Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3678 |
| ensemblid | ENSG00000161638.11 |
| hgncid | 6141 |
| symbol | ITGA5 |
| name | integrin subunit alpha 5 |
| refseq_nuc | NM_002205.5 |
| refseq_prot | NP_002196.4 |
| ensembl_nuc | ENST00000293379.9 |
| ensembl_prot | ENSP00000293379.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 54395261 |
| end | 54419266 |
| strand | - |
| ver | v1.2 |
| region | chr12:54395261-54419266 |
| region5000 | chr12:54390261-54424266 |
| regionname0 | ITGA5_chr12_54395261_54419266 |
| regionname5000 | ITGA5_chr12_54390261_54424266 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1049 | 315 | 85 | 69 | 108 | 12 | 39 | 74 | ITGA5_chr12_54390261_54424266 | ITGA5 | MGSRT others(1044): Show |
chr12 | 54390261 | 54424266 |
| a0002 | 0/0 | 1049 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | MGSRT others(1044): Show |
chr12 | 54390261 | 54424266 |
| a0003 | 0/0 | 1049 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | MGSRT others(1044): Show |
chr12 | 54390261 | 54424266 |
| a0004 | 0/0 | 1049 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | MGSRT others(1044): Show |
chr12 | 54390261 | 54424266 |
| a0005 | 0/0 | 1049 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | MGSRT others(1044): Show |
chr12 | 54390261 | 54424266 |
| a0006 | 0/0 | 1049 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | MGSRT others(1044): Show |
chr12 | 54390261 | 54424266 |
| a0007 | 0/0 | 1049 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | MGSRT others(1044): Show |
chr12 | 54390261 | 54424266 |
| a0008 | 0/0 | 1049 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | MGSRT others(1044): Show |
chr12 | 54390261 | 54424266 |
| a0009 | 0/0 | 1049 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | MGSRT others(1044): Show |
chr12 | 54390261 | 54424266 |
| a0010 | 0/0 | 1049 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | MGSRT others(1044): Show |
chr12 | 54390261 | 54424266 |
| a0011 | 0/0 | 1049 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | MGSRT others(1044): Show |
chr12 | 54390261 | 54424266 |
| a0012 | 0/0 | 1049 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | MGSRT others(1044): Show |
chr12 | 54390261 | 54424266 |
| a0013 | 0/0 | 1049 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | MGSRT others(1044): Show |
chr12 | 54390261 | 54424266 |
| a0014 | 0/0 | 1049 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | MGSRT others(1044): Show |
chr12 | 54390261 | 54424266 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3147 | 284 | 62 | 69 | 108 | 11 | 32 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATGGG others(3142): Show |
chr12 | 54390261 | 54424266 | ||
| a0001c0002 | 0/0 | 3147 | 12 | 5 | 0 | 0 | 0 | 7 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATGGG others(3142): Show |
chr12 | 54390261 | 54424266 | ||
| a0001c0003 | 0/0 | 3147 | 8 | 8 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATGGG others(3142): Show |
chr12 | 54390261 | 54424266 | ||
| a0001c0005 | 0/0 | 3147 | 3 | 3 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATGGG others(3142): Show |
chr12 | 54390261 | 54424266 | ||
| a0001c0006 | 0/0 | 3147 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATGGG others(3142): Show |
chr12 | 54390261 | 54424266 | ||
| a0001c0007 | 0/0 | 3147 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATGGG others(3142): Show |
chr12 | 54390261 | 54424266 | ||
| a0001c0015 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATGGG others(3142): Show |
chr12 | 54390261 | 54424266 | ||
| a0001c0018 | 0/0 | 3147 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATGGG others(3142): Show |
chr12 | 54390261 | 54424266 | ||
| a0001c0019 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATGGG others(3142): Show |
chr12 | 54390261 | 54424266 | ||
| a0001c0021 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATGGG others(3142): Show |
chr12 | 54390261 | 54424266 | ||
| a0002c0004 | 0/0 | 3147 | 3 | 3 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATGGG others(3142): Show |
chr12 | 54390261 | 54424266 | ||
| a0003c0008 | 0/0 | 3147 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATGGG others(3142): Show |
chr12 | 54390261 | 54424266 | ||
| a0004c0016 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATGGG others(3142): Show |
chr12 | 54390261 | 54424266 | ||
| a0005c0014 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATGGG others(3142): Show |
chr12 | 54390261 | 54424266 | ||
| a0006c0017 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATGGG others(3142): Show |
chr12 | 54390261 | 54424266 | ||
| a0007c0020 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATGGG others(3142): Show |
chr12 | 54390261 | 54424266 | ||
| a0008c0012 | 0/0 | 3147 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATGGG others(3142): Show |
chr12 | 54390261 | 54424266 | ||
| a0009c0009 | 0/0 | 3147 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATGGG others(3142): Show |
chr12 | 54390261 | 54424266 | ||
| a0010c0023 | 0/0 | 3147 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATGGG others(3142): Show |
chr12 | 54390261 | 54424266 | ||
| a0011c0010 | 0/0 | 3147 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATGGG others(3142): Show |
chr12 | 54390261 | 54424266 | ||
| a0012c0013 | 0/0 | 3147 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATGGG others(3142): Show |
chr12 | 54390261 | 54424266 | ||
| a0013c0022 | 0/0 | 3147 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATGGG others(3142): Show |
chr12 | 54390261 | 54424266 | ||
| a0014c0011 | 0/0 | 3147 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATGGG others(3142): Show |
chr12 | 54390261 | 54424266 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4250 | 268 | 61 | 68 | 94 | 11 | 32 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4245): Show |
chr12 | 54390261 | 54424266 |
| a0001c0001t0002 | 0/0 | 4250 | 14 | 0 | 0 | 14 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4245): Show |
chr12 | 54390261 | 54424266 |
| a0001c0001t0005 | 0/0 | 4250 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4245): Show |
chr12 | 54390261 | 54424266 |
| a0001c0001t0008 | 0/0 | 4250 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4245): Show |
chr12 | 54390261 | 54424266 |
| a0001c0002t0003 | 0/0 | 4242 | 12 | 5 | 0 | 0 | 0 | 7 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4237): Show |
chr12 | 54390261 | 54424266 |
| a0001c0003t0001 | 0/0 | 4250 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4245): Show |
chr12 | 54390261 | 54424266 |
| a0001c0003t0004 | 0/0 | 4250 | 6 | 6 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4245): Show |
chr12 | 54390261 | 54424266 |
| a0001c0005t0001 | 0/0 | 4250 | 3 | 3 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4245): Show |
chr12 | 54390261 | 54424266 |
| a0001c0006t0001 | 0/0 | 4250 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4245): Show |
chr12 | 54390261 | 54424266 |
| a0001c0006t0006 | 0/0 | 4250 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4245): Show |
chr12 | 54390261 | 54424266 |
| a0001c0007t0001 | 0/0 | 4250 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4245): Show |
chr12 | 54390261 | 54424266 |
| a0001c0015t0003 | 0/0 | 4242 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4237): Show |
chr12 | 54390261 | 54424266 |
| a0001c0018t0001 | 0/0 | 4250 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4245): Show |
chr12 | 54390261 | 54424266 |
| a0001c0019t0004 | 0/0 | 4250 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4245): Show |
chr12 | 54390261 | 54424266 |
| a0001c0021t0001 | 0/0 | 4250 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4245): Show |
chr12 | 54390261 | 54424266 |
| a0002c0004t0001 | 0/0 | 4250 | 3 | 3 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4245): Show |
chr12 | 54390261 | 54424266 |
| a0003c0008t0001 | 0/0 | 4250 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4245): Show |
chr12 | 54390261 | 54424266 |
| a0004c0016t0007 | 0/0 | 4250 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4245): Show |
chr12 | 54390261 | 54424266 |
| a0005c0014t0001 | 0/0 | 4250 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4245): Show |
chr12 | 54390261 | 54424266 |
| a0006c0017t0001 | 0/0 | 4250 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4245): Show |
chr12 | 54390261 | 54424266 |
| a0007c0020t0001 | 0/0 | 4250 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4245): Show |
chr12 | 54390261 | 54424266 |
| a0008c0012t0001 | 0/0 | 4250 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4245): Show |
chr12 | 54390261 | 54424266 |
| a0009c0009t0001 | 0/0 | 4250 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4245): Show |
chr12 | 54390261 | 54424266 |
| a0010c0023t0001 | 0/0 | 4250 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4245): Show |
chr12 | 54390261 | 54424266 |
| a0011c0010t0001 | 0/0 | 4250 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4245): Show |
chr12 | 54390261 | 54424266 |
| a0012c0013t0001 | 0/0 | 4250 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4245): Show |
chr12 | 54390261 | 54424266 |
| a0013c0022t0003 | 0/0 | 4242 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4237): Show |
chr12 | 54390261 | 54424266 |
| a0014c0011t0001 | 0/0 | 4250 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | ATTCG others(4245): Show |
chr12 | 54390261 | 54424266 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 46 | 11 | 4 | 27 | 0 | 4 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0002 | 0/0 | 20 | 6 | 6 | 3 | 1 | 4 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0003 | 0/0 | 19 | 1 | 3 | 8 | 5 | 2 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0004 | 0/0 | 16 | 0 | 2 | 11 | 0 | 3 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0005 | 0/0 | 15 | 3 | 6 | 0 | 3 | 3 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0007 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0008 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0013 | 0/0 | 4 | 3 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0019 | 0/1 | 3 | 0 | 2 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0020 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0032 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0002g0006 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0001t0008g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0002t0003g0009 | 0/0 | 6 | 1 | 0 | 0 | 0 | 5 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0002t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0002t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0002t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0002t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0002t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0003t0004g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0003t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0003t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0003t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0003t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0005t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0005t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0005t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0006t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0006t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0007t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0007t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0015t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0018t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0019t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0001c0021t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0002c0004t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0002c0004t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0002c0004t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0003c0008t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0004c0016t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0005c0014t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0006c0017t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0007c0020t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0008c0012t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0009c0009t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0010c0023t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0011c0010t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0012c0013t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0013c0022t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| a0014c0011t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0018 | t0001 | g0108 | EUR | GBR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0091 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01361 | hp2 | a0003 | c0008 | t0001 | g0077 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01884 | hp2 | a0001 | c0002 | t0003 | g0037 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0143 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02145 | hp1 | a0001 | c0006 | t0006 | g0136 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02145 | hp2 | a0004 | c0016 | t0007 | g0063 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CDX | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02280 | hp2 | a0001 | c0003 | t0004 | g0021 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0141 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02572 | hp2 | a0001 | c0007 | t0001 | g0138 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02615 | hp1 | a0001 | c0002 | t0003 | g0059 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02622 | hp1 | a0001 | c0005 | t0001 | g0135 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02622 | hp2 | a0005 | c0014 | t0001 | g0053 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02630 | hp1 | a0006 | c0017 | t0001 | g0097 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02698 | hp1 | a0001 | c0002 | t0003 | g0058 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02809 | hp1 | a0002 | c0004 | t0001 | g0085 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02886 | hp2 | a0001 | c0005 | t0001 | g0039 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02895 | hp2 | a0001 | c0003 | t0004 | g0145 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02897 | hp2 | a0001 | c0003 | t0004 | g0144 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03017 | hp2 | a0001 | c0002 | t0003 | g0009 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03041 | hp2 | a0001 | c0021 | t0001 | g0048 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03130 | hp2 | a0001 | c0002 | t0003 | g0057 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0142 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03239 | hp1 | a0001 | c0002 | t0003 | g0009 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03453 | hp1 | a0001 | c0002 | t0003 | g0061 | AFR | MSL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03453 | hp2 | a0002 | c0004 | t0001 | g0084 | AFR | MSL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03490 | hp1 | a0001 | c0002 | t0003 | g0009 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03492 | hp1 | a0001 | c0002 | t0003 | g0009 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03540 | hp2 | a0001 | c0006 | t0001 | g0094 | AFR | GWD | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03579 | hp1 | a0001 | c0003 | t0004 | g0034 | AFR | MSL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03579 | hp2 | a0001 | c0005 | t0001 | g0137 | AFR | MSL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | STU | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03710 | hp1 | a0008 | c0012 | t0001 | g0036 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03710 | hp2 | a0009 | c0009 | t0001 | g0110 | SAS | PJL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03834 | hp1 | a0001 | c0002 | t0003 | g0009 | SAS | BEB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG04115 | hp1 | a0001 | c0002 | t0003 | g0056 | SAS | STU | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG04115 | hp2 | a0010 | c0023 | t0001 | g0147 | SAS | STU | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | STU | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | STU | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | YRI | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18906 | hp1 | a0001 | c0002 | t0003 | g0009 | AFR | YRI | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | YRI | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18941 | hp2 | a0011 | c0010 | t0001 | g0045 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18966 | hp1 | a0012 | c0013 | t0001 | g0086 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18972 | hp1 | a0013 | c0022 | t0003 | g0060 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18982 | hp1 | a0014 | c0011 | t0001 | g0081 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19030 | hp1 | a0002 | c0004 | t0001 | g0099 | AFR | LWK | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19030 | hp2 | a0001 | c0003 | t0004 | g0021 | AFR | LWK | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | LWK | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19240 | hp1 | a0001 | c0003 | t0004 | g0146 | AFR | YRI | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA19240 | hp2 | a0001 | c0007 | t0001 | g0139 | AFR | YRI | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ASW | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | TSI | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | GIH | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG02559 | hp2 | a0001 | c0019 | t0004 | g0054 | AFR | ACB | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG03471 | hp2 | a0007 | c0020 | t0001 | g0047 | AFR | MSL | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | USA | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA21309 | hp1 | a0001 | c0015 | t0003 | g0050 | AFR | LWK | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0019 | REF | REF | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0032 | REF | REF | ITGA5_chr12_54390261_54424266 | ITGA5 | chr12 | 54390261 | 54424266 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:54401387 | G | A | 1 | a0004 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.2479C>T | p.His827Tyr | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 24/30 | 2547/4250 | 2479/3150 | 827/1049 | chr12 | 54401387 | |||
| chr12:54401420 | G | A | 1 | a0006 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.2446C>T | p.Pro816Ser | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 24/30 | 2514/4250 | 2446/3150 | 816/1049 | chr12 | 54401420 | |||
| chr12:54403258 | G | T | 1 | a0005 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.1843C>A | p.Gln615Lys | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 18/30 | 1911/4250 | 1843/3150 | 615/1049 | chr12 | 54403258 | |||
| chr12:54403702 | G | T | 1 | a0012 | 1 | NA18966.hp1 | missense_variant | MODERATE | c.1699C>A | p.Gln567Lys | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 17/30 | 1767/4250 | 1699/3150 | 567/1049 | chr12 | 54403702 | |||
| chr12:54404227 | C | T | 1 | a0002 | 3 | HG02809.hp1 HG03453.hp2 NA19030.hp1 |
missense_variant | MODERATE | c.1483G>A | p.Ala495Thr | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 15/30 | 1551/4250 | 1483/3150 | 495/1049 | chr12 | 54404227 | |||
| chr12:54404469 | A | G | 1 | a0008 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.1424T>C | p.Ile475Thr | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 14/30 | 1492/4250 | 1424/3150 | 475/1049 | chr12 | 54404469 | |||
| chr12:54404841 | C | T | 1 | a0014 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.1279G>A | p.Val427Ile | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 13/30 | 1347/4250 | 1279/3150 | 427/1049 | chr12 | 54404841 | |||
| chr12:54405193 | C | T | 1 | a0011 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.1198G>A | p.Gly400Arg | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 12/30 | 1266/4250 | 1198/3150 | 400/1049 | chr12 | 54405193 | |||
| chr12:54405369 | T | C | 1 | a0013 | 1 | NA18972.hp1 | missense_variant | MODERATE | c.1022A>G | p.Asp341Gly | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 12/30 | 1090/4250 | 1022/3150 | 341/1049 | chr12 | 54405369 | |||
| chr12:54405665 | C | T | 1 | a0007 | 1 | HG03471.hp2 | missense_variant&splice_region_variant | MODERATE | c.1015G>A | p.Gly339Arg | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 11/30 | 1083/4250 | 1015/3150 | 339/1049 | chr12 | 54405665 | |||
| chr12:54405898 | C | T | 1 | a0009 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.935G>A | p.Arg312Gln | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 10/30 | 1003/4250 | 935/3150 | 312/1049 | chr12 | 54405898 | |||
| chr12:54408904 | C | T | 1 | a0003 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.634G>A | p.Glu212Lys | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 5/30 | 702/4250 | 634/3150 | 212/1049 | chr12 | 54408904 | |||
| chr12:54419099 | G | A | 1 | a0010 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.100C>T | p.Pro34Ser | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/30 | 168/4250 | 100/3150 | 34/1049 | chr12 | 54419099 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:54399717 | G | A | 3 | a0001c0005 a0001c0021 a0007c0020 |
5 | HG02622.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
synonymous_variant | LOW | c.2769C>T | p.Leu923Leu | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 27/30 | 2837/4250 | 2769/3150 | 923/1049 | chr12 | 54399717 | |||
| chr12:54401626 | A | G | 5 | a0001c0002 a0001c0003 a0001c0015 others(2): Show |
23 | HG01884.hp2 HG01891.hp2 HG02280.hp2 others(20): Show |
synonymous_variant | LOW | c.2346T>C | p.Phe782Phe | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 23/30 | 2414/4250 | 2346/3150 | 782/1049 | chr12 | 54401626 | |||
| chr12:54402061 | G | A | 1 | a0001c0019 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.2166C>T | p.Ala722Ala | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 21/30 | 2234/4250 | 2166/3150 | 722/1049 | chr12 | 54402061 | |||
| chr12:54403214 | A | G | 4 | a0001c0002 a0001c0015 a0001c0019 others(1): Show |
15 | HG01884.hp2 HG02559.hp2 HG02615.hp1 others(12): Show |
synonymous_variant | LOW | c.1887T>C | p.Tyr629Tyr | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 18/30 | 1955/4250 | 1887/3150 | 629/1049 | chr12 | 54403214 | |||
| chr12:54403238 | G | A | 1 | a0001c0018 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.1863C>T | p.His621His | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 18/30 | 1931/4250 | 1863/3150 | 621/1049 | chr12 | 54403238 | |||
| chr12:54404225 | A | G | 3 | a0001c0006 a0001c0007 a0001c0019 |
5 | HG02145.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
synonymous_variant | LOW | c.1485T>C | p.Ala495Ala | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 15/30 | 1553/4250 | 1485/3150 | 495/1049 | chr12 | 54404225 | |||
| chr12:54404228 | G | A | 3 | a0001c0006 a0001c0007 a0001c0019 |
5 | HG02145.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
synonymous_variant | LOW | c.1482C>T | p.Ser494Ser | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 15/30 | 1550/4250 | 1482/3150 | 494/1049 | chr12 | 54404228 | |||
| chr12:54405666 | G | A | 1 | a0001c0007 | 2 | HG02572.hp2 NA19240.hp2 |
splice_region_variant&synonymous_variant | LOW | c.1014C>T | p.Asp338Asp | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 11/30 | 1082/4250 | 1014/3150 | 338/1049 | chr12 | 54405666 | |||
| chr12:54408796 | G | A | 4 | a0001c0002 a0001c0021 a0007c0020 others(1): Show |
15 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(12): Show |
synonymous_variant | LOW | c.651C>T | p.Gly217Gly | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 6/30 | 719/4250 | 651/3150 | 217/1049 | chr12 | 54408796 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:54395372 | T | G | 5 | a0001c0002t0003 a0001c0003t0004 a0001c0015t0003 others(2): Show |
21 | HG01884.hp2 HG02280.hp2 HG02559.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*921A>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 30/30 | 921 | chr12 | 54395372 | ||||||
| chr12:54395710 | TCTGGGCC | T | 3 | a0001c0002t0003 a0001c0015t0003 a0013c0022t0003 |
14 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*576_*582delGGCCCA others(1): Show |
ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 30/30 | 576 | chr12 | 54395710 | ||||||
| chr12:54395839 | C | T | 1 | a0004c0016t0007 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*454G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 30/30 | 454 | chr12 | 54395839 | ||||||
| chr12:54395952 | A | G | 1 | a0001c0006t0006 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*341T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 30/30 | 341 | chr12 | 54395952 | ||||||
| chr12:54395969 | TC | T | 3 | a0001c0002t0003 a0001c0015t0003 a0013c0022t0003 |
14 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*323delG | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 30/30 | 323 | chr12 | 54395969 | ||||||
| chr12:54396057 | T | C | 1 | a0001c0001t0008 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*236A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 30/30 | 236 | chr12 | 54396057 | ||||||
| chr12:54396183 | C | T | 1 | a0001c0001t0002 | 14 | HG00597.hp2 HG02056.hp2 HG02523.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*110G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 30/30 | 110 | chr12 | 54396183 | ||||||
| chr12:54396189 | C | T | 1 | a0001c0001t0005 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*104G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 30/30 | 104 | chr12 | 54396189 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:54396517 | A | T | 1 | a0001c0001t0001g0093 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3067-141T>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 29/29 | chr12 | 54396517 | |||||||
| chr12:54396526 | C | T | 1 | a0001c0005t0001g0135 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3067-150G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 29/29 | chr12 | 54396526 | |||||||
| chr12:54396858 | G | GT | 9 | a0001c0001t0001g0051 a0001c0001t0001g0088 a0001c0002t0003g0009 others(6): Show |
14 | HG02135.hp1 HG02135.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.3067-483dupA | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 29/29 | chr12 | 54396858 | |||||||
| chr12:54396879 | T | C | 1 | a0001c0001t0001g0030 | 2 | HG03688.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.3066+486A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 29/29 | chr12 | 54396879 | |||||||
| chr12:54396885 | T | C | 1 | a0001c0001t0001g0015 | 3 | HG02896.hp1 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3066+480A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 29/29 | chr12 | 54396885 | |||||||
| chr12:54397199 | A | AG | 7 | a0001c0002t0003g0009 a0001c0002t0003g0037 a0001c0002t0003g0057 others(4): Show |
12 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(9): Show |
intron_variant | MODIFIER | c.3066+165dupC | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 29/29 | chr12 | 54397199 | |||||||
| chr12:54397213 | T | C | 5 | a0001c0002t0003g0009 a0001c0002t0003g0056 a0001c0002t0003g0058 others(2): Show |
10 | HG02698.hp1 HG03017.hp2 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.3066+152A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 29/29 | chr12 | 54397213 | |||||||
| chr12:54397321 | G | C | 1 | a0001c0015t0003g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3066+44C>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 29/29 | chr12 | 54397321 | |||||||
| chr12:54397712 | C | T | 20 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(17): Show |
65 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.2944-225G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 28/29 | chr12 | 54397712 | |||||||
| chr12:54397844 | T | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0122 |
2 | HG00423.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.2944-357A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 28/29 | chr12 | 54397844 | |||||||
| chr12:54397902 | A | AT | 17 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0023 others(14): Show |
39 | HG00733.hp1 HG00741.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.2944-416dupA | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 28/29 | chr12 | 54397902 | |||||||
| chr12:54397902 | AT | A | 10 | a0001c0001t0001g0012 a0001c0001t0001g0070 a0001c0001t0001g0092 others(7): Show |
13 | HG00423.hp2 HG00597.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.2944-416delA | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 28/29 | chr12 | 54397902 | |||||||
| chr12:54397924 | G | T | 1 | a0001c0002t0003g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2944-437C>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 28/29 | chr12 | 54397924 | |||||||
| chr12:54398279 | T | G | 4 | a0001c0003t0004g0021 a0001c0003t0004g0034 a0001c0003t0004g0144 others(1): Show |
5 | HG02280.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2943+318A>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 28/29 | chr12 | 54398279 | |||||||
| chr12:54398294 | C | T | 2 | a0001c0002t0003g0057 a0001c0002t0003g0059 |
2 | HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2943+303G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 28/29 | chr12 | 54398294 | |||||||
| chr12:54398402 | T | A | 1 | a0001c0001t0001g0042 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2943+195A>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 28/29 | chr12 | 54398402 | |||||||
| chr12:54398409 | A | G | 1 | a0001c0015t0003g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2943+188T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 28/29 | chr12 | 54398409 | |||||||
| chr12:54398789 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2842-91G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 27/29 | chr12 | 54398789 | |||||||
| chr12:54398833 | C | CTT | 6 | a0001c0002t0003g0009 a0001c0002t0003g0037 a0001c0002t0003g0056 others(3): Show |
11 | HG01884.hp2 HG02698.hp1 HG03017.hp2 others(8): Show |
intron_variant | MODIFIER | c.2842-136_2842-135i others(4): Show |
ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 27/29 | chr12 | 54398833 | |||||||
| chr12:54398834 | TC | T | 8 | a0001c0001t0001g0031 a0001c0001t0001g0123 a0001c0003t0004g0146 others(5): Show |
9 | HG01109.hp2 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2842-137delG | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 27/29 | chr12 | 54398834 | |||||||
| chr12:54398835 | C | CT | 8 | a0001c0001t0001g0051 a0001c0001t0001g0072 a0001c0001t0001g0087 others(5): Show |
8 | HG01175.hp2 HG02135.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.2842-138dupA | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 27/29 | chr12 | 54398835 | |||||||
| chr12:54398835 | C | T | 16 | a0001c0002t0003g0009 a0001c0002t0003g0037 a0001c0002t0003g0056 others(13): Show |
21 | HG01884.hp2 HG02572.hp2 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.2842-137G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 27/29 | chr12 | 54398835 | |||||||
| chr12:54398835 | CT | C | 21 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0022 others(18): Show |
46 | HG00558.hp2 HG00733.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.2842-138delA | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 27/29 | chr12 | 54398835 | |||||||
| chr12:54398837 | T | C | 1 | a0001c0003t0004g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2842-139A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 27/29 | chr12 | 54398837 | |||||||
| chr12:54398860 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2842-162C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 27/29 | chr12 | 54398860 | |||||||
| chr12:54399237 | T | A | 1 | a0001c0001t0001g0069 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2841+408A>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 27/29 | chr12 | 54399237 | |||||||
| chr12:54399247 | A | T | 16 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0025 others(13): Show |
36 | HG00099.hp1 HG00558.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.2841+398T>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 27/29 | chr12 | 54399247 | |||||||
| chr12:54399450 | A | G | 1 | a0001c0001t0001g0014 | 4 | HG00673.hp1 NA18747.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.2841+195T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 27/29 | chr12 | 54399450 | |||||||
| chr12:54399962 | G | T | 1 | a0001c0015t0003g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2644-15C>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 25/29 | chr12 | 54399962 | |||||||
| chr12:54400046 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2644-99T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 25/29 | chr12 | 54400046 | |||||||
| chr12:54400202 | A | C | 11 | a0001c0001t0008g0141 a0001c0002t0003g0009 a0001c0002t0003g0037 others(8): Show |
16 | HG01884.hp2 HG02451.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.2644-255T>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 25/29 | chr12 | 54400202 | |||||||
| chr12:54400457 | C | T | 9 | a0001c0002t0003g0009 a0001c0002t0003g0037 a0001c0002t0003g0056 others(6): Show |
14 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(11): Show |
intron_variant | MODIFIER | c.2643+389G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 25/29 | chr12 | 54400457 | |||||||
| chr12:54400553 | G | T | 1 | a0001c0019t0004g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2643+293C>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 25/29 | chr12 | 54400553 | |||||||
| chr12:54400663 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2643+183G>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 25/29 | chr12 | 54400663 | |||||||
| chr12:54400805 | G | A | 1 | a0001c0019t0004g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2643+41C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 25/29 | chr12 | 54400805 | |||||||
| chr12:54400806 | A | G | 1 | a0001c0019t0004g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2643+40T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 25/29 | chr12 | 54400806 | |||||||
| chr12:54401049 | A | G | 12 | a0001c0002t0003g0009 a0001c0002t0003g0037 a0001c0002t0003g0056 others(9): Show |
17 | HG01884.hp2 HG02559.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.2494-54T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 24/29 | chr12 | 54401049 | |||||||
| chr12:54401143 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2494-148G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 24/29 | chr12 | 54401143 | |||||||
| chr12:54401170 | C | T | 1 | a0001c0001t0001g0027 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2494-175G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 24/29 | chr12 | 54401170 | |||||||
| chr12:54401197 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2493+176A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 24/29 | chr12 | 54401197 | |||||||
| chr12:54401251 | A | G | 1 | a0001c0002t0003g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2493+122T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 24/29 | chr12 | 54401251 | |||||||
| chr12:54401483 | G | GGAGGAGG others(8): Show |
1 | a0001c0019t0004g0054 | 1 | HG02559.hp2 | splice_region_variant&intron_variant | LOW | c.2388-20_2388-6dupT others(14): Show |
ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 23/29 | chr12 | 54401483 | |||||||
| chr12:54401489 | G | GGGTGGTT others(7): Show |
9 | a0001c0002t0003g0009 a0001c0002t0003g0037 a0001c0002t0003g0056 others(6): Show |
14 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(11): Show |
intron_variant | MODIFIER | c.2388-25_2388-12dup others(14): Show |
ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 23/29 | chr12 | 54401489 | |||||||
| chr12:54401935 | G | A | 1 | a0001c0019t0004g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2226+66C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 21/29 | chr12 | 54401935 | |||||||
| chr12:54402168 | G | A | 1 | a0001c0019t0004g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2133+12C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 20/29 | chr12 | 54402168 | |||||||
| chr12:54402361 | G | A | 1 | a0001c0001t0002g0035 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1983-31C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 19/29 | chr12 | 54402361 | |||||||
| chr12:54402658 | C | T | 1 | a0001c0001t0008g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1982+325G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 19/29 | chr12 | 54402658 | |||||||
| chr12:54402696 | G | A | 1 | a0001c0002t0003g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1982+287C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 19/29 | chr12 | 54402696 | |||||||
| chr12:54402743 | C | T | 12 | a0001c0002t0003g0009 a0001c0002t0003g0037 a0001c0002t0003g0056 others(9): Show |
17 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(14): Show |
intron_variant | MODIFIER | c.1982+240G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 19/29 | chr12 | 54402743 | |||||||
| chr12:54402809 | C | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0130 others(3): Show |
15 | HG00735.hp1 HG01346.hp2 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.1982+174G>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 19/29 | chr12 | 54402809 | |||||||
| chr12:54402859 | A | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0080 a0001c0001t0001g0101 others(1): Show |
12 | HG02257.hp2 HG02451.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1982+124T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 19/29 | chr12 | 54402859 | |||||||
| chr12:54402973 | C | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0041 others(3): Show |
22 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.1982+10G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 19/29 | chr12 | 54402973 | |||||||
| chr12:54403531 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1776+94A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 17/29 | chr12 | 54403531 | |||||||
| chr12:54403543 | G | A | 1 | a0001c0019t0004g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1776+82C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 17/29 | chr12 | 54403543 | |||||||
| chr12:54403544 | T | C | 9 | a0001c0002t0003g0009 a0001c0002t0003g0037 a0001c0002t0003g0056 others(6): Show |
14 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(11): Show |
intron_variant | MODIFIER | c.1776+81A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 17/29 | chr12 | 54403544 | |||||||
| chr12:54403556 | C | T | 1 | a0001c0019t0004g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1776+69G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 17/29 | chr12 | 54403556 | |||||||
| chr12:54403609 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0041 |
4 | HG00639.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1776+16C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 17/29 | chr12 | 54403609 | |||||||
| chr12:54403787 | C | G | 15 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0025 others(12): Show |
35 | HG00099.hp1 HG00558.hp2 HG00673.hp1 others(32): Show |
splice_region_variant&intron_variant | LOW | c.1622-8G>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 16/29 | chr12 | 54403787 | |||||||
| chr12:54403797 | T | A | 1 | a0001c0006t0006g0136 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1622-18A>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 16/29 | chr12 | 54403797 | |||||||
| chr12:54404264 | G | A | 9 | a0001c0002t0003g0009 a0001c0002t0003g0037 a0001c0002t0003g0056 others(6): Show |
14 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(11): Show |
intron_variant | MODIFIER | c.1464-18C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 14/29 | chr12 | 54404264 | |||||||
| chr12:54404303 | A | G | 2 | a0001c0001t0001g0083 a0001c0001t0001g0098 |
2 | HG02165.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.1464-57T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 14/29 | chr12 | 54404303 | |||||||
| chr12:54404353 | C | T | 1 | a0001c0002t0003g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1463+77G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 14/29 | chr12 | 54404353 | |||||||
| chr12:54404380 | C | T | 1 | a0001c0019t0004g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1463+50G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 14/29 | chr12 | 54404380 | |||||||
| chr12:54404507 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1418-32G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 13/29 | chr12 | 54404507 | |||||||
| chr12:54404909 | A | G | 9 | a0001c0002t0003g0009 a0001c0002t0003g0037 a0001c0002t0003g0056 others(6): Show |
14 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(11): Show |
intron_variant | MODIFIER | c.1226-15T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 12/29 | chr12 | 54404909 | |||||||
| chr12:54404968 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1226-74C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 12/29 | chr12 | 54404968 | |||||||
| chr12:54405451 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1017-77C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 11/29 | chr12 | 54405451 | |||||||
| chr12:54405939 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.907-13C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54405939 | |||||||
| chr12:54406080 | A | G | 2 | a0001c0015t0003g0050 a0001c0019t0004g0054 |
2 | HG02559.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.907-154T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54406080 | |||||||
| chr12:54406126 | C | G | 1 | a0001c0019t0004g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.907-200G>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54406126 | |||||||
| chr12:54406140 | C | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.907-214G>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54406140 | |||||||
| chr12:54406140 | C | T | 2 | a0001c0003t0004g0144 a0001c0003t0004g0145 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.907-214G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54406140 | |||||||
| chr12:54406329 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.907-403G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54406329 | |||||||
| chr12:54406764 | T | C | 8 | a0001c0002t0003g0009 a0001c0002t0003g0037 a0001c0002t0003g0056 others(5): Show |
13 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(10): Show |
intron_variant | MODIFIER | c.907-838A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54406764 | |||||||
| chr12:54406830 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.906+819T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54406830 | |||||||
| chr12:54406881 | G | A | 1 | a0006c0017t0001g0097 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.906+768C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54406881 | |||||||
| chr12:54406887 | C | T | 11 | a0001c0001t0002g0124 a0001c0002t0003g0009 a0001c0002t0003g0037 others(8): Show |
16 | HG01884.hp2 HG02523.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.906+762G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54406887 | |||||||
| chr12:54406902 | T | C | 1 | a0001c0019t0004g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.906+747A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54406902 | |||||||
| chr12:54407076 | G | T | 7 | a0001c0002t0003g0009 a0001c0002t0003g0056 a0001c0002t0003g0057 others(4): Show |
12 | HG02615.hp1 HG02698.hp1 HG03017.hp2 others(9): Show |
intron_variant | MODIFIER | c.906+573C>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54407076 | |||||||
| chr12:54407393 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.906+256G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54407393 | |||||||
| chr12:54407420 | G | A | 8 | a0001c0002t0003g0009 a0001c0002t0003g0037 a0001c0002t0003g0056 others(5): Show |
13 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(10): Show |
intron_variant | MODIFIER | c.906+229C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54407420 | |||||||
| chr12:54407495 | G | C | 1 | a0001c0001t0001g0133 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.906+154C>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54407495 | |||||||
| chr12:54407591 | C | T | 2 | a0001c0015t0003g0050 a0001c0019t0004g0054 |
2 | HG02559.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.906+58G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54407591 | |||||||
| chr12:54407592 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG02486.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.906+57C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54407592 | |||||||
| chr12:54407592 | G | T | 3 | a0001c0003t0004g0144 a0001c0003t0004g0145 a0001c0003t0004g0146 |
3 | HG02895.hp2 HG02897.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.906+57C>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 9/29 | chr12 | 54407592 | |||||||
| chr12:54407741 | A | G | 10 | a0001c0002t0003g0009 a0001c0002t0003g0037 a0001c0002t0003g0056 others(7): Show |
15 | HG01884.hp2 HG02559.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.863-49T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 8/29 | chr12 | 54407741 | |||||||
| chr12:54408246 | T | G | 12 | a0001c0002t0003g0009 a0001c0002t0003g0037 a0001c0002t0003g0056 others(9): Show |
17 | HG01884.hp2 HG02559.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.692-11A>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 6/29 | chr12 | 54408246 | |||||||
| chr12:54408306 | C | A | 13 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
35 | HG00733.hp1 HG00741.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.692-71G>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 6/29 | chr12 | 54408306 | |||||||
| chr12:54408392 | T | C | 1 | a0001c0003t0004g0146 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.692-157A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 6/29 | chr12 | 54408392 | |||||||
| chr12:54408482 | C | T | 8 | a0001c0002t0003g0009 a0001c0002t0003g0037 a0001c0002t0003g0056 others(5): Show |
13 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(10): Show |
intron_variant | MODIFIER | c.692-247G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 6/29 | chr12 | 54408482 | |||||||
| chr12:54408666 | T | C | 12 | a0001c0002t0003g0009 a0001c0002t0003g0037 a0001c0002t0003g0056 others(9): Show |
17 | HG01884.hp2 HG02559.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.691+90A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 6/29 | chr12 | 54408666 | |||||||
| chr12:54408709 | C | CA | 20 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0069 others(17): Show |
22 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.691+46dupT | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 6/29 | chr12 | 54408709 | |||||||
| chr12:54408709 | C | CAA | 5 | a0001c0001t0001g0044 a0001c0003t0004g0021 a0001c0003t0004g0034 others(2): Show |
6 | HG01109.hp1 HG02280.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.691+45_691+46dupTT | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 6/29 | chr12 | 54408709 | |||||||
| chr12:54408709 | C | CAAAA | 3 | a0001c0002t0003g0009 a0001c0002t0003g0037 a0001c0002t0003g0061 |
8 | HG01884.hp2 HG03017.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.691+43_691+46dupTT others(2): Show |
ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 6/29 | chr12 | 54408709 | |||||||
| chr12:54408854 | A | G | 10 | a0001c0002t0003g0009 a0001c0002t0003g0037 a0001c0002t0003g0056 others(7): Show |
15 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(12): Show |
intron_variant | MODIFIER | c.645+39T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 5/29 | chr12 | 54408854 | |||||||
| chr12:54408875 | C | T | 1 | a0001c0001t0002g0124 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.645+18G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 5/29 | chr12 | 54408875 | |||||||
| chr12:54408886 | C | G | 10 | a0001c0002t0003g0009 a0001c0002t0003g0037 a0001c0002t0003g0056 others(7): Show |
15 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.645+7G>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 5/29 | chr12 | 54408886 | |||||||
| chr12:54408983 | G | A | 10 | a0001c0002t0003g0009 a0001c0002t0003g0037 a0001c0002t0003g0056 others(7): Show |
15 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(12): Show |
intron_variant | MODIFIER | c.584-29C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 4/29 | chr12 | 54408983 | |||||||
| chr12:54409056 | G | C | 1 | a0001c0001t0001g0107 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.584-102C>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 4/29 | chr12 | 54409056 | |||||||
| chr12:54409067 | G | C | 16 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0025 others(13): Show |
36 | HG00099.hp1 HG00558.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.584-113C>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 4/29 | chr12 | 54409067 | |||||||
| chr12:54409088 | G | C | 8 | a0001c0002t0003g0009 a0001c0002t0003g0037 a0001c0002t0003g0056 others(5): Show |
13 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(10): Show |
intron_variant | MODIFIER | c.584-134C>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 4/29 | chr12 | 54409088 | |||||||
| chr12:54409144 | T | C | 1 | a0001c0005t0001g0137 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.583+88A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 4/29 | chr12 | 54409144 | |||||||
| chr12:54409478 | C | T | 1 | a0001c0001t0002g0124 | 1 | HG02523.hp2 | splice_region_variant&intron_variant | LOW | c.462+7G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 3/29 | chr12 | 54409478 | |||||||
| chr12:54409611 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0075 |
4 | HG00735.hp2 HG00738.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.350-14C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54409611 | |||||||
| chr12:54409820 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.350-223T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54409820 | |||||||
| chr12:54409843 | C | T | 3 | a0001c0019t0004g0054 a0001c0021t0001g0048 a0007c0020t0001g0047 |
3 | HG02559.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.350-246G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54409843 | |||||||
| chr12:54409913 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.350-316C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54409913 | |||||||
| chr12:54409918 | A | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(129): Show |
292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.350-321T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54409918 | |||||||
| chr12:54409927 | G | A | 8 | a0001c0002t0003g0009 a0001c0002t0003g0037 a0001c0002t0003g0056 others(5): Show |
13 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(10): Show |
intron_variant | MODIFIER | c.350-330C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54409927 | |||||||
| chr12:54409942 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0062 a0001c0015t0003g0050 |
7 | HG01071.hp1 HG01243.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.350-345G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54409942 | |||||||
| chr12:54410014 | A | G | 15 | a0001c0002t0003g0009 a0001c0002t0003g0037 a0001c0002t0003g0056 others(12): Show |
20 | HG01884.hp2 HG02559.hp2 HG02615.hp1 others(17): Show |
intron_variant | MODIFIER | c.350-417T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410014 | |||||||
| chr12:54410095 | C | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(129): Show |
292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.350-498G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410095 | |||||||
| chr12:54410153 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.350-556C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410153 | |||||||
| chr12:54410188 | G | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(87): Show |
225 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.350-591C>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410188 | |||||||
| chr12:54410234 | C | T | 12 | a0001c0002t0003g0009 a0001c0002t0003g0037 a0001c0002t0003g0056 others(9): Show |
17 | HG01884.hp2 HG02559.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.350-637G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410234 | |||||||
| chr12:54410331 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.350-734G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410331 | |||||||
| chr12:54410347 | C | CT | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
271 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.350-751dupA | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410347 | |||||||
| chr12:54410347 | C | CTT | 12 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0026 others(9): Show |
17 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.350-752_350-751dup others(2): Show |
ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410347 | |||||||
| chr12:54410503 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.350-906C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410503 | |||||||
| chr12:54410552 | A | AT | 9 | a0001c0001t0001g0072 a0001c0002t0003g0009 a0001c0002t0003g0056 others(6): Show |
14 | HG02145.hp1 HG02615.hp1 HG02698.hp1 others(11): Show |
intron_variant | MODIFIER | c.350-956dupA | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410552 | |||||||
| chr12:54410552 | AT | A | 6 | a0001c0001t0001g0040 a0001c0001t0001g0046 a0001c0001t0001g0118 others(3): Show |
6 | HG02922.hp2 HG02976.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.350-956delA | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410552 | |||||||
| chr12:54410679 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.350-1082G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410679 | |||||||
| chr12:54410725 | A | AT | 17 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0071 others(14): Show |
25 | HG01256.hp2 HG01258.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.349+1108dupA | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410725 | |||||||
| chr12:54410898 | T | A | 3 | a0001c0003t0004g0144 a0001c0003t0004g0145 a0001c0003t0004g0146 |
3 | HG02895.hp2 HG02897.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.349+936A>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54410898 | |||||||
| chr12:54411031 | C | G | 1 | a0001c0006t0006g0136 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.349+803G>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54411031 | |||||||
| chr12:54411160 | C | T | 9 | a0001c0001t0001g0015 a0001c0002t0003g0009 a0001c0002t0003g0037 others(6): Show |
16 | HG01884.hp2 HG02615.hp1 HG02698.hp1 others(13): Show |
intron_variant | MODIFIER | c.349+674G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54411160 | |||||||
| chr12:54411209 | T | G | 9 | a0001c0003t0004g0021 a0001c0003t0004g0034 a0001c0003t0004g0144 others(6): Show |
10 | HG02280.hp2 HG02559.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.349+625A>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54411209 | |||||||
| chr12:54411590 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0121 |
6 | HG00099.hp2 HG00639.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.349+244A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54411590 | |||||||
| chr12:54411731 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.349+103G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 2/29 | chr12 | 54411731 | |||||||
| chr12:54411969 | G | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(112): Show |
268 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(265): Show |
splice_region_variant&intron_variant | LOW | c.219-5C>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54411969 | |||||||
| chr12:54411981 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(104): Show |
260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.219-17G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54411981 | |||||||
| chr12:54412085 | C | A | 1 | a0001c0003t0004g0146 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.219-121G>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412085 | |||||||
| chr12:54412086 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.219-122C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412086 | |||||||
| chr12:54412158 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0123 |
3 | HG01109.hp2 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.219-194C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412158 | |||||||
| chr12:54412165 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.219-201G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412165 | |||||||
| chr12:54412253 | T | C | 1 | a0001c0001t0001g0020 | 3 | HG01192.hp1 HG04199.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.219-289A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412253 | |||||||
| chr12:54412283 | C | A | 5 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(2): Show |
6 | HG02280.hp2 HG02572.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-319G>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412283 | |||||||
| chr12:54412328 | A | G | 2 | a0001c0001t0002g0124 a0001c0002t0003g0037 |
2 | HG01884.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.219-364T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412328 | |||||||
| chr12:54412584 | G | A | 1 | a0001c0001t0002g0124 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.219-620C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412584 | |||||||
| chr12:54412754 | A | G | 2 | a0001c0001t0001g0022 a0001c0005t0001g0039 |
3 | HG02559.hp1 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.219-790T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412754 | |||||||
| chr12:54412834 | C | A | 10 | a0001c0001t0001g0140 a0001c0002t0003g0037 a0001c0003t0004g0144 others(7): Show |
10 | HG01884.hp2 HG02145.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-870G>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412834 | |||||||
| chr12:54412834 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.219-870G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412834 | |||||||
| chr12:54412925 | C | G | 1 | a0001c0002t0003g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.219-961G>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412925 | |||||||
| chr12:54412943 | T | C | 2 | a0001c0003t0004g0144 a0001c0003t0004g0145 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.219-979A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412943 | |||||||
| chr12:54412985 | C | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(129): Show |
292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.219-1021G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412985 | |||||||
| chr12:54412992 | C | G | 1 | a0001c0001t0001g0067 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.219-1028G>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54412992 | |||||||
| chr12:54413081 | G | GGTTTCTG others(314): Show |
1 | a0001c0001t0002g0124 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.219-1118_219-1117i others(323): Show |
ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54413081 | |||||||
| chr12:54413169 | A | G | 1 | a0001c0001t0001g0015 | 3 | HG02896.hp1 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.219-1205T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54413169 | |||||||
| chr12:54413261 | C | T | 1 | a0001c0001t0001g0015 | 3 | HG02896.hp1 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.219-1297G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54413261 | |||||||
| chr12:54413420 | T | C | 1 | a0001c0001t0001g0020 | 3 | HG01192.hp1 HG04199.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.219-1456A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54413420 | |||||||
| chr12:54413511 | A | G | 1 | a0001c0001t0001g0066 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.219-1547T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54413511 | |||||||
| chr12:54413646 | C | T | 7 | a0001c0001t0001g0140 a0001c0002t0003g0037 a0001c0005t0001g0135 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.219-1682G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54413646 | |||||||
| chr12:54413709 | A | C | 1 | a0001c0001t0001g0038 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.219-1745T>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54413709 | |||||||
| chr12:54413830 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.219-1866A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54413830 | |||||||
| chr12:54414102 | G | T | 1 | a0001c0002t0003g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.219-2138C>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414102 | |||||||
| chr12:54414119 | T | G | 1 | a0001c0001t0001g0128 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.219-2155A>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414119 | |||||||
| chr12:54414175 | C | T | 1 | a0001c0002t0003g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.219-2211G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414175 | |||||||
| chr12:54414212 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.219-2248G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414212 | |||||||
| chr12:54414226 | C | T | 1 | a0001c0005t0001g0135 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.219-2262G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414226 | |||||||
| chr12:54414557 | G | T | 1 | a0001c0001t0001g0015 | 3 | HG02896.hp1 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.219-2593C>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414557 | |||||||
| chr12:54414587 | CTGTAATC others(295): Show |
C | 7 | a0001c0002t0003g0009 a0001c0002t0003g0056 a0001c0002t0003g0057 others(4): Show |
12 | HG02615.hp1 HG02698.hp1 HG03017.hp2 others(9): Show |
intron_variant | MODIFIER | c.219-2925_219-2624d others(2): Show |
ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414587 | |||||||
| chr12:54414618 | GGGCAGAT others(295): Show |
G | 1 | a0001c0015t0003g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.219-2956_219-2655d others(2): Show |
ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414618 | |||||||
| chr12:54414673 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.219-2709G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414673 | |||||||
| chr12:54414676 | C | T | 1 | a0004c0016t0007g0063 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.219-2712G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414676 | |||||||
| chr12:54414708 | G | A | 6 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(3): Show |
7 | HG02280.hp2 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.219-2744C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414708 | |||||||
| chr12:54414803 | C | T | 2 | a0001c0003t0004g0144 a0001c0003t0004g0145 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.219-2839G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414803 | |||||||
| chr12:54414827 | C | T | 10 | a0001c0001t0001g0140 a0001c0002t0003g0037 a0001c0005t0001g0135 others(7): Show |
10 | HG01884.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.219-2863G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414827 | |||||||
| chr12:54414829 | G | C | 6 | a0001c0001t0001g0140 a0001c0005t0001g0135 a0001c0005t0001g0137 others(3): Show |
6 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-2865C>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414829 | |||||||
| chr12:54414832 | C | T | 3 | a0001c0003t0004g0144 a0001c0003t0004g0145 a0001c0003t0004g0146 |
3 | HG02895.hp2 HG02897.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.219-2868G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54414832 | |||||||
| chr12:54415008 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.219-3044G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54415008 | |||||||
| chr12:54415143 | C | T | 2 | a0001c0001t0002g0006 a0001c0001t0002g0035 |
13 | HG00597.hp2 HG02056.hp2 NA18939.hp2 others(10): Show |
intron_variant | MODIFIER | c.219-3179G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54415143 | |||||||
| chr12:54415144 | G | A | 2 | a0001c0021t0001g0048 a0007c0020t0001g0047 |
2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.219-3180C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54415144 | |||||||
| chr12:54415401 | G | A | 1 | a0001c0001t0001g0015 | 3 | HG02896.hp1 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.219-3437C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54415401 | |||||||
| chr12:54415404 | G | T | 1 | a0001c0001t0001g0062 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.219-3440C>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54415404 | |||||||
| chr12:54415513 | C | T | 1 | a0001c0001t0001g0015 | 3 | HG02896.hp1 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.218+3468G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54415513 | |||||||
| chr12:54415615 | T | C | 14 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0023 others(11): Show |
36 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.218+3366A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54415615 | |||||||
| chr12:54415711 | G | A | 21 | a0001c0001t0001g0015 a0001c0001t0001g0140 a0001c0002t0003g0009 others(18): Show |
28 | HG01891.hp2 HG02145.hp1 HG02559.hp2 others(25): Show |
intron_variant | MODIFIER | c.218+3270C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54415711 | |||||||
| chr12:54415774 | A | G | 1 | a0001c0002t0003g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.218+3207T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54415774 | |||||||
| chr12:54415800 | T | C | 21 | a0001c0001t0001g0015 a0001c0001t0001g0140 a0001c0002t0003g0009 others(18): Show |
28 | HG01891.hp2 HG02145.hp1 HG02559.hp2 others(25): Show |
intron_variant | MODIFIER | c.218+3181A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54415800 | |||||||
| chr12:54415880 | GGAGCT | G | 6 | a0001c0001t0001g0140 a0001c0005t0001g0135 a0001c0005t0001g0137 others(3): Show |
6 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+3096_218+3100d others(7): Show |
ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54415880 | |||||||
| chr12:54416195 | G | A | 8 | a0001c0002t0003g0009 a0001c0002t0003g0056 a0001c0002t0003g0057 others(5): Show |
13 | HG02615.hp1 HG02698.hp1 HG03017.hp2 others(10): Show |
intron_variant | MODIFIER | c.218+2786C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54416195 | |||||||
| chr12:54416236 | A | C | 2 | a0001c0003t0001g0142 a0001c0003t0001g0143 |
2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.218+2745T>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54416236 | |||||||
| chr12:54416542 | G | GGAGAACT others(4): Show |
21 | a0001c0001t0001g0015 a0001c0001t0001g0140 a0001c0002t0003g0009 others(18): Show |
28 | HG01891.hp2 HG02145.hp1 HG02559.hp2 others(25): Show |
intron_variant | MODIFIER | c.218+2438_218+2439i others(13): Show |
ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54416542 | |||||||
| chr12:54416546 | C | T | 21 | a0001c0001t0001g0015 a0001c0001t0001g0140 a0001c0002t0003g0009 others(18): Show |
28 | HG01891.hp2 HG02145.hp1 HG02559.hp2 others(25): Show |
intron_variant | MODIFIER | c.218+2435G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54416546 | |||||||
| chr12:54416551 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.218+2430G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54416551 | |||||||
| chr12:54416609 | G | A | 2 | a0001c0021t0001g0048 a0007c0020t0001g0047 |
2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.218+2372C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54416609 | |||||||
| chr12:54416735 | C | A | 1 | a0001c0001t0001g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.218+2246G>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54416735 | |||||||
| chr12:54416981 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0130 a0001c0001t0001g0131 others(2): Show |
12 | HG00735.hp1 HG01346.hp2 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.218+2000C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54416981 | |||||||
| chr12:54416981 | G | T | 1 | a0001c0019t0004g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.218+2000C>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54416981 | |||||||
| chr12:54416991 | C | T | 1 | a0005c0014t0001g0053 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.218+1990G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54416991 | |||||||
| chr12:54417053 | A | T | 1 | a0001c0001t0001g0052 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.218+1928T>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54417053 | |||||||
| chr12:54417070 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.218+1911C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54417070 | |||||||
| chr12:54417220 | C | G | 2 | a0001c0003t0001g0142 a0001c0003t0001g0143 |
2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.218+1761G>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54417220 | |||||||
| chr12:54417331 | G | A | 6 | a0001c0001t0001g0140 a0001c0005t0001g0135 a0001c0005t0001g0137 others(3): Show |
6 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+1650C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54417331 | |||||||
| chr12:54417439 | C | G | 1 | a0001c0001t0001g0051 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.218+1542G>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54417439 | |||||||
| chr12:54417538 | T | C | 1 | a0001c0001t0008g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.218+1443A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54417538 | |||||||
| chr12:54417671 | A | C | 1 | a0001c0015t0003g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.218+1310T>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54417671 | |||||||
| chr12:54417688 | G | A | 17 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0023 others(14): Show |
39 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.218+1293C>T | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54417688 | |||||||
| chr12:54417700 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.218+1281T>C | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54417700 | |||||||
| chr12:54417881 | C | T | 1 | a0008c0012t0001g0036 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.218+1100G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54417881 | |||||||
| chr12:54417924 | C | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0023 others(14): Show |
39 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.218+1057G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54417924 | |||||||
| chr12:54418016 | T | C | 2 | a0001c0003t0001g0142 a0001c0003t0001g0143 |
2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.218+965A>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54418016 | |||||||
| chr12:54418175 | A | T | 1 | a0001c0001t0002g0035 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.218+806T>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54418175 | |||||||
| chr12:54418585 | G | C | 3 | a0001c0003t0004g0144 a0001c0003t0004g0145 a0001c0003t0004g0146 |
3 | HG02895.hp2 HG02897.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.218+396C>G | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54418585 | |||||||
| chr12:54418691 | C | T | 2 | a0001c0003t0004g0021 a0001c0003t0004g0034 |
3 | HG02280.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.218+290G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54418691 | |||||||
| chr12:54418919 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.218+62G>A | ITGA5 | ENSG00000161638.11 | transcript | ENST00000293379.9 | protein_coding | 1/29 | chr12 | 54418919 |