0005g0223others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(11): Show |
intron_variant | MODIFIER | c.593+5966C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189403 | ||||||
| chr2:160189442
|
G | A | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.593+5927C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189442 | ||||||
| chr2:160189468
|
A | G | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.593+5901T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189468 | ||||||
| chr2:160189540
|
G | A | 13 | a0001c0001t0001g0008a0001c0001t0001g0102a0001c0001t0001g0103others(10): Show | 14 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.593+5829C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189540 | ||||||
| chr2:160189540
|
G | C | 8 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(5): Show | 8 | HG02145.hp1 HG02258.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.593+5829C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189540 | ||||||
| chr2:160189606
|
G | C | 5 | a0001c0001t0001g0013a0001c0001t0001g0309a0001c0006t0008g0305others(2): Show | 6 | HG02486.hp1 HG02572.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.593+5763C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189606 | ||||||
| chr2:160189634
|
C | G | 1 | a0001c0002t0002g0085 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.593+5735G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189634 | ||||||
| chr2:160189681
|
G | A | 92 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(89): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.593+5688C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189681 | ||||||
| chr2:160189861
|
C | T | 30 | a0001c0001t0004g0009a0001c0001t0004g0105a0001c0001t0004g0106others(27): Show | 31 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.593+5508G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189861 | ||||||
| chr2:160189905
|
A | C | 1 | a0001c0002t0002g0025 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.593+5464T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189905 | ||||||
| chr2:160189917
|
C | T | 1 | a0001c0003t0003g0146 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.593+5452G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189917 | ||||||
| chr2:160189951
|
C | A | 1 | a0001c0001t0001g0215 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.593+5418G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189951 | ||||||
| chr2:160190051
|
G | T | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.593+5318C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190051 | ||||||
| chr2:160190056
|
A | G | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.593+5313T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190056 | ||||||
| chr2:160190062
|
A | G | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.593+5307T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190062 | ||||||
| chr2:160190136
|
T | C | 1 | a0001c0001t0004g0119 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.593+5233A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190136 | ||||||
| chr2:160190137
|
G | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(225): Show | 245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.593+5232C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190137 | ||||||
| chr2:160190139
|
A | G | 336 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(333): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.593+5230T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190139 | ||||||
| chr2:160190163
|
A | G | 5 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(2): Show | 5 | HG00733.hp2 HG01099.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.593+5206T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190163 | ||||||
| chr2:160190261
|
G | A | 5 | a0001c0006t0008g0092a0001c0006t0008g0093a0001c0006t0008g0305others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.593+5108C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190261 | ||||||
| chr2:160190299
|
A | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(101): Show | 114 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.593+5070T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190299 | ||||||
| chr2:160190634
|
C | A | 1 | a0001c0003t0003g0206 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.593+4735G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190634 | ||||||
| chr2:160190681
|
A | G | 2 | a0001c0003t0003g0144a0001c0018t0003g0145 | 2 | HG02027.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.593+4688T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190681 | ||||||
| chr2:160190750
|
G | A | 1 | a0001c0002t0002g0076 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.593+4619C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190750 | ||||||
| chr2:160190886
|
A | G | 5 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.593+4483T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190886 | ||||||
| chr2:160190961
|
G | C | 1 | a0001c0001t0016g0299 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.593+4408C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190961 | ||||||
| chr2:160190995
|
T | A | 1 | a0001c0002t0002g0075 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.593+4374A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190995 | ||||||
| chr2:160191202
|
A | T | 3 | a0001c0005t0004g0019a0001c0005t0004g0020a0001c0005t0004g0021 | 3 | HG00639.hp2 HG00642.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.593+4167T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160191202 | ||||||
| chr2:160191375
|
C | T | 17 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(14): Show | 18 | HG01168.hp2 HG01169.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.593+3994G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160191375 | ||||||
| chr2:160191483
|
T | A | 3 | a0001c0001t0004g0118a0001c0001t0004g0119a0001c0003t0003g0207 | 3 | HG02145.hp2 NA18906.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.593+3886A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160191483 | ||||||
| chr2:160191524
|
G | C | 1 | a0001c0001t0001g0100 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.593+3845C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160191524 | ||||||
| chr2:160191626
|
A | G | 8 | a0001c0001t0001g0001a0001c0001t0001g0244a0001c0001t0001g0245others(5): Show | 13 | HG02080.hp2 NA18941.hp2 NA18948.hp2 others(10): Show |
intron_variant | MODIFIER | c.593+3743T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160191626 | ||||||
| chr2:160191671
|
C | A | 1 | a0001c0002t0002g0076 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.593+3698G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160191671 | ||||||
| chr2:160191924
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.593+3445T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160191924 | ||||||
| chr2:160191936
|
T | A | 1 | a0001c0005t0004g0084 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.593+3433A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160191936 | ||||||
| chr2:160192191
|
AG | A | 3 | a0001c0001t0004g0140a0001c0001t0004g0141a0001c0001t0004g0142 | 3 | HG00323.hp2 HG01081.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.593+3177delC | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160192191 | ||||||
| chr2:160192198
|
A | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(119): Show | 133 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(130): Show |
intron_variant | MODIFIER | c.593+3171T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160192198 | ||||||
| chr2:160192200
|
G | T | 5 | a0001c0001t0004g0238a0001c0001t0004g0239a0001c0001t0004g0240others(2): Show | 5 | NA18945.hp1 NA18962.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.593+3169C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160192200 | ||||||
| chr2:160192263
|
A | G | 12 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(9): Show | 13 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.593+3106T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160192263 | ||||||
| chr2:160192324
|
T | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0013others(80): Show | 92 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.593+3045A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160192324 | ||||||
| chr2:160192502
|
G | A | 9 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(6): Show | 9 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.593+2867C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160192502 | ||||||
| chr2:160192549
|
T | A | 2 | a0001c0004t0001g0300a0001c0004t0001g0301 | 2 | NA18963.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.593+2820A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160192549 | ||||||
| chr2:160192590
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(124): Show | 138 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.593+2779G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160192590 | ||||||
| chr2:160192661
|
G | A | 1 | a0001c0001t0014g0302 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.593+2708C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160192661 | ||||||
| chr2:160192818
|
A | G | 1 | a0001c0003t0003g0143 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.593+2551T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160192818 | ||||||
| chr2:160192884
|
G | A | 14 | a0001c0005t0005g0015a0001c0005t0005g0016a0001c0005t0005g0223others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(11): Show |
intron_variant | MODIFIER | c.593+2485C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160192884 | ||||||
| chr2:160193049
|
T | C | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.593+2320A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160193049 | ||||||
| chr2:160193521
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.593+1848T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160193521 | ||||||
| chr2:160193615
|
A | G | 1 | a0001c0002t0002g0024 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.593+1754T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160193615 | ||||||
| chr2:160193634
|
G | A | 17 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(14): Show | 18 | HG01168.hp2 HG01169.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.593+1735C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160193634 | ||||||
| chr2:160193723
|
A | G | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.593+1646T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160193723 | ||||||
| chr2:160193936
|
C | T | 1 | a0001c0002t0002g0023 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.593+1433G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160193936 | ||||||
| chr2:160194038
|
T | C | 1 | a0001c0004t0001g0208 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.593+1331A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160194038 | ||||||
| chr2:160194243
|
A | G | 1 | a0001c0001t0004g0233 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.593+1126T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160194243 | ||||||
| chr2:160194253
|
A | C | 1 | a0001c0005t0005g0323 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.593+1116T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160194253 | ||||||
| chr2:160194261
|
T | C | 1 | a0001c0003t0001g0209 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.593+1108A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160194261 | ||||||
| chr2:160194365
|
T | C | 5 | a0001c0001t0001g0008a0001c0001t0001g0101a0001c0001t0001g0102others(2): Show | 6 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.593+1004A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160194365 | ||||||
| chr2:160194552
|
C | G | 9 | a0001c0001t0004g0111a0001c0001t0004g0112a0001c0001t0004g0113others(6): Show | 9 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.593+817G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160194552 | ||||||
| chr2:160194612
|
A | G | 17 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(14): Show | 18 | HG01168.hp2 HG01169.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.593+757T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160194612 | ||||||
| chr2:160194652
|
C | A | 7 | a0001c0002t0002g0077a0001c0002t0002g0078a0001c0002t0002g0079others(4): Show | 7 | HG01069.hp2 HG01192.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.593+717G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160194652 | ||||||
| chr2:160194737
|
C | T | 12 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(9): Show | 13 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.593+632G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160194737 | ||||||
| chr2:160194852
|
C | T | 258 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(255): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.593+517G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160194852 | ||||||
| chr2:160194863
|
G | C | 1 | a0001c0005t0004g0084 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.593+506C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160194863 | ||||||
| chr2:160195008
|
G | A | 7 | a0001c0002t0002g0085a0001c0002t0002g0087a0001c0002t0002g0089others(4): Show | 9 | HG00140.hp2 HG00735.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.593+361C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160195008 | ||||||
| chr2:160195099
|
G | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(118): Show | 132 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(129): Show |
intron_variant | MODIFIER | c.593+270C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160195099 | ||||||
| chr2:160195205
|
A | C | 1 | a0001c0021t0003g0334 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.593+164T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160195205 | ||||||
| chr2:160195342
|
A | G | 88 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(85): Show | 98 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.593+27T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160195342 | ||||||
| chr2:160195683
|
G | T | 1 | a0001c0001t0004g0210 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.347-68C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 3/14 | chr2 | 160195683 | ||||||
| chr2:160195687
|
G | C | 1 | a0001c0001t0004g0210 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.347-72C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 3/14 | chr2 | 160195687 | ||||||
| chr2:160195886
|
TTG | T | 5 | a0001c0001t0004g0105a0001c0001t0004g0106a0001c0001t0004g0107others(2): Show | 5 | HG01256.hp1 HG01258.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.347-273_347-272del others(2): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 3/14 | chr2 | 160195886 | ||||||
| chr2:160195944
|
A | G | 6 | a0001c0004t0001g0227a0001c0004t0001g0228a0001c0004t0001g0230others(3): Show | 6 | NA18951.hp2 NA18961.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.346+272T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 3/14 | chr2 | 160195944 | ||||||
| chr2:160196037
|
G | A | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.346+179C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 3/14 | chr2 | 160196037 | ||||||
| chr2:160196040
|
G | A | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0213others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.346+176C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 3/14 | chr2 | 160196040 | ||||||
| chr2:160196063
|
G | A | 2 | a0001c0005t0005g0223a0001c0005t0005g0333 | 2 | HG01099.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.346+153C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 3/14 | chr2 | 160196063 | ||||||
| chr2:160196088
|
C | T | 1 | a0001c0001t0001g0317 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.346+128G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 3/14 | chr2 | 160196088 | ||||||
| chr2:160196441
|
C | A | 1 | a0001c0001t0004g0224 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.142-21G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160196441 | ||||||
| chr2:160196564
|
T | C | 2 | a0001c0003t0003g0225a0001c0003t0003g0226 | 2 | HG01081.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.142-144A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160196564 | ||||||
| chr2:160196679
|
A | ATG | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-261_142-260dup others(2): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160196679 | ||||||
| chr2:160196744
|
C | T | 4 | a0001c0002t0002g0022a0001c0005t0004g0019a0001c0005t0004g0020others(1): Show | 4 | HG00639.hp2 HG00642.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-324G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160196744 | ||||||
| chr2:160196869
|
T | C | 2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.142-449A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160196869 | ||||||
| chr2:160196937
|
T | G | 2 | a0001c0006t0008g0306a0001c0006t0008g0307 | 2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.142-517A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160196937 | ||||||
| chr2:160196961
|
A | G | 5 | a0001c0001t0007g0311a0001c0001t0007g0312a0001c0001t0007g0313others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-541T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160196961 | ||||||
| chr2:160196999
|
C | A | 1 | a0001c0001t0004g0308 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.142-579G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160196999 | ||||||
| chr2:160197184
|
T | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0309a0001c0001t0001g0335 | 4 | HG01261.hp1 HG03516.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-764A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160197184 | ||||||
| chr2:160197221
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(91): Show | 105 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.142-801C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160197221 | ||||||
| chr2:160197281
|
G | T | 12 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0095others(9): Show | 13 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.142-861C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160197281 | ||||||
| chr2:160197313
|
T | C | 1 | a0001c0001t0001g0310 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.142-893A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160197313 | ||||||
| chr2:160197369
|
T | C | 5 | a0001c0001t0007g0311a0001c0001t0007g0312a0001c0001t0007g0313others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-949A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160197369 | ||||||
| chr2:160197679
|
G | A | 1 | a0001c0003t0003g0316 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.142-1259C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160197679 | ||||||
| chr2:160198149
|
A | AT | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.141+1029dupA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160198149 | ||||||
| chr2:160198218
|
G | C | 6 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.141+961C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160198218 | ||||||
| chr2:160198237
|
G | A | 91 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(88): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.141+942C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160198237 | ||||||
| chr2:160198264
|
A | G | 2 | a0001c0006t0008g0092a0001c0006t0008g0093 | 2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.141+915T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160198264 | ||||||
| chr2:160198451
|
T | G | 1 | a0001c0002t0002g0091 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.141+728A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160198451 | ||||||
| chr2:160198704
|
A | G | 1 | a0001c0002t0002g0018 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.141+475T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160198704 | ||||||
| chr2:160198804
|
A | G | 78 | a0001c0002t0002g0002a0001c0002t0002g0006a0001c0002t0002g0007others(75): Show | 84 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.141+375T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160198804 | ||||||
| chr2:160199164
|
G | C | 1 | a0001c0021t0003g0334 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.141+15C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160199164 | ||||||
| chr2:160199494
|
T | C | 1 | a0001c0001t0001g0335 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.62-236A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 1/14 | chr2 | 160199494 | ||||||
| chr2:160199530
|
T | C | 1 | a0001c0004t0018g0017 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.62-272A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 1/14 | chr2 | 160199530 | ||||||
| chr2:160199609
|
C | T | 1 | a0001c0004t0018g0017 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.62-351G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 1/14 | chr2 | 160199609 | ||||||
| chr2:160199991
|
C | T | 2 | a0001c0005t0005g0015a0001c0005t0005g0016 | 2 | HG00140.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.61+12G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 1/14 | chr2 | 160199991 |