Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1170 | 208 | 45 | 52 | 84 | 11 | 14 | 53 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0002 | 0/0 | 1170 | 92 | 34 | 15 | 19 | 5 | 19 | 13 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0003 | 0/0 | 1170 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0004 | 0/0 | 1170 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0005 | 0/0 | 1170 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0006 | 0/0 | 1170 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0007 | 0/0 | 1170 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0008 | 0/0 | 1170 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0009 | 0/0 | 1170 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0010 | 0/0 | 1170 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0011 | 0/0 | 1170 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0012 | 0/0 | 1170 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0013 | 0/0 | 1170 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0014 | 0/0 | 1170 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 3513 | 185 | 29 | 51 | 82 | 11 | 10 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| c0002 | 0/0 | 3513 | 73 | 19 | 12 | 18 | 5 | 19 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| c0003 | 0/0 | 3513 | 10 | 10 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| c0004 | 0/0 | 3513 | 8 | 8 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| c0005 | 0/0 | 3513 | 8 | 7 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| c0006 | 0/0 | 3513 | 5 | 4 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| c0007 | 0/0 | 3513 | 4 | 0 | 3 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| c0008 | 0/0 | 3513 | 3 | 3 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| c0009 | 0/0 | 3513 | 3 | 0 | 0 | 0 | 0 | 3 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| c0010 | 0/0 | 3513 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| c0011 | 0/0 | 3513 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| c0012 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| c0013 | 0/0 | 3513 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| c0014 | 0/0 | 3513 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| c0015 | 0/0 | 3513 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| c0016 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| c0017 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| c0018 | 0/0 | 3513 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| c0019 | 0/0 | 3513 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| c0020 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| c0021 | 0/0 | 3513 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| c0022 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| c0023 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| c0024 | 0/0 | 3513 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| c0025 | 0/0 | 3513 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| c0026 | 0/0 | 3513 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| c0027 | 0/0 | 3513 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1617 | 291 | 63 | 72 | 105 | 15 | 34 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| t0002 | 0/0 | 1617 | 7 | 7 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| t0003 | 0/0 | 1617 | 7 | 7 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| t0004 | 0/0 | 1617 | 5 | 5 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| t0005 | 0/0 | 1617 | 3 | 3 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| t0006 | 0/0 | 1617 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| t0007 | 0/0 | 1617 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| t0008 | 0/0 | 1617 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| t0009 | 0/0 | 1617 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0225 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0262 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3513 | 185 | 29 | 51 | 82 | 11 | 10 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0001c0004 | 0/0 | 3513 | 8 | 8 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0001c0005 | 0/0 | 3513 | 8 | 7 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0001c0009 | 0/0 | 3513 | 3 | 0 | 0 | 0 | 0 | 3 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0001c0014 | 0/0 | 3513 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0001c0015 | 0/0 | 3513 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0001c0017 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0001c0025 | 0/0 | 3513 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0002c0002 | 0/0 | 3513 | 73 | 19 | 12 | 18 | 5 | 19 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0002c0003 | 0/0 | 3513 | 10 | 10 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0002c0007 | 0/0 | 3513 | 4 | 0 | 3 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0002c0008 | 0/0 | 3513 | 3 | 3 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0002c0016 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0002c0023 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0003c0006 | 0/0 | 3513 | 5 | 4 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0003c0020 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0004c0010 | 0/0 | 3513 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0005c0012 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0006c0022 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0007c0021 | 0/0 | 3513 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0008c0018 | 0/0 | 3513 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0009c0019 | 0/0 | 3513 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0010c0013 | 0/0 | 3513 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0011c0024 | 0/0 | 3513 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0012c0027 | 0/0 | 3513 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0013c0026 | 0/0 | 3513 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0014c0011 | 0/0 | 3513 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | 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 | copy fasta | chr16 | 30467742 | 30528185 |
| a0001c0001t0002 | 0/0 | 5129 | 4 | 4 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0001c0001t0003 | 0/0 | 5129 | 7 | 7 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0001c0001t0004 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0001c0001t0007 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0001c0001t0008 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0001c0001t0009 | 0/0 | 5129 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0001c0004t0001 | 0/0 | 5129 | 8 | 8 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0001c0005t0001 | 0/0 | 5129 | 6 | 5 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0001c0005t0004 | 0/0 | 5129 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0001c0009t0001 | 0/0 | 5129 | 3 | 0 | 0 | 0 | 0 | 3 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0001c0014t0001 | 0/0 | 5129 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0001c0015t0001 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0001c0017t0006 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0001c0025t0001 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0002c0002t0001 | 0/0 | 5129 | 70 | 16 | 12 | 18 | 5 | 19 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0002c0002t0002 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0002c0002t0004 | 0/0 | 5129 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0002c0003t0001 | 0/0 | 5129 | 5 | 5 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0002c0003t0002 | 0/0 | 5129 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0002c0003t0005 | 0/0 | 5129 | 3 | 3 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0002c0007t0001 | 0/0 | 5129 | 4 | 0 | 3 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0002c0008t0001 | 0/0 | 5129 | 3 | 3 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0002c0016t0006 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0002c0023t0001 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0003c0006t0001 | 0/0 | 5129 | 5 | 4 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0003c0020t0001 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0004c0010t0001 | 0/0 | 5129 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0005c0012t0001 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0006c0022t0001 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0007c0021t0001 | 0/0 | 5129 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0008c0018t0001 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0009c0019t0001 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0010c0013t0001 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0011c0024t0001 | 0/0 | 5129 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0012c0027t0001 | 0/0 | 5129 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0013c0026t0001 | 0/0 | 5129 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| a0014c0011t0001 | 0/0 | 5129 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | copy fasta | chr16 | 30467742 | 30528185 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0064 | 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 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0071 | 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 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0122 | 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 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0155 | 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 |
| 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 |
| 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 |
| a0001c0001t0001g0166 | 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 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0225 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0262 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0008g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0001t0009g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0004t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0004t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0004t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0004t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0004t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0004t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0004t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0004t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0005t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0005t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0005t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0005t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0005t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0005t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0005t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0005t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0009t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0009t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0009t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0014t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0015t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0017t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0001c0025t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0018 | 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 |
| a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0040 | 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 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0177 | 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 |
| a0002c0002t0001g0184 | 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 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0218 | 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 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0002c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0002t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0003t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0003t0001g0307 | 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 |
| a0002c0003t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0003t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0003t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0003t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0003t0005g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0003t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0007t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0007t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0007t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0007t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0008t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0008t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0008t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0016t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0002c0023t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0003c0006t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0003c0006t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0003c0006t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0003c0006t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0003c0006t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0003c0020t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0004c0010t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0004c0010t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0005c0012t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0006c0022t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0007c0021t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0008c0018t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0009c0019t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0010c0013t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0011c0024t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0012c0027t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0013c0026t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| a0014c0011t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | g0232 | EUR | GBR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | GBR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0253 | EUR | GBR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00140 | hp2 | a0001 | c0001 | t0009 | g0210 | EUR | GBR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0217 | EUR | FIN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | FIN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0209 | EUR | FIN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | FIN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00597 | hp2 | a0001 | c0025 | t0001 | g0123 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0251 | 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 | g0029 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0226 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0080 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01071 | hp2 | a0011 | c0024 | t0001 | g0079 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0028 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01099 | hp1 | a0012 | c0027 | t0001 | g0139 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01106 | hp1 | a0001 | c0005 | t0001 | g0266 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0175 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01109 | hp1 | a0003 | c0006 | t0001 | g0197 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0219 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0212 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01243 | hp1 | a0002 | c0007 | t0001 | g0026 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0047 | AMR | PUR | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0269 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01256 | hp1 | a0013 | c0026 | t0001 | g0136 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01258 | hp1 | a0002 | c0007 | t0001 | g0133 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01346 | hp1 | a0002 | c0007 | t0001 | g0228 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0049 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0218 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01496 | hp2 | a0007 | c0021 | t0001 | g0312 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0239 | EUR | IBS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0034 | 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 | g0033 | EUR | IBS | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01884 | hp1 | a0001 | c0005 | t0001 | g0233 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01884 | hp2 | a0002 | c0008 | t0001 | g0272 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01891 | hp1 | a0002 | c0003 | t0001 | g0308 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01891 | hp2 | a0006 | c0022 | t0001 | g0241 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0211 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0205 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02055 | hp1 | a0005 | c0012 | t0001 | g0267 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02055 | hp2 | a0002 | c0003 | t0002 | g0311 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02056 | hp2 | a0002 | c0007 | t0001 | g0238 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02132 | hp1 | a0009 | c0019 | t0001 | g0102 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | KHV | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02145 | hp2 | a0002 | c0002 | t0004 | g0200 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CDX | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CDX | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CDX | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CDX | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02257 | hp1 | a0002 | c0003 | t0001 | g0235 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02280 | hp1 | a0002 | c0003 | t0001 | g0306 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02280 | hp2 | a0002 | c0003 | t0002 | g0300 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02451 | hp1 | a0001 | c0005 | t0001 | g0298 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0250 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0024 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02602 | hp2 | a0001 | c0009 | t0001 | g0042 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02615 | hp1 | a0001 | c0004 | t0001 | g0292 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0286 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0247 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0202 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02630 | hp1 | a0001 | c0005 | t0001 | g0265 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02630 | hp2 | a0002 | c0016 | t0006 | g0240 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0236 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02647 | hp2 | a0001 | c0005 | t0001 | g0260 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02683 | hp1 | a0001 | c0014 | t0001 | g0221 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0050 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0044 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02698 | hp2 | a0001 | c0009 | t0001 | g0056 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02717 | hp1 | a0001 | c0004 | t0001 | g0295 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0268 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02723 | hp1 | a0001 | c0004 | t0001 | g0293 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0246 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0040 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02809 | hp1 | a0003 | c0006 | t0001 | g0008 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02809 | hp2 | a0001 | c0004 | t0001 | g0309 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0201 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0277 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0244 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0243 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0230 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0258 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02965 | hp1 | a0004 | c0010 | t0001 | g0314 | AFR | ESN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ESN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02970 | hp1 | a0002 | c0008 | t0001 | g0229 | AFR | ESN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0264 | AFR | ESN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0011 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0274 | AFR | MSL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03098 | hp2 | a0001 | c0004 | t0001 | g0310 | AFR | MSL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03130 | hp1 | a0001 | c0004 | t0001 | g0294 | AFR | ESN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03130 | hp2 | a0003 | c0020 | t0001 | g0234 | AFR | ESN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03139 | hp1 | a0004 | c0010 | t0001 | g0313 | AFR | ESN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03139 | hp2 | a0002 | c0003 | t0005 | g0304 | AFR | ESN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0290 | AFR | ESN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03195 | hp2 | a0001 | c0004 | t0001 | g0296 | AFR | ESN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0245 | AFR | MSL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0257 | AFR | MSL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03239 | hp1 | a0001 | c0009 | t0001 | g0055 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03453 | hp1 | a0002 | c0008 | t0001 | g0280 | AFR | MSL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0279 | AFR | MSL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03486 | hp1 | a0002 | c0023 | t0001 | g0195 | AFR | MSL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03486 | hp2 | a0001 | c0005 | t0001 | g0046 | AFR | MSL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0030 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0021 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0035 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03516 | hp1 | a0003 | c0006 | t0001 | g0198 | AFR | ESN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0287 | AFR | ESN | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03540 | hp1 | a0002 | c0002 | t0004 | g0199 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0171 | AFR | GWD | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03579 | hp1 | a0003 | c0006 | t0001 | g0010 | AFR | MSL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03579 | hp2 | a0001 | c0017 | t0006 | g0006 | AFR | MSL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0213 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0025 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0015 | SAS | PJL | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0016 | SAS | BEB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0207 | SAS | BEB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0037 | SAS | BEB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0038 | SAS | BEB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG04199 | hp1 | a0014 | c0011 | t0001 | g0019 | SAS | STU | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0020 | SAS | STU | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18522 | hp1 | a0001 | c0004 | t0001 | g0297 | AFR | YRI | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18522 | hp2 | a0002 | c0003 | t0001 | g0315 | AFR | YRI | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | CHB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18906 | hp1 | a0003 | c0006 | t0001 | g0009 | AFR | YRI | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0255 | AFR | YRI | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18939 | hp2 | a0001 | c0001 | t0008 | g0160 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18960 | hp2 | a0008 | c0018 | t0001 | g0065 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18974 | hp2 | a0001 | c0015 | t0001 | g0157 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | LWK | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | LWK | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19043 | hp1 | a0002 | c0003 | t0005 | g0305 | AFR | LWK | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0275 | AFR | LWK | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19091 | hp2 | a0010 | c0013 | t0001 | g0051 | EAS | JPT | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19240 | hp1 | a0002 | c0003 | t0005 | g0291 | AFR | YRI | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | YRI | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ASW | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA20129 | hp2 | a0002 | c0003 | t0001 | g0307 | AFR | ASW | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | TSI | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0237 | EUR | TSI | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0014 | EUR | TSI | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0273 | EUR | TSI | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0018 | SAS | GIH | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0052 | SAS | GIH | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0263 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0288 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02486 | hp1 | a0001 | c0005 | t0004 | g0303 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | USA | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0301 | AFR | USA | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0242 | AFR | USA | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA20300 | hp2 | a0001 | c0005 | t0004 | g0299 | AFR | USA | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | LWK | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | LWK | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0225 | REF | REF | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0262 | REF | REF | ITGAL_chr16_30467742_30528185 | ITGAL | chr16 | 30467742 | 30528185 |
| 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 | a0014 | 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 | a0005 | 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 | a0012a0013 | 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 | a0011 | 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 | a0006 | 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 | a0010 | 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 | a0009 | 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 | a0008 | 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 | a0003a0004 | 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 | a0002a0004a0005others(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 | a0005a0007 | 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 |
| 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 | a0001c0004a0001c0005a0002c0003others(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 | a0002c0007a0013c0026 | 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 | a0001c0017a0002c0016 | 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 |
| 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 | a0001c0001t0004a0001c0005t0004a0002c0002t0004 | 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 | a0001c0001t0003a0001c0017t0006a0002c0016t0006 | 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 | a0001c0001t0002a0002c0002t0002a0002c0003t0002 | 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 | a0001c0017t0006a0002c0016t0006 | 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 |
| 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 | a0002c0002t0001g0003 | 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 | a0001c0001t0001g0316 | 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 | 196 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(193): 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 | a0001c0001t0001g0302a0001c0001t0002g0290a0001c0004t0001g0292others(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 | 159 | a0001c0001t0001g0054a0001c0001t0001g0057a0001c0001t0001g0058others(156): 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 | a0002c0002t0001g0196a0002c0003t0001g0315 | 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 | 2 | a0003c0006t0001g0197a0003c0006t0001g0198 | 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 | 276 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(273): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(274): 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 | a0002c0002t0004g0199a0002c0002t0004g0200 | 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 | a0001c0001t0001g0239 | 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 | 65 | a0001c0001t0001g0043a0001c0001t0001g0048a0001c0001t0001g0172others(62): Show | 65 | HG00323.hp2 HG00621.hp1 HG00621.hp2 others(62): 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 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0003g0230others(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 | a0001c0001t0001g0237a0001c0001t0001g0289a0001c0001t0003g0288others(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 | a0001c0001t0002g0201a0001c0001t0003g0202a0002c0002t0001g0004others(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 | a0001c0001t0001g0227 | 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 | a0001c0001t0001g0005a0002c0002t0001g0196 | 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 | 44 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(41): 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 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(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 | a0002c0002t0004g0199a0002c0002t0004g0200 | 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 | a0001c0001t0003g0202 | 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 | a0001c0001t0001g0172a0001c0001t0001g0173 | 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 | 59 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0023others(56): 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 | a0001c0001t0001g0302a0001c0004t0001g0292a0001c0004t0001g0293others(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 | a0002c0002t0001g0218 | 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 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0174 | 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 | 25 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0206others(22): Show | 25 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(22): 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 | a0001c0001t0001g0054a0001c0001t0001g0057a0001c0001t0001g0163others(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 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0281others(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 | 2 | a0003c0006t0001g0197a0003c0006t0001g0198 | 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 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0281others(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 | a0002c0003t0005g0291a0007c0021t0001g0312 | 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 | 3 | a0001c0001t0001g0225a0002c0002t0001g0217a0002c0002t0001g0226 | 3 | HG00280.hp1 HG00741.hp1 homoSapiens_chm13v2.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 | a0001c0001t0001g0302a0001c0004t0001g0292a0001c0004t0001g0293others(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 | a0002c0002t0001g0243 | 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 | a0001c0001t0001g0159a0001c0001t0001g0161a0001c0001t0001g0162others(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 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0158others(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 | 275 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(272): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(273): 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 | 223 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(220): Show | 224 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(221): 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 | a0001c0001t0001g0048a0002c0002t0001g0047 | 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 | a0001c0001t0001g0149 | 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 | a0002c0002t0001g0175 | 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 | a0001c0001t0001g0237a0001c0001t0001g0302a0001c0001t0003g0230others(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 | 27 | a0001c0001t0001g0206a0001c0001t0001g0208a0001c0001t0001g0209others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(24): 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 | a0001c0001t0001g0215a0001c0001t0001g0222a0001c0001t0001g0223others(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 | 47 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(44): 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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0158others(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 | 133 | a0001c0001t0001g0054a0001c0001t0001g0057a0001c0001t0001g0061others(130): 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 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(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 | a0004c0010t0001g0313a0004c0010t0001g0314 | 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 | 107 | a0001c0001t0001g0054a0001c0001t0001g0058a0001c0001t0001g0059others(104): 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 | a0001c0001t0001g0237a0002c0002t0001g0232a0002c0007t0001g0228others(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 | a0001c0001t0002g0201a0001c0001t0003g0202 | 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 | a0002c0002t0004g0199a0002c0002t0004g0200 | 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 | a0001c0005t0004g0299a0001c0005t0004g0303a0002c0003t0002g0300others(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 | 29 | a0001c0001t0001g0098a0001c0001t0001g0225a0001c0001t0001g0259others(26): Show | 29 | HG00280.hp1 HG00741.hp1 HG01106.hp1 others(26): 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 | 72 | a0001c0001t0001g0002a0001c0001t0001g0058a0001c0001t0001g0059others(69): 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 | a0001c0001t0001g0062a0001c0001t0001g0163a0001c0001t0001g0188others(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 | a0001c0001t0001g0061a0001c0001t0001g0270a0002c0002t0001g0242others(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 | a0005c0012t0001g0267 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0060a0001c0001t0001g0164a0001c0001t0001g0179others(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 | a0001c0001t0001g0043a0001c0001t0001g0048a0001c0001t0001g0107others(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 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0023others(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 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0036others(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 | a0001c0001t0001g0105a0002c0002t0004g0199a0002c0002t0004g0200others(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 | a0001c0001t0001g0271a0002c0002t0001g0244a0002c0002t0001g0258 | 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 | a0001c0004t0001g0309 | 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 | a0002c0002t0001g0007a0002c0002t0001g0011 | 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 | 245 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(242): Show | 246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): 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 | a0001c0001t0001g0041 | 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 | 104 | a0001c0001t0001g0054a0001c0001t0001g0058a0001c0001t0001g0059others(101): 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 | 40 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(37): 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 | a0002c0023t0001g0195 | 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 | a0001c0001t0002g0201a0001c0001t0003g0202 | 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 | a0002c0002t0001g0245 | 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 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0057others(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 | 292 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(289): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.722+828A>G | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 7/30 | chr16 | 30482412 | ||||||
| chr16:30482560
|
T | C | 218 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(215): 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 | 5 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(2): 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 | a0001c0001t0001g0254 | 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 | a0001c0001t0001g0281 | 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 | 255 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(252): 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 | 107 | a0001c0001t0001g0054a0001c0001t0001g0057a0001c0001t0001g0058others(104): 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 | 255 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(252): 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 | a0001c0001t0004g0275 | 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 | a0001c0004t0001g0292a0001c0004t0001g0293a0001c0004t0001g0294others(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 | a0001c0001t0001g0183 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0002c0002t0001g0242a0002c0002t0001g0245a0002c0002t0001g0246others(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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0063 | 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 | 75 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(72): 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 | a0001c0004t0001g0292a0001c0004t0001g0293a0001c0004t0001g0294others(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 | a0001c0001t0001g0064a0001c0001t0001g0117a0001c0001t0001g0118others(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 |
183 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0054others(180): 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 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0282others(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 | 51 | a0001c0001t0001g0130a0001c0001t0001g0147a0001c0001t0001g0168others(48): Show | 51 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(48): 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 | 251 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(248): 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 | a0005c0012t0001g0267 | 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 | a0001c0001t0001g0036 | 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 | a0001c0001t0001g0062 | 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 | 25 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0206others(22): Show | 25 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(22): Show |
intron_variant | MODIFIER | c.1006+2013G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 9/30 | chr16 | 30486276 | ||||||
| chr16:30486408
|
C | CA | 85 | a0001c0001t0001g0012a0001c0001t0001g0054a0001c0001t0001g0058others(82): 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 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0057others(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 | a0001c0001t0001g0117a0001c0001t0001g0130a0001c0001t0001g0154others(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 | a0001c0001t0001g0239a0001c0001t0001g0254a0001c0001t0001g0256others(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 | a0001c0001t0001g0206a0001c0001t0001g0208a0001c0001t0001g0223others(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 | a0008c0018t0001g0065 | 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 | a0001c0001t0001g0043a0002c0002t0001g0049a0002c0002t0001g0050 | 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 | a0001c0017t0006g0006 | 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 | a0002c0002t0001g0025 | 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 | a0001c0001t0001g0066a0001c0001t0001g0188 | 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 | a0002c0002t0002g0301 | 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 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0092others(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 | a0001c0001t0001g0185a0001c0005t0001g0233a0002c0002t0001g0053others(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 | a0010c0013t0001g0051 | 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 | a0003c0006t0001g0008a0003c0006t0001g0009a0003c0006t0001g0010others(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 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0054others(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 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0054others(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 | a0002c0002t0001g0015a0002c0002t0001g0016 | 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 | a0001c0001t0002g0201a0002c0002t0004g0199a0002c0002t0004g0200 | 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 | a0001c0001t0001g0115a0001c0001t0001g0116 | 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 | a0001c0001t0001g0012a0001c0001t0001g0169a0001c0015t0001g0157others(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 | 27 | a0001c0001t0001g0057a0001c0001t0001g0203a0001c0001t0001g0204others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(24): 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 | 66 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0062others(63): 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 | a0002c0003t0001g0315 | 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 | a0001c0005t0001g0233a0002c0003t0001g0235a0003c0020t0001g0234 | 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 | a0002c0002t0001g0037 | 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 | 145 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(142): 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 | 164 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0023others(161): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): 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 | a0001c0001t0001g0012a0001c0001t0001g0048a0001c0001t0001g0070others(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 | a0001c0001t0001g0209 | 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 | a0001c0001t0003g0202 | 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 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0054others(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 | a0001c0001t0001g0091 | 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 | 261 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(258): 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 | a0002c0002t0001g0236 | 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 | 286 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(283): Show | 287 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(284): 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 | a0002c0002t0001g0186 | 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 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0054others(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 | 132 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(129): 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 | a0001c0001t0001g0036a0001c0001t0001g0071a0001c0001t0001g0072others(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 | 260 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(257): 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 | 23 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0206others(20): Show | 23 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(20): 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 | a0001c0001t0002g0201a0002c0002t0004g0199a0002c0002t0004g0200 | 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 | a0001c0001t0002g0201a0002c0002t0004g0199a0002c0002t0004g0200 | 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 | 25 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0206others(22): Show | 25 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(22): 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 | a0001c0001t0002g0201a0002c0002t0004g0199a0002c0002t0004g0200 | 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 | a0002c0003t0001g0315 | 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 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0054others(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 | a0001c0001t0001g0091 | 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 | 11 | a0001c0001t0001g0091a0001c0001t0001g0225a0001c0001t0003g0230others(8): Show | 11 | HG00280.hp1 HG00741.hp1 HG01884.hp1 others(8): 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 | a0001c0001t0001g0237a0002c0002t0001g0232a0002c0007t0001g0228others(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 | a0001c0001t0002g0201a0002c0002t0004g0199a0002c0002t0004g0200 | 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 | a0010c0013t0001g0051 | 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 | a0001c0001t0002g0201a0002c0002t0004g0199a0002c0002t0004g0200 | 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 | a0002c0002t0001g0138a0002c0002t0001g0180a0002c0002t0001g0191 | 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 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0054others(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 | 267 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(264): 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 | a0001c0001t0001g0097a0001c0001t0001g0150a0001c0001t0003g0230others(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 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284others(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 | 35 | a0001c0001t0001g0058a0001c0001t0001g0062a0001c0001t0001g0063others(32): 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 | a0001c0001t0001g0185a0002c0002t0001g0053 | 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 | a0001c0001t0002g0201 | 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 | 23 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0206others(20): Show | 23 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(20): 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 | a0001c0001t0001g0144 | 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 | 269 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(266): 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 | a0001c0001t0003g0230a0001c0001t0003g0231a0001c0005t0001g0233others(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 | a0001c0001t0003g0230a0001c0001t0003g0231a0001c0005t0001g0233others(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 | 154 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0054others(151): 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 | a0001c0001t0001g0206a0001c0001t0001g0239a0001c0001t0001g0254others(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 |
71 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0031others(68): Show | 71 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(68): 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 | a0001c0001t0001g0220a0001c0001t0001g0224a0001c0005t0001g0260others(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 | a0002c0003t0001g0307a0002c0003t0001g0315 | 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 | a0001c0005t0004g0299 | 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 | a0001c0001t0001g0023a0001c0001t0001g0039a0001c0001t0001g0041others(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 | a0001c0001t0001g0012a0002c0002t0001g0017a0002c0002t0001g0050 | 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 | a0001c0001t0001g0048a0002c0002t0001g0047 | 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 | a0001c0001t0001g0112 | 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 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0140others(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 | a0001c0001t0003g0230a0001c0001t0003g0231a0001c0005t0001g0233others(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 | a0001c0001t0002g0201a0002c0002t0004g0199a0002c0002t0004g0200 | 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 | a0001c0001t0001g0086 | 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 | a0002c0002t0001g0131 | 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 | a0002c0002t0001g0232a0002c0007t0001g0228 | 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 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0120 | 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 | 108 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(105): 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 | 262 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(259): 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 | 5 | a0001c0001t0001g0225a0002c0002t0001g0213a0002c0002t0001g0217others(2): Show | 5 | HG00280.hp1 HG00741.hp1 HG01175.hp2 others(2): 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 | a0002c0002t0004g0199a0002c0002t0004g0200 | 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 | a0010c0013t0001g0051 | 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 | a0001c0001t0001g0278a0001c0001t0002g0277a0001c0001t0002g0279others(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 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0054others(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 | a0002c0002t0001g0053 | 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 | a0001c0001t0001g0109 | 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 | a0001c0005t0001g0265 | 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 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0111others(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 | a0001c0001t0001g0289 | 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 | 262 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(259): 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 | a0001c0001t0001g0289 | 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 | a0001c0001t0001g0278a0001c0001t0001g0289a0001c0001t0002g0277others(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 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0054others(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 | a0001c0001t0001g0027a0001c0001t0001g0029a0002c0007t0001g0026 | 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 | 245 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(242): 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 | a0001c0001t0001g0067a0001c0001t0001g0129a0001c0001t0001g0156others(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 | a0001c0001t0001g0278a0001c0001t0002g0277a0001c0001t0002g0279others(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 | a0001c0001t0001g0215 | 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 | a0001c0017t0006g0006 | 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 | 152 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(149): 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 | a0006c0022t0001g0241 | 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 | a0002c0007t0001g0238 | 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 | a0001c0001t0001g0105a0001c0001t0001g0165a0001c0001t0001g0166others(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 | a0002c0002t0001g0020a0002c0002t0001g0021a0002c0002t0001g0040others(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 | a0002c0002t0001g0014a0002c0002t0001g0044a0002c0002t0001g0171 | 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 | a0002c0002t0001g0205a0002c0002t0001g0211a0002c0002t0001g0212others(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 | a0002c0002t0001g0244a0002c0002t0001g0258 | 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 | a0002c0002t0001g0244a0002c0002t0001g0258 | 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 | a0001c0001t0001g0113a0001c0001t0001g0149a0001c0001t0001g0164others(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 | a0001c0001t0001g0043a0001c0001t0001g0278a0001c0001t0001g0289others(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 | 47 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0140others(44): Show | 47 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(44): 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 | 76 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0031others(73): 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 | 101 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0031others(98): 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 | a0001c0001t0001g0239a0001c0001t0001g0256a0001c0001t0001g0270others(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 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0029others(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 | a0001c0001t0001g0278a0001c0001t0002g0277a0001c0001t0002g0279others(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 | 149 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0023others(146): 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 | 243 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(240): 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 | a0001c0005t0001g0233 | 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 | a0001c0001t0001g0237 | 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 | a0001c0005t0001g0233 | 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 | a0001c0005t0001g0298 | 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 | a0001c0001t0002g0201a0002c0002t0004g0199a0002c0002t0004g0200 | 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 | a0002c0002t0001g0044a0002c0002t0001g0047 | 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 | a0002c0002t0001g0024 | 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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0029others(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 | a0001c0005t0001g0298 | 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 | a0001c0001t0001g0023a0001c0001t0001g0039a0002c0002t0001g0022 | 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 | a0002c0002t0001g0024a0002c0002t0001g0044a0002c0002t0001g0047 | 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 | a0001c0001t0001g0081 | 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 | a0002c0002t0001g0274 | 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 |
82 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0036others(79): 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 |
12 | a0001c0001t0001g0013a0001c0001t0001g0031a0001c0001t0001g0064others(9): 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 | a0002c0002t0001g0177 | 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 | a0002c0023t0001g0195 | 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 | a0001c0001t0003g0230a0001c0001t0003g0231 | 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 | a0002c0002t0001g0030a0002c0002t0001g0035 | 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 | a0003c0020t0001g0234 | 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 | a0001c0001t0001g0112a0001c0001t0001g0215a0001c0001t0001g0281 | 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 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0083others(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 | a0001c0001t0002g0201a0002c0002t0004g0199a0002c0002t0004g0200 | 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 | a0001c0001t0001g0122 | 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 | a0001c0001t0002g0201a0002c0002t0004g0199a0002c0002t0004g0200 | 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0185a0001c0001t0001g0254a0001c0001t0001g0282others(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 | a0001c0001t0001g0278a0001c0001t0002g0277a0001c0001t0002g0279others(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 | 4 | a0001c0001t0001g0225a0001c0001t0002g0201a0002c0002t0001g0217others(1): Show | 4 | HG00280.hp1 HG00741.hp1 HG02818.hp1 others(1): Show |
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 | a0002c0003t0002g0300a0002c0003t0002g0311a0006c0022t0001g0241 | 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 | a0001c0001t0001g0091a0001c0001t0001g0094a0001c0001t0001g0101others(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 | a0001c0001t0001g0041a0001c0001t0001g0064a0001c0001t0001g0179others(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 | a0002c0003t0001g0315 | 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 | a0002c0002t0001g0001 | 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 | a0002c0002t0001g0016a0002c0002t0001g0020a0002c0002t0001g0021others(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 | a0001c0005t0001g0046a0001c0005t0001g0265a0001c0005t0001g0266others(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 | a0002c0016t0006g0240 | 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 | a0001c0001t0001g0185a0002c0002t0001g0050 | 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 | a0001c0001t0001g0254a0001c0001t0001g0283a0001c0001t0001g0289others(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 | a0002c0003t0001g0306a0002c0003t0001g0307a0002c0003t0005g0305 | 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 | a0002c0008t0001g0272 | 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 | a0001c0001t0001g0282a0001c0004t0001g0310 | 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 | a0002c0003t0005g0291 | 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 | a0002c0008t0001g0229 | 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 | a0002c0002t0001g0090 | 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 | 36 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0031others(33): 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 | 117 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0043others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): 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 | a0001c0001t0001g0122a0001c0001t0001g0129a0001c0001t0001g0162others(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 | a0005c0012t0001g0267 | 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 | a0001c0001t0001g0002a0001c0001t0001g0105a0001c0001t0001g0110others(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 | a0001c0001t0001g0071a0001c0001t0001g0087a0001c0001t0001g0095others(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 | 115 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0032others(112): Show | 116 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(113): 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 | a0001c0001t0001g0075a0002c0002t0001g0171a0002c0002t0004g0199others(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 | 16 | a0001c0001t0001g0068a0001c0001t0001g0076a0001c0001t0001g0077others(13): 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 | a0002c0002t0001g0142 | 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 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0041 | 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 | a0001c0004t0001g0297 | 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 | a0002c0002t0001g0205a0002c0002t0001g0211a0002c0002t0001g0212others(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 | a0001c0001t0001g0054 | 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 | 72 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0031others(69): 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 | 245 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(242): 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 | a0001c0001t0001g0106 | 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 | 287 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(284): Show | 288 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(285): 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 | a0001c0001t0002g0201a0002c0002t0004g0199a0002c0002t0004g0200 | 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 | a0001c0001t0001g0278a0001c0001t0002g0277a0001c0001t0002g0279others(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 | a0002c0002t0001g0007a0002c0002t0001g0011 | 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 | a0001c0001t0001g0058a0001c0001t0001g0063a0001c0001t0001g0068others(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 | a0001c0001t0002g0201a0002c0002t0004g0199a0002c0002t0004g0200 | 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 | 253 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(250): 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 | a0002c0002t0001g0004 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0278a0001c0001t0002g0277a0001c0001t0002g0279others(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 | 240 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(237): 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 | 314 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(311): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0271 | 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 | a0001c0001t0002g0201a0001c0001t0003g0202a0002c0002t0004g0199others(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 | a0002c0008t0001g0229 | 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 | a0002c0008t0001g0229 | 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 | 6 | a0001c0001t0001g0225a0002c0002t0001g0213a0002c0002t0001g0217others(3): Show | 6 | HG00280.hp1 HG00741.hp1 HG01175.hp2 others(3): 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 | a0002c0003t0001g0315 | 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 | a0001c0001t0003g0202a0007c0021t0001g0312 | 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 | a0001c0001t0001g0081a0001c0001t0001g0096a0001c0001t0001g0237others(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 | a0001c0001t0001g0239a0001c0001t0001g0254a0001c0001t0001g0256others(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 | a0001c0001t0001g0220a0001c0001t0001g0224 | 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 | a0001c0001t0001g0023a0001c0001t0001g0039a0001c0001t0001g0041others(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 | a0002c0008t0001g0229 | 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 | a0002c0002t0001g0236 | 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 | a0001c0001t0001g0076a0001c0001t0001g0189a0001c0001t0001g0203others(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 | 140 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(137): 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 | a0002c0002t0001g0007a0002c0002t0001g0011a0002c0003t0001g0235 | 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 | a0001c0001t0001g0023a0001c0001t0001g0039a0001c0001t0001g0041others(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 | a0001c0001t0001g0278a0001c0001t0002g0277a0001c0001t0002g0279others(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 | a0002c0002t0001g0022 | 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 | a0001c0001t0001g0206a0001c0001t0001g0208a0001c0001t0001g0223others(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 | a0001c0001t0001g0005a0001c0001t0001g0088a0001c0001t0001g0110others(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 | a0001c0001t0001g0067a0001c0001t0001g0107a0001c0001t0001g0159others(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 | 142 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(139): 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 | 138 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(135): 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 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0113others(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 | 138 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(135): 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 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0113others(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 | a0001c0001t0003g0264 | 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 | 254 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(251): 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 | a0002c0002t0001g0004 | 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 | 254 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(251): 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 | a0002c0008t0001g0229 | 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 | 254 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(251): 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 | a0002c0002t0001g0263 | 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 | 145 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0039others(142): 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 | 96 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0027others(93): 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 | a0002c0002t0001g0232 | 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 | a0002c0003t0005g0305 | 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 | a0001c0004t0001g0292 | 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 | a0002c0002t0004g0199 | 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 | a0001c0001t0001g0054a0001c0001t0001g0067a0001c0001t0001g0069others(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 | a0001c0001t0001g0023a0001c0001t0001g0039a0001c0001t0001g0041others(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 | a0002c0003t0001g0315 | 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 | a0001c0005t0001g0233a0003c0020t0001g0234a0004c0010t0001g0313others(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 | a0001c0001t0001g0145a0001c0001t0001g0190 | 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 | 149 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0039others(146): 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 | a0001c0001t0001g0256a0001c0001t0001g0302a0001c0001t0004g0275others(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 | 129 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0039others(126): 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 | a0001c0001t0001g0145a0001c0001t0001g0190 | 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 | 99 | a0001c0001t0001g0023a0001c0001t0001g0039a0001c0001t0001g0041others(96): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(97): 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 | a0001c0001t0001g0069a0001c0001t0001g0089a0001c0001t0001g0239others(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 | 193 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0023others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): 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 | a0001c0001t0001g0239a0001c0001t0001g0254a0001c0001t0001g0270others(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 | a0001c0001t0001g0066a0001c0001t0001g0084a0001c0001t0001g0085others(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 | a0012c0027t0001g0139 | 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 | a0001c0001t0001g0067a0001c0001t0001g0069a0008c0018t0001g0065 | 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 | 257 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0023others(254): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(255): 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 | a0001c0001t0003g0202a0001c0001t0003g0230a0001c0001t0003g0231others(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 | a0002c0002t0001g0243 | 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 | a0002c0002t0001g0196 | 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 | 68 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0057others(65): 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 | a0002c0002t0001g0236a0002c0002t0001g0243 | 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 | 91 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0057others(88): 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 | 66 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0112others(63): Show | 66 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(63): 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 | a0001c0001t0001g0039a0001c0001t0001g0041a0002c0002t0001g0001others(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 | a0002c0002t0001g0040a0002c0002t0001g0218a0002c0002t0001g0242others(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 | a0001c0004t0001g0293 | 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 | 126 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0112others(123): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): 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 | a0001c0005t0001g0298 | 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 | a0001c0001t0001g0089 | 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 | a0001c0001t0001g0209 | 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 | 63 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0057others(60): 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 | a0001c0001t0001g0063a0001c0001t0001g0118a0001c0001t0001g0120others(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 | a0001c0001t0001g0005a0001c0001t0001g0048a0001c0001t0001g0060others(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 | a0002c0002t0001g0022a0002c0002t0001g0119a0002c0002t0001g0177others(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 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(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 | a0002c0002t0001g0017a0002c0002t0001g0021a0002c0002t0001g0090others(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 | 34 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0115others(31): Show | 34 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(31): 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 | a0002c0002t0001g0003a0002c0002t0001g0018a0002c0002t0001g0038 | 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 | a0002c0003t0001g0306a0002c0003t0005g0291a0002c0003t0005g0304others(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 | a0002c0002t0001g0196 | 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 | a0001c0001t0001g0073a0001c0001t0001g0099a0001c0001t0001g0114others(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 | a0001c0001t0001g0239a0001c0001t0001g0270 | 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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0003g0202others(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 | a0001c0004t0001g0295 | 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0064a0001c0001t0001g0254a0001c0001t0001g0256others(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 | a0002c0002t0001g0038 | 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 | a0001c0001t0001g0012a0001c0001t0001g0135a0001c0001t0001g0239others(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 | a0001c0001t0001g0164 | 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 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(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 | a0001c0001t0001g0057a0001c0001t0001g0072a0001c0001t0001g0104others(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 | 114 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0115others(111): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): 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 | 8 | a0001c0001t0001g0043a0001c0005t0001g0260a0003c0006t0001g0008others(5): 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 | 134 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0115others(131): Show | 135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): 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 | a0001c0001t0001g0054a0001c0001t0001g0067a0001c0001t0001g0069others(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 | a0002c0002t0001g0007a0002c0002t0001g0011a0002c0002t0001g0274others(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 | a0002c0002t0001g0007a0002c0002t0001g0011a0002c0002t0001g0274others(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 | a0002c0002t0001g0213a0002c0002t0001g0219a0002c0002t0001g0269 | 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 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(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 | a0002c0002t0001g0038 | 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 | a0002c0002t0001g0080a0011c0024t0001g0079 | 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 | a0001c0005t0001g0298 | 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 | a0002c0002t0001g0017 | 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 | a0003c0006t0001g0009 | 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 | a0001c0001t0001g0066a0001c0001t0001g0071a0001c0001t0001g0159others(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 | a0001c0001t0001g0069a0001c0001t0001g0097a0001c0001t0001g0116others(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 | a0002c0007t0001g0026a0002c0007t0001g0133a0002c0007t0001g0228others(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 | a0001c0001t0001g0278a0001c0001t0002g0277a0001c0001t0002g0279others(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 | a0001c0001t0003g0202 | 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 | 33 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0115others(30): Show | 33 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(30): 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 | a0001c0001t0001g0012a0001c0001t0001g0105a0001c0001t0001g0165others(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 | a0002c0008t0001g0229a0002c0008t0001g0272a0002c0008t0001g0280 | 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 | a0001c0001t0001g0118a0001c0001t0001g0120 | 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 | 127 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0115others(124): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): 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 | a0001c0001t0003g0257a0001c0001t0003g0264a0002c0002t0001g0037others(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 | a0001c0001t0001g0092a0001c0001t0001g0095 | 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 | 31 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0115others(28): Show | 31 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(28): 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 | a0001c0001t0001g0086 | 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 | 5 | a0003c0006t0001g0008a0003c0006t0001g0009a0003c0006t0001g0010others(2): 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 | a0002c0002t0001g0052a0002c0002t0001g0174 | 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 | a0001c0001t0003g0202 | 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 | a0002c0002t0001g0274 | 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 | a0002c0002t0001g0018 | 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 | a0001c0001t0001g0285a0001c0005t0001g0046a0001c0005t0001g0265others(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 | 34 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0115others(31): Show | 34 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(31): 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 | a0001c0001t0001g0278a0001c0001t0001g0302a0001c0001t0002g0277others(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 | a0002c0002t0001g0138a0002c0002t0001g0142a0002c0002t0001g0177others(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 | a0001c0005t0004g0299 | 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 | a0001c0001t0001g0012a0001c0001t0001g0023a0001c0001t0001g0027others(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 | a0002c0002t0001g0049 | 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 | a0001c0001t0001g0057a0001c0001t0001g0068a0001c0001t0001g0076others(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 | a0002c0002t0001g0138a0002c0002t0001g0180a0002c0002t0001g0191 | 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 | 203 | a0001c0001t0001g0012a0001c0001t0001g0023a0001c0001t0001g0027others(200): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): 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 | a0001c0001t0001g0012a0001c0001t0001g0167a0001c0001t0001g0170 | 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 | a0002c0002t0001g0255 | 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 | a0001c0001t0001g0068a0001c0001t0001g0249a0001c0001t0001g0285others(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 | a0002c0002t0001g0020 | 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 | a0001c0001t0001g0289 | 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 | a0001c0001t0001g0083 | 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 | a0001c0001t0003g0257a0001c0001t0003g0264a0002c0002t0001g0245 | 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 | a0002c0002t0001g0244a0002c0002t0001g0255a0002c0002t0001g0258others(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 | a0003c0020t0001g0234 | 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 | a0001c0001t0003g0202 | 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 | a0001c0001t0002g0201 | 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 | a0002c0002t0001g0175 | 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 | a0001c0001t0001g0104a0001c0001t0001g0129a0001c0001t0001g0188others(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 | a0001c0001t0001g0066a0001c0001t0001g0071a0001c0001t0001g0084others(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 | a0001c0001t0001g0089 | 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 | a0001c0001t0001g0117a0001c0001t0001g0159a0001c0001t0001g0161others(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 | 13 | a0001c0001t0003g0230a0001c0001t0003g0231a0001c0005t0001g0260others(10): 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 | a0001c0001t0003g0257a0001c0001t0003g0264 | 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 | a0002c0002t0001g0028a0002c0002t0001g0047 | 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 | a0001c0001t0001g0276a0001c0009t0001g0042a0001c0009t0001g0055others(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 | a0001c0001t0001g0002a0001c0001t0001g0248a0001c0001t0001g0252others(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 | a0001c0001t0001g0057a0001c0001t0001g0143 | 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 | 37 | a0001c0001t0001g0002a0001c0001t0001g0248a0001c0001t0001g0252others(34): 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 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0073others(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 | a0001c0001t0001g0071 | 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 | a0002c0007t0001g0026 | 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 | 8 | a0001c0001t0002g0201a0001c0001t0003g0202a0002c0023t0001g0195others(5): 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 | 9 | a0001c0001t0001g0058a0001c0001t0001g0063a0001c0001t0001g0070others(6): 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 | a0001c0001t0001g0124 | 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 | a0001c0001t0001g0164 | 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 | a0001c0001t0001g0023 | 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 | a0001c0001t0001g0183a0001c0001t0001g0276a0001c0005t0001g0260others(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 | a0001c0001t0001g0194a0002c0002t0001g0007a0002c0002t0001g0011others(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 | a0001c0001t0001g0057a0001c0001t0001g0143 | 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 | a0006c0022t0001g0241 | 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 | a0001c0001t0001g0203a0001c0001t0001g0204 | 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 | a0001c0001t0003g0202 | 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 | a0002c0003t0001g0306 | 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 | a0001c0001t0003g0202 | 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 | a0002c0003t0005g0291 | 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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 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 | a0001c0001t0001g0062 | 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 | a0002c0002t0001g0243 | 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 | a0001c0001t0001g0115a0001c0001t0001g0116a0002c0002t0001g0219 | 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 | a0001c0001t0001g0064a0001c0001t0001g0183 | 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 | 237 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0023others(234): 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 | a0001c0001t0003g0230a0001c0001t0003g0231a0001c0001t0003g0257others(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 | a0001c0009t0001g0055 | 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 | 4 | a0001c0001t0001g0060a0001c0001t0001g0225a0001c0001t0001g0239others(1): Show | 4 | HG01168.hp2 HG01515.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.3340-476G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 30/30 | chr16 | 30521016 | ||||||
| chr16:30521134
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0190 | 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 | a0001c0001t0001g0043 | 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 | a0001c0001t0007g0250 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3340-23G>A | ITGAL | ENSG00000005844.19 | transcript | ENST00000356798.11 | protein_coding | 30/30 | chr16 | 30521469 |