Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3683 |
| ensemblid | ENSG00000005844.19 |
| hgncid | 6148 |
| symbol | ITGAL |
| name | integrin subunit alpha L |
| refseq_nuc | NM_002209.3 |
| refseq_prot | NP_002200.2 |
| ensembl_nuc | ENST00000356798.11 |
| ensembl_prot | ENSP00000349252.5 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 30472742 |
| end | 30523185 |
| strand | + |
| ver | v1.2 |
| region | chr16:30472742-30523185 |
| region5000 | chr16:30467742-30528185 |
| regionname0 | ITGAL_chr16_30472742_30523185 |
| regionname5000 | ITGAL_chr16_30467742_30528185 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1170 | 208 | 45 | 52 | 84 | 11 | 14 | 53 | ITGAL_chr16_30467742_30528185 | ITGAL | MKDSC others(1165): Show |
chr16 | 30467742 | 30528185 |
| a0002 | 0/0 | 1170 | 92 | 34 | 15 | 19 | 5 | 19 | 13 | ITGAL_chr16_30467742_30528185 | ITGAL | MKDSC others(1165): Show |
chr16 | 30467742 | 30528185 |
| a0003 | 0/0 | 1170 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | MKDSC others(1165): Show |
chr16 | 30467742 | 30528185 |
| a0004 | 0/0 | 1170 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | MKDSC others(1165): Show |
chr16 | 30467742 | 30528185 |
| a0005 | 0/0 | 1170 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | MKDSC others(1165): Show |
chr16 | 30467742 | 30528185 |
| a0006 | 0/0 | 1170 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | MKDSC others(1165): Show |
chr16 | 30467742 | 30528185 |
| a0007 | 0/0 | 1170 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | MKDSC others(1165): Show |
chr16 | 30467742 | 30528185 |
| a0008 | 0/0 | 1170 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | MKDSC others(1165): Show |
chr16 | 30467742 | 30528185 |
| a0009 | 0/0 | 1170 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | MKDSC others(1165): Show |
chr16 | 30467742 | 30528185 |
| a0010 | 0/0 | 1170 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | MKDSC others(1165): Show |
chr16 | 30467742 | 30528185 |
| a0011 | 0/0 | 1170 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | MKDSC others(1165): Show |
chr16 | 30467742 | 30528185 |
| a0012 | 0/0 | 1170 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | MKDSR others(1165): Show |
chr16 | 30467742 | 30528185 |
| a0013 | 0/0 | 1170 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | MKDSC others(1165): Show |
chr16 | 30467742 | 30528185 |
| a0014 | 0/0 | 1170 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | MKDSC others(1165): Show |
chr16 | 30467742 | 30528185 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3510 | 185 | 29 | 51 | 82 | 11 | 10 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 | ||
| a0001c0004 | 0/0 | 3510 | 8 | 8 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 | ||
| a0001c0005 | 0/0 | 3510 | 8 | 7 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 | ||
| a0001c0009 | 0/0 | 3510 | 3 | 0 | 0 | 0 | 0 | 3 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 | ||
| a0001c0014 | 0/0 | 3510 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 | ||
| a0001c0015 | 0/0 | 3510 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 | ||
| a0001c0017 | 0/0 | 3510 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 | ||
| a0001c0025 | 0/0 | 3510 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 | ||
| a0002c0002 | 0/0 | 3510 | 73 | 19 | 12 | 18 | 5 | 19 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 | ||
| a0002c0003 | 0/0 | 3510 | 10 | 10 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 | ||
| a0002c0007 | 0/0 | 3510 | 4 | 0 | 3 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 | ||
| a0002c0008 | 0/0 | 3510 | 3 | 3 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 | ||
| a0002c0016 | 0/0 | 3510 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 | ||
| a0002c0023 | 0/0 | 3510 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 | ||
| a0003c0006 | 0/0 | 3510 | 5 | 4 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 | ||
| a0003c0020 | 0/0 | 3510 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 | ||
| a0004c0010 | 0/0 | 3510 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 | ||
| a0005c0024 | 0/0 | 3510 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 | ||
| a0006c0027 | 0/0 | 3510 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 | ||
| a0007c0026 | 0/0 | 3510 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 | ||
| a0008c0021 | 0/0 | 3510 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 | ||
| a0009c0022 | 0/0 | 3510 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 | ||
| a0010c0012 | 0/0 | 3510 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 | ||
| a0011c0019 | 0/0 | 3510 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 | ||
| a0012c0011 | 0/0 | 3510 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 | ||
| a0013c0018 | 0/0 | 3510 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 | ||
| a0014c0013 | 0/0 | 3510 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATGAA others(3505): Show |
chr16 | 30467742 | 30528185 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5129 | 170 | 16 | 51 | 81 | 10 | 10 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0001c0001t0002 | 0/0 | 5129 | 4 | 4 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0001c0001t0003 | 0/0 | 5129 | 7 | 7 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0001c0001t0004 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0001c0001t0007 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0001c0001t0008 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0001c0001t0009 | 0/0 | 5129 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0001c0004t0001 | 0/0 | 5129 | 8 | 8 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0001c0005t0001 | 0/0 | 5129 | 6 | 5 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0001c0005t0004 | 0/0 | 5129 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0001c0009t0001 | 0/0 | 5129 | 3 | 0 | 0 | 0 | 0 | 3 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0001c0014t0001 | 0/0 | 5129 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0001c0015t0001 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0001c0017t0006 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0001c0025t0001 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0002c0002t0001 | 0/0 | 5129 | 70 | 16 | 12 | 18 | 5 | 19 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0002c0002t0002 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0002c0002t0004 | 0/0 | 5129 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0002c0003t0001 | 0/0 | 5129 | 5 | 5 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0002c0003t0002 | 0/0 | 5129 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0002c0003t0005 | 0/0 | 5129 | 3 | 3 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0002c0007t0001 | 0/0 | 5129 | 4 | 0 | 3 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0002c0008t0001 | 0/0 | 5129 | 3 | 3 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0002c0016t0006 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0002c0023t0001 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0003c0006t0001 | 0/0 | 5129 | 5 | 4 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0003c0020t0001 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0004c0010t0001 | 0/0 | 5129 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0005c0024t0001 | 0/0 | 5129 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0006c0027t0001 | 0/0 | 5129 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0007c0026t0001 | 0/0 | 5129 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0008c0021t0001 | 0/0 | 5129 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0009c0022t0001 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0010c0012t0001 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0011c0019t0001 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0012c0011t0001 | 0/0 | 5129 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0013c0018t0001 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| a0014c0013t0001 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | ATCAT others(5124): Show |
chr16 | 30467742 | 30528185 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0004 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0218 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0246 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0007g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0008g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0009g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0004t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0004t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0004t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0004t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0004t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0004t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0004t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0004t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0005t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0005t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0005t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0005t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0005t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0005t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0005t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0005t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0009t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0009t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0009t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0014t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0015t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0017t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0025t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0003t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0003t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0003t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0003t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0003t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0003t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0003t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0003t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0003t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0003t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0007t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0007t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0007t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0007t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0008t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0008t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0008t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0016t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0023t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0003c0006t0001g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0003c0006t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0003c0006t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0003c0006t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0003c0020t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0004c0010t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0004c0010t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0005c0024t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0006c0027t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0007c0026t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0008c0021t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0009c0022t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0010c0012t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0011c0019t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0012c0011t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0013c0018t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0014c0013t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0225 | EUR | GBR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | GBR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0244 | EUR | GBR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00140 | hp2 | a0001 | c0001 | t0009 | g0203 | EUR | GBR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0210 | EUR | FIN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | FIN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0201 | EUR | FIN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | FIN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00597 | hp2 | a0001 | c0025 | t0001 | g0006 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0219 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0085 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01071 | hp2 | a0005 | c0024 | t0001 | g0083 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0039 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01099 | hp1 | a0006 | c0027 | t0001 | g0136 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01106 | hp1 | a0001 | c0005 | t0001 | g0259 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0170 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01109 | hp1 | a0003 | c0006 | t0001 | g0007 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0212 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0206 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01243 | hp1 | a0002 | c0007 | t0001 | g0037 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0051 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0261 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01256 | hp1 | a0007 | c0026 | t0001 | g0132 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01258 | hp1 | a0002 | c0007 | t0001 | g0128 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01346 | hp1 | a0002 | c0007 | t0001 | g0221 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0053 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0211 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01496 | hp2 | a0008 | c0021 | t0001 | g0305 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0232 | EUR | IBS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0027 | EUR | IBS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0182 | EUR | IBS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0026 | EUR | IBS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01884 | hp1 | a0001 | c0005 | t0001 | g0226 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01884 | hp2 | a0002 | c0008 | t0001 | g0265 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01891 | hp1 | a0002 | c0003 | t0001 | g0301 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01891 | hp2 | a0009 | c0022 | t0001 | g0234 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0205 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0200 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02055 | hp1 | a0010 | c0012 | t0001 | g0260 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02055 | hp2 | a0002 | c0003 | t0002 | g0304 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02056 | hp2 | a0002 | c0007 | t0001 | g0231 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02132 | hp1 | a0011 | c0019 | t0001 | g0097 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02145 | hp2 | a0002 | c0002 | t0004 | g0193 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CDX | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CDX | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CDX | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02257 | hp1 | a0002 | c0003 | t0001 | g0228 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02280 | hp1 | a0002 | c0003 | t0001 | g0299 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02280 | hp2 | a0002 | c0003 | t0002 | g0293 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02451 | hp1 | a0001 | c0005 | t0001 | g0291 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0241 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0033 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02602 | hp2 | a0001 | c0009 | t0001 | g0046 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02615 | hp1 | a0001 | c0004 | t0001 | g0285 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0279 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0248 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0195 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02630 | hp1 | a0001 | c0005 | t0001 | g0258 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02630 | hp2 | a0002 | c0016 | t0006 | g0233 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0229 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02647 | hp2 | a0001 | c0005 | t0001 | g0256 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02683 | hp1 | a0001 | c0014 | t0001 | g0214 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0054 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0049 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02698 | hp2 | a0001 | c0009 | t0001 | g0061 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02717 | hp1 | a0001 | c0004 | t0001 | g0289 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0262 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02723 | hp1 | a0001 | c0004 | t0001 | g0286 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0249 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0044 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02809 | hp1 | a0003 | c0006 | t0001 | g0014 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02809 | hp2 | a0001 | c0004 | t0001 | g0303 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0271 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0237 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0236 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0224 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0223 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0257 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02965 | hp1 | a0004 | c0010 | t0001 | g0307 | AFR | ESN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ESN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02970 | hp1 | a0002 | c0008 | t0001 | g0222 | AFR | ESN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0255 | AFR | ESN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0264 | AFR | MSL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03098 | hp2 | a0001 | c0004 | t0001 | g0302 | AFR | MSL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03130 | hp1 | a0001 | c0004 | t0001 | g0288 | AFR | ESN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03130 | hp2 | a0003 | c0020 | t0001 | g0227 | AFR | ESN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03139 | hp1 | a0004 | c0010 | t0001 | g0306 | AFR | ESN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03139 | hp2 | a0002 | c0003 | t0005 | g0297 | AFR | ESN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0283 | AFR | ESN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03195 | hp2 | a0001 | c0004 | t0001 | g0287 | AFR | ESN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0238 | AFR | MSL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0254 | AFR | MSL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03239 | hp1 | a0001 | c0009 | t0001 | g0060 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0010 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03453 | hp1 | a0002 | c0008 | t0001 | g0274 | AFR | MSL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0272 | AFR | MSL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03486 | hp1 | a0002 | c0023 | t0001 | g0190 | AFR | MSL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03486 | hp2 | a0001 | c0005 | t0001 | g0050 | AFR | MSL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0019 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0030 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0028 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03516 | hp1 | a0003 | c0006 | t0001 | g0007 | AFR | ESN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0280 | AFR | ESN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03540 | hp1 | a0002 | c0002 | t0004 | g0192 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0166 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03579 | hp1 | a0003 | c0006 | t0001 | g0016 | AFR | MSL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03579 | hp2 | a0001 | c0017 | t0006 | g0012 | AFR | MSL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0009 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0204 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0034 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0020 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0021 | SAS | BEB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0198 | SAS | BEB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0041 | SAS | BEB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0042 | SAS | BEB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG04199 | hp1 | a0012 | c0011 | t0001 | g0024 | SAS | STU | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0029 | SAS | STU | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18522 | hp1 | a0001 | c0004 | t0001 | g0290 | AFR | YRI | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18522 | hp2 | a0002 | c0003 | t0001 | g0308 | AFR | YRI | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | CHB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18906 | hp1 | a0003 | c0006 | t0001 | g0015 | AFR | YRI | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0251 | AFR | YRI | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18939 | hp2 | a0001 | c0001 | t0008 | g0155 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18960 | hp2 | a0013 | c0018 | t0001 | g0071 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18974 | hp2 | a0001 | c0015 | t0001 | g0152 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | LWK | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | LWK | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19043 | hp1 | a0002 | c0003 | t0005 | g0298 | AFR | LWK | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0267 | AFR | LWK | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19091 | hp2 | a0014 | c0013 | t0001 | g0055 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19240 | hp1 | a0002 | c0003 | t0005 | g0284 | AFR | YRI | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | YRI | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ASW | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA20129 | hp2 | a0002 | c0003 | t0001 | g0300 | AFR | ASW | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0140 | EUR | TSI | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0230 | EUR | TSI | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0036 | EUR | TSI | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0263 | EUR | TSI | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0023 | SAS | GIH | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0056 | SAS | GIH | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0252 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0281 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02486 | hp1 | a0001 | c0005 | t0004 | g0296 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | USA | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0295 | AFR | USA | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0235 | AFR | USA | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA20300 | hp2 | a0001 | c0005 | t0004 | g0292 | AFR | USA | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | LWK | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | LWK | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0218 | REF | REF | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0246 | REF | REF | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:30472850 | T | C | 1 | a0012 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.13T>C | p.Cys5Arg | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 1/31 | 109/5129 | 13/3513 | 5/1170 | chr16 | 30472850 | |||
| chr16:30479194 | G | A | 1 | a0010 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.431G>A | p.Arg144His | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 5/31 | 527/5129 | 431/3513 | 144/1170 | chr16 | 30479194 | |||
| chr16:30481502 | C | T | 2 | a0006 a0007 |
2 | HG01099.hp1 HG01256.hp1 |
missense_variant | MODERATE | c.640C>T | p.Arg214Trp | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 7/31 | 736/5129 | 640/3513 | 214/1170 | chr16 | 30481502 | |||
| chr16:30483885 | A | G | 1 | a0005 | 1 | HG01071.hp2 | missense_variant | MODERATE | c.781A>G | p.Ile261Val | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 8/31 | 877/5129 | 781/3513 | 261/1170 | chr16 | 30483885 | |||
| chr16:30484134 | A | G | 1 | a0009 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.877A>G | p.Lys293Glu | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/31 | 973/5129 | 877/3513 | 293/1170 | chr16 | 30484134 | |||
| chr16:30489273 | C | A | 1 | a0014 | 1 | NA19091.hp2 | missense_variant | MODERATE | c.1100C>A | p.Ala367Glu | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/31 | 1196/5129 | 1100/3513 | 367/1170 | chr16 | 30489273 | |||
| chr16:30489284 | A | C | 1 | a0011 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.1111A>C | p.Lys371Gln | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/31 | 1207/5129 | 1111/3513 | 371/1170 | chr16 | 30489284 | |||
| chr16:30499168 | A | C | 1 | a0013 | 1 | NA18960.hp2 | missense_variant | MODERATE | c.1927A>C | p.Lys643Gln | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 16/31 | 2023/5129 | 1927/3513 | 643/1170 | chr16 | 30499168 | |||
| chr16:30505244 | C | A | 2 | a0003 a0004 |
8 | HG01109.hp1 HG02809.hp1 HG02965.hp1 others(5): Show |
missense_variant&splice_region_variant | MODERATE | c.2236C>A | p.Gln746Lys | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 19/31 | 2332/5129 | 2236/3513 | 746/1170 | chr16 | 30505244 | |||
| chr16:30506720 | G | C | 8 | a0002 a0004 a0005 others(5): Show |
100 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(97): Show |
missense_variant | MODERATE | c.2372G>C | p.Arg791Thr | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/31 | 2468/5129 | 2372/3513 | 791/1170 | chr16 | 30506720 | |||
| chr16:30517822 | G | A | 2 | a0008 a0010 |
2 | HG01496.hp2 HG02055.hp1 |
missense_variant | MODERATE | c.3059G>A | p.Arg1020His | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 28/31 | 3155/5129 | 3059/3513 | 1020/1170 | chr16 | 30517822 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:30483857 | C | T | 1 | a0001c0025 | 1 | HG00597.hp2 | synonymous_variant | LOW | c.753C>T | p.Ala251Ala | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 8/31 | 849/5129 | 753/3513 | 251/1170 | chr16 | 30483857 | |||
| chr16:30483923 | C | T | 1 | a0002c0023 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.819C>T | p.Ile273Ile | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 8/31 | 915/5129 | 819/3513 | 273/1170 | chr16 | 30483923 | |||
| chr16:30484175 | C | T | 6 | a0001c0004 a0001c0005 a0002c0003 others(3): Show |
30 | HG01106.hp1 HG01496.hp2 HG01884.hp1 others(27): Show |
synonymous_variant | LOW | c.918C>T | p.Pro306Pro | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/31 | 1014/5129 | 918/3513 | 306/1170 | chr16 | 30484175 | |||
| chr16:30484178 | G | A | 1 | a0001c0004 | 8 | HG02615.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
synonymous_variant | LOW | c.921G>A | p.Ala307Ala | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/31 | 1017/5129 | 921/3513 | 307/1170 | chr16 | 30484178 | |||
| chr16:30489361 | A | T | 1 | a0001c0009 | 3 | HG02602.hp2 HG02698.hp2 HG03239.hp1 |
synonymous_variant | LOW | c.1188A>T | p.Thr396Thr | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/31 | 1284/5129 | 1188/3513 | 396/1170 | chr16 | 30489361 | |||
| chr16:30499489 | G | A | 1 | a0001c0014 | 1 | HG02683.hp1 | splice_region_variant&synonymous_variant | LOW | c.2145G>A | p.Pro715Pro | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/31 | 2241/5129 | 2145/3513 | 715/1170 | chr16 | 30499489 | |||
| chr16:30505415 | G | A | 1 | a0001c0015 | 1 | NA18974.hp2 | synonymous_variant | LOW | c.2319G>A | p.Glu773Glu | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 20/31 | 2415/5129 | 2319/3513 | 773/1170 | chr16 | 30505415 | |||
| chr16:30506775 | C | T | 2 | a0002c0007 a0007c0026 |
5 | HG01243.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
synonymous_variant | LOW | c.2427C>T | p.Asn809Asn | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/31 | 2523/5129 | 2427/3513 | 809/1170 | chr16 | 30506775 | |||
| chr16:30510934 | G | T | 1 | a0002c0008 | 3 | HG01884.hp2 HG02970.hp1 HG03453.hp1 |
synonymous_variant | LOW | c.2673G>T | p.Ser891Ser | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 23/31 | 2769/5129 | 2673/3513 | 891/1170 | chr16 | 30510934 | |||
| chr16:30521608 | C | T | 2 | a0001c0017 a0002c0016 |
2 | HG02630.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.3456C>T | p.Pro1152Pro | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 31/31 | 3552/5129 | 3456/3513 | 1152/1170 | chr16 | 30521608 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:30521804 | T | C | 1 | a0001c0001t0007 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*139T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 31/31 | 139 | chr16 | 30521804 | ||||||
| chr16:30521899 | C | G | 3 | a0001c0001t0004 a0001c0005t0004 a0002c0002t0004 |
5 | HG02145.hp2 HG02486.hp1 HG03540.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*234C>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 31/31 | 234 | chr16 | 30521899 | ||||||
| chr16:30521904 | C | T | 1 | a0002c0003t0005 | 3 | HG03139.hp2 NA19043.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*239C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 31/31 | 239 | chr16 | 30521904 | ||||||
| chr16:30522401 | C | T | 1 | a0001c0001t0009 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*736C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 31/31 | 736 | chr16 | 30522401 | ||||||
| chr16:30522581 | A | G | 3 | a0001c0001t0003 a0001c0017t0006 a0002c0016t0006 |
9 | HG02109.hp2 HG02615.hp2 HG02622.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*916A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 31/31 | 916 | chr16 | 30522581 | ||||||
| chr16:30522634 | A | G | 1 | a0001c0001t0008 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*969A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 31/31 | 969 | chr16 | 30522634 | ||||||
| chr16:30522771 | C | T | 3 | a0001c0001t0002 a0002c0002t0002 a0002c0003t0002 |
7 | HG02055.hp2 HG02280.hp2 HG02818.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1106C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 31/31 | 1106 | chr16 | 30522771 | ||||||
| chr16:30523115 | G | A | 2 | a0001c0017t0006 a0002c0016t0006 |
2 | HG02630.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1450G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 31/31 | 1450 | chr16 | 30523115 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:30473158 | G | A | 1 | a0002c0002t0001g0009 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.61+260G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 1/30 | chr16 | 30473158 | |||||||
| chr16:30473883 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.62-313C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 1/30 | chr16 | 30473883 | |||||||
| chr16:30474072 | G | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(188): Show |
197 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.62-124G>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 1/30 | chr16 | 30474072 | |||||||
| chr16:30474846 | C | CT | 26 | a0001c0001t0001g0294 a0001c0001t0002g0283 a0001c0004t0001g0285 others(23): Show |
26 | HG01496.hp2 HG01891.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.165-447dupT | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr16 | 30474846 | ||||||
| chr16:30474860 | C | CT | 155 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(152): Show |
159 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.165-432dupT | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr16 | 30474860 | ||||||
| chr16:30474860 | C | T | 2 | a0002c0002t0001g0191 a0002c0003t0001g0308 |
2 | NA18522.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.165-446C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 2/30 | chr16 | 30474860 | |||||||
| chr16:30474898 | G | A | 1 | a0003c0006t0001g0007 | 2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.165-408G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 2/30 | chr16 | 30474898 | |||||||
| chr16:30475015 | T | C | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(267): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.165-291T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 2/30 | chr16 | 30475015 | |||||||
| chr16:30475110 | C | A | 2 | a0002c0002t0004g0192 a0002c0002t0004g0193 |
2 | HG02145.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.165-196C>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 2/30 | chr16 | 30475110 | |||||||
| chr16:30475111 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.165-195G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 2/30 | chr16 | 30475111 | |||||||
| chr16:30475734 | C | CT | 64 | a0001c0001t0001g0048 a0001c0001t0001g0052 a0001c0001t0001g0167 others(61): Show |
64 | HG00323.hp2 HG00621.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.327+180dupT | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr16 | 30475734 | ||||||
| chr16:30475734 | C | CTT | 19 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0003g0223 others(16): Show |
19 | HG00099.hp1 HG01346.hp1 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.327+179_327+180dup others(2): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr16 | 30475734 | ||||||
| chr16:30475734 | C | CTTT | 7 | a0001c0001t0001g0230 a0001c0001t0001g0282 a0001c0001t0003g0281 others(4): Show |
7 | HG02056.hp2 HG02109.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.327+178_327+180dup others(3): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr16 | 30475734 | ||||||
| chr16:30475734 | CT | C | 6 | a0001c0001t0002g0194 a0001c0001t0003g0195 a0002c0002t0001g0010 others(3): Show |
6 | HG01891.hp2 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.327+180delT | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr16 | 30475734 | ||||||
| chr16:30475782 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.327+202A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | chr16 | 30475782 | |||||||
| chr16:30475812 | G | A | 2 | a0001c0001t0001g0011 a0002c0002t0001g0191 |
2 | NA18952.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.327+232G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | chr16 | 30475812 | |||||||
| chr16:30476066 | C | T | 43 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(40): Show |
45 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.327+486C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | chr16 | 30476066 | |||||||
| chr16:30476182 | C | T | 6 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(3): Show |
6 | NA18945.hp2 NA18968.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.327+602C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | chr16 | 30476182 | |||||||
| chr16:30476229 | C | T | 2 | a0002c0002t0004g0192 a0002c0002t0004g0193 |
2 | HG02145.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.327+649C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | chr16 | 30476229 | |||||||
| chr16:30476386 | C | T | 1 | a0001c0001t0003g0195 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.327+806C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | chr16 | 30476386 | |||||||
| chr16:30476435 | C | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | NA18999.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.327+855C>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | chr16 | 30476435 | |||||||
| chr16:30476633 | C | CT | 58 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0025 others(55): Show |
60 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.327+1069dupT | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr16 | 30476633 | ||||||
| chr16:30476703 | G | A | 24 | a0001c0001t0001g0294 a0001c0004t0001g0285 a0001c0004t0001g0286 others(21): Show |
24 | HG01496.hp2 HG01891.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.327+1123G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | chr16 | 30476703 | |||||||
| chr16:30476885 | C | T | 1 | a0002c0002t0001g0211 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.327+1305C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | chr16 | 30476885 | |||||||
| chr16:30477045 | T | C | 3 | a0002c0002t0001g0056 a0002c0002t0001g0057 a0002c0002t0001g0169 |
3 | HG02132.hp2 NA18962.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.327+1465T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | chr16 | 30477045 | |||||||
| chr16:30477373 | C | A | 24 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0199 others(21): Show |
24 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.328-1718C>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | chr16 | 30477373 | |||||||
| chr16:30477378 | C | CA | 10 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0158 others(7): Show |
10 | HG01346.hp1 HG02071.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.328-1699dupA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr16 | 30477378 | ||||||
| chr16:30477606 | C | T | 16 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0273 others(13): Show |
16 | HG02109.hp2 HG02615.hp2 HG02738.hp1 others(13): Show |
intron_variant | MODIFIER | c.328-1485C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | chr16 | 30477606 | |||||||
| chr16:30477940 | C | T | 1 | a0003c0006t0001g0007 | 2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.328-1151C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | chr16 | 30477940 | |||||||
| chr16:30478121 | G | A | 7 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0273 others(4): Show |
7 | HG02738.hp1 HG02818.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.328-970G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | chr16 | 30478121 | |||||||
| chr16:30478125 | G | A | 2 | a0002c0003t0005g0284 a0008c0021t0001g0305 |
2 | HG01496.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.328-966G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | chr16 | 30478125 | |||||||
| chr16:30478159 | C | T | 2 | a0002c0002t0001g0210 a0002c0002t0001g0219 |
2 | HG00280.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.328-932C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | chr16 | 30478159 | |||||||
| chr16:30478391 | G | T | 22 | a0001c0001t0001g0294 a0001c0004t0001g0285 a0001c0004t0001g0286 others(19): Show |
22 | HG01496.hp2 HG01891.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.328-700G>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | chr16 | 30478391 | |||||||
| chr16:30478465 | G | A | 1 | a0002c0002t0001g0236 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.328-626G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | chr16 | 30478465 | |||||||
| chr16:30478552 | G | T | 6 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0001t0001g0157 others(3): Show |
6 | NA18939.hp2 NA18950.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.328-539G>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | chr16 | 30478552 | |||||||
| chr16:30478667 | A | G | 5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0153 others(2): Show |
5 | NA18612.hp2 NA18974.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-424A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | chr16 | 30478667 | |||||||
| chr16:30478684 | GA | G | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(266): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.328-405delA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr16 | 30478684 | ||||||
| chr16:30478697 | C | CA | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
223 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.328-376dupA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr16 | 30478697 | ||||||
| chr16:30478729 | A | C | 2 | a0001c0001t0001g0052 a0002c0002t0001g0051 |
2 | HG01070.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.328-362A>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | chr16 | 30478729 | |||||||
| chr16:30478949 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.328-142A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | chr16 | 30478949 | |||||||
| chr16:30479012 | G | A | 1 | a0002c0002t0001g0170 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.328-79G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 4/30 | chr16 | 30479012 | |||||||
| chr16:30479533 | G | A | 34 | a0001c0001t0001g0230 a0001c0001t0001g0294 a0001c0001t0003g0223 others(31): Show |
34 | HG00099.hp1 HG01346.hp1 HG01496.hp2 others(31): Show |
intron_variant | MODIFIER | c.576+72G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | chr16 | 30479533 | |||||||
| chr16:30479648 | C | CT | 26 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(23): Show |
26 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.576+216dupT | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 30479648 | ||||||
| chr16:30479648 | C | CTT | 10 | a0001c0001t0001g0208 a0001c0001t0001g0215 a0001c0001t0001g0216 others(7): Show |
10 | HG00280.hp2 HG00741.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.576+215_576+216dup others(2): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 30479648 | ||||||
| chr16:30479648 | CT | C | 46 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(43): Show |
48 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.576+216delT | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 30479648 | ||||||
| chr16:30479648 | CTTTTTTT others(1): Show |
C | 15 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0153 others(12): Show |
15 | HG00642.hp1 HG02109.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.576+209_576+216del others(8): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 30479648 | ||||||
| chr16:30479648 | CTTTTTTT others(2): Show |
C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
133 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.576+208_576+216del others(9): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 30479648 | ||||||
| chr16:30479648 | CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
4 | HG01192.hp1 HG02155.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+207_576+216del others(10): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 30479648 | ||||||
| chr16:30479648 | CTTTTTTT others(5): Show |
C | 2 | a0004c0010t0001g0306 a0004c0010t0001g0307 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.576+205_576+216del others(12): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 30479648 | ||||||
| chr16:30479843 | T | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
107 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.576+382T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | chr16 | 30479843 | |||||||
| chr16:30480462 | T | C | 5 | a0001c0001t0001g0230 a0002c0002t0001g0225 a0002c0007t0001g0221 others(2): Show |
5 | HG00099.hp1 HG01346.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.577-977T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | chr16 | 30480462 | |||||||
| chr16:30480503 | G | A | 2 | a0001c0001t0002g0194 a0001c0001t0003g0195 |
2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.577-936G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | chr16 | 30480503 | |||||||
| chr16:30480965 | C | A | 2 | a0002c0002t0004g0192 a0002c0002t0004g0193 |
2 | HG02145.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.577-474C>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | chr16 | 30480965 | |||||||
| chr16:30481056 | C | T | 4 | a0001c0005t0004g0292 a0001c0005t0004g0296 a0002c0003t0002g0293 others(1): Show |
4 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-383C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | chr16 | 30481056 | |||||||
| chr16:30481143 | A | AAC | 28 | a0001c0001t0001g0077 a0001c0001t0001g0247 a0001c0001t0001g0273 others(25): Show |
28 | HG00280.hp1 HG00741.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.577-257_577-256dup others(2): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 30481143 | ||||||
| chr16:30481143 | A | AACAC | 69 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(66): Show |
73 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.577-259_577-256dup others(4): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 30481143 | ||||||
| chr16:30481143 | A | AACACAC | 9 | a0001c0001t0001g0098 a0001c0001t0001g0158 a0001c0001t0001g0183 others(6): Show |
9 | HG01515.hp1 HG02071.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.577-261_577-256dup others(6): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 30481143 | ||||||
| chr16:30481143 | A | AACACACA others(1): Show |
6 | a0001c0001t0001g0069 a0001c0001t0001g0266 a0002c0002t0001g0235 others(3): Show |
6 | HG00423.hp2 HG01168.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.577-263_577-256dup others(8): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 30481143 | ||||||
| chr16:30481143 | A | AACACACA others(3): Show |
1 | a0010c0012t0001g0260 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.577-265_577-256dup others(10): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 30481143 | ||||||
| chr16:30481143 | A | C | 1 | a0001c0001t0001g0058 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.577-296A>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | chr16 | 30481143 | |||||||
| chr16:30481143 | AAC | A | 34 | a0001c0001t0001g0064 a0001c0001t0001g0159 a0001c0001t0001g0179 others(31): Show |
34 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(31): Show |
intron_variant | MODIFIER | c.577-257_577-256del others(2): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 30481143 | ||||||
| chr16:30481143 | AACAC | A | 32 | a0001c0001t0001g0048 a0001c0001t0001g0052 a0001c0001t0001g0110 others(29): Show |
32 | HG00323.hp2 HG00639.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.577-259_577-256del others(4): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 30481143 | ||||||
| chr16:30481143 | AACACAC | A | 89 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0018 others(86): Show |
89 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.577-261_577-256del others(6): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 30481143 | ||||||
| chr16:30481143 | AACACACA others(1): Show |
A | 13 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0035 others(10): Show |
14 | HG00673.hp1 HG01069.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.577-263_577-256del others(8): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 30481143 | ||||||
| chr16:30481143 | AACACACA others(3): Show |
A | 4 | a0001c0001t0001g0070 a0002c0002t0004g0192 a0002c0002t0004g0193 others(1): Show |
4 | HG01891.hp1 HG02145.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-265_577-256del others(10): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 30481143 | ||||||
| chr16:30481202 | C | T | 3 | a0001c0001t0001g0268 a0002c0002t0001g0237 a0002c0002t0001g0257 |
3 | HG02895.hp2 HG02897.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.577-237C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | chr16 | 30481202 | |||||||
| chr16:30481228 | C | T | 1 | a0001c0004t0001g0303 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.577-211C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | chr16 | 30481228 | |||||||
| chr16:30481271 | G | A | 2 | a0002c0002t0001g0013 a0002c0002t0001g0017 |
2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.577-168G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | chr16 | 30481271 | |||||||
| chr16:30481345 | TA | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(236): Show |
245 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.577-72delA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | 30481345 | ||||||
| chr16:30481360 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.577-79A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | chr16 | 30481360 | |||||||
| chr16:30481369 | A | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(97): Show |
104 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.577-70A>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 6/30 | chr16 | 30481369 | |||||||
| chr16:30481679 | G | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(36): Show |
41 | HG00323.hp2 HG00438.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.722+95G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 7/30 | chr16 | 30481679 | |||||||
| chr16:30481758 | A | G | 1 | a0002c0023t0001g0190 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.722+174A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 7/30 | chr16 | 30481758 | |||||||
| chr16:30482096 | T | C | 2 | a0001c0001t0002g0194 a0001c0001t0003g0195 |
2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.722+512T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 7/30 | chr16 | 30482096 | |||||||
| chr16:30482133 | G | A | 1 | a0002c0002t0001g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.722+549G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 7/30 | chr16 | 30482133 | |||||||
| chr16:30482309 | G | A | 85 | a0001c0001t0001g0006 a0001c0001t0001g0038 a0001c0001t0001g0040 others(82): Show |
85 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.722+725G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 7/30 | chr16 | 30482309 | |||||||
| chr16:30482412 | A | G | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(283): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.722+828A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 7/30 | chr16 | 30482412 | |||||||
| chr16:30482560 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(210): Show |
219 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.722+976T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 7/30 | chr16 | 30482560 | |||||||
| chr16:30482789 | C | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0099 a0001c0001t0001g0100 others(1): Show |
5 | HG00423.hp1 HG00558.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.723-1038C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 7/30 | chr16 | 30482789 | |||||||
| chr16:30483538 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.723-289G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 7/30 | chr16 | 30483538 | |||||||
| chr16:30483558 | T | C | 1 | a0001c0001t0001g0270 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.723-269T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 7/30 | chr16 | 30483558 | |||||||
| chr16:30484091 | T | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(247): Show |
256 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(253): Show |
intron_variant | MODIFIER | c.856-22T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 8/30 | chr16 | 30484091 | |||||||
| chr16:30484331 | G | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(100): Show |
107 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1006+68G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484331 | |||||||
| chr16:30484336 | T | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(247): Show |
256 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(253): Show |
intron_variant | MODIFIER | c.1006+73T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484336 | |||||||
| chr16:30484646 | C | T | 1 | a0001c0001t0004g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1006+383C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484646 | |||||||
| chr16:30484647 | G | A | 30 | a0001c0004t0001g0285 a0001c0004t0001g0286 a0001c0004t0001g0287 others(27): Show |
30 | HG01106.hp1 HG01496.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1006+384G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484647 | |||||||
| chr16:30484748 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1006+485G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484748 | |||||||
| chr16:30484836 | T | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+573T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484836 | |||||||
| chr16:30484841 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+578C>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484841 | |||||||
| chr16:30484848 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+585G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484848 | |||||||
| chr16:30484850 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+587C>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484850 | |||||||
| chr16:30484865 | G | GCACCCCC others(4): Show |
1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+603_1006+604i others(13): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr16 | 30484865 | ||||||
| chr16:30484871 | A | C | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+608A>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484871 | |||||||
| chr16:30484872 | T | A | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+609T>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484872 | |||||||
| chr16:30484873 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+610G>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484873 | |||||||
| chr16:30484878 | A | C | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+615A>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484878 | |||||||
| chr16:30484917 | C | CAAACA | 5 | a0002c0002t0001g0235 a0002c0002t0001g0238 a0002c0002t0001g0248 others(2): Show |
5 | HG02622.hp1 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006+673_1006+677d others(7): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr16 | 30484917 | ||||||
| chr16:30484931 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+668C>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484931 | |||||||
| chr16:30484936 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+673C>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484936 | |||||||
| chr16:30484944 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+681C>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484944 | |||||||
| chr16:30484960 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+697C>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484960 | |||||||
| chr16:30484961 | T | A | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+698T>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484961 | |||||||
| chr16:30484963 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+700G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484963 | |||||||
| chr16:30484966 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+703C>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484966 | |||||||
| chr16:30484968 | T | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+705T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484968 | |||||||
| chr16:30484969 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+706C>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484969 | |||||||
| chr16:30484970 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+707C>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484970 | |||||||
| chr16:30484971 | T | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+708T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484971 | |||||||
| chr16:30484973 | T | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+710T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484973 | |||||||
| chr16:30484974 | T | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+711T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484974 | |||||||
| chr16:30484979 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+716A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484979 | |||||||
| chr16:30484980 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+717C>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484980 | |||||||
| chr16:30484982 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+719C>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484982 | |||||||
| chr16:30484984 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+721A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484984 | |||||||
| chr16:30484987 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+724A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484987 | |||||||
| chr16:30484988 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+725A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484988 | |||||||
| chr16:30484989 | T | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+726T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484989 | |||||||
| chr16:30484990 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+727A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484990 | |||||||
| chr16:30484992 | T | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+729T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484992 | |||||||
| chr16:30484993 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+730A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484993 | |||||||
| chr16:30484998 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+735C>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484998 | |||||||
| chr16:30484999 | T | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+736T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30484999 | |||||||
| chr16:30485000 | T | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+737T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30485000 | |||||||
| chr16:30485002 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+739C>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30485002 | |||||||
| chr16:30485003 | T | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+740T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30485003 | |||||||
| chr16:30485014 | T | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+751T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30485014 | |||||||
| chr16:30485015 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+752C>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30485015 | |||||||
| chr16:30485016 | T | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+753T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30485016 | |||||||
| chr16:30485017 | T | A | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+754T>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30485017 | |||||||
| chr16:30485019 | T | A | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+756T>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30485019 | |||||||
| chr16:30485021 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+758C>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30485021 | |||||||
| chr16:30485022 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+759C>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30485022 | |||||||
| chr16:30485023 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+760A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30485023 | |||||||
| chr16:30485028 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+765C>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30485028 | |||||||
| chr16:30485029 | T | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+766T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30485029 | |||||||
| chr16:30485030 | T | A | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+767T>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30485030 | |||||||
| chr16:30485032 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+769C>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30485032 | |||||||
| chr16:30485033 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+770C>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30485033 | |||||||
| chr16:30485036 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+773A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30485036 | |||||||
| chr16:30485039 | A | C | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+776A>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30485039 | |||||||
| chr16:30485041 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+778A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30485041 | |||||||
| chr16:30485043 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1006+780C>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30485043 | |||||||
| chr16:30485090 | T | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(71): Show |
76 | HG00323.hp2 HG00438.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.1006+827T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30485090 | |||||||
| chr16:30485151 | C | T | 30 | a0001c0004t0001g0285 a0001c0004t0001g0286 a0001c0004t0001g0287 others(27): Show |
30 | HG01106.hp1 HG01496.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1006+888C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30485151 | |||||||
| chr16:30485276 | G | GAGTGCAG others(22): Show |
6 | a0001c0001t0001g0068 a0001c0001t0001g0106 a0001c0001t0001g0107 others(3): Show |
6 | HG00408.hp1 NA18612.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.1006+1020_1006+102 others(33): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr16 | 30485276 | ||||||
| chr16:30485276 | G | GAGTGCAG others(22): Show |
179 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
183 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.1006+1015_1006+104 others(33): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr16 | 30485276 | ||||||
| chr16:30485442 | A | G | 5 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0275 others(2): Show |
5 | HG02886.hp2 HG02965.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006+1179A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30485442 | |||||||
| chr16:30485678 | AT | A | 49 | a0001c0001t0001g0124 a0001c0001t0001g0142 a0001c0001t0001g0163 others(46): Show |
50 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(47): Show |
intron_variant | MODIFIER | c.1006+1432delT | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr16 | 30485678 | ||||||
| chr16:30485678 | ATT | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(243): Show |
252 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.1006+1431_1006+143 others(6): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr16 | 30485678 | ||||||
| chr16:30485786 | G | A | 1 | a0010c0012t0001g0260 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1006+1523G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30485786 | |||||||
| chr16:30485851 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1006+1588C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30485851 | |||||||
| chr16:30486184 | C | G | 1 | a0001c0001t0001g0098 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1006+1921C>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30486184 | |||||||
| chr16:30486276 | G | A | 24 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0199 others(21): Show |
24 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.1006+2013G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30486276 | |||||||
| chr16:30486408 | C | CA | 81 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(78): Show |
85 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.1006+2161dupA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr16 | 30486408 | ||||||
| chr16:30486408 | C | CAA | 92 | a0001c0001t0001g0006 a0001c0001t0001g0038 a0001c0001t0001g0040 others(89): Show |
92 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1006+2160_1006+216 others(6): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr16 | 30486408 | ||||||
| chr16:30486408 | C | CAAA | 7 | a0001c0001t0001g0106 a0001c0001t0001g0124 a0001c0001t0001g0149 others(4): Show |
7 | HG00735.hp2 HG01175.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.1006+2159_1006+216 others(7): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr16 | 30486408 | ||||||
| chr16:30486495 | T | A | 31 | a0001c0001t0001g0232 a0001c0001t0001g0250 a0001c0001t0001g0253 others(28): Show |
31 | HG01168.hp2 HG01515.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1006+2232T>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30486495 | |||||||
| chr16:30486633 | C | T | 5 | a0001c0001t0001g0199 a0001c0001t0001g0202 a0001c0001t0001g0215 others(2): Show |
5 | HG00099.hp2 HG00140.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006+2370C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30486633 | |||||||
| chr16:30486664 | G | C | 1 | a0013c0018t0001g0071 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1006+2401G>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30486664 | |||||||
| chr16:30486931 | G | C | 3 | a0001c0001t0001g0048 a0002c0002t0001g0053 a0002c0002t0001g0054 |
3 | HG00323.hp2 HG01346.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1007-2151G>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30486931 | |||||||
| chr16:30486988 | A | C | 1 | a0001c0017t0006g0012 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1007-2094A>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30486988 | |||||||
| chr16:30487003 | C | T | 1 | a0002c0002t0001g0034 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1007-2079C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30487003 | |||||||
| chr16:30487012 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0183 |
2 | NA19000.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1007-2070G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30487012 | |||||||
| chr16:30487105 | C | T | 1 | a0002c0002t0002g0295 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1007-1977C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30487105 | |||||||
| chr16:30487142 | C | CA | 16 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0099 others(13): Show |
16 | HG00408.hp1 HG00423.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.1007-1918dupA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr16 | 30487142 | ||||||
| chr16:30487267 | C | T | 5 | a0001c0001t0001g0178 a0001c0005t0001g0226 a0002c0002t0001g0057 others(2): Show |
5 | HG00621.hp2 HG01884.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1007-1815C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30487267 | |||||||
| chr16:30487271 | C | G | 1 | a0014c0013t0001g0055 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1007-1811C>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30487271 | |||||||
| chr16:30487404 | T | TTTTTG | 4 | a0003c0006t0001g0014 a0003c0006t0001g0015 a0003c0006t0001g0016 others(1): Show |
4 | HG02809.hp1 HG03579.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1007-1658_1007-165 others(9): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr16 | 30487404 | ||||||
| chr16:30487462 | T | C | 110 | a0001c0001t0001g0006 a0001c0001t0001g0038 a0001c0001t0001g0040 others(107): Show |
110 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1007-1620T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30487462 | |||||||
| chr16:30487503 | C | T | 103 | a0001c0001t0001g0006 a0001c0001t0001g0038 a0001c0001t0001g0040 others(100): Show |
103 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1007-1579C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30487503 | |||||||
| chr16:30487504 | G | A | 2 | a0002c0002t0001g0020 a0002c0002t0001g0021 |
2 | HG03710.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1007-1578G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30487504 | |||||||
| chr16:30487614 | A | G | 3 | a0001c0001t0002g0194 a0002c0002t0004g0192 a0002c0002t0004g0193 |
3 | HG02145.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1007-1468A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30487614 | |||||||
| chr16:30487690 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1007-1392G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30487690 | |||||||
| chr16:30487710 | C | CT | 6 | a0001c0001t0001g0018 a0001c0001t0001g0164 a0001c0015t0001g0152 others(3): Show |
6 | HG00408.hp2 NA18968.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.1007-1360dupT | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr16 | 30487710 | ||||||
| chr16:30488194 | C | CA | 26 | a0001c0001t0001g0059 a0001c0001t0001g0196 a0001c0001t0001g0197 others(23): Show |
26 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.1007-874dupA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr16 | 30488194 | ||||||
| chr16:30488442 | G | C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(59): Show |
66 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.1007-640G>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30488442 | |||||||
| chr16:30488478 | C | T | 1 | a0002c0003t0001g0308 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1007-604C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30488478 | |||||||
| chr16:30488638 | G | A | 3 | a0001c0005t0001g0226 a0002c0003t0001g0228 a0003c0020t0001g0227 |
3 | HG01884.hp1 HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1007-444G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30488638 | |||||||
| chr16:30488669 | C | A | 1 | a0002c0002t0001g0041 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1007-413C>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30488669 | |||||||
| chr16:30488679 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(137): Show |
146 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.1007-403G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30488679 | |||||||
| chr16:30488702 | C | CA | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(155): Show |
164 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.1007-355dupA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr16 | 30488702 | ||||||
| chr16:30488702 | C | CAA | 17 | a0001c0001t0001g0018 a0001c0001t0001g0052 a0001c0001t0001g0076 others(14): Show |
17 | HG00423.hp1 HG01070.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.1007-356_1007-355d others(4): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr16 | 30488702 | ||||||
| chr16:30488834 | G | T | 1 | a0001c0001t0001g0201 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1007-248G>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30488834 | |||||||
| chr16:30489160 | G | A | 1 | a0001c0001t0003g0195 | 1 | HG02622.hp2 | splice_region_variant&intron_variant | LOW | c.1080+5G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 10/30 | chr16 | 30489160 | |||||||
| chr16:30489440 | G | A | 110 | a0001c0001t0001g0006 a0001c0001t0001g0038 a0001c0001t0001g0040 others(107): Show |
110 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1213+54G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30489440 | |||||||
| chr16:30489645 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1213+259A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30489645 | |||||||
| chr16:30489664 | A | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(253): Show |
262 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.1213+278A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30489664 | |||||||
| chr16:30489753 | T | C | 1 | a0002c0002t0001g0229 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1213+367T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30489753 | |||||||
| chr16:30489895 | A | C | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(277): Show |
286 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.1213+509A>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30489895 | |||||||
| chr16:30490220 | T | A | 1 | a0002c0002t0001g0180 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1213+834T>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30490220 | |||||||
| chr16:30490226 | T | TA | 99 | a0001c0001t0001g0006 a0001c0001t0001g0038 a0001c0001t0001g0040 others(96): Show |
99 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.1213+840_1213+841i others(3): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30490226 | |||||||
| chr16:30490226 | T | TAA | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(124): Show |
133 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.1213+840_1213+841i others(4): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30490226 | |||||||
| chr16:30490226 | T | TAAA | 18 | a0001c0001t0001g0035 a0001c0001t0001g0078 a0001c0001t0001g0079 others(15): Show |
18 | HG00597.hp1 HG01255.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1213+840_1213+841i others(5): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30490226 | |||||||
| chr16:30490227 | T | A | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(252): Show |
261 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.1213+841T>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30490227 | |||||||
| chr16:30490227 | T | TA | 22 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0199 others(19): Show |
22 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.1213+861dupA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | 30490227 | ||||||
| chr16:30490232 | A | AC | 3 | a0001c0001t0002g0194 a0002c0002t0004g0192 a0002c0002t0004g0193 |
3 | HG02145.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1213+846_1213+847i others(3): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30490232 | |||||||
| chr16:30490238 | A | C | 3 | a0001c0001t0002g0194 a0002c0002t0004g0192 a0002c0002t0004g0193 |
3 | HG02145.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1213+852A>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30490238 | |||||||
| chr16:30490288 | C | T | 24 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0199 others(21): Show |
24 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.1213+902C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30490288 | |||||||
| chr16:30490435 | T | G | 3 | a0001c0001t0002g0194 a0002c0002t0004g0192 a0002c0002t0004g0193 |
3 | HG02145.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1213+1049T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30490435 | |||||||
| chr16:30490461 | C | T | 1 | a0002c0003t0001g0308 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1213+1075C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30490461 | |||||||
| chr16:30490831 | G | T | 110 | a0001c0001t0001g0006 a0001c0001t0001g0038 a0001c0001t0001g0040 others(107): Show |
110 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1213+1445G>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30490831 | |||||||
| chr16:30490871 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1213+1485G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30490871 | |||||||
| chr16:30490969 | C | CA | 10 | a0001c0001t0001g0096 a0001c0001t0003g0223 a0001c0001t0003g0224 others(7): Show |
10 | HG00280.hp1 HG00741.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1213+1599dupA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | 30490969 | ||||||
| chr16:30491237 | T | C | 5 | a0001c0001t0001g0230 a0002c0002t0001g0225 a0002c0007t0001g0221 others(2): Show |
5 | HG00099.hp1 HG01346.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.1213+1851T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30491237 | |||||||
| chr16:30491597 | ACT | A | 3 | a0001c0001t0002g0194 a0002c0002t0004g0192 a0002c0002t0004g0193 |
3 | HG02145.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1213+2215_1213+221 others(6): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | 30491597 | ||||||
| chr16:30491837 | T | G | 1 | a0014c0013t0001g0055 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1214-2375T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30491837 | |||||||
| chr16:30491951 | TACG | T | 3 | a0001c0001t0002g0194 a0002c0002t0004g0192 a0002c0002t0004g0193 |
3 | HG02145.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1214-2258_1214-225 others(7): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | 30491951 | ||||||
| chr16:30491970 | T | C | 3 | a0002c0002t0001g0133 a0002c0002t0001g0174 a0002c0002t0001g0186 |
3 | NA18953.hp2 NA18971.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1214-2242T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30491970 | |||||||
| chr16:30492093 | T | G | 103 | a0001c0001t0001g0006 a0001c0001t0001g0038 a0001c0001t0001g0040 others(100): Show |
103 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1214-2119T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30492093 | |||||||
| chr16:30492255 | CT | C | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(259): Show |
268 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.1214-1942delT | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | 30492255 | ||||||
| chr16:30492255 | CTT | C | 7 | a0001c0001t0001g0102 a0001c0001t0001g0145 a0001c0001t0003g0223 others(4): Show |
7 | HG01167.hp2 HG01884.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.1214-1943_1214-194 others(6): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | 30492255 | ||||||
| chr16:30492407 | C | T | 29 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(26): Show |
29 | HG01106.hp1 HG01496.hp2 HG02109.hp2 others(26): Show |
intron_variant | MODIFIER | c.1214-1805C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30492407 | |||||||
| chr16:30492492 | T | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(28): Show |
35 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.1214-1720T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30492492 | |||||||
| chr16:30492531 | C | T | 2 | a0001c0001t0001g0178 a0002c0002t0001g0057 |
2 | HG00621.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.1214-1681C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30492531 | |||||||
| chr16:30492630 | C | T | 1 | a0001c0001t0002g0194 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1214-1582C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30492630 | |||||||
| chr16:30492725 | T | C | 22 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0199 others(19): Show |
22 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(19): Show |
intron_variant | MODIFIER | c.1214-1487T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30492725 | |||||||
| chr16:30492892 | T | A | 1 | a0001c0001t0001g0134 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1214-1320T>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30492892 | |||||||
| chr16:30493023 | T | C | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(261): Show |
270 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.1214-1189T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30493023 | |||||||
| chr16:30493078 | G | C | 4 | a0001c0001t0003g0223 a0001c0001t0003g0224 a0001c0005t0001g0226 others(1): Show |
4 | HG01884.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1214-1134G>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30493078 | |||||||
| chr16:30493238 | TA | T | 4 | a0001c0001t0003g0223 a0001c0001t0003g0224 a0001c0005t0001g0226 others(1): Show |
4 | HG01884.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1214-973delA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30493238 | |||||||
| chr16:30493245 | C | CATTTT | 150 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(147): Show |
154 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.1214-932_1214-928d others(7): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | 30493245 | ||||||
| chr16:30493245 | C | CATTTTAT others(3): Show |
27 | a0001c0001t0001g0202 a0001c0001t0001g0232 a0001c0001t0001g0250 others(24): Show |
27 | HG01168.hp2 HG01515.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1214-937_1214-928d others(12): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | 30493245 | ||||||
| chr16:30493245 | C | CATTTTAT others(8): Show |
68 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0025 others(65): Show |
70 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.1214-942_1214-928d others(17): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | 30493245 | ||||||
| chr16:30493245 | C | CATTTTAT others(13): Show |
23 | a0001c0001t0001g0213 a0001c0001t0001g0217 a0001c0005t0001g0256 others(20): Show |
24 | HG00099.hp1 HG01346.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.1214-947_1214-928d others(22): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | 30493245 | ||||||
| chr16:30493245 | C | CATTTTAT others(18): Show |
2 | a0002c0003t0001g0300 a0002c0003t0001g0308 |
2 | NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1214-952_1214-928d others(27): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | 30493245 | ||||||
| chr16:30493245 | C | CATTTTAT others(23): Show |
1 | a0001c0005t0004g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1214-957_1214-928d others(32): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | 30493245 | ||||||
| chr16:30493245 | C | CATTTTAT others(9): Show |
16 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0045 others(13): Show |
16 | HG00323.hp2 HG00438.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.1214-957_1214-956i others(18): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | 30493245 | ||||||
| chr16:30493245 | C | CATTTTAT others(14): Show |
3 | a0001c0001t0001g0018 a0002c0002t0001g0022 a0002c0002t0001g0054 |
3 | HG02683.hp2 NA18942.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1214-957_1214-956i others(23): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | 30493245 | ||||||
| chr16:30493245 | C | CATTTTAT others(19): Show |
2 | a0001c0001t0001g0052 a0002c0002t0001g0051 |
2 | HG01070.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1214-957_1214-956i others(28): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | 30493245 | ||||||
| chr16:30493245 | CATTTTAT others(8): Show |
C | 1 | a0001c0001t0001g0125 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1214-942_1214-928d others(17): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | 30493245 | ||||||
| chr16:30493310 | C | T | 6 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0137 others(3): Show |
6 | HG00642.hp1 HG01081.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.1214-902C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30493310 | |||||||
| chr16:30493322 | C | T | 4 | a0001c0001t0003g0223 a0001c0001t0003g0224 a0001c0005t0001g0226 others(1): Show |
4 | HG01884.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1214-890C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30493322 | |||||||
| chr16:30493339 | G | A | 3 | a0001c0001t0002g0194 a0002c0002t0004g0192 a0002c0002t0004g0193 |
3 | HG02145.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1214-873G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30493339 | |||||||
| chr16:30493403 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1214-809A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30493403 | |||||||
| chr16:30493470 | G | A | 1 | a0002c0002t0001g0126 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1214-742G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30493470 | |||||||
| chr16:30493611 | C | T | 2 | a0002c0002t0001g0225 a0002c0007t0001g0221 |
2 | HG00099.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.1214-601C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30493611 | |||||||
| chr16:30493961 | C | T | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0109 |
3 | HG00408.hp1 NA18612.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1214-251C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30493961 | |||||||
| chr16:30494191 | C | T | 107 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(104): Show |
109 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1214-21C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30494191 | |||||||
| chr16:30494192 | A | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
263 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.1214-20A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 11/30 | chr16 | 30494192 | |||||||
| chr16:30494500 | C | T | 4 | a0002c0002t0001g0204 a0002c0002t0001g0210 a0002c0002t0001g0212 others(1): Show |
4 | HG00280.hp1 HG00741.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.1365+137C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 12/30 | chr16 | 30494500 | |||||||
| chr16:30494579 | A | G | 2 | a0002c0002t0004g0192 a0002c0002t0004g0193 |
2 | HG02145.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1366-134A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 12/30 | chr16 | 30494579 | |||||||
| chr16:30494608 | C | G | 1 | a0014c0013t0001g0055 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1366-105C>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 12/30 | chr16 | 30494608 | |||||||
| chr16:30494635 | G | A | 5 | a0001c0001t0001g0273 a0001c0001t0002g0271 a0001c0001t0002g0272 others(2): Show |
5 | HG02818.hp2 HG02886.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1366-78G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 12/30 | chr16 | 30494635 | |||||||
| chr16:30495211 | C | G | 110 | a0001c0001t0001g0006 a0001c0001t0001g0038 a0001c0001t0001g0040 others(107): Show |
110 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1503+361C>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 13/30 | chr16 | 30495211 | |||||||
| chr16:30495504 | C | T | 1 | a0002c0002t0001g0057 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1504-593C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 13/30 | chr16 | 30495504 | |||||||
| chr16:30495505 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1504-592C>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 13/30 | chr16 | 30495505 | |||||||
| chr16:30495814 | A | T | 1 | a0001c0005t0001g0258 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1504-283A>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 13/30 | chr16 | 30495814 | |||||||
| chr16:30495875 | A | G | 5 | a0001c0001t0001g0111 a0001c0001t0001g0122 a0001c0001t0001g0123 others(2): Show |
5 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1504-222A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 13/30 | chr16 | 30495875 | |||||||
| chr16:30495907 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1504-190G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 13/30 | chr16 | 30495907 | |||||||
| chr16:30495944 | T | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
263 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.1504-153T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 13/30 | chr16 | 30495944 | |||||||
| chr16:30495952 | G | T | 1 | a0001c0001t0001g0282 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1504-145G>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 13/30 | chr16 | 30495952 | |||||||
| chr16:30496018 | C | T | 6 | a0001c0001t0001g0273 a0001c0001t0001g0282 a0001c0001t0002g0271 others(3): Show |
6 | HG02818.hp2 HG02886.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1504-79C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 13/30 | chr16 | 30496018 | |||||||
| chr16:30496651 | T | C | 110 | a0001c0001t0001g0006 a0001c0001t0001g0038 a0001c0001t0001g0040 others(107): Show |
110 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1832+85T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 15/30 | chr16 | 30496651 | |||||||
| chr16:30496727 | G | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0002c0007t0001g0037 |
3 | HG00639.hp2 HG00738.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1832+161G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 15/30 | chr16 | 30496727 | |||||||
| chr16:30496808 | A | AT | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(237): Show |
246 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.1832+258dupT | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 30496808 | ||||||
| chr16:30496808 | A | ATT | 15 | a0001c0001t0001g0073 a0001c0001t0001g0121 a0001c0001t0001g0151 others(12): Show |
15 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.1832+257_1832+258d others(4): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 30496808 | ||||||
| chr16:30496911 | C | T | 5 | a0001c0001t0001g0273 a0001c0001t0002g0271 a0001c0001t0002g0272 others(2): Show |
5 | HG02818.hp2 HG02886.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1832+345C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 15/30 | chr16 | 30496911 | |||||||
| chr16:30497160 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1832+594C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 15/30 | chr16 | 30497160 | |||||||
| chr16:30497175 | T | G | 1 | a0001c0017t0006g0012 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1832+609T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 15/30 | chr16 | 30497175 | |||||||
| chr16:30497247 | G | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(144): Show |
153 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1832+681G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 15/30 | chr16 | 30497247 | |||||||
| chr16:30497291 | C | T | 1 | a0009c0022t0001g0234 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1832+725C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 15/30 | chr16 | 30497291 | |||||||
| chr16:30497318 | G | A | 1 | a0002c0007t0001g0231 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1832+752G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 15/30 | chr16 | 30497318 | |||||||
| chr16:30497321 | T | C | 6 | a0001c0001t0001g0070 a0001c0001t0001g0160 a0001c0001t0001g0161 others(3): Show |
6 | NA18944.hp2 NA18945.hp2 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.1832+755T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 15/30 | chr16 | 30497321 | |||||||
| chr16:30497337 | C | T | 4 | a0002c0002t0001g0029 a0002c0002t0001g0030 a0002c0002t0001g0044 others(1): Show |
4 | HG02738.hp2 HG03491.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1832+771C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 15/30 | chr16 | 30497337 | |||||||
| chr16:30497539 | C | T | 3 | a0002c0002t0001g0036 a0002c0002t0001g0049 a0002c0002t0001g0166 |
3 | HG02698.hp1 HG03540.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1832+973C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 15/30 | chr16 | 30497539 | |||||||
| chr16:30497613 | A | T | 4 | a0002c0002t0001g0200 a0002c0002t0001g0205 a0002c0002t0001g0206 others(1): Show |
4 | HG01192.hp2 HG01361.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.1832+1047A>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 15/30 | chr16 | 30497613 | |||||||
| chr16:30498120 | T | G | 2 | a0002c0002t0001g0237 a0002c0002t0001g0257 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1833-954T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 15/30 | chr16 | 30498120 | |||||||
| chr16:30498123 | A | G | 2 | a0002c0002t0001g0237 a0002c0002t0001g0257 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1833-951A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 15/30 | chr16 | 30498123 | |||||||
| chr16:30498263 | C | CA | 9 | a0001c0001t0001g0140 a0001c0001t0001g0144 a0001c0001t0001g0159 others(6): Show |
9 | HG00323.hp1 HG02074.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1833-794dupA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 30498263 | ||||||
| chr16:30498263 | C | CAA | 8 | a0001c0001t0001g0048 a0001c0001t0001g0273 a0001c0001t0001g0282 others(5): Show |
8 | HG00323.hp2 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1833-795_1833-794d others(4): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 30498263 | ||||||
| chr16:30498263 | C | CAAA | 45 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0137 others(42): Show |
46 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(43): Show |
intron_variant | MODIFIER | c.1833-796_1833-794d others(5): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr16 | 30498263 | ||||||
| chr16:30498402 | A | G | 75 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0032 others(72): Show |
77 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.1833-672A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 15/30 | chr16 | 30498402 | |||||||
| chr16:30498669 | C | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0032 others(97): Show |
102 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(99): Show |
intron_variant | MODIFIER | c.1833-405C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 15/30 | chr16 | 30498669 | |||||||
| chr16:30498715 | A | G | 16 | a0001c0001t0001g0232 a0001c0001t0001g0253 a0001c0001t0001g0266 others(13): Show |
16 | HG01168.hp2 HG01515.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1833-359A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 15/30 | chr16 | 30498715 | |||||||
| chr16:30499250 | C | T | 98 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0038 others(95): Show |
98 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1993+16C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 16/30 | chr16 | 30499250 | |||||||
| chr16:30499649 | G | C | 5 | a0001c0001t0001g0273 a0001c0001t0002g0271 a0001c0001t0002g0272 others(2): Show |
5 | HG02818.hp2 HG02886.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2145+160G>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30499649 | |||||||
| chr16:30499657 | T | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(141): Show |
150 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.2145+168T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30499657 | |||||||
| chr16:30499663 | T | TTA | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(235): Show |
244 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(241): Show |
intron_variant | MODIFIER | c.2145+184_2145+185d others(4): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499663 | ||||||
| chr16:30499673 | A | ATATGTGT others(19): Show |
1 | a0001c0005t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2145+185_2145+186i others(28): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499673 | ||||||
| chr16:30499675 | G | GTGTATAT others(29): Show |
1 | a0001c0001t0001g0230 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2145+198_2145+233d others(38): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499675 | ||||||
| chr16:30499677 | G | A | 1 | a0001c0005t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2145+188G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30499677 | |||||||
| chr16:30499687 | G | GTATATAT others(19): Show |
1 | a0001c0005t0001g0291 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2145+221_2145+222i others(28): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499687 | ||||||
| chr16:30499701 | A | G | 3 | a0001c0001t0002g0194 a0002c0002t0004g0192 a0002c0002t0004g0193 |
3 | HG02145.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2145+212A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30499701 | |||||||
| chr16:30499707 | A | ATATGTAT others(25): Show |
2 | a0002c0002t0001g0049 a0002c0002t0001g0051 |
2 | HG01243.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.2145+221_2145+222i others(34): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499707 | ||||||
| chr16:30499709 | A | ATGTATAT others(23): Show |
1 | a0002c0002t0001g0033 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2145+221_2145+222i others(32): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499709 | ||||||
| chr16:30499711 | A | ATATGTAT others(23): Show |
1 | a0001c0001t0001g0134 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2145+223_2145+224i others(32): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499711 | ||||||
| chr16:30499711 | A | ATGTATAT others(21): Show |
52 | a0001c0001t0001g0018 a0001c0001t0001g0038 a0001c0001t0001g0040 others(49): Show |
52 | HG00639.hp2 HG00673.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.2145+233_2145+234i others(30): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499711 | ||||||
| chr16:30499712 | T | C | 1 | a0001c0005t0001g0291 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2145+223T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30499712 | |||||||
| chr16:30499712 | T | TGTATATA others(21): Show |
3 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0002c0002t0001g0031 |
3 | HG00438.hp2 NA18939.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2145+235_2145+236i others(30): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499712 | ||||||
| chr16:30499713 | G | A | 3 | a0002c0002t0001g0033 a0002c0002t0001g0049 a0002c0002t0001g0051 |
3 | HG01243.hp2 HG02602.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.2145+224G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30499713 | |||||||
| chr16:30499713 | G | GTATATAT others(23): Show |
1 | a0001c0001t0001g0086 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2145+235_2145+236i others(32): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499713 | ||||||
| chr16:30499713 | G | GTATATAT others(25): Show |
1 | a0002c0002t0001g0264 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2145+235_2145+236i others(34): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499713 | ||||||
| chr16:30499713 | G | GTATATAT others(27): Show |
78 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(75): Show |
82 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.2145+235_2145+236i others(36): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499713 | ||||||
| chr16:30499713 | G | GTATATAT others(29): Show |
11 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0005t0004g0292 others(8): Show |
12 | HG00408.hp2 HG00642.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.2145+235_2145+236i others(38): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499713 | ||||||
| chr16:30499713 | G | GTATATAT others(31): Show |
1 | a0002c0002t0001g0172 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2145+235_2145+236i others(40): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499713 | ||||||
| chr16:30499713 | G | GTATATAT others(37): Show |
1 | a0002c0023t0001g0190 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2145+235_2145+236i others(46): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499713 | ||||||
| chr16:30499713 | G | GTATATAT others(21): Show |
2 | a0001c0001t0003g0223 a0001c0001t0003g0224 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2145+233_2145+234i others(30): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499713 | ||||||
| chr16:30499713 | G | GTATATAT others(25): Show |
2 | a0002c0002t0001g0019 a0002c0002t0001g0028 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2145+233_2145+234i others(34): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499713 | ||||||
| chr16:30499713 | G | GTATATAT others(21): Show |
1 | a0003c0020t0001g0227 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2145+233_2145+234i others(30): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499713 | ||||||
| chr16:30499713 | G | GTATATAT others(23): Show |
3 | a0001c0001t0001g0125 a0001c0001t0001g0208 a0001c0001t0001g0270 |
3 | HG00280.hp2 HG00639.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.2145+233_2145+234i others(32): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499713 | ||||||
| chr16:30499715 | A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0045 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2145+235_2145+236i others(31): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499715 | ||||||
| chr16:30499715 | A | ATATATAT others(21): Show |
37 | a0001c0001t0001g0006 a0001c0001t0001g0065 a0001c0001t0001g0069 others(34): Show |
37 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.2145+233_2145+234i others(30): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499715 | ||||||
| chr16:30499715 | A | G | 3 | a0001c0001t0002g0194 a0002c0002t0004g0192 a0002c0002t0004g0193 |
3 | HG02145.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2145+226A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30499715 | |||||||
| chr16:30499717 | A | ATATATGT others(19): Show |
1 | a0001c0001t0001g0115 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2145+233_2145+234i others(28): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499717 | ||||||
| chr16:30499717 | A | G | 3 | a0001c0001t0002g0194 a0002c0002t0004g0192 a0002c0002t0004g0193 |
3 | HG02145.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2145+228A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30499717 | |||||||
| chr16:30499721 | A | ATATGTGT others(27): Show |
1 | a0001c0001t0001g0087 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2145+235_2145+236i others(36): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499721 | ||||||
| chr16:30499723 | A | ATGTG | 37 | a0001c0001t0001g0178 a0001c0001t0001g0250 a0001c0001t0001g0275 others(34): Show |
38 | HG00621.hp2 HG01106.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.2145+235_2145+236i others(6): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499723 | ||||||
| chr16:30499730 | TA | T | 5 | a0001c0001t0001g0273 a0001c0001t0002g0271 a0001c0001t0002g0272 others(2): Show |
5 | HG02818.hp2 HG02886.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2145+242delA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30499730 | |||||||
| chr16:30499731 | A | AT | 3 | a0001c0001t0002g0194 a0002c0002t0001g0210 a0002c0002t0001g0219 |
3 | HG00280.hp1 HG00741.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2145+243dupT | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499731 | ||||||
| chr16:30499731 | A | ATT | 3 | a0002c0003t0002g0293 a0002c0003t0002g0304 a0009c0022t0001g0234 |
3 | HG01891.hp2 HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.2145+243_2145+244i others(4): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499731 | ||||||
| chr16:30499731 | A | T | 20 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0096 others(17): Show |
20 | HG00558.hp1 HG00673.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2145+242A>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30499731 | |||||||
| chr16:30499733 | A | AT | 12 | a0001c0001t0001g0045 a0001c0001t0001g0068 a0001c0001t0001g0179 others(9): Show |
12 | HG00408.hp2 HG00735.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.2145+257dupT | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499733 | ||||||
| chr16:30499733 | A | ATACATAT others(23): Show |
1 | a0002c0003t0001g0308 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2145+245_2145+246i others(32): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499733 | ||||||
| chr16:30499733 | A | ATACGTAT others(28): Show |
1 | a0002c0002t0001g0003 | 2 | HG02040.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.2145+245_2145+246i others(37): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499733 | ||||||
| chr16:30499733 | A | ATACGTAT others(26): Show |
10 | a0002c0002t0001g0021 a0002c0002t0001g0029 a0002c0002t0001g0030 others(7): Show |
10 | HG02132.hp2 HG02738.hp2 HG03491.hp1 others(7): Show |
intron_variant | MODIFIER | c.2145+245_2145+246i others(35): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499733 | ||||||
| chr16:30499733 | A | ATACGTAT others(28): Show |
4 | a0001c0005t0001g0050 a0001c0005t0001g0258 a0001c0005t0001g0259 others(1): Show |
4 | HG01106.hp1 HG02486.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2145+245_2145+246i others(37): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499733 | ||||||
| chr16:30499733 | A | ATACGTAT others(25): Show |
1 | a0002c0016t0006g0233 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2145+245_2145+246i others(34): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499733 | ||||||
| chr16:30499733 | A | ATACGTAT others(26): Show |
2 | a0001c0001t0001g0178 a0002c0002t0001g0054 |
2 | HG00621.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.2145+245_2145+246i others(35): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499733 | ||||||
| chr16:30499733 | A | ATACGTAT others(28): Show |
10 | a0001c0001t0001g0250 a0001c0001t0001g0275 a0001c0001t0001g0282 others(7): Show |
10 | HG02615.hp1 HG02717.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2145+245_2145+246i others(37): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499733 | ||||||
| chr16:30499733 | A | ATACGTAT others(22): Show |
3 | a0002c0003t0001g0299 a0002c0003t0001g0300 a0002c0003t0005g0298 |
3 | HG02280.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2145+245_2145+246i others(31): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499733 | ||||||
| chr16:30499733 | A | ATACGTAT others(23): Show |
1 | a0002c0008t0001g0265 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2145+245_2145+246i others(32): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499733 | ||||||
| chr16:30499733 | A | ATACGTAT others(28): Show |
2 | a0001c0001t0001g0276 a0001c0004t0001g0302 |
2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2145+245_2145+246i others(37): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499733 | ||||||
| chr16:30499733 | A | ATACGTAT others(22): Show |
1 | a0002c0003t0005g0284 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2145+245_2145+246i others(31): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499733 | ||||||
| chr16:30499733 | A | ATATGTAT others(23): Show |
1 | a0002c0008t0001g0222 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2145+245_2145+246i others(32): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499733 | ||||||
| chr16:30499733 | A | ATGTATAT others(52): Show |
1 | a0002c0002t0001g0095 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2145+245_2145+246i others(61): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499733 | ||||||
| chr16:30499733 | A | ATTT | 35 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0032 others(32): Show |
36 | HG00438.hp2 HG00642.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.2145+255_2145+257d others(5): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30499733 | ||||||
| chr16:30499733 | A | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(109): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.2145+244A>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30499733 | |||||||
| chr16:30499734 | T | TA | 6 | a0001c0001t0001g0115 a0001c0001t0001g0121 a0001c0001t0001g0157 others(3): Show |
6 | HG01261.hp2 HG01928.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.2145+245_2145+246i others(3): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30499734 | |||||||
| chr16:30499734 | T | TATGTATA others(18): Show |
1 | a0010c0012t0001g0260 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2145+245_2145+246i others(27): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30499734 | |||||||
| chr16:30499735 | T | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0070 a0001c0001t0001g0122 others(5): Show |
9 | HG00140.hp1 HG00741.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.2145+246T>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30499735 | |||||||
| chr16:30500057 | A | ATTAT | 21 | a0001c0001t0001g0066 a0001c0001t0001g0078 a0001c0001t0001g0079 others(18): Show |
21 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.2145+611_2145+614d others(6): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30500057 | ||||||
| chr16:30500057 | ATTAT | A | 114 | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0035 others(111): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2145+611_2145+614d others(6): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30500057 | ||||||
| chr16:30500057 | ATTATTTA others(1): Show |
A | 4 | a0001c0001t0001g0001 a0002c0002t0001g0166 a0002c0002t0004g0192 others(1): Show |
4 | HG01943.hp1 HG02145.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2145+607_2145+614d others(10): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30500057 | ||||||
| chr16:30500057 | ATTATTTA others(5): Show |
A | 14 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0074 others(11): Show |
16 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.2145+603_2145+614d others(14): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30500057 | ||||||
| chr16:30500061 | T | G | 1 | a0002c0002t0001g0139 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2145+572T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30500061 | |||||||
| chr16:30500072 | A | T | 1 | a0001c0001t0001g0045 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2145+583A>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30500072 | |||||||
| chr16:30500073 | T | G | 1 | a0001c0001t0001g0045 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2145+584T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30500073 | |||||||
| chr16:30500074 | T | A | 1 | a0001c0001t0001g0045 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2145+585T>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30500074 | |||||||
| chr16:30500076 | A | T | 1 | a0001c0001t0001g0045 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2145+587A>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30500076 | |||||||
| chr16:30500078 | T | C | 1 | a0001c0001t0001g0045 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2145+589T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30500078 | |||||||
| chr16:30500188 | C | T | 1 | a0001c0004t0001g0290 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2145+699C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30500188 | |||||||
| chr16:30500227 | A | G | 4 | a0002c0002t0001g0200 a0002c0002t0001g0205 a0002c0002t0001g0206 others(1): Show |
4 | HG01192.hp2 HG01361.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.2145+738A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30500227 | |||||||
| chr16:30500303 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2145+814C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30500303 | |||||||
| chr16:30500308 | A | C | 71 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0032 others(68): Show |
73 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.2145+819A>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30500308 | |||||||
| chr16:30500419 | T | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(237): Show |
246 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.2145+930T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30500419 | |||||||
| chr16:30500521 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2145+1032T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30500521 | |||||||
| chr16:30500527 | G | T | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(278): Show |
287 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.2145+1038G>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30500527 | |||||||
| chr16:30500531 | T | C | 3 | a0001c0001t0002g0194 a0002c0002t0004g0192 a0002c0002t0004g0193 |
3 | HG02145.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2145+1042T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30500531 | |||||||
| chr16:30500541 | T | A | 5 | a0001c0001t0001g0273 a0001c0001t0002g0271 a0001c0001t0002g0272 others(2): Show |
5 | HG02818.hp2 HG02886.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2145+1052T>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30500541 | |||||||
| chr16:30500863 | G | A | 2 | a0002c0002t0001g0013 a0002c0002t0001g0017 |
2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2145+1374G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30500863 | |||||||
| chr16:30501004 | C | CA | 12 | a0001c0001t0001g0062 a0001c0001t0001g0067 a0001c0001t0001g0074 others(9): Show |
12 | HG01192.hp1 HG01258.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.2145+1529dupA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30501004 | ||||||
| chr16:30501106 | A | G | 3 | a0001c0001t0002g0194 a0002c0002t0004g0192 a0002c0002t0004g0193 |
3 | HG02145.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2145+1617A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30501106 | |||||||
| chr16:30501122 | G | A | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(245): Show |
254 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(251): Show |
intron_variant | MODIFIER | c.2145+1633G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30501122 | |||||||
| chr16:30501342 | G | A | 1 | a0002c0002t0001g0010 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2145+1853G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30501342 | |||||||
| chr16:30501399 | A | T | 1 | a0001c0001t0001g0058 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2145+1910A>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30501399 | |||||||
| chr16:30501469 | TG | T | 5 | a0001c0001t0001g0273 a0001c0001t0002g0271 a0001c0001t0002g0272 others(2): Show |
5 | HG02818.hp2 HG02886.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2145+1983delG | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30501469 | ||||||
| chr16:30501577 | CA | C | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(232): Show |
241 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.2145+2105delA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30501577 | ||||||
| chr16:30501684 | G | GT | 307 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(304): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2145+2195_2145+219 others(5): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30501684 | |||||||
| chr16:30501685 | A | T | 1 | a0001c0001t0001g0045 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2145+2196A>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30501685 | |||||||
| chr16:30501686 | T | A | 1 | a0001c0001t0001g0045 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2145+2197T>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30501686 | |||||||
| chr16:30501767 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2145+2278C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30501767 | |||||||
| chr16:30501910 | G | A | 4 | a0001c0001t0002g0194 a0001c0001t0003g0195 a0002c0002t0004g0192 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2146-2265G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30501910 | |||||||
| chr16:30502129 | G | A | 1 | a0002c0008t0001g0222 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2146-2046G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30502129 | |||||||
| chr16:30502131 | C | A | 1 | a0002c0008t0001g0222 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2146-2044C>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30502131 | |||||||
| chr16:30502164 | A | G | 5 | a0002c0002t0001g0204 a0002c0002t0001g0210 a0002c0002t0001g0212 others(2): Show |
5 | HG00280.hp1 HG00741.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.2146-2011A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30502164 | |||||||
| chr16:30502175 | A | C | 1 | a0002c0003t0001g0308 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2146-2000A>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30502175 | |||||||
| chr16:30502185 | G | C | 2 | a0001c0001t0003g0195 a0008c0021t0001g0305 |
2 | HG01496.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2146-1990G>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30502185 | |||||||
| chr16:30502193 | T | C | 10 | a0001c0001t0001g0086 a0001c0001t0001g0101 a0001c0001t0001g0230 others(7): Show |
10 | HG00099.hp1 HG01346.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.2146-1982T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30502193 | |||||||
| chr16:30502193 | T | G | 29 | a0001c0001t0001g0232 a0001c0001t0001g0250 a0001c0001t0001g0253 others(26): Show |
29 | HG01106.hp1 HG01168.hp2 HG01515.hp1 others(26): Show |
intron_variant | MODIFIER | c.2146-1982T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30502193 | |||||||
| chr16:30502198 | C | T | 2 | a0001c0001t0001g0213 a0001c0001t0001g0217 |
2 | HG01358.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2146-1977C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30502198 | |||||||
| chr16:30502229 | C | T | 96 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0045 others(93): Show |
97 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.2146-1946C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30502229 | |||||||
| chr16:30502253 | T | C | 1 | a0002c0008t0001g0222 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2146-1922T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30502253 | |||||||
| chr16:30502314 | A | G | 1 | a0002c0002t0001g0229 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2146-1861A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30502314 | |||||||
| chr16:30502396 | C | CA | 6 | a0001c0001t0001g0082 a0001c0001t0001g0184 a0001c0001t0001g0196 others(3): Show |
6 | HG00642.hp1 HG01928.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.2146-1755dupA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30502396 | ||||||
| chr16:30502396 | CA | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(132): Show |
140 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.2146-1755delA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30502396 | ||||||
| chr16:30502396 | CAAAAAAA others(6): Show |
C | 3 | a0002c0002t0001g0013 a0002c0002t0001g0017 a0002c0003t0001g0228 |
3 | HG02257.hp1 HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2146-1767_2146-175 others(17): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30502396 | ||||||
| chr16:30502396 | CAAAAAAA others(9): Show |
C | 96 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0045 others(93): Show |
97 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.2146-1770_2146-175 others(20): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30502396 | ||||||
| chr16:30502423 | A | C | 5 | a0001c0001t0001g0273 a0001c0001t0002g0271 a0001c0001t0002g0272 others(2): Show |
5 | HG02818.hp2 HG02886.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2146-1752A>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30502423 | |||||||
| chr16:30502667 | G | A | 1 | a0002c0002t0001g0031 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2146-1508G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30502667 | |||||||
| chr16:30502720 | C | G | 5 | a0001c0001t0001g0199 a0001c0001t0001g0202 a0001c0001t0001g0215 others(2): Show |
5 | HG00099.hp2 HG00140.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.2146-1455C>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30502720 | |||||||
| chr16:30502748 | C | CA | 11 | a0001c0001t0001g0011 a0001c0001t0001g0093 a0001c0001t0001g0122 others(8): Show |
11 | HG00438.hp1 HG02080.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.2146-1412dupA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30502748 | ||||||
| chr16:30502748 | CA | C | 8 | a0001c0001t0001g0073 a0001c0001t0001g0110 a0001c0001t0001g0154 others(5): Show |
8 | HG01168.hp2 HG01515.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.2146-1412delA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30502748 | ||||||
| chr16:30502782 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(134): Show |
142 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.2146-1393G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30502782 | |||||||
| chr16:30502816 | AC | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(130): Show |
138 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.2146-1358delC | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30502816 | |||||||
| chr16:30502816 | ACT | A | 4 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0140 others(1): Show |
4 | HG00639.hp2 HG00738.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.2146-1358_2146-135 others(6): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30502816 | |||||||
| chr16:30502818 | T | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(130): Show |
138 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.2146-1357T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30502818 | |||||||
| chr16:30502819 | T | G | 4 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0140 others(1): Show |
4 | HG00639.hp2 HG00738.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.2146-1356T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30502819 | |||||||
| chr16:30502922 | C | T | 1 | a0001c0001t0003g0255 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2146-1253C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30502922 | |||||||
| chr16:30502975 | T | C | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(246): Show |
255 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(252): Show |
intron_variant | MODIFIER | c.2146-1200T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30502975 | |||||||
| chr16:30503002 | A | G | 1 | a0002c0002t0001g0010 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2146-1173A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30503002 | |||||||
| chr16:30503149 | C | T | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(246): Show |
255 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(252): Show |
intron_variant | MODIFIER | c.2146-1026C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30503149 | |||||||
| chr16:30503155 | A | G | 1 | a0002c0008t0001g0222 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2146-1020A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30503155 | |||||||
| chr16:30503402 | C | T | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(246): Show |
255 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(252): Show |
intron_variant | MODIFIER | c.2146-773C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30503402 | |||||||
| chr16:30503422 | C | T | 1 | a0002c0002t0001g0252 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2146-753C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30503422 | |||||||
| chr16:30503441 | C | CT | 141 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
146 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.2146-721dupT | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30503441 | ||||||
| chr16:30503441 | CT | C | 95 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0018 others(92): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.2146-721delT | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30503441 | ||||||
| chr16:30503455 | C | A | 1 | a0002c0002t0001g0225 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2146-720C>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30503455 | |||||||
| chr16:30503465 | G | A | 1 | a0002c0003t0005g0298 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2146-710G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30503465 | |||||||
| chr16:30503485 | A | G | 1 | a0001c0004t0001g0285 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2146-690A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30503485 | |||||||
| chr16:30503530 | G | A | 1 | a0002c0002t0004g0192 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2146-645G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | chr16 | 30503530 | |||||||
| chr16:30503543 | AAGGG | A | 4 | a0001c0001t0001g0058 a0001c0001t0001g0073 a0001c0001t0001g0075 others(1): Show |
4 | HG03831.hp1 NA18941.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.2146-616_2146-613d others(6): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr16 | 30503543 | ||||||
| chr16:30504328 | C | T | 65 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0045 others(62): Show |
66 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.2235+64C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 18/30 | chr16 | 30504328 | |||||||
| chr16:30504336 | G | T | 1 | a0002c0003t0001g0308 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2235+72G>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 18/30 | chr16 | 30504336 | |||||||
| chr16:30504443 | C | T | 4 | a0001c0005t0001g0226 a0003c0020t0001g0227 a0004c0010t0001g0306 others(1): Show |
4 | HG01884.hp1 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2235+179C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 18/30 | chr16 | 30504443 | |||||||
| chr16:30504572 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0185 |
2 | HG00673.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.2235+308G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 18/30 | chr16 | 30504572 | |||||||
| chr16:30504718 | A | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
150 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.2235+454A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 18/30 | chr16 | 30504718 | |||||||
| chr16:30504721 | A | G | 10 | a0001c0001t0001g0253 a0001c0001t0001g0294 a0001c0001t0004g0267 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.2235+457A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 18/30 | chr16 | 30504721 | |||||||
| chr16:30504827 | C | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(122): Show |
130 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.2236-417C>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 18/30 | chr16 | 30504827 | |||||||
| chr16:30504870 | A | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0185 |
2 | HG00673.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.2236-374A>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 18/30 | chr16 | 30504870 | |||||||
| chr16:30505018 | T | TA | 97 | a0001c0001t0001g0032 a0001c0001t0001g0043 a0001c0001t0001g0045 others(94): Show |
99 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.2236-208dupA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr16 | 30505018 | ||||||
| chr16:30505018 | TA | T | 6 | a0001c0001t0001g0075 a0001c0001t0001g0092 a0001c0001t0001g0232 others(3): Show |
6 | HG00558.hp2 HG01069.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.2236-208delA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr16 | 30505018 | ||||||
| chr16:30505171 | A | G | 190 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(187): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.2236-73A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 18/30 | chr16 | 30505171 | |||||||
| chr16:30505210 | C | T | 19 | a0001c0001t0001g0232 a0001c0001t0001g0250 a0001c0001t0001g0266 others(16): Show |
19 | HG01106.hp1 HG01168.hp2 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.2236-34C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 18/30 | chr16 | 30505210 | |||||||
| chr16:30505316 | G | A | 4 | a0001c0001t0001g0072 a0001c0001t0001g0089 a0001c0001t0001g0090 others(1): Show |
4 | NA18990.hp2 NA19000.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.2292+16G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 19/30 | chr16 | 30505316 | |||||||
| chr16:30505617 | C | T | 1 | a0006c0027t0001g0136 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2366+155C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 20/30 | chr16 | 30505617 | |||||||
| chr16:30505655 | G | C | 3 | a0001c0001t0001g0073 a0001c0001t0001g0075 a0013c0018t0001g0071 |
3 | NA18941.hp2 NA18960.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.2366+193G>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 20/30 | chr16 | 30505655 | |||||||
| chr16:30505769 | A | G | 253 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(250): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.2366+307A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 20/30 | chr16 | 30505769 | |||||||
| chr16:30505918 | A | G | 6 | a0001c0001t0003g0195 a0001c0001t0003g0223 a0001c0001t0003g0224 others(3): Show |
6 | HG01884.hp2 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2366+456A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 20/30 | chr16 | 30505918 | |||||||
| chr16:30505986 | G | A | 1 | a0002c0002t0001g0236 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2366+524G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 20/30 | chr16 | 30505986 | |||||||
| chr16:30506002 | A | G | 1 | a0002c0002t0001g0191 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2366+540A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 20/30 | chr16 | 30506002 | |||||||
| chr16:30506123 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(62): Show |
69 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.2367-592G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 20/30 | chr16 | 30506123 | |||||||
| chr16:30506222 | T | C | 2 | a0002c0002t0001g0229 a0002c0002t0001g0236 |
2 | HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.2367-493T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 20/30 | chr16 | 30506222 | |||||||
| chr16:30506262 | T | TA | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
92 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.2367-437dupA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr16 | 30506262 | ||||||
| chr16:30506262 | T | TAA | 65 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0111 others(62): Show |
65 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.2367-438_2367-437d others(4): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr16 | 30506262 | ||||||
| chr16:30506262 | T | TAAA | 62 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0002c0002t0001g0003 others(59): Show |
63 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.2367-439_2367-437d others(5): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr16 | 30506262 | ||||||
| chr16:30506262 | T | TAAAA | 12 | a0002c0002t0001g0044 a0002c0002t0001g0211 a0002c0002t0001g0235 others(9): Show |
12 | HG01361.hp2 HG02622.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.2367-440_2367-437d others(6): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr16 | 30506262 | ||||||
| chr16:30506308 | C | A | 1 | a0001c0004t0001g0286 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2367-407C>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 20/30 | chr16 | 30506308 | |||||||
| chr16:30506397 | CA | C | 125 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0111 others(122): Show |
126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.2367-306delA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr16 | 30506397 | ||||||
| chr16:30506418 | G | T | 1 | a0001c0005t0001g0291 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2367-297G>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 20/30 | chr16 | 30506418 | |||||||
| chr16:30506436 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2367-279G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 20/30 | chr16 | 30506436 | |||||||
| chr16:30506452 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2367-263G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 20/30 | chr16 | 30506452 | |||||||
| chr16:30506558 | C | CA | 61 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0045 others(58): Show |
64 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.2367-121dupA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr16 | 30506558 | ||||||
| chr16:30506558 | C | CAA | 19 | a0001c0001t0001g0067 a0001c0001t0001g0107 a0001c0001t0001g0109 others(16): Show |
19 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.2367-122_2367-121d others(4): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr16 | 30506558 | ||||||
| chr16:30506558 | CA | C | 14 | a0001c0001t0001g0011 a0001c0001t0001g0052 a0001c0001t0001g0064 others(11): Show |
14 | HG01070.hp2 HG01106.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.2367-121delA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr16 | 30506558 | ||||||
| chr16:30506558 | CAAAAAAA others(4): Show |
C | 6 | a0002c0002t0001g0031 a0002c0002t0001g0108 a0002c0002t0001g0172 others(3): Show |
6 | HG00741.hp1 HG02055.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.2367-131_2367-121d others(13): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr16 | 30506558 | ||||||
| chr16:30506558 | CAAAAAAA others(5): Show |
C | 84 | a0002c0002t0001g0003 a0002c0002t0001g0009 a0002c0002t0001g0010 others(81): Show |
85 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.2367-132_2367-121d others(14): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr16 | 30506558 | ||||||
| chr16:30506558 | CAAAAAAA others(6): Show |
C | 9 | a0002c0002t0001g0022 a0002c0002t0001g0030 a0002c0002t0001g0095 others(6): Show |
9 | HG01891.hp2 HG01943.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.2367-133_2367-121d others(15): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr16 | 30506558 | ||||||
| chr16:30506558 | CAAAAAAA others(8): Show |
C | 33 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0111 others(30): Show |
33 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.2367-135_2367-121d others(17): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr16 | 30506558 | ||||||
| chr16:30506860 | G | A | 3 | a0002c0002t0001g0009 a0002c0002t0001g0023 a0002c0002t0001g0042 |
3 | HG03654.hp1 HG04184.hp1 NA20905.hp1 |
splice_region_variant&intron_variant | LOW | c.2508+4G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30506860 | |||||||
| chr16:30506983 | C | T | 4 | a0002c0003t0001g0299 a0002c0003t0005g0284 a0002c0003t0005g0297 others(1): Show |
4 | HG02280.hp1 HG03139.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2508+127C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30506983 | |||||||
| chr16:30507251 | A | G | 1 | a0002c0002t0001g0191 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2508+395A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30507251 | |||||||
| chr16:30507337 | T | C | 7 | a0001c0001t0001g0078 a0001c0001t0001g0081 a0001c0001t0001g0103 others(4): Show |
7 | HG00597.hp1 HG01496.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.2508+481T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30507337 | |||||||
| chr16:30507376 | A | G | 2 | a0001c0001t0001g0232 a0001c0001t0001g0266 |
2 | HG01168.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.2508+520A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30507376 | |||||||
| chr16:30507450 | T | G | 1 | a0001c0001t0001g0188 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2508+594T>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30507450 | |||||||
| chr16:30507457 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0140 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2508+623_2508+634d others(14): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr16 | 30507457 | ||||||
| chr16:30507468 | C | CA | 6 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0003g0195 others(3): Show |
6 | HG00140.hp1 HG01192.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.2508+623dupA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr16 | 30507468 | ||||||
| chr16:30507476 | A | G | 1 | a0001c0004t0001g0289 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2508+620A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30507476 | |||||||
| chr16:30507479 | A | C | 1 | a0001c0001t0001g0147 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2508+623A>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30507479 | |||||||
| chr16:30507480 | C | CA | 7 | a0001c0001t0001g0068 a0001c0001t0001g0250 a0001c0001t0001g0253 others(4): Show |
7 | HG02258.hp2 NA18990.hp1 NA19000.hp1 others(4): Show |
intron_variant | MODIFIER | c.2508+634dupA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr16 | 30507480 | ||||||
| chr16:30507631 | T | C | 1 | a0002c0002t0001g0042 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2508+775T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30507631 | |||||||
| chr16:30507649 | CA | C | 15 | a0001c0001t0001g0018 a0001c0001t0001g0131 a0001c0001t0001g0232 others(12): Show |
15 | HG01256.hp2 HG01515.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.2508+806delA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr16 | 30507649 | ||||||
| chr16:30507939 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2508+1083C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30507939 | |||||||
| chr16:30508027 | G | T | 68 | a0002c0002t0001g0003 a0002c0002t0001g0009 a0002c0002t0001g0010 others(65): Show |
69 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.2508+1171G>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30508027 | |||||||
| chr16:30508209 | A | AT | 17 | a0001c0001t0001g0059 a0001c0001t0001g0066 a0001c0001t0001g0080 others(14): Show |
17 | HG02056.hp1 HG02074.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.2508+1374dupT | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr16 | 30508209 | ||||||
| chr16:30508209 | AT | A | 113 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0111 others(110): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.2508+1374delT | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr16 | 30508209 | ||||||
| chr16:30508300 | G | A | 7 | a0001c0001t0001g0048 a0001c0005t0001g0256 a0003c0006t0001g0007 others(4): Show |
8 | HG00323.hp2 HG01109.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2508+1444G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30508300 | |||||||
| chr16:30508307 | A | G | 133 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0111 others(130): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.2508+1451A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30508307 | |||||||
| chr16:30508488 | C | T | 4 | a0001c0001t0001g0058 a0001c0001t0001g0073 a0001c0001t0001g0075 others(1): Show |
4 | HG03831.hp1 NA18941.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.2508+1632C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30508488 | |||||||
| chr16:30508533 | C | T | 4 | a0002c0002t0001g0013 a0002c0002t0001g0017 a0002c0002t0001g0264 others(1): Show |
4 | HG02257.hp1 HG02486.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2508+1677C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30508533 | |||||||
| chr16:30508564 | G | C | 5 | a0002c0002t0001g0013 a0002c0002t0001g0017 a0002c0002t0001g0264 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2508+1708G>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30508564 | |||||||
| chr16:30508573 | C | T | 3 | a0002c0002t0001g0204 a0002c0002t0001g0212 a0002c0002t0001g0261 |
3 | HG01175.hp2 HG01255.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.2508+1717C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30508573 | |||||||
| chr16:30508749 | C | T | 8 | a0001c0001t0001g0065 a0001c0001t0001g0110 a0001c0001t0001g0116 others(5): Show |
8 | HG01175.hp1 HG01978.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.2509-1612C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30508749 | |||||||
| chr16:30508837 | C | T | 1 | a0002c0002t0001g0042 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2509-1524C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30508837 | |||||||
| chr16:30508890 | A | T | 2 | a0002c0002t0001g0085 a0005c0024t0001g0083 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2509-1471A>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30508890 | |||||||
| chr16:30508914 | C | T | 1 | a0001c0005t0001g0291 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2509-1447C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30508914 | |||||||
| chr16:30509035 | G | A | 1 | a0002c0002t0001g0022 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2509-1326G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30509035 | |||||||
| chr16:30509168 | C | T | 1 | a0003c0006t0001g0015 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2509-1193C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30509168 | |||||||
| chr16:30509176 | C | CA | 7 | a0001c0001t0001g0072 a0001c0001t0001g0079 a0001c0001t0001g0154 others(4): Show |
7 | HG02257.hp1 HG02486.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.2509-1169dupA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr16 | 30509176 | ||||||
| chr16:30509176 | CA | C | 10 | a0001c0001t0001g0075 a0001c0001t0001g0102 a0001c0001t0001g0105 others(7): Show |
10 | HG01099.hp2 HG01167.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.2509-1169delA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr16 | 30509176 | ||||||
| chr16:30509191 | A | G | 5 | a0002c0007t0001g0037 a0002c0007t0001g0128 a0002c0007t0001g0221 others(2): Show |
5 | HG01243.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.2509-1170A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30509191 | |||||||
| chr16:30509467 | C | T | 4 | a0001c0001t0001g0273 a0001c0001t0002g0271 a0001c0001t0002g0272 others(1): Show |
4 | HG02818.hp2 HG02886.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2509-894C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30509467 | |||||||
| chr16:30509491 | C | T | 1 | a0001c0001t0003g0195 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2509-870C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30509491 | |||||||
| chr16:30509535 | C | T | 32 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0111 others(29): Show |
32 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.2509-826C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30509535 | |||||||
| chr16:30509717 | C | T | 7 | a0001c0001t0001g0018 a0001c0001t0001g0070 a0001c0001t0001g0160 others(4): Show |
7 | NA18944.hp2 NA18945.hp2 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.2509-644C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30509717 | |||||||
| chr16:30510040 | A | T | 3 | a0002c0008t0001g0222 a0002c0008t0001g0265 a0002c0008t0001g0274 |
3 | HG01884.hp2 HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2509-321A>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30510040 | |||||||
| chr16:30510053 | A | T | 2 | a0001c0001t0001g0107 a0001c0001t0001g0109 |
2 | HG00408.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.2509-308A>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30510053 | |||||||
| chr16:30510053 | AT | A | 126 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0111 others(123): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.2509-300delT | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr16 | 30510053 | ||||||
| chr16:30510054 | T | A | 5 | a0001c0001t0003g0254 a0001c0001t0003g0255 a0002c0002t0001g0041 others(2): Show |
5 | HG02132.hp1 HG02970.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2509-307T>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 21/30 | chr16 | 30510054 | |||||||
| chr16:30510811 | T | C | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG00423.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.2620-70T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 22/30 | chr16 | 30510811 | |||||||
| chr16:30510831 | G | A | 30 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0111 others(27): Show |
30 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.2620-50G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 22/30 | chr16 | 30510831 | |||||||
| chr16:30511022 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2700-28C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 23/30 | chr16 | 30511022 | |||||||
| chr16:30511466 | C | T | 4 | a0003c0006t0001g0007 a0003c0006t0001g0014 a0003c0006t0001g0015 others(1): Show |
5 | HG01109.hp1 HG02809.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.2786+330C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 24/30 | chr16 | 30511466 | |||||||
| chr16:30511487 | A | T | 2 | a0002c0002t0001g0056 a0002c0002t0001g0169 |
2 | HG02132.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2786+351A>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 24/30 | chr16 | 30511487 | |||||||
| chr16:30511518 | A | G | 1 | a0001c0001t0003g0195 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2786+382A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 24/30 | chr16 | 30511518 | |||||||
| chr16:30511749 | C | T | 1 | a0002c0002t0001g0264 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2786+613C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 24/30 | chr16 | 30511749 | |||||||
| chr16:30511838 | C | A | 1 | a0002c0002t0001g0023 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2786+702C>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 24/30 | chr16 | 30511838 | |||||||
| chr16:30511925 | A | G | 4 | a0001c0001t0001g0278 a0001c0005t0001g0050 a0001c0005t0001g0258 others(1): Show |
4 | HG01106.hp1 HG02630.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2786+789A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 24/30 | chr16 | 30511925 | |||||||
| chr16:30512587 | A | G | 33 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0111 others(30): Show |
33 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.2787-1184A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 24/30 | chr16 | 30512587 | |||||||
| chr16:30512782 | C | T | 5 | a0001c0001t0001g0273 a0001c0001t0001g0294 a0001c0001t0002g0271 others(2): Show |
5 | HG02818.hp2 HG02886.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2787-989C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 24/30 | chr16 | 30512782 | |||||||
| chr16:30512979 | G | A | 5 | a0002c0002t0001g0133 a0002c0002t0001g0139 a0002c0002t0001g0172 others(2): Show |
5 | HG00408.hp2 NA18950.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.2787-792G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 24/30 | chr16 | 30512979 | |||||||
| chr16:30512990 | C | T | 1 | a0001c0005t0004g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2787-781C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 24/30 | chr16 | 30512990 | |||||||
| chr16:30513355 | C | T | 70 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0032 others(67): Show |
70 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.2787-416C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 24/30 | chr16 | 30513355 | |||||||
| chr16:30513478 | G | C | 1 | a0002c0002t0001g0053 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2787-293G>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 24/30 | chr16 | 30513478 | |||||||
| chr16:30514277 | A | AT | 8 | a0001c0001t0001g0059 a0001c0001t0001g0074 a0001c0001t0001g0082 others(5): Show |
8 | HG01261.hp1 HG01928.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.2862+448dupT | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 25/30 | INFO_REALIGN_3_PRIME | chr16 | 30514277 | ||||||
| chr16:30514410 | GGGATTAC others(1): Show |
G | 3 | a0002c0002t0001g0133 a0002c0002t0001g0174 a0002c0002t0001g0186 |
3 | NA18953.hp2 NA18971.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.2862+567_2862+574d others(10): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 25/30 | INFO_REALIGN_3_PRIME | chr16 | 30514410 | ||||||
| chr16:30514526 | CGT | C | 202 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0032 others(199): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.2862+682_2862+683d others(4): Show |
ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 25/30 | INFO_REALIGN_3_PRIME | chr16 | 30514526 | ||||||
| chr16:30514613 | G | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0161 a0001c0001t0001g0165 |
3 | NA18979.hp1 NA19010.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.2862+767G>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 25/30 | chr16 | 30514613 | |||||||
| chr16:30514756 | C | T | 1 | a0002c0002t0001g0251 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2862+910C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 25/30 | chr16 | 30514756 | |||||||
| chr16:30514825 | CT | C | 99 | a0001c0001t0001g0074 a0001c0001t0001g0240 a0001c0001t0001g0278 others(96): Show |
100 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.2862+996delT | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 25/30 | INFO_REALIGN_3_PRIME | chr16 | 30514825 | ||||||
| chr16:30514934 | C | T | 1 | a0002c0002t0001g0029 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2862+1088C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 25/30 | chr16 | 30514934 | |||||||
| chr16:30514984 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2862+1138C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 25/30 | chr16 | 30514984 | |||||||
| chr16:30515076 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2862+1230C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 25/30 | chr16 | 30515076 | |||||||
| chr16:30515459 | C | T | 3 | a0001c0001t0003g0254 a0001c0001t0003g0255 a0002c0002t0001g0238 |
3 | HG02970.hp2 HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2863-1514C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 25/30 | chr16 | 30515459 | |||||||
| chr16:30515476 | C | T | 6 | a0002c0002t0001g0237 a0002c0002t0001g0251 a0002c0002t0001g0257 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2863-1497C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 25/30 | chr16 | 30515476 | |||||||
| chr16:30515478 | C | G | 1 | a0003c0020t0001g0227 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2863-1495C>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 25/30 | chr16 | 30515478 | |||||||
| chr16:30515516 | C | G | 1 | a0001c0001t0003g0195 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2863-1457C>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 25/30 | chr16 | 30515516 | |||||||
| chr16:30515690 | G | T | 1 | a0001c0001t0002g0194 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2863-1283G>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 25/30 | chr16 | 30515690 | |||||||
| chr16:30515788 | A | G | 1 | a0002c0002t0001g0170 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2863-1185A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 25/30 | chr16 | 30515788 | |||||||
| chr16:30515970 | T | TA | 6 | a0001c0001t0001g0066 a0001c0001t0001g0121 a0001c0001t0001g0183 others(3): Show |
6 | HG01978.hp2 HG02738.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2863-987dupA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 25/30 | INFO_REALIGN_3_PRIME | chr16 | 30515970 | ||||||
| chr16:30516010 | A | G | 5 | a0001c0001t0001g0072 a0001c0001t0001g0079 a0001c0001t0001g0089 others(2): Show |
5 | NA18968.hp2 NA18990.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.2863-963A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 25/30 | chr16 | 30516010 | |||||||
| chr16:30516077 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2863-896C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 25/30 | chr16 | 30516077 | |||||||
| chr16:30516232 | AT | A | 7 | a0001c0001t0001g0106 a0001c0001t0001g0154 a0001c0001t0001g0156 others(4): Show |
7 | HG02258.hp2 NA18939.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.2863-726delT | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 25/30 | INFO_REALIGN_3_PRIME | chr16 | 30516232 | ||||||
| chr16:30516269 | G | A | 12 | a0001c0001t0003g0223 a0001c0001t0003g0224 a0001c0005t0001g0256 others(9): Show |
13 | HG01109.hp1 HG02145.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2863-704G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 25/30 | chr16 | 30516269 | |||||||
| chr16:30516419 | G | A | 2 | a0001c0001t0003g0254 a0001c0001t0003g0255 |
2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2863-554G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 25/30 | chr16 | 30516419 | |||||||
| chr16:30516673 | G | A | 2 | a0002c0002t0001g0039 a0002c0002t0001g0051 |
2 | HG01074.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.2863-300G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 25/30 | chr16 | 30516673 | |||||||
| chr16:30516758 | C | T | 7 | a0001c0001t0001g0269 a0001c0009t0001g0046 a0001c0009t0001g0060 others(4): Show |
7 | HG01256.hp1 HG01258.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.2863-215C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 25/30 | chr16 | 30516758 | |||||||
| chr16:30516811 | C | T | 26 | a0001c0001t0001g0008 a0001c0001t0001g0239 a0001c0001t0001g0243 others(23): Show |
27 | HG00140.hp1 HG00741.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.2863-162C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 25/30 | chr16 | 30516811 | |||||||
| chr16:30516851 | G | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0113 |
2 | HG02071.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.2863-122G>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 25/30 | chr16 | 30516851 | |||||||
| chr16:30516951 | C | A | 36 | a0001c0001t0001g0008 a0001c0001t0001g0239 a0001c0001t0001g0243 others(33): Show |
38 | HG00140.hp1 HG00741.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.2863-22C>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 25/30 | chr16 | 30516951 | |||||||
| chr16:30517290 | A | G | 80 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0081 others(77): Show |
81 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.2976+204A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 26/30 | chr16 | 30517290 | |||||||
| chr16:30517434 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2977-215G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 26/30 | chr16 | 30517434 | |||||||
| chr16:30517900 | T | C | 1 | a0002c0007t0001g0037 | 1 | HG01243.hp1 | splice_region_variant&intron_variant | LOW | c.3132+5T>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 28/30 | chr16 | 30517900 | |||||||
| chr16:30517994 | G | C | 7 | a0001c0001t0002g0194 a0001c0001t0003g0195 a0002c0023t0001g0190 others(4): Show |
8 | HG01109.hp1 HG02622.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.3132+99G>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 28/30 | chr16 | 30517994 | |||||||
| chr16:30518046 | C | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0062 a0001c0001t0001g0067 others(5): Show |
9 | HG00558.hp1 HG00673.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.3132+151C>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 28/30 | chr16 | 30518046 | |||||||
| chr16:30518083 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3132+188G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 28/30 | chr16 | 30518083 | |||||||
| chr16:30518098 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3132+203C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 28/30 | chr16 | 30518098 | |||||||
| chr16:30518273 | C | A | 1 | a0001c0001t0001g0032 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3133-351C>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 28/30 | chr16 | 30518273 | |||||||
| chr16:30518448 | C | CA | 6 | a0001c0001t0001g0175 a0001c0001t0001g0269 a0001c0005t0001g0256 others(3): Show |
6 | HG00621.hp1 HG01192.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.3133-160dupA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 28/30 | INFO_REALIGN_3_PRIME | chr16 | 30518448 | ||||||
| chr16:30518448 | CA | C | 7 | a0001c0001t0001g0189 a0002c0002t0001g0013 a0002c0002t0001g0017 others(4): Show |
7 | HG01517.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.3133-160delA | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 28/30 | INFO_REALIGN_3_PRIME | chr16 | 30518448 | ||||||
| chr16:30518801 | G | C | 2 | a0001c0001t0001g0059 a0001c0001t0001g0113 |
2 | HG02071.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.3228+82G>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 29/30 | chr16 | 30518801 | |||||||
| chr16:30518871 | C | T | 1 | a0009c0022t0001g0234 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3228+152C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 29/30 | chr16 | 30518871 | |||||||
| chr16:30518945 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3228+226C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 29/30 | chr16 | 30518945 | |||||||
| chr16:30519003 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG02080.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.3228+284C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 29/30 | chr16 | 30519003 | |||||||
| chr16:30519014 | A | G | 1 | a0001c0001t0003g0195 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3228+295A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 29/30 | chr16 | 30519014 | |||||||
| chr16:30519380 | C | G | 1 | a0002c0003t0001g0299 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3229-477C>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 29/30 | chr16 | 30519380 | |||||||
| chr16:30519547 | A | C | 1 | a0001c0001t0003g0195 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3229-310A>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 29/30 | chr16 | 30519547 | |||||||
| chr16:30519831 | C | T | 1 | a0002c0003t0005g0284 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3229-26C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 29/30 | chr16 | 30519831 | |||||||
| chr16:30520126 | G | T | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 |
3 | NA18956.hp1 NA18983.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.3339+159G>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 30/30 | chr16 | 30520126 | |||||||
| chr16:30520174 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3339+207C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 30/30 | chr16 | 30520174 | |||||||
| chr16:30520239 | G | C | 1 | a0002c0002t0001g0236 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3339+272G>C | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 30/30 | chr16 | 30520239 | |||||||
| chr16:30520277 | T | A | 3 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0002c0002t0001g0212 |
3 | HG01175.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3339+310T>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 30/30 | chr16 | 30520277 | |||||||
| chr16:30520325 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0175 |
2 | HG00621.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.3339+358C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 30/30 | chr16 | 30520325 | |||||||
| chr16:30520539 | G | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(229): Show |
238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.3339+572G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 30/30 | chr16 | 30520539 | |||||||
| chr16:30520833 | C | T | 4 | a0001c0001t0003g0223 a0001c0001t0003g0224 a0001c0001t0003g0254 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.3340-659C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 30/30 | chr16 | 30520833 | |||||||
| chr16:30520834 | G | A | 1 | a0001c0009t0001g0060 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3340-658G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 30/30 | chr16 | 30520834 | |||||||
| chr16:30521016 | G | A | 3 | a0001c0001t0001g0064 a0001c0001t0001g0232 a0001c0001t0001g0266 |
3 | HG01168.hp2 HG01515.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.3340-476G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 30/30 | chr16 | 30521016 | |||||||
| chr16:30521134 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0185 |
2 | NA18941.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.3340-358C>T | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 30/30 | chr16 | 30521134 | |||||||
| chr16:30521372 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3340-120A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 30/30 | chr16 | 30521372 | |||||||
| chr16:30521469 | G | A | 1 | a0001c0001t0007g0241 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3340-23G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 30/30 | chr16 | 30521469 |