Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3676 |
| ensemblid | ENSG00000115232.14 |
| hgncid | 6140 |
| symbol | ITGA4 |
| name | integrin subunit alpha 4 |
| refseq_nuc | NM_000885.6 |
| refseq_prot | NP_000876.3 |
| ensembl_nuc | ENST00000397033.7 |
| ensembl_prot | ENSP00000380227.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 181457386 |
| end | 181538940 |
| strand | + |
| ver | v1.2 |
| region | chr2:181457386-181538940 |
| region5000 | chr2:181452386-181543940 |
| regionname0 | ITGA4_chr2_181457386_181538940 |
| regionname5000 | ITGA4_chr2_181452386_181543940 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1032 | 274 | 58 | 48 | 139 | 8 | 20 | 106 | ITGA4_chr2_181452386_181543940 | ITGA4 | MAWEA others(1027): Show |
chr2 | 181452386 | 181543940 |
| a0002 | 1/0 | 1032 | 81 | 19 | 15 | 38 | 4 | 4 | 32 | ITGA4_chr2_181452386_181543940 | ITGA4 | MAWEA others(1027): Show |
chr2 | 181452386 | 181543940 |
| a0003 | 0/0 | 1032 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | MAWEA others(1027): Show |
chr2 | 181452386 | 181543940 |
| a0004 | 0/0 | 1032 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | MAWEA others(1027): Show |
chr2 | 181452386 | 181543940 |
| a0005 | 0/0 | 1032 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | MAWEA others(1027): Show |
chr2 | 181452386 | 181543940 |
| a0006 | 0/0 | 1032 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | MAWEA others(1027): Show |
chr2 | 181452386 | 181543940 |
| a0007 | 0/0 | 1032 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | MAWEA others(1027): Show |
chr2 | 181452386 | 181543940 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3096 | 194 | 44 | 31 | 96 | 5 | 17 | ITGA4_chr2_181452386_181543940 | ITGA4 | ATGGC others(3091): Show |
chr2 | 181452386 | 181543940 | ||
| a0001c0002 | 0/0 | 3096 | 75 | 13 | 17 | 42 | 2 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | ATGGC others(3091): Show |
chr2 | 181452386 | 181543940 | ||
| a0001c0007 | 0/0 | 3096 | 2 | 0 | 0 | 0 | 1 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | ATGGC others(3091): Show |
chr2 | 181452386 | 181543940 | ||
| a0001c0009 | 0/0 | 3096 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | ATGGC others(3091): Show |
chr2 | 181452386 | 181543940 | ||
| a0001c0013 | 0/0 | 3096 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | ATGGC others(3091): Show |
chr2 | 181452386 | 181543940 | ||
| a0001c0015 | 0/0 | 3096 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | ATGGC others(3091): Show |
chr2 | 181452386 | 181543940 | ||
| a0002c0003 | 0/0 | 3096 | 69 | 10 | 14 | 38 | 3 | 4 | ITGA4_chr2_181452386_181543940 | ITGA4 | ATGGC others(3091): Show |
chr2 | 181452386 | 181543940 | ||
| a0002c0005 | 0/0 | 3096 | 8 | 8 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | ATGGC others(3091): Show |
chr2 | 181452386 | 181543940 | ||
| a0002c0006 | 1/0 | 3096 | 2 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | ATGGC others(3091): Show |
chr2 | 181452386 | 181543940 | ||
| a0002c0011 | 0/0 | 3096 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | ATGGC others(3091): Show |
chr2 | 181452386 | 181543940 | ||
| a0002c0016 | 0/0 | 3096 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | ATGGC others(3091): Show |
chr2 | 181452386 | 181543940 | ||
| a0003c0004 | 0/0 | 3096 | 8 | 8 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | ATGGC others(3091): Show |
chr2 | 181452386 | 181543940 | ||
| a0003c0012 | 0/0 | 3096 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | ATGGC others(3091): Show |
chr2 | 181452386 | 181543940 | ||
| a0004c0014 | 0/0 | 3096 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | ATGGC others(3091): Show |
chr2 | 181452386 | 181543940 | ||
| a0005c0010 | 0/0 | 3096 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | ATGGC others(3091): Show |
chr2 | 181452386 | 181543940 | ||
| a0006c0017 | 0/0 | 3096 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | ATGGC others(3091): Show |
chr2 | 181452386 | 181543940 | ||
| a0007c0008 | 0/0 | 3096 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | ATGGC others(3091): Show |
chr2 | 181452386 | 181543940 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 6785 | 74 | 24 | 14 | 27 | 1 | 7 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| a0001c0001t0002 | 0/0 | 6785 | 69 | 15 | 12 | 32 | 3 | 7 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| a0001c0001t0006 | 0/0 | 6785 | 18 | 1 | 1 | 15 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| a0001c0001t0007 | 0/0 | 6785 | 7 | 0 | 1 | 5 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| a0001c0001t0010 | 0/0 | 6785 | 4 | 0 | 0 | 4 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| a0001c0001t0015 | 0/0 | 6785 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| a0001c0001t0019 | 0/0 | 6824 | 2 | 0 | 1 | 0 | 1 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6819): Show |
chr2 | 181452386 | 181543940 |
| a0001c0001t0020 | 0/0 | 6785 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| a0001c0001t0021 | 0/0 | 6785 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| a0001c0001t0024 | 0/0 | 6785 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| a0001c0001t0030 | 0/0 | 6785 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| a0001c0001t0032 | 0/0 | 6822 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6817): Show |
chr2 | 181452386 | 181543940 |
| a0001c0001t0033 | 0/0 | 6769 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6764): Show |
chr2 | 181452386 | 181543940 |
| a0001c0001t0035 | 0/0 | 6785 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| a0001c0001t0036 | 0/0 | 6785 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| a0001c0001t0037 | 0/0 | 6785 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| a0001c0001t0038 | 0/0 | 6785 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| a0001c0001t0039 | 0/0 | 6785 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| a0001c0001t0041 | 0/0 | 6785 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| a0001c0001t0051 | 0/0 | 6785 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| a0001c0001t0054 | 0/0 | 6785 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| a0001c0001t0057 | 0/0 | 6785 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| a0001c0002t0003 | 0/0 | 6780 | 49 | 2 | 15 | 31 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6775): Show |
chr2 | 181452386 | 181543940 |
| a0001c0002t0009 | 0/0 | 6780 | 5 | 0 | 1 | 4 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6775): Show |
chr2 | 181452386 | 181543940 |
| a0001c0002t0012 | 0/0 | 6780 | 4 | 4 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6775): Show |
chr2 | 181452386 | 181543940 |
| a0001c0002t0013 | 0/0 | 6793 | 4 | 0 | 0 | 4 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6788): Show |
chr2 | 181452386 | 181543940 |
| a0001c0002t0014 | 0/0 | 6780 | 3 | 3 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6775): Show |
chr2 | 181452386 | 181543940 |
| a0001c0002t0022 | 0/0 | 6780 | 2 | 0 | 0 | 0 | 2 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6775): Show |
chr2 | 181452386 | 181543940 |
| a0001c0002t0028 | 0/0 | 6780 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6775): Show |
chr2 | 181452386 | 181543940 |
| a0001c0002t0029 | 0/0 | 6793 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6788): Show |
chr2 | 181452386 | 181543940 |
| a0001c0002t0031 | 0/0 | 6781 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6776): Show |
chr2 | 181452386 | 181543940 |
| a0001c0002t0034 | 0/0 | 6781 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6776): Show |
chr2 | 181452386 | 181543940 |
| a0001c0002t0046 | 0/0 | 6780 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6775): Show |
chr2 | 181452386 | 181543940 |
| a0001c0002t0047 | 0/0 | 6780 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6775): Show |
chr2 | 181452386 | 181543940 |
| a0001c0002t0048 | 0/0 | 6781 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6776): Show |
chr2 | 181452386 | 181543940 |
| a0001c0002t0056 | 0/0 | 6781 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6776): Show |
chr2 | 181452386 | 181543940 |
| a0001c0007t0002 | 0/0 | 6785 | 2 | 0 | 0 | 0 | 1 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| a0001c0009t0002 | 0/0 | 6785 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| a0001c0013t0002 | 0/0 | 6785 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| a0001c0015t0040 | 0/0 | 6797 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6792): Show |
chr2 | 181452386 | 181543940 |
| a0002c0003t0004 | 0/0 | 6787 | 29 | 3 | 7 | 14 | 2 | 3 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6782): Show |
chr2 | 181452386 | 181543940 |
| a0002c0003t0005 | 0/0 | 6787 | 22 | 4 | 2 | 14 | 1 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6782): Show |
chr2 | 181452386 | 181543940 |
| a0002c0003t0011 | 0/0 | 6787 | 4 | 0 | 1 | 3 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6782): Show |
chr2 | 181452386 | 181543940 |
| a0002c0003t0017 | 0/0 | 6781 | 3 | 3 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6776): Show |
chr2 | 181452386 | 181543940 |
| a0002c0003t0018 | 0/0 | 6757 | 3 | 0 | 0 | 3 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6752): Show |
chr2 | 181452386 | 181543940 |
| a0002c0003t0023 | 0/0 | 6771 | 2 | 0 | 2 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6766): Show |
chr2 | 181452386 | 181543940 |
| a0002c0003t0025 | 0/0 | 6787 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6782): Show |
chr2 | 181452386 | 181543940 |
| a0002c0003t0026 | 0/0 | 6757 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6752): Show |
chr2 | 181452386 | 181543940 |
| a0002c0003t0027 | 0/0 | 6787 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6782): Show |
chr2 | 181452386 | 181543940 |
| a0002c0003t0044 | 0/0 | 6787 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6782): Show |
chr2 | 181452386 | 181543940 |
| a0002c0003t0045 | 0/0 | 6787 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6782): Show |
chr2 | 181452386 | 181543940 |
| a0002c0003t0055 | 0/0 | 6787 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6782): Show |
chr2 | 181452386 | 181543940 |
| a0002c0005t0001 | 0/0 | 6785 | 5 | 5 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| a0002c0005t0016 | 0/0 | 6785 | 3 | 3 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| a0002c0006t0052 | 0/0 | 6781 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6776): Show |
chr2 | 181452386 | 181543940 |
| a0002c0006t0053 | 1/0 | 6781 | 1 | 0 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6776): Show |
chr2 | 181452386 | 181543940 |
| a0002c0011t0043 | 0/0 | 6775 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6770): Show |
chr2 | 181452386 | 181543940 |
| a0002c0016t0004 | 0/0 | 6787 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6782): Show |
chr2 | 181452386 | 181543940 |
| a0003c0004t0008 | 0/0 | 6767 | 6 | 6 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6762): Show |
chr2 | 181452386 | 181543940 |
| a0003c0004t0049 | 0/0 | 6767 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6762): Show |
chr2 | 181452386 | 181543940 |
| a0003c0004t0050 | 0/0 | 6767 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6762): Show |
chr2 | 181452386 | 181543940 |
| a0003c0012t0021 | 0/0 | 6785 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| a0004c0014t0002 | 0/0 | 6785 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| a0005c0010t0042 | 0/0 | 6787 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6782): Show |
chr2 | 181452386 | 181543940 |
| a0006c0017t0005 | 0/0 | 6787 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6782): Show |
chr2 | 181452386 | 181543940 |
| a0007c0008t0001 | 0/0 | 6785 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | GAAGC others(6780): Show |
chr2 | 181452386 | 181543940 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0075 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0002g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0006g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0006g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0006g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0006g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0006g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0006g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0006g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0006g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0006g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0006g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0006g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0006g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0006g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0006g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0006g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0006g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0006g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0007g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0007g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0007g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0007g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0007g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0007g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0007g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0010g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0010g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0010g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0010g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0015g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0015g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0015g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0019g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0019g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0020g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0020g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0021g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0024g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0024g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0030g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0032g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0033g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0035g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0036g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0037g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0038g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0039g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0041g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0051g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0054g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0001t0057g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0009g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0009g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0009g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0009g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0009g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0012g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0012g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0012g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0012g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0013g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0013g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0013g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0013g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0014g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0014g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0014g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0022g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0028g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0029g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0031g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0034g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0046g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0047g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0048g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0002t0056g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0007t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0007t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0009t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0013t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0001c0015t0040g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0004g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0005g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0005g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0005g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0005g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0005g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0005g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0005g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0011g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0011g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0011g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0017g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0017g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0017g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0018g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0018g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0018g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0023g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0023g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0025g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0026g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0027g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0044g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0045g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0003t0055g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0005t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0005t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0005t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0005t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0005t0016g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0006t0052g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0006t0053g0275 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0011t0043g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0002c0016t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0003c0004t0008g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0003c0004t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0003c0004t0008g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0003c0004t0008g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0003c0004t0008g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0003c0004t0049g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0003c0004t0050g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0003c0012t0021g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0004c0014t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0005c0010t0042g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0006c0017t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| a0007c0008t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0283 | EUR | GBR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00099 | hp2 | a0002 | c0003 | t0005 | g0269 | EUR | GBR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0066 | EUR | GBR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00140 | hp2 | a0002 | c0003 | t0004 | g0342 | EUR | GBR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | FIN | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00323 | hp2 | a0001 | c0001 | t0019 | g0095 | EUR | FIN | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00408 | hp2 | a0001 | c0002 | t0003 | g0175 | EAS | CHS | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00423 | hp1 | a0001 | c0002 | t0003 | g0193 | EAS | CHS | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00423 | hp2 | a0001 | c0001 | t0006 | g0250 | EAS | CHS | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00438 | hp1 | a0001 | c0002 | t0003 | g0090 | EAS | CHS | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | CHS | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | CHS | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00544 | hp2 | a0002 | c0003 | t0004 | g0140 | EAS | CHS | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | CHS | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00558 | hp2 | a0001 | c0002 | t0003 | g0318 | EAS | CHS | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00597 | hp1 | a0001 | c0001 | t0007 | g0266 | EAS | CHS | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00597 | hp2 | a0001 | c0002 | t0009 | g0218 | EAS | CHS | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00609 | hp1 | a0001 | c0002 | t0013 | g0300 | EAS | CHS | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00609 | hp2 | a0002 | c0003 | t0018 | g0324 | EAS | CHS | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00621 | hp1 | a0002 | c0003 | t0018 | g0146 | EAS | CHS | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | CHS | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00642 | hp1 | a0002 | c0003 | t0004 | g0126 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00642 | hp2 | a0002 | c0003 | t0044 | g0078 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00673 | hp2 | a0004 | c0014 | t0002 | g0070 | EAS | CHS | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00733 | hp1 | a0001 | c0001 | t0007 | g0258 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0346 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00735 | hp2 | a0002 | c0003 | t0023 | g0004 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00738 | hp1 | a0002 | c0003 | t0005 | g0239 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00738 | hp2 | a0001 | c0002 | t0009 | g0267 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0284 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG00741 | hp2 | a0001 | c0002 | t0003 | g0046 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01070 | hp1 | a0002 | c0003 | t0023 | g0057 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01070 | hp2 | a0001 | c0002 | t0003 | g0015 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0015 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01081 | hp1 | a0001 | c0002 | t0034 | g0345 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01081 | hp2 | a0002 | c0003 | t0004 | g0059 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01099 | hp2 | a0001 | c0001 | t0036 | g0162 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01106 | hp1 | a0002 | c0003 | t0004 | g0169 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01106 | hp2 | a0001 | c0002 | t0003 | g0170 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01109 | hp1 | a0002 | c0003 | t0004 | g0125 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01109 | hp2 | a0001 | c0001 | t0019 | g0292 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01175 | hp1 | a0002 | c0003 | t0004 | g0004 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0260 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01243 | hp2 | a0002 | c0016 | t0004 | g0116 | AMR | PUR | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01257 | hp1 | a0001 | c0002 | t0003 | g0014 | AMR | CLM | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0074 | AMR | CLM | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01258 | hp1 | a0001 | c0002 | t0003 | g0014 | AMR | CLM | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01361 | hp1 | a0001 | c0002 | t0003 | g0073 | AMR | CLM | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01496 | hp1 | a0002 | c0003 | t0027 | g0268 | AMR | CLM | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01516 | hp1 | a0001 | c0007 | t0002 | g0079 | EUR | IBS | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01516 | hp2 | a0001 | c0002 | t0022 | g0018 | EUR | IBS | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01517 | hp1 | a0001 | c0002 | t0022 | g0018 | EUR | IBS | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01517 | hp2 | a0002 | c0003 | t0004 | g0038 | EUR | IBS | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01884 | hp2 | a0003 | c0004 | t0008 | g0023 | AFR | ACB | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01891 | hp1 | a0002 | c0005 | t0001 | g0197 | AFR | ACB | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01934 | hp1 | a0001 | c0002 | t0003 | g0210 | AMR | PEL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01943 | hp2 | a0001 | c0002 | t0003 | g0061 | AMR | PEL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | PEL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01952 | hp2 | a0001 | c0001 | t0033 | g0005 | AMR | PEL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01975 | hp1 | a0002 | c0003 | t0005 | g0237 | AMR | PEL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01978 | hp1 | a0002 | c0003 | t0004 | g0221 | AMR | PEL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01978 | hp2 | a0001 | c0002 | t0003 | g0106 | AMR | PEL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01981 | hp2 | a0001 | c0002 | t0003 | g0180 | AMR | PEL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02004 | hp2 | a0002 | c0003 | t0011 | g0257 | AMR | PEL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02015 | hp1 | a0001 | c0001 | t0057 | g0108 | EAS | KHV | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02015 | hp2 | a0002 | c0003 | t0005 | g0235 | EAS | KHV | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02040 | hp1 | a0001 | c0001 | t0041 | g0021 | EAS | KHV | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02040 | hp2 | a0001 | c0002 | t0003 | g0178 | EAS | KHV | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02055 | hp1 | a0003 | c0004 | t0008 | g0196 | AFR | ACB | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0313 | AFR | ACB | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | KHV | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02071 | hp1 | a0001 | c0001 | t0007 | g0256 | EAS | KHV | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02071 | hp2 | a0001 | c0001 | t0035 | g0307 | EAS | KHV | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02129 | hp1 | a0002 | c0003 | t0005 | g0234 | EAS | KHV | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | KHV | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02132 | hp1 | a0001 | c0002 | t0003 | g0334 | EAS | KHV | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02132 | hp2 | a0001 | c0001 | t0015 | g0233 | EAS | KHV | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | ACB | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02148 | hp2 | a0001 | c0002 | t0003 | g0211 | AMR | PEL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | CDX | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CDX | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | CDX | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02165 | hp2 | a0002 | c0003 | t0004 | g0198 | EAS | CDX | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02257 | hp1 | a0002 | c0005 | t0001 | g0173 | AFR | ACB | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PEL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02273 | hp2 | a0001 | c0002 | t0003 | g0311 | AMR | PEL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | ACB | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02293 | hp2 | a0001 | c0002 | t0003 | g0172 | AMR | PEL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02300 | hp1 | a0005 | c0010 | t0042 | g0065 | AMR | PEL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02300 | hp2 | a0001 | c0002 | t0003 | g0222 | AMR | PEL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02451 | hp1 | a0002 | c0005 | t0016 | g0002 | AFR | ACB | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02451 | hp2 | a0001 | c0002 | t0012 | g0335 | AFR | ACB | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02523 | hp1 | a0001 | c0001 | t0010 | g0135 | EAS | KHV | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | KHV | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02572 | hp1 | a0002 | c0003 | t0004 | g0131 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02615 | hp1 | a0001 | c0002 | t0048 | g0273 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02622 | hp1 | a0001 | c0002 | t0003 | g0010 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02622 | hp2 | a0002 | c0005 | t0001 | g0282 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02630 | hp2 | a0002 | c0003 | t0005 | g0259 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02647 | hp1 | a0003 | c0004 | t0008 | g0007 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02683 | hp2 | a0001 | c0009 | t0002 | g0195 | SAS | PJL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02717 | hp1 | a0002 | c0003 | t0017 | g0039 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02717 | hp2 | a0001 | c0002 | t0003 | g0010 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02723 | hp1 | a0001 | c0002 | t0014 | g0279 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02723 | hp2 | a0002 | c0003 | t0017 | g0164 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | PJL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02735 | hp2 | a0002 | c0003 | t0004 | g0060 | SAS | PJL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02809 | hp1 | a0002 | c0003 | t0004 | g0286 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02818 | hp2 | a0002 | c0005 | t0016 | g0002 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02896 | hp1 | a0002 | c0005 | t0016 | g0002 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02922 | hp1 | a0001 | c0001 | t0021 | g0115 | AFR | ESN | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0225 | AFR | ESN | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ESN | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | ESN | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02976 | hp1 | a0002 | c0003 | t0005 | g0223 | AFR | ESN | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02976 | hp2 | a0003 | c0012 | t0021 | g0274 | AFR | ESN | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03041 | hp1 | a0001 | c0002 | t0031 | g0220 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03041 | hp2 | a0003 | c0004 | t0008 | g0103 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | MSL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03130 | hp2 | a0003 | c0004 | t0049 | g0098 | AFR | ESN | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03139 | hp1 | a0001 | c0015 | t0040 | g0111 | AFR | ESN | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03195 | hp2 | a0001 | c0002 | t0014 | g0278 | AFR | ESN | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | MSL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03209 | hp2 | a0002 | c0003 | t0005 | g0224 | AFR | MSL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | MSL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03239 | hp2 | a0002 | c0003 | t0005 | g0238 | SAS | PJL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03453 | hp1 | a0001 | c0002 | t0012 | g0338 | AFR | MSL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03453 | hp2 | a0002 | c0005 | t0001 | g0009 | AFR | MSL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03486 | hp1 | a0002 | c0003 | t0017 | g0129 | AFR | MSL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0309 | SAS | PJL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03540 | hp1 | a0001 | c0001 | t0037 | g0089 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0341 | AFR | GWD | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03579 | hp1 | a0002 | c0005 | t0001 | g0009 | AFR | MSL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03654 | hp1 | a0001 | c0001 | t0007 | g0236 | SAS | PJL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0293 | SAS | PJL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03669 | hp1 | a0002 | c0003 | t0004 | g0161 | SAS | PJL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0308 | SAS | PJL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03704 | hp1 | a0001 | c0001 | t0032 | g0321 | SAS | PJL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03710 | hp2 | a0001 | c0001 | t0006 | g0216 | SAS | PJL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03942 | hp2 | a0001 | c0007 | t0002 | g0080 | SAS | BEB | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG04199 | hp1 | a0001 | c0002 | t0003 | g0297 | SAS | STU | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | STU | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | STU | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG04204 | hp2 | a0002 | c0003 | t0004 | g0058 | SAS | STU | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18612 | hp1 | a0001 | c0001 | t0010 | g0165 | EAS | CHB | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHB | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18747 | hp1 | a0001 | c0002 | t0003 | g0305 | EAS | CHB | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18747 | hp2 | a0001 | c0001 | t0030 | g0215 | EAS | CHB | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | YRI | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18939 | hp1 | a0001 | c0002 | t0003 | g0314 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18940 | hp1 | a0002 | c0003 | t0004 | g0137 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18940 | hp2 | a0001 | c0002 | t0003 | g0204 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18941 | hp2 | a0001 | c0002 | t0003 | g0171 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18943 | hp1 | a0001 | c0002 | t0003 | g0319 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18944 | hp2 | a0001 | c0002 | t0003 | g0177 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18945 | hp1 | a0002 | c0003 | t0004 | g0132 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18946 | hp2 | a0001 | c0002 | t0003 | g0331 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18950 | hp1 | a0006 | c0017 | t0005 | g0229 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18950 | hp2 | a0001 | c0002 | t0028 | g0130 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18951 | hp1 | a0002 | c0003 | t0005 | g0255 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18951 | hp2 | a0001 | c0001 | t0006 | g0251 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18954 | hp1 | a0002 | c0003 | t0005 | g0001 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18957 | hp2 | a0002 | c0003 | t0011 | g0016 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18959 | hp1 | a0001 | c0002 | t0003 | g0020 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18959 | hp2 | a0001 | c0001 | t0024 | g0067 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18964 | hp2 | a0002 | c0003 | t0005 | g0001 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18966 | hp2 | a0002 | c0003 | t0004 | g0206 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18968 | hp1 | a0002 | c0003 | t0011 | g0016 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18968 | hp2 | a0001 | c0001 | t0006 | g0262 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18969 | hp1 | a0001 | c0001 | t0006 | g0249 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18969 | hp2 | a0001 | c0002 | t0003 | g0190 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18970 | hp2 | a0002 | c0003 | t0004 | g0212 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18971 | hp1 | a0001 | c0001 | t0051 | g0299 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18971 | hp2 | a0001 | c0001 | t0006 | g0230 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18972 | hp1 | a0001 | c0001 | t0006 | g0185 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18972 | hp2 | a0001 | c0002 | t0003 | g0287 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18974 | hp1 | a0001 | c0002 | t0003 | g0332 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18975 | hp2 | a0002 | c0003 | t0004 | g0181 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18977 | hp1 | a0001 | c0001 | t0006 | g0270 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18977 | hp2 | a0002 | c0003 | t0005 | g0240 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18983 | hp1 | a0002 | c0003 | t0005 | g0241 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18983 | hp2 | a0001 | c0013 | t0002 | g0163 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18984 | hp1 | a0001 | c0001 | t0006 | g0227 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18984 | hp2 | a0002 | c0003 | t0004 | g0168 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18986 | hp1 | a0002 | c0003 | t0025 | g0265 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18987 | hp1 | a0001 | c0002 | t0013 | g0298 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18987 | hp2 | a0001 | c0001 | t0006 | g0124 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18989 | hp2 | a0001 | c0002 | t0003 | g0316 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18990 | hp2 | a0001 | c0002 | t0003 | g0243 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18991 | hp1 | a0001 | c0002 | t0003 | g0179 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18993 | hp1 | a0002 | c0003 | t0005 | g0231 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18995 | hp1 | a0001 | c0001 | t0006 | g0214 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18995 | hp2 | a0001 | c0002 | t0009 | g0188 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18998 | hp1 | a0001 | c0001 | t0006 | g0261 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19000 | hp1 | a0001 | c0001 | t0006 | g0263 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19000 | hp2 | a0001 | c0002 | t0003 | g0203 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19001 | hp1 | a0001 | c0002 | t0003 | g0150 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19001 | hp2 | a0002 | c0003 | t0005 | g0271 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19002 | hp1 | a0001 | c0001 | t0054 | g0081 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19003 | hp1 | a0002 | c0003 | t0026 | g0254 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19003 | hp2 | a0001 | c0002 | t0029 | g0343 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19004 | hp1 | a0002 | c0003 | t0004 | g0205 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19004 | hp2 | a0001 | c0001 | t0006 | g0186 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19005 | hp1 | a0001 | c0001 | t0020 | g0322 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19007 | hp1 | a0001 | c0001 | t0015 | g0122 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19007 | hp2 | a0001 | c0002 | t0003 | g0199 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19010 | hp2 | a0002 | c0003 | t0004 | g0194 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19011 | hp1 | a0002 | c0003 | t0011 | g0133 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19030 | hp1 | a0002 | c0003 | t0005 | g0247 | AFR | LWK | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19030 | hp2 | a0002 | c0006 | t0052 | g0272 | AFR | LWK | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19043 | hp1 | a0001 | c0001 | t0039 | g0339 | AFR | LWK | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19043 | hp2 | a0001 | c0002 | t0046 | g0158 | AFR | LWK | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19054 | hp2 | a0002 | c0003 | t0045 | g0019 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19056 | hp1 | a0001 | c0002 | t0013 | g0295 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19057 | hp1 | a0001 | c0002 | t0009 | g0226 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19057 | hp2 | a0001 | c0001 | t0020 | g0142 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19060 | hp1 | a0001 | c0001 | t0010 | g0091 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19060 | hp2 | a0001 | c0002 | t0009 | g0264 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19062 | hp1 | a0002 | c0003 | t0004 | g0294 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19063 | hp1 | a0002 | c0003 | t0005 | g0001 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19063 | hp2 | a0001 | c0002 | t0003 | g0289 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19064 | hp1 | a0001 | c0001 | t0007 | g0213 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19064 | hp2 | a0001 | c0002 | t0003 | g0157 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19066 | hp1 | a0001 | c0001 | t0007 | g0123 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19068 | hp1 | a0001 | c0001 | t0007 | g0217 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19068 | hp2 | a0002 | c0003 | t0005 | g0001 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19072 | hp1 | a0001 | c0001 | t0006 | g0248 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19072 | hp2 | a0002 | c0003 | t0004 | g0317 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19074 | hp1 | a0001 | c0002 | t0003 | g0315 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19074 | hp2 | a0002 | c0003 | t0005 | g0253 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19075 | hp1 | a0001 | c0001 | t0015 | g0228 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19075 | hp2 | a0001 | c0002 | t0003 | g0291 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19076 | hp2 | a0001 | c0002 | t0003 | g0191 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19078 | hp2 | a0001 | c0002 | t0013 | g0192 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19079 | hp1 | a0001 | c0001 | t0024 | g0069 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19079 | hp2 | a0001 | c0002 | t0003 | g0302 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19080 | hp1 | a0001 | c0002 | t0003 | g0288 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19080 | hp2 | a0002 | c0003 | t0004 | g0301 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19082 | hp2 | a0002 | c0003 | t0055 | g0019 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19084 | hp2 | a0001 | c0002 | t0047 | g0306 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19086 | hp1 | a0001 | c0001 | t0010 | g0325 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19088 | hp2 | a0002 | c0003 | t0018 | g0092 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19089 | hp1 | a0002 | c0003 | t0005 | g0187 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19089 | hp2 | a0007 | c0008 | t0001 | g0120 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19091 | hp1 | a0001 | c0002 | t0003 | g0207 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA19091 | hp2 | a0002 | c0003 | t0005 | g0232 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ASW | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA20129 | hp2 | a0003 | c0004 | t0050 | g0285 | AFR | ASW | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA20805 | hp1 | a0002 | c0011 | t0043 | g0119 | EUR | TSI | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0312 | EUR | TSI | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01123 | hp1 | a0002 | c0003 | t0004 | g0056 | AMR | CLM | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0333 | AMR | CLM | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02109 | hp1 | a0001 | c0002 | t0014 | g0277 | AFR | ACB | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02109 | hp2 | a0003 | c0004 | t0008 | g0166 | AFR | ACB | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02486 | hp1 | a0001 | c0002 | t0056 | g0160 | AFR | ACB | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02559 | hp1 | a0002 | c0003 | t0004 | g0344 | AFR | ACB | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03471 | hp1 | a0001 | c0002 | t0012 | g0337 | AFR | MSL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18955 | hp1 | a0002 | c0003 | t0004 | g0323 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA18955 | hp2 | a0001 | c0001 | t0006 | g0252 | EAS | JPT | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA20300 | hp1 | a0001 | c0002 | t0012 | g0336 | AFR | USA | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | USA | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA21309 | hp1 | a0003 | c0004 | t0008 | g0007 | AFR | LWK | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| NA21309 | hp2 | a0001 | c0001 | t0038 | g0110 | AFR | LWK | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0075 | REF | REF | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| homoSapiens | grch38p0 | a0002 | c0006 | t0053 | g0275 | REF | REF | ITGA4_chr2_181452386_181543940 | ITGA4 | chr2 | 181452386 | 181543940 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:181481625 | G | A | 1 | a0007 | 1 | NA19089.hp2 | missense_variant | MODERATE | c.782G>A | p.Arg261Gln | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 7/28 | 1051/6781 | 782/3099 | 261/1032 | chr2 | 181481625 | |||
| chr2:181509740 | C | T | 1 | a0006 | 1 | NA18950.hp1 | missense_variant | MODERATE | c.1778C>T | p.Thr593Ile | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 16/28 | 2047/6781 | 1778/3099 | 593/1032 | chr2 | 181509740 | |||
| chr2:181511753 | T | A | 1 | a0003 | 9 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
missense_variant | MODERATE | c.1900T>A | p.Ser634Thr | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/28 | 2169/6781 | 1900/3099 | 634/1032 | chr2 | 181511753 | |||
| chr2:181530618 | G | A | 4 | a0001 a0003 a0004 others(1): Show |
284 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(281): Show |
missense_variant | MODERATE | c.2633G>A | p.Arg878Gln | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 24/28 | 2902/6781 | 2633/3099 | 878/1032 | chr2 | 181530618 | |||
| chr2:181531730 | C | A | 1 | a0005 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.2738C>A | p.Ala913Asp | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/28 | 3007/6781 | 2738/3099 | 913/1032 | chr2 | 181531730 | |||
| chr2:181534901 | T | C | 1 | a0004 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.2969T>C | p.Ile990Thr | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 27/28 | 3238/6781 | 2969/3099 | 990/1032 | chr2 | 181534901 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:181509807 | A | G | 9 | a0001c0001 a0001c0007 a0001c0013 others(6): Show |
209 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(206): Show |
splice_region_variant&synonymous_variant | LOW | c.1845A>G | p.Thr615Thr | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 16/28 | 2114/6781 | 1845/3099 | 615/1032 | chr2 | 181509807 | |||
| chr2:181530647 | T | C | 1 | a0001c0013 | 1 | NA18983.hp2 | splice_region_variant&synonymous_variant | LOW | c.2662T>C | p.Leu888Leu | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 24/28 | 2931/6781 | 2662/3099 | 888/1032 | chr2 | 181530647 | |||
| chr2:181534370 | T | C | 9 | a0001c0001 a0001c0007 a0001c0009 others(6): Show |
209 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(206): Show |
splice_region_variant&synonymous_variant | LOW | c.2883T>C | p.His961His | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 26/28 | 3152/6781 | 2883/3099 | 961/1032 | chr2 | 181534370 | |||
| chr2:181534911 | A | G | 16 | a0001c0001 a0001c0002 a0001c0007 others(13): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
synonymous_variant | LOW | c.2979A>G | p.Leu993Leu | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 27/28 | 3248/6781 | 2979/3099 | 993/1032 | chr2 | 181534911 | |||
| chr2:181535506 | C | T | 1 | a0001c0007 | 2 | HG01516.hp1 HG03942.hp2 |
synonymous_variant | LOW | c.3078C>T | p.Asn1026Asn | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 3347/6781 | 3078/3099 | 1026/1032 | chr2 | 181535506 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:181457441 | CG | C | 1 | a0001c0002t0014 | 3 | HG02109.hp1 HG02723.hp1 HG03195.hp2 |
5_prime_UTR_variant | MODIFIER | c.-211delG | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 1/28 | 211 | INFO_REALIGN_3_PRIME | chr2 | 181457441 | |||||
| chr2:181457476 | G | T | 1 | a0001c0001t0057 | 1 | HG02015.hp1 | 5_prime_UTR_variant | MODIFIER | c.-179G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 1/28 | 179 | chr2 | 181457476 | ||||||
| chr2:181457493 | C | A | 12 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0015 others(9): Show |
62 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(59): Show |
5_prime_UTR_variant | MODIFIER | c.-162C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 1/28 | 162 | chr2 | 181457493 | ||||||
| chr2:181457600 | C | T | 1 | a0001c0002t0056 | 1 | HG02486.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-55C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 1/28 | chr2 | 181457600 | |||||||
| chr2:181457622 | C | T | 1 | a0001c0001t0030 | 1 | NA18747.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-33C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 1/28 | chr2 | 181457622 | |||||||
| chr2:181457641 | C | G | 1 | a0001c0001t0024 | 2 | NA18959.hp2 NA19079.hp1 |
5_prime_UTR_variant | MODIFIER | c.-14C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 1/28 | 14 | chr2 | 181457641 | ||||||
| chr2:181535718 | G | A | 1 | a0001c0002t0031 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*191G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 191 | chr2 | 181535718 | ||||||
| chr2:181535736 | A | C | 1 | a0002c0003t0055 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*209A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 209 | chr2 | 181535736 | ||||||
| chr2:181536014 | C | T | 1 | a0001c0001t0054 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*487C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 487 | chr2 | 181536014 | ||||||
| chr2:181536033 | TTAAAGCC others(9): Show |
T | 1 | a0002c0003t0023 | 2 | HG00735.hp2 HG01070.hp1 |
3_prime_UTR_variant | MODIFIER | c.*510_*525delAGCCCT others(10): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 510 | INFO_REALIGN_3_PRIME | chr2 | 181536033 | |||||
| chr2:181536037 | A | C | 1 | a0001c0001t0006 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*510A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 510 | chr2 | 181536037 | ||||||
| chr2:181536104 | G | GAATATTA others(30): Show |
1 | a0001c0001t0032 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*578_*614dupAATATT others(31): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 615 | INFO_REALIGN_3_PRIME | chr2 | 181536104 | |||||
| chr2:181536178 | T | G | 64 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(61): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
3_prime_UTR_variant | MODIFIER | c.*651T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 651 | chr2 | 181536178 | ||||||
| chr2:181536217 | C | T | 1 | a0001c0001t0051 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*690C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 690 | chr2 | 181536217 | ||||||
| chr2:181536310 | G | A | 1 | a0002c0005t0016 | 3 | HG02451.hp1 HG02818.hp2 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*783G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 783 | chr2 | 181536310 | ||||||
| chr2:181536382 | T | TGATACA | 15 | a0002c0003t0004 a0002c0003t0005 a0002c0003t0011 others(12): Show |
70 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*856_*861dupGATACA | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 862 | INFO_REALIGN_3_PRIME | chr2 | 181536382 | |||||
| chr2:181536389 | C | T | 14 | a0001c0002t0003 a0001c0002t0009 a0001c0002t0012 others(11): Show |
78 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*862C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 862 | chr2 | 181536389 | ||||||
| chr2:181536521 | T | A | 1 | a0002c0006t0052 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*994T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 994 | chr2 | 181536521 | ||||||
| chr2:181536543 | C | CTTTACAA others(9): Show |
30 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(27): Show |
208 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(205): Show |
3_prime_UTR_variant | MODIFIER | c.*1019_*1034dupTACA others(12): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 1035 | INFO_REALIGN_3_PRIME | chr2 | 181536543 | |||||
| chr2:181536585 | AAAATTCA others(7): Show |
A | 3 | a0003c0004t0008 a0003c0004t0049 a0003c0004t0050 |
8 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1074_*1087delAATT others(10): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 1074 | INFO_REALIGN_3_PRIME | chr2 | 181536585 | |||||
| chr2:181536661 | C | T | 6 | a0001c0001t0021 a0001c0001t0041 a0001c0002t0014 others(3): Show |
8 | HG01081.hp1 HG02040.hp1 HG02109.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1134C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 1134 | chr2 | 181536661 | ||||||
| chr2:181536688 | A | AATATTTT others(9): Show |
1 | a0001c0001t0019 | 2 | HG00323.hp2 HG01109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1162_*1177dupATAT others(12): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 1178 | INFO_REALIGN_3_PRIME | chr2 | 181536688 | |||||
| chr2:181536839 | C | T | 64 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(61): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
3_prime_UTR_variant | MODIFIER | c.*1312C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 1312 | chr2 | 181536839 | ||||||
| chr2:181536860 | C | T | 1 | a0002c0003t0027 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1333C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 1333 | chr2 | 181536860 | ||||||
| chr2:181536924 | G | GGAAAGAT others(6): Show |
2 | a0001c0002t0013 a0001c0002t0029 |
5 | HG00609.hp1 NA18987.hp1 NA19003.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1398_*1410dupGAAA others(9): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 1411 | INFO_REALIGN_3_PRIME | chr2 | 181536924 | |||||
| chr2:181537025 | G | A | 18 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0010 others(15): Show |
112 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*1498G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 1498 | chr2 | 181537025 | ||||||
| chr2:181537139 | C | T | 3 | a0001c0002t0014 a0001c0002t0031 a0001c0002t0034 |
5 | HG01081.hp1 HG02109.hp1 HG02723.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1612C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 1612 | chr2 | 181537139 | ||||||
| chr2:181537140 | G | A | 3 | a0003c0004t0008 a0003c0004t0049 a0005c0010t0042 |
8 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1613G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 1613 | chr2 | 181537140 | ||||||
| chr2:181537230 | G | T | 17 | a0001c0002t0003 a0001c0002t0009 a0001c0002t0012 others(14): Show |
83 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*1703G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 1703 | chr2 | 181537230 | ||||||
| chr2:181537269 | G | C | 3 | a0003c0004t0008 a0003c0004t0049 a0003c0004t0050 |
8 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1742G>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 1742 | chr2 | 181537269 | ||||||
| chr2:181537304 | C | T | 64 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(61): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
3_prime_UTR_variant | MODIFIER | c.*1777C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 1777 | chr2 | 181537304 | ||||||
| chr2:181537418 | T | TCAACTTA others(16): Show |
1 | a0001c0001t0019 | 2 | HG00323.hp2 HG01109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1892_*1914dupCAAC others(19): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 1915 | INFO_REALIGN_3_PRIME | chr2 | 181537418 | |||||
| chr2:181537427 | T | C | 1 | a0001c0001t0037 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1900T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 1900 | chr2 | 181537427 | ||||||
| chr2:181537489 | C | CT | 6 | a0001c0002t0048 a0001c0002t0056 a0001c0015t0040 others(3): Show |
11 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1968dupT | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 1969 | INFO_REALIGN_3_PRIME | chr2 | 181537489 | |||||
| chr2:181537611 | T | C | 1 | a0002c0003t0017 | 3 | HG02717.hp1 HG02723.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2084T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 2084 | chr2 | 181537611 | ||||||
| chr2:181537617 | A | G | 3 | a0001c0001t0015 a0001c0001t0020 a0001c0001t0030 |
6 | HG02132.hp2 NA18747.hp2 NA19005.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2090A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 2090 | chr2 | 181537617 | ||||||
| chr2:181537710 | GT | G | 15 | a0001c0002t0003 a0001c0002t0009 a0001c0002t0012 others(12): Show |
79 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*2190delT | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 2190 | INFO_REALIGN_3_PRIME | chr2 | 181537710 | |||||
| chr2:181537712 | T | A | 1 | a0001c0001t0010 | 4 | HG02523.hp1 NA18612.hp1 NA19060.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2185T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 2185 | chr2 | 181537712 | ||||||
| chr2:181537716 | T | G | 1 | a0001c0002t0046 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2189T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 2189 | chr2 | 181537716 | ||||||
| chr2:181537764 | C | T | 18 | a0001c0002t0003 a0001c0002t0009 a0001c0002t0012 others(15): Show |
84 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*2237C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 2237 | chr2 | 181537764 | ||||||
| chr2:181537837 | T | C | 4 | a0001c0015t0040 a0003c0004t0008 a0003c0004t0049 others(1): Show |
9 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2310T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 2310 | chr2 | 181537837 | ||||||
| chr2:181537853 | C | T | 1 | a0001c0002t0047 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2326C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 2326 | chr2 | 181537853 | ||||||
| chr2:181537854 | G | A | 1 | a0001c0002t0012 | 4 | HG02451.hp2 HG03453.hp1 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2327G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 2327 | chr2 | 181537854 | ||||||
| chr2:181537889 | C | T | 1 | a0001c0001t0036 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2362C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 2362 | chr2 | 181537889 | ||||||
| chr2:181537908 | C | A | 2 | a0001c0002t0022 a0001c0002t0028 |
3 | HG01516.hp2 HG01517.hp1 NA18950.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2381C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 2381 | chr2 | 181537908 | ||||||
| chr2:181538024 | A | C | 1 | a0001c0001t0035 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2497A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 2497 | chr2 | 181538024 | ||||||
| chr2:181538063 | G | A | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(34): Show |
271 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*2536G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 2536 | chr2 | 181538063 | ||||||
| chr2:181538126 | CCACATTT others(23): Show |
C | 2 | a0002c0003t0018 a0002c0003t0026 |
4 | HG00609.hp2 HG00621.hp1 NA19003.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2600_*2629delCACA others(26): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 2600 | chr2 | 181538126 | ||||||
| chr2:181538227 | A | G | 1 | a0001c0001t0038 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2700A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 2700 | chr2 | 181538227 | ||||||
| chr2:181538461 | A | G | 1 | a0002c0003t0045 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2934A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 2934 | chr2 | 181538461 | ||||||
| chr2:181538495 | TGCCTCTA others(5): Show |
T | 31 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(28): Show |
209 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*2969_*2980delGCCT others(8): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 2969 | chr2 | 181538495 | ||||||
| chr2:181538537 | T | G | 1 | a0001c0002t0012 | 4 | HG02451.hp2 HG03453.hp1 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3010T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 3010 | chr2 | 181538537 | ||||||
| chr2:181538660 | T | G | 9 | a0001c0002t0003 a0001c0002t0009 a0001c0002t0013 others(6): Show |
65 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*3133T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 3133 | chr2 | 181538660 | ||||||
| chr2:181538799 | C | T | 1 | a0003c0004t0049 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3272C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 3272 | chr2 | 181538799 | ||||||
| chr2:181538867 | C | T | 2 | a0002c0003t0011 a0002c0003t0025 |
5 | HG02004.hp2 NA18957.hp2 NA18968.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3340C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 28/28 | 3340 | chr2 | 181538867 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:181457912 | A | G | 2 | a0001c0001t0002g0346 a0001c0002t0034g0345 |
2 | HG00735.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.197+61A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 1/27 | chr2 | 181457912 | |||||||
| chr2:181458065 | C | G | 1 | a0001c0002t0029g0343 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.198-131C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 1/27 | chr2 | 181458065 | |||||||
| chr2:181458065 | C | T | 1 | a0002c0003t0004g0344 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.198-131C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 1/27 | chr2 | 181458065 | |||||||
| chr2:181458341 | G | T | 1 | a0002c0003t0004g0342 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.319+24G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181458341 | |||||||
| chr2:181458370 | C | T | 2 | a0001c0001t0002g0341 a0002c0005t0016g0002 |
4 | HG02451.hp1 HG02818.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.319+53C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181458370 | |||||||
| chr2:181458407 | C | T | 6 | a0001c0001t0001g0340 a0001c0001t0039g0339 a0001c0002t0012g0335 others(3): Show |
6 | HG02451.hp2 HG03225.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.319+90C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181458407 | |||||||
| chr2:181458564 | C | G | 1 | a0001c0001t0001g0340 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.319+247C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181458564 | |||||||
| chr2:181458647 | T | G | 1 | a0001c0002t0003g0020 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.319+330T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181458647 | |||||||
| chr2:181458688 | A | G | 1 | a0001c0002t0003g0334 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.319+371A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181458688 | |||||||
| chr2:181458790 | G | A | 1 | a0001c0001t0041g0021 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.319+473G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181458790 | |||||||
| chr2:181458938 | C | T | 52 | a0001c0001t0001g0290 a0001c0001t0001g0303 a0001c0001t0001g0304 others(49): Show |
53 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.319+621C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181458938 | |||||||
| chr2:181459039 | G | A | 164 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(161): Show |
175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.319+722G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181459039 | |||||||
| chr2:181459085 | T | A | 1 | a0001c0001t0001g0022 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.319+768T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181459085 | |||||||
| chr2:181459088 | T | A | 1 | a0001c0001t0001g0022 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.319+771T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181459088 | |||||||
| chr2:181459097 | T | A | 1 | a0001c0001t0001g0022 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.319+780T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181459097 | |||||||
| chr2:181459100 | T | G | 1 | a0001c0001t0001g0022 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.319+783T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181459100 | |||||||
| chr2:181459249 | T | C | 1 | a0003c0004t0008g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.319+932T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181459249 | |||||||
| chr2:181459253 | T | A | 1 | a0007c0008t0001g0120 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.319+936T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181459253 | |||||||
| chr2:181459256 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.319+939G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181459256 | |||||||
| chr2:181459315 | G | GT | 164 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(161): Show |
175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.319+998_319+999ins others(1): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181459315 | |||||||
| chr2:181459438 | T | A | 1 | a0001c0002t0022g0018 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.319+1121T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181459438 | |||||||
| chr2:181459459 | CTT | C | 163 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(160): Show |
174 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.319+1144_319+1145d others(4): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 181459459 | ||||||
| chr2:181459745 | C | T | 2 | a0002c0003t0004g0286 a0003c0004t0050g0285 |
2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.319+1428C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181459745 | |||||||
| chr2:181459775 | C | T | 2 | a0001c0001t0002g0283 a0001c0001t0002g0284 |
2 | HG00099.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.319+1458C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181459775 | |||||||
| chr2:181459778 | G | A | 1 | a0001c0002t0034g0345 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.319+1461G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181459778 | |||||||
| chr2:181459821 | T | C | 3 | a0001c0002t0003g0287 a0001c0002t0003g0288 a0001c0002t0003g0289 |
3 | NA18972.hp2 NA19063.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.319+1504T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181459821 | |||||||
| chr2:181459940 | T | A | 5 | a0001c0001t0001g0340 a0001c0002t0012g0335 a0001c0002t0012g0336 others(2): Show |
5 | HG02451.hp2 HG03225.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.319+1623T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181459940 | |||||||
| chr2:181459941 | TA | T | 5 | a0001c0001t0001g0340 a0001c0002t0012g0335 a0001c0002t0012g0336 others(2): Show |
5 | HG02451.hp2 HG03225.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.319+1627delA | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 181459941 | ||||||
| chr2:181459977 | ATTGT | A | 7 | a0001c0001t0001g0340 a0001c0001t0002g0346 a0001c0002t0012g0335 others(4): Show |
7 | HG00735.hp1 HG01081.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.319+1664_319+1667d others(6): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 181459977 | ||||||
| chr2:181460173 | A | C | 1 | a0001c0001t0001g0118 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.319+1856A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460173 | |||||||
| chr2:181460201 | C | T | 2 | a0002c0003t0004g0286 a0003c0004t0050g0285 |
2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.319+1884C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460201 | |||||||
| chr2:181460286 | C | G | 1 | a0002c0003t0004g0344 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.319+1969C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460286 | |||||||
| chr2:181460429 | C | G | 1 | a0002c0005t0001g0282 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.319+2112C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460429 | |||||||
| chr2:181460566 | A | AAT | 54 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0101 others(51): Show |
59 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.319+2249_319+2250i others(4): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460566 | |||||||
| chr2:181460566 | A | AATATGTG others(9): Show |
1 | a0002c0003t0004g0344 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.319+2249_319+2250i others(18): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460566 | |||||||
| chr2:181460566 | A | AATGT | 16 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0112 others(13): Show |
19 | HG01099.hp2 HG01123.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.319+2249_319+2250i others(6): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460566 | |||||||
| chr2:181460566 | A | AATGTGT | 14 | a0001c0001t0002g0167 a0001c0001t0002g0283 a0001c0001t0002g0284 others(11): Show |
14 | HG00099.hp1 HG00735.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.319+2249_319+2250i others(8): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460566 | |||||||
| chr2:181460566 | A | AATGTGTG others(1): Show |
13 | a0001c0001t0001g0174 a0001c0001t0001g0182 a0001c0001t0001g0183 others(10): Show |
13 | HG00408.hp2 HG01081.hp1 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.319+2249_319+2250i others(10): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460566 | |||||||
| chr2:181460566 | A | AATGTGTG others(3): Show |
33 | a0001c0001t0001g0184 a0001c0001t0001g0189 a0001c0001t0001g0208 others(30): Show |
34 | HG00423.hp1 HG01257.hp1 HG01258.hp1 others(31): Show |
intron_variant | MODIFIER | c.319+2249_319+2250i others(12): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460566 | |||||||
| chr2:181460566 | A | AATGTGTG others(5): Show |
11 | a0001c0001t0002g0219 a0001c0001t0006g0214 a0001c0001t0006g0216 others(8): Show |
12 | HG00597.hp2 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.319+2249_319+2250i others(14): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460566 | |||||||
| chr2:181460566 | A | AATGTGTG others(7): Show |
26 | a0001c0001t0001g0017 a0001c0001t0002g0242 a0001c0001t0002g0244 others(23): Show |
28 | HG00738.hp1 HG01975.hp1 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.319+2249_319+2250i others(16): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460566 | |||||||
| chr2:181460566 | A | AATGTGTG others(9): Show |
15 | a0001c0001t0001g0246 a0001c0001t0006g0248 a0001c0001t0006g0249 others(12): Show |
15 | HG00423.hp2 HG00733.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.319+2249_319+2250i others(18): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460566 | |||||||
| chr2:181460566 | A | AATGTGTG others(11): Show |
10 | a0001c0001t0006g0261 a0001c0001t0006g0262 a0001c0001t0006g0263 others(7): Show |
13 | HG00099.hp2 HG00597.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.319+2249_319+2250i others(20): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460566 | |||||||
| chr2:181460566 | A | AATGTGTG others(13): Show |
2 | a0001c0001t0006g0270 a0002c0003t0005g0271 |
2 | NA18977.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.319+2249_319+2250i others(22): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460566 | |||||||
| chr2:181460566 | A | AGTGTGTG others(5): Show |
1 | a0001c0001t0002g0280 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.319+2275_319+2286d others(14): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 181460566 | ||||||
| chr2:181460566 | A | AGTGTGTG others(7): Show |
1 | a0001c0001t0002g0281 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.319+2273_319+2286d others(16): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 181460566 | ||||||
| chr2:181460566 | AGT | A | 50 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0044 others(47): Show |
52 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.319+2285_319+2286d others(4): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 181460566 | ||||||
| chr2:181460566 | AGTGT | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(13): Show |
17 | HG00323.hp1 HG01517.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.319+2283_319+2286d others(6): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 181460566 | ||||||
| chr2:181460566 | AGTGTGT | A | 6 | a0001c0001t0001g0029 a0001c0001t0002g0026 a0001c0001t0002g0027 others(3): Show |
6 | HG01891.hp2 HG02647.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.319+2281_319+2286d others(8): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 181460566 | ||||||
| chr2:181460566 | AGTGTGTG others(1): Show |
A | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0015g0122 |
3 | HG02818.hp1 HG03098.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.319+2279_319+2286d others(10): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 181460566 | ||||||
| chr2:181460567 | G | A | 69 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0097 others(66): Show |
70 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.319+2250G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460567 | |||||||
| chr2:181460569 | G | A | 50 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0044 others(47): Show |
52 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.319+2252G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460569 | |||||||
| chr2:181460571 | G | A | 18 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(15): Show |
19 | HG00323.hp1 HG00735.hp1 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.319+2254G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460571 | |||||||
| chr2:181460573 | G | A | 9 | a0001c0001t0001g0029 a0001c0001t0001g0340 a0001c0001t0002g0026 others(6): Show |
9 | HG01891.hp2 HG02451.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.319+2256G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460573 | |||||||
| chr2:181460575 | G | A | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0015g0122 |
3 | HG02818.hp1 HG03098.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.319+2258G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460575 | |||||||
| chr2:181460583 | G | A | 1 | a0001c0001t0039g0339 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.319+2266G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460583 | |||||||
| chr2:181460648 | G | T | 1 | a0001c0001t0021g0115 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.319+2331G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460648 | |||||||
| chr2:181460765 | G | T | 56 | a0001c0001t0001g0017 a0001c0001t0001g0182 a0001c0001t0001g0183 others(53): Show |
59 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.319+2448G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460765 | |||||||
| chr2:181460766 | C | T | 56 | a0001c0001t0001g0017 a0001c0001t0001g0182 a0001c0001t0001g0183 others(53): Show |
59 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.319+2449C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460766 | |||||||
| chr2:181460779 | A | G | 1 | a0001c0002t0056g0160 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.319+2462A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460779 | |||||||
| chr2:181460801 | A | G | 2 | a0001c0001t0001g0097 a0003c0004t0049g0098 |
2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.319+2484A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460801 | |||||||
| chr2:181460827 | A | G | 59 | a0001c0001t0006g0124 a0001c0001t0006g0185 a0001c0001t0006g0186 others(56): Show |
63 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.319+2510A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460827 | |||||||
| chr2:181460846 | T | C | 1 | a0003c0004t0008g0166 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.319+2529T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460846 | |||||||
| chr2:181460924 | C | G | 2 | a0001c0001t0002g0346 a0001c0002t0034g0345 |
2 | HG00735.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.319+2607C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181460924 | |||||||
| chr2:181461180 | C | T | 62 | a0001c0001t0006g0124 a0001c0001t0006g0185 a0001c0001t0006g0186 others(59): Show |
66 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.319+2863C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181461180 | |||||||
| chr2:181461281 | A | G | 1 | a0001c0001t0002g0327 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.319+2964A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181461281 | |||||||
| chr2:181461332 | T | A | 1 | a0001c0002t0056g0160 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.319+3015T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181461332 | |||||||
| chr2:181461409 | C | G | 56 | a0001c0001t0001g0017 a0001c0001t0001g0182 a0001c0001t0001g0183 others(53): Show |
59 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.319+3092C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181461409 | |||||||
| chr2:181461489 | C | T | 3 | a0001c0001t0021g0115 a0001c0001t0038g0110 a0001c0015t0040g0111 |
3 | HG02922.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.319+3172C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181461489 | |||||||
| chr2:181461571 | A | G | 1 | a0002c0003t0004g0212 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.319+3254A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181461571 | |||||||
| chr2:181461664 | T | A | 1 | a0001c0002t0034g0345 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.319+3347T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181461664 | |||||||
| chr2:181461785 | G | C | 1 | a0001c0001t0006g0225 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.319+3468G>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181461785 | |||||||
| chr2:181461797 | C | A | 38 | a0001c0001t0001g0121 a0001c0001t0001g0127 a0001c0001t0001g0128 others(35): Show |
39 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.319+3480C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181461797 | |||||||
| chr2:181461861 | C | T | 1 | a0001c0002t0003g0157 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.319+3544C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181461861 | |||||||
| chr2:181461879 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.319+3562G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181461879 | |||||||
| chr2:181462128 | G | A | 1 | a0001c0001t0038g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.319+3811G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181462128 | |||||||
| chr2:181462237 | C | T | 1 | a0001c0001t0002g0109 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.319+3920C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181462237 | |||||||
| chr2:181462315 | G | C | 2 | a0001c0007t0002g0079 a0001c0007t0002g0080 |
2 | HG01516.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.319+3998G>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181462315 | |||||||
| chr2:181462336 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.319+4019T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181462336 | |||||||
| chr2:181462582 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.319+4265T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181462582 | |||||||
| chr2:181462622 | A | G | 3 | a0002c0003t0005g0223 a0002c0003t0005g0224 a0002c0003t0005g0247 |
3 | HG02976.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.319+4305A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181462622 | |||||||
| chr2:181462765 | A | G | 7 | a0001c0001t0006g0186 a0001c0002t0009g0188 a0001c0002t0009g0218 others(4): Show |
7 | HG00597.hp2 NA18977.hp2 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+4448A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181462765 | |||||||
| chr2:181462812 | T | C | 1 | a0001c0002t0003g0010 | 2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.319+4495T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181462812 | |||||||
| chr2:181462984 | A | T | 1 | a0001c0001t0039g0339 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.319+4667A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181462984 | |||||||
| chr2:181463051 | C | T | 1 | a0001c0001t0010g0165 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.319+4734C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181463051 | |||||||
| chr2:181463148 | G | A | 1 | a0002c0003t0004g0294 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.319+4831G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181463148 | |||||||
| chr2:181463179 | C | T | 1 | a0001c0001t0039g0339 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.319+4862C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181463179 | |||||||
| chr2:181463230 | G | A | 60 | a0001c0001t0006g0124 a0001c0001t0006g0185 a0001c0001t0006g0186 others(57): Show |
64 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.319+4913G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181463230 | |||||||
| chr2:181463265 | C | T | 1 | a0002c0005t0001g0009 | 2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.319+4948C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181463265 | |||||||
| chr2:181463315 | G | A | 25 | a0001c0001t0006g0227 a0001c0001t0006g0230 a0001c0001t0006g0248 others(22): Show |
28 | HG00423.hp2 NA18950.hp1 NA18951.hp1 others(25): Show |
intron_variant | MODIFIER | c.319+4998G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181463315 | |||||||
| chr2:181463487 | G | A | 163 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(160): Show |
174 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.319+5170G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181463487 | |||||||
| chr2:181463656 | C | CA | 13 | a0001c0001t0001g0174 a0001c0001t0001g0184 a0001c0001t0001g0246 others(10): Show |
13 | HG00099.hp1 HG00741.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.319+5343dupA | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 181463656 | ||||||
| chr2:181463671 | C | T | 14 | a0001c0001t0001g0121 a0001c0001t0001g0127 a0001c0001t0001g0128 others(11): Show |
15 | HG00408.hp1 HG01943.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.319+5354C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181463671 | |||||||
| chr2:181463778 | A | C | 1 | a0001c0001t0038g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.319+5461A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181463778 | |||||||
| chr2:181463895 | G | A | 1 | a0001c0002t0013g0295 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.319+5578G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181463895 | |||||||
| chr2:181463895 | G | T | 1 | a0001c0001t0001g0174 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.319+5578G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181463895 | |||||||
| chr2:181464066 | G | A | 1 | a0001c0002t0046g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.319+5749G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181464066 | |||||||
| chr2:181464265 | G | A | 1 | a0001c0001t0002g0296 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.319+5948G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181464265 | |||||||
| chr2:181464378 | T | G | 1 | a0001c0001t0054g0081 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.319+6061T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181464378 | |||||||
| chr2:181464501 | T | C | 1 | a0001c0001t0001g0149 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.319+6184T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181464501 | |||||||
| chr2:181464733 | C | T | 60 | a0001c0001t0006g0124 a0001c0001t0006g0185 a0001c0001t0006g0186 others(57): Show |
64 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.319+6416C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181464733 | |||||||
| chr2:181464756 | A | G | 1 | a0002c0003t0004g0344 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.319+6439A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181464756 | |||||||
| chr2:181464809 | A | T | 56 | a0001c0001t0001g0017 a0001c0001t0001g0182 a0001c0001t0001g0183 others(53): Show |
59 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.319+6492A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181464809 | |||||||
| chr2:181464892 | A | G | 6 | a0001c0001t0001g0340 a0001c0001t0002g0346 a0001c0002t0012g0335 others(3): Show |
6 | HG00735.hp1 HG01081.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.319+6575A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181464892 | |||||||
| chr2:181464920 | T | G | 246 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(243): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.319+6603T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181464920 | |||||||
| chr2:181465181 | G | A | 1 | a0001c0002t0056g0160 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.319+6864G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181465181 | |||||||
| chr2:181465277 | C | A | 1 | a0001c0002t0003g0175 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.319+6960C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181465277 | |||||||
| chr2:181465294 | C | T | 2 | a0001c0001t0002g0346 a0001c0002t0034g0345 |
2 | HG00735.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.319+6977C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181465294 | |||||||
| chr2:181465452 | A | G | 1 | a0001c0001t0001g0017 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.319+7135A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181465452 | |||||||
| chr2:181465770 | A | G | 1 | a0001c0001t0002g0096 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.319+7453A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181465770 | |||||||
| chr2:181465856 | T | C | 62 | a0001c0001t0001g0017 a0001c0001t0001g0182 a0001c0001t0001g0183 others(59): Show |
65 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.319+7539T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181465856 | |||||||
| chr2:181465954 | A | T | 1 | a0001c0002t0003g0175 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.319+7637A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181465954 | |||||||
| chr2:181465974 | G | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(2): Show |
6 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.319+7657G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181465974 | |||||||
| chr2:181466095 | G | T | 1 | a0001c0001t0019g0095 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.319+7778G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181466095 | |||||||
| chr2:181466117 | A | C | 1 | a0002c0003t0004g0344 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.319+7800A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181466117 | |||||||
| chr2:181466183 | C | T | 1 | a0001c0001t0057g0108 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.319+7866C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181466183 | |||||||
| chr2:181466296 | T | C | 1 | a0001c0001t0002g0035 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.319+7979T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181466296 | |||||||
| chr2:181466296 | T | TA | 5 | a0001c0001t0002g0036 a0001c0001t0002g0100 a0001c0002t0003g0046 others(2): Show |
5 | HG00741.hp2 HG02145.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.319+7988dupA | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 181466296 | ||||||
| chr2:181466368 | G | A | 1 | a0001c0002t0003g0297 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.319+8051G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181466368 | |||||||
| chr2:181466538 | G | A | 301 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(298): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.319+8221G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181466538 | |||||||
| chr2:181466590 | A | G | 7 | a0001c0001t0006g0186 a0001c0002t0009g0188 a0001c0002t0009g0218 others(4): Show |
7 | HG00597.hp2 NA18977.hp2 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+8273A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181466590 | |||||||
| chr2:181466998 | A | T | 1 | a0007c0008t0001g0120 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.320-7962A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181466998 | |||||||
| chr2:181467061 | A | G | 7 | a0001c0002t0009g0264 a0002c0003t0005g0001 a0002c0003t0005g0231 others(4): Show |
10 | NA18951.hp1 NA18954.hp1 NA18964.hp2 others(7): Show |
intron_variant | MODIFIER | c.320-7899A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181467061 | |||||||
| chr2:181467113 | A | G | 3 | a0002c0003t0005g0223 a0002c0003t0005g0224 a0002c0003t0005g0247 |
3 | HG02976.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.320-7847A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181467113 | |||||||
| chr2:181467225 | T | TA | 169 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(166): Show |
180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.320-7725dupA | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 181467225 | ||||||
| chr2:181467253 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG01074.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.320-7707A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181467253 | |||||||
| chr2:181467283 | C | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0031 a0001c0001t0001g0032 others(7): Show |
11 | HG01884.hp2 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.320-7677C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181467283 | |||||||
| chr2:181467419 | G | A | 13 | a0001c0001t0001g0174 a0001c0001t0001g0340 a0001c0001t0002g0167 others(10): Show |
13 | HG00735.hp1 HG01081.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.320-7541G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181467419 | |||||||
| chr2:181467436 | A | G | 1 | a0002c0005t0001g0009 | 2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.320-7524A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181467436 | |||||||
| chr2:181467623 | T | C | 7 | a0001c0001t0001g0174 a0001c0001t0002g0167 a0001c0002t0012g0338 others(4): Show |
7 | HG02109.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.320-7337T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181467623 | |||||||
| chr2:181467696 | C | A | 1 | a0001c0002t0048g0273 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.320-7264C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181467696 | |||||||
| chr2:181468075 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.320-6885G>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181468075 | |||||||
| chr2:181468234 | A | G | 39 | a0001c0001t0001g0121 a0001c0001t0001g0127 a0001c0001t0001g0128 others(36): Show |
40 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.320-6726A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181468234 | |||||||
| chr2:181468340 | C | G | 4 | a0001c0002t0003g0014 a0001c0002t0003g0210 a0001c0002t0003g0211 others(1): Show |
5 | HG01257.hp1 HG01258.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.320-6620C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181468340 | |||||||
| chr2:181468375 | T | C | 4 | a0001c0001t0007g0256 a0001c0001t0007g0266 a0002c0003t0005g0234 others(1): Show |
4 | HG00597.hp1 HG02015.hp2 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.320-6585T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181468375 | |||||||
| chr2:181468409 | T | C | 1 | a0002c0003t0004g0132 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.320-6551T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181468409 | |||||||
| chr2:181468720 | A | G | 232 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(229): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.320-6240A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181468720 | |||||||
| chr2:181469092 | T | C | 1 | a0001c0001t0001g0290 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.320-5868T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181469092 | |||||||
| chr2:181469376 | G | A | 1 | a0001c0002t0003g0150 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.320-5584G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181469376 | |||||||
| chr2:181469617 | G | A | 1 | a0001c0001t0002g0346 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.320-5343G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181469617 | |||||||
| chr2:181469629 | C | T | 4 | a0001c0001t0002g0006 a0001c0001t0002g0093 a0001c0001t0002g0094 others(1): Show |
5 | NA18946.hp1 NA18979.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.320-5331C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181469629 | |||||||
| chr2:181469780 | T | C | 1 | a0002c0005t0001g0009 | 2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.320-5180T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181469780 | |||||||
| chr2:181469957 | C | T | 168 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(165): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.320-5003C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181469957 | |||||||
| chr2:181470021 | A | G | 3 | a0001c0001t0002g0341 a0002c0005t0001g0009 a0002c0005t0016g0002 |
6 | HG02451.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.320-4939A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181470021 | |||||||
| chr2:181470026 | G | T | 166 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(163): Show |
177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.320-4934G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181470026 | |||||||
| chr2:181470078 | G | T | 36 | a0001c0001t0001g0121 a0001c0001t0001g0127 a0001c0001t0001g0128 others(33): Show |
37 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.320-4882G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181470078 | |||||||
| chr2:181470146 | T | C | 71 | a0001c0001t0001g0017 a0001c0001t0001g0174 a0001c0001t0001g0182 others(68): Show |
74 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.320-4814T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181470146 | |||||||
| chr2:181470339 | G | A | 1 | a0001c0001t0002g0093 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.320-4621G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181470339 | |||||||
| chr2:181470362 | A | C | 1 | a0002c0003t0004g0132 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.320-4598A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181470362 | |||||||
| chr2:181470475 | T | C | 1 | a0002c0003t0011g0133 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.320-4485T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181470475 | |||||||
| chr2:181470684 | ACTT | A | 7 | a0001c0001t0001g0340 a0001c0001t0039g0339 a0001c0002t0012g0335 others(4): Show |
7 | HG02451.hp2 HG03225.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.320-4270_320-4268d others(5): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 181470684 | ||||||
| chr2:181471144 | C | T | 1 | a0001c0002t0012g0338 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.320-3816C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181471144 | |||||||
| chr2:181471152 | T | A | 1 | a0001c0001t0001g0011 | 2 | HG01361.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.320-3808T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181471152 | |||||||
| chr2:181471153 | T | A | 1 | a0001c0001t0001g0011 | 2 | HG01361.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.320-3807T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181471153 | |||||||
| chr2:181471226 | A | G | 1 | a0002c0005t0001g0009 | 2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.320-3734A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181471226 | |||||||
| chr2:181471241 | G | A | 1 | a0001c0002t0056g0160 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.320-3719G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181471241 | |||||||
| chr2:181471261 | G | A | 1 | a0001c0001t0006g0185 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.320-3699G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181471261 | |||||||
| chr2:181471353 | G | C | 3 | a0001c0001t0002g0346 a0002c0003t0004g0286 a0003c0004t0050g0285 |
3 | HG00735.hp1 HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.320-3607G>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181471353 | |||||||
| chr2:181471488 | G | A | 1 | a0001c0002t0012g0335 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.320-3472G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181471488 | |||||||
| chr2:181471610 | C | G | 1 | a0001c0001t0002g0341 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.320-3350C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181471610 | |||||||
| chr2:181471710 | C | G | 39 | a0001c0001t0001g0045 a0001c0001t0001g0326 a0001c0001t0002g0117 others(36): Show |
40 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.320-3250C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181471710 | |||||||
| chr2:181471718 | C | T | 60 | a0001c0001t0001g0017 a0001c0001t0001g0182 a0001c0001t0001g0183 others(57): Show |
65 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.320-3242C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181471718 | |||||||
| chr2:181471747 | T | C | 73 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0022 others(70): Show |
78 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.320-3213T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181471747 | |||||||
| chr2:181471753 | C | T | 1 | a0001c0001t0020g0322 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.320-3207C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181471753 | |||||||
| chr2:181471988 | G | A | 2 | a0002c0003t0004g0286 a0002c0003t0017g0039 |
2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.320-2972G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181471988 | |||||||
| chr2:181472005 | CT | C | 58 | a0001c0001t0001g0017 a0001c0001t0001g0182 a0001c0001t0001g0189 others(55): Show |
64 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.320-2954delT | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181472005 | |||||||
| chr2:181472070 | G | A | 3 | a0002c0003t0004g0301 a0002c0003t0045g0019 a0002c0003t0055g0019 |
3 | NA19054.hp2 NA19080.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.320-2890G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181472070 | |||||||
| chr2:181472078 | T | G | 164 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0031 others(161): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.320-2882T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181472078 | |||||||
| chr2:181472157 | A | G | 108 | a0001c0001t0001g0017 a0001c0001t0001g0102 a0001c0001t0001g0182 others(105): Show |
115 | HG00099.hp2 HG00408.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.320-2803A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181472157 | |||||||
| chr2:181472294 | A | G | 1 | a0001c0001t0039g0339 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.320-2666A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181472294 | |||||||
| chr2:181472412 | G | A | 1 | a0001c0001t0006g0124 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.320-2548G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181472412 | |||||||
| chr2:181472516 | A | G | 1 | a0002c0003t0005g0224 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.320-2444A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181472516 | |||||||
| chr2:181472651 | A | T | 1 | a0002c0003t0004g0286 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.320-2309A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181472651 | |||||||
| chr2:181472720 | G | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0031 others(78): Show |
88 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.320-2240G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181472720 | |||||||
| chr2:181472789 | T | C | 1 | a0001c0001t0002g0082 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.320-2171T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181472789 | |||||||
| chr2:181472927 | C | G | 1 | a0001c0001t0006g0227 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.320-2033C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181472927 | |||||||
| chr2:181473147 | A | G | 6 | a0001c0001t0001g0029 a0001c0001t0002g0026 a0001c0001t0002g0027 others(3): Show |
6 | HG01891.hp2 HG02451.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.320-1813A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181473147 | |||||||
| chr2:181473264 | T | G | 1 | a0007c0008t0001g0120 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.320-1696T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181473264 | |||||||
| chr2:181473300 | T | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(174): Show |
192 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.320-1660T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181473300 | |||||||
| chr2:181473791 | A | AC | 6 | a0002c0003t0004g0294 a0002c0003t0004g0301 a0002c0003t0004g0317 others(3): Show |
6 | HG00738.hp1 NA19054.hp2 NA19062.hp1 others(3): Show |
intron_variant | MODIFIER | c.320-1164dupC | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr2 | 181473791 | ||||||
| chr2:181473802 | T | G | 2 | a0001c0002t0012g0335 a0001c0002t0012g0336 |
2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.320-1158T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181473802 | |||||||
| chr2:181473908 | T | C | 2 | a0001c0002t0012g0335 a0001c0002t0012g0336 |
2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.320-1052T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181473908 | |||||||
| chr2:181474009 | C | G | 2 | a0001c0001t0006g0225 a0003c0004t0008g0023 |
2 | HG01884.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.320-951C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181474009 | |||||||
| chr2:181474076 | G | A | 1 | a0002c0003t0004g0212 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.320-884G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181474076 | |||||||
| chr2:181474192 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.320-768T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181474192 | |||||||
| chr2:181474242 | A | T | 5 | a0002c0003t0004g0294 a0002c0003t0004g0301 a0002c0003t0004g0317 others(2): Show |
5 | NA19054.hp2 NA19062.hp1 NA19072.hp2 others(2): Show |
intron_variant | MODIFIER | c.320-718A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181474242 | |||||||
| chr2:181474294 | A | C | 1 | a0001c0002t0003g0314 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.320-666A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181474294 | |||||||
| chr2:181474583 | G | T | 2 | a0001c0002t0003g0207 a0002c0003t0004g0206 |
2 | NA18966.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.320-377G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181474583 | |||||||
| chr2:181474594 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.320-366A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181474594 | |||||||
| chr2:181474792 | G | C | 1 | a0001c0001t0002g0026 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.320-168G>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181474792 | |||||||
| chr2:181474926 | A | T | 3 | a0001c0001t0001g0208 a0001c0002t0003g0020 a0001c0002t0003g0331 |
3 | NA18946.hp2 NA18959.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.320-34A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 2/27 | chr2 | 181474926 | |||||||
| chr2:181475410 | C | A | 3 | a0001c0002t0003g0190 a0001c0002t0003g0191 a0001c0002t0003g0302 |
3 | NA18969.hp2 NA19076.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.556+122C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181475410 | |||||||
| chr2:181475463 | A | G | 1 | a0001c0002t0003g0010 | 2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.556+175A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181475463 | |||||||
| chr2:181475486 | A | C | 1 | a0001c0002t0003g0046 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.556+198A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181475486 | |||||||
| chr2:181475487 | A | T | 197 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(194): Show |
212 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.556+199A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181475487 | |||||||
| chr2:181475500 | A | G | 1 | a0003c0004t0008g0166 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.556+212A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181475500 | |||||||
| chr2:181475653 | T | G | 1 | a0001c0002t0028g0130 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.556+365T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181475653 | |||||||
| chr2:181475717 | G | A | 5 | a0001c0002t0003g0015 a0001c0002t0003g0046 a0001c0002t0003g0073 others(2): Show |
6 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.556+429G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181475717 | |||||||
| chr2:181475773 | G | A | 3 | a0001c0002t0003g0190 a0001c0002t0003g0191 a0001c0002t0003g0302 |
3 | NA18969.hp2 NA19076.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.556+485G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181475773 | |||||||
| chr2:181475930 | C | A | 1 | a0001c0002t0003g0170 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.556+642C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181475930 | |||||||
| chr2:181475987 | A | ACT | 55 | a0001c0001t0001g0102 a0001c0001t0001g0159 a0001c0001t0002g0346 others(52): Show |
56 | HG00099.hp2 HG00609.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.556+701_556+702dup others(2): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr2 | 181475987 | ||||||
| chr2:181475987 | A | T | 1 | a0003c0004t0008g0166 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.556+699A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181475987 | |||||||
| chr2:181476515 | T | A | 1 | a0001c0007t0002g0079 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.556+1227T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181476515 | |||||||
| chr2:181476689 | T | C | 8 | a0001c0001t0006g0260 a0001c0001t0007g0236 a0001c0002t0009g0267 others(5): Show |
8 | HG00738.hp2 HG01243.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.556+1401T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181476689 | |||||||
| chr2:181476842 | A | G | 2 | a0001c0002t0012g0335 a0001c0002t0012g0336 |
2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.556+1554A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181476842 | |||||||
| chr2:181476927 | T | C | 200 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(197): Show |
215 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.556+1639T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181476927 | |||||||
| chr2:181476947 | T | C | 252 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(249): Show |
268 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.556+1659T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181476947 | |||||||
| chr2:181476990 | C | G | 252 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(249): Show |
268 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.556+1702C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181476990 | |||||||
| chr2:181477011 | A | G | 1 | a0003c0004t0008g0166 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.556+1723A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181477011 | |||||||
| chr2:181477125 | T | G | 2 | a0002c0003t0005g0234 a0002c0003t0005g0235 |
2 | HG02015.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.557-1632T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181477125 | |||||||
| chr2:181477133 | T | A | 1 | a0001c0001t0041g0021 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.557-1624T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181477133 | |||||||
| chr2:181477185 | G | C | 252 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(249): Show |
268 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.557-1572G>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181477185 | |||||||
| chr2:181477244 | C | T | 11 | a0001c0001t0002g0346 a0001c0002t0014g0277 a0001c0002t0014g0278 others(8): Show |
11 | HG00735.hp1 HG01081.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.557-1513C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181477244 | |||||||
| chr2:181477380 | A | G | 15 | a0001c0001t0001g0182 a0001c0002t0003g0203 a0001c0002t0003g0204 others(12): Show |
18 | HG00544.hp2 NA18940.hp2 NA18951.hp1 others(15): Show |
intron_variant | MODIFIER | c.557-1377A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181477380 | |||||||
| chr2:181477396 | G | A | 51 | a0001c0001t0001g0102 a0001c0001t0002g0346 a0001c0001t0006g0230 others(48): Show |
52 | HG00099.hp2 HG00609.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.557-1361G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181477396 | |||||||
| chr2:181477400 | G | A | 2 | a0001c0002t0012g0338 a0001c0002t0031g0220 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.557-1357G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181477400 | |||||||
| chr2:181477449 | G | A | 13 | a0001c0001t0002g0346 a0001c0002t0012g0338 a0001c0002t0014g0277 others(10): Show |
13 | HG00735.hp1 HG01081.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.557-1308G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181477449 | |||||||
| chr2:181477451 | A | G | 1 | a0001c0002t0003g0334 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.557-1306A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181477451 | |||||||
| chr2:181477499 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.557-1258C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181477499 | |||||||
| chr2:181477507 | C | T | 2 | a0001c0002t0012g0338 a0001c0002t0031g0220 |
2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.557-1250C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181477507 | |||||||
| chr2:181477729 | C | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0031 others(78): Show |
88 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.557-1028C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181477729 | |||||||
| chr2:181477897 | G | A | 38 | a0001c0001t0001g0102 a0001c0001t0006g0230 a0001c0001t0006g0260 others(35): Show |
39 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.557-860G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181477897 | |||||||
| chr2:181477992 | A | G | 209 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(206): Show |
224 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.557-765A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181477992 | |||||||
| chr2:181478039 | A | T | 209 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(206): Show |
224 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.557-718A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181478039 | |||||||
| chr2:181478105 | G | A | 1 | a0001c0001t0010g0091 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.557-652G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181478105 | |||||||
| chr2:181478106 | T | G | 1 | a0001c0001t0007g0123 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.557-651T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181478106 | |||||||
| chr2:181478214 | A | T | 1 | a0001c0001t0001g0105 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.557-543A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181478214 | |||||||
| chr2:181478218 | G | GAAGATGT others(6): Show |
11 | a0001c0001t0002g0346 a0001c0002t0014g0277 a0001c0002t0014g0278 others(8): Show |
11 | HG00735.hp1 HG01081.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.557-528_557-516dup others(13): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr2 | 181478218 | ||||||
| chr2:181478328 | G | A | 5 | a0001c0001t0001g0044 a0001c0001t0001g0138 a0001c0001t0001g0159 others(2): Show |
5 | HG00733.hp1 HG01071.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.557-429G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181478328 | |||||||
| chr2:181478398 | A | C | 11 | a0001c0001t0002g0006 a0001c0001t0002g0093 a0001c0001t0002g0094 others(8): Show |
12 | HG00673.hp2 HG01243.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.557-359A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181478398 | |||||||
| chr2:181478470 | A | C | 1 | a0001c0001t0002g0167 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.557-287A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181478470 | |||||||
| chr2:181478510 | A | T | 1 | a0001c0002t0031g0220 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.557-247A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181478510 | |||||||
| chr2:181478551 | A | G | 247 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(244): Show |
263 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.557-206A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181478551 | |||||||
| chr2:181478613 | T | A | 1 | a0001c0002t0031g0220 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.557-144T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181478613 | |||||||
| chr2:181478623 | A | G | 1 | a0001c0002t0031g0220 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.557-134A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181478623 | |||||||
| chr2:181478658 | A | G | 8 | a0001c0001t0002g0346 a0001c0002t0014g0277 a0001c0002t0014g0278 others(5): Show |
8 | HG00735.hp1 HG01081.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.557-99A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 4/27 | chr2 | 181478658 | |||||||
| chr2:181479197 | T | C | 40 | a0001c0001t0001g0102 a0001c0001t0001g0159 a0001c0001t0006g0230 others(37): Show |
41 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.624+373T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 5/27 | chr2 | 181479197 | |||||||
| chr2:181479306 | A | G | 1 | a0001c0002t0031g0220 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.624+482A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 5/27 | chr2 | 181479306 | |||||||
| chr2:181479336 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.624+512C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 5/27 | chr2 | 181479336 | |||||||
| chr2:181479488 | CAGTTTA | C | 196 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(193): Show |
211 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.625-644_625-639del others(6): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr2 | 181479488 | ||||||
| chr2:181479599 | T | C | 1 | a0001c0001t0039g0339 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.625-538T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 5/27 | chr2 | 181479599 | |||||||
| chr2:181479813 | G | A | 11 | a0001c0001t0002g0346 a0001c0002t0014g0277 a0001c0002t0014g0278 others(8): Show |
11 | HG00735.hp1 HG01081.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.625-324G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 5/27 | chr2 | 181479813 | |||||||
| chr2:181480079 | G | A | 1 | a0001c0002t0056g0160 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.625-58G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 5/27 | chr2 | 181480079 | |||||||
| chr2:181480094 | T | G | 1 | a0001c0001t0010g0091 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.625-43T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 5/27 | chr2 | 181480094 | |||||||
| chr2:181480119 | G | GT | 254 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(251): Show |
270 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(267): Show |
splice_region_variant&intron_variant | LOW | c.625-8dupT | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr2 | 181480119 | ||||||
| chr2:181480276 | A | C | 4 | a0001c0001t0001g0029 a0001c0001t0002g0026 a0001c0001t0002g0027 others(1): Show |
4 | HG01891.hp2 HG02647.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.754+10A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 6/27 | chr2 | 181480276 | |||||||
| chr2:181480442 | CA | C | 2 | a0001c0001t0002g0341 a0002c0005t0016g0002 |
4 | HG02451.hp1 HG02818.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.754+177delA | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 6/27 | chr2 | 181480442 | |||||||
| chr2:181480662 | A | G | 254 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(251): Show |
270 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.754+396A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 6/27 | chr2 | 181480662 | |||||||
| chr2:181480785 | G | A | 2 | a0001c0002t0012g0335 a0001c0002t0012g0336 |
2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.754+519G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 6/27 | chr2 | 181480785 | |||||||
| chr2:181480813 | T | C | 2 | a0001c0002t0012g0335 a0001c0002t0012g0336 |
2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.754+547T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 6/27 | chr2 | 181480813 | |||||||
| chr2:181480905 | C | G | 1 | a0001c0001t0002g0167 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.754+639C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 6/27 | chr2 | 181480905 | |||||||
| chr2:181480920 | A | C | 1 | a0001c0002t0003g0157 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.754+654A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 6/27 | chr2 | 181480920 | |||||||
| chr2:181480927 | G | T | 1 | a0001c0001t0002g0313 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.754+661G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 6/27 | chr2 | 181480927 | |||||||
| chr2:181480934 | A | C | 1 | a0002c0003t0017g0039 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.755-664A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 6/27 | chr2 | 181480934 | |||||||
| chr2:181481034 | CTCTT | C | 6 | a0001c0001t0001g0083 a0001c0001t0002g0341 a0002c0005t0001g0009 others(3): Show |
10 | HG01884.hp1 HG02451.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.755-556_755-553del others(4): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr2 | 181481034 | ||||||
| chr2:181481038 | T | C | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.755-560T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 6/27 | chr2 | 181481038 | |||||||
| chr2:181481128 | C | A | 343 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(340): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.755-470C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 6/27 | chr2 | 181481128 | |||||||
| chr2:181481148 | T | A | 42 | a0001c0001t0001g0102 a0001c0001t0001g0159 a0001c0001t0006g0230 others(39): Show |
43 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.755-450T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 6/27 | chr2 | 181481148 | |||||||
| chr2:181481153 | C | G | 1 | a0001c0002t0031g0220 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.755-445C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 6/27 | chr2 | 181481153 | |||||||
| chr2:181481275 | A | G | 3 | a0002c0003t0004g0125 a0002c0003t0004g0126 a0005c0010t0042g0065 |
3 | HG00642.hp1 HG01109.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.755-323A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 6/27 | chr2 | 181481275 | |||||||
| chr2:181481374 | G | A | 1 | a0001c0001t0020g0322 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.755-224G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 6/27 | chr2 | 181481374 | |||||||
| chr2:181481399 | C | G | 1 | a0001c0002t0031g0220 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.755-199C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 6/27 | chr2 | 181481399 | |||||||
| chr2:181481419 | T | C | 42 | a0001c0001t0001g0102 a0001c0001t0001g0159 a0001c0001t0006g0230 others(39): Show |
43 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.755-179T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 6/27 | chr2 | 181481419 | |||||||
| chr2:181481450 | A | G | 2 | a0001c0002t0012g0335 a0001c0002t0012g0336 |
2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.755-148A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 6/27 | chr2 | 181481450 | |||||||
| chr2:181481493 | A | T | 11 | a0001c0001t0002g0346 a0001c0002t0014g0277 a0001c0002t0014g0278 others(8): Show |
11 | HG00735.hp1 HG01081.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.755-105A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 6/27 | chr2 | 181481493 | |||||||
| chr2:181481801 | A | G | 1 | a0001c0001t0002g0312 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.840+118A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 7/27 | chr2 | 181481801 | |||||||
| chr2:181481817 | T | C | 39 | a0001c0001t0001g0102 a0001c0001t0001g0159 a0001c0001t0006g0230 others(36): Show |
40 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.840+134T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 7/27 | chr2 | 181481817 | |||||||
| chr2:181481838 | T | C | 1 | a0001c0001t0006g0227 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.840+155T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 7/27 | chr2 | 181481838 | |||||||
| chr2:181481888 | A | C | 1 | a0002c0003t0005g0224 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.840+205A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 7/27 | chr2 | 181481888 | |||||||
| chr2:181482210 | C | T | 39 | a0001c0001t0001g0102 a0001c0001t0001g0159 a0001c0001t0006g0230 others(36): Show |
40 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.841-150C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 7/27 | chr2 | 181482210 | |||||||
| chr2:181482227 | C | T | 248 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(245): Show |
264 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.841-133C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 7/27 | chr2 | 181482227 | |||||||
| chr2:181482345 | T | C | 42 | a0001c0001t0001g0102 a0001c0001t0001g0159 a0001c0001t0006g0230 others(39): Show |
43 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.841-15T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 7/27 | chr2 | 181482345 | |||||||
| chr2:181483174 | G | A | 1 | a0001c0002t0056g0160 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1041+523G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 9/27 | chr2 | 181483174 | |||||||
| chr2:181483327 | G | A | 1 | a0001c0002t0056g0160 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1041+676G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 9/27 | chr2 | 181483327 | |||||||
| chr2:181483414 | G | GAA | 42 | a0001c0001t0001g0102 a0001c0001t0001g0159 a0001c0001t0006g0230 others(39): Show |
43 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.1041+764_1041+765d others(4): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 181483414 | ||||||
| chr2:181483615 | G | A | 41 | a0001c0001t0001g0102 a0001c0001t0001g0159 a0001c0001t0006g0230 others(38): Show |
42 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.1041+964G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 9/27 | chr2 | 181483615 | |||||||
| chr2:181483648 | G | A | 3 | a0001c0002t0003g0177 a0001c0002t0003g0178 a0001c0002t0003g0179 |
3 | HG02040.hp2 NA18944.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1041+997G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 9/27 | chr2 | 181483648 | |||||||
| chr2:181483683 | G | A | 1 | a0001c0001t0057g0108 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1041+1032G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 9/27 | chr2 | 181483683 | |||||||
| chr2:181483827 | G | A | 40 | a0001c0001t0001g0102 a0001c0001t0006g0230 a0001c0001t0006g0260 others(37): Show |
41 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1041+1176G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 9/27 | chr2 | 181483827 | |||||||
| chr2:181484139 | G | C | 240 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(237): Show |
256 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.1041+1488G>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 9/27 | chr2 | 181484139 | |||||||
| chr2:181484216 | G | A | 1 | a0002c0003t0004g0161 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1041+1565G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 9/27 | chr2 | 181484216 | |||||||
| chr2:181484336 | T | G | 15 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0184 others(12): Show |
15 | HG01074.hp1 HG02056.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.1042-1545T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 9/27 | chr2 | 181484336 | |||||||
| chr2:181484406 | T | C | 1 | a0001c0002t0003g0177 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1042-1475T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 9/27 | chr2 | 181484406 | |||||||
| chr2:181484439 | G | A | 1 | a0001c0002t0003g0318 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1042-1442G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 9/27 | chr2 | 181484439 | |||||||
| chr2:181484682 | G | A | 36 | a0001c0001t0001g0102 a0001c0001t0006g0230 a0001c0001t0006g0260 others(33): Show |
37 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.1042-1199G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 9/27 | chr2 | 181484682 | |||||||
| chr2:181484820 | A | C | 2 | a0001c0002t0012g0335 a0001c0002t0012g0336 |
2 | HG02451.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1042-1061A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 9/27 | chr2 | 181484820 | |||||||
| chr2:181484851 | G | T | 1 | a0001c0002t0003g0020 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1042-1030G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 9/27 | chr2 | 181484851 | |||||||
| chr2:181484979 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1042-902G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 9/27 | chr2 | 181484979 | |||||||
| chr2:181485360 | T | A | 200 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(197): Show |
215 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.1042-521T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 9/27 | chr2 | 181485360 | |||||||
| chr2:181485369 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1042-512A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 9/27 | chr2 | 181485369 | |||||||
| chr2:181485403 | A | AT | 196 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(193): Show |
211 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.1042-466dupT | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | 181485403 | ||||||
| chr2:181485418 | G | A | 242 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(239): Show |
258 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.1042-463G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 9/27 | chr2 | 181485418 | |||||||
| chr2:181485545 | A | C | 1 | a0001c0001t0001g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1042-336A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 9/27 | chr2 | 181485545 | |||||||
| chr2:181485553 | G | A | 1 | a0001c0002t0056g0160 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1042-328G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 9/27 | chr2 | 181485553 | |||||||
| chr2:181485720 | A | G | 201 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(198): Show |
216 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.1042-161A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 9/27 | chr2 | 181485720 | |||||||
| chr2:181485745 | T | C | 4 | a0001c0001t0002g0030 a0001c0001t0002g0036 a0001c0001t0002g0040 others(1): Show |
4 | HG02145.hp1 HG02280.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042-136T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 9/27 | chr2 | 181485745 | |||||||
| chr2:181485762 | T | C | 38 | a0001c0001t0001g0102 a0001c0001t0006g0230 a0001c0001t0006g0260 others(35): Show |
39 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.1042-119T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 9/27 | chr2 | 181485762 | |||||||
| chr2:181485875 | A | G | 2 | a0001c0002t0012g0337 a0001c0002t0012g0338 |
2 | HG03453.hp1 HG03471.hp1 |
splice_region_variant&intron_variant | LOW | c.1042-6A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 9/27 | chr2 | 181485875 | |||||||
| chr2:181486016 | A | G | 245 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(242): Show |
261 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.1153+24A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181486016 | |||||||
| chr2:181486386 | A | G | 1 | a0001c0002t0056g0160 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1153+394A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181486386 | |||||||
| chr2:181486445 | T | G | 39 | a0001c0001t0001g0102 a0001c0001t0006g0230 a0001c0001t0006g0260 others(36): Show |
40 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1153+453T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181486445 | |||||||
| chr2:181486457 | C | T | 86 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(83): Show |
93 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.1153+465C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181486457 | |||||||
| chr2:181486489 | T | C | 200 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(197): Show |
215 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.1153+497T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181486489 | |||||||
| chr2:181486552 | T | C | 1 | a0001c0002t0056g0160 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1153+560T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181486552 | |||||||
| chr2:181486585 | C | A | 241 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(238): Show |
257 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.1153+593C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181486585 | |||||||
| chr2:181486625 | G | T | 200 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(197): Show |
215 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.1153+633G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181486625 | |||||||
| chr2:181486812 | T | G | 1 | a0001c0002t0012g0336 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1153+820T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181486812 | |||||||
| chr2:181487053 | A | G | 230 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(227): Show |
246 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.1153+1061A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181487053 | |||||||
| chr2:181487153 | G | A | 1 | a0001c0002t0056g0160 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1153+1161G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181487153 | |||||||
| chr2:181487160 | C | T | 1 | a0002c0003t0004g0060 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1153+1168C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181487160 | |||||||
| chr2:181487242 | T | A | 2 | a0001c0001t0006g0230 a0001c0001t0006g0263 |
2 | NA18971.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1153+1250T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181487242 | |||||||
| chr2:181487286 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1153+1294C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181487286 | |||||||
| chr2:181487297 | C | A | 3 | a0002c0003t0017g0039 a0002c0003t0017g0129 a0002c0003t0017g0164 |
3 | HG02717.hp1 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1153+1305C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181487297 | |||||||
| chr2:181487429 | G | A | 20 | a0001c0001t0001g0121 a0001c0001t0001g0127 a0001c0001t0001g0139 others(17): Show |
20 | HG00408.hp1 HG00673.hp1 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.1153+1437G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181487429 | |||||||
| chr2:181487569 | G | A | 14 | a0001c0001t0002g0346 a0001c0002t0012g0338 a0001c0002t0014g0277 others(11): Show |
14 | HG00735.hp1 HG01081.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1153+1577G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181487569 | |||||||
| chr2:181487656 | A | G | 1 | a0001c0002t0056g0160 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1153+1664A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181487656 | |||||||
| chr2:181487742 | A | G | 50 | a0001c0001t0001g0045 a0001c0001t0001g0102 a0001c0001t0006g0260 others(47): Show |
51 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.1153+1750A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181487742 | |||||||
| chr2:181487841 | T | C | 168 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0011 others(165): Show |
184 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.1153+1849T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181487841 | |||||||
| chr2:181487952 | A | G | 59 | a0001c0001t0001g0045 a0001c0001t0001g0102 a0001c0001t0002g0346 others(56): Show |
60 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.1153+1960A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181487952 | |||||||
| chr2:181488011 | T | C | 1 | a0003c0004t0008g0196 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1153+2019T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181488011 | |||||||
| chr2:181488064 | G | A | 64 | a0001c0001t0001g0045 a0001c0001t0001g0102 a0001c0001t0001g0276 others(61): Show |
65 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.1153+2072G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181488064 | |||||||
| chr2:181488242 | C | T | 16 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0184 others(13): Show |
16 | HG01074.hp1 HG02056.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.1153+2250C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181488242 | |||||||
| chr2:181488255 | T | C | 6 | a0001c0001t0001g0044 a0001c0001t0001g0138 a0001c0001t0001g0159 others(3): Show |
6 | HG00733.hp1 HG01071.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.1153+2263T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181488255 | |||||||
| chr2:181488472 | C | T | 2 | a0003c0004t0049g0098 a0003c0004t0050g0285 |
2 | HG03130.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1153+2480C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181488472 | |||||||
| chr2:181488519 | T | C | 3 | a0002c0003t0017g0039 a0002c0003t0017g0129 a0002c0003t0017g0164 |
3 | HG02717.hp1 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1153+2527T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181488519 | |||||||
| chr2:181488526 | A | G | 1 | a0002c0003t0005g0224 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1153+2534A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181488526 | |||||||
| chr2:181488532 | C | T | 1 | a0001c0002t0003g0193 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1153+2540C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181488532 | |||||||
| chr2:181488540 | A | G | 62 | a0001c0001t0001g0045 a0001c0001t0001g0101 a0001c0001t0002g0346 others(59): Show |
63 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1153+2548A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181488540 | |||||||
| chr2:181488589 | C | T | 77 | a0001c0001t0001g0005 a0001c0001t0001g0045 a0001c0001t0001g0062 others(74): Show |
79 | HG00140.hp2 HG00609.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.1153+2597C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181488589 | |||||||
| chr2:181488659 | T | C | 3 | a0001c0001t0001g0134 a0001c0001t0020g0322 a0001c0002t0003g0291 |
3 | NA19005.hp1 NA19075.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1153+2667T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181488659 | |||||||
| chr2:181488704 | A | G | 1 | a0002c0005t0001g0282 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1153+2712A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181488704 | |||||||
| chr2:181488713 | C | T | 2 | a0001c0002t0048g0273 a0001c0002t0056g0160 |
2 | HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1153+2721C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181488713 | |||||||
| chr2:181488716 | C | T | 1 | a0002c0005t0001g0282 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1153+2724C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181488716 | |||||||
| chr2:181488718 | C | T | 1 | a0001c0001t0041g0021 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1153+2726C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181488718 | |||||||
| chr2:181488719 | A | C | 12 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(9): Show |
12 | HG01167.hp2 HG01175.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.1153+2727A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181488719 | |||||||
| chr2:181488726 | T | C | 1 | a0003c0012t0021g0274 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1153+2734T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181488726 | |||||||
| chr2:181488739 | T | C | 3 | a0001c0002t0046g0158 a0003c0004t0049g0098 a0003c0004t0050g0285 |
3 | HG03130.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1153+2747T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181488739 | |||||||
| chr2:181488749 | A | G | 48 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0048 others(45): Show |
48 | HG00423.hp2 HG01074.hp1 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.1153+2757A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181488749 | |||||||
| chr2:181488838 | A | G | 3 | a0001c0001t0001g0304 a0001c0001t0001g0326 a0001c0001t0007g0266 |
3 | HG00597.hp1 HG02129.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1153+2846A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181488838 | |||||||
| chr2:181488847 | T | C | 2 | a0001c0001t0039g0339 a0003c0012t0021g0274 |
2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1153+2855T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181488847 | |||||||
| chr2:181488849 | C | T | 2 | a0001c0001t0039g0339 a0003c0012t0021g0274 |
2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1153+2857C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181488849 | |||||||
| chr2:181488850 | A | G | 2 | a0001c0001t0039g0339 a0003c0012t0021g0274 |
2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1153+2858A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181488850 | |||||||
| chr2:181488877 | T | C | 53 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0045 others(50): Show |
54 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.1153+2885T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181488877 | |||||||
| chr2:181488894 | G | A | 52 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0045 others(49): Show |
53 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.1153+2902G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181488894 | |||||||
| chr2:181489069 | ATCTTC | A | 12 | a0001c0001t0002g0341 a0001c0001t0006g0225 a0001c0002t0014g0277 others(9): Show |
12 | HG01081.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1153+3082_1153+308 others(9): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 181489069 | ||||||
| chr2:181489206 | T | C | 1 | a0003c0004t0049g0098 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1153+3214T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181489206 | |||||||
| chr2:181489391 | G | GA | 346 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(343): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.1153+3405dupA | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 181489391 | ||||||
| chr2:181489399 | C | T | 346 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(343): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.1153+3407C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181489399 | |||||||
| chr2:181489425 | A | T | 2 | a0001c0001t0002g0341 a0002c0003t0004g0286 |
2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1153+3433A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181489425 | |||||||
| chr2:181489444 | A | AT | 12 | a0001c0001t0002g0341 a0001c0001t0039g0339 a0001c0002t0012g0337 others(9): Show |
12 | HG01081.hp1 HG02109.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1153+3458dupT | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 181489444 | ||||||
| chr2:181489541 | TCTGA | T | 254 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(251): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1153+3550_1153+355 others(8): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181489541 | |||||||
| chr2:181489542 | C | T | 84 | a0001c0001t0001g0017 a0001c0001t0001g0189 a0001c0001t0002g0030 others(81): Show |
88 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1153+3550C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181489542 | |||||||
| chr2:181489546 | A | T | 254 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(251): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1153+3554A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181489546 | |||||||
| chr2:181489636 | G | A | 1 | a0002c0005t0001g0197 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1153+3644G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181489636 | |||||||
| chr2:181489716 | GC | G | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0100 |
3 | HG02145.hp2 HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1154-3608delC | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181489716 | |||||||
| chr2:181489801 | A | T | 73 | a0001c0001t0001g0017 a0001c0001t0001g0189 a0001c0001t0002g0200 others(70): Show |
77 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.1154-3524A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181489801 | |||||||
| chr2:181489887 | A | G | 1 | a0001c0001t0007g0123 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1154-3438A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181489887 | |||||||
| chr2:181490146 | A | G | 340 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(337): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1154-3179A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181490146 | |||||||
| chr2:181490298 | T | C | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1154-3027T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181490298 | |||||||
| chr2:181490390 | G | A | 1 | a0001c0002t0046g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1154-2935G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181490390 | |||||||
| chr2:181490395 | A | G | 1 | a0001c0001t0001g0017 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1154-2930A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181490395 | |||||||
| chr2:181490455 | AT | A | 328 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(325): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1154-2858delT | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 181490455 | ||||||
| chr2:181490455 | ATT | A | 12 | a0001c0002t0003g0020 a0001c0002t0003g0193 a0001c0002t0003g0207 others(9): Show |
13 | HG00423.hp1 HG01516.hp2 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.1154-2859_1154-285 others(6): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 181490455 | ||||||
| chr2:181490484 | CGT | C | 12 | a0001c0001t0001g0083 a0001c0001t0001g0102 a0001c0001t0001g0184 others(9): Show |
12 | HG00099.hp2 HG01884.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.1154-2800_1154-279 others(6): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 181490484 | ||||||
| chr2:181490484 | CGTGT | C | 42 | a0001c0001t0001g0045 a0001c0001t0001g0071 a0001c0001t0001g0208 others(39): Show |
42 | HG00621.hp2 HG00733.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.1154-2802_1154-279 others(8): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 181490484 | ||||||
| chr2:181490484 | CGTGTGT | C | 190 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(187): Show |
204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.1154-2804_1154-279 others(10): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 181490484 | ||||||
| chr2:181490484 | CGTGTGTG others(1): Show |
C | 48 | a0001c0001t0002g0281 a0001c0001t0002g0328 a0001c0002t0003g0015 others(45): Show |
50 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.1154-2806_1154-279 others(12): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 181490484 | ||||||
| chr2:181490484 | CGTGTGTG others(3): Show |
C | 17 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0084 others(14): Show |
19 | HG00099.hp1 HG00741.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.1154-2808_1154-279 others(14): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 181490484 | ||||||
| chr2:181490484 | CGTGTGTG others(5): Show |
C | 1 | a0001c0002t0003g0010 | 2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1154-2810_1154-279 others(16): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 181490484 | ||||||
| chr2:181490484 | CGTGTGTG others(15): Show |
C | 4 | a0001c0002t0003g0177 a0001c0002t0003g0178 a0001c0002t0003g0179 others(1): Show |
4 | HG02040.hp2 NA18944.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154-2820_1154-279 others(26): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 181490484 | ||||||
| chr2:181490511 | GTGTGTGT others(9): Show |
G | 1 | a0001c0001t0051g0299 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1154-2803_1154-278 others(20): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 181490511 | ||||||
| chr2:181490515 | G | C | 1 | a0001c0001t0001g0045 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1154-2810G>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181490515 | |||||||
| chr2:181490515 | GTGTGTGT others(5): Show |
G | 21 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0037 others(18): Show |
21 | HG00323.hp1 HG01167.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.1154-2799_1154-278 others(16): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 181490515 | ||||||
| chr2:181490517 | GTGTGTGT others(3): Show |
G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0062 |
2 | HG02004.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1154-2798_1154-278 others(14): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 181490517 | ||||||
| chr2:181490533 | G | C | 24 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0037 others(21): Show |
24 | HG00323.hp1 HG01167.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.1154-2792G>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181490533 | |||||||
| chr2:181490784 | G | A | 47 | a0001c0001t0002g0013 a0001c0001t0002g0050 a0001c0001t0002g0051 others(44): Show |
48 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.1154-2541G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181490784 | |||||||
| chr2:181491063 | C | T | 5 | a0001c0002t0014g0277 a0001c0002t0014g0278 a0001c0002t0014g0279 others(2): Show |
5 | HG01081.hp1 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1154-2262C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181491063 | |||||||
| chr2:181491064 | G | A | 1 | a0001c0001t0002g0109 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1154-2261G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181491064 | |||||||
| chr2:181491130 | T | C | 204 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(201): Show |
215 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1154-2195T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181491130 | |||||||
| chr2:181491244 | TAAGAATT others(308): Show |
T | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1154-2068_1154-175 others(4): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 181491244 | ||||||
| chr2:181491606 | A | G | 1 | a0001c0002t0014g0278 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1154-1719A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181491606 | |||||||
| chr2:181491683 | TA | T | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1154-1638delA | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 181491683 | ||||||
| chr2:181491756 | C | T | 1 | a0001c0002t0003g0010 | 2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1154-1569C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181491756 | |||||||
| chr2:181491774 | C | G | 6 | a0002c0003t0004g0131 a0003c0004t0008g0023 a0003c0004t0008g0166 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1154-1551C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181491774 | |||||||
| chr2:181491805 | T | A | 2 | a0001c0002t0048g0273 a0001c0002t0056g0160 |
2 | HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1154-1520T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181491805 | |||||||
| chr2:181491960 | A | G | 2 | a0001c0001t0002g0024 a0001c0001t0002g0025 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1154-1365A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181491960 | |||||||
| chr2:181491963 | G | A | 1 | a0001c0001t0036g0162 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1154-1362G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181491963 | |||||||
| chr2:181492036 | T | C | 2 | a0001c0002t0003g0046 a0001c0002t0003g0073 |
2 | HG00741.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1154-1289T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181492036 | |||||||
| chr2:181492095 | A | G | 62 | a0001c0001t0002g0281 a0001c0001t0024g0069 a0001c0002t0003g0014 others(59): Show |
65 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.1154-1230A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181492095 | |||||||
| chr2:181492184 | T | A | 1 | a0001c0001t0001g0062 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1154-1141T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181492184 | |||||||
| chr2:181492185 | G | T | 1 | a0001c0001t0001g0062 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1154-1140G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181492185 | |||||||
| chr2:181492186 | G | GAATAAAC others(25): Show |
1 | a0001c0001t0001g0062 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1154-1139_1154-113 others(36): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181492186 | |||||||
| chr2:181492187 | G | T | 1 | a0001c0001t0001g0062 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1154-1138G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181492187 | |||||||
| chr2:181492260 | GTAAATA | G | 33 | a0001c0001t0001g0012 a0001c0001t0001g0044 a0001c0001t0001g0071 others(30): Show |
34 | HG00408.hp1 HG00597.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.1154-1062_1154-105 others(10): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | 181492260 | ||||||
| chr2:181492299 | A | T | 1 | a0001c0001t0019g0292 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1154-1026A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181492299 | |||||||
| chr2:181492387 | C | A | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1154-938C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181492387 | |||||||
| chr2:181492556 | AT | A | 265 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(262): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1154-768delT | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181492556 | |||||||
| chr2:181492590 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1154-735G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181492590 | |||||||
| chr2:181492701 | A | T | 346 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(343): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.1154-624A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181492701 | |||||||
| chr2:181492807 | A | G | 67 | a0001c0001t0002g0281 a0001c0001t0024g0069 a0001c0002t0003g0010 others(64): Show |
71 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1154-518A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181492807 | |||||||
| chr2:181493011 | A | G | 346 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(343): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.1154-314A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181493011 | |||||||
| chr2:181493077 | C | T | 6 | a0002c0003t0004g0131 a0003c0004t0008g0023 a0003c0004t0008g0166 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1154-248C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181493077 | |||||||
| chr2:181493197 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1154-128G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 10/27 | chr2 | 181493197 | |||||||
| chr2:181493544 | G | A | 5 | a0001c0002t0014g0277 a0001c0002t0014g0278 a0001c0002t0014g0279 others(2): Show |
5 | HG01081.hp1 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1248+125G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 11/27 | chr2 | 181493544 | |||||||
| chr2:181493728 | A | T | 67 | a0001c0001t0002g0281 a0001c0001t0024g0069 a0001c0002t0003g0010 others(64): Show |
71 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1248+309A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 11/27 | chr2 | 181493728 | |||||||
| chr2:181493891 | C | A | 4 | a0001c0002t0003g0190 a0001c0002t0003g0191 a0001c0002t0003g0302 others(1): Show |
4 | HG00597.hp2 NA18969.hp2 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.1248+472C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 11/27 | chr2 | 181493891 | |||||||
| chr2:181493931 | GA | G | 266 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(263): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.1248+520delA | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr2 | 181493931 | ||||||
| chr2:181493988 | G | T | 1 | a0002c0003t0004g0206 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1248+569G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 11/27 | chr2 | 181493988 | |||||||
| chr2:181494155 | A | C | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1249-567A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 11/27 | chr2 | 181494155 | |||||||
| chr2:181494406 | A | G | 67 | a0001c0001t0002g0281 a0001c0001t0024g0069 a0001c0002t0003g0010 others(64): Show |
71 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1249-316A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 11/27 | chr2 | 181494406 | |||||||
| chr2:181494433 | C | T | 1 | a0001c0002t0003g0177 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1249-289C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 11/27 | chr2 | 181494433 | |||||||
| chr2:181494438 | C | T | 346 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(343): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.1249-284C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 11/27 | chr2 | 181494438 | |||||||
| chr2:181494554 | C | G | 1 | a0001c0002t0003g0150 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1249-168C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 11/27 | chr2 | 181494554 | |||||||
| chr2:181494694 | C | G | 1 | a0001c0001t0001g0049 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1249-28C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 11/27 | chr2 | 181494694 | |||||||
| chr2:181494865 | T | C | 37 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0029 others(34): Show |
41 | HG00323.hp1 HG01167.hp2 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.1339+53T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 12/27 | chr2 | 181494865 | |||||||
| chr2:181494886 | G | A | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1339+74G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 12/27 | chr2 | 181494886 | |||||||
| chr2:181494969 | A | G | 3 | a0001c0002t0003g0020 a0001c0002t0003g0207 a0001c0002t0003g0331 |
3 | NA18946.hp2 NA18959.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1339+157A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 12/27 | chr2 | 181494969 | |||||||
| chr2:181494985 | G | T | 1 | a0002c0016t0004g0116 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1339+173G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 12/27 | chr2 | 181494985 | |||||||
| chr2:181495455 | T | C | 49 | a0001c0001t0002g0013 a0001c0001t0002g0050 a0001c0001t0002g0051 others(46): Show |
50 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.1385+39T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 13/27 | chr2 | 181495455 | |||||||
| chr2:181495562 | T | C | 6 | a0001c0001t0002g0219 a0001c0001t0002g0242 a0001c0001t0002g0245 others(3): Show |
6 | HG00544.hp1 HG00621.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.1385+146T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 13/27 | chr2 | 181495562 | |||||||
| chr2:181495565 | C | T | 1 | a0001c0001t0021g0115 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1385+149C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 13/27 | chr2 | 181495565 | |||||||
| chr2:181495588 | T | C | 1 | a0001c0001t0002g0035 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1385+172T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 13/27 | chr2 | 181495588 | |||||||
| chr2:181495770 | A | G | 2 | a0003c0004t0008g0007 a0003c0004t0008g0103 |
3 | HG02647.hp1 HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1386-13A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 13/27 | chr2 | 181495770 | |||||||
| chr2:181496024 | C | T | 1 | a0001c0001t0002g0052 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1540+87C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 14/27 | chr2 | 181496024 | |||||||
| chr2:181496103 | G | A | 1 | a0001c0001t0015g0233 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1540+166G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 14/27 | chr2 | 181496103 | |||||||
| chr2:181496833 | T | C | 1 | a0001c0002t0013g0295 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1540+896T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 14/27 | chr2 | 181496833 | |||||||
| chr2:181496876 | C | T | 1 | a0001c0002t0003g0316 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1540+939C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 14/27 | chr2 | 181496876 | |||||||
| chr2:181497723 | A | T | 1 | a0001c0002t0022g0018 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1541-900A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 14/27 | chr2 | 181497723 | |||||||
| chr2:181497916 | A | G | 3 | a0001c0001t0002g0013 a0001c0001t0002g0141 a0001c0001t0006g0186 |
4 | HG02056.hp2 NA18966.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.1541-707A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 14/27 | chr2 | 181497916 | |||||||
| chr2:181498116 | T | A | 269 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(266): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.1541-507T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 14/27 | chr2 | 181498116 | |||||||
| chr2:181498313 | T | A | 5 | a0003c0004t0008g0023 a0003c0004t0008g0166 a0003c0004t0008g0196 others(2): Show |
5 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1541-310T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 14/27 | chr2 | 181498313 | |||||||
| chr2:181498393 | T | C | 1 | a0005c0010t0042g0065 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1541-230T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 14/27 | chr2 | 181498393 | |||||||
| chr2:181498850 | G | C | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG01074.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1695+73G>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181498850 | |||||||
| chr2:181498886 | T | A | 339 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(336): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1695+109T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181498886 | |||||||
| chr2:181499157 | G | C | 1 | a0003c0004t0008g0166 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1695+380G>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181499157 | |||||||
| chr2:181499352 | G | A | 1 | a0001c0002t0003g0243 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1695+575G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181499352 | |||||||
| chr2:181499459 | G | T | 1 | a0001c0002t0003g0170 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1695+682G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181499459 | |||||||
| chr2:181499482 | T | G | 2 | a0001c0002t0048g0273 a0001c0002t0056g0160 |
2 | HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1695+705T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181499482 | |||||||
| chr2:181499510 | C | A | 1 | a0001c0002t0003g0334 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1695+733C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181499510 | |||||||
| chr2:181499510 | C | T | 2 | a0001c0002t0048g0273 a0001c0002t0056g0160 |
2 | HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1695+733C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181499510 | |||||||
| chr2:181499558 | A | G | 1 | a0002c0003t0004g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1695+781A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181499558 | |||||||
| chr2:181499610 | C | G | 1 | a0001c0002t0003g0314 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1695+833C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181499610 | |||||||
| chr2:181499769 | G | A | 1 | a0001c0001t0002g0117 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1695+992G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181499769 | |||||||
| chr2:181499781 | A | T | 1 | a0001c0001t0002g0072 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1695+1004A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181499781 | |||||||
| chr2:181499796 | C | T | 1 | a0001c0001t0001g0304 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1695+1019C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181499796 | |||||||
| chr2:181499797 | G | A | 2 | a0002c0003t0004g0194 a0002c0003t0005g0187 |
2 | NA19010.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1695+1020G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181499797 | |||||||
| chr2:181499839 | C | A | 339 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(336): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1695+1062C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181499839 | |||||||
| chr2:181499916 | G | T | 65 | a0001c0002t0003g0010 a0001c0002t0003g0014 a0001c0002t0003g0015 others(62): Show |
69 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1695+1139G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181499916 | |||||||
| chr2:181499946 | G | A | 62 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(59): Show |
66 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.1695+1169G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181499946 | |||||||
| chr2:181500062 | C | T | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1695+1285C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181500062 | |||||||
| chr2:181500076 | G | A | 339 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(336): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1695+1299G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181500076 | |||||||
| chr2:181500268 | C | A | 4 | a0001c0002t0012g0335 a0001c0002t0012g0336 a0001c0002t0012g0337 others(1): Show |
4 | HG02451.hp2 HG03453.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1695+1491C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181500268 | |||||||
| chr2:181500424 | T | C | 6 | a0002c0003t0004g0131 a0003c0004t0008g0023 a0003c0004t0008g0166 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1695+1647T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181500424 | |||||||
| chr2:181500510 | G | A | 1 | a0002c0016t0004g0116 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1695+1733G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181500510 | |||||||
| chr2:181500511 | C | T | 3 | a0001c0001t0001g0326 a0001c0001t0007g0256 a0001c0001t0007g0266 |
3 | HG00597.hp1 HG02071.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1695+1734C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181500511 | |||||||
| chr2:181500727 | T | A | 1 | a0002c0005t0001g0009 | 2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1695+1950T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181500727 | |||||||
| chr2:181500849 | T | G | 2 | a0001c0002t0048g0273 a0001c0002t0056g0160 |
2 | HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1695+2072T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181500849 | |||||||
| chr2:181500943 | A | G | 9 | a0001c0001t0002g0030 a0001c0001t0002g0036 a0001c0001t0002g0040 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1695+2166A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181500943 | |||||||
| chr2:181500981 | C | T | 46 | a0001c0001t0002g0013 a0001c0001t0002g0050 a0001c0001t0002g0051 others(43): Show |
47 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.1695+2204C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181500981 | |||||||
| chr2:181501008 | A | G | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1695+2231A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181501008 | |||||||
| chr2:181501380 | G | C | 266 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(263): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.1695+2603G>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181501380 | |||||||
| chr2:181501388 | T | A | 62 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(59): Show |
66 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.1695+2611T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181501388 | |||||||
| chr2:181501700 | C | T | 2 | a0001c0002t0048g0273 a0001c0002t0056g0160 |
2 | HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1695+2923C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181501700 | |||||||
| chr2:181501814 | T | A | 66 | a0001c0002t0003g0010 a0001c0002t0003g0014 a0001c0002t0003g0015 others(63): Show |
70 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1695+3037T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181501814 | |||||||
| chr2:181501922 | A | G | 5 | a0003c0004t0008g0023 a0003c0004t0008g0166 a0003c0004t0008g0196 others(2): Show |
5 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1695+3145A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181501922 | |||||||
| chr2:181501940 | C | T | 2 | a0002c0003t0005g0223 a0002c0003t0005g0247 |
2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1695+3163C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181501940 | |||||||
| chr2:181501991 | G | A | 1 | a0002c0005t0001g0173 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1695+3214G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181501991 | |||||||
| chr2:181502073 | AGT | A | 112 | a0001c0001t0001g0134 a0001c0001t0001g0151 a0001c0001t0001g0189 others(109): Show |
114 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.1695+3300_1695+330 others(6): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 181502073 | ||||||
| chr2:181502184 | T | G | 159 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(156): Show |
172 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.1695+3407T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181502184 | |||||||
| chr2:181502204 | GT | G | 70 | a0001c0001t0001g0189 a0001c0001t0002g0200 a0001c0001t0002g0201 others(67): Show |
74 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1695+3428delT | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181502204 | |||||||
| chr2:181502239 | G | A | 1 | a0001c0002t0009g0267 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1695+3462G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181502239 | |||||||
| chr2:181502263 | G | A | 1 | a0001c0001t0007g0236 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1695+3486G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181502263 | |||||||
| chr2:181502326 | C | G | 1 | a0001c0002t0003g0010 | 2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1695+3549C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181502326 | |||||||
| chr2:181502354 | T | C | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1695+3577T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181502354 | |||||||
| chr2:181502464 | G | A | 1 | a0001c0001t0002g0329 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1695+3687G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181502464 | |||||||
| chr2:181502577 | A | C | 4 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0028 others(1): Show |
4 | HG01891.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1695+3800A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181502577 | |||||||
| chr2:181502594 | G | A | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1695+3817G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181502594 | |||||||
| chr2:181502748 | G | T | 1 | a0001c0001t0020g0142 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1695+3971G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181502748 | |||||||
| chr2:181502917 | C | T | 3 | a0002c0003t0017g0039 a0002c0003t0017g0129 a0002c0003t0017g0164 |
3 | HG02717.hp1 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1695+4140C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181502917 | |||||||
| chr2:181502977 | G | A | 2 | a0001c0001t0002g0052 a0001c0001t0002g0085 |
2 | HG01258.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1695+4200G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181502977 | |||||||
| chr2:181503063 | C | T | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1695+4286C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181503063 | |||||||
| chr2:181503074 | C | T | 4 | a0002c0003t0018g0092 a0002c0003t0018g0146 a0002c0003t0018g0324 others(1): Show |
4 | HG00609.hp2 HG00621.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.1695+4297C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181503074 | |||||||
| chr2:181503142 | A | G | 339 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(336): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1695+4365A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181503142 | |||||||
| chr2:181503233 | T | C | 346 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(343): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.1695+4456T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181503233 | |||||||
| chr2:181503443 | C | T | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1695+4666C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181503443 | |||||||
| chr2:181503484 | C | T | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1695+4707C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181503484 | |||||||
| chr2:181503565 | CTTT | C | 18 | a0001c0002t0003g0061 a0001c0002t0003g0177 a0001c0002t0003g0243 others(15): Show |
18 | HG00140.hp2 HG00735.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.1695+4809_1695+481 others(7): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 181503565 | ||||||
| chr2:181503565 | CTTTT | C | 123 | a0001c0001t0002g0055 a0001c0001t0002g0281 a0001c0001t0030g0215 others(120): Show |
133 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.1695+4808_1695+481 others(8): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 181503565 | ||||||
| chr2:181503565 | CTTTTT | C | 193 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(190): Show |
202 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.1695+4807_1695+481 others(9): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 181503565 | ||||||
| chr2:181503565 | CTTTTTT | C | 7 | a0001c0001t0001g0134 a0001c0001t0001g0340 a0001c0001t0006g0124 others(4): Show |
7 | HG02523.hp1 HG03225.hp1 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.1695+4806_1695+481 others(10): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 181503565 | ||||||
| chr2:181503600 | T | A | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1695+4823T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181503600 | |||||||
| chr2:181503761 | G | A | 5 | a0001c0002t0013g0192 a0001c0002t0013g0295 a0001c0002t0013g0298 others(2): Show |
5 | HG00609.hp1 NA18987.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.1695+4984G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181503761 | |||||||
| chr2:181503824 | G | GA | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1695+5051dupA | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 181503824 | ||||||
| chr2:181503859 | C | T | 5 | a0003c0004t0008g0023 a0003c0004t0008g0166 a0003c0004t0008g0196 others(2): Show |
5 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1695+5082C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181503859 | |||||||
| chr2:181504105 | G | A | 2 | a0001c0002t0048g0273 a0001c0002t0056g0160 |
2 | HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1695+5328G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181504105 | |||||||
| chr2:181504210 | G | A | 1 | a0001c0002t0014g0279 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1695+5433G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181504210 | |||||||
| chr2:181504219 | G | A | 72 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(69): Show |
76 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1696-5439G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181504219 | |||||||
| chr2:181504309 | A | C | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1696-5349A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181504309 | |||||||
| chr2:181504391 | C | T | 1 | a0001c0001t0020g0142 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1696-5267C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181504391 | |||||||
| chr2:181504418 | T | C | 1 | a0001c0001t0032g0321 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1696-5240T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181504418 | |||||||
| chr2:181504449 | G | A | 269 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(266): Show |
284 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.1696-5209G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181504449 | |||||||
| chr2:181504571 | G | A | 4 | a0002c0003t0004g0004 a0002c0003t0004g0056 a0002c0003t0023g0004 others(1): Show |
4 | HG00735.hp2 HG01070.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.1696-5087G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181504571 | |||||||
| chr2:181504641 | C | G | 2 | a0001c0002t0048g0273 a0001c0002t0056g0160 |
2 | HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1696-5017C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181504641 | |||||||
| chr2:181504810 | G | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0076 |
3 | HG02572.hp2 HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1696-4848G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181504810 | |||||||
| chr2:181504816 | T | C | 1 | a0001c0001t0002g0308 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1696-4842T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181504816 | |||||||
| chr2:181504827 | G | A | 1 | a0002c0011t0043g0119 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1696-4831G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181504827 | |||||||
| chr2:181504941 | T | C | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1696-4717T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181504941 | |||||||
| chr2:181505058 | C | A | 1 | a0001c0001t0002g0082 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1696-4600C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181505058 | |||||||
| chr2:181505166 | A | G | 1 | a0001c0001t0039g0339 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1696-4492A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181505166 | |||||||
| chr2:181505189 | T | G | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1696-4469T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181505189 | |||||||
| chr2:181505218 | A | T | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1696-4440A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181505218 | |||||||
| chr2:181505266 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1696-4392A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181505266 | |||||||
| chr2:181505334 | C | T | 1 | a0003c0012t0021g0274 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1696-4324C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181505334 | |||||||
| chr2:181505415 | A | G | 346 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(343): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.1696-4243A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181505415 | |||||||
| chr2:181505447 | C | T | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1696-4211C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181505447 | |||||||
| chr2:181505632 | G | A | 1 | a0003c0012t0021g0274 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1696-4026G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181505632 | |||||||
| chr2:181505720 | G | A | 1 | a0001c0001t0002g0293 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1696-3938G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181505720 | |||||||
| chr2:181505833 | G | A | 5 | a0001c0002t0012g0335 a0001c0002t0012g0336 a0001c0002t0012g0337 others(2): Show |
5 | HG02451.hp2 HG03453.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1696-3825G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181505833 | |||||||
| chr2:181506003 | C | T | 5 | a0001c0002t0014g0277 a0001c0002t0014g0278 a0001c0002t0014g0279 others(2): Show |
5 | HG01081.hp1 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1696-3655C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181506003 | |||||||
| chr2:181506019 | T | G | 1 | a0001c0001t0001g0083 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1696-3639T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181506019 | |||||||
| chr2:181506031 | T | G | 2 | a0001c0002t0048g0273 a0001c0002t0056g0160 |
2 | HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1696-3627T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181506031 | |||||||
| chr2:181506049 | T | C | 2 | a0002c0003t0004g0221 a0002c0003t0005g0269 |
2 | HG00099.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1696-3609T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181506049 | |||||||
| chr2:181506103 | C | A | 1 | a0002c0003t0005g0259 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1696-3555C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181506103 | |||||||
| chr2:181506242 | T | A | 33 | a0001c0001t0001g0012 a0001c0001t0001g0044 a0001c0001t0001g0071 others(30): Show |
34 | HG00408.hp1 HG00597.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.1696-3416T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181506242 | |||||||
| chr2:181506279 | C | T | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1696-3379C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181506279 | |||||||
| chr2:181506416 | A | G | 339 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(336): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1696-3242A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181506416 | |||||||
| chr2:181506419 | T | C | 339 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(336): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1696-3239T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181506419 | |||||||
| chr2:181506513 | A | G | 1 | a0003c0004t0050g0285 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1696-3145A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181506513 | |||||||
| chr2:181506514 | C | T | 339 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(336): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1696-3144C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181506514 | |||||||
| chr2:181506590 | C | T | 339 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(336): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1696-3068C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181506590 | |||||||
| chr2:181506719 | A | T | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1696-2939A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181506719 | |||||||
| chr2:181506847 | A | G | 1 | a0001c0001t0002g0026 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1696-2811A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181506847 | |||||||
| chr2:181506999 | T | C | 1 | a0002c0003t0005g0224 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1696-2659T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181506999 | |||||||
| chr2:181507078 | T | C | 2 | a0001c0002t0048g0273 a0001c0002t0056g0160 |
2 | HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1696-2580T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181507078 | |||||||
| chr2:181507079 | A | G | 7 | a0001c0001t0001g0083 a0001c0001t0001g0276 a0002c0005t0001g0009 others(4): Show |
10 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1696-2579A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181507079 | |||||||
| chr2:181507332 | G | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG01074.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1696-2326G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181507332 | |||||||
| chr2:181507374 | C | G | 1 | a0001c0002t0003g0203 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1696-2284C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181507374 | |||||||
| chr2:181507409 | A | G | 4 | a0001c0001t0001g0189 a0001c0001t0002g0200 a0001c0001t0002g0201 others(1): Show |
4 | NA18945.hp2 NA18960.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-2249A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181507409 | |||||||
| chr2:181507424 | G | C | 266 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(263): Show |
280 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.1696-2234G>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181507424 | |||||||
| chr2:181507553 | A | T | 73 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(70): Show |
78 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1696-2105A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181507553 | |||||||
| chr2:181507556 | C | A | 73 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(70): Show |
78 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1696-2102C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181507556 | |||||||
| chr2:181507560 | G | A | 4 | a0001c0001t0002g0030 a0001c0001t0002g0036 a0001c0001t0002g0040 others(1): Show |
4 | HG02145.hp1 HG02280.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-2098G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181507560 | |||||||
| chr2:181507577 | C | T | 73 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(70): Show |
78 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1696-2081C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181507577 | |||||||
| chr2:181507692 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1696-1966A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181507692 | |||||||
| chr2:181507770 | A | G | 73 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(70): Show |
78 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1696-1888A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181507770 | |||||||
| chr2:181507771 | T | A | 1 | a0001c0001t0002g0308 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1696-1887T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181507771 | |||||||
| chr2:181508021 | AT | A | 67 | a0001c0001t0001g0149 a0001c0001t0007g0217 a0002c0003t0004g0004 others(64): Show |
71 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.1696-1630delT | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 181508021 | ||||||
| chr2:181508028 | T | A | 1 | a0001c0001t0002g0312 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1696-1630T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181508028 | |||||||
| chr2:181508066 | T | A | 73 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(70): Show |
78 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1696-1592T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181508066 | |||||||
| chr2:181508070 | T | A | 1 | a0001c0002t0012g0336 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1696-1588T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181508070 | |||||||
| chr2:181508272 | G | A | 1 | a0001c0002t0003g0210 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1696-1386G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181508272 | |||||||
| chr2:181508636 | T | C | 73 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(70): Show |
78 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1696-1022T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181508636 | |||||||
| chr2:181508702 | AAAAT | A | 73 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(70): Show |
78 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1696-936_1696-933d others(6): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 181508702 | ||||||
| chr2:181508739 | A | T | 6 | a0001c0001t0001g0054 a0001c0001t0001g0183 a0001c0001t0001g0290 others(3): Show |
6 | NA18957.hp1 NA18979.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1696-919A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181508739 | |||||||
| chr2:181508758 | C | T | 2 | a0001c0001t0002g0077 a0001c0001t0002g0341 |
2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1696-900C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181508758 | |||||||
| chr2:181508770 | A | G | 1 | a0001c0001t0002g0109 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1696-888A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181508770 | |||||||
| chr2:181508968 | C | T | 66 | a0001c0001t0002g0281 a0001c0002t0003g0010 a0001c0002t0003g0014 others(63): Show |
70 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1696-690C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181508968 | |||||||
| chr2:181509061 | G | A | 66 | a0001c0002t0003g0010 a0001c0002t0003g0014 a0001c0002t0003g0015 others(63): Show |
70 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1696-597G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181509061 | |||||||
| chr2:181509135 | TAAAAAAA others(6): Show |
T | 2 | a0003c0004t0008g0103 a0003c0004t0049g0098 |
2 | HG03041.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1696-488_1696-476d others(15): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 181509135 | ||||||
| chr2:181509135 | TAAAAAAA others(7): Show |
T | 3 | a0001c0002t0012g0338 a0002c0003t0004g0131 a0003c0004t0008g0007 |
4 | HG02572.hp1 HG02647.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1696-489_1696-476d others(16): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 181509135 | ||||||
| chr2:181509135 | TAAAAAAA others(8): Show |
T | 12 | a0001c0002t0003g0010 a0001c0002t0012g0336 a0001c0002t0012g0337 others(9): Show |
13 | HG00621.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1696-490_1696-476d others(17): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 181509135 | ||||||
| chr2:181509135 | TAAAAAAA others(9): Show |
T | 18 | a0001c0002t0003g0090 a0001c0002t0003g0106 a0001c0002t0003g0172 others(15): Show |
18 | HG00423.hp1 HG00438.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.1696-491_1696-476d others(18): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 181509135 | ||||||
| chr2:181509135 | TAAAAAAA others(10): Show |
T | 107 | a0001c0001t0002g0281 a0001c0002t0003g0014 a0001c0002t0003g0015 others(104): Show |
114 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1696-492_1696-476d others(19): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 181509135 | ||||||
| chr2:181509135 | TAAAAAAA others(11): Show |
T | 7 | a0001c0001t0001g0104 a0001c0001t0002g0050 a0001c0001t0037g0089 others(4): Show |
7 | HG01070.hp1 HG01081.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.1696-493_1696-476d others(20): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 181509135 | ||||||
| chr2:181509135 | TAAAAAAA others(12): Show |
T | 28 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0034 others(25): Show |
30 | HG00323.hp1 HG01123.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.1696-494_1696-476d others(21): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 181509135 | ||||||
| chr2:181509135 | TAAAAAAA others(14): Show |
T | 5 | a0001c0001t0001g0054 a0001c0001t0001g0121 a0001c0001t0001g0304 others(2): Show |
5 | HG02922.hp2 NA18939.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.1696-496_1696-476d others(23): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | 181509135 | ||||||
| chr2:181509149 | A | T | 2 | a0003c0004t0008g0103 a0003c0004t0049g0098 |
2 | HG03041.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1696-509A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181509149 | |||||||
| chr2:181509150 | A | T | 2 | a0002c0003t0004g0131 a0003c0004t0008g0007 |
3 | HG02572.hp1 HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1696-508A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181509150 | |||||||
| chr2:181509151 | A | T | 8 | a0002c0003t0017g0039 a0002c0003t0017g0129 a0002c0003t0017g0164 others(5): Show |
8 | HG00621.hp1 HG01884.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1696-507A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181509151 | |||||||
| chr2:181509152 | A | T | 5 | a0002c0003t0004g0004 a0002c0003t0004g0125 a0002c0003t0004g0301 others(2): Show |
5 | HG00735.hp2 HG01109.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1696-506A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181509152 | |||||||
| chr2:181509153 | A | T | 54 | a0002c0003t0004g0038 a0002c0003t0004g0056 a0002c0003t0004g0058 others(51): Show |
58 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.1696-505A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181509153 | |||||||
| chr2:181509154 | A | T | 3 | a0002c0003t0004g0317 a0002c0003t0005g0238 a0002c0003t0023g0057 |
3 | HG01070.hp1 HG03239.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1696-504A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181509154 | |||||||
| chr2:181509169 | A | C | 1 | a0001c0002t0003g0061 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1696-489A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181509169 | |||||||
| chr2:181509170 | A | C | 1 | a0002c0003t0018g0324 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1696-488A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181509170 | |||||||
| chr2:181509207 | T | A | 2 | a0001c0002t0048g0273 a0001c0002t0056g0160 |
2 | HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1696-451T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181509207 | |||||||
| chr2:181509254 | T | C | 268 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(265): Show |
282 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.1696-404T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181509254 | |||||||
| chr2:181509315 | A | G | 199 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(196): Show |
209 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.1696-343A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181509315 | |||||||
| chr2:181509316 | A | G | 3 | a0002c0003t0018g0092 a0002c0003t0018g0324 a0002c0003t0026g0254 |
3 | HG00609.hp2 NA19003.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1696-342A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181509316 | |||||||
| chr2:181509335 | G | T | 2 | a0001c0002t0048g0273 a0001c0002t0056g0160 |
2 | HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1696-323G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181509335 | |||||||
| chr2:181509409 | A | C | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1696-249A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181509409 | |||||||
| chr2:181509452 | T | C | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1696-206T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181509452 | |||||||
| chr2:181509453 | T | C | 1 | a0001c0001t0002g0346 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1696-205T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181509453 | |||||||
| chr2:181509601 | T | A | 74 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(71): Show |
79 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.1696-57T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181509601 | |||||||
| chr2:181509615 | C | T | 1 | a0001c0002t0003g0170 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1696-43C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 15/27 | chr2 | 181509615 | |||||||
| chr2:181509826 | A | T | 75 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(72): Show |
80 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.1845+19A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 16/27 | chr2 | 181509826 | |||||||
| chr2:181509840 | A | G | 75 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(72): Show |
80 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.1845+33A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 16/27 | chr2 | 181509840 | |||||||
| chr2:181509899 | G | A | 3 | a0001c0001t0002g0066 a0001c0001t0019g0095 a0001c0001t0019g0292 |
3 | HG00140.hp1 HG00323.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.1845+92G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 16/27 | chr2 | 181509899 | |||||||
| chr2:181509915 | C | T | 1 | a0001c0002t0003g0297 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1845+108C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 16/27 | chr2 | 181509915 | |||||||
| chr2:181509917 | A | G | 1 | a0001c0002t0009g0267 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1845+110A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 16/27 | chr2 | 181509917 | |||||||
| chr2:181509933 | A | T | 66 | a0001c0001t0002g0281 a0001c0002t0003g0010 a0001c0002t0003g0014 others(63): Show |
70 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1845+126A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 16/27 | chr2 | 181509933 | |||||||
| chr2:181510049 | A | G | 1 | a0001c0001t0021g0115 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1845+242A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 16/27 | chr2 | 181510049 | |||||||
| chr2:181510145 | T | C | 1 | a0001c0002t0003g0178 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1845+338T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 16/27 | chr2 | 181510145 | |||||||
| chr2:181510199 | C | G | 3 | a0002c0003t0017g0039 a0002c0003t0017g0129 a0002c0003t0017g0164 |
3 | HG02717.hp1 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1845+392C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 16/27 | chr2 | 181510199 | |||||||
| chr2:181510444 | A | G | 1 | a0001c0001t0002g0144 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1845+637A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 16/27 | chr2 | 181510444 | |||||||
| chr2:181510477 | G | T | 346 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(343): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.1845+670G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 16/27 | chr2 | 181510477 | |||||||
| chr2:181510715 | CAT | C | 197 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(194): Show |
207 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1845+911_1845+912d others(4): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr2 | 181510715 | ||||||
| chr2:181510797 | G | A | 8 | a0003c0004t0008g0007 a0003c0004t0008g0023 a0003c0004t0008g0103 others(5): Show |
9 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1846-902G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 16/27 | chr2 | 181510797 | |||||||
| chr2:181510888 | A | T | 2 | a0001c0001t0002g0072 a0001c0001t0035g0307 |
2 | HG02071.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1846-811A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 16/27 | chr2 | 181510888 | |||||||
| chr2:181510916 | GA | G | 76 | a0001c0001t0001g0048 a0001c0007t0002g0080 a0002c0003t0004g0004 others(73): Show |
81 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1846-774delA | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr2 | 181510916 | ||||||
| chr2:181511068 | C | T | 74 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(71): Show |
79 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.1846-631C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 16/27 | chr2 | 181511068 | |||||||
| chr2:181511107 | T | C | 74 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(71): Show |
79 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.1846-592T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 16/27 | chr2 | 181511107 | |||||||
| chr2:181511184 | G | A | 265 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(262): Show |
279 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.1846-515G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 16/27 | chr2 | 181511184 | |||||||
| chr2:181511205 | CCTTA | C | 198 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(195): Show |
208 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1846-489_1846-486d others(6): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr2 | 181511205 | ||||||
| chr2:181511234 | C | A | 265 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(262): Show |
279 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.1846-465C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 16/27 | chr2 | 181511234 | |||||||
| chr2:181511331 | C | T | 74 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(71): Show |
79 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.1846-368C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 16/27 | chr2 | 181511331 | |||||||
| chr2:181511336 | T | G | 74 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(71): Show |
79 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.1846-363T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 16/27 | chr2 | 181511336 | |||||||
| chr2:181511380 | A | G | 10 | a0001c0001t0002g0030 a0001c0001t0002g0036 a0001c0001t0002g0040 others(7): Show |
10 | HG02145.hp1 HG02165.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1846-319A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 16/27 | chr2 | 181511380 | |||||||
| chr2:181511819 | T | G | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1922+44T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181511819 | |||||||
| chr2:181512136 | C | T | 1 | a0001c0001t0015g0233 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1922+361C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181512136 | |||||||
| chr2:181512295 | A | G | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1922+520A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181512295 | |||||||
| chr2:181512308 | G | A | 197 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(194): Show |
207 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1922+533G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181512308 | |||||||
| chr2:181512360 | G | A | 1 | a0001c0001t0002g0077 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1922+585G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181512360 | |||||||
| chr2:181512604 | A | T | 1 | a0001c0002t0003g0319 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1922+829A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181512604 | |||||||
| chr2:181512684 | A | G | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1922+909A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181512684 | |||||||
| chr2:181512729 | G | A | 4 | a0001c0001t0002g0030 a0001c0001t0002g0036 a0001c0001t0002g0040 others(1): Show |
4 | HG02145.hp1 HG02280.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1922+954G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181512729 | |||||||
| chr2:181512734 | G | A | 2 | a0003c0004t0050g0285 a0003c0012t0021g0274 |
2 | HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1922+959G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181512734 | |||||||
| chr2:181512814 | G | A | 66 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(63): Show |
70 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1922+1039G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181512814 | |||||||
| chr2:181512988 | T | A | 1 | a0002c0003t0005g0239 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1922+1213T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181512988 | |||||||
| chr2:181513046 | T | C | 267 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(264): Show |
281 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.1922+1271T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181513046 | |||||||
| chr2:181513070 | T | A | 1 | a0001c0002t0003g0207 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1922+1295T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181513070 | |||||||
| chr2:181513112 | C | G | 1 | a0001c0002t0012g0335 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1922+1337C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181513112 | |||||||
| chr2:181513141 | G | A | 1 | a0002c0003t0005g0240 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1922+1366G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181513141 | |||||||
| chr2:181513163 | C | A | 8 | a0003c0004t0008g0007 a0003c0004t0008g0023 a0003c0004t0008g0103 others(5): Show |
9 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1922+1388C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181513163 | |||||||
| chr2:181513337 | A | G | 1 | a0001c0001t0001g0011 | 2 | HG01361.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1922+1562A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181513337 | |||||||
| chr2:181513349 | A | G | 6 | a0001c0001t0002g0068 a0001c0001t0006g0251 a0001c0001t0006g0270 others(3): Show |
6 | NA18951.hp2 NA18959.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.1922+1574A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181513349 | |||||||
| chr2:181513419 | T | C | 1 | a0001c0002t0046g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1922+1644T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181513419 | |||||||
| chr2:181513656 | A | C | 1 | a0001c0001t0001g0105 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1922+1881A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181513656 | |||||||
| chr2:181513911 | A | G | 346 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(343): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.1922+2136A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181513911 | |||||||
| chr2:181514144 | G | A | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1922+2369G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181514144 | |||||||
| chr2:181514152 | G | A | 1 | a0001c0001t0001g0017 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1922+2377G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181514152 | |||||||
| chr2:181514318 | G | C | 2 | a0001c0002t0012g0337 a0001c0002t0012g0338 |
2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1922+2543G>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181514318 | |||||||
| chr2:181514319 | G | A | 198 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(195): Show |
208 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1922+2544G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181514319 | |||||||
| chr2:181514464 | A | G | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1922+2689A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181514464 | |||||||
| chr2:181514524 | G | GT | 76 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(73): Show |
81 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1922+2750dupT | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr2 | 181514524 | ||||||
| chr2:181514619 | G | GT | 65 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(62): Show |
69 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1922+2849dupT | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr2 | 181514619 | ||||||
| chr2:181514890 | T | C | 8 | a0003c0004t0008g0007 a0003c0004t0008g0023 a0003c0004t0008g0103 others(5): Show |
9 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1922+3115T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181514890 | |||||||
| chr2:181514996 | T | C | 76 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(73): Show |
81 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1922+3221T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181514996 | |||||||
| chr2:181515062 | A | G | 2 | a0001c0001t0002g0030 a0001c0001t0002g0040 |
2 | HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1922+3287A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181515062 | |||||||
| chr2:181515193 | T | A | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1922+3418T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181515193 | |||||||
| chr2:181515344 | A | G | 66 | a0001c0001t0002g0281 a0001c0002t0003g0010 a0001c0002t0003g0014 others(63): Show |
70 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1922+3569A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181515344 | |||||||
| chr2:181515411 | A | C | 2 | a0002c0003t0005g0234 a0002c0003t0005g0235 |
2 | HG02015.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1922+3636A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181515411 | |||||||
| chr2:181515454 | C | T | 2 | a0001c0001t0002g0024 a0001c0001t0002g0025 |
2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1922+3679C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181515454 | |||||||
| chr2:181515483 | C | T | 198 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(195): Show |
208 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1922+3708C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181515483 | |||||||
| chr2:181515484 | A | C | 65 | a0001c0001t0002g0281 a0001c0002t0003g0010 a0001c0002t0003g0014 others(62): Show |
69 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1922+3709A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181515484 | |||||||
| chr2:181515902 | C | T | 1 | a0001c0001t0036g0162 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1922+4127C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181515902 | |||||||
| chr2:181515958 | A | G | 1 | a0001c0002t0003g0203 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1922+4183A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181515958 | |||||||
| chr2:181515978 | C | T | 198 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(195): Show |
208 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1922+4203C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181515978 | |||||||
| chr2:181516011 | C | CTTCA | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1922+4238_1922+423 others(8): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr2 | 181516011 | ||||||
| chr2:181516193 | C | T | 1 | a0001c0002t0046g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1922+4418C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181516193 | |||||||
| chr2:181516256 | A | G | 8 | a0003c0004t0008g0007 a0003c0004t0008g0023 a0003c0004t0008g0103 others(5): Show |
9 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1922+4481A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181516256 | |||||||
| chr2:181516323 | A | G | 199 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(196): Show |
209 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.1922+4548A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181516323 | |||||||
| chr2:181516444 | T | C | 5 | a0001c0002t0014g0277 a0001c0002t0014g0278 a0001c0002t0014g0279 others(2): Show |
5 | HG01081.hp1 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1922+4669T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181516444 | |||||||
| chr2:181516511 | G | T | 2 | a0001c0002t0048g0273 a0001c0002t0056g0160 |
2 | HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1922+4736G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181516511 | |||||||
| chr2:181516516 | G | C | 1 | a0001c0001t0001g0208 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1922+4741G>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181516516 | |||||||
| chr2:181516580 | C | T | 198 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(195): Show |
208 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1922+4805C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181516580 | |||||||
| chr2:181516651 | T | G | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1922+4876T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181516651 | |||||||
| chr2:181516676 | T | C | 1 | a0002c0003t0004g0060 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1922+4901T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181516676 | |||||||
| chr2:181516797 | C | T | 17 | a0001c0001t0001g0121 a0001c0001t0001g0127 a0001c0001t0001g0134 others(14): Show |
17 | HG00408.hp1 HG00597.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.1922+5022C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181516797 | |||||||
| chr2:181516822 | C | T | 198 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(195): Show |
208 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1922+5047C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181516822 | |||||||
| chr2:181516834 | T | G | 1 | a0001c0001t0001g0174 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1922+5059T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181516834 | |||||||
| chr2:181516877 | T | G | 1 | a0001c0002t0003g0305 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1922+5102T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181516877 | |||||||
| chr2:181516903 | G | C | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1922+5128G>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181516903 | |||||||
| chr2:181517242 | A | G | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1923-4949A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181517242 | |||||||
| chr2:181517404 | C | T | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1923-4787C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181517404 | |||||||
| chr2:181517589 | G | A | 65 | a0001c0001t0001g0304 a0001c0002t0003g0010 a0001c0002t0003g0014 others(62): Show |
69 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.1923-4602G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181517589 | |||||||
| chr2:181517640 | G | T | 66 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(63): Show |
70 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1923-4551G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181517640 | |||||||
| chr2:181517804 | T | C | 1 | a0001c0002t0003g0297 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1923-4387T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181517804 | |||||||
| chr2:181518056 | G | T | 2 | a0003c0004t0050g0285 a0003c0012t0021g0274 |
2 | HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1923-4135G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181518056 | |||||||
| chr2:181518061 | G | T | 3 | a0002c0003t0017g0039 a0002c0003t0017g0129 a0002c0003t0017g0164 |
3 | HG02717.hp1 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1923-4130G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181518061 | |||||||
| chr2:181518312 | G | A | 8 | a0003c0004t0008g0007 a0003c0004t0008g0023 a0003c0004t0008g0103 others(5): Show |
9 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1923-3879G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181518312 | |||||||
| chr2:181518364 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1923-3827C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181518364 | |||||||
| chr2:181518689 | T | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0076 |
2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1923-3502T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181518689 | |||||||
| chr2:181518771 | T | C | 2 | a0001c0001t0002g0077 a0001c0001t0024g0067 |
2 | HG02886.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1923-3420T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181518771 | |||||||
| chr2:181518906 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1923-3285G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181518906 | |||||||
| chr2:181519033 | C | T | 2 | a0003c0004t0050g0285 a0003c0012t0021g0274 |
2 | HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1923-3158C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181519033 | |||||||
| chr2:181519278 | T | C | 1 | a0001c0001t0002g0242 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1923-2913T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181519278 | |||||||
| chr2:181519529 | G | C | 17 | a0001c0001t0002g0219 a0001c0001t0002g0242 a0001c0001t0002g0245 others(14): Show |
17 | HG00438.hp2 HG00544.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.1923-2662G>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181519529 | |||||||
| chr2:181519565 | T | G | 63 | a0001c0001t0002g0281 a0001c0002t0003g0010 a0001c0002t0003g0014 others(60): Show |
67 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1923-2626T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181519565 | |||||||
| chr2:181519580 | G | A | 2 | a0001c0002t0003g0046 a0001c0002t0003g0073 |
2 | HG00741.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1923-2611G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181519580 | |||||||
| chr2:181519601 | C | G | 198 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(195): Show |
208 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1923-2590C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181519601 | |||||||
| chr2:181519698 | T | G | 1 | a0003c0004t0008g0103 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1923-2493T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181519698 | |||||||
| chr2:181519850 | C | CAGAA | 3 | a0001c0001t0002g0066 a0001c0001t0019g0095 a0001c0001t0019g0292 |
3 | HG00140.hp1 HG00323.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.1923-2341_1923-234 others(8): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181519850 | |||||||
| chr2:181520011 | C | T | 1 | a0001c0002t0012g0336 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1923-2180C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181520011 | |||||||
| chr2:181520140 | T | C | 3 | a0001c0001t0001g0083 a0001c0001t0038g0110 a0001c0015t0040g0111 |
3 | HG01884.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1923-2051T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181520140 | |||||||
| chr2:181520141 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0076 |
2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1923-2050A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181520141 | |||||||
| chr2:181520305 | C | T | 1 | a0005c0010t0042g0065 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1923-1886C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181520305 | |||||||
| chr2:181520390 | C | A | 1 | a0001c0002t0003g0287 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1923-1801C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181520390 | |||||||
| chr2:181520403 | G | A | 3 | a0002c0003t0017g0039 a0002c0003t0017g0129 a0002c0003t0017g0164 |
3 | HG02717.hp1 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1923-1788G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181520403 | |||||||
| chr2:181520588 | G | A | 2 | a0001c0002t0048g0273 a0001c0002t0056g0160 |
2 | HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1923-1603G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181520588 | |||||||
| chr2:181520785 | A | G | 3 | a0002c0003t0017g0039 a0002c0003t0017g0129 a0002c0003t0017g0164 |
3 | HG02717.hp1 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1923-1406A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181520785 | |||||||
| chr2:181520862 | T | C | 1 | a0001c0001t0002g0346 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1923-1329T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181520862 | |||||||
| chr2:181520916 | A | G | 66 | a0001c0002t0003g0010 a0001c0002t0003g0014 a0001c0002t0003g0015 others(63): Show |
70 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1923-1275A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181520916 | |||||||
| chr2:181520932 | C | T | 74 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(71): Show |
79 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.1923-1259C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181520932 | |||||||
| chr2:181521013 | A | G | 1 | a0001c0002t0009g0267 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1923-1178A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181521013 | |||||||
| chr2:181521054 | CATT | C | 8 | a0003c0004t0008g0007 a0003c0004t0008g0023 a0003c0004t0008g0103 others(5): Show |
9 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1923-1133_1923-113 others(7): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr2 | 181521054 | ||||||
| chr2:181521188 | G | T | 10 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(7): Show |
10 | HG00140.hp2 HG00735.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.1923-1003G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181521188 | |||||||
| chr2:181521228 | A | G | 74 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(71): Show |
79 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.1923-963A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181521228 | |||||||
| chr2:181521261 | C | T | 198 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(195): Show |
208 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1923-930C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181521261 | |||||||
| chr2:181521315 | A | G | 2 | a0001c0002t0012g0337 a0001c0002t0012g0338 |
2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1923-876A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181521315 | |||||||
| chr2:181521534 | G | A | 10 | a0002c0003t0017g0039 a0002c0003t0017g0129 a0002c0003t0017g0164 others(7): Show |
11 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1923-657G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181521534 | |||||||
| chr2:181521643 | G | A | 1 | a0001c0001t0036g0162 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1923-548G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181521643 | |||||||
| chr2:181521942 | C | T | 4 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0028 others(1): Show |
4 | HG01891.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1923-249C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181521942 | |||||||
| chr2:181522022 | T | A | 65 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(62): Show |
69 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1923-169T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181522022 | |||||||
| chr2:181522171 | T | C | 2 | a0002c0003t0017g0129 a0002c0003t0017g0164 |
2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1923-20T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 17/27 | chr2 | 181522171 | |||||||
| chr2:181522406 | A | G | 200 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(197): Show |
210 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.2073+65A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 18/27 | chr2 | 181522406 | |||||||
| chr2:181522812 | C | T | 1 | a0002c0003t0017g0129 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2073+471C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 18/27 | chr2 | 181522812 | |||||||
| chr2:181522844 | G | A | 1 | a0002c0003t0018g0146 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2073+503G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 18/27 | chr2 | 181522844 | |||||||
| chr2:181523173 | C | A | 2 | a0001c0001t0015g0233 a0001c0001t0030g0215 |
2 | HG02132.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.2074-264C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 18/27 | chr2 | 181523173 | |||||||
| chr2:181523231 | C | CAT | 72 | a0001c0001t0002g0281 a0001c0002t0003g0010 a0001c0002t0003g0014 others(69): Show |
76 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.2074-198_2074-197d others(4): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 18/27 | INFO_REALIGN_3_PRIME | chr2 | 181523231 | ||||||
| chr2:181523901 | A | G | 67 | a0001c0001t0002g0281 a0001c0002t0003g0010 a0001c0002t0003g0014 others(64): Show |
71 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.2170-270A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 19/27 | chr2 | 181523901 | |||||||
| chr2:181523949 | G | A | 5 | a0001c0001t0002g0006 a0001c0001t0002g0093 a0001c0001t0002g0094 others(2): Show |
6 | NA18946.hp1 NA18955.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.2170-222G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 19/27 | chr2 | 181523949 | |||||||
| chr2:181524289 | C | G | 5 | a0001c0002t0014g0277 a0001c0002t0014g0278 a0001c0002t0014g0279 others(2): Show |
5 | HG01081.hp1 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2249+39C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 20/27 | chr2 | 181524289 | |||||||
| chr2:181524338 | A | G | 1 | a0001c0001t0002g0088 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2249+88A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 20/27 | chr2 | 181524338 | |||||||
| chr2:181524576 | T | C | 62 | a0001c0001t0002g0281 a0001c0002t0003g0010 a0001c0002t0003g0014 others(59): Show |
66 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.2249+326T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 20/27 | chr2 | 181524576 | |||||||
| chr2:181524786 | A | T | 5 | a0001c0002t0014g0277 a0001c0002t0014g0278 a0001c0002t0014g0279 others(2): Show |
5 | HG01081.hp1 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2250-416A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 20/27 | chr2 | 181524786 | |||||||
| chr2:181524837 | T | C | 193 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(190): Show |
200 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.2250-365T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 20/27 | chr2 | 181524837 | |||||||
| chr2:181524959 | T | TAA | 8 | a0001c0001t0002g0281 a0001c0002t0003g0010 a0001c0002t0003g0175 others(5): Show |
9 | HG00408.hp2 HG02622.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.2250-231_2250-230d others(4): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 181524959 | ||||||
| chr2:181524959 | T | TAAA | 52 | a0001c0002t0003g0014 a0001c0002t0003g0015 a0001c0002t0003g0020 others(49): Show |
55 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.2250-232_2250-230d others(5): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 181524959 | ||||||
| chr2:181524959 | TA | T | 14 | a0001c0001t0002g0136 a0001c0001t0006g0124 a0001c0001t0015g0233 others(11): Show |
15 | HG01516.hp1 HG02132.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.2250-230delA | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 181524959 | ||||||
| chr2:181524959 | TAA | T | 9 | a0001c0002t0014g0277 a0001c0002t0014g0278 a0001c0002t0014g0279 others(6): Show |
9 | HG01081.hp1 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2250-231_2250-230d others(4): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr2 | 181524959 | ||||||
| chr2:181524973 | T | A | 1 | a0001c0001t0021g0115 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2250-229T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 20/27 | chr2 | 181524973 | |||||||
| chr2:181525063 | A | G | 4 | a0002c0003t0018g0092 a0002c0003t0018g0146 a0002c0003t0018g0324 others(1): Show |
4 | HG00609.hp2 HG00621.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.2250-139A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 20/27 | chr2 | 181525063 | |||||||
| chr2:181525380 | A | AT | 5 | a0001c0002t0014g0277 a0001c0002t0014g0278 a0001c0002t0014g0279 others(2): Show |
5 | HG01081.hp1 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2339+96dupT | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181525380 | ||||||
| chr2:181525380 | A | T | 60 | a0001c0002t0003g0010 a0001c0002t0003g0014 a0001c0002t0003g0015 others(57): Show |
64 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.2339+89A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | chr2 | 181525380 | |||||||
| chr2:181525400 | A | G | 8 | a0003c0004t0008g0007 a0003c0004t0008g0023 a0003c0004t0008g0103 others(5): Show |
9 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2339+109A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | chr2 | 181525400 | |||||||
| chr2:181525728 | T | C | 263 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(260): Show |
274 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.2339+437T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | chr2 | 181525728 | |||||||
| chr2:181525745 | C | A | 262 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(259): Show |
273 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.2339+454C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | chr2 | 181525745 | |||||||
| chr2:181526010 | T | C | 5 | a0001c0002t0014g0277 a0001c0002t0014g0278 a0001c0002t0014g0279 others(2): Show |
5 | HG01081.hp1 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2339+719T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | chr2 | 181526010 | |||||||
| chr2:181526113 | T | G | 1 | a0001c0001t0002g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2339+822T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | chr2 | 181526113 | |||||||
| chr2:181526226 | G | T | 261 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(258): Show |
272 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.2339+935G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | chr2 | 181526226 | |||||||
| chr2:181526273 | T | C | 5 | a0001c0002t0014g0277 a0001c0002t0014g0278 a0001c0002t0014g0279 others(2): Show |
5 | HG01081.hp1 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2339+982T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | chr2 | 181526273 | |||||||
| chr2:181526563 | G | T | 1 | a0001c0001t0002g0202 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2340-734G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | chr2 | 181526563 | |||||||
| chr2:181526602 | A | G | 60 | a0001c0002t0003g0010 a0001c0002t0003g0014 a0001c0002t0003g0015 others(57): Show |
64 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.2340-695A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | chr2 | 181526602 | |||||||
| chr2:181526821 | C | CTTTTTT | 35 | a0001c0001t0002g0293 a0002c0003t0004g0038 a0002c0003t0004g0056 others(32): Show |
39 | HG00099.hp2 HG00642.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.2340-449_2340-444d others(8): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181526821 | ||||||
| chr2:181526821 | C | CTTTTTTT | 19 | a0001c0001t0007g0256 a0001c0001t0035g0307 a0002c0003t0004g0004 others(16): Show |
19 | HG00140.hp2 HG00609.hp2 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.2340-450_2340-444d others(9): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181526821 | ||||||
| chr2:181526821 | C | CTTTTTTT others(1): Show |
8 | a0002c0003t0004g0125 a0002c0003t0004g0140 a0002c0003t0004g0317 others(5): Show |
8 | HG00544.hp2 HG01109.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.2340-451_2340-444d others(10): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181526821 | ||||||
| chr2:181526821 | C | CTTTTTTT others(3): Show |
1 | a0002c0003t0004g0194 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2340-453_2340-444d others(12): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181526821 | ||||||
| chr2:181526821 | C | CTTTTTTT others(4): Show |
5 | a0001c0001t0001g0139 a0001c0001t0002g0209 a0001c0001t0002g0219 others(2): Show |
5 | HG02523.hp2 HG03710.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.2340-454_2340-444d others(13): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181526821 | ||||||
| chr2:181526821 | C | CTTTTTTT others(5): Show |
8 | a0001c0001t0001g0037 a0001c0001t0001g0054 a0001c0001t0001g0063 others(5): Show |
8 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(5): Show |
intron_variant | MODIFIER | c.2340-455_2340-444d others(14): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181526821 | ||||||
| chr2:181526821 | C | CTTTTTTT others(6): Show |
30 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0045 others(27): Show |
31 | HG00099.hp1 HG00323.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.2340-456_2340-444d others(15): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181526821 | ||||||
| chr2:181526821 | C | CTTTTTTT others(7): Show |
21 | a0001c0001t0001g0049 a0001c0001t0001g0113 a0001c0001t0001g0118 others(18): Show |
21 | HG00544.hp1 HG00597.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.2340-457_2340-444d others(16): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181526821 | ||||||
| chr2:181526821 | C | CTTTTTTT others(8): Show |
27 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0043 others(24): Show |
29 | HG00140.hp1 HG00621.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.2340-458_2340-444d others(17): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181526821 | ||||||
| chr2:181526821 | C | CTTTTTTT others(9): Show |
11 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0076 others(8): Show |
12 | HG00408.hp1 HG02145.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.2340-459_2340-444d others(18): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181526821 | ||||||
| chr2:181526821 | C | CTTTTTTT others(10): Show |
11 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0326 others(8): Show |
11 | HG01516.hp1 HG01891.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.2340-460_2340-444d others(19): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181526821 | ||||||
| chr2:181526821 | C | CTTTTTTT others(11): Show |
13 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0084 others(10): Show |
15 | HG00423.hp2 HG00438.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.2340-461_2340-444d others(20): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181526821 | ||||||
| chr2:181526821 | C | CTTTTTTT others(12): Show |
7 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0104 others(4): Show |
7 | HG01257.hp2 HG02647.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2340-462_2340-444d others(21): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181526821 | ||||||
| chr2:181526821 | C | CTTTTTTT others(13): Show |
5 | a0001c0001t0001g0099 a0001c0001t0001g0114 a0001c0001t0002g0313 others(2): Show |
5 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2340-463_2340-444d others(22): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181526821 | ||||||
| chr2:181526821 | C | CTTTTTTT others(14): Show |
1 | a0001c0009t0002g0195 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2340-464_2340-444d others(23): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181526821 | ||||||
| chr2:181526821 | C | CTTTTTTT others(15): Show |
2 | a0001c0001t0001g0033 a0001c0001t0002g0117 |
2 | HG02615.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2340-465_2340-444d others(24): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181526821 | ||||||
| chr2:181526821 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0001g0121 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2340-467_2340-444d others(26): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181526821 | ||||||
| chr2:181526821 | CTT | C | 7 | a0001c0001t0001g0304 a0001c0001t0002g0024 a0001c0001t0002g0025 others(4): Show |
7 | HG02723.hp1 HG02818.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.2340-445_2340-444d others(4): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181526821 | ||||||
| chr2:181526821 | CTTTT | C | 9 | a0001c0001t0001g0102 a0001c0001t0001g0127 a0001c0001t0002g0144 others(6): Show |
9 | HG01081.hp1 HG01981.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2340-447_2340-444d others(6): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181526821 | ||||||
| chr2:181526821 | CTTTTT | C | 7 | a0001c0001t0001g0148 a0001c0001t0001g0246 a0001c0001t0002g0035 others(4): Show |
7 | HG02683.hp1 HG03239.hp1 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.2340-448_2340-444d others(7): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181526821 | ||||||
| chr2:181526821 | CTTTTTTT others(2): Show |
C | 58 | a0001c0001t0002g0036 a0001c0001t0002g0041 a0001c0002t0003g0010 others(55): Show |
62 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.2340-452_2340-444d others(11): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181526821 | ||||||
| chr2:181526821 | CTTTTTTT others(3): Show |
C | 3 | a0001c0002t0003g0190 a0001c0002t0003g0191 a0001c0002t0003g0302 |
3 | NA18969.hp2 NA19076.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.2340-453_2340-444d others(12): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181526821 | ||||||
| chr2:181526821 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0159 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2340-455_2340-444d others(14): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181526821 | ||||||
| chr2:181526821 | CTTTTTTT others(9): Show |
C | 6 | a0001c0001t0039g0339 a0001c0002t0012g0335 a0001c0002t0012g0336 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2340-459_2340-444d others(18): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181526821 | ||||||
| chr2:181526821 | CTTTTTTT others(10): Show |
C | 7 | a0001c0001t0001g0276 a0001c0002t0048g0273 a0002c0005t0001g0009 others(4): Show |
10 | HG01891.hp1 HG02257.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.2340-460_2340-444d others(19): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181526821 | ||||||
| chr2:181526821 | CTTTTTTT others(11): Show |
C | 8 | a0003c0004t0008g0007 a0003c0004t0008g0023 a0003c0004t0008g0103 others(5): Show |
9 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2340-461_2340-444d others(20): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | 181526821 | ||||||
| chr2:181526890 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2340-407G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | chr2 | 181526890 | |||||||
| chr2:181526967 | T | G | 1 | a0001c0001t0002g0346 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2340-330T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | chr2 | 181526967 | |||||||
| chr2:181526972 | C | A | 1 | a0001c0002t0031g0220 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2340-325C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | chr2 | 181526972 | |||||||
| chr2:181526988 | C | T | 4 | a0001c0002t0012g0335 a0001c0002t0012g0336 a0001c0002t0012g0337 others(1): Show |
4 | HG02451.hp2 HG03453.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2340-309C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | chr2 | 181526988 | |||||||
| chr2:181527108 | T | C | 11 | a0001c0001t0001g0276 a0001c0001t0002g0030 a0001c0001t0002g0036 others(8): Show |
14 | HG00735.hp1 HG01891.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.2340-189T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | chr2 | 181527108 | |||||||
| chr2:181527251 | G | A | 8 | a0003c0004t0008g0007 a0003c0004t0008g0023 a0003c0004t0008g0103 others(5): Show |
9 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2340-46G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 21/27 | chr2 | 181527251 | |||||||
| chr2:181527416 | G | C | 65 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(62): Show |
69 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.2430+29G>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 22/27 | chr2 | 181527416 | |||||||
| chr2:181527519 | C | T | 4 | a0001c0002t0012g0335 a0001c0002t0012g0336 a0001c0002t0012g0337 others(1): Show |
4 | HG02451.hp2 HG03453.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2430+132C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 22/27 | chr2 | 181527519 | |||||||
| chr2:181527712 | A | AG | 69 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(66): Show |
73 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.2430+328dupG | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr2 | 181527712 | ||||||
| chr2:181527947 | A | G | 1 | a0001c0001t0002g0176 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2430+560A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 22/27 | chr2 | 181527947 | |||||||
| chr2:181528247 | T | C | 2 | a0001c0002t0048g0273 a0001c0002t0056g0160 |
2 | HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.2430+860T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 22/27 | chr2 | 181528247 | |||||||
| chr2:181528256 | C | A | 1 | a0002c0003t0027g0268 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2430+869C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 22/27 | chr2 | 181528256 | |||||||
| chr2:181528341 | A | G | 259 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(256): Show |
270 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.2430+954A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 22/27 | chr2 | 181528341 | |||||||
| chr2:181528382 | C | T | 264 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(261): Show |
275 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.2430+995C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 22/27 | chr2 | 181528382 | |||||||
| chr2:181528478 | C | A | 5 | a0001c0002t0014g0277 a0001c0002t0014g0278 a0001c0002t0014g0279 others(2): Show |
5 | HG01081.hp1 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2431-1063C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 22/27 | chr2 | 181528478 | |||||||
| chr2:181528553 | G | A | 1 | a0001c0002t0003g0193 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2431-988G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 22/27 | chr2 | 181528553 | |||||||
| chr2:181528879 | A | G | 1 | a0002c0003t0004g0137 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2431-662A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 22/27 | chr2 | 181528879 | |||||||
| chr2:181528924 | C | T | 2 | a0001c0002t0014g0277 a0001c0002t0014g0278 |
2 | HG02109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2431-617C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 22/27 | chr2 | 181528924 | |||||||
| chr2:181529032 | C | T | 272 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(269): Show |
284 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.2431-509C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 22/27 | chr2 | 181529032 | |||||||
| chr2:181529248 | T | A | 1 | a0001c0001t0010g0325 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2431-293T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 22/27 | chr2 | 181529248 | |||||||
| chr2:181529251 | TTA | T | 108 | a0001c0001t0002g0006 a0001c0001t0002g0013 a0001c0001t0002g0024 others(105): Show |
110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.2431-288_2431-287d others(4): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr2 | 181529251 | ||||||
| chr2:181529312 | T | C | 1 | a0001c0001t0002g0312 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2431-229T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 22/27 | chr2 | 181529312 | |||||||
| chr2:181529418 | C | T | 272 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(269): Show |
284 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.2431-123C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 22/27 | chr2 | 181529418 | |||||||
| chr2:181529492 | C | T | 5 | a0001c0002t0014g0277 a0001c0002t0014g0278 a0001c0002t0014g0279 others(2): Show |
5 | HG01081.hp1 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2431-49C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 22/27 | chr2 | 181529492 | |||||||
| chr2:181529770 | C | T | 1 | a0001c0001t0001g0017 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2538+122C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 23/27 | chr2 | 181529770 | |||||||
| chr2:181529840 | A | G | 268 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(265): Show |
280 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.2538+192A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 23/27 | chr2 | 181529840 | |||||||
| chr2:181529841 | T | C | 1 | a0002c0003t0004g0205 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2538+193T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 23/27 | chr2 | 181529841 | |||||||
| chr2:181529971 | T | A | 5 | a0001c0002t0014g0277 a0001c0002t0014g0278 a0001c0002t0014g0279 others(2): Show |
5 | HG01081.hp1 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2538+323T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 23/27 | chr2 | 181529971 | |||||||
| chr2:181530039 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2538+391C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 23/27 | chr2 | 181530039 | |||||||
| chr2:181530127 | A | G | 4 | a0001c0001t0002g0030 a0001c0001t0002g0036 a0001c0001t0002g0040 others(1): Show |
4 | HG02145.hp1 HG02280.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2539-397A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 23/27 | chr2 | 181530127 | |||||||
| chr2:181530214 | C | T | 1 | a0001c0013t0002g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2539-310C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 23/27 | chr2 | 181530214 | |||||||
| chr2:181530227 | A | G | 205 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(202): Show |
213 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.2539-297A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 23/27 | chr2 | 181530227 | |||||||
| chr2:181530385 | C | CA | 4 | a0001c0002t0003g0177 a0001c0002t0003g0178 a0001c0002t0003g0179 others(1): Show |
4 | HG02040.hp2 NA18944.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.2539-132dupA | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr2 | 181530385 | ||||||
| chr2:181530436 | A | C | 1 | a0001c0001t0001g0097 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2539-88A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 23/27 | chr2 | 181530436 | |||||||
| chr2:181530514 | G | T | 2 | a0002c0003t0004g0286 a0002c0003t0004g0344 |
2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2539-10G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 23/27 | chr2 | 181530514 | |||||||
| chr2:181530519 | C | T | 2 | a0001c0002t0003g0190 a0001c0002t0003g0302 |
2 | NA18969.hp2 NA19079.hp2 |
splice_region_variant&intron_variant | LOW | c.2539-5C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 23/27 | chr2 | 181530519 | |||||||
| chr2:181530716 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2664+67G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 24/27 | chr2 | 181530716 | |||||||
| chr2:181530845 | T | C | 5 | a0001c0002t0014g0277 a0001c0002t0014g0278 a0001c0002t0014g0279 others(2): Show |
5 | HG01081.hp1 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2664+196T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 24/27 | chr2 | 181530845 | |||||||
| chr2:181531058 | T | G | 2 | a0001c0001t0002g0283 a0001c0001t0002g0284 |
2 | HG00099.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.2664+409T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 24/27 | chr2 | 181531058 | |||||||
| chr2:181531120 | G | GA | 66 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(63): Show |
70 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.2664+482dupA | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 181531120 | ||||||
| chr2:181531120 | GA | G | 9 | a0001c0001t0001g0304 a0001c0001t0010g0091 a0001c0001t0010g0135 others(6): Show |
9 | HG02523.hp1 NA18612.hp1 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.2664+482delA | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr2 | 181531120 | ||||||
| chr2:181531164 | T | G | 4 | a0001c0002t0012g0335 a0001c0002t0012g0336 a0001c0002t0012g0337 others(1): Show |
4 | HG02451.hp2 HG03453.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2665-493T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 24/27 | chr2 | 181531164 | |||||||
| chr2:181531252 | T | C | 3 | a0002c0003t0017g0039 a0002c0003t0017g0129 a0002c0003t0017g0164 |
3 | HG02717.hp1 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2665-405T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 24/27 | chr2 | 181531252 | |||||||
| chr2:181531297 | G | A | 1 | a0001c0002t0014g0279 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2665-360G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 24/27 | chr2 | 181531297 | |||||||
| chr2:181531305 | T | G | 267 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(264): Show |
279 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.2665-352T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 24/27 | chr2 | 181531305 | |||||||
| chr2:181531327 | C | T | 267 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(264): Show |
279 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.2665-330C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 24/27 | chr2 | 181531327 | |||||||
| chr2:181531368 | T | C | 1 | a0001c0002t0003g0010 | 2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2665-289T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 24/27 | chr2 | 181531368 | |||||||
| chr2:181531588 | T | C | 1 | a0001c0001t0006g0260 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2665-69T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 24/27 | chr2 | 181531588 | |||||||
| chr2:181531599 | T | G | 1 | a0001c0002t0034g0345 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2665-58T>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 24/27 | chr2 | 181531599 | |||||||
| chr2:181531841 | A | G | 60 | a0001c0002t0003g0010 a0001c0002t0003g0014 a0001c0002t0003g0015 others(57): Show |
64 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.2784+65A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | chr2 | 181531841 | |||||||
| chr2:181532056 | C | T | 1 | a0001c0001t0007g0217 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2784+280C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | chr2 | 181532056 | |||||||
| chr2:181532065 | A | G | 60 | a0001c0002t0003g0010 a0001c0002t0003g0014 a0001c0002t0003g0015 others(57): Show |
64 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.2784+289A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | chr2 | 181532065 | |||||||
| chr2:181532148 | C | G | 268 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(265): Show |
280 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.2784+372C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | chr2 | 181532148 | |||||||
| chr2:181532160 | G | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0053 a0001c0001t0001g0189 |
3 | NA18944.hp1 NA18960.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.2784+384G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | chr2 | 181532160 | |||||||
| chr2:181532188 | G | C | 8 | a0003c0004t0008g0007 a0003c0004t0008g0023 a0003c0004t0008g0103 others(5): Show |
9 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2784+412G>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | chr2 | 181532188 | |||||||
| chr2:181532247 | T | C | 82 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(79): Show |
87 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.2784+471T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | chr2 | 181532247 | |||||||
| chr2:181532287 | T | C | 341 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(338): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.2784+511T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | chr2 | 181532287 | |||||||
| chr2:181532516 | G | A | 1 | a0001c0001t0007g0258 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2784+740G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | chr2 | 181532516 | |||||||
| chr2:181532566 | C | T | 3 | a0001c0001t0002g0244 a0001c0001t0006g0249 a0001c0001t0006g0262 |
3 | NA18968.hp2 NA18969.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.2784+790C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | chr2 | 181532566 | |||||||
| chr2:181532638 | A | C | 1 | a0001c0001t0002g0329 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2784+862A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | chr2 | 181532638 | |||||||
| chr2:181532674 | A | G | 268 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(265): Show |
280 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.2784+898A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | chr2 | 181532674 | |||||||
| chr2:181532689 | G | A | 1 | a0001c0001t0002g0026 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2784+913G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | chr2 | 181532689 | |||||||
| chr2:181532829 | A | C | 1 | a0001c0001t0002g0329 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2784+1053A>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | chr2 | 181532829 | |||||||
| chr2:181533051 | CAT | C | 74 | a0001c0002t0003g0010 a0001c0002t0003g0014 a0001c0002t0003g0015 others(71): Show |
79 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.2785-1218_2785-121 others(6): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 181533051 | ||||||
| chr2:181533123 | G | A | 5 | a0001c0002t0014g0277 a0001c0002t0014g0278 a0001c0002t0014g0279 others(2): Show |
5 | HG01081.hp1 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2785-1149G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | chr2 | 181533123 | |||||||
| chr2:181533132 | G | A | 1 | a0001c0001t0002g0088 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2785-1140G>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | chr2 | 181533132 | |||||||
| chr2:181533207 | T | A | 1 | a0001c0001t0002g0329 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2785-1065T>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | chr2 | 181533207 | |||||||
| chr2:181533215 | C | A | 191 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(188): Show |
198 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.2785-1057C>A | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | chr2 | 181533215 | |||||||
| chr2:181533422 | C | T | 1 | a0001c0002t0003g0073 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2785-850C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | chr2 | 181533422 | |||||||
| chr2:181533433 | G | T | 7 | a0003c0004t0008g0007 a0003c0004t0008g0023 a0003c0004t0008g0103 others(4): Show |
8 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2785-839G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | chr2 | 181533433 | |||||||
| chr2:181533602 | A | G | 61 | a0001c0002t0003g0010 a0001c0002t0003g0014 a0001c0002t0003g0015 others(58): Show |
65 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.2785-670A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | chr2 | 181533602 | |||||||
| chr2:181533738 | C | G | 8 | a0003c0004t0008g0007 a0003c0004t0008g0023 a0003c0004t0008g0103 others(5): Show |
9 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2785-534C>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | chr2 | 181533738 | |||||||
| chr2:181533746 | A | G | 60 | a0001c0002t0003g0010 a0001c0002t0003g0014 a0001c0002t0003g0015 others(57): Show |
64 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.2785-526A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | chr2 | 181533746 | |||||||
| chr2:181533791 | C | T | 1 | a0002c0003t0004g0206 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2785-481C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | chr2 | 181533791 | |||||||
| chr2:181533966 | C | T | 1 | a0001c0002t0022g0018 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2785-306C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | chr2 | 181533966 | |||||||
| chr2:181534028 | ATATTTAA others(38): Show |
A | 1 | a0001c0001t0002g0025 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2785-242_2785-198d others(47): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr2 | 181534028 | ||||||
| chr2:181534603 | AG | A | 60 | a0001c0002t0003g0010 a0001c0002t0003g0014 a0001c0002t0003g0015 others(57): Show |
64 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.2884-211delG | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr2 | 181534603 | ||||||
| chr2:181534720 | T | C | 1 | a0001c0001t0020g0142 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2884-96T>C | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 26/27 | chr2 | 181534720 | |||||||
| chr2:181534759 | G | T | 75 | a0001c0002t0003g0010 a0001c0002t0003g0014 a0001c0002t0003g0015 others(72): Show |
80 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.2884-57G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 26/27 | chr2 | 181534759 | |||||||
| chr2:181534770 | A | AT | 14 | a0001c0002t0014g0277 a0001c0002t0014g0278 a0001c0002t0014g0279 others(11): Show |
15 | HG01081.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2884-35dupT | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr2 | 181534770 | ||||||
| chr2:181534770 | A | ATT | 264 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(261): Show |
278 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.2884-36_2884-35dup others(2): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr2 | 181534770 | ||||||
| chr2:181534787 | T | TTGAG | 61 | a0001c0002t0003g0010 a0001c0002t0003g0014 a0001c0002t0003g0015 others(58): Show |
65 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.2884-27_2884-24dup others(4): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr2 | 181534787 | ||||||
| chr2:181534958 | C | T | 68 | a0002c0003t0004g0004 a0002c0003t0004g0038 a0002c0003t0004g0056 others(65): Show |
72 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.3003+23C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 27/27 | chr2 | 181534958 | |||||||
| chr2:181535035 | G | T | 64 | a0001c0002t0003g0010 a0001c0002t0003g0014 a0001c0002t0003g0015 others(61): Show |
68 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.3003+100G>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 27/27 | chr2 | 181535035 | |||||||
| chr2:181535092 | G | GTCTT | 5 | a0001c0002t0014g0277 a0001c0002t0014g0278 a0001c0002t0014g0279 others(2): Show |
5 | HG01081.hp1 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.3003+161_3003+164d others(6): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr2 | 181535092 | ||||||
| chr2:181535130 | AAGAC | A | 5 | a0001c0002t0014g0277 a0001c0002t0014g0278 a0001c0002t0014g0279 others(2): Show |
5 | HG01081.hp1 HG02109.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.3003+200_3003+203d others(6): Show |
ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr2 | 181535130 | ||||||
| chr2:181535138 | C | T | 8 | a0001c0001t0001g0121 a0001c0001t0001g0151 a0001c0001t0001g0154 others(5): Show |
8 | HG00408.hp1 HG00597.hp1 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.3003+203C>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 27/27 | chr2 | 181535138 | |||||||
| chr2:181535259 | A | G | 267 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(264): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.3004-173A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 27/27 | chr2 | 181535259 | |||||||
| chr2:181535259 | A | T | 1 | a0001c0001t0037g0089 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3004-173A>T | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 27/27 | chr2 | 181535259 | |||||||
| chr2:181535365 | A | G | 4 | a0001c0001t0001g0064 a0001c0001t0001g0174 a0001c0001t0001g0276 others(1): Show |
4 | HG01255.hp2 HG02257.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.3004-67A>G | ITGA4 | ENSG00000115232.14 | transcript | ENST00000397033.7 | protein_coding | 27/27 | chr2 | 181535365 |