| geneid | 3673 |
|---|---|
| ensemblid | ENSG00000164171.11 |
| hgncid | 6137 |
| symbol | ITGA2 |
| name | integrin subunit alpha 2 |
| refseq_nuc | NM_002203.4 |
| refseq_prot | NP_002194.2 |
| ensembl_nuc | ENST00000296585.10 |
| ensembl_prot | ENSP00000296585.5 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 52989352 |
| end | 53094779 |
| strand | + |
| ver | v1.2 |
| region | chr5:52989352-53094779 |
| region5000 | chr5:52984352-53099779 |
| regionname0 | ITGA2_chr5_52989352_53094779 |
| regionname5000 | ITGA2_chr5_52984352_53099779 |
| 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 | 1181 | 330 | 74 | 64 | 144 | 13 | 33 | 112 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0002 | 0/0 | 1181 | 37 | 15 | 6 | 12 | 3 | 1 | 8 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0003 | 0/0 | 1181 | 10 | 0 | 0 | 10 | 0 | 0 | 9 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0004 | 0/0 | 1181 | 7 | 0 | 0 | 7 | 0 | 0 | 7 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0005 | 0/0 | 1181 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0006 | 0/0 | 1181 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0007 | 0/0 | 1181 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0008 | 0/0 | 1181 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0009 | 0/0 | 1181 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0010 | 0/0 | 1181 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0011 | 0/0 | 1181 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0012 | 0/0 | 1181 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0013 | 0/0 | 1181 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0014 | 0/0 | 1181 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0015 | 0/0 | 1181 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0016 | 0/0 | 1181 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 3546 | 173 | 25 | 36 | 85 | 7 | 19 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0002 | 0/1 | 3546 | 120 | 20 | 26 | 56 | 5 | 12 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0003 | 0/0 | 3546 | 29 | 10 | 6 | 9 | 3 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0004 | 0/0 | 3546 | 23 | 22 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0005 | 0/0 | 3546 | 10 | 0 | 0 | 10 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0006 | 0/0 | 3546 | 6 | 0 | 0 | 6 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0007 | 0/0 | 3546 | 5 | 5 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0008 | 0/0 | 3546 | 5 | 5 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0009 | 0/0 | 3546 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0010 | 0/0 | 3546 | 3 | 0 | 3 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0011 | 0/0 | 3546 | 3 | 1 | 1 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0012 | 0/0 | 3546 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0013 | 0/0 | 3546 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0014 | 0/0 | 3546 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0015 | 0/0 | 3546 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0016 | 0/0 | 3546 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0017 | 0/0 | 3546 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0018 | 0/0 | 3546 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0019 | 0/0 | 3546 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0020 | 0/0 | 3546 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0021 | 0/0 | 3546 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0022 | 0/0 | 3546 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0023 | 0/0 | 3546 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0024 | 0/0 | 3546 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0025 | 0/0 | 3546 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0026 | 0/0 | 3546 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0027 | 0/0 | 3546 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0028 | 0/0 | 3546 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| c0029 | 0/0 | 3546 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| 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 | 1/0 | 4298 | 76 | 15 | 10 | 45 | 1 | 4 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0002 | 0/0 | 4313 | 52 | 6 | 15 | 19 | 4 | 8 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0003 | 0/0 | 4331 | 52 | 1 | 6 | 39 | 2 | 4 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0004 | 0/0 | 4334 | 35 | 12 | 5 | 11 | 1 | 6 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0005 | 0/0 | 4298 | 30 | 3 | 10 | 9 | 2 | 6 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0006 | 0/0 | 4333 | 26 | 3 | 5 | 18 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0007 | 0/0 | 4312 | 23 | 7 | 4 | 8 | 3 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0008 | 0/0 | 4313 | 21 | 20 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0009 | 0/0 | 4332 | 6 | 0 | 0 | 5 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0010 | 0/0 | 4312 | 5 | 5 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0011 | 0/0 | 4331 | 5 | 0 | 5 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0012 | 0/0 | 4312 | 3 | 3 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0013 | 0/0 | 4297 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0014 | 0/0 | 4295 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0015 | 0/0 | 4313 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0016 | 0/0 | 4308 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0017 | 0/0 | 4307 | 3 | 1 | 2 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0018 | 0/0 | 4329 | 3 | 0 | 2 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0019 | 0/0 | 4335 | 3 | 0 | 2 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0020 | 0/0 | 4312 | 2 | 0 | 2 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0021 | 0/0 | 4312 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0022 | 0/0 | 4294 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0023 | 0/0 | 4313 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0024 | 0/0 | 4298 | 2 | 0 | 2 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0025 | 0/0 | 4313 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0026 | 0/0 | 4307 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0027 | 0/0 | 4331 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0028 | 0/1 | 4331 | 2 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0029 | 0/0 | 4313 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0030 | 0/0 | 4312 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0031 | 0/0 | 4313 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0032 | 0/0 | 4298 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0033 | 0/0 | 4298 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0034 | 0/0 | 4298 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0035 | 0/0 | 4297 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0036 | 0/0 | 4298 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0037 | 0/0 | 4313 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0038 | 0/0 | 4313 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0039 | 0/0 | 4313 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0040 | 0/0 | 4312 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0041 | 0/0 | 4329 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0042 | 0/0 | 4329 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0043 | 0/0 | 4331 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0044 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0045 | 0/0 | 4330 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0046 | 0/0 | 4330 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0047 | 0/0 | 4334 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0048 | 0/0 | 4334 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0049 | 0/0 | 4334 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0050 | 0/0 | 4334 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0051 | 0/0 | 4298 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0052 | 0/0 | 4313 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| t0053 | 0/0 | 4313 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0004 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0016 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0357 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3546 | 173 | 25 | 36 | 85 | 7 | 19 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0002 | 0/1 | 3546 | 120 | 20 | 26 | 56 | 5 | 12 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0004 | 0/0 | 3546 | 23 | 22 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0008 | 0/0 | 3546 | 5 | 5 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0011 | 0/0 | 3546 | 3 | 1 | 1 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0013 | 0/0 | 3546 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0014 | 0/0 | 3546 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0016 | 0/0 | 3546 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0021 | 0/0 | 3546 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0022 | 0/0 | 3546 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0028 | 0/0 | 3546 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0002c0003 | 0/0 | 3546 | 29 | 10 | 6 | 9 | 3 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0002c0007 | 0/0 | 3546 | 5 | 5 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0002c0009 | 0/0 | 3546 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0003c0005 | 0/0 | 3546 | 10 | 0 | 0 | 10 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0004c0006 | 0/0 | 3546 | 6 | 0 | 0 | 6 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0004c0020 | 0/0 | 3546 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0005c0010 | 0/0 | 3546 | 3 | 0 | 3 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0006c0012 | 0/0 | 3546 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0007c0024 | 0/0 | 3546 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0008c0018 | 0/0 | 3546 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0009c0017 | 0/0 | 3546 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0010c0027 | 0/0 | 3546 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0011c0023 | 0/0 | 3546 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0012c0026 | 0/0 | 3546 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0013c0019 | 0/0 | 3546 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0014c0025 | 0/0 | 3546 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0015c0015 | 0/0 | 3546 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0016c0029 | 0/0 | 3546 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 7843 | 74 | 15 | 9 | 44 | 1 | 4 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0001t0002 | 0/0 | 7858 | 45 | 5 | 12 | 19 | 3 | 6 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0001t0005 | 0/0 | 7843 | 28 | 3 | 10 | 8 | 2 | 5 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0001t0013 | 0/0 | 7842 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0001t0014 | 0/0 | 7840 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0001t0015 | 0/0 | 7858 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0001t0020 | 0/0 | 7857 | 2 | 0 | 2 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0001t0022 | 0/0 | 7839 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0001t0023 | 0/0 | 7858 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0001t0024 | 0/0 | 7843 | 2 | 0 | 2 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0001t0025 | 0/0 | 7858 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0001t0029 | 0/0 | 7858 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0001t0032 | 0/0 | 7843 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0001t0033 | 0/0 | 7843 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0001t0036 | 0/0 | 7843 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0001t0038 | 0/0 | 7858 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0001t0039 | 0/0 | 7858 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0001t0051 | 0/0 | 7843 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0002t0003 | 0/0 | 7876 | 34 | 1 | 6 | 22 | 2 | 3 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0002t0004 | 0/0 | 7879 | 34 | 12 | 5 | 10 | 1 | 6 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0002t0006 | 0/0 | 7878 | 25 | 3 | 5 | 17 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0002t0009 | 0/0 | 7877 | 6 | 0 | 0 | 5 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0002t0011 | 0/0 | 7876 | 5 | 0 | 5 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0002t0018 | 0/0 | 7874 | 3 | 0 | 2 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0002t0019 | 0/0 | 7880 | 3 | 0 | 2 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0002t0028 | 0/1 | 7876 | 2 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0002t0041 | 0/0 | 7874 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0002t0042 | 0/0 | 7874 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0002t0043 | 0/0 | 7876 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0002t0044 | 0/0 | 7880 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0002t0046 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0002t0047 | 0/0 | 7879 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0002t0048 | 0/0 | 7879 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0002t0049 | 0/0 | 7879 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0004t0002 | 0/0 | 7858 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0004t0008 | 0/0 | 7858 | 21 | 20 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0004t0031 | 0/0 | 7858 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0008t0012 | 0/0 | 7857 | 3 | 3 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0008t0021 | 0/0 | 7857 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0011t0002 | 0/0 | 7858 | 2 | 0 | 1 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0011t0034 | 0/0 | 7843 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0013t0001 | 0/0 | 7843 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0014t0003 | 0/0 | 7876 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0016t0005 | 0/0 | 7843 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0021t0050 | 0/0 | 7879 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0022t0002 | 0/0 | 7858 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0001c0028t0004 | 0/0 | 7879 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0002c0003t0007 | 0/0 | 7857 | 23 | 7 | 4 | 8 | 3 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0002c0003t0017 | 0/0 | 7852 | 3 | 1 | 2 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0002c0003t0026 | 0/0 | 7852 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0002c0003t0040 | 0/0 | 7857 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0002c0007t0010 | 0/0 | 7857 | 5 | 5 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0002c0009t0016 | 0/0 | 7853 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0003c0005t0003 | 0/0 | 7876 | 7 | 0 | 0 | 7 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0003c0005t0027 | 0/0 | 7876 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0003c0005t0045 | 0/0 | 7875 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0004c0006t0003 | 0/0 | 7876 | 6 | 0 | 0 | 6 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0004c0020t0003 | 0/0 | 7876 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0005c0010t0002 | 0/0 | 7858 | 2 | 0 | 2 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0005c0010t0053 | 0/0 | 7858 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0006c0012t0003 | 0/0 | 7876 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0007c0024t0005 | 0/0 | 7843 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0008c0018t0037 | 0/0 | 7858 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0009c0017t0052 | 0/0 | 7858 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0010c0027t0006 | 0/0 | 7878 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0011c0023t0035 | 0/0 | 7842 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0012c0026t0003 | 0/0 | 7876 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0013c0019t0030 | 0/0 | 7857 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0014c0025t0003 | 0/0 | 7876 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0015c0015t0002 | 0/0 | 7858 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| a0016c0029t0001 | 0/0 | 7843 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | copy fasta | chr5 | 52984352 | 53099779 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0357 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0004 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0005g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0013g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0013g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0013g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0014g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0014g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0014g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0015g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0015g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0015g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0020g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0020g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0022g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0022g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0023g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0023g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0024g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0024g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0025g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0025g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0029g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0032g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0033g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0036g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0038g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0039g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0001t0051g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0004g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0006g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0009g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0009g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0009g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0009g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0009g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0009g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0011g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0011g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0011g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0011g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0011g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0018g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0018g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0018g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0019g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0019g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0019g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0028g0016 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0041g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0042g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0043g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0044g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0046g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0047g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0048g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0002t0049g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0008g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0004t0031g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0008t0012g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0008t0012g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0008t0012g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0008t0021g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0011t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0011t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0011t0034g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0013t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0014t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0016t0005g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0021t0050g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0022t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0001c0028t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0007g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0017g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0017g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0017g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0026g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0026g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0003t0040g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0007t0010g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0007t0010g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0007t0010g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0007t0010g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0007t0010g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0009t0016g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0009t0016g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0002c0009t0016g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0003c0005t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0003c0005t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0003c0005t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0003c0005t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0003c0005t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0003c0005t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0003c0005t0027g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0003c0005t0027g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0003c0005t0045g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0004c0006t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0004c0006t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0004c0006t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0004c0006t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0004c0006t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0004c0020t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0005c0010t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0005c0010t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0005c0010t0053g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0006c0012t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0007c0024t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0008c0018t0037g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0009c0017t0052g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0010c0027t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0011c0023t0035g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0012c0026t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0013c0019t0030g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0014c0025t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0015c0015t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| a0016c0029t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0028 | g0016 | EUR | GBR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0010 | EUR | GBR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0328 | EUR | FIN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00280 | hp2 | a0001 | c0002 | t0009 | g0210 | EUR | FIN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00323 | hp1 | a0001 | c0001 | t0029 | g0139 | EUR | FIN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00323 | hp2 | a0002 | c0003 | t0007 | g0334 | EUR | FIN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00408 | hp1 | a0001 | c0002 | t0006 | g0331 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00544 | hp1 | a0001 | c0013 | t0001 | g0268 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00544 | hp2 | a0002 | c0003 | t0007 | g0078 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00597 | hp1 | a0001 | c0001 | t0023 | g0352 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00597 | hp2 | a0001 | c0002 | t0006 | g0037 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00609 | hp1 | a0001 | c0002 | t0003 | g0183 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00609 | hp2 | a0001 | c0014 | t0003 | g0064 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00621 | hp1 | a0002 | c0003 | t0007 | g0079 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00621 | hp2 | a0001 | c0002 | t0006 | g0035 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00639 | hp1 | a0005 | c0010 | t0053 | g0244 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00642 | hp1 | a0001 | c0002 | t0018 | g0120 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00673 | hp1 | a0002 | c0009 | t0016 | g0216 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00733 | hp1 | a0001 | c0002 | t0006 | g0034 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00733 | hp2 | a0001 | c0011 | t0002 | g0158 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00735 | hp1 | a0001 | c0002 | t0004 | g0265 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0288 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG00741 | hp2 | a0001 | c0002 | t0003 | g0170 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01069 | hp1 | a0001 | c0001 | t0020 | g0140 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01069 | hp2 | a0001 | c0001 | t0024 | g0300 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01070 | hp1 | a0002 | c0003 | t0007 | g0286 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01071 | hp2 | a0001 | c0001 | t0020 | g0131 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01074 | hp1 | a0001 | c0002 | t0019 | g0238 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01081 | hp1 | a0001 | c0002 | t0003 | g0031 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01081 | hp2 | a0001 | c0002 | t0019 | g0237 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0287 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01099 | hp2 | a0001 | c0002 | t0004 | g0256 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01109 | hp2 | a0001 | c0004 | t0008 | g0369 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0317 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01167 | hp2 | a0001 | c0002 | t0041 | g0332 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0316 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01175 | hp1 | a0001 | c0002 | t0018 | g0103 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01175 | hp2 | a0001 | c0002 | t0006 | g0054 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01192 | hp1 | a0002 | c0003 | t0007 | g0346 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0017 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0327 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01243 | hp2 | a0002 | c0003 | t0017 | g0022 | AMR | PUR | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01256 | hp1 | a0016 | c0029 | t0001 | g0304 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01256 | hp2 | a0001 | c0002 | t0004 | g0233 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01257 | hp2 | a0001 | c0002 | t0006 | g0038 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01258 | hp2 | a0001 | c0002 | t0004 | g0240 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01261 | hp1 | a0002 | c0003 | t0017 | g0021 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0321 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01346 | hp1 | a0001 | c0001 | t0032 | g0092 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01358 | hp1 | a0002 | c0003 | t0007 | g0333 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0291 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0213 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0326 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01496 | hp2 | a0001 | c0002 | t0006 | g0005 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01515 | hp1 | a0001 | c0002 | t0003 | g0200 | EUR | IBS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01515 | hp2 | a0001 | c0011 | t0002 | g0114 | EUR | IBS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01516 | hp1 | a0002 | c0003 | t0007 | g0018 | EUR | IBS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0248 | EUR | IBS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01517 | hp1 | a0002 | c0003 | t0007 | g0018 | EUR | IBS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01517 | hp2 | a0001 | c0002 | t0003 | g0199 | EUR | IBS | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01884 | hp2 | a0002 | c0003 | t0007 | g0019 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01891 | hp2 | a0001 | c0004 | t0008 | g0374 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01928 | hp1 | a0005 | c0010 | t0002 | g0124 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01928 | hp2 | a0001 | c0002 | t0011 | g0168 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01975 | hp1 | a0002 | c0003 | t0007 | g0343 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01975 | hp2 | a0001 | c0002 | t0011 | g0215 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01978 | hp1 | a0005 | c0010 | t0002 | g0143 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01978 | hp2 | a0001 | c0002 | t0011 | g0202 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01981 | hp2 | a0001 | c0002 | t0003 | g0189 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01993 | hp1 | a0001 | c0002 | t0003 | g0190 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01993 | hp2 | a0001 | c0001 | t0024 | g0214 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02004 | hp1 | a0001 | c0001 | t0005 | g0217 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02004 | hp2 | a0001 | c0002 | t0011 | g0187 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02015 | hp1 | a0006 | c0012 | t0003 | g0206 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02015 | hp2 | a0001 | c0002 | t0006 | g0042 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02027 | hp1 | a0001 | c0002 | t0004 | g0266 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02040 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02040 | hp2 | a0001 | c0001 | t0005 | g0301 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02055 | hp1 | a0001 | c0004 | t0008 | g0373 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02055 | hp2 | a0002 | c0003 | t0007 | g0285 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02056 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02071 | hp1 | a0001 | c0001 | t0005 | g0330 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02071 | hp2 | a0003 | c0005 | t0003 | g0178 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02074 | hp1 | a0001 | c0028 | t0004 | g0074 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02132 | hp1 | a0002 | c0003 | t0007 | g0080 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02145 | hp2 | a0001 | c0002 | t0044 | g0223 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | CDX | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02165 | hp2 | a0001 | c0002 | t0003 | g0192 | EAS | CDX | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02257 | hp1 | a0002 | c0003 | t0017 | g0023 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02273 | hp1 | a0001 | c0002 | t0011 | g0191 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02273 | hp2 | a0001 | c0001 | t0005 | g0218 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02280 | hp1 | a0002 | c0007 | t0010 | g0260 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02280 | hp2 | a0001 | c0002 | t0042 | g0311 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02293 | hp1 | a0001 | c0002 | t0004 | g0145 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02293 | hp2 | a0001 | c0001 | t0005 | g0219 | AMR | PEL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02451 | hp1 | a0001 | c0004 | t0008 | g0309 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02451 | hp2 | a0002 | c0003 | t0026 | g0274 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02572 | hp1 | a0001 | c0004 | t0008 | g0372 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02602 | hp1 | a0001 | c0002 | t0004 | g0229 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02602 | hp2 | a0001 | c0022 | t0002 | g0245 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02615 | hp1 | a0001 | c0002 | t0004 | g0247 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02615 | hp2 | a0001 | c0004 | t0008 | g0306 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02622 | hp1 | a0001 | c0004 | t0008 | g0365 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02622 | hp2 | a0002 | c0003 | t0007 | g0283 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02630 | hp1 | a0001 | c0001 | t0025 | g0281 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02647 | hp1 | a0001 | c0002 | t0004 | g0102 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02647 | hp2 | a0001 | c0021 | t0050 | g0280 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0126 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02683 | hp2 | a0001 | c0001 | t0051 | g0071 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02698 | hp1 | a0001 | c0002 | t0003 | g0194 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02698 | hp2 | a0001 | c0002 | t0004 | g0106 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02717 | hp1 | a0001 | c0002 | t0006 | g0367 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02717 | hp2 | a0001 | c0004 | t0002 | g0344 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02723 | hp1 | a0001 | c0008 | t0021 | g0013 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02723 | hp2 | a0002 | c0003 | t0007 | g0359 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02809 | hp1 | a0001 | c0004 | t0008 | g0310 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02809 | hp2 | a0001 | c0002 | t0004 | g0259 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02818 | hp1 | a0002 | c0003 | t0007 | g0284 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02818 | hp2 | a0002 | c0007 | t0010 | g0167 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02886 | hp1 | a0001 | c0004 | t0008 | g0362 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02886 | hp2 | a0001 | c0002 | t0004 | g0246 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02895 | hp2 | a0001 | c0002 | t0004 | g0235 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02896 | hp1 | a0001 | c0004 | t0008 | g0307 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02896 | hp2 | a0002 | c0003 | t0007 | g0356 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02897 | hp1 | a0001 | c0004 | t0008 | g0313 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02897 | hp2 | a0001 | c0002 | t0004 | g0242 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02965 | hp2 | a0001 | c0008 | t0012 | g0164 | AFR | ESN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02970 | hp1 | a0002 | c0003 | t0026 | g0275 | AFR | ESN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02970 | hp2 | a0002 | c0007 | t0010 | g0165 | AFR | ESN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02976 | hp1 | a0001 | c0002 | t0047 | g0061 | AFR | ESN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02976 | hp2 | a0001 | c0002 | t0004 | g0236 | AFR | ESN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03098 | hp1 | a0001 | c0002 | t0049 | g0338 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03130 | hp1 | a0001 | c0008 | t0012 | g0162 | AFR | ESN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03130 | hp2 | a0001 | c0004 | t0008 | g0305 | AFR | ESN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03139 | hp1 | a0001 | c0008 | t0012 | g0163 | AFR | ESN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03139 | hp2 | a0002 | c0003 | t0007 | g0019 | AFR | ESN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03195 | hp1 | a0001 | c0004 | t0008 | g0312 | AFR | ESN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03195 | hp2 | a0001 | c0002 | t0004 | g0241 | AFR | ESN | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03209 | hp1 | a0001 | c0004 | t0008 | g0308 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03209 | hp2 | a0001 | c0002 | t0006 | g0112 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03225 | hp1 | a0001 | c0004 | t0008 | g0364 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0262 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03239 | hp1 | a0001 | c0002 | t0019 | g0230 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03453 | hp2 | a0001 | c0004 | t0008 | g0370 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03486 | hp2 | a0001 | c0004 | t0031 | g0363 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03490 | hp1 | a0012 | c0026 | t0003 | g0204 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03490 | hp2 | a0001 | c0001 | t0005 | g0314 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03492 | hp1 | a0001 | c0002 | t0004 | g0257 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0004 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0315 | AFR | GWD | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03579 | hp1 | a0009 | c0017 | t0052 | g0263 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03654 | hp1 | a0001 | c0001 | t0039 | g0121 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03654 | hp2 | a0001 | c0016 | t0005 | g0104 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03688 | hp1 | a0001 | c0002 | t0004 | g0116 | SAS | STU | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03688 | hp2 | a0001 | c0002 | t0048 | g0239 | SAS | STU | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03704 | hp2 | a0001 | c0001 | t0036 | g0296 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03710 | hp1 | a0001 | c0002 | t0018 | g0105 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0004 | SAS | PJL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03831 | hp1 | a0002 | c0003 | t0007 | g0349 | SAS | BEB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03831 | hp2 | a0015 | c0015 | t0002 | g0278 | SAS | BEB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | BEB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03927 | hp2 | a0001 | c0002 | t0004 | g0115 | SAS | BEB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03942 | hp1 | a0001 | c0002 | t0003 | g0201 | SAS | BEB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03942 | hp2 | a0001 | c0001 | t0038 | g0129 | SAS | BEB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0133 | SAS | STU | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG04184 | hp1 | a0001 | c0002 | t0003 | g0113 | SAS | BEB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0122 | SAS | BEB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG04199 | hp1 | a0001 | c0001 | t0005 | g0299 | SAS | STU | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG04199 | hp2 | a0001 | c0002 | t0004 | g0282 | SAS | STU | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | YRI | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18522 | hp2 | a0001 | c0002 | t0004 | g0099 | AFR | YRI | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18612 | hp1 | a0001 | c0002 | t0003 | g0185 | EAS | CHB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18939 | hp2 | a0001 | c0001 | t0014 | g0294 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18940 | hp1 | a0001 | c0001 | t0005 | g0135 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18942 | hp1 | a0001 | c0001 | t0015 | g0152 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18942 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0302 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18947 | hp1 | a0004 | c0006 | t0003 | g0174 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18947 | hp2 | a0001 | c0001 | t0033 | g0353 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18948 | hp1 | a0001 | c0002 | t0003 | g0063 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18950 | hp2 | a0002 | c0003 | t0040 | g0342 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18951 | hp1 | a0007 | c0024 | t0005 | g0130 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18951 | hp2 | a0001 | c0001 | t0014 | g0295 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18954 | hp2 | a0001 | c0002 | t0003 | g0179 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18956 | hp2 | a0001 | c0002 | t0004 | g0253 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18957 | hp2 | a0001 | c0002 | t0006 | g0001 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18959 | hp1 | a0001 | c0001 | t0013 | g0009 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18959 | hp2 | a0001 | c0002 | t0006 | g0040 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18961 | hp1 | a0002 | c0009 | t0016 | g0272 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18961 | hp2 | a0001 | c0002 | t0003 | g0182 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18962 | hp1 | a0001 | c0001 | t0013 | g0340 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18962 | hp2 | a0001 | c0002 | t0006 | g0050 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18963 | hp2 | a0001 | c0002 | t0003 | g0110 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18964 | hp1 | a0003 | c0005 | t0003 | g0015 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18964 | hp2 | a0001 | c0002 | t0006 | g0041 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18965 | hp1 | a0001 | c0002 | t0006 | g0045 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18965 | hp2 | a0003 | c0005 | t0027 | g0211 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18970 | hp2 | a0004 | c0006 | t0003 | g0014 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18971 | hp1 | a0001 | c0002 | t0003 | g0111 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0303 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18972 | hp1 | a0001 | c0001 | t0005 | g0293 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18972 | hp2 | a0001 | c0002 | t0006 | g0052 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18973 | hp2 | a0003 | c0005 | t0003 | g0176 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18975 | hp2 | a0001 | c0002 | t0006 | g0048 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18979 | hp1 | a0014 | c0025 | t0003 | g0173 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18980 | hp2 | a0001 | c0002 | t0004 | g0251 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18981 | hp2 | a0001 | c0002 | t0006 | g0039 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18983 | hp1 | a0001 | c0001 | t0022 | g0044 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18983 | hp2 | a0003 | c0005 | t0003 | g0290 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18986 | hp1 | a0003 | c0005 | t0045 | g0205 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18988 | hp1 | a0004 | c0006 | t0003 | g0014 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18989 | hp1 | a0001 | c0002 | t0003 | g0197 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18989 | hp2 | a0002 | c0003 | t0007 | g0337 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18991 | hp2 | a0001 | c0002 | t0006 | g0043 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18993 | hp1 | a0002 | c0003 | t0007 | g0072 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18993 | hp2 | a0001 | c0001 | t0023 | g0354 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18994 | hp1 | a0010 | c0027 | t0006 | g0036 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18994 | hp2 | a0001 | c0002 | t0003 | g0108 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18995 | hp1 | a0001 | c0002 | t0009 | g0208 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18995 | hp2 | a0002 | c0009 | t0016 | g0271 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18999 | hp1 | a0003 | c0005 | t0003 | g0270 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19000 | hp1 | a0001 | c0002 | t0006 | g0053 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19002 | hp2 | a0004 | c0020 | t0003 | g0132 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19003 | hp1 | a0001 | c0002 | t0004 | g0252 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19003 | hp2 | a0001 | c0002 | t0009 | g0207 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19004 | hp1 | a0001 | c0002 | t0003 | g0198 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19005 | hp2 | a0001 | c0002 | t0009 | g0209 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19007 | hp1 | a0001 | c0002 | t0003 | g0196 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19009 | hp1 | a0001 | c0002 | t0003 | g0171 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19010 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19010 | hp2 | a0003 | c0005 | t0027 | g0347 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19012 | hp2 | a0001 | c0002 | t0003 | g0184 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19030 | hp1 | a0002 | c0007 | t0010 | g0261 | AFR | LWK | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19030 | hp2 | a0001 | c0004 | t0008 | g0319 | AFR | LWK | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19043 | hp1 | a0001 | c0004 | t0008 | g0366 | AFR | LWK | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19043 | hp2 | a0001 | c0002 | t0004 | g0232 | AFR | LWK | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19054 | hp1 | a0001 | c0001 | t0022 | g0046 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19054 | hp2 | a0001 | c0002 | t0003 | g0186 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19055 | hp2 | a0001 | c0001 | t0015 | g0160 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19056 | hp1 | a0001 | c0002 | t0003 | g0157 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19056 | hp2 | a0002 | c0003 | t0007 | g0355 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19057 | hp2 | a0001 | c0001 | t0015 | g0249 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19060 | hp2 | a0001 | c0002 | t0006 | g0001 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19063 | hp1 | a0001 | c0002 | t0009 | g0027 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19065 | hp1 | a0001 | c0002 | t0046 | g0002 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19065 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19066 | hp2 | a0004 | c0006 | t0003 | g0169 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19068 | hp1 | a0001 | c0002 | t0004 | g0255 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19068 | hp2 | a0001 | c0002 | t0003 | g0069 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19070 | hp2 | a0004 | c0006 | t0003 | g0172 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19075 | hp1 | a0001 | c0001 | t0013 | g0141 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19075 | hp2 | a0001 | c0002 | t0006 | g0049 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19076 | hp1 | a0001 | c0002 | t0009 | g0212 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19076 | hp2 | a0001 | c0001 | t0014 | g0279 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19079 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19080 | hp2 | a0004 | c0006 | t0003 | g0175 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19082 | hp1 | a0001 | c0002 | t0004 | g0254 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19082 | hp2 | a0002 | c0003 | t0007 | g0348 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19084 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19084 | hp2 | a0002 | c0003 | t0007 | g0360 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19085 | hp2 | a0001 | c0002 | t0006 | g0001 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19086 | hp1 | a0001 | c0002 | t0003 | g0203 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19087 | hp2 | a0003 | c0005 | t0003 | g0177 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19088 | hp2 | a0003 | c0005 | t0003 | g0015 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19090 | hp1 | a0001 | c0002 | t0003 | g0193 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19091 | hp1 | a0001 | c0002 | t0043 | g0109 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19091 | hp2 | a0001 | c0002 | t0004 | g0258 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | YRI | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA19240 | hp2 | a0001 | c0002 | t0004 | g0231 | AFR | YRI | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA20129 | hp1 | a0001 | c0002 | t0006 | g0005 | AFR | ASW | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA20129 | hp2 | a0013 | c0019 | t0030 | g0033 | AFR | ASW | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | TSI | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0329 | EUR | TSI | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA20805 | hp1 | a0001 | c0002 | t0004 | g0234 | EUR | TSI | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0017 | EUR | TSI | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | GIH | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0004 | SAS | GIH | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01123 | hp1 | a0001 | c0002 | t0006 | g0051 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG01123 | hp2 | a0001 | c0002 | t0003 | g0180 | AMR | CLM | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02109 | hp1 | a0001 | c0004 | t0008 | g0361 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02109 | hp2 | a0001 | c0008 | t0021 | g0013 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02486 | hp1 | a0001 | c0002 | t0004 | g0087 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02486 | hp2 | a0001 | c0004 | t0008 | g0371 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02559 | hp1 | a0001 | c0004 | t0008 | g0368 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG02559 | hp2 | a0001 | c0001 | t0025 | g0276 | AFR | ACB | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03471 | hp1 | a0008 | c0018 | t0037 | g0277 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG03471 | hp2 | a0002 | c0007 | t0010 | g0166 | AFR | MSL | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG06807 | hp1 | a0001 | c0011 | t0034 | g0084 | AFR | USA | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| HG06807 | hp2 | a0001 | c0002 | t0003 | g0195 | AFR | USA | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18955 | hp1 | a0011 | c0023 | t0035 | g0292 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA18955 | hp2 | a0001 | c0002 | t0003 | g0188 | EAS | JPT | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0358 | AFR | USA | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0318 | AFR | USA | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0264 | AFR | LWK | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0267 | AFR | LWK | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0028 | g0016 | REF | REF | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0357 | REF | REF | ITGA2_chr5_52984352_53099779 | ITGA2 | chr5 | 52984352 | 53099779 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:53045032
|
G | A | 1 | a0006 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.327G>A | p.Met109Ile | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/30 | 444/7843 | 327/3546 | 109/1181 | chr5 | 53045032 | ||
| chr5:53048657
|
A | G | 1 | a0016 | 1 | HG01256.hp1 | missense_variant | MODERATE | c.517A>G | p.Ile173Val | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/30 | 634/7843 | 517/3546 | 173/1181 | chr5 | 53048657 | ||
| chr5:53051540
|
G | A | 1 | a0015 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.760G>A | p.Gly254Arg | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/30 | 877/7843 | 760/3546 | 254/1181 | chr5 | 53051540 | ||
| chr5:53056008
|
G | A | 1 | a0005 | 3 | HG00639.hp1 HG01928.hp1 HG01978.hp1 |
missense_variant | MODERATE | c.955G>A | p.Ala319Thr | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/30 | 1072/7843 | 955/3546 | 319/1181 | chr5 | 53056008 | ||
| chr5:53056144
|
T | C | 1 | a0014 | 1 | NA18979.hp1 | missense_variant | MODERATE | c.1091T>C | p.Ile364Thr | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/30 | 1208/7843 | 1091/3546 | 364/1181 | chr5 | 53056144 | ||
| chr5:53058045
|
A | G | 1 | a0007 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.1117A>G | p.Asn373Asp | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/30 | 1234/7843 | 1117/3546 | 373/1181 | chr5 | 53058045 | ||
| chr5:53062927
|
G | A | 2 | a0002a0013 | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
missense_variant&splice_region_variant | MODERATE | c.1600G>A | p.Glu534Lys | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/30 | 1717/7843 | 1600/3546 | 534/1181 | chr5 | 53062927 | ||
| chr5:53070124
|
T | C | 1 | a0012 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.2099T>C | p.Ile700Thr | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/30 | 2216/7843 | 2099/3546 | 700/1181 | chr5 | 53070124 | ||
| chr5:53072643
|
G | A | 2 | a0004a0014 | 8 | NA18947.hp1 NA18970.hp2 NA18979.hp1 others(5): Show |
missense_variant | MODERATE | c.2377G>A | p.Gly793Arg | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 19/30 | 2494/7843 | 2377/3546 | 793/1181 | chr5 | 53072643 | ||
| chr5:53072695
|
A | G | 1 | a0011 | 1 | NA18955.hp1 | missense_variant&splice_region_variant | MODERATE | c.2429A>G | p.Gln810Arg | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 19/30 | 2546/7843 | 2429/3546 | 810/1181 | chr5 | 53072695 | ||
| chr5:53074418
|
G | A | 1 | a0013 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.2605G>A | p.Ala869Thr | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 21/30 | 2722/7843 | 2605/3546 | 869/1181 | chr5 | 53074418 | ||
| chr5:53074449
|
G | T | 1 | a0010 | 1 | NA18994.hp1 | missense_variant | MODERATE | c.2636G>T | p.Gly879Val | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 21/30 | 2753/7843 | 2636/3546 | 879/1181 | chr5 | 53074449 | ||
| chr5:53075070
|
A | C | 1 | a0008 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.2674A>C | p.Thr892Pro | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 22/30 | 2791/7843 | 2674/3546 | 892/1181 | chr5 | 53075070 | ||
| chr5:53075259
|
A | G | 1 | a0003 | 10 | HG02071.hp2 NA18964.hp1 NA18965.hp2 others(7): Show |
missense_variant | MODERATE | c.2780A>G | p.Asn927Ser | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/30 | 2897/7843 | 2780/3546 | 927/1181 | chr5 | 53075259 | ||
| chr5:53078840
|
A | G | 1 | a0006 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.2894A>G | p.Glu965Gly | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/30 | 3011/7843 | 2894/3546 | 965/1181 | chr5 | 53078840 | ||
| chr5:53089976
|
A | C | 2 | a0008a0009 | 2 | HG03471.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.3379A>C | p.Lys1127Gln | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 29/30 | 3496/7843 | 3379/3546 | 1127/1181 | chr5 | 53089976 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:53051413
|
G | A | 2 | a0001c0013a0001c0014 | 2 | HG00544.hp1 HG00609.hp2 |
splice_region_variant&synonymous_variant | LOW | c.633G>A | p.Val211Val | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/30 | 750/7843 | 633/3546 | 211/1181 | chr5 | 53051413 | ||
| chr5:53051539
|
C | T | 9 | a0001c0002a0001c0011a0001c0028others(6): Show | 144 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
synonymous_variant | LOW | c.759C>T | p.Phe253Phe | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/30 | 876/7843 | 759/3546 | 253/1181 | chr5 | 53051539 | ||
| chr5:53055547
|
T | C | 3 | a0001c0016a0002c0003a0002c0009 | 33 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(30): Show |
synonymous_variant | LOW | c.789T>C | p.Ala263Ala | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 8/30 | 906/7843 | 789/3546 | 263/1181 | chr5 | 53055547 | ||
| chr5:53055583
|
G | A | 11 | a0001c0002a0001c0011a0001c0028others(8): Show | 146 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(143): Show |
synonymous_variant | LOW | c.825G>A | p.Thr275Thr | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 8/30 | 942/7843 | 825/3546 | 275/1181 | chr5 | 53055583 | ||
| chr5:53055607
|
C | T | 1 | a0001c0004 | 23 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
synonymous_variant | LOW | c.849C>T | p.Asp283Asp | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 8/30 | 966/7843 | 849/3546 | 283/1181 | chr5 | 53055607 | ||
| chr5:53056046
|
A | G | 3 | a0001c0016a0002c0003a0002c0009 | 33 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(30): Show |
synonymous_variant | LOW | c.993A>G | p.Ala331Ala | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/30 | 1110/7843 | 993/3546 | 331/1181 | chr5 | 53056046 | ||
| chr5:53059927
|
C | G | 1 | a0001c0028 | 1 | HG02074.hp1 | synonymous_variant | LOW | c.1227C>G | p.Val409Val | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 11/30 | 1344/7843 | 1227/3546 | 409/1181 | chr5 | 53059927 | ||
| chr5:53072642
|
C | T | 6 | a0002c0003a0002c0007a0002c0009others(3): Show | 40 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(37): Show |
synonymous_variant | LOW | c.2376C>T | p.Asp792Asp | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 19/30 | 2493/7843 | 2376/3546 | 792/1181 | chr5 | 53072642 | ||
| chr5:53073172
|
G | A | 4 | a0002c0003a0002c0007a0002c0009others(1): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
synonymous_variant | LOW | c.2484G>A | p.Thr828Thr | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/30 | 2601/7843 | 2484/3546 | 828/1181 | chr5 | 53073172 | ||
| chr5:53073256
|
G | A | 3 | a0002c0003a0002c0007a0013c0019 | 35 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(32): Show |
synonymous_variant | LOW | c.2568G>A | p.Leu856Leu | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/30 | 2685/7843 | 2568/3546 | 856/1181 | chr5 | 53073256 | ||
| chr5:53075114
|
G | A | 2 | a0001c0008a0001c0021 | 6 | HG02109.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
synonymous_variant | LOW | c.2718G>A | p.Ala906Ala | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 22/30 | 2835/7843 | 2718/3546 | 906/1181 | chr5 | 53075114 | ||
| chr5:53083447
|
C | T | 11 | a0001c0002a0001c0014a0001c0021others(8): Show | 144 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
synonymous_variant | LOW | c.3252C>T | p.Phe1084Phe | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/30 | 3369/7843 | 3252/3546 | 1084/1181 | chr5 | 53083447 | ||
| chr5:53090521
|
C | T | 1 | a0001c0022 | 1 | HG02602.hp2 | splice_region_variant&synonymous_variant | LOW | c.3468C>T | p.Leu1156Leu | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3585/7843 | 3468/3546 | 1156/1181 | chr5 | 53090521 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:52989415
|
C | T | 1 | a0005c0010t0053 | 1 | HG00639.hp1 | 5_prime_UTR_variant | MODIFIER | c.-54C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/30 | 54 | chr5 | 52989415 | |||||
| chr5:52989456
|
G | A | 2 | a0001c0001t0020a0001c0001t0029 | 3 | HG00323.hp1 HG01069.hp1 HG01071.hp2 |
5_prime_UTR_variant | MODIFIER | c.-13G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/30 | 13 | chr5 | 52989456 | |||||
| chr5:53090634
|
A | C | 1 | a0001c0002t0028 | 2 | HG00140.hp1 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*35A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 35 | chr5 | 53090634 | |||||
| chr5:53090667
|
A | G | 1 | a0009c0017t0052 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*68A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 68 | chr5 | 53090667 | |||||
| chr5:53090686
|
A | AT | 1 | a0001c0002t0009 | 6 | HG00280.hp2 NA18995.hp1 NA19003.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*95dupT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 96 | INFO_REALIGN_3_PRIME | chr5 | 53090686 | ||||
| chr5:53090736
|
C | G | 1 | a0001c0001t0051 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*137C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 137 | chr5 | 53090736 | |||||
| chr5:53090807
|
G | A | 2 | a0002c0007t0010a0013c0019t0030 | 6 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*208G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 208 | chr5 | 53090807 | |||||
| chr5:53090830
|
TG | T | 2 | a0001c0008t0012a0001c0008t0021 | 5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*236delG | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 236 | INFO_REALIGN_3_PRIME | chr5 | 53090830 | ||||
| chr5:53091060
|
A | C | 1 | a0001c0021t0050 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*461A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 461 | chr5 | 53091060 | |||||
| chr5:53091071
|
TAAC | T | 28 | a0001c0002t0003a0001c0002t0004a0001c0002t0006others(25): Show | 144 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*475_*477delCAA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 475 | INFO_REALIGN_3_PRIME | chr5 | 53091071 | ||||
| chr5:53091306
|
G | C | 1 | a0001c0004t0031 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*707G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 707 | chr5 | 53091306 | |||||
| chr5:53091320
|
A | C | 61 | a0001c0001t0002a0001c0001t0005a0001c0001t0014others(58): Show | 311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
3_prime_UTR_variant | MODIFIER | c.*721A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 721 | chr5 | 53091320 | |||||
| chr5:53091357
|
C | CATTT | 7 | a0002c0003t0007a0002c0003t0017a0002c0003t0026others(4): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*760_*761insTTAT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 761 | INFO_REALIGN_3_PRIME | chr5 | 53091357 | ||||
| chr5:53091408
|
G | C | 1 | a0001c0001t0032 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*809G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 809 | chr5 | 53091408 | |||||
| chr5:53091493
|
C | T | 54 | a0001c0001t0002a0001c0001t0015a0001c0001t0020others(51): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
3_prime_UTR_variant | MODIFIER | c.*894C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 894 | chr5 | 53091493 | |||||
| chr5:53091836
|
A | G | 1 | a0001c0011t0034 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1237A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 1237 | chr5 | 53091836 | |||||
| chr5:53091851
|
G | A | 7 | a0002c0003t0007a0002c0003t0017a0002c0003t0026others(4): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1252G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 1252 | chr5 | 53091851 | |||||
| chr5:53092240
|
C | G | 1 | a0002c0003t0017 | 3 | HG01243.hp2 HG01261.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1641C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 1641 | chr5 | 53092240 | |||||
| chr5:53092356
|
GA | G | 3 | a0001c0002t0006a0001c0002t0049a0010c0027t0006 | 27 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1764delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 1764 | INFO_REALIGN_3_PRIME | chr5 | 53092356 | ||||
| chr5:53092481
|
G | A | 1 | a0001c0008t0012 | 3 | HG02965.hp2 HG03130.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1882G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 1882 | chr5 | 53092481 | |||||
| chr5:53092496
|
A | T | 1 | a0001c0001t0033 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1897A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 1897 | chr5 | 53092496 | |||||
| chr5:53092514
|
G | A | 1 | a0011c0023t0035 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1915G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 1915 | chr5 | 53092514 | |||||
| chr5:53092520
|
G | T | 1 | a0002c0003t0017 | 3 | HG01243.hp2 HG01261.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1921G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 1921 | chr5 | 53092520 | |||||
| chr5:53092624
|
TA | T | 12 | a0001c0001t0013a0001c0001t0020a0001c0002t0004others(9): Show | 72 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*2041delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2041 | INFO_REALIGN_3_PRIME | chr5 | 53092624 | ||||
| chr5:53092624
|
TAAA | T | 7 | a0002c0003t0007a0002c0003t0017a0002c0003t0026others(4): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2039_*2041delAAA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2039 | INFO_REALIGN_3_PRIME | chr5 | 53092624 | ||||
| chr5:53092650
|
A | G | 1 | a0001c0001t0039 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2051A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2051 | chr5 | 53092650 | |||||
| chr5:53092687
|
A | G | 1 | a0001c0001t0015 | 3 | NA18942.hp1 NA19055.hp2 NA19057.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2088A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2088 | chr5 | 53092687 | |||||
| chr5:53092750
|
A | G | 2 | a0001c0008t0012a0001c0008t0021 | 5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2151A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2151 | chr5 | 53092750 | |||||
| chr5:53092797
|
T | C | 1 | a0002c0003t0040 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2198T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2198 | chr5 | 53092797 | |||||
| chr5:53092928
|
TGAAACCC others(16): Show |
T | 7 | a0002c0003t0007a0002c0003t0017a0002c0003t0026others(4): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2330_*2352delGAAA others(19): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2330 | chr5 | 53092928 | |||||
| chr5:53093103
|
TCAAA | T | 19 | a0001c0001t0022a0001c0002t0003a0001c0002t0009others(16): Show | 77 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*2517_*2520delCAAA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2517 | INFO_REALIGN_3_PRIME | chr5 | 53093103 | ||||
| chr5:53093115
|
A | C | 7 | a0002c0003t0007a0002c0003t0017a0002c0003t0026others(4): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2516A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2516 | chr5 | 53093115 | |||||
| chr5:53093116
|
C | A | 7 | a0002c0003t0007a0002c0003t0017a0002c0003t0026others(4): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2517C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2517 | chr5 | 53093116 | |||||
| chr5:53093118
|
A | T | 7 | a0002c0003t0007a0002c0003t0017a0002c0003t0026others(4): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2519A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2519 | chr5 | 53093118 | |||||
| chr5:53093120
|
A | C | 1 | a0001c0002t0044 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2521A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2521 | chr5 | 53093120 | |||||
| chr5:53093169
|
C | A | 1 | a0001c0002t0011 | 5 | HG01928.hp2 HG01975.hp2 HG01978.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2570C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2570 | chr5 | 53093169 | |||||
| chr5:53093169
|
C | T | 13 | a0001c0001t0002a0001c0001t0015a0001c0001t0020others(10): Show | 63 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*2570C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2570 | chr5 | 53093169 | |||||
| chr5:53093173
|
C | G | 7 | a0002c0003t0007a0002c0003t0017a0002c0003t0026others(4): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2574C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2574 | chr5 | 53093173 | |||||
| chr5:53093322
|
G | C | 2 | a0003c0005t0027a0003c0005t0045 | 3 | NA18965.hp2 NA18986.hp1 NA19010.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2723G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2723 | chr5 | 53093322 | |||||
| chr5:53093381
|
C | G | 1 | a0001c0002t0043 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2782C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2782 | chr5 | 53093381 | |||||
| chr5:53093481
|
G | GGTATGTT others(4): Show |
55 | a0001c0001t0002a0001c0001t0015a0001c0001t0020others(52): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
3_prime_UTR_variant | MODIFIER | c.*2883_*2893dupGTAT others(7): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2894 | INFO_REALIGN_3_PRIME | chr5 | 53093481 | ||||
| chr5:53093538
|
C | T | 7 | a0002c0003t0007a0002c0003t0017a0002c0003t0026others(4): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2939C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2939 | chr5 | 53093538 | |||||
| chr5:53093539
|
G | A | 28 | a0001c0002t0003a0001c0002t0004a0001c0002t0006others(25): Show | 144 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*2940G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2940 | chr5 | 53093539 | |||||
| chr5:53093598
|
A | G | 23 | a0001c0002t0003a0001c0002t0004a0001c0002t0009others(20): Show | 115 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*2999A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 2999 | chr5 | 53093598 | |||||
| chr5:53093625
|
A | G | 55 | a0001c0001t0002a0001c0001t0015a0001c0001t0020others(52): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
3_prime_UTR_variant | MODIFIER | c.*3026A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3026 | chr5 | 53093625 | |||||
| chr5:53093647
|
G | A | 2 | a0008c0018t0037a0009c0017t0052 | 2 | HG03471.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3048G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3048 | chr5 | 53093647 | |||||
| chr5:53093763
|
G | A | 7 | a0002c0003t0007a0002c0003t0017a0002c0003t0026others(4): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*3164G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3164 | chr5 | 53093763 | |||||
| chr5:53093769
|
A | G | 1 | a0001c0001t0025 | 2 | HG02559.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3170A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3170 | chr5 | 53093769 | |||||
| chr5:53093904
|
ACTC | A | 1 | a0001c0001t0014 | 3 | NA18939.hp2 NA18951.hp2 NA19076.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3308_*3310delCCT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3308 | INFO_REALIGN_3_PRIME | chr5 | 53093904 | ||||
| chr5:53093914
|
G | T | 1 | a0001c0001t0038 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3315G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3315 | chr5 | 53093914 | |||||
| chr5:53093930
|
A | G | 1 | a0013c0019t0030 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3331A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3331 | chr5 | 53093930 | |||||
| chr5:53093967
|
A | T | 1 | a0001c0002t0042 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3368A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3368 | chr5 | 53093967 | |||||
| chr5:53093981
|
T | TAAAG | 55 | a0001c0001t0002a0001c0001t0015a0001c0001t0020others(52): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
3_prime_UTR_variant | MODIFIER | c.*3385_*3386insGAAA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3386 | INFO_REALIGN_3_PRIME | chr5 | 53093981 | ||||
| chr5:53093997
|
T | G | 1 | a0001c0002t0041 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3398T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3398 | chr5 | 53093997 | |||||
| chr5:53094191
|
A | AATTTAT | 2 | a0002c0003t0017a0002c0003t0026 | 5 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3593_*3594insTTTA others(2): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3594 | INFO_REALIGN_3_PRIME | chr5 | 53094191 | ||||
| chr5:53094196
|
A | AACTTTGT others(6): Show |
2 | a0002c0003t0017a0002c0003t0026 | 5 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3598_*3599insCTTT others(9): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3599 | INFO_REALIGN_3_PRIME | chr5 | 53094196 | ||||
| chr5:53094196
|
A | AATTATAT others(18): Show |
28 | a0001c0002t0003a0001c0002t0004a0001c0002t0006others(25): Show | 144 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*3599_*3600insTATA others(21): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3600 | INFO_REALIGN_3_PRIME | chr5 | 53094196 | ||||
| chr5:53094196
|
A | AATTTATA others(17): Show |
4 | a0002c0003t0007a0002c0003t0040a0002c0007t0010others(1): Show | 30 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3599_*3600insTTAT others(20): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3600 | INFO_REALIGN_3_PRIME | chr5 | 53094196 | ||||
| chr5:53094196
|
A | AATTTATA others(17): Show |
1 | a0002c0009t0016 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3599_*3600insTTAT others(20): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3600 | INFO_REALIGN_3_PRIME | chr5 | 53094196 | ||||
| chr5:53094360
|
TAA | T | 3 | a0001c0002t0018a0001c0002t0041a0001c0002t0042 | 5 | HG00642.hp1 HG01167.hp2 HG01175.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3763_*3764delAA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3763 | INFO_REALIGN_3_PRIME | chr5 | 53094360 | ||||
| chr5:53094373
|
G | T | 1 | a0001c0001t0036 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3774G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3774 | chr5 | 53094373 | |||||
| chr5:53094488
|
A | G | 1 | a0001c0002t0048 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3889A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3889 | chr5 | 53094488 | |||||
| chr5:53094517
|
G | C | 7 | a0002c0003t0007a0002c0003t0017a0002c0003t0026others(4): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*3918G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3918 | chr5 | 53094517 | |||||
| chr5:53094585
|
A | C | 29 | a0001c0001t0024a0001c0002t0003a0001c0002t0004others(26): Show | 146 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*3986A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 3986 | chr5 | 53094585 | |||||
| chr5:53094639
|
CAGTTAGT | C | 1 | a0002c0009t0016 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4045_*4051delAGTA others(3): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 4045 | INFO_REALIGN_3_PRIME | chr5 | 53094639 | ||||
| chr5:53094642
|
TTAG | T | 6 | a0002c0003t0007a0002c0003t0017a0002c0003t0026others(3): Show | 35 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*4048_*4050delAGT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 4048 | INFO_REALIGN_3_PRIME | chr5 | 53094642 | ||||
| chr5:53094697
|
C | G | 7 | a0002c0003t0007a0002c0003t0017a0002c0003t0026others(4): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*4098C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 30/30 | 4098 | chr5 | 53094697 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:52989557
|
C | A | 3 | a0002c0003t0017g0021a0002c0003t0017g0022a0002c0003t0017g0023 | 3 | HG01243.hp2 HG01261.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.64+25C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52989557 | ||||||
| chr5:52989559
|
G | A | 2 | a0001c0001t0002g0024a0001c0001t0002g0025 | 2 | HG01952.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.64+27G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52989559 | ||||||
| chr5:52989623
|
G | A | 7 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0029others(4): Show | 7 | HG00673.hp2 HG01081.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+91G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52989623 | ||||||
| chr5:52989678
|
C | A | 25 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0047others(22): Show | 30 | HG00597.hp2 HG00621.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.64+146C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52989678 | ||||||
| chr5:52989680
|
T | G | 25 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0047others(22): Show | 30 | HG00597.hp2 HG00621.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.64+148T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52989680 | ||||||
| chr5:52989814
|
G | GCA | 116 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0029others(113): Show | 122 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(119): Show |
intron_variant | MODIFIER | c.64+303_64+304dupCA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 52989814 | |||||
| chr5:52989814
|
G | GCACA | 91 | a0001c0001t0001g0009a0001c0001t0001g0085a0001c0001t0001g0086others(88): Show | 95 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.64+301_64+304dupCA others(2): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 52989814 | |||||
| chr5:52989814
|
G | GCACACAC others(1): Show |
23 | a0001c0001t0001g0062a0001c0001t0001g0065a0001c0001t0001g0066others(20): Show | 23 | HG00544.hp2 HG00558.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.64+297_64+304dupCA others(6): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 52989814 | |||||
| chr5:52989814
|
G | GCACACAC others(3): Show |
8 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(5): Show | 9 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+295_64+304dupCA others(8): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 52989814 | |||||
| chr5:52989814
|
G | GCACACAC others(5): Show |
1 | a0001c0002t0006g0054 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.64+293_64+304dupCA others(10): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 52989814 | |||||
| chr5:52989833
|
CACAG | C | 48 | a0001c0001t0001g0289a0001c0001t0001g0297a0001c0001t0001g0298others(45): Show | 52 | HG00280.hp1 HG00735.hp2 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.64+309_64+312delGA others(2): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 52989833 | |||||
| chr5:52989835
|
CAG | C | 29 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0047others(26): Show | 34 | HG00597.hp2 HG00621.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.64+305_64+306delGA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 52989835 | |||||
| chr5:52989837
|
G | C | 250 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0026others(247): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.64+305G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52989837 | ||||||
| chr5:52990007
|
G | C | 50 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(47): Show | 51 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.64+475G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990007 | ||||||
| chr5:52990079
|
C | T | 25 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0047others(22): Show | 30 | HG00597.hp2 HG00621.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.64+547C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990079 | ||||||
| chr5:52990081
|
A | G | 4 | a0001c0011t0034g0084a0002c0007t0010g0165a0002c0007t0010g0166others(1): Show | 4 | HG02818.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+549A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990081 | ||||||
| chr5:52990134
|
A | G | 3 | a0001c0008t0012g0162a0001c0008t0012g0163a0001c0008t0012g0164 | 3 | HG02965.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.64+602A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990134 | ||||||
| chr5:52990150
|
A | C | 3 | a0002c0007t0010g0165a0002c0007t0010g0166a0002c0007t0010g0167 | 3 | HG02818.hp2 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.64+618A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990150 | ||||||
| chr5:52990180
|
C | T | 211 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(208): Show | 223 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(220): Show |
intron_variant | MODIFIER | c.64+648C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990180 | ||||||
| chr5:52990274
|
G | T | 3 | a0001c0001t0002g0273a0002c0003t0026g0274a0002c0003t0026g0275 | 3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+742G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990274 | ||||||
| chr5:52990283
|
G | A | 3 | a0001c0001t0002g0273a0002c0003t0026g0274a0002c0003t0026g0275 | 3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+751G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990283 | ||||||
| chr5:52990291
|
C | T | 1 | a0001c0001t0002g0161 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.64+759C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990291 | ||||||
| chr5:52990503
|
A | T | 3 | a0001c0001t0002g0273a0002c0003t0026g0274a0002c0003t0026g0275 | 3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+971A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990503 | ||||||
| chr5:52990522
|
C | A | 3 | a0001c0001t0002g0273a0002c0003t0026g0274a0002c0003t0026g0275 | 3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+990C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990522 | ||||||
| chr5:52990567
|
G | GTGGT | 3 | a0001c0008t0012g0162a0001c0008t0012g0163a0001c0008t0012g0164 | 3 | HG02965.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.64+1035_64+1036ins others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990567 | ||||||
| chr5:52990568
|
G | T | 3 | a0001c0008t0012g0162a0001c0008t0012g0163a0001c0008t0012g0164 | 3 | HG02965.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.64+1036G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990568 | ||||||
| chr5:52990568
|
GT | G | 128 | a0001c0001t0001g0009a0001c0001t0001g0083a0001c0001t0001g0118others(125): Show | 133 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.64+1054delT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 52990568 | |||||
| chr5:52990568
|
GTT | G | 187 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(184): Show | 201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.64+1053_64+1054del others(2): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 52990568 | |||||
| chr5:52990622
|
T | G | 1 | a0013c0019t0030g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.64+1090T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990622 | ||||||
| chr5:52990701
|
C | T | 1 | a0001c0002t0006g0052 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.64+1169C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990701 | ||||||
| chr5:52990702
|
T | C | 1 | a0001c0002t0006g0052 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.64+1170T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52990702 | ||||||
| chr5:52991025
|
A | G | 1 | a0001c0002t0004g0265 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.64+1493A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52991025 | ||||||
| chr5:52991417
|
TAC | T | 15 | a0001c0001t0002g0012a0001c0001t0002g0146a0001c0001t0002g0147others(12): Show | 16 | HG00558.hp2 NA18942.hp1 NA18957.hp1 others(13): Show |
intron_variant | MODIFIER | c.64+1901_64+1902del others(2): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 52991417 | |||||
| chr5:52991559
|
T | C | 1 | a0001c0001t0025g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.64+2027T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52991559 | ||||||
| chr5:52991575
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.64+2043C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52991575 | ||||||
| chr5:52991753
|
C | T | 14 | a0001c0002t0006g0367a0001c0004t0008g0361a0001c0004t0008g0362others(11): Show | 14 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.64+2221C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52991753 | ||||||
| chr5:52991794
|
A | G | 47 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(44): Show | 48 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.64+2262A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52991794 | ||||||
| chr5:52991795
|
T | C | 1 | a0001c0002t0018g0103 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.64+2263T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52991795 | ||||||
| chr5:52991993
|
G | A | 1 | a0001c0001t0025g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.64+2461G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52991993 | ||||||
| chr5:52991998
|
T | TCCACC | 121 | a0001c0001t0001g0009a0001c0001t0001g0118a0001c0001t0001g0136others(118): Show | 129 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.64+2468_64+2472dup others(5): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 52991998 | |||||
| chr5:52992007
|
G | C | 1 | a0001c0002t0006g0034 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.64+2475G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52992007 | ||||||
| chr5:52992075
|
G | A | 57 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(54): Show | 59 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.64+2543G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52992075 | ||||||
| chr5:52992086
|
C | A | 4 | a0001c0008t0012g0162a0001c0008t0012g0163a0001c0008t0012g0164others(1): Show | 5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+2554C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52992086 | ||||||
| chr5:52992233
|
G | A | 3 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0222 | 3 | HG02129.hp1 HG02132.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.64+2701G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52992233 | ||||||
| chr5:52992265
|
T | C | 1 | a0001c0001t0001g0062 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.64+2733T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52992265 | ||||||
| chr5:52992301
|
C | G | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+2769C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52992301 | ||||||
| chr5:52992319
|
A | G | 3 | a0001c0008t0012g0162a0001c0008t0012g0163a0001c0008t0012g0164 | 3 | HG02965.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.64+2787A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52992319 | ||||||
| chr5:52992343
|
A | G | 52 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(49): Show | 53 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.64+2811A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52992343 | ||||||
| chr5:52992537
|
A | G | 4 | a0001c0001t0002g0326a0001c0001t0002g0328a0001c0001t0005g0327others(1): Show | 4 | HG00280.hp1 HG01243.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+3005A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52992537 | ||||||
| chr5:52992547
|
C | T | 1 | a0009c0017t0052g0263 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64+3015C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52992547 | ||||||
| chr5:52992641
|
C | A | 1 | a0001c0002t0044g0223 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.64+3109C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52992641 | ||||||
| chr5:52992652
|
T | C | 88 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0026others(85): Show | 97 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.64+3120T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52992652 | ||||||
| chr5:52992653
|
G | A | 1 | a0001c0002t0006g0035 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.64+3121G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52992653 | ||||||
| chr5:52992834
|
G | GGTAC | 3 | a0001c0001t0002g0273a0002c0003t0026g0274a0002c0003t0026g0275 | 3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+3303_64+3306dup others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 52992834 | |||||
| chr5:52993094
|
A | G | 1 | a0002c0003t0007g0360 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.64+3562A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993094 | ||||||
| chr5:52993160
|
T | G | 2 | a0001c0002t0018g0105a0001c0016t0005g0104 | 2 | HG03654.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.64+3628T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993160 | ||||||
| chr5:52993183
|
G | A | 45 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(42): Show | 47 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.64+3651G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993183 | ||||||
| chr5:52993241
|
G | A | 2 | a0001c0001t0002g0146a0001c0001t0002g0147 | 2 | NA18978.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.64+3709G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993241 | ||||||
| chr5:52993243
|
C | T | 4 | a0001c0008t0012g0162a0001c0008t0012g0163a0001c0008t0012g0164others(1): Show | 5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+3711C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993243 | ||||||
| chr5:52993362
|
G | T | 1 | a0002c0003t0007g0359 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.64+3830G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993362 | ||||||
| chr5:52993389
|
G | A | 1 | a0001c0002t0011g0168 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.64+3857G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993389 | ||||||
| chr5:52993547
|
T | C | 332 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(329): Show | 352 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.64+4015T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993547 | ||||||
| chr5:52993582
|
G | A | 5 | a0001c0001t0005g0262a0002c0007t0010g0260a0002c0007t0010g0261others(2): Show | 5 | HG02280.hp1 HG03225.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+4050G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993582 | ||||||
| chr5:52993601
|
C | G | 1 | a0001c0002t0009g0212 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.64+4069C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993601 | ||||||
| chr5:52993636
|
A | C | 2 | a0001c0001t0002g0159a0001c0001t0002g0267 | 2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.64+4104A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993636 | ||||||
| chr5:52993690
|
G | T | 1 | a0003c0005t0027g0211 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.64+4158G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993690 | ||||||
| chr5:52993880
|
CAA | C | 63 | a0001c0001t0001g0009a0001c0001t0001g0118a0001c0001t0001g0136others(60): Show | 66 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.64+4349_64+4350del others(2): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993880 | ||||||
| chr5:52993904
|
G | A | 2 | a0001c0002t0006g0037a0010c0027t0006g0036 | 2 | HG00597.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.64+4372G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993904 | ||||||
| chr5:52993924
|
G | T | 1 | a0002c0003t0007g0018 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.64+4392G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993924 | ||||||
| chr5:52993936
|
T | G | 206 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(203): Show | 219 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.64+4404T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52993936 | ||||||
| chr5:52994074
|
A | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.64+4542A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52994074 | ||||||
| chr5:52994264
|
A | T | 52 | a0001c0001t0002g0107a0001c0001t0002g0220a0001c0001t0002g0221others(49): Show | 54 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.64+4732A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52994264 | ||||||
| chr5:52994288
|
C | G | 3 | a0001c0001t0002g0273a0002c0003t0026g0274a0002c0003t0026g0275 | 3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+4756C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52994288 | ||||||
| chr5:52994430
|
G | C | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.64+4898G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52994430 | ||||||
| chr5:52994447
|
C | T | 4 | a0001c0008t0012g0162a0001c0008t0012g0163a0001c0008t0012g0164others(1): Show | 5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+4915C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52994447 | ||||||
| chr5:52994466
|
G | A | 2 | a0002c0003t0007g0018a0002c0003t0007g0286 | 3 | HG01070.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.64+4934G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52994466 | ||||||
| chr5:52994595
|
C | T | 1 | a0001c0002t0006g0051 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.64+5063C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52994595 | ||||||
| chr5:52994604
|
C | T | 62 | a0001c0001t0001g0009a0001c0001t0001g0118a0001c0001t0001g0136others(59): Show | 65 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.64+5072C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52994604 | ||||||
| chr5:52994806
|
G | T | 64 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0029others(61): Show | 68 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.64+5274G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52994806 | ||||||
| chr5:52995040
|
A | C | 1 | a0001c0002t0004g0259 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.64+5508A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995040 | ||||||
| chr5:52995049
|
C | T | 5 | a0001c0002t0004g0145a0001c0008t0012g0162a0001c0008t0012g0163others(2): Show | 6 | HG02109.hp2 HG02293.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+5517C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995049 | ||||||
| chr5:52995050
|
G | A | 51 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(48): Show | 52 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.64+5518G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995050 | ||||||
| chr5:52995099
|
C | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | NA18991.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.64+5567C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995099 | ||||||
| chr5:52995151
|
C | T | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+5619C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995151 | ||||||
| chr5:52995228
|
C | A | 64 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0029others(61): Show | 68 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.64+5696C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995228 | ||||||
| chr5:52995286
|
G | A | 1 | a0001c0002t0004g0229 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.64+5754G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995286 | ||||||
| chr5:52995357
|
T | C | 50 | a0001c0001t0001g0289a0001c0001t0001g0297a0001c0001t0001g0298others(47): Show | 54 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.64+5825T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995357 | ||||||
| chr5:52995401
|
A | T | 2 | a0001c0001t0025g0276a0001c0002t0047g0061 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.64+5869A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995401 | ||||||
| chr5:52995449
|
G | T | 53 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(50): Show | 54 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.64+5917G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995449 | ||||||
| chr5:52995515
|
A | G | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+5983A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995515 | ||||||
| chr5:52995567
|
G | A | 91 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0026others(88): Show | 100 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.64+6035G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995567 | ||||||
| chr5:52995661
|
G | A | 2 | a0002c0003t0007g0333a0002c0003t0007g0334 | 2 | HG00323.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.64+6129G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995661 | ||||||
| chr5:52995709
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.64+6177C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52995709 | ||||||
| chr5:52996244
|
T | A | 1 | a0001c0001t0001g0076 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.64+6712T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52996244 | ||||||
| chr5:52996407
|
T | C | 203 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(200): Show | 216 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.64+6875T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52996407 | ||||||
| chr5:52996575
|
A | T | 120 | a0001c0001t0001g0009a0001c0001t0001g0118a0001c0001t0001g0136others(117): Show | 127 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.64+7043A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52996575 | ||||||
| chr5:52996624
|
T | C | 1 | a0004c0006t0003g0169 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.64+7092T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52996624 | ||||||
| chr5:52996647
|
T | C | 64 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0029others(61): Show | 68 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.64+7115T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52996647 | ||||||
| chr5:52996725
|
T | G | 233 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0055others(230): Show | 244 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.64+7193T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52996725 | ||||||
| chr5:52996893
|
G | A | 5 | a0001c0002t0004g0115a0001c0002t0004g0116a0001c0002t0004g0145others(2): Show | 5 | HG00733.hp2 HG01515.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+7361G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52996893 | ||||||
| chr5:52997019
|
G | T | 1 | a0001c0001t0001g0075 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.64+7487G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52997019 | ||||||
| chr5:52997153
|
T | C | 9 | a0001c0001t0002g0107a0001c0001t0005g0262a0001c0002t0004g0102others(6): Show | 9 | HG01175.hp1 HG01433.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+7621T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52997153 | ||||||
| chr5:52997220
|
A | G | 3 | a0001c0001t0002g0273a0002c0003t0026g0274a0002c0003t0026g0275 | 3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+7688A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52997220 | ||||||
| chr5:52997257
|
T | C | 120 | a0001c0001t0001g0009a0001c0001t0001g0118a0001c0001t0001g0136others(117): Show | 127 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.64+7725T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52997257 | ||||||
| chr5:52997417
|
T | G | 374 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(371): Show | 396 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(393): Show |
intron_variant | MODIFIER | c.64+7885T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52997417 | ||||||
| chr5:52997652
|
A | G | 2 | a0001c0001t0001g0324a0001c0001t0001g0325 | 2 | NA18956.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.64+8120A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52997652 | ||||||
| chr5:52997779
|
A | T | 3 | a0002c0003t0017g0021a0002c0003t0017g0022a0002c0003t0017g0023 | 3 | HG01243.hp2 HG01261.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.64+8247A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52997779 | ||||||
| chr5:52997788
|
C | T | 1 | a0001c0001t0025g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.64+8256C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52997788 | ||||||
| chr5:52997891
|
A | G | 324 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(321): Show | 344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.64+8359A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52997891 | ||||||
| chr5:52997932
|
T | G | 1 | a0001c0002t0019g0230 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.64+8400T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52997932 | ||||||
| chr5:52997980
|
C | G | 2 | a0001c0002t0004g0229a0001c0002t0004g0257 | 2 | HG02602.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.64+8448C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52997980 | ||||||
| chr5:52998212
|
G | A | 49 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(46): Show | 50 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.64+8680G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52998212 | ||||||
| chr5:52998266
|
AC | A | 3 | a0001c0002t0004g0102a0002c0007t0010g0260a0002c0007t0010g0261 | 3 | HG02280.hp1 HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.64+8735delC | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52998266 | ||||||
| chr5:52998386
|
G | A | 1 | a0001c0001t0005g0262 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.64+8854G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52998386 | ||||||
| chr5:52998446
|
C | T | 3 | a0001c0004t0008g0372a0001c0004t0008g0373a0001c0004t0008g0374 | 3 | HG01891.hp2 HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.64+8914C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52998446 | ||||||
| chr5:52998483
|
A | G | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.64+8951A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52998483 | ||||||
| chr5:52998599
|
A | G | 233 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0055others(230): Show | 244 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.64+9067A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52998599 | ||||||
| chr5:52998721
|
T | G | 54 | a0001c0001t0002g0107a0001c0001t0002g0220a0001c0001t0002g0221others(51): Show | 56 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.64+9189T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52998721 | ||||||
| chr5:52998727
|
T | C | 2 | a0001c0001t0025g0276a0001c0002t0047g0061 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.64+9195T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52998727 | ||||||
| chr5:52998842
|
G | A | 1 | a0001c0002t0004g0231 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.64+9310G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52998842 | ||||||
| chr5:52998940
|
T | G | 1 | a0001c0002t0009g0212 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.64+9408T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52998940 | ||||||
| chr5:52998996
|
G | C | 2 | a0001c0002t0006g0037a0010c0027t0006g0036 | 2 | HG00597.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.64+9464G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52998996 | ||||||
| chr5:52999026
|
T | C | 51 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(48): Show | 52 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.64+9494T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52999026 | ||||||
| chr5:52999054
|
T | TAGTAACA others(10): Show |
1 | a0001c0002t0004g0232 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64+9522_64+9523ins others(17): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52999054 | ||||||
| chr5:52999101
|
T | C | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+9569T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52999101 | ||||||
| chr5:52999754
|
C | A | 3 | a0002c0003t0017g0021a0002c0003t0017g0022a0002c0003t0017g0023 | 3 | HG01243.hp2 HG01261.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.64+10222C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52999754 | ||||||
| chr5:52999874
|
T | C | 58 | a0001c0001t0002g0107a0001c0001t0002g0220a0001c0001t0002g0221others(55): Show | 61 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.64+10342T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 52999874 | ||||||
| chr5:53000047
|
G | A | 64 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0029others(61): Show | 68 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.64+10515G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53000047 | ||||||
| chr5:53000139
|
GATT | G | 3 | a0001c0001t0002g0273a0002c0003t0026g0274a0002c0003t0026g0275 | 3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+10609_64+10611d others(5): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53000139 | |||||
| chr5:53000401
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.64+10869T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53000401 | ||||||
| chr5:53000485
|
C | T | 3 | a0001c0001t0002g0273a0002c0003t0026g0274a0002c0003t0026g0275 | 3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+10953C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53000485 | ||||||
| chr5:53000573
|
T | A | 1 | a0002c0007t0010g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.64+11041T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53000573 | ||||||
| chr5:53000654
|
G | A | 2 | a0001c0001t0001g0335a0001c0001t0001g0336 | 2 | NA18980.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.64+11122G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53000654 | ||||||
| chr5:53000654
|
G | T | 233 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0055others(230): Show | 244 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.64+11122G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53000654 | ||||||
| chr5:53000804
|
C | A | 1 | a0002c0003t0007g0337 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.64+11272C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53000804 | ||||||
| chr5:53000896
|
TG | T | 6 | a0001c0002t0009g0207a0001c0002t0009g0208a0001c0002t0009g0209others(3): Show | 6 | HG00280.hp2 HG06807.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+11365delG | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53000896 | ||||||
| chr5:53000897
|
G | GT | 57 | a0001c0001t0001g0094a0001c0001t0001g0289a0001c0001t0001g0297others(54): Show | 61 | HG00673.hp1 HG01069.hp2 HG01070.hp1 others(58): Show |
intron_variant | MODIFIER | c.64+11386dupT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53000897 | |||||
| chr5:53000897
|
G | GTT | 12 | a0001c0001t0001g0073a0001c0001t0002g0326a0001c0001t0002g0328others(9): Show | 13 | HG00280.hp1 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.64+11385_64+11386d others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53000897 | |||||
| chr5:53000897
|
G | T | 14 | a0001c0001t0001g0088a0001c0001t0001g0095a0001c0001t0001g0096others(11): Show | 14 | HG01099.hp2 HG01891.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.64+11365G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53000897 | ||||||
| chr5:53000897
|
GT | G | 62 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(59): Show | 66 | HG00140.hp1 HG00609.hp1 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.64+11386delT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53000897 | |||||
| chr5:53000897
|
GTT | G | 5 | a0001c0001t0001g0026a0001c0008t0012g0162a0001c0008t0012g0163others(2): Show | 6 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+11385_64+11386d others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53000897 | |||||
| chr5:53000978
|
T | C | 60 | a0001c0001t0001g0009a0001c0001t0001g0118a0001c0001t0001g0136others(57): Show | 63 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.64+11446T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53000978 | ||||||
| chr5:53001057
|
A | G | 4 | a0001c0008t0012g0162a0001c0008t0012g0163a0001c0008t0012g0164others(1): Show | 5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+11525A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53001057 | ||||||
| chr5:53001059
|
G | A | 11 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0029others(8): Show | 11 | HG00673.hp2 HG01081.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.64+11527G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53001059 | ||||||
| chr5:53001163
|
A | G | 3 | a0001c0001t0002g0273a0002c0003t0026g0274a0002c0003t0026g0275 | 3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+11631A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53001163 | ||||||
| chr5:53001290
|
C | T | 1 | a0001c0002t0003g0113 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.64+11758C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53001290 | ||||||
| chr5:53001412
|
C | T | 259 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(256): Show | 275 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.64+11880C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53001412 | ||||||
| chr5:53001538
|
G | A | 1 | a0001c0002t0004g0265 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.64+12006G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53001538 | ||||||
| chr5:53001558
|
G | A | 1 | a0001c0001t0002g0142 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.64+12026G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53001558 | ||||||
| chr5:53001744
|
G | A | 53 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0222others(50): Show | 55 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.64+12212G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53001744 | ||||||
| chr5:53001813
|
T | TA | 45 | a0001c0001t0001g0289a0001c0001t0001g0297a0001c0001t0001g0298others(42): Show | 49 | HG00280.hp1 HG00621.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.64+12304dupA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53001813 | |||||
| chr5:53001813
|
TA | T | 108 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(105): Show | 111 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.64+12304delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53001813 | |||||
| chr5:53001842
|
C | G | 1 | a0004c0006t0003g0169 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.64+12310C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53001842 | ||||||
| chr5:53002053
|
A | T | 2 | a0001c0001t0005g0302a0001c0001t0005g0303 | 2 | NA18946.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.64+12521A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53002053 | ||||||
| chr5:53002102
|
G | T | 1 | a0001c0002t0028g0016 | 2 | HG00140.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.64+12570G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53002102 | ||||||
| chr5:53002121
|
A | G | 42 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0222others(39): Show | 44 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.64+12589A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53002121 | ||||||
| chr5:53002126
|
A | T | 2 | a0001c0001t0005g0301a0001c0001t0005g0330 | 2 | HG02040.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.64+12594A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53002126 | ||||||
| chr5:53002458
|
C | A | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+12926C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53002458 | ||||||
| chr5:53002784
|
C | T | 3 | a0001c0001t0002g0273a0002c0003t0026g0274a0002c0003t0026g0275 | 3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+13252C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53002784 | ||||||
| chr5:53002967
|
A | T | 1 | a0009c0017t0052g0263 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64+13435A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53002967 | ||||||
| chr5:53003059
|
A | G | 3 | a0001c0001t0002g0273a0002c0003t0026g0274a0002c0003t0026g0275 | 3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+13527A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53003059 | ||||||
| chr5:53003227
|
G | A | 2 | a0001c0001t0025g0276a0001c0002t0047g0061 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.64+13695G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53003227 | ||||||
| chr5:53003348
|
T | C | 6 | a0004c0006t0003g0014a0004c0006t0003g0169a0004c0006t0003g0172others(3): Show | 7 | NA18947.hp1 NA18970.hp2 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.64+13816T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53003348 | ||||||
| chr5:53003796
|
C | T | 4 | a0001c0001t0005g0004a0001c0001t0005g0299a0001c0001t0005g0314others(1): Show | 6 | HG01069.hp2 HG03490.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+14264C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53003796 | ||||||
| chr5:53003847
|
G | A | 3 | a0001c0008t0012g0162a0001c0008t0012g0163a0001c0008t0012g0164 | 3 | HG02965.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.64+14315G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53003847 | ||||||
| chr5:53003884
|
G | A | 1 | a0001c0002t0018g0103 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.64+14352G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53003884 | ||||||
| chr5:53003941
|
C | T | 2 | a0001c0002t0018g0103a0001c0002t0018g0105 | 2 | HG01175.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.64+14409C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53003941 | ||||||
| chr5:53004083
|
T | G | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+14551T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004083 | ||||||
| chr5:53004093
|
A | G | 1 | a0001c0001t0002g0137 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.64+14561A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004093 | ||||||
| chr5:53004188
|
A | T | 1 | a0002c0003t0026g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.64+14656A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004188 | ||||||
| chr5:53004275
|
G | T | 1 | a0001c0002t0004g0116 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.64+14743G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004275 | ||||||
| chr5:53004367
|
G | A | 4 | a0001c0008t0012g0162a0001c0008t0012g0163a0001c0008t0012g0164others(1): Show | 5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+14835G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004367 | ||||||
| chr5:53004416
|
T | C | 370 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(367): Show | 391 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.64+14884T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004416 | ||||||
| chr5:53004444
|
G | A | 3 | a0001c0001t0002g0273a0002c0003t0026g0274a0002c0003t0026g0275 | 3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+14912G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004444 | ||||||
| chr5:53004743
|
AGCAGTTG others(5): Show |
A | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+15213_64+15224d others(14): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004743 | |||||
| chr5:53004783
|
T | C | 2 | a0002c0003t0007g0333a0002c0003t0007g0334 | 2 | HG00323.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.64+15251T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004783 | ||||||
| chr5:53004894
|
G | GT | 21 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0030others(18): Show | 22 | HG00673.hp2 HG01175.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.64+15401dupT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | |||||
| chr5:53004894
|
G | GTT | 7 | a0001c0001t0001g0350a0001c0001t0001g0351a0001c0001t0023g0354others(4): Show | 7 | HG01978.hp2 HG02015.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+15400_64+15401d others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | |||||
| chr5:53004894
|
G | GTTTTTTT others(3): Show |
1 | a0009c0017t0052g0263 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64+15392_64+15401d others(12): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | |||||
| chr5:53004894
|
G | T | 1 | a0001c0001t0001g0020 | 2 | NA18975.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.64+15362G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004894 | ||||||
| chr5:53004894
|
GT | G | 32 | a0001c0001t0001g0181a0001c0001t0005g0262a0001c0002t0003g0031others(29): Show | 33 | HG00280.hp2 HG00609.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.64+15401delT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | |||||
| chr5:53004894
|
GTTTTTT | G | 8 | a0002c0009t0016g0271a0003c0005t0003g0015a0003c0005t0003g0176others(5): Show | 9 | HG02071.hp2 NA18964.hp1 NA18965.hp2 others(6): Show |
intron_variant | MODIFIER | c.64+15396_64+15401d others(8): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | |||||
| chr5:53004894
|
GTTTTTTT others(2): Show |
G | 11 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0083others(8): Show | 12 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.64+15393_64+15401d others(11): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | |||||
| chr5:53004894
|
GTTTTTTT others(3): Show |
G | 43 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(40): Show | 44 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.64+15392_64+15401d others(12): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | |||||
| chr5:53004894
|
GTTTTTTT others(4): Show |
G | 6 | a0001c0001t0001g0094a0001c0001t0001g0224a0001c0004t0008g0313others(3): Show | 6 | HG02897.hp1 HG03098.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+15391_64+15401d others(13): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | |||||
| chr5:53004894
|
GTTTTTTT others(5): Show |
G | 14 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0005g0303others(11): Show | 14 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.64+15390_64+15401d others(14): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | |||||
| chr5:53004894
|
GTTTTTTT others(6): Show |
G | 46 | a0001c0001t0001g0136a0001c0001t0001g0289a0001c0001t0001g0324others(43): Show | 50 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.64+15389_64+15401d others(15): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | |||||
| chr5:53004894
|
GTTTTTTT others(7): Show |
G | 65 | a0001c0001t0001g0009a0001c0001t0001g0047a0001c0001t0001g0118others(62): Show | 68 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.64+15388_64+15401d others(16): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | |||||
| chr5:53004894
|
GTTTTTTT others(8): Show |
G | 22 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0002g0148others(19): Show | 27 | HG00408.hp1 HG00733.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.64+15387_64+15401d others(17): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | |||||
| chr5:53004894
|
GTTTTTTT others(9): Show |
G | 8 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0222others(5): Show | 8 | HG01516.hp2 HG02074.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.64+15386_64+15401d others(18): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | |||||
| chr5:53004894
|
GTTTTTTT others(10): Show |
G | 32 | a0001c0001t0002g0243a0001c0002t0004g0003a0001c0002t0004g0106others(29): Show | 34 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.64+15385_64+15401d others(19): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | |||||
| chr5:53004894
|
GTTTTTTT others(12): Show |
G | 1 | a0002c0003t0026g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.64+15383_64+15401d others(21): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53004894 | |||||
| chr5:53004902
|
T | G | 3 | a0002c0003t0007g0283a0002c0003t0007g0284a0002c0003t0007g0285 | 3 | HG02055.hp2 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.64+15370T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004902 | ||||||
| chr5:53004908
|
T | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(4): Show | 8 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.64+15376T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004908 | ||||||
| chr5:53004909
|
T | G | 1 | a0002c0003t0007g0283 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.64+15377T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004909 | ||||||
| chr5:53004918
|
T | G | 1 | a0001c0001t0024g0214 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.64+15386T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004918 | ||||||
| chr5:53004925
|
T | C | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+15393T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53004925 | ||||||
| chr5:53005021
|
T | C | 3 | a0001c0001t0001g0289a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | NA18963.hp1 NA19012.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.64+15489T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005021 | ||||||
| chr5:53005037
|
A | T | 56 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0222others(53): Show | 59 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.64+15505A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005037 | ||||||
| chr5:53005060
|
T | C | 6 | a0001c0001t0005g0262a0001c0002t0004g0102a0002c0007t0010g0260others(3): Show | 6 | HG02280.hp1 HG02647.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+15528T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005060 | ||||||
| chr5:53005121
|
G | C | 1 | a0015c0015t0002g0278 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.64+15589G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005121 | ||||||
| chr5:53005123
|
T | C | 3 | a0001c0001t0002g0273a0002c0003t0026g0274a0002c0003t0026g0275 | 3 | HG02451.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.64+15591T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005123 | ||||||
| chr5:53005217
|
G | A | 2 | a0001c0001t0002g0146a0001c0001t0002g0147 | 2 | NA18978.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.64+15685G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005217 | ||||||
| chr5:53005247
|
A | G | 4 | a0001c0008t0012g0162a0001c0008t0012g0163a0001c0008t0012g0164others(1): Show | 5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.64+15715A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005247 | ||||||
| chr5:53005252
|
C | T | 1 | a0001c0002t0004g0247 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.64+15720C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005252 | ||||||
| chr5:53005261
|
C | T | 41 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0222others(38): Show | 43 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.64+15729C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005261 | ||||||
| chr5:53005580
|
C | CA | 6 | a0001c0001t0002g0222a0001c0008t0012g0162a0001c0008t0012g0163others(3): Show | 7 | HG02109.hp2 HG02523.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.64+16064dupA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53005580 | |||||
| chr5:53005580
|
C | CAA | 45 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0243others(42): Show | 47 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.64+16063_64+16064d others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53005580 | |||||
| chr5:53005580
|
CA | C | 265 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(262): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.64+16064delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53005580 | |||||
| chr5:53005625
|
C | T | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+16093C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005625 | ||||||
| chr5:53005709
|
C | T | 1 | a0001c0001t0005g0262 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.64+16177C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005709 | ||||||
| chr5:53005730
|
G | T | 1 | a0001c0001t0002g0142 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.64+16198G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005730 | ||||||
| chr5:53005786
|
T | C | 3 | a0002c0003t0017g0021a0002c0003t0017g0022a0002c0003t0017g0023 | 3 | HG01243.hp2 HG01261.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.64+16254T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005786 | ||||||
| chr5:53005886
|
C | T | 91 | a0001c0001t0001g0289a0001c0001t0001g0297a0001c0001t0001g0298others(88): Show | 98 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.64+16354C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005886 | ||||||
| chr5:53005918
|
C | T | 1 | a0001c0001t0002g0250 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.64+16386C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005918 | ||||||
| chr5:53005983
|
G | T | 4 | a0001c0001t0002g0273a0001c0001t0025g0276a0001c0002t0047g0061others(1): Show | 4 | HG02559.hp2 HG02970.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+16451G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53005983 | ||||||
| chr5:53006012
|
T | C | 2 | a0001c0002t0003g0179a0001c0002t0003g0203 | 2 | NA18954.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.64+16480T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53006012 | ||||||
| chr5:53006029
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.64+16497C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53006029 | ||||||
| chr5:53006030
|
G | A | 1 | a0013c0019t0030g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.64+16498G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53006030 | ||||||
| chr5:53006212
|
A | T | 1 | a0001c0002t0004g0087 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.64+16680A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53006212 | ||||||
| chr5:53006224
|
A | G | 1 | a0001c0001t0002g0117 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.64+16692A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53006224 | ||||||
| chr5:53006497
|
A | AAGAGG | 3 | a0001c0001t0001g0009a0001c0001t0001g0118a0001c0001t0013g0009 | 3 | NA18959.hp1 NA18981.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.64+16967_64+16971d others(7): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53006497 | |||||
| chr5:53006598
|
AATT | A | 3 | a0001c0008t0012g0162a0001c0008t0012g0163a0001c0008t0012g0164 | 3 | HG02965.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.64+17073_64+17075d others(5): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53006598 | |||||
| chr5:53006663
|
C | G | 14 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(11): Show | 14 | HG01346.hp1 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.64+17131C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53006663 | ||||||
| chr5:53006709
|
T | C | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+17177T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53006709 | ||||||
| chr5:53006857
|
A | G | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+17325A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53006857 | ||||||
| chr5:53006863
|
A | C | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+17331A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53006863 | ||||||
| chr5:53007385
|
G | T | 1 | a0001c0001t0005g0318 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.64+17853G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53007385 | ||||||
| chr5:53007456
|
G | A | 2 | a0001c0002t0018g0103a0001c0002t0018g0105 | 2 | HG01175.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.64+17924G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53007456 | ||||||
| chr5:53007467
|
T | C | 2 | a0001c0001t0005g0327a0001c0001t0005g0329 | 2 | HG01243.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.64+17935T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53007467 | ||||||
| chr5:53007515
|
G | A | 63 | a0001c0001t0001g0009a0001c0001t0001g0118a0001c0001t0001g0320others(60): Show | 66 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.64+17983G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53007515 | ||||||
| chr5:53007596
|
T | C | 1 | a0001c0001t0001g0320 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.64+18064T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53007596 | ||||||
| chr5:53007674
|
A | G | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+18142A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53007674 | ||||||
| chr5:53007721
|
G | A | 8 | a0003c0005t0003g0015a0003c0005t0003g0176a0003c0005t0003g0177others(5): Show | 9 | HG02071.hp2 NA18964.hp1 NA18965.hp2 others(6): Show |
intron_variant | MODIFIER | c.64+18189G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53007721 | ||||||
| chr5:53007733
|
A | C | 1 | a0002c0007t0010g0261 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.64+18201A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53007733 | ||||||
| chr5:53007826
|
G | A | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.64+18294G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53007826 | ||||||
| chr5:53008087
|
G | A | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.64+18555G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53008087 | ||||||
| chr5:53008095
|
A | G | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+18563A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53008095 | ||||||
| chr5:53008130
|
G | C | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.64+18598G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53008130 | ||||||
| chr5:53008248
|
C | T | 3 | a0002c0007t0010g0165a0002c0007t0010g0166a0002c0007t0010g0167 | 3 | HG02818.hp2 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-18500C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53008248 | ||||||
| chr5:53008289
|
G | A | 1 | a0001c0001t0025g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.65-18459G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53008289 | ||||||
| chr5:53008301
|
G | A | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.65-18447G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53008301 | ||||||
| chr5:53008423
|
G | A | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-18325G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53008423 | ||||||
| chr5:53008523
|
C | T | 1 | a0001c0002t0004g0246 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.65-18225C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53008523 | ||||||
| chr5:53008625
|
G | T | 2 | a0001c0001t0005g0316a0001c0001t0005g0317 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.65-18123G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53008625 | ||||||
| chr5:53008642
|
GTC | G | 256 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(253): Show | 272 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.65-18094_65-18093d others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53008642 | |||||
| chr5:53009166
|
A | G | 116 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0055others(113): Show | 120 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.65-17582A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53009166 | ||||||
| chr5:53009489
|
A | T | 1 | a0004c0020t0003g0132 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.65-17259A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53009489 | ||||||
| chr5:53009643
|
G | T | 5 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0222others(2): Show | 5 | HG02080.hp2 HG02129.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-17105G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53009643 | ||||||
| chr5:53009651
|
A | G | 1 | a0002c0003t0007g0080 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.65-17097A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53009651 | ||||||
| chr5:53009721
|
A | C | 3 | a0001c0002t0003g0199a0001c0002t0003g0200a0001c0002t0003g0201 | 3 | HG01515.hp1 HG01517.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.65-17027A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53009721 | ||||||
| chr5:53009807
|
C | G | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-16941C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53009807 | ||||||
| chr5:53009975
|
C | T | 1 | a0001c0001t0001g0345 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.65-16773C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53009975 | ||||||
| chr5:53009976
|
G | A | 3 | a0001c0002t0004g0102a0002c0007t0010g0260a0002c0007t0010g0261 | 3 | HG02280.hp1 HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.65-16772G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53009976 | ||||||
| chr5:53010055
|
T | C | 1 | a0001c0002t0006g0034 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.65-16693T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53010055 | ||||||
| chr5:53010183
|
C | A | 63 | a0001c0001t0001g0009a0001c0001t0001g0118a0001c0001t0001g0320others(60): Show | 66 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.65-16565C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53010183 | ||||||
| chr5:53010214
|
A | T | 49 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0222others(46): Show | 51 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.65-16534A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53010214 | ||||||
| chr5:53010549
|
C | T | 5 | a0002c0003t0017g0021a0002c0003t0017g0022a0002c0003t0017g0023others(2): Show | 5 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-16199C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53010549 | ||||||
| chr5:53010550
|
C | G | 1 | a0001c0001t0002g0264 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.65-16198C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53010550 | ||||||
| chr5:53010760
|
G | A | 54 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(51): Show | 55 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.65-15988G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53010760 | ||||||
| chr5:53010863
|
G | C | 2 | a0001c0002t0006g0037a0010c0027t0006g0036 | 2 | HG00597.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.65-15885G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53010863 | ||||||
| chr5:53011007
|
C | G | 1 | a0001c0001t0025g0281 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.65-15741C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53011007 | ||||||
| chr5:53011316
|
A | G | 1 | a0003c0005t0003g0290 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65-15432A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53011316 | ||||||
| chr5:53011342
|
G | A | 2 | a0001c0001t0002g0159a0001c0001t0002g0267 | 2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.65-15406G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53011342 | ||||||
| chr5:53011454
|
C | T | 2 | a0001c0001t0002g0273a0001c0002t0047g0061 | 2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.65-15294C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53011454 | ||||||
| chr5:53011455
|
G | C | 1 | a0001c0001t0013g0141 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.65-15293G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53011455 | ||||||
| chr5:53011540
|
C | T | 55 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0222others(52): Show | 57 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.65-15208C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53011540 | ||||||
| chr5:53011736
|
T | TG | 52 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0222others(49): Show | 54 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.65-15005dupG | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53011736 | |||||
| chr5:53011795
|
C | T | 1 | a0001c0001t0001g0345 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.65-14953C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53011795 | ||||||
| chr5:53012235
|
G | A | 1 | a0001c0001t0025g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.65-14513G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53012235 | ||||||
| chr5:53012544
|
T | C | 128 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0028others(125): Show | 134 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.65-14204T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53012544 | ||||||
| chr5:53012554
|
A | G | 1 | a0002c0003t0007g0079 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.65-14194A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53012554 | ||||||
| chr5:53012605
|
G | A | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-14143G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53012605 | ||||||
| chr5:53012660
|
C | A | 3 | a0001c0002t0004g0232a0001c0002t0004g0236a0001c0002t0004g0247 | 3 | HG02615.hp1 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.65-14088C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53012660 | ||||||
| chr5:53012758
|
CA | C | 4 | a0001c0008t0012g0162a0001c0008t0012g0163a0001c0008t0012g0164others(1): Show | 5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-13989delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53012758 | ||||||
| chr5:53012805
|
G | A | 4 | a0001c0002t0004g0265a0001c0002t0019g0230a0001c0002t0019g0237others(1): Show | 4 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-13943G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53012805 | ||||||
| chr5:53013024
|
C | T | 1 | a0001c0001t0015g0160 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.65-13724C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013024 | ||||||
| chr5:53013097
|
T | C | 2 | a0001c0001t0005g0004a0001c0001t0005g0314 | 4 | HG03490.hp2 HG03492.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-13651T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013097 | ||||||
| chr5:53013185
|
C | T | 128 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0028others(125): Show | 134 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.65-13563C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013185 | ||||||
| chr5:53013190
|
T | C | 1 | a0001c0002t0004g0115 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.65-13558T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013190 | ||||||
| chr5:53013374
|
C | CT | 61 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(58): Show | 63 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.65-13361dupT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53013374 | |||||
| chr5:53013397
|
G | T | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-13351G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013397 | ||||||
| chr5:53013459
|
T | C | 1 | a0001c0001t0002g0117 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.65-13289T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013459 | ||||||
| chr5:53013491
|
T | C | 1 | a0001c0004t0008g0305 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.65-13257T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013491 | ||||||
| chr5:53013557
|
G | C | 2 | a0001c0013t0001g0268a0001c0014t0003g0064 | 2 | HG00544.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.65-13191G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013557 | ||||||
| chr5:53013663
|
G | C | 38 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0222others(35): Show | 40 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.65-13085G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013663 | ||||||
| chr5:53013808
|
A | T | 1 | a0001c0001t0005g0262 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.65-12940A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013808 | ||||||
| chr5:53013812
|
C | A | 1 | a0001c0001t0002g0161 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.65-12936C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013812 | ||||||
| chr5:53013841
|
A | G | 2 | a0002c0003t0026g0274a0002c0003t0026g0275 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.65-12907A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013841 | ||||||
| chr5:53013845
|
A | G | 61 | a0001c0001t0001g0289a0001c0001t0001g0297a0001c0001t0001g0298others(58): Show | 65 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.65-12903A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013845 | ||||||
| chr5:53013909
|
G | A | 65 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0029others(62): Show | 69 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.65-12839G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53013909 | ||||||
| chr5:53014041
|
T | C | 5 | a0002c0003t0017g0021a0002c0003t0017g0022a0002c0003t0017g0023others(2): Show | 5 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-12707T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53014041 | ||||||
| chr5:53014103
|
T | C | 5 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0222others(2): Show | 5 | HG02080.hp2 HG02129.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-12645T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53014103 | ||||||
| chr5:53014147
|
C | G | 8 | a0001c0011t0034g0084a0002c0003t0017g0021a0002c0003t0017g0022others(5): Show | 8 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.65-12601C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53014147 | ||||||
| chr5:53014168
|
G | A | 6 | a0001c0011t0034g0084a0002c0003t0017g0021a0002c0003t0017g0022others(3): Show | 6 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-12580G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53014168 | ||||||
| chr5:53014345
|
C | T | 50 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0222others(47): Show | 52 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.65-12403C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53014345 | ||||||
| chr5:53014523
|
G | A | 6 | a0001c0011t0034g0084a0002c0003t0017g0021a0002c0003t0017g0022others(3): Show | 6 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-12225G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53014523 | ||||||
| chr5:53014580
|
C | A | 1 | a0001c0002t0006g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.65-12168C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53014580 | ||||||
| chr5:53014719
|
G | T | 26 | a0001c0002t0042g0311a0001c0004t0002g0344a0001c0004t0008g0305others(23): Show | 26 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.65-12029G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53014719 | ||||||
| chr5:53014823
|
A | C | 57 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(54): Show | 59 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.65-11925A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53014823 | ||||||
| chr5:53015146
|
T | C | 49 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0222others(46): Show | 51 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.65-11602T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53015146 | ||||||
| chr5:53015162
|
G | A | 1 | a0001c0001t0025g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.65-11586G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53015162 | ||||||
| chr5:53015333
|
A | G | 344 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(341): Show | 364 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.65-11415A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53015333 | ||||||
| chr5:53015471
|
AT | A | 331 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(328): Show | 352 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.65-11266delT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53015471 | |||||
| chr5:53015471
|
ATT | A | 9 | a0001c0001t0005g0262a0001c0002t0004g0102a0002c0007t0010g0165others(6): Show | 9 | HG02280.hp1 HG02647.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.65-11267_65-11266d others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53015471 | |||||
| chr5:53015493
|
G | A | 33 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0222others(30): Show | 35 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.65-11255G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53015493 | ||||||
| chr5:53015786
|
C | T | 11 | a0001c0001t0001g0228a0001c0002t0003g0171a0001c0002t0003g0179others(8): Show | 11 | HG00609.hp1 NA18612.hp1 NA18954.hp2 others(8): Show |
intron_variant | MODIFIER | c.65-10962C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53015786 | ||||||
| chr5:53015908
|
T | C | 1 | a0001c0001t0002g0159 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.65-10840T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53015908 | ||||||
| chr5:53015926
|
CT | C | 51 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(48): Show | 52 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.65-10821delT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53015926 | ||||||
| chr5:53016019
|
C | T | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-10729C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016019 | ||||||
| chr5:53016086
|
C | T | 1 | a0002c0003t0007g0080 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.65-10662C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016086 | ||||||
| chr5:53016136
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.65-10612T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016136 | ||||||
| chr5:53016173
|
A | G | 1 | a0001c0002t0003g0182 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.65-10575A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016173 | ||||||
| chr5:53016404
|
T | C | 6 | a0001c0011t0034g0084a0002c0003t0017g0021a0002c0003t0017g0022others(3): Show | 6 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-10344T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016404 | ||||||
| chr5:53016521
|
G | T | 65 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0029others(62): Show | 69 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.65-10227G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016521 | ||||||
| chr5:53016592
|
A | G | 194 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0055others(191): Show | 203 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.65-10156A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016592 | ||||||
| chr5:53016613
|
T | C | 49 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(46): Show | 50 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.65-10135T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016613 | ||||||
| chr5:53016667
|
T | C | 1 | a0001c0001t0002g0159 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.65-10081T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016667 | ||||||
| chr5:53016673
|
A | G | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-10075A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016673 | ||||||
| chr5:53016792
|
T | C | 1 | a0002c0003t0026g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.65-9956T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016792 | ||||||
| chr5:53016800
|
C | T | 1 | a0001c0001t0036g0296 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.65-9948C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016800 | ||||||
| chr5:53016880
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.65-9868T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016880 | ||||||
| chr5:53016969
|
T | C | 5 | a0002c0003t0017g0021a0002c0003t0017g0022a0002c0003t0017g0023others(2): Show | 5 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-9779T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016969 | ||||||
| chr5:53016985
|
A | G | 3 | a0001c0002t0003g0186a0001c0002t0003g0197a0001c0002t0003g0198 | 3 | NA18989.hp1 NA19004.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.65-9763A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53016985 | ||||||
| chr5:53017448
|
T | A | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.65-9300T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53017448 | ||||||
| chr5:53017681
|
G | T | 2 | a0001c0001t0001g0085a0001c0002t0004g0087 | 2 | HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.65-9067G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53017681 | ||||||
| chr5:53017734
|
G | A | 129 | a0001c0001t0001g0009a0001c0001t0001g0118a0001c0001t0001g0289others(126): Show | 136 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.65-9014G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53017734 | ||||||
| chr5:53017760
|
T | C | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-8988T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53017760 | ||||||
| chr5:53017991
|
G | A | 1 | a0001c0002t0003g0031 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.65-8757G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53017991 | ||||||
| chr5:53017998
|
A | G | 38 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0222others(35): Show | 40 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.65-8750A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53017998 | ||||||
| chr5:53018217
|
C | T | 45 | a0001c0001t0001g0320a0001c0001t0001g0322a0001c0001t0001g0323others(42): Show | 47 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.65-8531C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53018217 | ||||||
| chr5:53018222
|
G | A | 2 | a0001c0001t0002g0273a0001c0002t0047g0061 | 2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.65-8526G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53018222 | ||||||
| chr5:53018474
|
T | G | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-8274T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53018474 | ||||||
| chr5:53018494
|
C | G | 1 | a0001c0001t0033g0353 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.65-8254C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53018494 | ||||||
| chr5:53018552
|
A | T | 65 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0029others(62): Show | 69 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.65-8196A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53018552 | ||||||
| chr5:53018829
|
C | T | 1 | a0001c0001t0005g0288 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.65-7919C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53018829 | ||||||
| chr5:53018861
|
C | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0269 | 2 | NA18946.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.65-7887C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53018861 | ||||||
| chr5:53018962
|
G | A | 2 | a0001c0001t0005g0302a0001c0001t0005g0303 | 2 | NA18946.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.65-7786G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53018962 | ||||||
| chr5:53018972
|
G | C | 1 | a0001c0001t0051g0071 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.65-7776G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53018972 | ||||||
| chr5:53018993
|
G | A | 61 | a0001c0001t0001g0289a0001c0001t0001g0297a0001c0001t0001g0298others(58): Show | 65 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.65-7755G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53018993 | ||||||
| chr5:53019011
|
C | T | 1 | a0001c0002t0006g0045 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.65-7737C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53019011 | ||||||
| chr5:53019065
|
A | AAAAT | 61 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(58): Show | 63 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.65-7659_65-7656dup others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53019065 | |||||
| chr5:53019065
|
A | AAAATAAA others(1): Show |
3 | a0002c0003t0017g0021a0002c0003t0017g0022a0002c0003t0017g0023 | 3 | HG01243.hp2 HG01261.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.65-7663_65-7656dup others(8): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53019065 | |||||
| chr5:53019094
|
G | A | 12 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0038others(9): Show | 15 | HG01257.hp2 HG01496.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.65-7654G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53019094 | ||||||
| chr5:53019147
|
TA | T | 6 | a0001c0011t0034g0084a0002c0003t0017g0021a0002c0003t0017g0022others(3): Show | 6 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-7594delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53019147 | |||||
| chr5:53019282
|
T | C | 52 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0222others(49): Show | 54 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.65-7466T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53019282 | ||||||
| chr5:53019283
|
A | G | 1 | a0002c0003t0017g0023 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.65-7465A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53019283 | ||||||
| chr5:53019563
|
T | C | 1 | a0001c0002t0004g0258 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.65-7185T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53019563 | ||||||
| chr5:53019668
|
G | C | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-7080G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53019668 | ||||||
| chr5:53019673
|
G | A | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.65-7075G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53019673 | ||||||
| chr5:53019723
|
C | G | 1 | a0002c0003t0007g0349 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.65-7025C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53019723 | ||||||
| chr5:53019757
|
C | T | 4 | a0001c0001t0005g0011a0001c0001t0005g0135a0004c0020t0003g0132others(1): Show | 5 | HG02040.hp1 NA18940.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-6991C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53019757 | ||||||
| chr5:53019762
|
G | T | 1 | a0002c0003t0007g0018 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.65-6986G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53019762 | ||||||
| chr5:53019852
|
G | A | 2 | a0001c0002t0018g0103a0001c0002t0018g0105 | 2 | HG01175.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.65-6896G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53019852 | ||||||
| chr5:53019994
|
A | G | 1 | a0014c0025t0003g0173 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.65-6754A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53019994 | ||||||
| chr5:53020189
|
C | T | 1 | a0001c0002t0004g0256 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.65-6559C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53020189 | ||||||
| chr5:53020211
|
A | C | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-6537A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53020211 | ||||||
| chr5:53020342
|
C | T | 129 | a0001c0001t0001g0009a0001c0001t0001g0118a0001c0001t0001g0289others(126): Show | 136 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.65-6406C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53020342 | ||||||
| chr5:53020486
|
C | T | 3 | a0001c0001t0001g0181a0001c0002t0003g0194a0001c0002t0003g0195 | 3 | HG01106.hp2 HG02698.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.65-6262C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53020486 | ||||||
| chr5:53020655
|
C | T | 1 | a0001c0002t0003g0180 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.65-6093C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53020655 | ||||||
| chr5:53020689
|
T | A | 45 | a0001c0001t0001g0339a0001c0001t0002g0220a0001c0001t0002g0221others(42): Show | 47 | HG00280.hp2 HG00609.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.65-6059T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53020689 | ||||||
| chr5:53020848
|
A | AT | 13 | a0001c0001t0001g0070a0001c0001t0001g0093a0001c0001t0002g0161others(10): Show | 13 | HG01074.hp1 HG02015.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.65-5882dupT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53020848 | |||||
| chr5:53020985
|
G | A | 1 | a0001c0002t0004g0116 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.65-5763G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53020985 | ||||||
| chr5:53021137
|
G | A | 1 | a0001c0001t0051g0071 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.65-5611G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53021137 | ||||||
| chr5:53021182
|
A | G | 3 | a0001c0001t0014g0279a0001c0001t0014g0294a0001c0001t0014g0295 | 3 | NA18939.hp2 NA18951.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.65-5566A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53021182 | ||||||
| chr5:53021227
|
C | T | 1 | a0013c0019t0030g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.65-5521C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53021227 | ||||||
| chr5:53021269
|
T | C | 2 | a0002c0007t0010g0165a0002c0007t0010g0166 | 2 | HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-5479T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53021269 | ||||||
| chr5:53021318
|
A | G | 30 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0222others(27): Show | 32 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.65-5430A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53021318 | ||||||
| chr5:53021397
|
T | C | 1 | a0001c0001t0015g0249 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.65-5351T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53021397 | ||||||
| chr5:53021424
|
C | G | 1 | a0001c0001t0001g0085 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.65-5324C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53021424 | ||||||
| chr5:53021428
|
C | G | 1 | a0001c0004t0002g0344 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.65-5320C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53021428 | ||||||
| chr5:53021487
|
C | T | 2 | a0001c0001t0002g0273a0001c0002t0047g0061 | 2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.65-5261C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53021487 | ||||||
| chr5:53021775
|
C | G | 1 | a0001c0001t0022g0044 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.65-4973C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53021775 | ||||||
| chr5:53021883
|
C | T | 1 | a0001c0002t0004g0106 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.65-4865C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53021883 | ||||||
| chr5:53022009
|
T | C | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-4739T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53022009 | ||||||
| chr5:53022024
|
A | G | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-4724A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53022024 | ||||||
| chr5:53022083
|
A | G | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-4665A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53022083 | ||||||
| chr5:53022086
|
A | G | 1 | a0001c0002t0019g0237 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.65-4662A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53022086 | ||||||
| chr5:53022127
|
A | G | 3 | a0001c0002t0003g0170a0001c0002t0003g0182a0001c0002t0003g0213 | 3 | HG00741.hp2 HG01433.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.65-4621A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53022127 | ||||||
| chr5:53022208
|
A | AT | 112 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(109): Show | 123 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.65-4529dupT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53022208 | |||||
| chr5:53022218
|
T | TG | 3 | a0001c0001t0002g0243a0001c0001t0025g0276a0001c0002t0048g0239 | 3 | HG00642.hp2 HG02559.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.65-4530_65-4529ins others(1): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53022218 | ||||||
| chr5:53022219
|
T | G | 70 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0029others(67): Show | 74 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.65-4529T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53022219 | ||||||
| chr5:53022219
|
T | TG | 145 | a0001c0001t0001g0009a0001c0001t0001g0055a0001c0001t0001g0076others(142): Show | 150 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.65-4524dupG | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr5 | 53022219 | |||||
| chr5:53022342
|
G | C | 1 | a0001c0001t0002g0119 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.65-4406G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53022342 | ||||||
| chr5:53022777
|
GAC | G | 3 | a0001c0008t0012g0162a0001c0008t0012g0163a0001c0008t0012g0164 | 3 | HG02965.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.65-3970_65-3969del others(2): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53022777 | ||||||
| chr5:53022881
|
T | C | 1 | a0001c0001t0002g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.65-3867T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53022881 | ||||||
| chr5:53022916
|
A | G | 1 | a0001c0001t0005g0262 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.65-3832A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53022916 | ||||||
| chr5:53023076
|
G | T | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-3672G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53023076 | ||||||
| chr5:53023086
|
C | T | 66 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098others(63): Show | 70 | HG00280.hp1 HG00673.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.65-3662C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53023086 | ||||||
| chr5:53023226
|
T | G | 50 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0222others(47): Show | 52 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.65-3522T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53023226 | ||||||
| chr5:53023246
|
C | T | 195 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0055others(192): Show | 204 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.65-3502C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53023246 | ||||||
| chr5:53023412
|
C | A | 1 | a0013c0019t0030g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.65-3336C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53023412 | ||||||
| chr5:53023464
|
A | G | 1 | a0001c0001t0024g0300 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.65-3284A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53023464 | ||||||
| chr5:53023532
|
T | C | 1 | a0001c0001t0025g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.65-3216T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53023532 | ||||||
| chr5:53023661
|
T | A | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-3087T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53023661 | ||||||
| chr5:53023769
|
T | C | 6 | a0001c0002t0004g0102a0002c0007t0010g0165a0002c0007t0010g0166others(3): Show | 6 | HG02280.hp1 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-2979T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53023769 | ||||||
| chr5:53024020
|
T | C | 6 | a0001c0011t0034g0084a0002c0003t0017g0021a0002c0003t0017g0022others(3): Show | 6 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-2728T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53024020 | ||||||
| chr5:53024112
|
G | T | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.65-2636G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53024112 | ||||||
| chr5:53024199
|
A | G | 68 | a0001c0001t0001g0009a0001c0001t0001g0118a0001c0001t0001g0320others(65): Show | 71 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.65-2549A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53024199 | ||||||
| chr5:53024325
|
G | A | 2 | a0001c0001t0005g0327a0001c0001t0005g0329 | 2 | HG01243.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.65-2423G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53024325 | ||||||
| chr5:53024403
|
T | G | 4 | a0001c0001t0001g0341a0001c0001t0001g0350a0001c0001t0013g0340others(1): Show | 4 | HG00408.hp2 NA18962.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-2345T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53024403 | ||||||
| chr5:53024490
|
A | G | 3 | a0002c0003t0007g0283a0002c0003t0007g0284a0002c0003t0007g0285 | 3 | HG02055.hp2 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.65-2258A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53024490 | ||||||
| chr5:53024493
|
A | C | 2 | a0001c0001t0025g0281a0001c0021t0050g0280 | 2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.65-2255A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53024493 | ||||||
| chr5:53024501
|
T | A | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-2247T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53024501 | ||||||
| chr5:53024689
|
T | C | 1 | a0009c0017t0052g0263 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.65-2059T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53024689 | ||||||
| chr5:53024761
|
A | C | 1 | a0001c0002t0004g0256 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.65-1987A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53024761 | ||||||
| chr5:53024900
|
G | T | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-1848G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53024900 | ||||||
| chr5:53024919
|
T | C | 138 | a0001c0001t0001g0009a0001c0001t0001g0118a0001c0001t0001g0289others(135): Show | 145 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.65-1829T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53024919 | ||||||
| chr5:53025063
|
T | C | 274 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(271): Show | 290 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.65-1685T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53025063 | ||||||
| chr5:53025110
|
G | A | 57 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(54): Show | 59 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.65-1638G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53025110 | ||||||
| chr5:53025129
|
C | T | 2 | a0001c0001t0001g0136a0001c0001t0013g0141 | 2 | NA19000.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.65-1619C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53025129 | ||||||
| chr5:53025197
|
A | G | 3 | a0001c0002t0004g0102a0002c0007t0010g0260a0002c0007t0010g0261 | 3 | HG02280.hp1 HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.65-1551A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53025197 | ||||||
| chr5:53025209
|
T | C | 26 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0047others(23): Show | 31 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.65-1539T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53025209 | ||||||
| chr5:53025352
|
A | C | 1 | a0001c0001t0038g0129 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.65-1396A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53025352 | ||||||
| chr5:53025531
|
C | T | 7 | a0002c0003t0017g0021a0002c0003t0017g0022a0002c0003t0017g0023others(4): Show | 7 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-1217C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53025531 | ||||||
| chr5:53025591
|
A | G | 1 | a0001c0002t0006g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.65-1157A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53025591 | ||||||
| chr5:53025602
|
G | T | 53 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(50): Show | 54 | HG00544.hp1 HG00558.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.65-1146G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53025602 | ||||||
| chr5:53025978
|
A | G | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.65-770A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53025978 | ||||||
| chr5:53026045
|
T | C | 2 | a0001c0001t0002g0273a0001c0002t0047g0061 | 2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.65-703T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53026045 | ||||||
| chr5:53026217
|
C | A | 1 | a0003c0005t0003g0290 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65-531C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53026217 | ||||||
| chr5:53026280
|
G | A | 10 | a0001c0002t0003g0171a0001c0002t0003g0179a0001c0002t0003g0183others(7): Show | 10 | HG00609.hp1 NA18612.hp1 NA18954.hp2 others(7): Show |
intron_variant | MODIFIER | c.65-468G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53026280 | ||||||
| chr5:53026306
|
C | A | 2 | a0001c0001t0005g0301a0001c0001t0005g0330 | 2 | HG02040.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.65-442C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53026306 | ||||||
| chr5:53026366
|
C | T | 5 | a0002c0003t0017g0021a0002c0003t0017g0022a0002c0003t0017g0023others(2): Show | 5 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-382C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53026366 | ||||||
| chr5:53026412
|
A | T | 1 | a0001c0002t0004g0256 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.65-336A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53026412 | ||||||
| chr5:53026539
|
G | A | 6 | a0001c0002t0004g0233a0001c0002t0004g0240a0001c0002t0004g0265others(3): Show | 6 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-209G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53026539 | ||||||
| chr5:53026577
|
C | T | 4 | a0002c0003t0007g0337a0002c0003t0007g0348a0002c0003t0007g0355others(1): Show | 4 | NA18989.hp2 NA19056.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-171C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53026577 | ||||||
| chr5:53026691
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.65-57C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53026691 | ||||||
| chr5:53026694
|
C | T | 5 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0222others(2): Show | 5 | HG02080.hp2 HG02129.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-54C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 1/29 | chr5 | 53026694 | ||||||
| chr5:53026891
|
G | T | 92 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(89): Show | 97 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.185+23G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53026891 | ||||||
| chr5:53026956
|
G | C | 1 | a0001c0001t0001g0066 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.185+88G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53026956 | ||||||
| chr5:53027152
|
T | TGATA | 53 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0222others(50): Show | 55 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.185+287_185+290dup others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53027152 | |||||
| chr5:53027182
|
G | T | 5 | a0002c0003t0017g0021a0002c0003t0017g0022a0002c0003t0017g0023others(2): Show | 5 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.185+314G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53027182 | ||||||
| chr5:53027276
|
A | C | 1 | a0001c0002t0003g0063 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.185+408A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53027276 | ||||||
| chr5:53027414
|
G | A | 2 | a0001c0002t0006g0112a0001c0002t0006g0367 | 2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.185+546G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53027414 | ||||||
| chr5:53027623
|
C | A | 118 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0289others(115): Show | 124 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.185+755C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53027623 | ||||||
| chr5:53027738
|
A | G | 225 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(222): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.185+870A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53027738 | ||||||
| chr5:53027790
|
C | T | 4 | a0001c0011t0034g0084a0002c0009t0016g0271a0002c0009t0016g0272others(1): Show | 4 | HG06807.hp1 NA18961.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+922C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53027790 | ||||||
| chr5:53027890
|
G | C | 8 | a0001c0002t0004g0102a0002c0007t0010g0165a0002c0007t0010g0166others(5): Show | 8 | HG02280.hp1 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+1022G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53027890 | ||||||
| chr5:53027927
|
G | A | 306 | a0001c0001t0001g0009a0001c0001t0001g0028a0001c0001t0001g0029others(303): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.185+1059G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53027927 | ||||||
| chr5:53028099
|
A | C | 1 | a0013c0019t0030g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.185+1231A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53028099 | ||||||
| chr5:53028655
|
C | T | 1 | a0001c0002t0003g0170 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.185+1787C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53028655 | ||||||
| chr5:53028675
|
C | T | 8 | a0001c0002t0004g0102a0002c0007t0010g0165a0002c0007t0010g0166others(5): Show | 8 | HG02280.hp1 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+1807C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53028675 | ||||||
| chr5:53028724
|
C | T | 1 | a0001c0001t0005g0318 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.185+1856C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53028724 | ||||||
| chr5:53028829
|
C | T | 9 | a0001c0002t0003g0171a0001c0002t0003g0179a0001c0002t0003g0183others(6): Show | 9 | HG00609.hp1 NA18612.hp1 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.185+1961C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53028829 | ||||||
| chr5:53028851
|
T | A | 1 | a0001c0001t0002g0117 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.185+1983T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53028851 | ||||||
| chr5:53028868
|
C | T | 25 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(22): Show | 28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.185+2000C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53028868 | ||||||
| chr5:53028886
|
G | A | 1 | a0001c0001t0005g0262 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.185+2018G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53028886 | ||||||
| chr5:53029023
|
G | C | 5 | a0001c0002t0018g0103a0001c0002t0018g0105a0001c0002t0018g0120others(2): Show | 5 | HG00642.hp1 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.185+2155G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53029023 | ||||||
| chr5:53029141
|
G | A | 8 | a0001c0002t0004g0102a0002c0007t0010g0165a0002c0007t0010g0166others(5): Show | 8 | HG02280.hp1 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+2273G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53029141 | ||||||
| chr5:53029211
|
G | T | 2 | a0001c0002t0004g0233a0001c0002t0004g0240 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.185+2343G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53029211 | ||||||
| chr5:53029230
|
C | T | 3 | a0001c0001t0001g0070a0001c0001t0001g0076a0001c0001t0001g0077 | 3 | NA18940.hp2 NA18991.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.185+2362C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53029230 | ||||||
| chr5:53029239
|
T | A | 24 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(21): Show | 27 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.185+2371T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53029239 | ||||||
| chr5:53029484
|
G | A | 25 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(22): Show | 28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.185+2616G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53029484 | ||||||
| chr5:53029575
|
T | C | 26 | a0001c0016t0005g0104a0002c0003t0007g0019a0002c0003t0007g0072others(23): Show | 27 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.185+2707T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53029575 | ||||||
| chr5:53029582
|
A | G | 1 | a0001c0001t0002g0264 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.185+2714A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53029582 | ||||||
| chr5:53029945
|
C | T | 113 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(110): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.185+3077C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53029945 | ||||||
| chr5:53029955
|
C | T | 1 | a0001c0001t0025g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.185+3087C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53029955 | ||||||
| chr5:53030218
|
A | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(4): Show | 8 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+3350A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53030218 | ||||||
| chr5:53030468
|
T | C | 1 | a0001c0002t0006g0035 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.185+3600T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53030468 | ||||||
| chr5:53030613
|
C | T | 1 | a0013c0019t0030g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.185+3745C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53030613 | ||||||
| chr5:53030630
|
CAA | C | 8 | a0001c0002t0004g0102a0002c0007t0010g0165a0002c0007t0010g0166others(5): Show | 8 | HG02280.hp1 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+3763_185+3764d others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53030630 | ||||||
| chr5:53031305
|
C | T | 1 | a0001c0001t0025g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.185+4437C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53031305 | ||||||
| chr5:53031379
|
C | T | 1 | a0001c0008t0021g0013 | 2 | HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.185+4511C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53031379 | ||||||
| chr5:53031400
|
G | A | 104 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(101): Show | 110 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.185+4532G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53031400 | ||||||
| chr5:53031521
|
T | C | 4 | a0001c0008t0012g0162a0001c0008t0012g0163a0001c0008t0012g0164others(1): Show | 5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.185+4653T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53031521 | ||||||
| chr5:53031686
|
C | G | 2 | a0001c0001t0005g0218a0001c0001t0005g0219 | 2 | HG02273.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.185+4818C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53031686 | ||||||
| chr5:53031866
|
T | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | NA18991.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.185+4998T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53031866 | ||||||
| chr5:53031937
|
A | G | 8 | a0001c0002t0004g0102a0002c0007t0010g0165a0002c0007t0010g0166others(5): Show | 8 | HG02280.hp1 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+5069A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53031937 | ||||||
| chr5:53031977
|
C | G | 104 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(101): Show | 110 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.185+5109C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53031977 | ||||||
| chr5:53032173
|
TA | T | 73 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(70): Show | 76 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.185+5313delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53032173 | |||||
| chr5:53032363
|
A | G | 24 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(21): Show | 27 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.185+5495A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53032363 | ||||||
| chr5:53032379
|
T | C | 1 | a0001c0002t0004g0115 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.185+5511T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53032379 | ||||||
| chr5:53032402
|
C | G | 4 | a0001c0001t0005g0217a0001c0001t0005g0218a0001c0001t0005g0219others(1): Show | 4 | HG01993.hp2 HG02004.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+5534C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53032402 | ||||||
| chr5:53032570
|
C | T | 132 | a0001c0001t0002g0243a0001c0002t0003g0002a0001c0002t0003g0031others(129): Show | 141 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.185+5702C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53032570 | ||||||
| chr5:53032612
|
T | G | 1 | a0013c0019t0030g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.185+5744T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53032612 | ||||||
| chr5:53032824
|
A | G | 24 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(21): Show | 27 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.185+5956A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53032824 | ||||||
| chr5:53032983
|
C | T | 8 | a0001c0002t0004g0102a0002c0007t0010g0165a0002c0007t0010g0166others(5): Show | 8 | HG02280.hp1 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+6115C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53032983 | ||||||
| chr5:53032995
|
C | T | 103 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(100): Show | 109 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.185+6127C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53032995 | ||||||
| chr5:53033039
|
G | A | 9 | a0001c0001t0001g0358a0001c0002t0004g0102a0002c0007t0010g0165others(6): Show | 9 | HG02280.hp1 HG02647.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.185+6171G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033039 | ||||||
| chr5:53033046
|
T | C | 34 | a0001c0001t0005g0004a0001c0001t0005g0017a0001c0001t0005g0217others(31): Show | 38 | HG00673.hp1 HG00735.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.185+6178T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033046 | ||||||
| chr5:53033123
|
G | A | 1 | a0001c0001t0025g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.185+6255G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033123 | ||||||
| chr5:53033129
|
C | T | 25 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(22): Show | 28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.185+6261C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033129 | ||||||
| chr5:53033130
|
G | A | 79 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(76): Show | 83 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.185+6262G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033130 | ||||||
| chr5:53033132
|
G | A | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.185+6264G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033132 | ||||||
| chr5:53033136
|
G | A | 73 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(70): Show | 76 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.185+6268G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033136 | ||||||
| chr5:53033219
|
A | G | 1 | a0003c0005t0003g0178 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.185+6351A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033219 | ||||||
| chr5:53033268
|
CA | C | 160 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(157): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.185+6410delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53033268 | |||||
| chr5:53033302
|
A | G | 108 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(105): Show | 114 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.185+6434A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033302 | ||||||
| chr5:53033418
|
C | T | 3 | a0002c0007t0010g0165a0002c0007t0010g0166a0002c0007t0010g0167 | 3 | HG02818.hp2 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.185+6550C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033418 | ||||||
| chr5:53033511
|
A | G | 245 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(242): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.185+6643A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033511 | ||||||
| chr5:53033607
|
A | T | 39 | a0001c0001t0025g0276a0001c0002t0047g0061a0001c0008t0012g0162others(36): Show | 41 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.185+6739A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033607 | ||||||
| chr5:53033611
|
A | T | 219 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(216): Show | 230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.185+6743A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033611 | ||||||
| chr5:53033751
|
C | T | 1 | a0013c0019t0030g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.185+6883C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033751 | ||||||
| chr5:53033764
|
AT | A | 132 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(129): Show | 140 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.185+6913delT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53033764 | |||||
| chr5:53033764
|
ATT | A | 110 | a0001c0001t0029g0139a0001c0001t0039g0121a0001c0002t0003g0002others(107): Show | 116 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.185+6912_185+6913d others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53033764 | |||||
| chr5:53033786
|
C | T | 10 | a0001c0002t0003g0171a0001c0002t0003g0179a0001c0002t0003g0183others(7): Show | 10 | HG00609.hp1 HG00673.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.185+6918C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033786 | ||||||
| chr5:53033798
|
C | A | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.185+6930C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033798 | ||||||
| chr5:53033832
|
C | T | 1 | a0001c0001t0025g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.185+6964C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033832 | ||||||
| chr5:53033850
|
G | A | 1 | a0013c0019t0030g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.185+6982G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53033850 | ||||||
| chr5:53034000
|
A | G | 2 | a0001c0001t0005g0316a0001c0001t0005g0317 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.185+7132A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034000 | ||||||
| chr5:53034021
|
C | T | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.185+7153C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034021 | ||||||
| chr5:53034052
|
G | T | 1 | a0001c0002t0003g0193 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.185+7184G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034052 | ||||||
| chr5:53034183
|
A | T | 25 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(22): Show | 28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.185+7315A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034183 | ||||||
| chr5:53034193
|
A | G | 139 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(136): Show | 147 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.185+7325A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034193 | ||||||
| chr5:53034384
|
G | A | 1 | a0013c0019t0030g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.185+7516G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034384 | ||||||
| chr5:53034407
|
CA | C | 26 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(23): Show | 29 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.185+7553delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53034407 | |||||
| chr5:53034407
|
CAA | C | 112 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(109): Show | 117 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.185+7552_185+7553d others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53034407 | |||||
| chr5:53034501
|
A | G | 27 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(24): Show | 30 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.186-7611A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034501 | ||||||
| chr5:53034517
|
A | AT | 26 | a0001c0016t0005g0104a0002c0003t0007g0019a0002c0003t0007g0072others(23): Show | 27 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.186-7594dupT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53034517 | |||||
| chr5:53034529
|
C | T | 1 | a0001c0004t0008g0310 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.186-7583C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034529 | ||||||
| chr5:53034695
|
A | T | 1 | a0010c0027t0006g0036 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.186-7417A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034695 | ||||||
| chr5:53034751
|
A | G | 108 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(105): Show | 114 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.186-7361A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034751 | ||||||
| chr5:53034813
|
A | G | 26 | a0001c0016t0005g0104a0002c0003t0007g0019a0002c0003t0007g0072others(23): Show | 27 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.186-7299A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034813 | ||||||
| chr5:53034859
|
T | C | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.186-7253T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034859 | ||||||
| chr5:53034872
|
T | A | 1 | a0013c0019t0030g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.186-7240T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034872 | ||||||
| chr5:53034915
|
G | A | 245 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(242): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.186-7197G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034915 | ||||||
| chr5:53034962
|
C | A | 5 | a0002c0003t0017g0021a0002c0003t0017g0022a0002c0003t0017g0023others(2): Show | 5 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.186-7150C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53034962 | ||||||
| chr5:53035102
|
G | C | 25 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(22): Show | 28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.186-7010G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53035102 | ||||||
| chr5:53035195
|
A | C | 108 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(105): Show | 114 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.186-6917A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53035195 | ||||||
| chr5:53035263
|
G | C | 1 | a0001c0002t0003g0113 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.186-6849G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53035263 | ||||||
| chr5:53035304
|
C | T | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.186-6808C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53035304 | ||||||
| chr5:53035314
|
G | A | 25 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(22): Show | 28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.186-6798G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53035314 | ||||||
| chr5:53035372
|
G | A | 5 | a0002c0007t0010g0165a0002c0007t0010g0166a0002c0007t0010g0167others(2): Show | 5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-6740G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53035372 | ||||||
| chr5:53035623
|
A | G | 21 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(18): Show | 24 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.186-6489A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53035623 | ||||||
| chr5:53035660
|
C | T | 73 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(70): Show | 76 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.186-6452C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53035660 | ||||||
| chr5:53035665
|
A | G | 1 | a0001c0002t0004g0282 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.186-6447A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53035665 | ||||||
| chr5:53035674
|
G | A | 1 | a0001c0001t0002g0156 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.186-6438G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53035674 | ||||||
| chr5:53036032
|
G | A | 1 | a0004c0006t0003g0172 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.186-6080G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53036032 | ||||||
| chr5:53036044
|
T | TATTC | 28 | a0001c0001t0002g0138a0001c0001t0002g0155a0001c0002t0019g0238others(25): Show | 29 | HG01074.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.186-6036_186-6033d others(6): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53036044 | |||||
| chr5:53036044
|
T | TATTCATT others(1): Show |
101 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(98): Show | 106 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.186-6040_186-6033d others(10): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53036044 | |||||
| chr5:53036044
|
T | TATTCATT others(5): Show |
8 | a0001c0001t0001g0325a0001c0001t0002g0159a0001c0001t0039g0121others(5): Show | 8 | HG01099.hp2 HG02486.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.186-6044_186-6033d others(14): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53036044 | |||||
| chr5:53036044
|
TATTC | T | 13 | a0001c0002t0006g0034a0001c0002t0006g0035a0001c0002t0006g0037others(10): Show | 13 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.186-6036_186-6033d others(6): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53036044 | |||||
| chr5:53036259
|
G | C | 247 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(244): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.186-5853G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53036259 | ||||||
| chr5:53036271
|
T | C | 25 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(22): Show | 28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.186-5841T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53036271 | ||||||
| chr5:53036356
|
C | T | 133 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(130): Show | 142 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.186-5756C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53036356 | ||||||
| chr5:53036605
|
G | A | 270 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(267): Show | 285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.186-5507G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53036605 | ||||||
| chr5:53036678
|
A | G | 1 | a0001c0001t0001g0336 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.186-5434A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53036678 | ||||||
| chr5:53036756
|
C | CT | 65 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(62): Show | 69 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.186-5350dupT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53036756 | |||||
| chr5:53037303
|
A | G | 1 | a0001c0002t0003g0170 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.186-4809A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53037303 | ||||||
| chr5:53037383
|
T | G | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.186-4729T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53037383 | ||||||
| chr5:53037492
|
G | A | 7 | a0002c0007t0010g0165a0002c0007t0010g0166a0002c0007t0010g0167others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.186-4620G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53037492 | ||||||
| chr5:53037590
|
C | A | 133 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(130): Show | 142 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.186-4522C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53037590 | ||||||
| chr5:53037757
|
T | G | 1 | a0001c0001t0005g0262 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.186-4355T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53037757 | ||||||
| chr5:53037914
|
T | C | 222 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(219): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.186-4198T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53037914 | ||||||
| chr5:53038090
|
G | A | 2 | a0001c0002t0004g0229a0001c0002t0004g0257 | 2 | HG02602.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.186-4022G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038090 | ||||||
| chr5:53038109
|
A | G | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.186-4003A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038109 | ||||||
| chr5:53038207
|
T | TAAA | 87 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0108others(84): Show | 93 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.186-3892_186-3890d others(5): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53038207 | |||||
| chr5:53038207
|
T | TAAAA | 15 | a0001c0002t0003g0063a0001c0002t0003g0069a0001c0002t0003g0157others(12): Show | 15 | HG00642.hp1 HG01175.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.186-3893_186-3890d others(6): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53038207 | |||||
| chr5:53038207
|
TA | T | 86 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(83): Show | 90 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.186-3890delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53038207 | |||||
| chr5:53038207
|
TAA | T | 30 | a0001c0001t0002g0107a0001c0001t0002g0142a0001c0001t0002g0264others(27): Show | 32 | HG01192.hp1 HG01243.hp2 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.186-3891_186-3890d others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53038207 | |||||
| chr5:53038241
|
G | A | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.186-3871G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038241 | ||||||
| chr5:53038307
|
C | T | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.186-3805C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038307 | ||||||
| chr5:53038488
|
G | A | 109 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(106): Show | 115 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.186-3624G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038488 | ||||||
| chr5:53038514
|
A | G | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.186-3598A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038514 | ||||||
| chr5:53038662
|
A | G | 2 | a0008c0018t0037g0277a0009c0017t0052g0263 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.186-3450A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038662 | ||||||
| chr5:53038678
|
C | G | 222 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(219): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.186-3434C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038678 | ||||||
| chr5:53038693
|
C | T | 1 | a0001c0004t0008g0309 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.186-3419C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038693 | ||||||
| chr5:53038697
|
CGCACTTG others(7): Show |
C | 4 | a0002c0003t0007g0337a0002c0003t0007g0348a0002c0003t0007g0355others(1): Show | 4 | NA18989.hp2 NA19056.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-3414_186-3401d others(16): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038697 | ||||||
| chr5:53038701
|
C | A | 1 | a0001c0028t0004g0074 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.186-3411C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038701 | ||||||
| chr5:53038710
|
C | T | 1 | a0001c0001t0001g0341 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.186-3402C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038710 | ||||||
| chr5:53038745
|
A | G | 1 | a0001c0002t0041g0332 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.186-3367A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038745 | ||||||
| chr5:53038822
|
G | C | 2 | a0001c0001t0005g0327a0001c0001t0005g0329 | 2 | HG01243.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.186-3290G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038822 | ||||||
| chr5:53038832
|
A | T | 242 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(239): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.186-3280A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038832 | ||||||
| chr5:53038840
|
C | A | 31 | a0001c0001t0005g0004a0001c0001t0005g0017a0001c0001t0005g0217others(28): Show | 34 | HG00735.hp2 HG01069.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.186-3272C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038840 | ||||||
| chr5:53038841
|
A | G | 31 | a0001c0001t0005g0004a0001c0001t0005g0017a0001c0001t0005g0217others(28): Show | 34 | HG00735.hp2 HG01069.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.186-3271A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038841 | ||||||
| chr5:53038944
|
A | G | 35 | a0001c0002t0004g0003a0001c0002t0004g0087a0001c0002t0004g0099others(32): Show | 37 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.186-3168A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038944 | ||||||
| chr5:53038966
|
G | A | 5 | a0002c0007t0010g0165a0002c0007t0010g0166a0002c0007t0010g0167others(2): Show | 5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-3146G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53038966 | ||||||
| chr5:53039081
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.186-3031C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53039081 | ||||||
| chr5:53039208
|
T | G | 5 | a0002c0007t0010g0165a0002c0007t0010g0166a0002c0007t0010g0167others(2): Show | 5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-2904T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53039208 | ||||||
| chr5:53039309
|
GA | G | 106 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(103): Show | 112 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.186-2795delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53039309 | |||||
| chr5:53039342
|
C | T | 1 | a0001c0004t0008g0310 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.186-2770C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53039342 | ||||||
| chr5:53039401
|
G | A | 2 | a0008c0018t0037g0277a0009c0017t0052g0263 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.186-2711G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53039401 | ||||||
| chr5:53039531
|
G | A | 115 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(112): Show | 121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.186-2581G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53039531 | ||||||
| chr5:53039539
|
G | T | 1 | a0001c0022t0002g0245 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.186-2573G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53039539 | ||||||
| chr5:53039572
|
C | T | 79 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(76): Show | 83 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.186-2540C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53039572 | ||||||
| chr5:53039611
|
G | A | 3 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0032 | 3 | HG00673.hp2 HG02129.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.186-2501G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53039611 | ||||||
| chr5:53039664
|
C | T | 132 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(129): Show | 141 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.186-2448C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53039664 | ||||||
| chr5:53039720
|
A | G | 28 | a0001c0016t0005g0104a0002c0003t0007g0018a0002c0003t0007g0019others(25): Show | 30 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.186-2392A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53039720 | ||||||
| chr5:53039739
|
C | CA | 85 | a0001c0001t0001g0006a0001c0001t0001g0047a0001c0001t0001g0065others(82): Show | 90 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.186-2348dupA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53039739 | |||||
| chr5:53039739
|
C | CAA | 12 | a0001c0001t0001g0324a0001c0001t0001g0336a0001c0001t0002g0122others(9): Show | 12 | HG01261.hp2 HG01978.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.186-2349_186-2348d others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53039739 | |||||
| chr5:53039739
|
CA | C | 11 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0345others(8): Show | 11 | HG01168.hp2 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.186-2348delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53039739 | |||||
| chr5:53039739
|
CAAA | C | 23 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(20): Show | 26 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.186-2350_186-2348d others(5): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53039739 | |||||
| chr5:53039783
|
A | C | 1 | a0001c0001t0005g0287 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.186-2329A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53039783 | ||||||
| chr5:53039952
|
A | C | 10 | a0001c0002t0003g0063a0001c0002t0003g0069a0001c0002t0003g0157others(7): Show | 11 | HG02015.hp1 NA18947.hp1 NA18948.hp1 others(8): Show |
intron_variant | MODIFIER | c.186-2160A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53039952 | ||||||
| chr5:53040036
|
G | A | 3 | a0001c0002t0004g0087a0001c0002t0004g0232a0001c0002t0004g0236 | 3 | HG02486.hp1 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.186-2076G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53040036 | ||||||
| chr5:53040086
|
C | A | 1 | a0001c0001t0005g0318 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.186-2026C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53040086 | ||||||
| chr5:53040117
|
T | C | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.186-1995T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53040117 | ||||||
| chr5:53040237
|
G | T | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.186-1875G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53040237 | ||||||
| chr5:53040374
|
A | C | 1 | a0002c0009t0016g0271 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.186-1738A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53040374 | ||||||
| chr5:53040462
|
G | A | 1 | a0001c0004t0008g0362 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.186-1650G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53040462 | ||||||
| chr5:53040641
|
G | GA | 8 | a0001c0004t0008g0361a0001c0004t0008g0364a0001c0004t0008g0368others(5): Show | 8 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-1465dupA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53040641 | |||||
| chr5:53040703
|
C | A | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.186-1409C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53040703 | ||||||
| chr5:53040744
|
C | T | 117 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(114): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.186-1368C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53040744 | ||||||
| chr5:53040751
|
A | C | 222 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(219): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.186-1361A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53040751 | ||||||
| chr5:53040812
|
C | T | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.186-1300C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53040812 | ||||||
| chr5:53041010
|
G | A | 1 | a0002c0007t0010g0261 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.186-1102G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041010 | ||||||
| chr5:53041079
|
T | G | 219 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(216): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.186-1033T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041079 | ||||||
| chr5:53041100
|
T | G | 4 | a0001c0008t0012g0162a0001c0008t0012g0163a0001c0008t0012g0164others(1): Show | 5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-1012T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041100 | ||||||
| chr5:53041115
|
T | TA | 71 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(68): Show | 74 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.186-996dupA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr5 | 53041115 | |||||
| chr5:53041152
|
G | A | 219 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(216): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.186-960G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041152 | ||||||
| chr5:53041262
|
T | C | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.186-850T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041262 | ||||||
| chr5:53041314
|
C | T | 109 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(106): Show | 115 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.186-798C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041314 | ||||||
| chr5:53041325
|
T | C | 222 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(219): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.186-787T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041325 | ||||||
| chr5:53041426
|
C | T | 222 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(219): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.186-686C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041426 | ||||||
| chr5:53041496
|
G | T | 78 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(75): Show | 82 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.186-616G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041496 | ||||||
| chr5:53041573
|
G | C | 115 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(112): Show | 121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.186-539G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041573 | ||||||
| chr5:53041592
|
C | T | 27 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(24): Show | 30 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.186-520C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041592 | ||||||
| chr5:53041676
|
C | A | 1 | a0001c0001t0005g0262 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.186-436C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041676 | ||||||
| chr5:53041709
|
C | T | 2 | a0001c0001t0025g0281a0001c0021t0050g0280 | 2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.186-403C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041709 | ||||||
| chr5:53041926
|
A | G | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.186-186A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041926 | ||||||
| chr5:53041953
|
T | C | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.186-159T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53041953 | ||||||
| chr5:53042052
|
G | T | 1 | a0008c0018t0037g0277 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-60G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53042052 | ||||||
| chr5:53042078
|
C | T | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.186-34C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 2/29 | chr5 | 53042078 | ||||||
| chr5:53042253
|
T | G | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.295+32T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53042253 | ||||||
| chr5:53042310
|
A | G | 4 | a0002c0003t0007g0337a0002c0003t0007g0348a0002c0003t0007g0355others(1): Show | 4 | NA18989.hp2 NA19056.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.295+89A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53042310 | ||||||
| chr5:53042411
|
G | A | 73 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(70): Show | 76 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.295+190G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53042411 | ||||||
| chr5:53042446
|
T | C | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.295+225T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53042446 | ||||||
| chr5:53042521
|
T | C | 1 | a0001c0001t0002g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.295+300T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53042521 | ||||||
| chr5:53042834
|
T | G | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.295+613T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53042834 | ||||||
| chr5:53042837
|
G | T | 2 | a0008c0018t0037g0277a0009c0017t0052g0263 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.295+616G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53042837 | ||||||
| chr5:53042847
|
C | T | 20 | a0001c0016t0005g0104a0002c0003t0007g0018a0002c0003t0007g0019others(17): Show | 22 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.295+626C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53042847 | ||||||
| chr5:53042849
|
T | TA | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.295+635dupA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53042849 | |||||
| chr5:53042976
|
A | C | 247 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(244): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.295+755A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53042976 | ||||||
| chr5:53043026
|
T | C | 2 | a0001c0001t0005g0316a0001c0001t0005g0317 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.295+805T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53043026 | ||||||
| chr5:53043196
|
G | GTA | 6 | a0001c0001t0002g0119a0001c0002t0003g0031a0001c0002t0003g0108others(3): Show | 6 | HG00741.hp1 HG01081.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.295+991_295+992dup others(2): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53043196 | |||||
| chr5:53043240
|
GGAGT | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(4): Show | 8 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.295+1025_295+1028d others(6): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53043240 | |||||
| chr5:53043277
|
AT | A | 69 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(66): Show | 73 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.295+1060delT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53043277 | |||||
| chr5:53043284
|
T | C | 79 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(76): Show | 83 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.295+1063T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53043284 | ||||||
| chr5:53043380
|
G | T | 1 | a0002c0007t0010g0167 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.295+1159G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53043380 | ||||||
| chr5:53043540
|
G | T | 2 | a0008c0018t0037g0277a0009c0017t0052g0263 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.295+1319G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53043540 | ||||||
| chr5:53043660
|
T | C | 1 | a0001c0001t0005g0262 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.296-1341T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53043660 | ||||||
| chr5:53043715
|
G | A | 6 | a0001c0002t0009g0027a0001c0002t0009g0207a0001c0002t0009g0208others(3): Show | 6 | HG00280.hp2 NA18995.hp1 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.296-1286G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53043715 | ||||||
| chr5:53044013
|
G | A | 8 | a0001c0001t0005g0017a0001c0001t0005g0288a0001c0001t0005g0315others(5): Show | 9 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.296-988G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044013 | ||||||
| chr5:53044086
|
G | A | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.296-915G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044086 | ||||||
| chr5:53044128
|
A | G | 2 | a0008c0018t0037g0277a0009c0017t0052g0263 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.296-873A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044128 | ||||||
| chr5:53044143
|
T | C | 247 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(244): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.296-858T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044143 | ||||||
| chr5:53044199
|
C | T | 1 | a0002c0003t0007g0286 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.296-802C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044199 | ||||||
| chr5:53044200
|
G | A | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.296-801G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044200 | ||||||
| chr5:53044207
|
A | G | 25 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(22): Show | 28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.296-794A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044207 | ||||||
| chr5:53044249
|
T | C | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.296-752T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044249 | ||||||
| chr5:53044274
|
C | CA | 62 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(59): Show | 68 | HG00408.hp2 HG00544.hp1 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.296-695dupA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | |||||
| chr5:53044274
|
C | CAA | 44 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0029others(41): Show | 44 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.296-696_296-695dup others(2): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | |||||
| chr5:53044274
|
C | CAAA | 6 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0005g0291others(3): Show | 6 | HG01358.hp2 HG02071.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.296-697_296-695dup others(3): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | |||||
| chr5:53044274
|
C | CAAAAA | 5 | a0001c0001t0005g0017a0001c0001t0005g0288a0001c0001t0005g0316others(2): Show | 6 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.296-699_296-695dup others(5): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | |||||
| chr5:53044274
|
C | CAAAAAAA others(3): Show |
8 | a0002c0003t0007g0019a0002c0003t0007g0286a0002c0003t0007g0346others(5): Show | 9 | HG01070.hp1 HG01192.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.296-704_296-695dup others(10): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | |||||
| chr5:53044274
|
C | CAAAAAAA others(4): Show |
6 | a0001c0008t0021g0013a0002c0003t0007g0333a0002c0003t0007g0334others(3): Show | 7 | HG00323.hp2 HG01358.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.296-705_296-695dup others(11): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | |||||
| chr5:53044274
|
C | CAAAAAAA others(5): Show |
1 | a0001c0016t0005g0104 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.296-706_296-695dup others(12): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | |||||
| chr5:53044274
|
C | CAAAAAAA others(6): Show |
2 | a0002c0003t0007g0018a0002c0003t0007g0349 | 3 | HG01516.hp1 HG01517.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.296-707_296-695dup others(13): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | |||||
| chr5:53044274
|
C | CAAAAAAA others(7): Show |
1 | a0002c0003t0007g0343 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.296-708_296-695dup others(14): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | |||||
| chr5:53044274
|
C | CAAAAAAA others(8): Show |
4 | a0001c0008t0012g0163a0001c0008t0012g0164a0002c0003t0007g0079others(1): Show | 4 | HG00621.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-709_296-695dup others(15): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | |||||
| chr5:53044274
|
C | CAAAAAAA others(9): Show |
1 | a0001c0008t0012g0162 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.296-710_296-695dup others(16): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | |||||
| chr5:53044274
|
C | CAAAAAAA others(15): Show |
2 | a0002c0003t0007g0072a0002c0003t0007g0080 | 2 | HG02132.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.296-716_296-695dup others(22): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | |||||
| chr5:53044274
|
CAA | C | 11 | a0001c0002t0003g0108a0001c0002t0003g0188a0001c0002t0003g0189others(8): Show | 11 | HG00544.hp2 HG01978.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.296-696_296-695del others(2): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | |||||
| chr5:53044274
|
CAAA | C | 71 | a0001c0001t0001g0324a0001c0001t0002g0133a0001c0001t0002g0137others(68): Show | 75 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.296-697_296-695del others(3): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | |||||
| chr5:53044274
|
CAAAA | C | 97 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(94): Show | 102 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.296-698_296-695del others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | |||||
| chr5:53044274
|
CAAAAA | C | 6 | a0001c0001t0002g0117a0001c0001t0002g0138a0001c0001t0002g0154others(3): Show | 6 | HG00323.hp1 HG01168.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.296-699_296-695del others(5): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | |||||
| chr5:53044274
|
CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0025g0281a0001c0002t0004g0247a0001c0021t0050g0280 | 3 | HG02615.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.296-705_296-695del others(11): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | |||||
| chr5:53044274
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0002t0049g0338 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.296-707_296-695del others(13): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | |||||
| chr5:53044274
|
CAAAAAAA others(7): Show |
C | 22 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(19): Show | 25 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.296-708_296-695del others(14): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | |||||
| chr5:53044274
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0002t0006g0041 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.296-709_296-695del others(15): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | |||||
| chr5:53044274
|
CAAAAAAA others(12): Show |
C | 1 | a0002c0003t0026g0274 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.296-713_296-695del others(19): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr5 | 53044274 | |||||
| chr5:53044305
|
A | T | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.296-696A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044305 | ||||||
| chr5:53044311
|
G | C | 1 | a0001c0001t0001g0228 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.296-690G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044311 | ||||||
| chr5:53044443
|
T | A | 3 | a0001c0001t0001g0289a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | NA18963.hp1 NA19012.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.296-558T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044443 | ||||||
| chr5:53044470
|
T | C | 1 | a0002c0003t0007g0343 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.296-531T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044470 | ||||||
| chr5:53044481
|
C | T | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.296-520C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044481 | ||||||
| chr5:53044502
|
G | A | 28 | a0001c0001t0005g0004a0001c0001t0005g0017a0001c0001t0005g0217others(25): Show | 31 | HG00735.hp2 HG01069.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.296-499G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044502 | ||||||
| chr5:53044504
|
T | G | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.296-497T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044504 | ||||||
| chr5:53044536
|
G | A | 2 | a0001c0001t0025g0281a0001c0021t0050g0280 | 2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.296-465G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044536 | ||||||
| chr5:53044678
|
G | A | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.296-323G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044678 | ||||||
| chr5:53044704
|
G | A | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.296-297G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044704 | ||||||
| chr5:53044745
|
A | T | 1 | a0002c0003t0007g0359 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.296-256A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044745 | ||||||
| chr5:53044777
|
C | T | 1 | a0001c0001t0002g0107 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.296-224C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044777 | ||||||
| chr5:53044812
|
A | G | 1 | a0001c0011t0002g0114 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.296-189A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044812 | ||||||
| chr5:53044844
|
C | T | 25 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(22): Show | 28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.296-157C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 3/29 | chr5 | 53044844 | ||||||
| chr5:53045149
|
G | A | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.387+57G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045149 | ||||||
| chr5:53045234
|
A | G | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.387+142A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045234 | ||||||
| chr5:53045280
|
T | G | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.387+188T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045280 | ||||||
| chr5:53045391
|
A | G | 1 | a0001c0002t0004g0231 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.387+299A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045391 | ||||||
| chr5:53045529
|
C | T | 24 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(21): Show | 27 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.387+437C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045529 | ||||||
| chr5:53045564
|
T | A | 2 | a0008c0018t0037g0277a0009c0017t0052g0263 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.387+472T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045564 | ||||||
| chr5:53045572
|
C | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0047others(17): Show | 22 | HG00544.hp1 HG00609.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.387+480C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045572 | ||||||
| chr5:53045682
|
A | G | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.387+590A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045682 | ||||||
| chr5:53045762
|
G | C | 1 | a0001c0001t0005g0299 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.387+670G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045762 | ||||||
| chr5:53045903
|
TAGAG | T | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.387+814_387+817del others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr5 | 53045903 | |||||
| chr5:53045912
|
T | A | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.387+820T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045912 | ||||||
| chr5:53045913
|
G | T | 79 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(76): Show | 83 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.387+821G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045913 | ||||||
| chr5:53045916
|
C | T | 20 | a0001c0016t0005g0104a0002c0003t0007g0018a0002c0003t0007g0019others(17): Show | 22 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.387+824C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045916 | ||||||
| chr5:53045917
|
G | A | 51 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0117others(48): Show | 54 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.387+825G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045917 | ||||||
| chr5:53045926
|
C | T | 25 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(22): Show | 28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.387+834C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53045926 | ||||||
| chr5:53046006
|
C | A | 1 | a0001c0002t0006g0050 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.387+914C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046006 | ||||||
| chr5:53046020
|
A | G | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.387+928A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046020 | ||||||
| chr5:53046050
|
G | C | 25 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(22): Show | 28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.387+958G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046050 | ||||||
| chr5:53046136
|
A | G | 104 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(101): Show | 110 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.387+1044A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046136 | ||||||
| chr5:53046158
|
G | A | 25 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(22): Show | 28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.387+1066G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046158 | ||||||
| chr5:53046194
|
C | CA | 15 | a0001c0001t0001g0093a0001c0001t0001g0136a0001c0001t0001g0289others(12): Show | 17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.387+1123dupA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr5 | 53046194 | |||||
| chr5:53046194
|
CA | C | 15 | a0001c0001t0001g0082a0001c0001t0001g0320a0001c0001t0002g0125others(12): Show | 15 | HG01168.hp2 HG01243.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.387+1123delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr5 | 53046194 | |||||
| chr5:53046194
|
CAA | C | 201 | a0001c0001t0001g0066a0001c0001t0001g0322a0001c0001t0001g0323others(198): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.387+1122_387+1123d others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr5 | 53046194 | |||||
| chr5:53046194
|
CAAA | C | 25 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(22): Show | 28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.387+1121_387+1123d others(5): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr5 | 53046194 | |||||
| chr5:53046211
|
A | G | 104 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(101): Show | 110 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.387+1119A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046211 | ||||||
| chr5:53046250
|
AC | A | 25 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(22): Show | 28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.387+1159delC | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046250 | ||||||
| chr5:53046253
|
C | T | 132 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(129): Show | 141 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.387+1161C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046253 | ||||||
| chr5:53046278
|
G | A | 28 | a0001c0016t0005g0104a0002c0003t0007g0018a0002c0003t0007g0019others(25): Show | 30 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.387+1186G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046278 | ||||||
| chr5:53046282
|
T | C | 241 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(238): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.387+1190T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046282 | ||||||
| chr5:53046442
|
G | C | 2 | a0008c0018t0037g0277a0009c0017t0052g0263 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.387+1350G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046442 | ||||||
| chr5:53046489
|
C | G | 1 | a0001c0001t0025g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.387+1397C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046489 | ||||||
| chr5:53046496
|
G | A | 1 | a0002c0003t0007g0018 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.387+1404G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046496 | ||||||
| chr5:53046573
|
C | T | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.387+1481C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046573 | ||||||
| chr5:53046579
|
G | T | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.387+1487G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046579 | ||||||
| chr5:53046607
|
C | T | 2 | a0008c0018t0037g0277a0009c0017t0052g0263 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.387+1515C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046607 | ||||||
| chr5:53046668
|
A | G | 302 | a0001c0001t0001g0066a0001c0001t0001g0085a0001c0001t0001g0320others(299): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.387+1576A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046668 | ||||||
| chr5:53046700
|
G | A | 1 | a0002c0003t0007g0355 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.387+1608G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046700 | ||||||
| chr5:53046810
|
T | A | 1 | a0016c0029t0001g0304 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.388-1553T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046810 | ||||||
| chr5:53046930
|
A | T | 132 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(129): Show | 141 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.388-1433A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046930 | ||||||
| chr5:53046975
|
AG | A | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.388-1387delG | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53046975 | ||||||
| chr5:53047060
|
A | G | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.388-1303A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53047060 | ||||||
| chr5:53047250
|
A | G | 1 | a0001c0002t0049g0338 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.388-1113A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53047250 | ||||||
| chr5:53047349
|
A | G | 1 | a0001c0001t0002g0107 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.388-1014A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53047349 | ||||||
| chr5:53047358
|
T | G | 64 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(61): Show | 68 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.388-1005T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53047358 | ||||||
| chr5:53047359
|
G | A | 64 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(61): Show | 68 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.388-1004G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53047359 | ||||||
| chr5:53047526
|
C | G | 241 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(238): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.388-837C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53047526 | ||||||
| chr5:53047621
|
C | T | 25 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(22): Show | 28 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.388-742C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53047621 | ||||||
| chr5:53047731
|
A | G | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.388-632A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53047731 | ||||||
| chr5:53047798
|
A | G | 1 | a0001c0004t0008g0305 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.388-565A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53047798 | ||||||
| chr5:53047963
|
G | A | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.388-400G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53047963 | ||||||
| chr5:53047972
|
C | T | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.388-391C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53047972 | ||||||
| chr5:53048000
|
C | T | 1 | a0002c0003t0007g0079 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.388-363C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53048000 | ||||||
| chr5:53048071
|
C | T | 73 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(70): Show | 76 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.388-292C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53048071 | ||||||
| chr5:53048091
|
G | C | 1 | a0001c0004t0008g0365 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.388-272G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53048091 | ||||||
| chr5:53048120
|
A | G | 1 | a0001c0002t0003g0201 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.388-243A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53048120 | ||||||
| chr5:53048121
|
C | G | 1 | a0001c0001t0002g0153 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.388-242C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53048121 | ||||||
| chr5:53048150
|
C | A | 4 | a0002c0003t0026g0274a0002c0003t0026g0275a0008c0018t0037g0277others(1): Show | 4 | HG02451.hp2 HG02970.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-213C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53048150 | ||||||
| chr5:53048216
|
G | A | 107 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(104): Show | 113 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.388-147G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 4/29 | chr5 | 53048216 | ||||||
| chr5:53048626
|
C | T | 1 | a0001c0002t0003g0180 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.503-17C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 5/29 | chr5 | 53048626 | ||||||
| chr5:53048780
|
A | G | 270 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(267): Show | 285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.630+10A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53048780 | ||||||
| chr5:53048950
|
G | A | 31 | a0001c0002t0047g0061a0001c0016t0005g0104a0002c0003t0007g0018others(28): Show | 33 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.630+180G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53048950 | ||||||
| chr5:53048975
|
C | A | 1 | a0001c0004t0008g0362 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.630+205C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53048975 | ||||||
| chr5:53049005
|
G | A | 5 | a0001c0002t0003g0031a0001c0002t0003g0108a0001c0002t0003g0110others(2): Show | 5 | HG01081.hp1 NA18963.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.630+235G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049005 | ||||||
| chr5:53049007
|
C | T | 168 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(165): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.630+237C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049007 | ||||||
| chr5:53049012
|
C | CT | 8 | a0001c0001t0001g0098a0001c0001t0005g0219a0001c0002t0003g0171others(5): Show | 8 | HG02293.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.630+258dupT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr5 | 53049012 | |||||
| chr5:53049012
|
CT | C | 7 | a0001c0001t0001g0090a0001c0001t0002g0150a0001c0001t0002g0154others(4): Show | 7 | HG01081.hp2 HG02559.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.630+258delT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr5 | 53049012 | |||||
| chr5:53049012
|
CTT | C | 34 | a0001c0002t0047g0061a0001c0016t0005g0104a0002c0003t0007g0018others(31): Show | 36 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.630+257_630+258del others(2): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr5 | 53049012 | |||||
| chr5:53049115
|
G | T | 31 | a0001c0002t0047g0061a0001c0016t0005g0104a0002c0003t0007g0018others(28): Show | 33 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.630+345G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049115 | ||||||
| chr5:53049205
|
T | G | 70 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(67): Show | 73 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.630+435T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049205 | ||||||
| chr5:53049234
|
ACTC | A | 30 | a0001c0016t0005g0104a0002c0003t0007g0018a0002c0003t0007g0019others(27): Show | 32 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.630+467_630+469del others(3): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr5 | 53049234 | |||||
| chr5:53049243
|
C | T | 30 | a0001c0016t0005g0104a0002c0003t0007g0018a0002c0003t0007g0019others(27): Show | 32 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.630+473C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049243 | ||||||
| chr5:53049390
|
G | A | 135 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(132): Show | 144 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.630+620G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049390 | ||||||
| chr5:53049417
|
A | G | 31 | a0001c0016t0005g0104a0002c0003t0007g0018a0002c0003t0007g0019others(28): Show | 33 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.630+647A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049417 | ||||||
| chr5:53049434
|
A | T | 1 | a0001c0001t0005g0318 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.630+664A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049434 | ||||||
| chr5:53049500
|
C | T | 168 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(165): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.630+730C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049500 | ||||||
| chr5:53049502
|
G | C | 168 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(165): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.630+732G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049502 | ||||||
| chr5:53049503
|
C | A | 31 | a0001c0016t0005g0104a0002c0003t0007g0018a0002c0003t0007g0019others(28): Show | 33 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.630+733C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049503 | ||||||
| chr5:53049837
|
C | T | 9 | a0003c0005t0003g0015a0003c0005t0003g0176a0003c0005t0003g0177others(6): Show | 10 | HG02071.hp2 NA18964.hp1 NA18965.hp2 others(7): Show |
intron_variant | MODIFIER | c.630+1067C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049837 | ||||||
| chr5:53049852
|
G | GTTGACA | 31 | a0001c0016t0005g0104a0002c0003t0007g0018a0002c0003t0007g0019others(28): Show | 33 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.630+1084_630+1089d others(8): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr5 | 53049852 | |||||
| chr5:53049858
|
A | G | 2 | a0001c0002t0004g0116a0001c0011t0034g0084 | 2 | HG03688.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.630+1088A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049858 | ||||||
| chr5:53049947
|
T | C | 2 | a0008c0018t0037g0277a0009c0017t0052g0263 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.630+1177T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049947 | ||||||
| chr5:53049974
|
C | T | 2 | a0001c0002t0006g0112a0001c0002t0006g0367 | 2 | HG02717.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.630+1204C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53049974 | ||||||
| chr5:53050038
|
C | T | 30 | a0001c0016t0005g0104a0002c0003t0007g0018a0002c0003t0007g0019others(27): Show | 32 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.630+1268C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050038 | ||||||
| chr5:53050039
|
G | A | 1 | a0001c0002t0004g0282 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.630+1269G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050039 | ||||||
| chr5:53050112
|
T | C | 1 | a0001c0001t0023g0354 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.631-1299T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050112 | ||||||
| chr5:53050184
|
T | C | 31 | a0001c0016t0005g0104a0002c0003t0007g0018a0002c0003t0007g0019others(28): Show | 33 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.631-1227T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050184 | ||||||
| chr5:53050208
|
G | A | 1 | a0001c0001t0001g0323 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.631-1203G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050208 | ||||||
| chr5:53050219
|
C | T | 5 | a0001c0002t0018g0103a0001c0002t0018g0105a0001c0002t0018g0120others(2): Show | 5 | HG00642.hp1 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.631-1192C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050219 | ||||||
| chr5:53050273
|
C | T | 23 | a0001c0004t0002g0344a0001c0004t0008g0305a0001c0004t0008g0306others(20): Show | 23 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.631-1138C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050273 | ||||||
| chr5:53050283
|
T | C | 23 | a0001c0004t0002g0344a0001c0004t0008g0305a0001c0004t0008g0306others(20): Show | 23 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.631-1128T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050283 | ||||||
| chr5:53050347
|
G | C | 1 | a0001c0002t0043g0109 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.631-1064G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050347 | ||||||
| chr5:53050366
|
G | A | 168 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(165): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.631-1045G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050366 | ||||||
| chr5:53050562
|
C | T | 2 | a0008c0018t0037g0277a0009c0017t0052g0263 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.631-849C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050562 | ||||||
| chr5:53050697
|
G | A | 6 | a0001c0001t0002g0119a0001c0001t0002g0126a0001c0001t0002g0137others(3): Show | 6 | HG00741.hp1 HG01168.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.631-714G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050697 | ||||||
| chr5:53050724
|
T | C | 1 | a0001c0002t0003g0183 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.631-687T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050724 | ||||||
| chr5:53050773
|
T | C | 33 | a0001c0016t0005g0104a0002c0003t0007g0018a0002c0003t0007g0019others(30): Show | 35 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.631-638T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050773 | ||||||
| chr5:53050847
|
C | G | 23 | a0001c0016t0005g0104a0002c0003t0007g0018a0002c0003t0007g0019others(20): Show | 25 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.631-564C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050847 | ||||||
| chr5:53050929
|
C | T | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.631-482C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53050929 | ||||||
| chr5:53051029
|
C | T | 2 | a0008c0018t0037g0277a0009c0017t0052g0263 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.631-382C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53051029 | ||||||
| chr5:53051057
|
G | A | 2 | a0008c0018t0037g0277a0009c0017t0052g0263 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.631-354G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53051057 | ||||||
| chr5:53051206
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.631-205G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 6/29 | chr5 | 53051206 | ||||||
| chr5:53051684
|
AC | A | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.779+126delC | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53051684 | ||||||
| chr5:53051731
|
G | A | 135 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(132): Show | 144 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.779+172G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53051731 | ||||||
| chr5:53051784
|
C | T | 2 | a0008c0018t0037g0277a0009c0017t0052g0263 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.779+225C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53051784 | ||||||
| chr5:53051995
|
G | A | 1 | a0001c0001t0002g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.779+436G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53051995 | ||||||
| chr5:53052050
|
A | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.779+491A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052050 | ||||||
| chr5:53052068
|
AC | A | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.779+511delC | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr5 | 53052068 | |||||
| chr5:53052242
|
C | A | 1 | a0001c0002t0003g0110 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.779+683C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052242 | ||||||
| chr5:53052294
|
T | G | 135 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(132): Show | 144 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.779+735T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052294 | ||||||
| chr5:53052426
|
T | C | 135 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(132): Show | 144 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.779+867T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052426 | ||||||
| chr5:53052506
|
C | T | 1 | a0001c0002t0004g0258 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.779+947C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052506 | ||||||
| chr5:53052524
|
T | C | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.779+965T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052524 | ||||||
| chr5:53052537
|
C | G | 33 | a0001c0016t0005g0104a0002c0003t0007g0018a0002c0003t0007g0019others(30): Show | 35 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.779+978C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052537 | ||||||
| chr5:53052656
|
T | C | 168 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(165): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.779+1097T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052656 | ||||||
| chr5:53052801
|
T | A | 1 | a0002c0003t0007g0078 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.779+1242T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052801 | ||||||
| chr5:53052802
|
C | A | 1 | a0002c0003t0007g0078 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.779+1243C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052802 | ||||||
| chr5:53052821
|
C | T | 2 | a0008c0018t0037g0277a0009c0017t0052g0263 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.779+1262C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052821 | ||||||
| chr5:53052862
|
G | A | 1 | a0001c0002t0004g0266 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.779+1303G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052862 | ||||||
| chr5:53052868
|
G | C | 28 | a0001c0016t0005g0104a0002c0003t0007g0018a0002c0003t0007g0019others(25): Show | 30 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.779+1309G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052868 | ||||||
| chr5:53052918
|
A | G | 2 | a0002c0003t0007g0333a0002c0003t0007g0334 | 2 | HG00323.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.779+1359A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052918 | ||||||
| chr5:53052991
|
C | T | 28 | a0001c0001t0005g0004a0001c0001t0005g0017a0001c0001t0005g0217others(25): Show | 31 | HG00735.hp2 HG01069.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.779+1432C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53052991 | ||||||
| chr5:53053023
|
C | A | 1 | a0001c0001t0001g0075 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.779+1464C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53053023 | ||||||
| chr5:53053153
|
G | T | 23 | a0001c0004t0002g0344a0001c0004t0008g0305a0001c0004t0008g0306others(20): Show | 23 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.779+1594G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53053153 | ||||||
| chr5:53053235
|
G | A | 168 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(165): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.779+1676G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53053235 | ||||||
| chr5:53053242
|
G | A | 4 | a0001c0008t0012g0162a0001c0008t0012g0163a0001c0008t0012g0164others(1): Show | 5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.779+1683G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53053242 | ||||||
| chr5:53053258
|
G | C | 168 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(165): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.779+1699G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53053258 | ||||||
| chr5:53053559
|
T | G | 2 | a0001c0001t0002g0220a0001c0001t0002g0222 | 2 | HG02132.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.780-1979T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53053559 | ||||||
| chr5:53053575
|
T | C | 52 | a0001c0002t0003g0002a0001c0002t0003g0063a0001c0002t0003g0069others(49): Show | 55 | HG00280.hp2 HG00609.hp1 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.780-1963T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53053575 | ||||||
| chr5:53053831
|
T | A | 303 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(300): Show | 321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.780-1707T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53053831 | ||||||
| chr5:53053836
|
G | A | 2 | a0001c0004t0008g0306a0001c0004t0008g0312 | 2 | HG02615.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.780-1702G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53053836 | ||||||
| chr5:53053992
|
A | G | 6 | a0001c0001t0002g0156a0001c0001t0002g0220a0001c0001t0002g0221others(3): Show | 6 | HG02080.hp2 HG02129.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.780-1546A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53053992 | ||||||
| chr5:53054038
|
G | A | 168 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(165): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.780-1500G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054038 | ||||||
| chr5:53054163
|
G | A | 28 | a0001c0016t0005g0104a0002c0003t0007g0018a0002c0003t0007g0019others(25): Show | 30 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.780-1375G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054163 | ||||||
| chr5:53054186
|
T | G | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.780-1352T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054186 | ||||||
| chr5:53054254
|
C | T | 23 | a0001c0004t0002g0344a0001c0004t0008g0305a0001c0004t0008g0306others(20): Show | 23 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.780-1284C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054254 | ||||||
| chr5:53054266
|
T | A | 1 | a0001c0016t0005g0104 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.780-1272T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054266 | ||||||
| chr5:53054272
|
G | C | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.780-1266G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054272 | ||||||
| chr5:53054301
|
T | C | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.780-1237T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054301 | ||||||
| chr5:53054512
|
T | A | 1 | a0008c0018t0037g0277 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.780-1026T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054512 | ||||||
| chr5:53054557
|
T | G | 168 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(165): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.780-981T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054557 | ||||||
| chr5:53054583
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.780-955G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054583 | ||||||
| chr5:53054608
|
T | C | 28 | a0001c0016t0005g0104a0002c0003t0007g0018a0002c0003t0007g0019others(25): Show | 30 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.780-930T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054608 | ||||||
| chr5:53054691
|
G | A | 134 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(131): Show | 143 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.780-847G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054691 | ||||||
| chr5:53054781
|
G | A | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.780-757G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054781 | ||||||
| chr5:53054799
|
C | T | 1 | a0002c0003t0007g0359 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.780-739C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054799 | ||||||
| chr5:53054889
|
T | C | 4 | a0001c0002t0018g0103a0001c0002t0018g0105a0001c0002t0018g0120others(1): Show | 4 | HG00642.hp1 HG01175.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.780-649T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054889 | ||||||
| chr5:53054912
|
T | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0068 | 2 | NA18973.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.780-626T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054912 | ||||||
| chr5:53054985
|
G | A | 1 | a0016c0029t0001g0304 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.780-553G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53054985 | ||||||
| chr5:53055032
|
G | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0047 | 5 | HG02080.hp1 HG02523.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.780-506G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53055032 | ||||||
| chr5:53055313
|
G | A | 2 | a0001c0001t0002g0142a0001c0001t0002g0273 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.780-225G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53055313 | ||||||
| chr5:53055352
|
A | G | 5 | a0001c0002t0018g0103a0001c0002t0018g0105a0001c0002t0018g0120others(2): Show | 5 | HG00642.hp1 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.780-186A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53055352 | ||||||
| chr5:53055406
|
C | T | 4 | a0001c0002t0004g0265a0001c0002t0019g0230a0001c0002t0019g0237others(1): Show | 4 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.780-132C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53055406 | ||||||
| chr5:53055412
|
A | G | 168 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(165): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.780-126A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53055412 | ||||||
| chr5:53055527
|
A | T | 1 | a0001c0001t0005g0291 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.780-11A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 7/29 | chr5 | 53055527 | ||||||
| chr5:53055752
|
T | C | 1 | a0001c0002t0006g0053 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.930+64T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 8/29 | chr5 | 53055752 | ||||||
| chr5:53055916
|
G | A | 168 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(165): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.931-68G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 8/29 | chr5 | 53055916 | ||||||
| chr5:53056159
|
A | AT | 4 | a0001c0008t0012g0162a0001c0008t0012g0163a0001c0008t0012g0164others(1): Show | 5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1096+11dupT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr5 | 53056159 | |||||
| chr5:53056165
|
T | A | 11 | a0001c0001t0002g0012a0001c0001t0002g0146a0001c0001t0002g0147others(8): Show | 12 | HG00558.hp2 NA18957.hp1 NA18970.hp1 others(9): Show |
intron_variant | MODIFIER | c.1096+16T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53056165 | ||||||
| chr5:53056497
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1096+348C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53056497 | ||||||
| chr5:53056532
|
G | A | 1 | a0001c0001t0001g0320 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1096+383G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53056532 | ||||||
| chr5:53056546
|
G | T | 168 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(165): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.1096+397G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53056546 | ||||||
| chr5:53056548
|
A | T | 137 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(134): Show | 146 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.1096+399A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53056548 | ||||||
| chr5:53056740
|
T | C | 1 | a0004c0006t0003g0174 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1096+591T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53056740 | ||||||
| chr5:53056857
|
G | C | 28 | a0001c0016t0005g0104a0002c0003t0007g0018a0002c0003t0007g0019others(25): Show | 30 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1096+708G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53056857 | ||||||
| chr5:53056858
|
T | C | 28 | a0001c0016t0005g0104a0002c0003t0007g0018a0002c0003t0007g0019others(25): Show | 30 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1096+709T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53056858 | ||||||
| chr5:53057003
|
A | G | 167 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(164): Show | 178 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.1096+854A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53057003 | ||||||
| chr5:53057169
|
A | G | 1 | a0002c0003t0007g0286 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1097-856A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53057169 | ||||||
| chr5:53057195
|
T | C | 1 | a0001c0001t0001g0323 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1097-830T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53057195 | ||||||
| chr5:53057384
|
G | A | 28 | a0001c0016t0005g0104a0002c0003t0007g0018a0002c0003t0007g0019others(25): Show | 30 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1097-641G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53057384 | ||||||
| chr5:53057449
|
A | G | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1097-576A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53057449 | ||||||
| chr5:53057668
|
A | C | 1 | a0013c0019t0030g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1097-357A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53057668 | ||||||
| chr5:53057783
|
A | G | 168 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(165): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.1097-242A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53057783 | ||||||
| chr5:53058000
|
C | T | 1 | a0001c0002t0004g0115 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1097-25C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 9/29 | chr5 | 53058000 | ||||||
| chr5:53058129
|
T | C | 28 | a0001c0016t0005g0104a0002c0003t0007g0018a0002c0003t0007g0019others(25): Show | 30 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1173+28T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058129 | ||||||
| chr5:53058196
|
A | G | 1 | a0001c0001t0002g0107 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1173+95A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058196 | ||||||
| chr5:53058199
|
G | T | 1 | a0001c0002t0003g0184 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1173+98G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058199 | ||||||
| chr5:53058225
|
G | A | 1 | a0001c0001t0001g0320 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1173+124G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058225 | ||||||
| chr5:53058226
|
G | T | 1 | a0001c0002t0003g0194 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1173+125G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058226 | ||||||
| chr5:53058255
|
A | T | 3 | a0001c0008t0012g0162a0001c0008t0012g0163a0001c0008t0012g0164 | 3 | HG02965.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1173+154A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058255 | ||||||
| chr5:53058273
|
A | T | 301 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(298): Show | 319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.1173+172A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058273 | ||||||
| chr5:53058354
|
C | T | 1 | a0001c0001t0025g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1173+253C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058354 | ||||||
| chr5:53058473
|
G | A | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1173+372G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058473 | ||||||
| chr5:53058484
|
G | T | 270 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(267): Show | 285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.1173+383G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058484 | ||||||
| chr5:53058594
|
G | C | 64 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(61): Show | 68 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.1173+493G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058594 | ||||||
| chr5:53058638
|
T | C | 1 | a0002c0003t0007g0284 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1173+537T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058638 | ||||||
| chr5:53058644
|
T | G | 2 | a0008c0018t0037g0277a0009c0017t0052g0263 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1173+543T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058644 | ||||||
| chr5:53058693
|
A | G | 1 | a0013c0019t0030g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1173+592A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058693 | ||||||
| chr5:53058780
|
A | G | 168 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(165): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.1173+679A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058780 | ||||||
| chr5:53058782
|
C | T | 1 | a0001c0001t0002g0107 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1173+681C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058782 | ||||||
| chr5:53058982
|
C | G | 1 | a0001c0001t0002g0107 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1173+881C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53058982 | ||||||
| chr5:53059098
|
A | G | 24 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(21): Show | 27 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1174-776A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53059098 | ||||||
| chr5:53059103
|
C | T | 1 | a0001c0001t0036g0296 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1174-771C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53059103 | ||||||
| chr5:53059258
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1174-616T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53059258 | ||||||
| chr5:53059272
|
C | T | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1174-602C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53059272 | ||||||
| chr5:53059362
|
G | C | 2 | a0008c0018t0037g0277a0009c0017t0052g0263 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1174-512G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53059362 | ||||||
| chr5:53059395
|
G | T | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1174-479G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53059395 | ||||||
| chr5:53059405
|
C | T | 1 | a0001c0001t0002g0123 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1174-469C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53059405 | ||||||
| chr5:53059419
|
G | A | 1 | a0001c0001t0013g0141 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1174-455G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53059419 | ||||||
| chr5:53059627
|
G | A | 2 | a0001c0002t0003g0063a0001c0002t0003g0069 | 2 | NA18948.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1174-247G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53059627 | ||||||
| chr5:53059686
|
G | A | 8 | a0001c0001t0005g0017a0001c0001t0005g0288a0001c0001t0005g0315others(5): Show | 9 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1174-188G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53059686 | ||||||
| chr5:53059736
|
A | G | 37 | a0001c0016t0005g0104a0002c0003t0007g0018a0002c0003t0007g0019others(34): Show | 39 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1174-138A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 10/29 | chr5 | 53059736 | ||||||
| chr5:53060020
|
A | G | 1 | a0001c0001t0002g0107 | 1 | HG01433.hp1 | splice_region_variant&intron_variant | LOW | c.1312+8A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 11/29 | chr5 | 53060020 | ||||||
| chr5:53060024
|
T | C | 134 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(131): Show | 143 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.1312+12T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 11/29 | chr5 | 53060024 | ||||||
| chr5:53060176
|
C | T | 68 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(65): Show | 71 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.1312+164C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 11/29 | chr5 | 53060176 | ||||||
| chr5:53060184
|
C | T | 6 | a0002c0007t0010g0165a0002c0007t0010g0166a0002c0007t0010g0167others(3): Show | 6 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1312+172C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 11/29 | chr5 | 53060184 | ||||||
| chr5:53060376
|
T | C | 1 | a0001c0001t0002g0137 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1312+364T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 11/29 | chr5 | 53060376 | ||||||
| chr5:53060432
|
C | G | 1 | a0001c0002t0003g0195 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1312+420C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 11/29 | chr5 | 53060432 | ||||||
| chr5:53060440
|
T | C | 3 | a0002c0003t0007g0078a0002c0003t0007g0079a0002c0003t0007g0080 | 3 | HG00544.hp2 HG00621.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.1312+428T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 11/29 | chr5 | 53060440 | ||||||
| chr5:53060494
|
G | A | 4 | a0001c0008t0012g0162a0001c0008t0012g0163a0001c0008t0012g0164others(1): Show | 5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1313-407G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 11/29 | chr5 | 53060494 | ||||||
| chr5:53060602
|
C | T | 1 | a0013c0019t0030g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1313-299C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 11/29 | chr5 | 53060602 | ||||||
| chr5:53060694
|
C | T | 1 | a0002c0003t0007g0349 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1313-207C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 11/29 | chr5 | 53060694 | ||||||
| chr5:53060862
|
T | C | 24 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(21): Show | 27 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1313-39T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 11/29 | chr5 | 53060862 | ||||||
| chr5:53060871
|
T | G | 37 | a0001c0016t0005g0104a0002c0003t0007g0018a0002c0003t0007g0019others(34): Show | 39 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1313-30T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 11/29 | chr5 | 53060871 | ||||||
| chr5:53061135
|
G | A | 1 | a0005c0010t0002g0143 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1458+89G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53061135 | ||||||
| chr5:53061223
|
C | T | 1 | a0001c0001t0005g0299 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1458+177C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53061223 | ||||||
| chr5:53061336
|
A | G | 1 | a0001c0008t0021g0013 | 2 | HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1458+290A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53061336 | ||||||
| chr5:53061502
|
G | A | 2 | a0001c0001t0005g0302a0001c0001t0005g0303 | 2 | NA18946.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1458+456G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53061502 | ||||||
| chr5:53061645
|
C | T | 24 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(21): Show | 27 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1458+599C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53061645 | ||||||
| chr5:53061812
|
G | T | 1 | a0001c0008t0021g0013 | 2 | HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1458+766G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53061812 | ||||||
| chr5:53061879
|
C | T | 1 | a0001c0001t0001g0335 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1458+833C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53061879 | ||||||
| chr5:53062010
|
G | C | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1459-776G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53062010 | ||||||
| chr5:53062056
|
C | T | 1 | a0009c0017t0052g0263 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1459-730C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53062056 | ||||||
| chr5:53062084
|
T | C | 2 | a0001c0001t0001g0089a0001c0001t0001g0091 | 2 | HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1459-702T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53062084 | ||||||
| chr5:53062432
|
A | G | 31 | a0001c0016t0005g0104a0002c0003t0007g0018a0002c0003t0007g0019others(28): Show | 33 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1459-354A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53062432 | ||||||
| chr5:53062556
|
C | G | 1 | a0001c0001t0001g0098 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1459-230C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53062556 | ||||||
| chr5:53062650
|
G | A | 1 | a0001c0002t0004g0115 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1459-136G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53062650 | ||||||
| chr5:53062652
|
C | G | 1 | a0001c0002t0011g0202 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1459-134C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53062652 | ||||||
| chr5:53062747
|
T | A | 1 | a0001c0001t0002g0149 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1459-39T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 12/29 | chr5 | 53062747 | ||||||
| chr5:53062931
|
TA | T | 6 | a0001c0002t0003g0192a0002c0003t0017g0021a0002c0003t0017g0022others(3): Show | 6 | HG01243.hp2 HG01261.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.1602+15delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr5 | 53062931 | |||||
| chr5:53063049
|
A | G | 1 | a0001c0001t0005g0262 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1602+120A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53063049 | ||||||
| chr5:53063057
|
A | T | 19 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(16): Show | 21 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.1602+128A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53063057 | ||||||
| chr5:53063205
|
T | C | 6 | a0002c0007t0010g0165a0002c0007t0010g0166a0002c0007t0010g0167others(3): Show | 6 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1602+276T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53063205 | ||||||
| chr5:53063207
|
G | A | 27 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(24): Show | 29 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1602+278G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53063207 | ||||||
| chr5:53063273
|
G | T | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1602+344G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53063273 | ||||||
| chr5:53063304
|
C | G | 1 | a0001c0002t0009g0212 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1602+375C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53063304 | ||||||
| chr5:53063477
|
A | G | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1602+548A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53063477 | ||||||
| chr5:53063531
|
AT | A | 22 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(19): Show | 24 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1602+603delT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53063531 | ||||||
| chr5:53063687
|
A | G | 2 | a0008c0018t0037g0277a0009c0017t0052g0263 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1602+758A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53063687 | ||||||
| chr5:53063859
|
T | A | 7 | a0001c0002t0004g0003a0001c0002t0004g0251a0001c0002t0004g0252others(4): Show | 9 | NA18942.hp2 NA18956.hp2 NA18980.hp2 others(6): Show |
intron_variant | MODIFIER | c.1602+930T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53063859 | ||||||
| chr5:53063984
|
A | G | 23 | a0001c0004t0002g0344a0001c0004t0008g0305a0001c0004t0008g0306others(20): Show | 23 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1603-928A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53063984 | ||||||
| chr5:53064046
|
T | C | 6 | a0002c0007t0010g0165a0002c0007t0010g0166a0002c0007t0010g0167others(3): Show | 6 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1603-866T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53064046 | ||||||
| chr5:53064047
|
G | C | 1 | a0002c0003t0007g0286 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1603-865G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53064047 | ||||||
| chr5:53064104
|
A | G | 173 | a0001c0001t0001g0289a0001c0002t0003g0002a0001c0002t0003g0031others(170): Show | 184 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1603-808A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53064104 | ||||||
| chr5:53064261
|
T | A | 1 | a0012c0026t0003g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1603-651T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53064261 | ||||||
| chr5:53064269
|
A | G | 1 | a0001c0001t0001g0057 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1603-643A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53064269 | ||||||
| chr5:53064329
|
G | T | 1 | a0001c0001t0002g0264 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1603-583G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53064329 | ||||||
| chr5:53064349
|
G | C | 1 | a0001c0001t0014g0279 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1603-563G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53064349 | ||||||
| chr5:53064528
|
T | C | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1603-384T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53064528 | ||||||
| chr5:53064828
|
A | T | 5 | a0001c0001t0001g0062a0001c0001t0001g0068a0001c0001t0001g0075others(2): Show | 5 | HG03704.hp1 NA18973.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.1603-84A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53064828 | ||||||
| chr5:53064830
|
C | T | 1 | a0001c0002t0004g0087 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1603-82C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53064830 | ||||||
| chr5:53064876
|
T | C | 1 | a0001c0001t0005g0291 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1603-36T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 13/29 | chr5 | 53064876 | ||||||
| chr5:53065185
|
T | G | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1806+70T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 14/29 | chr5 | 53065185 | ||||||
| chr5:53065233
|
C | T | 2 | a0008c0018t0037g0277a0009c0017t0052g0263 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1806+118C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 14/29 | chr5 | 53065233 | ||||||
| chr5:53065250
|
G | T | 5 | a0001c0002t0003g0180a0001c0002t0003g0199a0001c0002t0003g0200others(2): Show | 6 | HG00140.hp1 HG01123.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.1806+135G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 14/29 | chr5 | 53065250 | ||||||
| chr5:53065346
|
T | C | 1 | a0001c0001t0025g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1806+231T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 14/29 | chr5 | 53065346 | ||||||
| chr5:53065389
|
A | G | 303 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(300): Show | 321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.1806+274A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 14/29 | chr5 | 53065389 | ||||||
| chr5:53065470
|
G | A | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1806+355G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 14/29 | chr5 | 53065470 | ||||||
| chr5:53065488
|
T | G | 1 | a0001c0001t0001g0085 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1807-353T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 14/29 | chr5 | 53065488 | ||||||
| chr5:53065573
|
C | A | 1 | a0001c0001t0005g0287 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1807-268C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 14/29 | chr5 | 53065573 | ||||||
| chr5:53065708
|
C | A | 1 | a0001c0004t0008g0362 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1807-133C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 14/29 | chr5 | 53065708 | ||||||
| chr5:53066521
|
C | T | 1 | a0015c0015t0002g0278 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1943+544C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 15/29 | chr5 | 53066521 | ||||||
| chr5:53066572
|
A | C | 1 | a0001c0002t0004g0116 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1944-546A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 15/29 | chr5 | 53066572 | ||||||
| chr5:53066575
|
CATTT | C | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1944-542_1944-539d others(6): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 15/29 | chr5 | 53066575 | ||||||
| chr5:53066859
|
C | T | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1944-259C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 15/29 | chr5 | 53066859 | ||||||
| chr5:53066935
|
A | T | 66 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(63): Show | 69 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.1944-183A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 15/29 | chr5 | 53066935 | ||||||
| chr5:53066936
|
A | T | 1 | a0001c0001t0002g0149 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1944-182A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 15/29 | chr5 | 53066936 | ||||||
| chr5:53067077
|
G | A | 1 | a0001c0002t0044g0223 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1944-41G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 15/29 | chr5 | 53067077 | ||||||
| chr5:53067352
|
T | C | 4 | a0001c0008t0012g0162a0001c0008t0012g0163a0001c0008t0012g0164others(1): Show | 5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2083+95T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53067352 | ||||||
| chr5:53067449
|
A | G | 3 | a0001c0001t0001g0341a0001c0001t0001g0350a0001c0001t0013g0340 | 3 | HG00408.hp2 NA18962.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2083+192A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53067449 | ||||||
| chr5:53067614
|
T | A | 1 | a0001c0002t0003g0069 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2083+357T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53067614 | ||||||
| chr5:53067627
|
A | G | 1 | a0001c0001t0001g0339 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2083+370A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53067627 | ||||||
| chr5:53067647
|
A | G | 33 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(30): Show | 35 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.2083+390A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53067647 | ||||||
| chr5:53067669
|
C | T | 269 | a0001c0001t0001g0066a0001c0001t0001g0320a0001c0001t0001g0322others(266): Show | 284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.2083+412C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53067669 | ||||||
| chr5:53067670
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0181 | 2 | HG01106.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.2083+413G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53067670 | ||||||
| chr5:53067742
|
T | C | 1 | a0001c0002t0004g0234 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2083+485T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53067742 | ||||||
| chr5:53067796
|
A | T | 60 | a0001c0002t0003g0002a0001c0002t0003g0063a0001c0002t0003g0069others(57): Show | 64 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.2083+539A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53067796 | ||||||
| chr5:53067929
|
A | G | 65 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(62): Show | 69 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.2083+672A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53067929 | ||||||
| chr5:53068256
|
T | G | 1 | a0001c0001t0001g0075 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2083+999T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53068256 | ||||||
| chr5:53068473
|
G | A | 23 | a0001c0004t0002g0344a0001c0004t0008g0305a0001c0004t0008g0306others(20): Show | 23 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.2083+1216G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53068473 | ||||||
| chr5:53068624
|
C | T | 1 | a0001c0001t0002g0024 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2083+1367C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53068624 | ||||||
| chr5:53068845
|
G | A | 1 | a0001c0004t0008g0372 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2084-1264G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53068845 | ||||||
| chr5:53068925
|
A | T | 2 | a0003c0005t0003g0015a0003c0005t0003g0270 | 3 | NA18964.hp1 NA18999.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2084-1184A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53068925 | ||||||
| chr5:53069270
|
G | A | 1 | a0001c0002t0003g0194 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2084-839G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53069270 | ||||||
| chr5:53069364
|
A | T | 3 | a0001c0002t0006g0040a0001c0002t0006g0041a0001c0002t0006g0045 | 3 | NA18959.hp2 NA18964.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.2084-745A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53069364 | ||||||
| chr5:53069541
|
A | G | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2084-568A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53069541 | ||||||
| chr5:53069555
|
A | C | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2084-554A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53069555 | ||||||
| chr5:53069663
|
G | T | 2 | a0001c0002t0004g0229a0001c0002t0004g0257 | 2 | HG02602.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2084-446G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53069663 | ||||||
| chr5:53069736
|
G | A | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2084-373G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53069736 | ||||||
| chr5:53069775
|
A | T | 1 | a0001c0001t0002g0273 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2084-334A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53069775 | ||||||
| chr5:53069810
|
AT | A | 23 | a0001c0004t0002g0344a0001c0004t0008g0305a0001c0004t0008g0306others(20): Show | 23 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.2084-296delT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr5 | 53069810 | |||||
| chr5:53069843
|
C | T | 1 | a0001c0002t0009g0208 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2084-266C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53069843 | ||||||
| chr5:53069974
|
A | G | 1 | a0001c0001t0005g0299 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2084-135A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53069974 | ||||||
| chr5:53070093
|
A | ATT | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
splice_region_variant&intron_variant | LOW | c.2084-9_2084-8dupTT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr5 | 53070093 | |||||
| chr5:53070102
|
A | G | 1 | a0001c0002t0018g0105 | 1 | HG03710.hp1 | splice_region_variant&intron_variant | LOW | c.2084-7A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 16/29 | chr5 | 53070102 | ||||||
| chr5:53070308
|
G | A | 261 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0024others(258): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.2235+48G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53070308 | ||||||
| chr5:53070332
|
G | A | 65 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(62): Show | 69 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.2235+72G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53070332 | ||||||
| chr5:53070343
|
A | C | 4 | a0001c0008t0012g0162a0001c0008t0012g0163a0001c0008t0012g0164others(1): Show | 5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2235+83A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53070343 | ||||||
| chr5:53070454
|
G | A | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2235+194G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53070454 | ||||||
| chr5:53070506
|
T | C | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2235+246T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53070506 | ||||||
| chr5:53070551
|
A | G | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2235+291A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53070551 | ||||||
| chr5:53070565
|
G | C | 19 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(16): Show | 21 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.2235+305G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53070565 | ||||||
| chr5:53070674
|
T | C | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2235+414T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53070674 | ||||||
| chr5:53070804
|
G | A | 23 | a0001c0004t0002g0344a0001c0004t0008g0305a0001c0004t0008g0306others(20): Show | 23 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.2235+544G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53070804 | ||||||
| chr5:53070887
|
T | A | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2235+627T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53070887 | ||||||
| chr5:53070890
|
C | CT | 22 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(19): Show | 24 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.2235+636dupT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr5 | 53070890 | |||||
| chr5:53070928
|
A | G | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2235+668A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53070928 | ||||||
| chr5:53070948
|
C | T | 1 | a0013c0019t0030g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2235+688C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53070948 | ||||||
| chr5:53070949
|
G | A | 40 | a0001c0002t0004g0003a0001c0002t0004g0087a0001c0002t0004g0099others(37): Show | 42 | HG00733.hp2 HG00735.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.2235+689G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53070949 | ||||||
| chr5:53071050
|
A | C | 173 | a0001c0001t0024g0214a0001c0002t0003g0002a0001c0002t0003g0031others(170): Show | 184 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.2235+790A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53071050 | ||||||
| chr5:53071066
|
T | C | 23 | a0001c0004t0002g0344a0001c0004t0008g0305a0001c0004t0008g0306others(20): Show | 23 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.2235+806T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53071066 | ||||||
| chr5:53071075
|
A | G | 31 | a0001c0001t0005g0004a0001c0001t0005g0017a0001c0001t0005g0217others(28): Show | 34 | HG00735.hp2 HG01069.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.2235+815A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53071075 | ||||||
| chr5:53071139
|
C | T | 3 | a0001c0001t0002g0159a0001c0001t0002g0267a0001c0002t0003g0031 | 3 | HG01081.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2236-799C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53071139 | ||||||
| chr5:53071259
|
G | GA | 4 | a0001c0008t0012g0162a0001c0008t0012g0163a0001c0008t0012g0164others(1): Show | 5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2236-673dupA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr5 | 53071259 | |||||
| chr5:53071316
|
C | T | 5 | a0001c0002t0018g0103a0001c0002t0018g0105a0001c0002t0018g0120others(2): Show | 5 | HG00642.hp1 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.2236-622C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53071316 | ||||||
| chr5:53071348
|
C | T | 27 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(24): Show | 29 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.2236-590C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53071348 | ||||||
| chr5:53071495
|
C | A | 1 | a0001c0002t0003g0203 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2236-443C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53071495 | ||||||
| chr5:53071719
|
T | C | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2236-219T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53071719 | ||||||
| chr5:53071836
|
A | T | 294 | a0001c0001t0001g0085a0001c0001t0002g0010a0001c0001t0002g0012others(291): Show | 312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.2236-102A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53071836 | ||||||
| chr5:53071876
|
T | C | 172 | a0001c0001t0024g0214a0001c0002t0003g0002a0001c0002t0003g0031others(169): Show | 183 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.2236-62T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53071876 | ||||||
| chr5:53071885
|
T | C | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2236-53T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 17/29 | chr5 | 53071885 | ||||||
| chr5:53072126
|
G | T | 14 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(11): Show | 14 | HG01346.hp1 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.2346+78G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 18/29 | chr5 | 53072126 | ||||||
| chr5:53072138
|
C | T | 1 | a0001c0001t0005g0217 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2346+90C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 18/29 | chr5 | 53072138 | ||||||
| chr5:53072394
|
G | A | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2347-219G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 18/29 | chr5 | 53072394 | ||||||
| chr5:53072416
|
TC | T | 40 | a0001c0002t0004g0003a0001c0002t0004g0087a0001c0002t0004g0099others(37): Show | 42 | HG00733.hp2 HG00735.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.2347-192delC | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr5 | 53072416 | |||||
| chr5:53072536
|
A | C | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2347-77A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 18/29 | chr5 | 53072536 | ||||||
| chr5:53072544
|
A | G | 2 | a0002c0009t0016g0271a0002c0009t0016g0272 | 2 | NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2347-69A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 18/29 | chr5 | 53072544 | ||||||
| chr5:53072562
|
T | C | 1 | a0002c0003t0017g0021 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2347-51T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 18/29 | chr5 | 53072562 | ||||||
| chr5:53072716
|
T | C | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2429+21T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 19/29 | chr5 | 53072716 | ||||||
| chr5:53072735
|
A | T | 19 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(16): Show | 21 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.2429+40A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 19/29 | chr5 | 53072735 | ||||||
| chr5:53072764
|
C | T | 35 | a0001c0001t0001g0065a0001c0001t0001g0269a0002c0003t0007g0018others(32): Show | 37 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.2429+69C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 19/29 | chr5 | 53072764 | ||||||
| chr5:53072765
|
G | C | 1 | a0001c0021t0050g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2429+70G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 19/29 | chr5 | 53072765 | ||||||
| chr5:53072896
|
G | C | 1 | a0001c0004t0008g0308 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2429+201G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 19/29 | chr5 | 53072896 | ||||||
| chr5:53073025
|
A | C | 1 | a0001c0002t0004g0236 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2430-93A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 19/29 | chr5 | 53073025 | ||||||
| chr5:53073087
|
G | A | 1 | a0001c0008t0021g0013 | 2 | HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2430-31G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 19/29 | chr5 | 53073087 | ||||||
| chr5:53073092
|
T | A | 135 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(132): Show | 144 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.2430-26T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 19/29 | chr5 | 53073092 | ||||||
| chr5:53073111
|
T | C | 1 | a0002c0003t0007g0348 | 1 | NA19082.hp2 | splice_region_variant&intron_variant | LOW | c.2430-7T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 19/29 | chr5 | 53073111 | ||||||
| chr5:53073363
|
A | G | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2571+104A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53073363 | ||||||
| chr5:53073505
|
A | G | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2571+246A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53073505 | ||||||
| chr5:53073547
|
C | G | 2 | a0001c0001t0005g0301a0001c0001t0005g0330 | 2 | HG02040.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.2571+288C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53073547 | ||||||
| chr5:53073665
|
C | T | 22 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(19): Show | 24 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.2571+406C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53073665 | ||||||
| chr5:53073790
|
T | C | 3 | a0002c0003t0017g0021a0002c0003t0017g0022a0002c0003t0017g0023 | 3 | HG01243.hp2 HG01261.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.2571+531T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53073790 | ||||||
| chr5:53073830
|
T | G | 1 | a0001c0001t0005g0299 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2572-555T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53073830 | ||||||
| chr5:53073834
|
G | A | 60 | a0001c0002t0003g0002a0001c0002t0003g0063a0001c0002t0003g0069others(57): Show | 64 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.2572-551G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53073834 | ||||||
| chr5:53073913
|
C | T | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2572-472C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53073913 | ||||||
| chr5:53073944
|
T | TA | 19 | a0001c0001t0001g0088a0001c0001t0001g0100a0001c0001t0001g0136others(16): Show | 19 | HG01106.hp1 HG01106.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.2572-419dupA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr5 | 53073944 | |||||
| chr5:53073944
|
TA | T | 6 | a0001c0001t0001g0060a0001c0001t0015g0160a0001c0002t0003g0063others(3): Show | 6 | HG00280.hp2 HG01257.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.2572-419delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr5 | 53073944 | |||||
| chr5:53073944
|
TAAAA | T | 27 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(24): Show | 29 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.2572-422_2572-419d others(6): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr5 | 53073944 | |||||
| chr5:53073944
|
TAAAAA | T | 6 | a0002c0007t0010g0165a0002c0007t0010g0166a0002c0007t0010g0167others(3): Show | 6 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2572-423_2572-419d others(7): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr5 | 53073944 | |||||
| chr5:53073960
|
A | C | 23 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(20): Show | 26 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.2572-425A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53073960 | ||||||
| chr5:53074005
|
T | C | 2 | a0001c0001t0005g0301a0001c0001t0005g0330 | 2 | HG02040.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.2572-380T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53074005 | ||||||
| chr5:53074037
|
A | G | 1 | a0001c0001t0002g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2572-348A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53074037 | ||||||
| chr5:53074098
|
C | T | 3 | a0001c0001t0002g0148a0001c0001t0002g0149a0001c0001t0002g0151 | 3 | NA18970.hp1 NA18985.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.2572-287C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53074098 | ||||||
| chr5:53074158
|
T | C | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2572-227T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53074158 | ||||||
| chr5:53074188
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2572-197C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53074188 | ||||||
| chr5:53074252
|
G | A | 4 | a0002c0003t0007g0337a0002c0003t0007g0348a0002c0003t0007g0355others(1): Show | 4 | NA18989.hp2 NA19056.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.2572-133G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53074252 | ||||||
| chr5:53074331
|
A | T | 1 | a0001c0001t0001g0341 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2572-54A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53074331 | ||||||
| chr5:53074344
|
G | A | 173 | a0001c0001t0025g0276a0001c0002t0003g0002a0001c0002t0003g0031others(170): Show | 184 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.2572-41G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 20/29 | chr5 | 53074344 | ||||||
| chr5:53074557
|
A | G | 3 | a0002c0003t0007g0283a0002c0003t0007g0284a0002c0003t0007g0285 | 3 | HG02055.hp2 HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2664+80A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 21/29 | chr5 | 53074557 | ||||||
| chr5:53074602
|
G | C | 33 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(30): Show | 35 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.2664+125G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 21/29 | chr5 | 53074602 | ||||||
| chr5:53074663
|
T | C | 1 | a0013c0019t0030g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2664+186T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 21/29 | chr5 | 53074663 | ||||||
| chr5:53074844
|
C | T | 1 | a0013c0019t0030g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2665-217C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 21/29 | chr5 | 53074844 | ||||||
| chr5:53074886
|
G | A | 1 | a0001c0002t0006g0052 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2665-175G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 21/29 | chr5 | 53074886 | ||||||
| chr5:53074902
|
G | T | 33 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(30): Show | 35 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.2665-159G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 21/29 | chr5 | 53074902 | ||||||
| chr5:53074909
|
A | G | 1 | a0003c0005t0003g0177 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2665-152A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 21/29 | chr5 | 53074909 | ||||||
| chr5:53074941
|
G | C | 14 | a0001c0002t0003g0002a0001c0002t0003g0170a0001c0002t0003g0182others(11): Show | 15 | HG00741.hp2 HG01433.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.2665-120G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 21/29 | chr5 | 53074941 | ||||||
| chr5:53075005
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2665-56C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 21/29 | chr5 | 53075005 | ||||||
| chr5:53075540
|
C | T | 172 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(169): Show | 183 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.2825+236C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53075540 | ||||||
| chr5:53075770
|
A | G | 1 | a0001c0001t0005g0262 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2825+466A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53075770 | ||||||
| chr5:53075837
|
C | T | 1 | a0001c0001t0002g0220 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2825+533C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53075837 | ||||||
| chr5:53075878
|
G | GT | 27 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(24): Show | 29 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.2825+580dupT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr5 | 53075878 | |||||
| chr5:53075978
|
T | C | 23 | a0001c0004t0002g0344a0001c0004t0008g0305a0001c0004t0008g0306others(20): Show | 23 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.2825+674T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53075978 | ||||||
| chr5:53076044
|
C | T | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2825+740C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53076044 | ||||||
| chr5:53076189
|
C | A | 1 | a0001c0001t0001g0225 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2825+885C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53076189 | ||||||
| chr5:53076217
|
G | A | 2 | a0001c0002t0006g0005a0001c0002t0006g0038 | 3 | HG01257.hp2 HG01496.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2825+913G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53076217 | ||||||
| chr5:53076232
|
C | T | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2825+928C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53076232 | ||||||
| chr5:53076321
|
C | G | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2825+1017C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53076321 | ||||||
| chr5:53076358
|
A | G | 1 | a0001c0001t0002g0264 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2825+1054A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53076358 | ||||||
| chr5:53076586
|
C | T | 2 | a0001c0001t0014g0294a0001c0001t0014g0295 | 2 | NA18939.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.2825+1282C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53076586 | ||||||
| chr5:53076620
|
C | T | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2825+1316C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53076620 | ||||||
| chr5:53076920
|
T | A | 1 | a0001c0002t0003g0063 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2825+1616T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53076920 | ||||||
| chr5:53077057
|
CAT | C | 33 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(30): Show | 35 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.2826-1714_2826-171 others(6): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53077057 | ||||||
| chr5:53077296
|
G | A | 14 | a0001c0002t0003g0002a0001c0002t0003g0170a0001c0002t0003g0182others(11): Show | 15 | HG00741.hp2 HG01433.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.2826-1476G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53077296 | ||||||
| chr5:53077382
|
T | TA | 5 | a0001c0002t0018g0103a0001c0002t0018g0105a0001c0002t0018g0120others(2): Show | 5 | HG00642.hp1 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.2826-1382dupA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr5 | 53077382 | |||||
| chr5:53077408
|
G | A | 136 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(133): Show | 145 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.2826-1364G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53077408 | ||||||
| chr5:53077411
|
A | G | 1 | a0001c0001t0002g0123 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2826-1361A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53077411 | ||||||
| chr5:53077446
|
A | G | 3 | a0001c0002t0003g0063a0001c0002t0003g0069a0001c0002t0003g0157 | 3 | NA18948.hp1 NA19056.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.2826-1326A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53077446 | ||||||
| chr5:53077453
|
T | A | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2826-1319T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53077453 | ||||||
| chr5:53077572
|
C | T | 1 | a0001c0001t0002g0264 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2826-1200C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53077572 | ||||||
| chr5:53077599
|
T | C | 136 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(133): Show | 145 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.2826-1173T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53077599 | ||||||
| chr5:53077622
|
C | G | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2826-1150C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53077622 | ||||||
| chr5:53077782
|
G | A | 1 | a0001c0001t0025g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2826-990G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53077782 | ||||||
| chr5:53077866
|
C | T | 24 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(21): Show | 27 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.2826-906C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53077866 | ||||||
| chr5:53077872
|
A | C | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2826-900A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53077872 | ||||||
| chr5:53077980
|
C | T | 59 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0024others(56): Show | 62 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.2826-792C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53077980 | ||||||
| chr5:53078258
|
T | C | 93 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0024others(90): Show | 97 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.2826-514T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078258 | ||||||
| chr5:53078366
|
A | T | 2 | a0001c0001t0001g0335a0001c0001t0001g0336 | 2 | NA18980.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.2826-406A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078366 | ||||||
| chr5:53078397
|
A | C | 68 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0024others(65): Show | 72 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.2826-375A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078397 | ||||||
| chr5:53078622
|
T | G | 1 | a0001c0021t0050g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2826-150T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078622 | ||||||
| chr5:53078690
|
AAGATACT others(5): Show |
A | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-80_2826-69del others(12): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr5 | 53078690 | |||||
| chr5:53078697
|
TTAAA | T | 5 | a0001c0002t0018g0103a0001c0002t0018g0105a0001c0002t0018g0120others(2): Show | 5 | HG00642.hp1 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.2826-70_2826-67del others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr5 | 53078697 | |||||
| chr5:53078706
|
A | G | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-66A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078706 | ||||||
| chr5:53078708
|
A | T | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-64A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078708 | ||||||
| chr5:53078711
|
T | A | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-61T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078711 | ||||||
| chr5:53078715
|
A | T | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-57A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078715 | ||||||
| chr5:53078718
|
C | T | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-54C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078718 | ||||||
| chr5:53078720
|
T | A | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-52T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078720 | ||||||
| chr5:53078721
|
C | T | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-51C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078721 | ||||||
| chr5:53078722
|
A | T | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-50A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078722 | ||||||
| chr5:53078725
|
A | T | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-47A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078725 | ||||||
| chr5:53078737
|
C | A | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-35C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078737 | ||||||
| chr5:53078743
|
T | C | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-29T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078743 | ||||||
| chr5:53078746
|
T | A | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-26T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078746 | ||||||
| chr5:53078750
|
C | G | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-22C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078750 | ||||||
| chr5:53078751
|
T | C | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-21T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078751 | ||||||
| chr5:53078763
|
A | G | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2826-9A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078763 | ||||||
| chr5:53078769
|
C | T | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | splice_region_variant&intron_variant | LOW | c.2826-3C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078769 | ||||||
| chr5:53078770
|
A | G | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.2826-2A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078770 | ||||||
| chr5:53078771
|
G | T | 1 | a0001c0002t0006g0039 | 1 | NA18981.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.2826-1G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 23/29 | chr5 | 53078771 | ||||||
| chr5:53079009
|
T | A | 1 | a0001c0002t0003g0190 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2928+135T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53079009 | ||||||
| chr5:53079120
|
A | T | 2 | a0001c0001t0001g0335a0001c0001t0001g0336 | 2 | NA18980.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.2928+246A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53079120 | ||||||
| chr5:53079152
|
T | C | 1 | a0001c0001t0001g0269 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2928+278T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53079152 | ||||||
| chr5:53079224
|
G | C | 1 | a0001c0002t0003g0171 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2928+350G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53079224 | ||||||
| chr5:53079290
|
G | A | 1 | a0001c0001t0002g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2928+416G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53079290 | ||||||
| chr5:53079529
|
G | A | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2928+655G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53079529 | ||||||
| chr5:53079552
|
A | G | 27 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(24): Show | 29 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.2928+678A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53079552 | ||||||
| chr5:53079645
|
TA | T | 7 | a0002c0007t0010g0165a0002c0007t0010g0166a0002c0007t0010g0167others(4): Show | 7 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.2928+779delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr5 | 53079645 | |||||
| chr5:53079706
|
G | A | 2 | a0001c0001t0002g0142a0001c0001t0002g0273 | 2 | HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2929-805G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53079706 | ||||||
| chr5:53079706
|
G | C | 24 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(21): Show | 27 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.2929-805G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53079706 | ||||||
| chr5:53079753
|
C | T | 4 | a0001c0008t0012g0162a0001c0008t0012g0163a0001c0008t0012g0164others(1): Show | 5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2929-758C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53079753 | ||||||
| chr5:53079754
|
G | A | 3 | a0001c0001t0002g0133a0001c0001t0038g0129a0001c0022t0002g0245 | 3 | HG02602.hp2 HG03942.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.2929-757G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53079754 | ||||||
| chr5:53079755
|
C | T | 1 | a0001c0001t0025g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2929-756C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53079755 | ||||||
| chr5:53079923
|
A | G | 1 | a0001c0001t0001g0350 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2929-588A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53079923 | ||||||
| chr5:53080097
|
C | T | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.2929-414C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53080097 | ||||||
| chr5:53080289
|
G | A | 33 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(30): Show | 35 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.2929-222G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53080289 | ||||||
| chr5:53080335
|
G | A | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2929-176G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53080335 | ||||||
| chr5:53080417
|
C | T | 1 | a0002c0003t0007g0283 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2929-94C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53080417 | ||||||
| chr5:53080438
|
C | T | 1 | a0001c0001t0005g0262 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2929-73C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53080438 | ||||||
| chr5:53080439
|
G | A | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2929-72G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53080439 | ||||||
| chr5:53080442
|
G | T | 1 | a0001c0001t0002g0117 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2929-69G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 24/29 | chr5 | 53080442 | ||||||
| chr5:53080694
|
G | A | 4 | a0001c0008t0012g0162a0001c0008t0012g0163a0001c0008t0012g0164others(1): Show | 5 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.3039+73G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 25/29 | chr5 | 53080694 | ||||||
| chr5:53080888
|
T | C | 1 | a0016c0029t0001g0304 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3039+267T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 25/29 | chr5 | 53080888 | ||||||
| chr5:53080931
|
T | C | 1 | a0001c0001t0002g0142 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3039+310T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 25/29 | chr5 | 53080931 | ||||||
| chr5:53080989
|
C | T | 1 | a0001c0011t0034g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3039+368C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 25/29 | chr5 | 53080989 | ||||||
| chr5:53080990
|
G | A | 33 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(30): Show | 35 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.3039+369G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 25/29 | chr5 | 53080990 | ||||||
| chr5:53081086
|
G | T | 293 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0024others(290): Show | 311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.3039+465G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 25/29 | chr5 | 53081086 | ||||||
| chr5:53081133
|
C | A | 1 | a0001c0001t0002g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3040-459C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 25/29 | chr5 | 53081133 | ||||||
| chr5:53081285
|
T | C | 3 | a0002c0003t0017g0021a0002c0003t0017g0022a0002c0003t0017g0023 | 3 | HG01243.hp2 HG01261.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.3040-307T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 25/29 | chr5 | 53081285 | ||||||
| chr5:53081347
|
A | G | 2 | a0002c0003t0007g0333a0002c0003t0007g0334 | 2 | HG00323.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.3040-245A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 25/29 | chr5 | 53081347 | ||||||
| chr5:53081351
|
T | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(4): Show | 8 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.3040-241T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 25/29 | chr5 | 53081351 | ||||||
| chr5:53081447
|
A | T | 3 | a0002c0003t0017g0021a0002c0003t0017g0022a0002c0003t0017g0023 | 3 | HG01243.hp2 HG01261.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.3040-145A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 25/29 | chr5 | 53081447 | ||||||
| chr5:53081524
|
A | G | 1 | a0001c0002t0003g0203 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.3040-68A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 25/29 | chr5 | 53081524 | ||||||
| chr5:53081783
|
T | C | 7 | a0004c0006t0003g0014a0004c0006t0003g0169a0004c0006t0003g0172others(4): Show | 8 | NA18947.hp1 NA18970.hp2 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.3144+87T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53081783 | ||||||
| chr5:53081784
|
C | A | 1 | a0001c0001t0001g0323 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.3144+88C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53081784 | ||||||
| chr5:53081818
|
A | G | 1 | a0001c0021t0050g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3144+122A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53081818 | ||||||
| chr5:53081886
|
G | A | 1 | a0001c0002t0041g0332 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3144+190G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53081886 | ||||||
| chr5:53082104
|
C | T | 1 | a0001c0001t0025g0281 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3144+408C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53082104 | ||||||
| chr5:53082407
|
T | C | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.3144+711T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53082407 | ||||||
| chr5:53082465
|
G | A | 136 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(133): Show | 145 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.3144+769G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53082465 | ||||||
| chr5:53082558
|
G | C | 1 | a0001c0001t0001g0068 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3145-782G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53082558 | ||||||
| chr5:53082606
|
C | T | 38 | a0001c0002t0004g0003a0001c0002t0004g0087a0001c0002t0004g0099others(35): Show | 40 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.3145-734C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53082606 | ||||||
| chr5:53082679
|
T | G | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.3145-661T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53082679 | ||||||
| chr5:53082692
|
A | G | 6 | a0002c0007t0010g0165a0002c0007t0010g0166a0002c0007t0010g0167others(3): Show | 6 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.3145-648A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53082692 | ||||||
| chr5:53082779
|
T | C | 5 | a0002c0007t0010g0165a0002c0007t0010g0166a0002c0007t0010g0167others(2): Show | 5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3145-561T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53082779 | ||||||
| chr5:53082843
|
C | T | 5 | a0001c0002t0018g0103a0001c0002t0018g0105a0001c0002t0018g0120others(2): Show | 5 | HG00642.hp1 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.3145-497C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53082843 | ||||||
| chr5:53082922
|
A | G | 1 | a0001c0002t0004g0266 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3145-418A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53082922 | ||||||
| chr5:53082961
|
T | C | 1 | a0001c0001t0002g0107 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3145-379T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53082961 | ||||||
| chr5:53083020
|
GT | G | 135 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(132): Show | 144 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.3145-313delT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr5 | 53083020 | |||||
| chr5:53083089
|
T | G | 5 | a0002c0007t0010g0165a0002c0007t0010g0166a0002c0007t0010g0167others(2): Show | 5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3145-251T>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53083089 | ||||||
| chr5:53083126
|
G | A | 57 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0024others(54): Show | 59 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.3145-214G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53083126 | ||||||
| chr5:53083130
|
T | C | 1 | a0001c0001t0001g0225 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3145-210T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53083130 | ||||||
| chr5:53083189
|
G | A | 168 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(165): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.3145-151G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53083189 | ||||||
| chr5:53083196
|
T | C | 5 | a0002c0007t0010g0165a0002c0007t0010g0166a0002c0007t0010g0167others(2): Show | 5 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3145-144T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53083196 | ||||||
| chr5:53083293
|
C | T | 1 | a0002c0009t0016g0216 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3145-47C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 26/29 | chr5 | 53083293 | ||||||
| chr5:53083670
|
A | G | 1 | a0001c0002t0003g0201 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3258+217A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53083670 | ||||||
| chr5:53084292
|
A | AT | 95 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0024others(92): Show | 101 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.3258+849dupT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr5 | 53084292 | |||||
| chr5:53084354
|
AT | A | 6 | a0002c0007t0010g0165a0002c0007t0010g0166a0002c0007t0010g0167others(3): Show | 6 | HG02280.hp1 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.3258+910delT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr5 | 53084354 | |||||
| chr5:53084677
|
GT | G | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3258+1226delT | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr5 | 53084677 | |||||
| chr5:53084765
|
T | C | 3 | a0001c0002t0003g0199a0001c0002t0003g0200a0001c0002t0003g0201 | 3 | HG01515.hp1 HG01517.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.3258+1312T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53084765 | ||||||
| chr5:53084791
|
CACTG | C | 19 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(16): Show | 21 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.3258+1343_3258+134 others(8): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr5 | 53084791 | |||||
| chr5:53085093
|
A | T | 38 | a0001c0002t0004g0003a0001c0002t0004g0087a0001c0002t0004g0099others(35): Show | 40 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.3258+1640A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53085093 | ||||||
| chr5:53085271
|
T | C | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3259-1681T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53085271 | ||||||
| chr5:53085290
|
G | A | 1 | a0001c0001t0002g0128 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3259-1662G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53085290 | ||||||
| chr5:53085291
|
G | C | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3259-1661G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53085291 | ||||||
| chr5:53085291
|
G | T | 1 | a0001c0001t0002g0128 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3259-1661G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53085291 | ||||||
| chr5:53085294
|
C | A | 1 | a0001c0001t0002g0128 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3259-1658C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53085294 | ||||||
| chr5:53085332
|
A | C | 30 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(27): Show | 32 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.3259-1620A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53085332 | ||||||
| chr5:53085334
|
C | G | 22 | a0001c0004t0008g0305a0001c0004t0008g0306a0001c0004t0008g0307others(19): Show | 22 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.3259-1618C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53085334 | ||||||
| chr5:53085386
|
T | C | 5 | a0001c0002t0018g0103a0001c0002t0018g0105a0001c0002t0018g0120others(2): Show | 5 | HG00642.hp1 HG01167.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.3259-1566T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53085386 | ||||||
| chr5:53085575
|
T | C | 1 | a0001c0001t0051g0071 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3259-1377T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53085575 | ||||||
| chr5:53085822
|
C | T | 1 | a0002c0003t0007g0286 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.3259-1130C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53085822 | ||||||
| chr5:53085922
|
T | C | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3259-1030T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53085922 | ||||||
| chr5:53086022
|
C | T | 1 | a0001c0001t0038g0129 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3259-930C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086022 | ||||||
| chr5:53086030
|
G | A | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.3259-922G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086030 | ||||||
| chr5:53086051
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3259-901C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086051 | ||||||
| chr5:53086072
|
T | C | 3 | a0002c0009t0016g0216a0002c0009t0016g0271a0002c0009t0016g0272 | 3 | HG00673.hp1 NA18961.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.3259-880T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086072 | ||||||
| chr5:53086103
|
T | C | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3259-849T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086103 | ||||||
| chr5:53086171
|
C | T | 2 | a0001c0001t0025g0276a0001c0001t0025g0281 | 2 | HG02559.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.3259-781C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086171 | ||||||
| chr5:53086375
|
G | T | 2 | a0002c0003t0007g0018a0002c0003t0007g0286 | 3 | HG01070.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3259-577G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086375 | ||||||
| chr5:53086388
|
C | G | 135 | a0001c0002t0003g0002a0001c0002t0003g0031a0001c0002t0003g0063others(132): Show | 144 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.3259-564C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086388 | ||||||
| chr5:53086455
|
T | A | 1 | a0001c0001t0001g0096 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3259-497T>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086455 | ||||||
| chr5:53086481
|
C | T | 23 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(20): Show | 26 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.3259-471C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086481 | ||||||
| chr5:53086519
|
T | C | 136 | a0001c0001t0024g0214a0001c0002t0003g0002a0001c0002t0003g0031others(133): Show | 145 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.3259-433T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086519 | ||||||
| chr5:53086587
|
A | G | 1 | a0001c0001t0029g0139 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3259-365A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086587 | ||||||
| chr5:53086612
|
G | A | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3259-340G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086612 | ||||||
| chr5:53086776
|
C | T | 1 | a0001c0001t0001g0358 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3259-176C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086776 | ||||||
| chr5:53086825
|
T | C | 33 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(30): Show | 35 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.3259-127T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086825 | ||||||
| chr5:53086873
|
T | C | 2 | a0001c0001t0002g0326a0001c0001t0002g0328 | 2 | HG00280.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.3259-79T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086873 | ||||||
| chr5:53086918
|
A | T | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3259-34A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 27/29 | chr5 | 53086918 | ||||||
| chr5:53087074
|
A | G | 22 | a0001c0004t0008g0305a0001c0004t0008g0306a0001c0004t0008g0307others(19): Show | 22 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.3348+33A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53087074 | ||||||
| chr5:53087095
|
C | T | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3348+54C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53087095 | ||||||
| chr5:53087235
|
C | T | 3 | a0002c0003t0007g0019a0002c0003t0007g0346a0002c0003t0007g0356 | 4 | HG01192.hp1 HG01884.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3348+194C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53087235 | ||||||
| chr5:53087278
|
C | G | 1 | a0001c0001t0001g0228 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.3348+237C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53087278 | ||||||
| chr5:53087321
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.3348+280A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53087321 | ||||||
| chr5:53087414
|
G | A | 1 | a0001c0002t0047g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3348+373G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53087414 | ||||||
| chr5:53087414
|
G | T | 1 | a0013c0019t0030g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3348+373G>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53087414 | ||||||
| chr5:53087463
|
T | C | 1 | a0001c0001t0002g0025 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3348+422T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53087463 | ||||||
| chr5:53087598
|
G | A | 1 | a0001c0001t0029g0139 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3348+557G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53087598 | ||||||
| chr5:53087624
|
T | TA | 46 | a0001c0001t0001g0289a0001c0002t0003g0186a0001c0002t0004g0003others(43): Show | 48 | HG00735.hp1 HG01074.hp1 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.3348+599dupA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr5 | 53087624 | |||||
| chr5:53087624
|
T | TAA | 86 | a0001c0002t0003g0002a0001c0002t0003g0063a0001c0002t0003g0069others(83): Show | 93 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.3348+598_3348+599d others(4): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr5 | 53087624 | |||||
| chr5:53087624
|
T | TAAA | 7 | a0001c0001t0024g0214a0001c0002t0003g0031a0001c0002t0003g0108others(4): Show | 7 | HG01081.hp1 HG01993.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.3348+597_3348+599d others(5): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr5 | 53087624 | |||||
| chr5:53087624
|
TA | T | 9 | a0001c0001t0001g0058a0001c0004t0008g0309a0001c0011t0034g0084others(6): Show | 9 | HG01070.hp2 HG01243.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.3348+599delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr5 | 53087624 | |||||
| chr5:53087721
|
C | T | 1 | a0001c0001t0005g0262 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3348+680C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53087721 | ||||||
| chr5:53087808
|
C | T | 24 | a0001c0002t0006g0001a0001c0002t0006g0005a0001c0002t0006g0034others(21): Show | 27 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.3348+767C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53087808 | ||||||
| chr5:53087888
|
C | G | 172 | a0001c0001t0024g0214a0001c0002t0003g0002a0001c0002t0003g0031others(169): Show | 183 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.3348+847C>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53087888 | ||||||
| chr5:53088002
|
T | C | 172 | a0001c0001t0024g0214a0001c0002t0003g0002a0001c0002t0003g0031others(169): Show | 183 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.3348+961T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088002 | ||||||
| chr5:53088005
|
G | A | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3348+964G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088005 | ||||||
| chr5:53088157
|
G | A | 72 | a0001c0001t0024g0214a0001c0002t0003g0002a0001c0002t0003g0031others(69): Show | 76 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.3348+1116G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088157 | ||||||
| chr5:53088175
|
A | T | 5 | a0002c0003t0017g0021a0002c0003t0017g0022a0002c0003t0017g0023others(2): Show | 5 | HG01243.hp2 HG01261.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.3348+1134A>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088175 | ||||||
| chr5:53088391
|
A | G | 1 | a0001c0001t0029g0139 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3348+1350A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088391 | ||||||
| chr5:53088412
|
A | G | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3348+1371A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088412 | ||||||
| chr5:53088462
|
A | G | 1 | a0001c0001t0001g0289 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.3348+1421A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088462 | ||||||
| chr5:53088484
|
G | C | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3348+1443G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088484 | ||||||
| chr5:53088511
|
A | C | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3349-1435A>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088511 | ||||||
| chr5:53088602
|
C | T | 1 | a0001c0004t0008g0319 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3349-1344C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088602 | ||||||
| chr5:53088613
|
G | A | 1 | a0001c0002t0004g0266 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3349-1333G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088613 | ||||||
| chr5:53088685
|
C | CA | 131 | a0001c0001t0001g0297a0001c0001t0001g0320a0001c0001t0024g0214others(128): Show | 141 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.3349-1242dupA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr5 | 53088685 | |||||
| chr5:53088685
|
C | CAA | 31 | a0001c0002t0003g0188a0001c0002t0009g0209a0002c0003t0007g0018others(28): Show | 33 | HG00323.hp2 HG00621.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.3349-1243_3349-124 others(6): Show |
ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr5 | 53088685 | |||||
| chr5:53088685
|
CA | C | 56 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0024others(53): Show | 58 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.3349-1242delA | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr5 | 53088685 | |||||
| chr5:53088712
|
G | A | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3349-1234G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088712 | ||||||
| chr5:53088833
|
G | C | 261 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0024others(258): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.3349-1113G>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088833 | ||||||
| chr5:53088849
|
C | T | 1 | a0001c0016t0005g0104 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3349-1097C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53088849 | ||||||
| chr5:53089056
|
C | A | 6 | a0001c0002t0009g0027a0001c0002t0009g0207a0001c0002t0009g0208others(3): Show | 6 | HG00280.hp2 NA18995.hp1 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.3349-890C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53089056 | ||||||
| chr5:53089182
|
C | A | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3349-764C>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53089182 | ||||||
| chr5:53089230
|
C | T | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3349-716C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53089230 | ||||||
| chr5:53089482
|
C | T | 4 | a0001c0002t0004g0115a0001c0002t0004g0145a0001c0002t0048g0239others(1): Show | 4 | HG02074.hp1 HG02293.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.3349-464C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53089482 | ||||||
| chr5:53089574
|
G | A | 1 | a0001c0001t0002g0138 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.3349-372G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53089574 | ||||||
| chr5:53089683
|
T | C | 1 | a0001c0004t0008g0308 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3349-263T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53089683 | ||||||
| chr5:53089715
|
T | C | 1 | a0001c0004t0008g0309 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3349-231T>C | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 28/29 | chr5 | 53089715 | ||||||
| chr5:53090123
|
A | G | 4 | a0001c0002t0004g0099a0001c0002t0004g0241a0001c0002t0004g0246others(1): Show | 4 | HG02809.hp2 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3465+61A>G | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 29/29 | chr5 | 53090123 | ||||||
| chr5:53090225
|
C | T | 1 | a0001c0008t0021g0013 | 2 | HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3465+163C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 29/29 | chr5 | 53090225 | ||||||
| chr5:53090401
|
C | T | 36 | a0002c0003t0007g0018a0002c0003t0007g0019a0002c0003t0007g0072others(33): Show | 38 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.3466-118C>T | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 29/29 | chr5 | 53090401 | ||||||
| chr5:53090441
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3466-78G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 29/29 | chr5 | 53090441 | ||||||
| chr5:53090485
|
G | A | 4 | a0001c0002t0003g0180a0001c0002t0003g0199a0001c0002t0003g0200others(1): Show | 4 | HG01123.hp2 HG01515.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.3466-34G>A | ITGA2 | ENSG00000164171.11 | transcript | ENST00000296585.10 | protein_coding | 29/29 | chr5 | 53090485 |