Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 116985 |
| ensemblid | ENSG00000186635.16 |
| hgncid | 16925 |
| symbol | ARAP1 |
| name | ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 1 |
| refseq_nuc | NM_001040118.3 |
| refseq_prot | NP_001035207.1 |
| ensembl_nuc | ENST00000393609.8 |
| ensembl_prot | ENSP00000377233.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 72685069 |
| end | 72752408 |
| strand | - |
| ver | v1.2 |
| region | chr11:72685069-72752408 |
| region5000 | chr11:72680069-72757408 |
| regionname0 | ARAP1_chr11_72685069_72752408 |
| regionname5000 | ARAP1_chr11_72680069_72757408 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1450 | 249 | 63 | 56 | 94 | 8 | 27 | 72 | ARAP1_chr11_72680069_72757408 | ARAP1 | MAEAG others(1445): Show |
chr11 | 72680069 | 72757408 |
| a0002 | 0/0 | 1450 | 68 | 24 | 15 | 19 | 2 | 8 | 11 | ARAP1_chr11_72680069_72757408 | ARAP1 | MAEAG others(1445): Show |
chr11 | 72680069 | 72757408 |
| a0003 | 0/0 | 1450 | 14 | 0 | 3 | 11 | 0 | 0 | 6 | ARAP1_chr11_72680069_72757408 | ARAP1 | MAEAG others(1445): Show |
chr11 | 72680069 | 72757408 |
| a0004 | 0/0 | 1450 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | MAEAG others(1445): Show |
chr11 | 72680069 | 72757408 |
| a0005 | 0/0 | 1450 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | ARAP1_chr11_72680069_72757408 | ARAP1 | MAEAG others(1445): Show |
chr11 | 72680069 | 72757408 |
| a0006 | 0/0 | 1450 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ARAP1_chr11_72680069_72757408 | ARAP1 | MAEAG others(1445): Show |
chr11 | 72680069 | 72757408 |
| a0007 | 0/0 | 1450 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | MAEAG others(1445): Show |
chr11 | 72680069 | 72757408 |
| a0008 | 0/0 | 1450 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | MAEAG others(1445): Show |
chr11 | 72680069 | 72757408 |
| a0009 | 0/0 | 1450 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | MAEAG others(1445): Show |
chr11 | 72680069 | 72757408 |
| a0010 | 0/0 | 1450 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | MAEAG others(1445): Show |
chr11 | 72680069 | 72757408 |
| a0011 | 0/0 | 1450 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | MAEAG others(1445): Show |
chr11 | 72680069 | 72757408 |
| a0012 | 0/0 | 1450 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | MAEAG others(1445): Show |
chr11 | 72680069 | 72757408 |
| a0013 | 0/0 | 1450 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | MAEAG others(1445): Show |
chr11 | 72680069 | 72757408 |
| a0014 | 0/0 | 1450 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | MAEAG others(1445): Show |
chr11 | 72680069 | 72757408 |
| a0015 | 0/0 | 1450 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | MAEAG others(1445): Show |
chr11 | 72680069 | 72757408 |
| a0016 | 0/0 | 1450 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | MAEAG others(1445): Show |
chr11 | 72680069 | 72757408 |
| a0017 | 0/0 | 1450 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | MAEAG others(1445): Show |
chr11 | 72680069 | 72757408 |
| a0018 | 0/0 | 1450 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | MAEAG others(1445): Show |
chr11 | 72680069 | 72757408 |
| a0019 | 0/0 | 1450 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | MAEAG others(1445): Show |
chr11 | 72680069 | 72757408 |
| a0020 | 0/0 | 1450 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | MAEAG others(1445): Show |
chr11 | 72680069 | 72757408 |
| a0021 | 0/1 | 1450 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | MAEAG others(1445): Show |
chr11 | 72680069 | 72757408 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 4350 | 109 | 51 | 18 | 29 | 2 | 8 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0001c0002 | 0/0 | 4350 | 84 | 2 | 29 | 36 | 6 | 11 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0001c0004 | 0/0 | 4350 | 32 | 6 | 5 | 15 | 0 | 6 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0001c0006 | 0/0 | 4350 | 7 | 0 | 0 | 7 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0001c0007 | 0/0 | 4350 | 6 | 0 | 1 | 5 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0001c0008 | 0/0 | 4350 | 4 | 3 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0001c0013 | 0/0 | 4350 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0001c0019 | 0/0 | 4350 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0001c0024 | 0/0 | 4350 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0001c0028 | 0/0 | 4350 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0001c0030 | 0/0 | 4350 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0001c0034 | 0/0 | 4350 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0001c0035 | 0/0 | 4350 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0002c0003 | 0/0 | 4350 | 64 | 21 | 14 | 19 | 2 | 8 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0002c0012 | 0/0 | 4350 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0002c0020 | 0/0 | 4350 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0002c0025 | 0/0 | 4350 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0003c0005 | 0/0 | 4350 | 14 | 0 | 3 | 11 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0004c0009 | 0/0 | 4350 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0005c0010 | 0/0 | 4350 | 3 | 0 | 0 | 3 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0006c0011 | 0/0 | 4350 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0007c0031 | 0/0 | 4350 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0008c0029 | 0/0 | 4350 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0009c0026 | 0/0 | 4350 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0010c0014 | 0/0 | 4350 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0011c0033 | 0/0 | 4350 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0012c0023 | 0/0 | 4350 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0013c0015 | 0/0 | 4350 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0014c0036 | 0/0 | 4350 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0015c0017 | 0/0 | 4350 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0016c0022 | 0/0 | 4350 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0017c0032 | 0/0 | 4350 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0018c0027 | 0/0 | 4350 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0019c0021 | 0/0 | 4350 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0020c0018 | 0/0 | 4350 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 | ||
| a0021c0016 | 0/1 | 4350 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | ATGGC others(4345): Show |
chr11 | 72680069 | 72757408 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5156 | 101 | 45 | 16 | 29 | 2 | 8 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0001c0001t0002 | 0/0 | 5156 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0001c0001t0003 | 0/0 | 5156 | 3 | 1 | 2 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0001c0001t0004 | 0/0 | 5156 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0001c0001t0007 | 0/0 | 5156 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0001c0002t0001 | 0/0 | 5156 | 83 | 2 | 29 | 36 | 6 | 10 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0001c0002t0002 | 0/0 | 5156 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0001c0004t0001 | 0/0 | 5156 | 31 | 6 | 5 | 14 | 0 | 6 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0001c0004t0006 | 0/0 | 5156 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0001c0006t0001 | 0/0 | 5156 | 7 | 0 | 0 | 7 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0001c0007t0001 | 0/0 | 5156 | 6 | 0 | 1 | 5 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0001c0008t0001 | 0/0 | 5156 | 4 | 3 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0001c0013t0001 | 0/0 | 5156 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0001c0019t0001 | 0/0 | 5156 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0001c0024t0001 | 0/0 | 5156 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0001c0028t0003 | 0/0 | 5156 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0001c0030t0001 | 0/0 | 5156 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0001c0034t0001 | 0/0 | 5156 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0001c0035t0001 | 0/0 | 5156 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0002c0003t0001 | 0/0 | 5156 | 43 | 21 | 7 | 13 | 0 | 2 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0002c0003t0002 | 0/0 | 5156 | 21 | 0 | 7 | 6 | 2 | 6 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0002c0012t0001 | 0/0 | 5156 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0002c0020t0002 | 0/0 | 5156 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0002c0025t0001 | 0/0 | 5156 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0003c0005t0001 | 0/0 | 5156 | 14 | 0 | 3 | 11 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0004c0009t0001 | 0/0 | 5156 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0005c0010t0002 | 0/0 | 5156 | 3 | 0 | 0 | 3 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0006c0011t0001 | 0/0 | 5156 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0007c0031t0001 | 0/0 | 5156 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0008c0029t0005 | 0/0 | 5156 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0009c0026t0001 | 0/0 | 5156 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0010c0014t0001 | 0/0 | 5156 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0011c0033t0001 | 0/0 | 5156 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0012c0023t0001 | 0/0 | 5156 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0013c0015t0001 | 0/0 | 5156 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0014c0036t0001 | 0/0 | 5156 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0015c0017t0001 | 0/0 | 5156 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0016c0022t0002 | 0/0 | 5156 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0017c0032t0001 | 0/0 | 5156 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0018c0027t0001 | 0/0 | 5156 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0019c0021t0001 | 0/0 | 5156 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0020c0018t0002 | 0/0 | 5156 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| a0021c0016t0001 | 0/1 | 5156 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | GCTGC others(5151): Show |
chr11 | 72680069 | 72757408 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0263 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0007g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0003 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0006t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0006t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0006t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0006t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0006t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0006t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0006t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0007t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0007t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0007t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0007t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0007t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0007t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0008t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0008t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0008t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0008t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0013t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0019t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0024t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0028t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0030t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0034t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0035t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0022 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0012t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0012t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0020t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0025t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0003c0005t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0003c0005t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0003c0005t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0003c0005t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0003c0005t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0003c0005t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0003c0005t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0003c0005t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0003c0005t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0003c0005t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0003c0005t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0003c0005t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0003c0005t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0004c0009t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0004c0009t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0004c0009t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0005c0010t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0005c0010t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0005c0010t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0006c0011t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0006c0011t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0007c0031t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0008c0029t0005g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0009c0026t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0010c0014t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0011c0033t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0012c0023t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0013c0015t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0014c0036t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0015c0017t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0016c0022t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0017c0032t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0018c0027t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0019c0021t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0020c0018t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0021c0016t0001g0111 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0040 | EUR | GBR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00099 | hp2 | a0002 | c0003 | t0002 | g0317 | EUR | GBR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0128 | EUR | GBR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00140 | hp2 | a0002 | c0003 | t0002 | g0022 | EUR | GBR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00438 | hp2 | a0002 | c0003 | t0001 | g0199 | EAS | CHS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00544 | hp1 | a0001 | c0004 | t0001 | g0053 | EAS | CHS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00544 | hp2 | a0002 | c0003 | t0002 | g0328 | EAS | CHS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00558 | hp1 | a0001 | c0007 | t0001 | g0072 | EAS | CHS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00558 | hp2 | a0002 | c0003 | t0002 | g0327 | EAS | CHS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00597 | hp1 | a0002 | c0003 | t0001 | g0209 | EAS | CHS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00597 | hp2 | a0001 | c0004 | t0001 | g0036 | EAS | CHS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00621 | hp1 | a0001 | c0004 | t0001 | g0034 | EAS | CHS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00621 | hp2 | a0001 | c0006 | t0001 | g0121 | EAS | CHS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0181 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0188 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0217 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0192 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | CHS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00735 | hp2 | a0001 | c0004 | t0001 | g0050 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0190 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0178 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0176 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01074 | hp1 | a0001 | c0008 | t0001 | g0288 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0180 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01099 | hp1 | a0001 | c0004 | t0001 | g0055 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0202 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01106 | hp2 | a0002 | c0003 | t0001 | g0208 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0225 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01167 | hp2 | a0001 | c0004 | t0001 | g0051 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01168 | hp2 | a0002 | c0003 | t0001 | g0244 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0224 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01175 | hp1 | a0008 | c0029 | t0005 | g0056 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01175 | hp2 | a0003 | c0005 | t0001 | g0216 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01243 | hp2 | a0002 | c0003 | t0002 | g0318 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0172 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01255 | hp2 | a0002 | c0003 | t0002 | g0313 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01258 | hp1 | a0002 | c0003 | t0002 | g0311 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0201 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01346 | hp1 | a0002 | c0003 | t0002 | g0309 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01346 | hp2 | a0001 | c0024 | t0001 | g0189 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01358 | hp1 | a0003 | c0005 | t0001 | g0030 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0173 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0184 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01361 | hp2 | a0001 | c0004 | t0001 | g0170 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01433 | hp1 | a0002 | c0020 | t0002 | g0319 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01433 | hp2 | a0001 | c0028 | t0003 | g0023 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01496 | hp1 | a0002 | c0003 | t0002 | g0315 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0175 | EUR | IBS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0016 | EUR | IBS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01884 | hp1 | a0001 | c0008 | t0001 | g0287 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01891 | hp1 | a0002 | c0003 | t0001 | g0021 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01891 | hp2 | a0002 | c0003 | t0001 | g0210 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01928 | hp1 | a0002 | c0003 | t0001 | g0017 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01928 | hp2 | a0002 | c0003 | t0001 | g0135 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01934 | hp2 | a0002 | c0003 | t0002 | g0312 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01943 | hp1 | a0003 | c0005 | t0001 | g0038 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0020 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01952 | hp1 | a0002 | c0003 | t0002 | g0323 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01975 | hp2 | a0002 | c0003 | t0001 | g0214 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01978 | hp2 | a0002 | c0003 | t0001 | g0017 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01993 | hp1 | a0001 | c0007 | t0001 | g0070 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0183 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0246 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02027 | hp2 | a0009 | c0026 | t0001 | g0242 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02040 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0254 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02056 | hp2 | a0010 | c0014 | t0001 | g0117 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02071 | hp1 | a0002 | c0003 | t0001 | g0241 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02074 | hp2 | a0001 | c0004 | t0001 | g0047 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02080 | hp1 | a0001 | c0004 | t0001 | g0156 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02080 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0236 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02083 | hp2 | a0003 | c0005 | t0001 | g0004 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02132 | hp1 | a0003 | c0005 | t0001 | g0035 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02132 | hp2 | a0002 | c0003 | t0002 | g0326 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0261 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02145 | hp1 | a0002 | c0003 | t0001 | g0276 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02148 | hp1 | a0001 | c0004 | t0001 | g0165 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02155 | hp1 | a0003 | c0005 | t0001 | g0029 | EAS | CDX | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02155 | hp2 | a0011 | c0033 | t0001 | g0155 | EAS | CDX | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CDX | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02165 | hp2 | a0003 | c0005 | t0001 | g0004 | EAS | CDX | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02258 | hp1 | a0004 | c0009 | t0001 | g0275 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02258 | hp2 | a0002 | c0003 | t0001 | g0087 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02293 | hp1 | a0002 | c0003 | t0001 | g0062 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0174 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02523 | hp1 | a0003 | c0005 | t0001 | g0267 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02523 | hp2 | a0002 | c0003 | t0001 | g0220 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02572 | hp2 | a0001 | c0004 | t0001 | g0084 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02602 | hp1 | a0002 | c0003 | t0001 | g0245 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02602 | hp2 | a0012 | c0023 | t0001 | g0166 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02615 | hp1 | a0004 | c0009 | t0001 | g0274 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02615 | hp2 | a0013 | c0015 | t0001 | g0043 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02622 | hp2 | a0001 | c0004 | t0001 | g0086 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0306 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02630 | hp2 | a0001 | c0004 | t0001 | g0101 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02723 | hp1 | a0002 | c0003 | t0001 | g0283 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0305 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0200 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02738 | hp2 | a0001 | c0004 | t0001 | g0052 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02886 | hp1 | a0002 | c0003 | t0001 | g0279 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02886 | hp2 | a0002 | c0012 | t0001 | g0285 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02895 | hp1 | a0014 | c0036 | t0001 | g0294 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0226 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02965 | hp1 | a0002 | c0003 | t0001 | g0282 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02970 | hp1 | a0002 | c0003 | t0001 | g0289 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02976 | hp1 | a0004 | c0009 | t0001 | g0271 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03017 | hp1 | a0002 | c0003 | t0002 | g0314 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03017 | hp2 | a0015 | c0017 | t0001 | g0230 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03041 | hp1 | a0002 | c0003 | t0001 | g0284 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0321 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03195 | hp1 | a0002 | c0003 | t0001 | g0195 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03195 | hp2 | a0002 | c0003 | t0001 | g0194 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03209 | hp2 | a0001 | c0004 | t0001 | g0044 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03225 | hp2 | a0002 | c0012 | t0001 | g0286 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0300 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03486 | hp1 | a0002 | c0003 | t0001 | g0281 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0239 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0191 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03516 | hp1 | a0002 | c0003 | t0001 | g0211 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03540 | hp1 | a0002 | c0003 | t0001 | g0076 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0079 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03579 | hp2 | a0002 | c0003 | t0001 | g0280 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0193 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03654 | hp2 | a0016 | c0022 | t0002 | g0310 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03688 | hp1 | a0002 | c0003 | t0002 | g0022 | SAS | STU | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | STU | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03831 | hp1 | a0001 | c0004 | t0001 | g0048 | SAS | BEB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03831 | hp2 | a0002 | c0003 | t0002 | g0329 | SAS | BEB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03834 | hp1 | a0001 | c0004 | t0001 | g0054 | SAS | BEB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0307 | SAS | BEB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03927 | hp1 | a0002 | c0003 | t0001 | g0196 | SAS | BEB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0182 | SAS | BEB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03942 | hp2 | a0001 | c0019 | t0001 | g0179 | SAS | BEB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG04115 | hp1 | a0001 | c0004 | t0001 | g0061 | SAS | STU | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG04115 | hp2 | a0002 | c0003 | t0002 | g0320 | SAS | STU | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0167 | SAS | BEB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG04199 | hp1 | a0001 | c0013 | t0001 | g0171 | SAS | STU | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG04199 | hp2 | a0002 | c0003 | t0002 | g0308 | SAS | STU | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG04204 | hp1 | a0002 | c0003 | t0002 | g0325 | SAS | STU | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0203 | SAS | STU | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | YRI | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | YRI | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18612 | hp1 | a0001 | c0006 | t0001 | g0148 | EAS | CHB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18612 | hp2 | a0002 | c0003 | t0001 | g0227 | EAS | CHB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18906 | hp1 | a0001 | c0035 | t0001 | g0269 | AFR | YRI | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | YRI | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18940 | hp1 | a0001 | c0004 | t0001 | g0045 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18940 | hp2 | a0002 | c0003 | t0002 | g0304 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18944 | hp1 | a0001 | c0006 | t0001 | g0141 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18944 | hp2 | a0001 | c0030 | t0001 | g0215 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18948 | hp1 | a0006 | c0011 | t0001 | g0151 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18954 | hp2 | a0003 | c0005 | t0001 | g0127 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18959 | hp1 | a0001 | c0004 | t0001 | g0059 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18960 | hp1 | a0003 | c0005 | t0001 | g0243 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18960 | hp2 | a0002 | c0003 | t0001 | g0228 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18963 | hp1 | a0001 | c0006 | t0001 | g0065 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18965 | hp2 | a0017 | c0032 | t0001 | g0266 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18966 | hp1 | a0001 | c0007 | t0001 | g0071 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18966 | hp2 | a0001 | c0004 | t0001 | g0060 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18967 | hp2 | a0003 | c0005 | t0001 | g0032 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18968 | hp1 | a0002 | c0003 | t0002 | g0324 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18969 | hp2 | a0002 | c0003 | t0001 | g0207 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18971 | hp1 | a0001 | c0004 | t0001 | g0132 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18973 | hp1 | a0005 | c0010 | t0002 | g0302 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18977 | hp2 | a0005 | c0010 | t0002 | g0301 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18980 | hp2 | a0002 | c0003 | t0001 | g0136 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18981 | hp1 | a0003 | c0005 | t0001 | g0033 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18981 | hp2 | a0002 | c0003 | t0001 | g0204 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18987 | hp1 | a0001 | c0034 | t0001 | g0299 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18987 | hp2 | a0002 | c0003 | t0002 | g0322 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18990 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18991 | hp1 | a0006 | c0011 | t0001 | g0112 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18992 | hp1 | a0003 | c0005 | t0001 | g0108 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18993 | hp1 | a0001 | c0007 | t0001 | g0081 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18994 | hp2 | a0018 | c0027 | t0001 | g0145 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18995 | hp1 | a0005 | c0010 | t0002 | g0303 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18995 | hp2 | a0002 | c0003 | t0001 | g0198 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18998 | hp2 | a0001 | c0006 | t0001 | g0218 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18999 | hp1 | a0002 | c0003 | t0001 | g0221 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19000 | hp1 | a0001 | c0004 | t0001 | g0126 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19003 | hp1 | a0001 | c0007 | t0001 | g0068 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19010 | hp1 | a0001 | c0006 | t0001 | g0122 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19010 | hp2 | a0002 | c0003 | t0001 | g0219 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19030 | hp1 | a0019 | c0021 | t0001 | g0268 | AFR | LWK | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19030 | hp2 | a0001 | c0008 | t0001 | g0291 | AFR | LWK | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | LWK | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19043 | hp2 | a0002 | c0003 | t0001 | g0080 | AFR | LWK | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19055 | hp2 | a0001 | c0004 | t0006 | g0058 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19056 | hp1 | a0002 | c0003 | t0001 | g0206 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19066 | hp1 | a0003 | c0005 | t0001 | g0031 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0264 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19077 | hp1 | a0001 | c0007 | t0001 | g0064 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19077 | hp2 | a0001 | c0004 | t0001 | g0256 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19090 | hp1 | a0001 | c0006 | t0001 | g0154 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19240 | hp1 | a0002 | c0003 | t0001 | g0088 | AFR | YRI | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19240 | hp2 | a0001 | c0008 | t0001 | g0290 | AFR | YRI | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA20129 | hp1 | a0020 | c0018 | t0002 | g0316 | AFR | ASW | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ASW | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0177 | EUR | TSI | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0233 | EUR | TSI | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0237 | EUR | TSI | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0240 | EUR | TSI | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA20905 | hp1 | a0001 | c0004 | t0001 | g0057 | SAS | GIH | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA20905 | hp2 | a0001 | c0004 | t0001 | g0049 | SAS | GIH | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0238 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01123 | hp2 | a0007 | c0031 | t0001 | g0037 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02486 | hp1 | a0002 | c0003 | t0001 | g0277 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02486 | hp2 | a0002 | c0003 | t0001 | g0270 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0113 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0085 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | USA | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG06807 | hp2 | a0002 | c0003 | t0001 | g0021 | AFR | USA | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA20300 | hp1 | a0002 | c0025 | t0001 | g0278 | AFR | USA | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | USA | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA21309 | hp1 | a0002 | c0003 | t0001 | g0119 | AFR | LWK | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA21309 | hp2 | a0001 | c0004 | t0001 | g0248 | AFR | LWK | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| homoSapiens | chm13v2 | a0021 | c0016 | t0001 | g0111 | REF | REF | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0263 | REF | REF | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:72686155 | C | T | 3 | a0003 a0007 a0009 |
16 | HG01123.hp2 HG01175.hp2 HG01358.hp1 others(13): Show |
missense_variant | MODERATE | c.4222G>A | p.Val1408Met | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 34/35 | 4430/5156 | 4222/4353 | 1408/1450 | chr11 | 72686155 | |||
| chr11:72693710 | C | A | 1 | a0012 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.3790G>T | p.Ala1264Ser | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 28/35 | 3998/5156 | 3790/4353 | 1264/1450 | chr11 | 72693710 | |||
| chr11:72697010 | G | C | 5 | a0002 a0009 a0015 others(2): Show |
72 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(69): Show |
missense_variant | MODERATE | c.3139C>G | p.Gln1047Glu | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 22/35 | 3347/5156 | 3139/4353 | 1047/1450 | chr11 | 72697010 | |||
| chr11:72698015 | C | T | 1 | a0016 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.2633G>A | p.Arg878Gln | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 19/35 | 2841/5156 | 2633/4353 | 878/1450 | chr11 | 72698015 | |||
| chr11:72698070 | G | A | 1 | a0008 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.2578C>T | p.Arg860Trp | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 19/35 | 2786/5156 | 2578/4353 | 860/1450 | chr11 | 72698070 | |||
| chr11:72699035 | C | G | 1 | a0019 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.2511G>C | p.Gln837His | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 18/35 | 2719/5156 | 2511/4353 | 837/1450 | chr11 | 72699035 | |||
| chr11:72702913 | C | A | 1 | a0018 | 1 | NA18994.hp2 | missense_variant | MODERATE | c.2159G>T | p.Arg720Leu | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 15/35 | 2367/5156 | 2159/4353 | 720/1450 | chr11 | 72702913 | |||
| chr11:72707313 | C | T | 1 | a0020 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.1585G>A | p.Ala529Thr | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 12/35 | 1793/5156 | 1585/4353 | 529/1450 | chr11 | 72707313 | |||
| chr11:72709888 | G | A | 1 | a0007 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.1505C>T | p.Thr502Met | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/35 | 1713/5156 | 1505/4353 | 502/1450 | chr11 | 72709888 | |||
| chr11:72709934 | C | T | 1 | a0015 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.1459G>A | p.Val487Met | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/35 | 1667/5156 | 1459/4353 | 487/1450 | chr11 | 72709934 | |||
| chr11:72709957 | C | A | 1 | a0017 | 1 | NA18965.hp2 | missense_variant | MODERATE | c.1436G>T | p.Gly479Val | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/35 | 1644/5156 | 1436/4353 | 479/1450 | chr11 | 72709957 | |||
| chr11:72710537 | G | A | 1 | a0011 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.1264C>T | p.Arg422Cys | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 10/35 | 1472/5156 | 1264/4353 | 422/1450 | chr11 | 72710537 | |||
| chr11:72711449 | C | T | 1 | a0004 | 3 | HG02258.hp1 HG02615.hp1 HG02976.hp1 |
missense_variant | MODERATE | c.1073G>A | p.Arg358Gln | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 8/35 | 1281/5156 | 1073/4353 | 358/1450 | chr11 | 72711449 | |||
| chr11:72712269 | C | T | 1 | a0013 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.949G>A | p.Gly317Arg | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 7/35 | 1157/5156 | 949/4353 | 317/1450 | chr11 | 72712269 | |||
| chr11:72712335 | C | T | 1 | a0006 | 2 | NA18948.hp1 NA18991.hp1 |
missense_variant | MODERATE | c.883G>A | p.Gly295Arg | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 7/35 | 1091/5156 | 883/4353 | 295/1450 | chr11 | 72712335 | |||
| chr11:72712555 | G | A | 1 | a0014 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.761C>T | p.Pro254Leu | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 6/35 | 969/5156 | 761/4353 | 254/1450 | chr11 | 72712555 | |||
| chr11:72712562 | G | A | 1 | a0005 | 3 | NA18973.hp1 NA18977.hp2 NA18995.hp1 |
missense_variant | MODERATE | c.754C>T | p.Pro252Ser | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 6/35 | 962/5156 | 754/4353 | 252/1450 | chr11 | 72712562 | |||
| chr11:72726632 | C | T | 1 | a0010 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.497G>A | p.Arg166His | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/35 | 705/5156 | 497/4353 | 166/1450 | chr11 | 72726632 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:72695041 | G | A | 1 | a0002c0012 | 2 | HG02886.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.3633C>T | p.Asn1211Asn | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 27/35 | 3841/5156 | 3633/4353 | 1211/1450 | chr11 | 72695041 | |||
| chr11:72695089 | T | C | 1 | a0001c0024 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.3585A>G | p.Ala1195Ala | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 27/35 | 3793/5156 | 3585/4353 | 1195/1450 | chr11 | 72695089 | |||
| chr11:72695718 | A | G | 1 | a0002c0025 | 1 | NA20300.hp1 | splice_region_variant&synonymous_variant | LOW | c.3420T>C | p.Ser1140Ser | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 24/35 | 3628/5156 | 3420/4353 | 1140/1450 | chr11 | 72695718 | |||
| chr11:72697032 | A | C | 1 | a0001c0008 | 4 | HG01074.hp1 HG01884.hp1 NA19030.hp2 others(1): Show |
synonymous_variant | LOW | c.3117T>G | p.Pro1039Pro | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 22/35 | 3325/5156 | 3117/4353 | 1039/1450 | chr11 | 72697032 | |||
| chr11:72697612 | C | T | 9 | a0001c0002 a0001c0007 a0001c0013 others(6): Show |
99 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(96): Show |
synonymous_variant | LOW | c.2775G>A | p.Leu925Leu | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 20/35 | 2983/5156 | 2775/4353 | 925/1450 | chr11 | 72697612 | |||
| chr11:72697948 | G | A | 1 | a0018c0027 | 1 | NA18994.hp2 | synonymous_variant | LOW | c.2700C>T | p.Cys900Cys | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 19/35 | 2908/5156 | 2700/4353 | 900/1450 | chr11 | 72697948 | |||
| chr11:72701764 | C | T | 2 | a0001c0019 a0002c0020 |
2 | HG01433.hp1 HG03942.hp2 |
synonymous_variant | LOW | c.2187G>A | p.Ser729Ser | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 16/35 | 2395/5156 | 2187/4353 | 729/1450 | chr11 | 72701764 | |||
| chr11:72704197 | G | A | 1 | a0001c0028 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.1947C>T | p.Tyr649Tyr | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 14/35 | 2155/5156 | 1947/4353 | 649/1450 | chr11 | 72704197 | |||
| chr11:72704284 | G | A | 6 | a0001c0004 a0001c0007 a0003c0005 others(3): Show |
55 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(52): Show |
synonymous_variant | LOW | c.1860C>T | p.Asn620Asn | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 14/35 | 2068/5156 | 1860/4353 | 620/1450 | chr11 | 72704284 | |||
| chr11:72707239 | G | A | 1 | a0001c0030 | 1 | NA18944.hp2 | synonymous_variant | LOW | c.1659C>T | p.Cys553Cys | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 12/35 | 1867/5156 | 1659/4353 | 553/1450 | chr11 | 72707239 | |||
| chr11:72709887 | C | T | 1 | a0001c0006 | 7 | HG00621.hp2 NA18612.hp1 NA18944.hp1 others(4): Show |
synonymous_variant | LOW | c.1506G>A | p.Thr502Thr | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/35 | 1714/5156 | 1506/4353 | 502/1450 | chr11 | 72709887 | |||
| chr11:72712458 | G | A | 1 | a0001c0034 | 1 | NA18987.hp1 | synonymous_variant | LOW | c.858C>T | p.His286His | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 6/35 | 1066/5156 | 858/4353 | 286/1450 | chr11 | 72712458 | |||
| chr11:72712512 | G | A | 1 | a0001c0035 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.804C>T | p.Ser268Ser | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 6/35 | 1012/5156 | 804/4353 | 268/1450 | chr11 | 72712512 | |||
| chr11:72726775 | C | T | 1 | a0001c0013 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.354G>A | p.Pro118Pro | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/35 | 562/5156 | 354/4353 | 118/1450 | chr11 | 72726775 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:72685078 | A | C | 1 | a0008c0029t0005 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*586T>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 35/35 | 586 | chr11 | 72685078 | ||||||
| chr11:72685093 | T | C | 1 | a0001c0004t0006 | 1 | NA19055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*571A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 35/35 | 571 | chr11 | 72685093 | ||||||
| chr11:72685431 | A | G | 1 | a0001c0001t0004 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*233T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 35/35 | 233 | chr11 | 72685431 | ||||||
| chr11:72685608 | T | A | 2 | a0001c0001t0003 a0001c0028t0003 |
4 | HG01168.hp1 HG01169.hp1 HG01433.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*56A>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 35/35 | 56 | chr11 | 72685608 | ||||||
| chr11:72752356 | A | T | 2 | a0001c0001t0003 a0001c0028t0003 |
4 | HG01168.hp1 HG01169.hp1 HG01433.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-156T>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/35 | 25228 | chr11 | 72752356 | ||||||
| chr11:72752362 | C | A | 1 | a0001c0001t0007 | 1 | HG03453.hp1 | 5_prime_UTR_variant | MODIFIER | c.-162G>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/35 | 25234 | chr11 | 72752362 | ||||||
| chr11:72752390 | G | A | 7 | a0001c0001t0002 a0001c0002t0002 a0002c0003t0002 others(4): Show |
31 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(28): Show |
5_prime_UTR_variant | MODIFIER | c.-190C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/35 | 25262 | chr11 | 72752390 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:72685754 | C | T | 4 | a0001c0001t0001g0089 a0002c0003t0001g0281 a0002c0003t0001g0283 others(1): Show |
4 | HG02723.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.4336-73G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 34/34 | chr11 | 72685754 | |||||||
| chr11:72685755 | A | G | 129 | a0001c0001t0001g0007 a0001c0001t0001g0077 a0001c0001t0001g0089 others(126): Show |
144 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.4336-74T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 34/34 | chr11 | 72685755 | |||||||
| chr11:72685945 | G | A | 129 | a0001c0001t0001g0007 a0001c0001t0001g0077 a0001c0001t0001g0089 others(126): Show |
144 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.4335+97C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 34/34 | chr11 | 72685945 | |||||||
| chr11:72685964 | A | G | 74 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0078 others(71): Show |
79 | HG00544.hp1 HG00558.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.4335+78T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 34/34 | chr11 | 72685964 | |||||||
| chr11:72686540 | AAAAGAAC others(11): Show |
A | 1 | a0001c0004t0001g0165 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.4186-367_4186-350d others(20): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 33/34 | chr11 | 72686540 | |||||||
| chr11:72686787 | C | T | 1 | a0001c0002t0001g0175 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.4186-596G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 33/34 | chr11 | 72686787 | |||||||
| chr11:72686810 | G | A | 25 | a0001c0002t0001g0002 a0001c0002t0001g0012 a0001c0002t0001g0013 others(22): Show |
29 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.4186-619C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 33/34 | chr11 | 72686810 | |||||||
| chr11:72686927 | A | C | 1 | a0001c0001t0001g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4185+512T>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 33/34 | chr11 | 72686927 | |||||||
| chr11:72687045 | G | A | 1 | a0001c0004t0001g0054 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.4185+394C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 33/34 | chr11 | 72687045 | |||||||
| chr11:72687252 | G | T | 1 | a0001c0002t0001g0213 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.4185+187C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 33/34 | chr11 | 72687252 | |||||||
| chr11:72687396 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4185+43G>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 33/34 | chr11 | 72687396 | |||||||
| chr11:72687665 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.4121+23G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 32/34 | chr11 | 72687665 | |||||||
| chr11:72687802 | C | G | 1 | a0001c0002t0001g0191 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.4071-64G>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 31/34 | chr11 | 72687802 | |||||||
| chr11:72687889 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4071-151C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 31/34 | chr11 | 72687889 | |||||||
| chr11:72687925 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4071-187G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 31/34 | chr11 | 72687925 | |||||||
| chr11:72687945 | C | T | 5 | a0001c0004t0001g0044 a0001c0004t0001g0084 a0001c0004t0001g0085 others(2): Show |
5 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.4071-207G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 31/34 | chr11 | 72687945 | |||||||
| chr11:72688007 | GT | G | 186 | a0001c0001t0001g0007 a0001c0001t0001g0046 a0001c0001t0001g0077 others(183): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.4071-270delA | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 31/34 | chr11 | 72688007 | |||||||
| chr11:72688010 | T | G | 74 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0078 others(71): Show |
79 | HG00544.hp1 HG00558.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.4071-272A>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 31/34 | chr11 | 72688010 | |||||||
| chr11:72688022 | T | C | 2 | a0001c0001t0003g0024 a0001c0001t0003g0025 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.4071-284A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 31/34 | chr11 | 72688022 | |||||||
| chr11:72688089 | T | C | 128 | a0001c0001t0001g0007 a0001c0001t0001g0046 a0001c0001t0001g0077 others(125): Show |
143 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.4071-351A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 31/34 | chr11 | 72688089 | |||||||
| chr11:72688101 | C | T | 5 | a0001c0004t0001g0044 a0001c0004t0001g0084 a0001c0004t0001g0085 others(2): Show |
5 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.4070+354G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 31/34 | chr11 | 72688101 | |||||||
| chr11:72688133 | G | A | 124 | a0001c0001t0001g0007 a0001c0001t0001g0077 a0001c0001t0001g0089 others(121): Show |
139 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(136): Show |
intron_variant | MODIFIER | c.4070+322C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 31/34 | chr11 | 72688133 | |||||||
| chr11:72688168 | A | G | 4 | a0002c0003t0001g0087 a0002c0003t0001g0088 a0002c0003t0001g0194 others(1): Show |
4 | HG02258.hp2 HG03195.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.4070+287T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 31/34 | chr11 | 72688168 | |||||||
| chr11:72688406 | A | G | 58 | a0001c0001t0001g0110 a0001c0001t0001g0134 a0001c0001t0001g0149 others(55): Show |
59 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.4070+49T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 31/34 | chr11 | 72688406 | |||||||
| chr11:72688446 | C | T | 1 | a0001c0002t0001g0192 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.4070+9G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 31/34 | chr11 | 72688446 | |||||||
| chr11:72688450 | C | A | 1 | a0001c0006t0001g0122 | 1 | NA19010.hp1 | splice_region_variant&intron_variant | LOW | c.4070+5G>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 31/34 | chr11 | 72688450 | |||||||
| chr11:72688562 | G | A | 126 | a0001c0001t0001g0007 a0001c0001t0001g0046 a0001c0001t0001g0077 others(123): Show |
141 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.3988-25C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72688562 | |||||||
| chr11:72688594 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3988-57C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72688594 | |||||||
| chr11:72688601 | C | T | 1 | a0001c0001t0002g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3988-64G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72688601 | |||||||
| chr11:72688602 | G | T | 1 | a0001c0001t0001g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3988-65C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72688602 | |||||||
| chr11:72688652 | C | T | 69 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0078 others(66): Show |
74 | HG00544.hp1 HG00558.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.3988-115G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72688652 | |||||||
| chr11:72688936 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0293 |
2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3988-399G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72688936 | |||||||
| chr11:72688956 | C | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0158 |
2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3988-419G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72688956 | |||||||
| chr11:72689037 | C | T | 22 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 others(19): Show |
23 | HG00639.hp2 HG00733.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.3988-500G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72689037 | |||||||
| chr11:72689206 | T | A | 1 | a0001c0001t0001g0159 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3988-669A>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72689206 | |||||||
| chr11:72689231 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0186 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3988-694G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72689231 | |||||||
| chr11:72689293 | G | T | 1 | a0002c0003t0002g0311 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.3988-756C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72689293 | |||||||
| chr11:72689419 | G | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0164 a0001c0002t0001g0169 |
4 | NA18941.hp2 NA18990.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.3988-882C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72689419 | |||||||
| chr11:72689450 | C | A | 2 | a0001c0006t0001g0065 a0001c0006t0001g0141 |
2 | NA18944.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.3988-913G>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72689450 | |||||||
| chr11:72689536 | G | C | 9 | a0001c0001t0001g0077 a0001c0001t0001g0295 a0001c0001t0001g0296 others(6): Show |
9 | HG01168.hp1 HG01169.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.3988-999C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72689536 | |||||||
| chr11:72689551 | A | G | 127 | a0001c0001t0001g0007 a0001c0001t0001g0077 a0001c0001t0001g0089 others(124): Show |
142 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.3988-1014T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72689551 | |||||||
| chr11:72689558 | G | A | 3 | a0005c0010t0002g0301 a0005c0010t0002g0302 a0005c0010t0002g0303 |
3 | NA18973.hp1 NA18977.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.3988-1021C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72689558 | |||||||
| chr11:72689654 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0186 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3988-1117C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72689654 | |||||||
| chr11:72689757 | T | A | 1 | a0001c0001t0001g0144 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3988-1220A>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72689757 | |||||||
| chr11:72689759 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3988-1222T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72689759 | |||||||
| chr11:72689812 | A | T | 125 | a0001c0001t0001g0007 a0001c0001t0001g0077 a0001c0001t0001g0089 others(122): Show |
140 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.3988-1275T>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72689812 | |||||||
| chr11:72689840 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0186 |
2 | HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3988-1303C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72689840 | |||||||
| chr11:72689864 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3988-1327G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72689864 | |||||||
| chr11:72689913 | G | T | 123 | a0001c0001t0001g0007 a0001c0001t0001g0077 a0001c0001t0001g0089 others(120): Show |
138 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.3988-1376C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72689913 | |||||||
| chr11:72689954 | C | T | 1 | a0001c0002t0001g0203 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3988-1417G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72689954 | |||||||
| chr11:72689957 | C | T | 7 | a0001c0002t0001g0002 a0001c0002t0001g0176 a0001c0002t0001g0177 others(4): Show |
9 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.3988-1420G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72689957 | |||||||
| chr11:72690030 | A | G | 1 | a0001c0001t0001g0251 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3988-1493T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72690030 | |||||||
| chr11:72690056 | T | C | 100 | a0001c0001t0001g0011 a0001c0001t0001g0078 a0001c0001t0001g0096 others(97): Show |
104 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.3988-1519A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72690056 | |||||||
| chr11:72690072 | G | T | 1 | a0001c0002t0001g0040 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3988-1535C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72690072 | |||||||
| chr11:72690250 | A | G | 91 | a0001c0001t0001g0007 a0001c0001t0001g0046 a0001c0001t0001g0077 others(88): Show |
95 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.3988-1713T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72690250 | |||||||
| chr11:72690290 | C | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0237 |
2 | HG01261.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.3988-1753G>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72690290 | |||||||
| chr11:72690305 | T | G | 1 | a0001c0001t0001g0118 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3988-1768A>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72690305 | |||||||
| chr11:72690309 | T | C | 9 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0110 others(6): Show |
9 | HG02647.hp2 HG02818.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.3988-1772A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72690309 | |||||||
| chr11:72690321 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0114 a0001c0001t0001g0115 |
4 | HG00738.hp1 HG01081.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.3988-1784C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72690321 | |||||||
| chr11:72690365 | C | G | 2 | a0014c0036t0001g0294 a0019c0021t0001g0268 |
2 | HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3988-1828G>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72690365 | |||||||
| chr11:72690768 | T | G | 68 | a0001c0001t0001g0015 a0001c0001t0001g0082 a0001c0001t0001g0083 others(65): Show |
72 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.3987+1985A>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72690768 | |||||||
| chr11:72690780 | C | A | 2 | a0001c0004t0001g0048 a0001c0004t0001g0049 |
2 | HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.3987+1973G>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72690780 | |||||||
| chr11:72690867 | G | A | 18 | a0001c0001t0001g0015 a0001c0001t0001g0082 a0001c0001t0001g0083 others(15): Show |
19 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.3987+1886C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72690867 | |||||||
| chr11:72690955 | T | C | 3 | a0001c0002t0001g0169 a0001c0002t0001g0212 a0001c0030t0001g0215 |
3 | NA18944.hp2 NA18993.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.3987+1798A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72690955 | |||||||
| chr11:72690959 | C | A | 11 | a0001c0001t0001g0011 a0001c0001t0001g0077 a0001c0001t0001g0163 others(8): Show |
12 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.3987+1794G>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72690959 | |||||||
| chr11:72691035 | C | T | 2 | a0006c0011t0001g0112 a0006c0011t0001g0151 |
2 | NA18948.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.3987+1718G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72691035 | |||||||
| chr11:72691064 | C | T | 3 | a0003c0005t0001g0031 a0003c0005t0001g0032 a0003c0005t0001g0033 |
3 | NA18967.hp2 NA18981.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.3987+1689G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72691064 | |||||||
| chr11:72691291 | A | G | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG02818.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3987+1462T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72691291 | |||||||
| chr11:72691344 | A | G | 237 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0046 others(234): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.3987+1409T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72691344 | |||||||
| chr11:72691617 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3987+1136G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72691617 | |||||||
| chr11:72691749 | A | G | 263 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0015 others(260): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.3987+1004T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72691749 | |||||||
| chr11:72691777 | T | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0158 |
2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3987+976A>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72691777 | |||||||
| chr11:72691899 | C | T | 263 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0015 others(260): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.3987+854G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72691899 | |||||||
| chr11:72691981 | G | A | 1 | a0001c0001t0003g0026 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3987+772C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72691981 | |||||||
| chr11:72692229 | G | A | 1 | a0001c0024t0001g0189 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3987+524C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72692229 | |||||||
| chr11:72692263 | G | A | 1 | a0001c0001t0001g0293 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3987+490C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72692263 | |||||||
| chr11:72692343 | C | T | 165 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0046 others(162): Show |
183 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(180): Show |
intron_variant | MODIFIER | c.3987+410G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72692343 | |||||||
| chr11:72692550 | T | C | 80 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0005 others(77): Show |
93 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.3987+203A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72692550 | |||||||
| chr11:72692585 | A | G | 9 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0089 others(6): Show |
9 | HG02055.hp1 HG02145.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.3987+168T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72692585 | |||||||
| chr11:72692659 | G | C | 1 | a0019c0021t0001g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3987+94C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 30/34 | chr11 | 72692659 | |||||||
| chr11:72692958 | A | G | 263 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0015 others(260): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.3955-173T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 29/34 | chr11 | 72692958 | |||||||
| chr11:72692971 | G | A | 1 | a0014c0036t0001g0294 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3955-186C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 29/34 | chr11 | 72692971 | |||||||
| chr11:72693154 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3954+171C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 29/34 | chr11 | 72693154 | |||||||
| chr11:72693260 | A | C | 4 | a0001c0001t0001g0046 a0001c0001t0001g0104 a0001c0001t0001g0105 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.3954+65T>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 29/34 | chr11 | 72693260 | |||||||
| chr11:72693518 | G | A | 1 | a0002c0003t0002g0314 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3809-48C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 28/34 | chr11 | 72693518 | |||||||
| chr11:72693848 | C | T | 35 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0018 others(32): Show |
40 | HG00673.hp2 HG00733.hp2 HG01943.hp2 others(37): Show |
intron_variant | MODIFIER | c.3695-43G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 27/34 | chr11 | 72693848 | |||||||
| chr11:72693913 | A | C | 264 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0015 others(261): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.3695-108T>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 27/34 | chr11 | 72693913 | |||||||
| chr11:72694062 | C | T | 1 | a0001c0001t0002g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3695-257G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 27/34 | chr11 | 72694062 | |||||||
| chr11:72694178 | T | C | 234 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0077 others(231): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.3695-373A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 27/34 | chr11 | 72694178 | |||||||
| chr11:72694179 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3695-374T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 27/34 | chr11 | 72694179 | |||||||
| chr11:72694227 | G | A | 1 | a0001c0004t0001g0050 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3695-422C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 27/34 | chr11 | 72694227 | |||||||
| chr11:72694270 | C | G | 1 | a0001c0004t0001g0034 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3695-465G>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 27/34 | chr11 | 72694270 | |||||||
| chr11:72694314 | C | T | 12 | a0001c0001t0001g0011 a0001c0001t0001g0077 a0001c0001t0001g0078 others(9): Show |
13 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.3695-509G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 27/34 | chr11 | 72694314 | |||||||
| chr11:72694405 | C | T | 71 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0002c0003t0001g0017 others(68): Show |
74 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.3694+575G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 27/34 | chr11 | 72694405 | |||||||
| chr11:72694472 | A | G | 4 | a0001c0001t0001g0046 a0001c0001t0001g0104 a0001c0001t0001g0105 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.3694+508T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 27/34 | chr11 | 72694472 | |||||||
| chr11:72694500 | A | C | 86 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0005 others(83): Show |
99 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.3694+480T>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 27/34 | chr11 | 72694500 | |||||||
| chr11:72694525 | C | T | 4 | a0001c0008t0001g0287 a0001c0008t0001g0288 a0001c0008t0001g0290 others(1): Show |
4 | HG01074.hp1 HG01884.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.3694+455G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 27/34 | chr11 | 72694525 | |||||||
| chr11:72694556 | A | G | 1 | a0009c0026t0001g0242 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3694+424T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 27/34 | chr11 | 72694556 | |||||||
| chr11:72694602 | G | A | 1 | a0011c0033t0001g0155 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3694+378C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 27/34 | chr11 | 72694602 | |||||||
| chr11:72694740 | A | C | 163 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0077 others(160): Show |
181 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.3694+240T>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 27/34 | chr11 | 72694740 | |||||||
| chr11:72694823 | C | T | 163 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0077 others(160): Show |
181 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.3694+157G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 27/34 | chr11 | 72694823 | |||||||
| chr11:72694865 | A | T | 1 | a0001c0001t0004g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3694+115T>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 27/34 | chr11 | 72694865 | |||||||
| chr11:72694869 | A | C | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG02818.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3694+111T>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 27/34 | chr11 | 72694869 | |||||||
| chr11:72694908 | G | C | 1 | a0001c0001t0001g0232 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.3694+72C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 27/34 | chr11 | 72694908 | |||||||
| chr11:72694961 | C | G | 1 | a0002c0003t0002g0326 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3694+19G>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 27/34 | chr11 | 72694961 | |||||||
| chr11:72694970 | C | T | 1 | a0001c0001t0002g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3694+10G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 27/34 | chr11 | 72694970 | |||||||
| chr11:72695142 | T | C | 1 | a0002c0003t0001g0196 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3577-45A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 26/34 | chr11 | 72695142 | |||||||
| chr11:72695156 | C | T | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG02818.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3577-59G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 26/34 | chr11 | 72695156 | |||||||
| chr11:72695249 | A | G | 1 | a0002c0012t0001g0286 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3576+138T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 26/34 | chr11 | 72695249 | |||||||
| chr11:72695252 | C | A | 163 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0077 others(160): Show |
181 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.3576+135G>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 26/34 | chr11 | 72695252 | |||||||
| chr11:72696049 | T | C | 1 | a0001c0035t0001g0269 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3273-184A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 23/34 | chr11 | 72696049 | |||||||
| chr11:72696117 | G | C | 163 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0077 others(160): Show |
181 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.3273-252C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 23/34 | chr11 | 72696117 | |||||||
| chr11:72696161 | C | T | 1 | a0001c0001t0003g0024 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.3273-296G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 23/34 | chr11 | 72696161 | |||||||
| chr11:72696162 | G | C | 1 | a0001c0001t0003g0024 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.3273-297C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 23/34 | chr11 | 72696162 | |||||||
| chr11:72696224 | A | G | 163 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0077 others(160): Show |
181 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.3272+325T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 23/34 | chr11 | 72696224 | |||||||
| chr11:72696412 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3272+137G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 23/34 | chr11 | 72696412 | |||||||
| chr11:72696490 | G | A | 1 | a0001c0002t0001g0193 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3272+59C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 23/34 | chr11 | 72696490 | |||||||
| chr11:72696712 | C | A | 1 | a0001c0001t0003g0024 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.3167-58G>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 22/34 | chr11 | 72696712 | |||||||
| chr11:72696725 | G | C | 163 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0077 others(160): Show |
181 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.3167-71C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 22/34 | chr11 | 72696725 | |||||||
| chr11:72696812 | T | G | 1 | a0001c0001t0003g0024 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.3167-158A>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 22/34 | chr11 | 72696812 | |||||||
| chr11:72696839 | C | T | 264 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0015 others(261): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.3166+144G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 22/34 | chr11 | 72696839 | |||||||
| chr11:72696896 | C | T | 16 | a0001c0001t0001g0015 a0001c0001t0001g0082 a0001c0001t0001g0083 others(13): Show |
17 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.3166+87G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 22/34 | chr11 | 72696896 | |||||||
| chr11:72696932 | C | A | 163 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0077 others(160): Show |
181 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.3166+51G>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 22/34 | chr11 | 72696932 | |||||||
| chr11:72697221 | C | T | 45 | a0001c0001t0001g0186 a0001c0004t0001g0001 a0001c0004t0001g0034 others(42): Show |
48 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.2954-26G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 21/34 | chr11 | 72697221 | |||||||
| chr11:72697248 | C | G | 1 | a0001c0001t0003g0024 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2954-53G>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 21/34 | chr11 | 72697248 | |||||||
| chr11:72697307 | T | C | 5 | a0001c0004t0001g0044 a0001c0004t0001g0084 a0001c0004t0001g0085 others(2): Show |
5 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2953+16A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 21/34 | chr11 | 72697307 | |||||||
| chr11:72697502 | T | A | 1 | a0001c0002t0001g0229 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2790-16A>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 20/34 | chr11 | 72697502 | |||||||
| chr11:72697511 | G | A | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0002g0321 |
3 | HG03098.hp1 HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2790-25C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 20/34 | chr11 | 72697511 | |||||||
| chr11:72697700 | A | G | 12 | a0001c0001t0001g0011 a0001c0001t0001g0077 a0001c0001t0001g0078 others(9): Show |
13 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2738-51T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 19/34 | chr11 | 72697700 | |||||||
| chr11:72697795 | AGGATGGC others(2): Show |
A | 10 | a0001c0002t0001g0016 a0001c0002t0001g0200 a0001c0002t0001g0201 others(7): Show |
11 | HG00642.hp1 HG01099.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.2737+107_2737+115d others(11): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 19/34 | chr11 | 72697795 | |||||||
| chr11:72698114 | A | G | 18 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 others(15): Show |
19 | HG00733.hp1 HG01071.hp2 HG01884.hp2 others(16): Show |
splice_region_variant&intron_variant | LOW | c.2542-8T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 18/34 | chr11 | 72698114 | |||||||
| chr11:72698123 | G | A | 2 | a0002c0012t0001g0286 a0003c0005t0001g0216 |
2 | HG01175.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2542-17C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 18/34 | chr11 | 72698123 | |||||||
| chr11:72698144 | C | T | 69 | a0002c0003t0001g0017 a0002c0003t0001g0021 a0002c0003t0001g0062 others(66): Show |
72 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.2542-38G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 18/34 | chr11 | 72698144 | |||||||
| chr11:72698215 | C | T | 163 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0077 others(160): Show |
181 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.2542-109G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 18/34 | chr11 | 72698215 | |||||||
| chr11:72698246 | A | C | 1 | a0002c0003t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2542-140T>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 18/34 | chr11 | 72698246 | |||||||
| chr11:72698297 | C | T | 4 | a0001c0002t0001g0124 a0001c0002t0001g0137 a0001c0002t0001g0138 others(1): Show |
4 | HG02135.hp2 NA18947.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.2542-191G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 18/34 | chr11 | 72698297 | |||||||
| chr11:72698399 | T | C | 1 | a0001c0002t0001g0128 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2542-293A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 18/34 | chr11 | 72698399 | |||||||
| chr11:72698406 | G | A | 1 | a0002c0003t0001g0208 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2542-300C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 18/34 | chr11 | 72698406 | |||||||
| chr11:72698421 | G | A | 4 | a0001c0008t0001g0287 a0001c0008t0001g0288 a0001c0008t0001g0290 others(1): Show |
4 | HG01074.hp1 HG01884.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2542-315C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 18/34 | chr11 | 72698421 | |||||||
| chr11:72698452 | T | A | 163 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0077 others(160): Show |
181 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.2542-346A>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 18/34 | chr11 | 72698452 | |||||||
| chr11:72698585 | G | T | 1 | a0003c0005t0001g0216 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2541+420C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 18/34 | chr11 | 72698585 | |||||||
| chr11:72698668 | T | G | 5 | a0001c0007t0001g0064 a0001c0007t0001g0068 a0001c0007t0001g0071 others(2): Show |
5 | HG00558.hp1 NA18966.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2541+337A>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 18/34 | chr11 | 72698668 | |||||||
| chr11:72698749 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2541+256C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 18/34 | chr11 | 72698749 | |||||||
| chr11:72698870 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2541+135C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 18/34 | chr11 | 72698870 | |||||||
| chr11:72698916 | C | T | 1 | a0002c0003t0001g0221 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2541+89G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 18/34 | chr11 | 72698916 | |||||||
| chr11:72698924 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2541+81G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 18/34 | chr11 | 72698924 | |||||||
| chr11:72699134 | G | A | 5 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0004c0009t0001g0271 others(2): Show |
5 | HG02258.hp1 HG02615.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2439-27C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 17/34 | chr11 | 72699134 | |||||||
| chr11:72699181 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2439-74C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 17/34 | chr11 | 72699181 | |||||||
| chr11:72699283 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2438+134G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 17/34 | chr11 | 72699283 | |||||||
| chr11:72699624 | G | A | 1 | a0001c0004t0001g0057 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2303-72C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 16/34 | chr11 | 72699624 | |||||||
| chr11:72700016 | A | T | 1 | a0001c0002t0001g0265 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2303-464T>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 16/34 | chr11 | 72700016 | |||||||
| chr11:72700037 | T | C | 163 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0077 others(160): Show |
181 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.2303-485A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 16/34 | chr11 | 72700037 | |||||||
| chr11:72700054 | C | T | 80 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0005 others(77): Show |
93 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.2303-502G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 16/34 | chr11 | 72700054 | |||||||
| chr11:72700172 | C | T | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG02818.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2303-620G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 16/34 | chr11 | 72700172 | |||||||
| chr11:72700446 | G | A | 1 | a0014c0036t0001g0294 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2303-894C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 16/34 | chr11 | 72700446 | |||||||
| chr11:72700619 | G | A | 153 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0077 others(150): Show |
170 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.2302+1030C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 16/34 | chr11 | 72700619 | |||||||
| chr11:72700642 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2302+1007C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 16/34 | chr11 | 72700642 | |||||||
| chr11:72700742 | G | A | 70 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0005 others(67): Show |
82 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.2302+907C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 16/34 | chr11 | 72700742 | |||||||
| chr11:72700798 | G | A | 6 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0297 others(3): Show |
6 | HG00438.hp1 NA18973.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.2302+851C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 16/34 | chr11 | 72700798 | |||||||
| chr11:72700809 | A | C | 1 | a0001c0001t0001g0078 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2302+840T>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 16/34 | chr11 | 72700809 | |||||||
| chr11:72700939 | G | A | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG02818.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2302+710C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 16/34 | chr11 | 72700939 | |||||||
| chr11:72700952 | C | T | 163 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0077 others(160): Show |
181 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.2302+697G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 16/34 | chr11 | 72700952 | |||||||
| chr11:72701180 | C | T | 3 | a0002c0003t0001g0087 a0002c0003t0001g0088 a0002c0003t0001g0195 |
3 | HG02258.hp2 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2302+469G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 16/34 | chr11 | 72701180 | |||||||
| chr11:72701263 | G | A | 1 | a0001c0002t0001g0191 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2302+386C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 16/34 | chr11 | 72701263 | |||||||
| chr11:72701302 | G | C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0118 a0001c0001t0001g0120 others(2): Show |
6 | HG01934.hp1 HG01952.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.2302+347C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 16/34 | chr11 | 72701302 | |||||||
| chr11:72701445 | C | G | 163 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0077 others(160): Show |
181 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.2302+204G>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 16/34 | chr11 | 72701445 | |||||||
| chr11:72701503 | T | C | 163 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0077 others(160): Show |
181 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.2302+146A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 16/34 | chr11 | 72701503 | |||||||
| chr11:72701630 | A | G | 163 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0077 others(160): Show |
181 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.2302+19T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 16/34 | chr11 | 72701630 | |||||||
| chr11:72701793 | C | T | 1 | a0001c0008t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2168-10G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 15/34 | chr11 | 72701793 | |||||||
| chr11:72702164 | T | C | 1 | a0002c0003t0001g0210 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2168-381A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 15/34 | chr11 | 72702164 | |||||||
| chr11:72702208 | G | T | 2 | a0002c0003t0001g0283 a0002c0003t0001g0284 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2168-425C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 15/34 | chr11 | 72702208 | |||||||
| chr11:72702592 | G | A | 1 | a0001c0004t0001g0051 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2167+313C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 15/34 | chr11 | 72702592 | |||||||
| chr11:72702639 | C | T | 68 | a0002c0003t0001g0017 a0002c0003t0001g0021 a0002c0003t0001g0062 others(65): Show |
71 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.2167+266G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 15/34 | chr11 | 72702639 | |||||||
| chr11:72702774 | C | T | 1 | a0001c0001t0001g0015 | 2 | HG01243.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2167+131G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 15/34 | chr11 | 72702774 | |||||||
| chr11:72702794 | A | T | 4 | a0001c0001t0001g0046 a0001c0001t0001g0104 a0001c0001t0001g0105 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.2167+111T>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 15/34 | chr11 | 72702794 | |||||||
| chr11:72703144 | G | A | 155 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0077 others(152): Show |
172 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(169): Show |
intron_variant | MODIFIER | c.1993-65C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 14/34 | chr11 | 72703144 | |||||||
| chr11:72703407 | C | CCGGGGG | 36 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0018 others(33): Show |
41 | HG00673.hp2 HG00733.hp2 HG01943.hp2 others(38): Show |
intron_variant | MODIFIER | c.1993-334_1993-329d others(8): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 14/34 | chr11 | 72703407 | |||||||
| chr11:72703408 | C | CGGGGGGC others(3): Show |
1 | a0001c0004t0001g0053 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1993-330_1993-329i others(12): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 14/34 | chr11 | 72703408 | |||||||
| chr11:72703408 | C | CGGGGGGG others(3): Show |
2 | a0001c0001t0001g0011 a0001c0001t0001g0296 |
3 | HG02257.hp2 HG02622.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1993-339_1993-330d others(12): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 14/34 | chr11 | 72703408 | |||||||
| chr11:72703408 | C | CGGGGGGG others(4): Show |
1 | a0001c0001t0001g0295 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1993-330_1993-329i others(13): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 14/34 | chr11 | 72703408 | |||||||
| chr11:72703408 | CG | C | 107 | a0001c0001t0001g0007 a0001c0001t0001g0046 a0001c0001t0001g0093 others(104): Show |
112 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1993-330delC | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 14/34 | chr11 | 72703408 | |||||||
| chr11:72703410 | G | A | 1 | a0002c0025t0001g0278 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1993-331C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 14/34 | chr11 | 72703410 | |||||||
| chr11:72703415 | G | C | 38 | a0001c0001t0001g0186 a0001c0002t0001g0005 a0001c0002t0001g0006 others(35): Show |
43 | HG00544.hp1 HG00673.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.1993-336C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 14/34 | chr11 | 72703415 | |||||||
| chr11:72703415 | G | GGGGGGC | 15 | a0001c0002t0001g0002 a0001c0002t0001g0014 a0001c0002t0001g0040 others(12): Show |
18 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.1993-337_1993-336i others(8): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 14/34 | chr11 | 72703415 | |||||||
| chr11:72703415 | G | GGGGGGGC | 19 | a0001c0002t0001g0003 a0001c0002t0001g0012 a0001c0002t0001g0172 others(16): Show |
22 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.1993-337_1993-336i others(9): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 14/34 | chr11 | 72703415 | |||||||
| chr11:72703415 | G | GGGGGGGG others(2): Show |
22 | a0001c0004t0001g0036 a0001c0004t0001g0044 a0001c0004t0001g0047 others(19): Show |
22 | HG00558.hp1 HG00597.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.1993-337_1993-336i others(11): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 14/34 | chr11 | 72703415 | |||||||
| chr11:72703415 | G | GGGGGGGG others(3): Show |
7 | a0001c0004t0001g0051 a0001c0004t0001g0052 a0001c0004t0001g0054 others(4): Show |
7 | HG01167.hp2 HG01358.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1993-337_1993-336i others(12): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 14/34 | chr11 | 72703415 | |||||||
| chr11:72703415 | G | GTGGGGGG others(1): Show |
7 | a0001c0004t0001g0001 a0001c0004t0001g0034 a0001c0004t0001g0045 others(4): Show |
9 | HG00621.hp1 HG02040.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.1993-337_1993-336i others(10): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 14/34 | chr11 | 72703415 | |||||||
| chr11:72703540 | C | T | 6 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0089 others(3): Show |
6 | HG02055.hp1 HG02145.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1993-461G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 14/34 | chr11 | 72703540 | |||||||
| chr11:72703565 | C | T | 1 | a0001c0004t0006g0058 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1993-486G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 14/34 | chr11 | 72703565 | |||||||
| chr11:72703578 | G | A | 9 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0089 others(6): Show |
9 | HG02055.hp1 HG02145.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1993-499C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 14/34 | chr11 | 72703578 | |||||||
| chr11:72703604 | T | TGGGAGGG others(9): Show |
5 | a0001c0007t0001g0064 a0001c0007t0001g0068 a0001c0007t0001g0071 others(2): Show |
5 | HG00558.hp1 NA18966.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1992+532_1993-526d others(18): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 14/34 | chr11 | 72703604 | |||||||
| chr11:72703630 | T | G | 1 | a0001c0001t0002g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1992+522A>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 14/34 | chr11 | 72703630 | |||||||
| chr11:72703681 | G | A | 2 | a0001c0004t0001g0156 a0011c0033t0001g0155 |
2 | HG02080.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1992+471C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 14/34 | chr11 | 72703681 | |||||||
| chr11:72703754 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1992+398C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 14/34 | chr11 | 72703754 | |||||||
| chr11:72704031 | T | G | 1 | a0001c0004t0001g0051 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1992+121A>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 14/34 | chr11 | 72704031 | |||||||
| chr11:72704096 | G | A | 1 | a0001c0004t0001g0248 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1992+56C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 14/34 | chr11 | 72704096 | |||||||
| chr11:72704483 | G | T | 88 | a0001c0001t0001g0015 a0001c0001t0001g0082 a0001c0001t0001g0083 others(85): Show |
101 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.1810-149C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 13/34 | chr11 | 72704483 | |||||||
| chr11:72704923 | A | C | 154 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0077 others(151): Show |
171 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.1810-589T>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 13/34 | chr11 | 72704923 | |||||||
| chr11:72704938 | C | G | 2 | a0014c0036t0001g0294 a0019c0021t0001g0268 |
2 | HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1810-604G>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 13/34 | chr11 | 72704938 | |||||||
| chr11:72705087 | C | T | 1 | a0002c0003t0001g0219 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1809+718G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 13/34 | chr11 | 72705087 | |||||||
| chr11:72705105 | G | A | 2 | a0001c0001t0001g0251 a0001c0001t0001g0262 |
2 | NA18947.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1809+700C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 13/34 | chr11 | 72705105 | |||||||
| chr11:72705227 | C | T | 1 | a0001c0002t0001g0236 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1809+578G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 13/34 | chr11 | 72705227 | |||||||
| chr11:72705280 | C | G | 154 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0077 others(151): Show |
171 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.1809+525G>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 13/34 | chr11 | 72705280 | |||||||
| chr11:72705356 | T | C | 51 | a0001c0004t0001g0001 a0001c0004t0001g0034 a0001c0004t0001g0036 others(48): Show |
54 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.1809+449A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 13/34 | chr11 | 72705356 | |||||||
| chr11:72705357 | G | A | 51 | a0001c0004t0001g0001 a0001c0004t0001g0034 a0001c0004t0001g0036 others(48): Show |
54 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.1809+448C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 13/34 | chr11 | 72705357 | |||||||
| chr11:72705454 | G | A | 1 | a0001c0004t0001g0060 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1809+351C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 13/34 | chr11 | 72705454 | |||||||
| chr11:72705522 | G | A | 1 | a0001c0006t0001g0218 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1809+283C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 13/34 | chr11 | 72705522 | |||||||
| chr11:72705575 | T | TA | 7 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0272 others(4): Show |
8 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1809+229dupT | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 13/34 | chr11 | 72705575 | |||||||
| chr11:72705687 | G | C | 79 | a0001c0001t0001g0046 a0001c0002t0001g0016 a0001c0002t0001g0200 others(76): Show |
83 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.1809+118C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 13/34 | chr11 | 72705687 | |||||||
| chr11:72705688 | G | T | 79 | a0001c0001t0001g0046 a0001c0002t0001g0016 a0001c0002t0001g0200 others(76): Show |
83 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.1809+117C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 13/34 | chr11 | 72705688 | |||||||
| chr11:72705789 | G | A | 1 | a0001c0004t0001g0047 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1809+16C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 13/34 | chr11 | 72705789 | |||||||
| chr11:72705938 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1724-48C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 12/34 | chr11 | 72705938 | |||||||
| chr11:72706069 | T | A | 70 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0005 others(67): Show |
82 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.1724-179A>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 12/34 | chr11 | 72706069 | |||||||
| chr11:72706264 | G | C | 2 | a0001c0001t0001g0251 a0001c0001t0001g0262 |
2 | NA18947.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1724-374C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 12/34 | chr11 | 72706264 | |||||||
| chr11:72706306 | T | C | 1 | a0001c0004t0001g0132 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1724-416A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 12/34 | chr11 | 72706306 | |||||||
| chr11:72706313 | A | G | 1 | a0001c0004t0001g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1724-423T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 12/34 | chr11 | 72706313 | |||||||
| chr11:72706551 | C | T | 2 | a0002c0003t0001g0088 a0002c0003t0001g0195 |
2 | HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1723+624G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 12/34 | chr11 | 72706551 | |||||||
| chr11:72706552 | G | A | 2 | a0001c0002t0001g0224 a0001c0002t0001g0225 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1723+623C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 12/34 | chr11 | 72706552 | |||||||
| chr11:72706570 | C | T | 1 | a0002c0003t0002g0320 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1723+605G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 12/34 | chr11 | 72706570 | |||||||
| chr11:72706598 | G | GATCCTGA others(3): Show |
1 | a0001c0001t0001g0249 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1723+567_1723+576d others(12): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 12/34 | chr11 | 72706598 | |||||||
| chr11:72706808 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1723+367C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 12/34 | chr11 | 72706808 | |||||||
| chr11:72706978 | G | A | 1 | a0001c0002t0001g0193 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1723+197C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 12/34 | chr11 | 72706978 | |||||||
| chr11:72707084 | C | T | 3 | a0003c0005t0001g0031 a0003c0005t0001g0032 a0003c0005t0001g0033 |
3 | NA18967.hp2 NA18981.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1723+91G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 12/34 | chr11 | 72707084 | |||||||
| chr11:72707135 | G | A | 3 | a0002c0003t0001g0087 a0002c0003t0001g0088 a0002c0003t0001g0195 |
3 | HG02258.hp2 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1723+40C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 12/34 | chr11 | 72707135 | |||||||
| chr11:72707575 | G | T | 1 | a0006c0011t0001g0151 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1524-201C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/34 | chr11 | 72707575 | |||||||
| chr11:72707600 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1524-226G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/34 | chr11 | 72707600 | |||||||
| chr11:72707731 | G | A | 10 | a0001c0001t0001g0011 a0001c0001t0001g0077 a0001c0001t0001g0078 others(7): Show |
11 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1524-357C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/34 | chr11 | 72707731 | |||||||
| chr11:72707869 | A | G | 1 | a0013c0015t0001g0043 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1524-495T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/34 | chr11 | 72707869 | |||||||
| chr11:72708075 | T | C | 1 | a0001c0002t0001g0212 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1524-701A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/34 | chr11 | 72708075 | |||||||
| chr11:72708237 | A | T | 1 | a0002c0003t0001g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1524-863T>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/34 | chr11 | 72708237 | |||||||
| chr11:72708271 | C | T | 3 | a0004c0009t0001g0271 a0004c0009t0001g0274 a0004c0009t0001g0275 |
3 | HG02258.hp1 HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1524-897G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/34 | chr11 | 72708271 | |||||||
| chr11:72708401 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1524-1027A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/34 | chr11 | 72708401 | |||||||
| chr11:72708469 | C | T | 25 | a0002c0003t0001g0135 a0002c0003t0001g0198 a0002c0003t0001g0204 others(22): Show |
26 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.1524-1095G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/34 | chr11 | 72708469 | |||||||
| chr11:72708477 | G | A | 1 | a0002c0003t0002g0323 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1524-1103C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/34 | chr11 | 72708477 | |||||||
| chr11:72708504 | A | T | 78 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0005 others(75): Show |
91 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.1524-1130T>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/34 | chr11 | 72708504 | |||||||
| chr11:72708598 | T | C | 266 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0015 others(263): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1524-1224A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/34 | chr11 | 72708598 | |||||||
| chr11:72708644 | G | T | 11 | a0002c0003t0001g0021 a0002c0003t0001g0270 a0002c0003t0001g0276 others(8): Show |
12 | HG01891.hp1 HG02145.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1523+1226C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/34 | chr11 | 72708644 | |||||||
| chr11:72708649 | G | A | 1 | a0001c0002t0001g0261 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1523+1221C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/34 | chr11 | 72708649 | |||||||
| chr11:72708670 | C | A | 1 | a0002c0003t0001g0276 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1523+1200G>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/34 | chr11 | 72708670 | |||||||
| chr11:72708776 | C | A | 5 | a0001c0002t0001g0200 a0001c0002t0001g0201 a0001c0002t0001g0202 others(2): Show |
5 | HG01099.hp2 HG01261.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1523+1094G>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/34 | chr11 | 72708776 | |||||||
| chr11:72709038 | CAAAAAGC others(6): Show |
C | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1523+819_1523+831d others(15): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/34 | chr11 | 72709038 | |||||||
| chr11:72709045 | C | CA | 42 | a0001c0001t0001g0015 a0001c0001t0001g0083 a0001c0001t0001g0094 others(39): Show |
45 | HG00621.hp1 HG00673.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.1523+824dupT | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/34 | chr11 | 72709045 | |||||||
| chr11:72709524 | G | A | 1 | a0001c0001t0001g0251 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1523+346C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/34 | chr11 | 72709524 | |||||||
| chr11:72709565 | C | T | 1 | a0001c0001t0001g0015 | 2 | HG01243.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1523+305G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/34 | chr11 | 72709565 | |||||||
| chr11:72709566 | G | A | 1 | a0002c0003t0002g0329 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1523+304C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/34 | chr11 | 72709566 | |||||||
| chr11:72709607 | G | A | 54 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(51): Show |
57 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.1523+263C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/34 | chr11 | 72709607 | |||||||
| chr11:72709614 | T | TGGGCAAC others(14): Show |
1 | a0001c0001t0001g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1523+235_1523+255d others(23): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 11/34 | chr11 | 72709614 | |||||||
| chr11:72710014 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1417-38C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 10/34 | chr11 | 72710014 | |||||||
| chr11:72710062 | C | T | 1 | a0015c0017t0001g0230 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1417-86G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 10/34 | chr11 | 72710062 | |||||||
| chr11:72710079 | G | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1417-103C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 10/34 | chr11 | 72710079 | |||||||
| chr11:72710080 | G | T | 1 | a0001c0001t0001g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1417-104C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 10/34 | chr11 | 72710080 | |||||||
| chr11:72710237 | A | G | 4 | a0001c0008t0001g0287 a0001c0008t0001g0288 a0001c0008t0001g0290 others(1): Show |
4 | HG01074.hp1 HG01884.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1416+148T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 10/34 | chr11 | 72710237 | |||||||
| chr11:72710663 | A | G | 30 | a0001c0002t0001g0016 a0001c0002t0001g0200 a0001c0002t0001g0201 others(27): Show |
32 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1214-76T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 9/34 | chr11 | 72710663 | |||||||
| chr11:72710721 | C | T | 51 | a0001c0004t0001g0001 a0001c0004t0001g0034 a0001c0004t0001g0036 others(48): Show |
54 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.1214-134G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 9/34 | chr11 | 72710721 | |||||||
| chr11:72710780 | C | T | 12 | a0001c0001t0001g0015 a0001c0001t0001g0082 a0001c0001t0001g0083 others(9): Show |
13 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1214-193G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 9/34 | chr11 | 72710780 | |||||||
| chr11:72710796 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1214-209A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 9/34 | chr11 | 72710796 | |||||||
| chr11:72710926 | C | G | 2 | a0014c0036t0001g0294 a0019c0021t0001g0268 |
2 | HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1213+95G>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 9/34 | chr11 | 72710926 | |||||||
| chr11:72710928 | G | A | 14 | a0001c0001t0001g0015 a0001c0001t0001g0082 a0001c0001t0001g0083 others(11): Show |
15 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1213+93C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 9/34 | chr11 | 72710928 | |||||||
| chr11:72711013 | C | T | 1 | a0019c0021t0001g0268 | 1 | NA19030.hp1 | splice_region_variant&intron_variant | LOW | c.1213+8G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 9/34 | chr11 | 72711013 | |||||||
| chr11:72711335 | C | T | 1 | a0001c0001t0002g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1092+95G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 8/34 | chr11 | 72711335 | |||||||
| chr11:72711694 | C | CT | 80 | a0001c0001t0001g0046 a0001c0001t0001g0095 a0001c0001t0001g0099 others(77): Show |
83 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.1023-196dupA | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 7/34 | chr11 | 72711694 | |||||||
| chr11:72711694 | C | CTT | 88 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0077 others(85): Show |
93 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1023-197_1023-196d others(4): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 7/34 | chr11 | 72711694 | |||||||
| chr11:72711694 | C | CTTT | 89 | a0001c0001t0001g0015 a0001c0001t0001g0083 a0001c0001t0001g0089 others(86): Show |
103 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.1023-198_1023-196d others(5): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 7/34 | chr11 | 72711694 | |||||||
| chr11:72711695 | T | TC | 4 | a0001c0008t0001g0287 a0001c0008t0001g0288 a0001c0008t0001g0290 others(1): Show |
4 | HG01074.hp1 HG01884.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1023-197_1023-196i others(3): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 7/34 | chr11 | 72711695 | |||||||
| chr11:72711742 | C | T | 1 | a0002c0003t0002g0309 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1023-243G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 7/34 | chr11 | 72711742 | |||||||
| chr11:72711823 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1023-324C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 7/34 | chr11 | 72711823 | |||||||
| chr11:72711830 | A | G | 264 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0015 others(261): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1023-331T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 7/34 | chr11 | 72711830 | |||||||
| chr11:72711884 | A | C | 2 | a0002c0003t0001g0283 a0002c0003t0001g0284 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1022+312T>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 7/34 | chr11 | 72711884 | |||||||
| chr11:72711897 | A | G | 46 | a0001c0004t0001g0001 a0001c0004t0001g0034 a0001c0004t0001g0036 others(43): Show |
49 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1022+299T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 7/34 | chr11 | 72711897 | |||||||
| chr11:72711928 | C | T | 1 | a0001c0002t0001g0260 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1022+268G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 7/34 | chr11 | 72711928 | |||||||
| chr11:72712062 | A | G | 2 | a0014c0036t0001g0294 a0019c0021t0001g0268 |
2 | HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1022+134T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 7/34 | chr11 | 72712062 | |||||||
| chr11:72712381 | A | G | 12 | a0001c0001t0001g0011 a0001c0001t0001g0077 a0001c0001t0001g0078 others(9): Show |
13 | HG02257.hp2 HG02258.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.879-42T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 6/34 | chr11 | 72712381 | |||||||
| chr11:72712391 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.878+47G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 6/34 | chr11 | 72712391 | |||||||
| chr11:72712712 | C | G | 1 | a0002c0003t0001g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.748-144G>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 5/34 | chr11 | 72712712 | |||||||
| chr11:72712773 | C | A | 1 | a0001c0001t0001g0298 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.748-205G>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 5/34 | chr11 | 72712773 | |||||||
| chr11:72712855 | C | T | 11 | a0001c0001t0001g0011 a0001c0001t0001g0077 a0001c0001t0001g0078 others(8): Show |
12 | HG00140.hp1 HG02257.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.748-287G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 5/34 | chr11 | 72712855 | |||||||
| chr11:72712890 | C | T | 1 | a0002c0003t0001g0199 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.747+286G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 5/34 | chr11 | 72712890 | |||||||
| chr11:72712924 | G | C | 1 | a0014c0036t0001g0294 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.747+252C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 5/34 | chr11 | 72712924 | |||||||
| chr11:72712967 | G | C | 18 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 others(15): Show |
19 | HG00733.hp1 HG01071.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.747+209C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 5/34 | chr11 | 72712967 | |||||||
| chr11:72713001 | C | T | 1 | a0001c0006t0001g0154 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.747+175G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 5/34 | chr11 | 72713001 | |||||||
| chr11:72713022 | C | A | 2 | a0001c0001t0002g0305 a0001c0001t0002g0306 |
2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.747+154G>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 5/34 | chr11 | 72713022 | |||||||
| chr11:72713031 | G | A | 2 | a0002c0012t0001g0285 a0002c0012t0001g0286 |
2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.747+145C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 5/34 | chr11 | 72713031 | |||||||
| chr11:72713052 | G | T | 1 | a0017c0032t0001g0266 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.747+124C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 5/34 | chr11 | 72713052 | |||||||
| chr11:72713258 | G | A | 1 | a0002c0003t0001g0194 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.680-15C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 4/34 | chr11 | 72713258 | |||||||
| chr11:72713329 | C | T | 1 | a0003c0005t0001g0031 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.680-86G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 4/34 | chr11 | 72713329 | |||||||
| chr11:72713434 | G | A | 1 | a0001c0028t0003g0023 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.680-191C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 4/34 | chr11 | 72713434 | |||||||
| chr11:72713471 | C | T | 251 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(248): Show |
266 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(263): Show |
intron_variant | MODIFIER | c.680-228G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 4/34 | chr11 | 72713471 | |||||||
| chr11:72713570 | A | G | 1 | a0009c0026t0001g0242 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.680-327T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 4/34 | chr11 | 72713570 | |||||||
| chr11:72713585 | T | C | 6 | a0001c0001t0001g0102 a0001c0001t0001g0106 a0001c0004t0001g0054 others(3): Show |
6 | HG02258.hp2 HG02970.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.680-342A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 4/34 | chr11 | 72713585 | |||||||
| chr11:72713589 | T | C | 32 | a0001c0001t0001g0046 a0001c0001t0001g0104 a0001c0001t0001g0105 others(29): Show |
33 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.680-346A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 4/34 | chr11 | 72713589 | |||||||
| chr11:72713618 | T | C | 1 | a0002c0003t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.680-375A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 4/34 | chr11 | 72713618 | |||||||
| chr11:72713644 | G | A | 12 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(9): Show |
12 | HG00733.hp1 HG01071.hp2 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.680-401C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 4/34 | chr11 | 72713644 | |||||||
| chr11:72713664 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.680-421C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 4/34 | chr11 | 72713664 | |||||||
| chr11:72713691 | C | T | 53 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(50): Show |
56 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.680-448G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 4/34 | chr11 | 72713691 | |||||||
| chr11:72713731 | C | T | 1 | a0001c0002t0001g0113 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.679+421G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 4/34 | chr11 | 72713731 | |||||||
| chr11:72713803 | C | A | 3 | a0001c0001t0001g0109 a0002c0003t0002g0325 a0019c0021t0001g0268 |
3 | HG02922.hp2 HG04204.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.679+349G>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 4/34 | chr11 | 72713803 | |||||||
| chr11:72713803 | C | T | 1 | a0001c0002t0001g0236 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.679+349G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 4/34 | chr11 | 72713803 | |||||||
| chr11:72713804 | A | G | 4 | a0001c0001t0001g0109 a0001c0002t0001g0236 a0002c0003t0002g0325 others(1): Show |
4 | HG02083.hp1 HG02922.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.679+348T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 4/34 | chr11 | 72713804 | |||||||
| chr11:72713846 | C | CA | 7 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0249 others(4): Show |
7 | HG02055.hp1 HG02572.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.679+305dupT | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 4/34 | chr11 | 72713846 | |||||||
| chr11:72713846 | CA | C | 75 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(72): Show |
79 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.679+305delT | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 4/34 | chr11 | 72713846 | |||||||
| chr11:72713864 | A | G | 4 | a0001c0002t0001g0205 a0002c0003t0001g0206 a0002c0003t0001g0227 others(1): Show |
4 | NA18612.hp2 NA18960.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.679+288T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 4/34 | chr11 | 72713864 | |||||||
| chr11:72713920 | C | T | 1 | a0002c0025t0001g0278 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.679+232G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 4/34 | chr11 | 72713920 | |||||||
| chr11:72714701 | G | C | 6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(3): Show |
6 | HG02451.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.510-380C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72714701 | |||||||
| chr11:72714721 | T | C | 1 | a0001c0001t0002g0306 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.510-400A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72714721 | |||||||
| chr11:72714830 | T | G | 1 | a0017c0032t0001g0266 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.510-509A>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72714830 | |||||||
| chr11:72715032 | C | G | 1 | a0001c0002t0002g0307 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.510-711G>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72715032 | |||||||
| chr11:72715179 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0104 a0001c0001t0001g0105 others(1): Show |
5 | HG02257.hp2 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-858C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72715179 | |||||||
| chr11:72715239 | T | G | 1 | a0017c0032t0001g0266 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.510-918A>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72715239 | |||||||
| chr11:72715261 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.510-940C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72715261 | |||||||
| chr11:72715316 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.510-995A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72715316 | |||||||
| chr11:72715364 | T | TG | 267 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(264): Show |
282 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(279): Show |
intron_variant | MODIFIER | c.510-1044dupC | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72715364 | |||||||
| chr11:72715570 | C | CT | 135 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(132): Show |
145 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.510-1250dupA | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72715570 | |||||||
| chr11:72715570 | C | CTT | 50 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0089 others(47): Show |
51 | HG00597.hp1 HG00642.hp1 HG01099.hp2 others(48): Show |
intron_variant | MODIFIER | c.510-1251_510-1250d others(4): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72715570 | |||||||
| chr11:72715570 | CT | C | 15 | a0001c0001t0001g0078 a0001c0001t0001g0103 a0001c0001t0001g0159 others(12): Show |
15 | HG00099.hp1 HG00639.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.510-1250delA | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72715570 | |||||||
| chr11:72715624 | G | A | 1 | a0002c0012t0001g0286 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.510-1303C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72715624 | |||||||
| chr11:72715955 | G | A | 1 | a0001c0002t0001g0203 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.510-1634C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72715955 | |||||||
| chr11:72715968 | C | T | 3 | a0001c0001t0001g0107 a0001c0001t0001g0292 a0001c0001t0001g0293 |
3 | HG02818.hp2 HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.510-1647G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72715968 | |||||||
| chr11:72716033 | C | T | 1 | a0001c0001t0002g0306 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.510-1712G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72716033 | |||||||
| chr11:72716034 | G | C | 1 | a0002c0003t0001g0289 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.510-1713C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72716034 | |||||||
| chr11:72716066 | A | G | 156 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0039 others(153): Show |
165 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.510-1745T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72716066 | |||||||
| chr11:72716103 | G | A | 1 | a0002c0003t0001g0194 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.510-1782C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72716103 | |||||||
| chr11:72716172 | C | CA | 82 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0083 others(79): Show |
89 | HG00558.hp1 HG00597.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.510-1852dupT | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72716172 | |||||||
| chr11:72716172 | C | CAA | 22 | a0001c0001t0001g0011 a0001c0001t0001g0046 a0001c0001t0001g0097 others(19): Show |
23 | HG02148.hp1 HG02257.hp2 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.510-1853_510-1852d others(4): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72716172 | |||||||
| chr11:72716172 | CA | C | 18 | a0001c0001t0001g0109 a0001c0001t0001g0115 a0001c0001t0001g0116 others(15): Show |
18 | HG01069.hp2 HG01168.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.510-1852delT | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72716172 | |||||||
| chr11:72716172 | CAAAAAAA others(3): Show |
C | 23 | a0001c0002t0001g0175 a0002c0003t0002g0022 a0002c0003t0002g0304 others(20): Show |
24 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.510-1861_510-1852d others(12): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72716172 | |||||||
| chr11:72716272 | A | C | 1 | a0017c0032t0001g0266 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.510-1951T>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72716272 | |||||||
| chr11:72716510 | G | A | 6 | a0002c0003t0002g0022 a0002c0003t0002g0313 a0002c0003t0002g0315 others(3): Show |
7 | HG00099.hp2 HG00140.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.510-2189C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72716510 | |||||||
| chr11:72716534 | A | G | 2 | a0001c0004t0001g0165 a0001c0004t0001g0170 |
2 | HG01361.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.510-2213T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72716534 | |||||||
| chr11:72716789 | G | T | 1 | a0002c0003t0002g0314 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.510-2468C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72716789 | |||||||
| chr11:72716804 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.510-2483G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72716804 | |||||||
| chr11:72716972 | G | A | 5 | a0001c0002t0001g0113 a0001c0002t0001g0174 a0001c0002t0001g0183 others(2): Show |
5 | HG01361.hp1 HG02004.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-2651C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72716972 | |||||||
| chr11:72716993 | T | G | 43 | a0001c0001t0001g0011 a0001c0001t0001g0046 a0001c0001t0001g0098 others(40): Show |
45 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.510-2672A>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72716993 | |||||||
| chr11:72717021 | T | G | 16 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0102 others(13): Show |
16 | HG00733.hp1 HG01071.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.510-2700A>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72717021 | |||||||
| chr11:72717103 | G | A | 46 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 others(43): Show |
48 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.510-2782C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72717103 | |||||||
| chr11:72717127 | A | G | 30 | a0001c0001t0001g0011 a0001c0001t0001g0104 a0001c0001t0001g0105 others(27): Show |
32 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.510-2806T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72717127 | |||||||
| chr11:72717213 | A | G | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG02818.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.510-2892T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72717213 | |||||||
| chr11:72717263 | G | A | 1 | a0002c0003t0001g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.510-2942C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72717263 | |||||||
| chr11:72717275 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01069.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.510-2954G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72717275 | |||||||
| chr11:72717433 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.510-3112T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72717433 | |||||||
| chr11:72717480 | C | T | 2 | a0002c0003t0001g0076 a0002c0003t0001g0277 |
2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.510-3159G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72717480 | |||||||
| chr11:72717531 | T | C | 1 | a0001c0004t0001g0248 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.510-3210A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72717531 | |||||||
| chr11:72717721 | G | C | 2 | a0002c0003t0001g0076 a0002c0003t0001g0277 |
2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.510-3400C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72717721 | |||||||
| chr11:72717805 | G | A | 3 | a0002c0003t0001g0021 a0002c0003t0001g0270 a0002c0003t0001g0280 |
4 | HG01891.hp1 HG02486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-3484C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72717805 | |||||||
| chr11:72718048 | C | T | 1 | a0002c0003t0001g0289 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.510-3727G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72718048 | |||||||
| chr11:72718091 | C | T | 2 | a0001c0004t0001g0048 a0001c0004t0001g0049 |
2 | HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.510-3770G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72718091 | |||||||
| chr11:72718096 | G | A | 136 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(133): Show |
144 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.510-3775C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72718096 | |||||||
| chr11:72718111 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.510-3790T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72718111 | |||||||
| chr11:72718198 | G | A | 1 | a0002c0003t0002g0325 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.510-3877C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72718198 | |||||||
| chr11:72718352 | G | A | 1 | a0001c0008t0001g0291 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.510-4031C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72718352 | |||||||
| chr11:72718383 | C | T | 1 | a0005c0010t0002g0302 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.510-4062G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72718383 | |||||||
| chr11:72718534 | G | A | 23 | a0001c0001t0002g0305 a0001c0001t0002g0306 a0002c0003t0002g0022 others(20): Show |
24 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.510-4213C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72718534 | |||||||
| chr11:72718751 | TGCA | T | 24 | a0001c0001t0002g0305 a0001c0001t0002g0306 a0002c0003t0002g0022 others(21): Show |
25 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.510-4433_510-4431d others(5): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72718751 | |||||||
| chr11:72718764 | A | G | 10 | a0001c0002t0001g0002 a0001c0002t0001g0176 a0001c0002t0001g0177 others(7): Show |
12 | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.510-4443T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72718764 | |||||||
| chr11:72719068 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.510-4747C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72719068 | |||||||
| chr11:72719152 | C | A | 3 | a0002c0003t0002g0326 a0002c0003t0002g0327 a0002c0003t0002g0328 |
3 | HG00544.hp2 HG00558.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.510-4831G>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72719152 | |||||||
| chr11:72719290 | AC | A | 7 | a0001c0008t0001g0287 a0001c0008t0001g0288 a0001c0008t0001g0290 others(4): Show |
7 | HG01074.hp1 HG01884.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.510-4970delG | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72719290 | |||||||
| chr11:72719323 | T | C | 6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(3): Show |
6 | HG02451.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.510-5002A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72719323 | |||||||
| chr11:72719544 | T | C | 1 | a0001c0034t0001g0299 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.510-5223A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72719544 | |||||||
| chr11:72719890 | C | T | 4 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0188 others(1): Show |
7 | HG00639.hp2 HG00741.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.510-5569G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72719890 | |||||||
| chr11:72720186 | T | G | 254 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(251): Show |
267 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(264): Show |
intron_variant | MODIFIER | c.510-5865A>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72720186 | |||||||
| chr11:72720516 | C | T | 1 | a0001c0002t0001g0175 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.509+6104G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72720516 | |||||||
| chr11:72720634 | T | C | 117 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(114): Show |
124 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.509+5986A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72720634 | |||||||
| chr11:72720836 | C | T | 1 | a0002c0003t0001g0196 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.509+5784G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72720836 | |||||||
| chr11:72720908 | C | T | 23 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 others(20): Show |
24 | HG00733.hp1 HG01071.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.509+5712G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72720908 | |||||||
| chr11:72721465 | C | A | 3 | a0002c0003t0001g0076 a0002c0003t0001g0277 a0002c0025t0001g0278 |
3 | HG02486.hp1 HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.509+5155G>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72721465 | |||||||
| chr11:72721666 | C | T | 5 | a0001c0002t0001g0205 a0001c0002t0001g0229 a0002c0003t0001g0206 others(2): Show |
5 | NA18612.hp2 NA18960.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+4954G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72721666 | |||||||
| chr11:72721868 | T | A | 6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(3): Show |
6 | HG02451.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.509+4752A>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72721868 | |||||||
| chr11:72721896 | G | A | 1 | a0001c0004t0001g0156 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.509+4724C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72721896 | |||||||
| chr11:72721904 | G | A | 1 | a0002c0003t0001g0281 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.509+4716C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72721904 | |||||||
| chr11:72721912 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.509+4708A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72721912 | |||||||
| chr11:72721937 | C | T | 1 | a0001c0004t0006g0058 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.509+4683G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72721937 | |||||||
| chr11:72721940 | G | A | 24 | a0001c0001t0002g0305 a0001c0001t0002g0306 a0002c0003t0002g0022 others(21): Show |
25 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.509+4680C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72721940 | |||||||
| chr11:72722053 | A | C | 22 | a0002c0003t0002g0022 a0002c0003t0002g0304 a0002c0003t0002g0308 others(19): Show |
23 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.509+4567T>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72722053 | |||||||
| chr11:72722138 | C | T | 2 | a0001c0001t0002g0305 a0001c0001t0002g0306 |
2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.509+4482G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72722138 | |||||||
| chr11:72722151 | C | CAG | 10 | a0001c0001t0001g0011 a0001c0001t0001g0104 a0001c0001t0001g0105 others(7): Show |
11 | HG01255.hp1 HG01358.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.509+4467_509+4468d others(4): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72722151 | |||||||
| chr11:72722151 | C | CAGAGAGA others(23): Show |
1 | a0003c0005t0001g0030 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.509+4468_509+4469i others(32): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72722151 | |||||||
| chr11:72722151 | CAG | C | 92 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(89): Show |
98 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.509+4467_509+4468d others(4): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72722151 | |||||||
| chr11:72722151 | CAGAG | C | 22 | a0001c0001t0002g0305 a0001c0001t0002g0306 a0002c0003t0002g0022 others(19): Show |
23 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.509+4465_509+4468d others(6): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72722151 | |||||||
| chr11:72722179 | G | A | 1 | a0001c0002t0001g0184 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.509+4441C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72722179 | |||||||
| chr11:72722182 | G | GGA | 85 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(82): Show |
91 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.509+4436_509+4437d others(4): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72722182 | |||||||
| chr11:72722215 | G | A | 1 | a0001c0002t0001g0128 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.509+4405C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72722215 | |||||||
| chr11:72722314 | T | C | 2 | a0001c0002t0001g0020 a0001c0002t0001g0265 |
3 | HG00733.hp2 HG01943.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.509+4306A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72722314 | |||||||
| chr11:72722383 | A | G | 1 | a0001c0001t0002g0305 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.509+4237T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72722383 | |||||||
| chr11:72722561 | G | A | 1 | a0001c0004t0001g0248 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.509+4059C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72722561 | |||||||
| chr11:72722875 | T | C | 116 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(113): Show |
123 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.509+3745A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72722875 | |||||||
| chr11:72723026 | T | G | 262 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(259): Show |
276 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.509+3594A>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72723026 | |||||||
| chr11:72723073 | C | T | 100 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(97): Show |
104 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.509+3547G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72723073 | |||||||
| chr11:72723327 | A | G | 262 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(259): Show |
276 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.509+3293T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72723327 | |||||||
| chr11:72723472 | T | C | 2 | a0002c0003t0001g0021 a0002c0003t0001g0270 |
3 | HG01891.hp1 HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.509+3148A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72723472 | |||||||
| chr11:72723613 | G | A | 1 | a0001c0004t0001g0060 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.509+3007C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72723613 | |||||||
| chr11:72723679 | G | A | 1 | a0001c0001t0001g0249 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.509+2941C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72723679 | |||||||
| chr11:72723934 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01069.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.509+2686T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72723934 | |||||||
| chr11:72723947 | C | T | 2 | a0002c0003t0001g0198 a0002c0003t0001g0204 |
2 | NA18981.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.509+2673G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72723947 | |||||||
| chr11:72723978 | G | A | 2 | a0001c0002t0001g0013 a0001c0002t0001g0185 |
3 | HG02040.hp2 NA18950.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.509+2642C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72723978 | |||||||
| chr11:72724143 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.509+2477C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72724143 | |||||||
| chr11:72724222 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.509+2398C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72724222 | |||||||
| chr11:72724269 | G | A | 76 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(73): Show |
82 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.509+2351C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72724269 | |||||||
| chr11:72724492 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.509+2128C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72724492 | |||||||
| chr11:72724890 | C | T | 7 | a0001c0001t0001g0249 a0001c0001t0001g0252 a0001c0001t0001g0255 others(4): Show |
7 | NA18941.hp1 NA18953.hp2 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+1730G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72724890 | |||||||
| chr11:72724938 | A | G | 106 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(103): Show |
113 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.509+1682T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72724938 | |||||||
| chr11:72724951 | A | G | 106 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(103): Show |
113 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.509+1669T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72724951 | |||||||
| chr11:72725295 | C | CCT | 26 | a0001c0001t0002g0305 a0001c0001t0002g0306 a0001c0002t0001g0188 others(23): Show |
27 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.509+1323_509+1324d others(4): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72725295 | |||||||
| chr11:72725295 | CCT | C | 79 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(76): Show |
85 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.509+1323_509+1324d others(4): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72725295 | |||||||
| chr11:72725295 | CCTCTCTC others(3): Show |
C | 2 | a0001c0002t0001g0041 a0001c0002t0001g0042 |
2 | NA18948.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.509+1315_509+1324d others(12): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72725295 | |||||||
| chr11:72725322 | T | C | 8 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0089 others(5): Show |
8 | HG02055.hp1 HG02145.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.509+1298A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72725322 | |||||||
| chr11:72725324 | C | T | 2 | a0001c0001t0001g0109 a0010c0014t0001g0117 |
2 | HG02056.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.509+1296G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72725324 | |||||||
| chr11:72725391 | G | A | 60 | a0001c0001t0001g0039 a0001c0001t0001g0046 a0001c0002t0001g0005 others(57): Show |
65 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.509+1229C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72725391 | |||||||
| chr11:72725666 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.509+954G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72725666 | |||||||
| chr11:72725867 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0152 |
2 | NA19056.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.509+753G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72725867 | |||||||
| chr11:72725959 | C | T | 4 | a0001c0004t0001g0084 a0001c0004t0001g0085 a0001c0004t0001g0086 others(1): Show |
4 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+661G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72725959 | |||||||
| chr11:72725973 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.509+647C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72725973 | |||||||
| chr11:72726069 | G | A | 7 | a0001c0008t0001g0287 a0001c0008t0001g0288 a0001c0008t0001g0290 others(4): Show |
7 | HG01074.hp1 HG01884.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+551C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72726069 | |||||||
| chr11:72726177 | C | A | 1 | a0001c0001t0001g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.509+443G>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72726177 | |||||||
| chr11:72726251 | C | A | 76 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(73): Show |
82 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.509+369G>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72726251 | |||||||
| chr11:72726353 | G | A | 124 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(121): Show |
130 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(127): Show |
intron_variant | MODIFIER | c.509+267C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72726353 | |||||||
| chr11:72726427 | C | T | 1 | a0001c0001t0002g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.509+193G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72726427 | |||||||
| chr11:72726587 | G | T | 1 | a0001c0001t0001g0107 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.509+33C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72726587 | |||||||
| chr11:72726591 | G | A | 1 | a0002c0003t0001g0195 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.509+29C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72726591 | |||||||
| chr11:72727661 | G | A | 6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(3): Show |
6 | HG02451.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44-489C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72727661 | |||||||
| chr11:72727698 | C | T | 1 | a0002c0003t0001g0062 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-44-526G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72727698 | |||||||
| chr11:72727781 | A | C | 6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(3): Show |
6 | HG02451.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44-609T>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72727781 | |||||||
| chr11:72727825 | A | G | 6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(3): Show |
6 | HG02451.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44-653T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72727825 | |||||||
| chr11:72727928 | A | T | 2 | a0001c0002t0001g0063 a0001c0002t0001g0067 |
2 | NA18963.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-44-756T>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72727928 | |||||||
| chr11:72727966 | G | C | 2 | a0001c0002t0001g0066 a0001c0002t0001g0075 |
2 | NA18969.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.-44-794C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72727966 | |||||||
| chr11:72728261 | G | T | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG02818.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-44-1089C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72728261 | |||||||
| chr11:72728351 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-44-1179G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72728351 | |||||||
| chr11:72728356 | G | A | 1 | a0002c0003t0002g0314 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-44-1184C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72728356 | |||||||
| chr11:72728384 | C | T | 1 | a0001c0004t0001g0170 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-44-1212G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72728384 | |||||||
| chr11:72728398 | C | T | 1 | a0001c0002t0001g0124 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-44-1226G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72728398 | |||||||
| chr11:72728454 | G | A | 1 | a0001c0001t0002g0306 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-44-1282C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72728454 | |||||||
| chr11:72728464 | C | T | 2 | a0001c0002t0001g0012 a0001c0002t0001g0191 |
3 | HG03490.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-44-1292G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72728464 | |||||||
| chr11:72728478 | G | T | 1 | a0002c0025t0001g0278 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-44-1306C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72728478 | |||||||
| chr11:72728530 | G | A | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG02818.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-44-1358C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72728530 | |||||||
| chr11:72728679 | G | T | 2 | a0001c0001t0001g0106 a0001c0004t0001g0248 |
2 | HG03130.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-44-1507C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72728679 | |||||||
| chr11:72728707 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-44-1535T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72728707 | |||||||
| chr11:72728931 | G | C | 1 | a0001c0001t0001g0232 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-44-1759C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72728931 | |||||||
| chr11:72728934 | G | A | 9 | a0002c0003t0001g0021 a0002c0003t0001g0270 a0002c0003t0001g0276 others(6): Show |
10 | HG01891.hp1 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-44-1762C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72728934 | |||||||
| chr11:72728979 | G | C | 1 | a0001c0002t0001g0167 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-44-1807C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72728979 | |||||||
| chr11:72729029 | A | G | 76 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(73): Show |
82 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.-44-1857T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72729029 | |||||||
| chr11:72729079 | C | G | 56 | a0001c0001t0001g0039 a0001c0001t0001g0046 a0001c0002t0001g0005 others(53): Show |
61 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.-44-1907G>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72729079 | |||||||
| chr11:72729186 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-44-2014T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72729186 | |||||||
| chr11:72729219 | C | T | 2 | a0001c0001t0002g0305 a0001c0001t0002g0306 |
2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-44-2047G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72729219 | |||||||
| chr11:72729450 | G | A | 1 | a0010c0014t0001g0117 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-44-2278C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72729450 | |||||||
| chr11:72729484 | T | C | 1 | a0001c0002t0001g0113 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-44-2312A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72729484 | |||||||
| chr11:72729553 | C | T | 1 | a0003c0005t0001g0127 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-44-2381G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72729553 | |||||||
| chr11:72729582 | T | G | 1 | a0001c0001t0002g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-44-2410A>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72729582 | |||||||
| chr11:72729611 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-44-2439C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72729611 | |||||||
| chr11:72729755 | T | TA | 77 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(74): Show |
83 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.-44-2584dupT | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72729755 | |||||||
| chr11:72729792 | G | A | 3 | a0001c0001t0001g0123 a0001c0001t0001g0129 a0001c0001t0001g0131 |
3 | HG02165.hp1 NA18971.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-44-2620C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72729792 | |||||||
| chr11:72729923 | TA | T | 247 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(244): Show |
260 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(257): Show |
intron_variant | MODIFIER | c.-45+2591delT | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72729923 | |||||||
| chr11:72730274 | C | T | 4 | a0001c0001t0001g0039 a0003c0005t0001g0031 a0003c0005t0001g0032 others(1): Show |
4 | NA18967.hp2 NA18981.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.-45+2241G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72730274 | |||||||
| chr11:72730371 | G | A | 1 | a0004c0009t0001g0275 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-45+2144C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72730371 | |||||||
| chr11:72730386 | T | C | 254 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(251): Show |
267 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(264): Show |
intron_variant | MODIFIER | c.-45+2129A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72730386 | |||||||
| chr11:72730450 | G | A | 83 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(80): Show |
89 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.-45+2065C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72730450 | |||||||
| chr11:72730494 | C | T | 1 | a0001c0004t0001g0248 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-45+2021G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72730494 | |||||||
| chr11:72730517 | T | C | 1 | a0006c0011t0001g0151 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-45+1998A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72730517 | |||||||
| chr11:72730560 | C | T | 6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(3): Show |
6 | HG02451.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-45+1955G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72730560 | |||||||
| chr11:72730708 | A | G | 1 | a0001c0002t0001g0254 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-45+1807T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72730708 | |||||||
| chr11:72730779 | T | C | 6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(3): Show |
6 | HG02451.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-45+1736A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72730779 | |||||||
| chr11:72730910 | G | A | 1 | a0001c0004t0001g0248 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-45+1605C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72730910 | |||||||
| chr11:72731095 | T | C | 5 | a0001c0004t0001g0001 a0001c0004t0001g0045 a0001c0004t0001g0059 others(2): Show |
7 | HG02040.hp1 HG02080.hp2 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.-45+1420A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72731095 | |||||||
| chr11:72731172 | G | A | 1 | a0002c0003t0001g0080 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-45+1343C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72731172 | |||||||
| chr11:72731478 | G | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0110 |
3 | HG02896.hp1 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-45+1037C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72731478 | |||||||
| chr11:72731489 | T | C | 1 | a0001c0001t0002g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-45+1026A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72731489 | |||||||
| chr11:72732045 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-45+470G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72732045 | |||||||
| chr11:72732132 | G | A | 56 | a0001c0001t0001g0039 a0001c0001t0001g0046 a0001c0002t0001g0005 others(53): Show |
61 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.-45+383C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72732132 | |||||||
| chr11:72732196 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-45+319C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72732196 | |||||||
| chr11:72732447 | C | T | 1 | a0001c0001t0002g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-45+68G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72732447 | |||||||
| chr11:72732495 | C | G | 1 | a0002c0003t0001g0227 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-45+20G>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72732495 | |||||||
| chr11:72732707 | G | A | 1 | a0002c0003t0001g0219 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-127-110C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72732707 | |||||||
| chr11:72732849 | A | G | 6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(3): Show |
6 | HG02451.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-127-252T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72732849 | |||||||
| chr11:72732855 | T | C | 6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(3): Show |
6 | HG02451.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-127-258A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72732855 | |||||||
| chr11:72733003 | GA | G | 6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(3): Show |
6 | HG02451.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-127-407delT | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72733003 | |||||||
| chr11:72733006 | G | C | 1 | a0001c0001t0001g0107 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-127-409C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72733006 | |||||||
| chr11:72733166 | T | C | 6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(3): Show |
6 | HG02451.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-127-569A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72733166 | |||||||
| chr11:72733212 | T | C | 6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(3): Show |
6 | HG02451.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-127-615A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72733212 | |||||||
| chr11:72733405 | C | T | 77 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(74): Show |
83 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.-127-808G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72733405 | |||||||
| chr11:72733538 | T | C | 115 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(112): Show |
122 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.-127-941A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72733538 | |||||||
| chr11:72733570 | A | G | 83 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(80): Show |
89 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.-127-973T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72733570 | |||||||
| chr11:72733604 | T | G | 1 | a0001c0002t0001g0169 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-127-1007A>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72733604 | |||||||
| chr11:72733631 | A | G | 104 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(101): Show |
111 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.-127-1034T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72733631 | |||||||
| chr11:72733636 | G | A | 1 | a0002c0003t0001g0241 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-127-1039C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72733636 | |||||||
| chr11:72733702 | T | C | 83 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(80): Show |
89 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.-127-1105A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72733702 | |||||||
| chr11:72733972 | C | T | 4 | a0001c0001t0001g0106 a0001c0001t0001g0109 a0001c0001t0001g0110 others(1): Show |
4 | HG02922.hp2 HG03130.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-127-1375G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72733972 | |||||||
| chr11:72733979 | C | T | 83 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(80): Show |
89 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.-127-1382G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72733979 | |||||||
| chr11:72734014 | C | T | 6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(3): Show |
6 | HG02451.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-127-1417G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72734014 | |||||||
| chr11:72734098 | G | T | 83 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(80): Show |
89 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.-127-1501C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72734098 | |||||||
| chr11:72734149 | C | T | 7 | a0001c0001t0001g0102 a0001c0004t0001g0084 a0001c0004t0001g0085 others(4): Show |
7 | HG02258.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-127-1552G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72734149 | |||||||
| chr11:72734246 | G | A | 1 | a0001c0004t0001g0248 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-127-1649C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72734246 | |||||||
| chr11:72734269 | T | C | 77 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(74): Show |
83 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.-127-1672A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72734269 | |||||||
| chr11:72734431 | A | G | 83 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(80): Show |
89 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.-127-1834T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72734431 | |||||||
| chr11:72734478 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-127-1881A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72734478 | |||||||
| chr11:72734582 | C | T | 6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(3): Show |
6 | HG02451.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-127-1985G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72734582 | |||||||
| chr11:72734692 | C | T | 1 | a0001c0004t0001g0132 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-127-2095G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72734692 | |||||||
| chr11:72734841 | C | CA | 7 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0187 others(4): Show |
7 | HG02451.hp2 HG02976.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-127-2245dupT | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72734841 | |||||||
| chr11:72734841 | C | CAAA | 75 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(72): Show |
81 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.-127-2247_-127-224 others(7): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72734841 | |||||||
| chr11:72734841 | CA | C | 45 | a0001c0001t0001g0011 a0001c0001t0001g0104 a0001c0001t0001g0105 others(42): Show |
47 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.-127-2245delT | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72734841 | |||||||
| chr11:72734857 | G | A | 6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(3): Show |
6 | HG02451.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-127-2260C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72734857 | |||||||
| chr11:72734978 | G | A | 12 | a0002c0003t0001g0021 a0002c0003t0001g0076 a0002c0003t0001g0270 others(9): Show |
13 | HG01891.hp1 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-127-2381C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72734978 | |||||||
| chr11:72735027 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-127-2430G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72735027 | |||||||
| chr11:72735137 | C | T | 45 | a0001c0001t0001g0197 a0001c0001t0001g0222 a0001c0001t0001g0223 others(42): Show |
46 | HG00438.hp2 HG00597.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.-127-2540G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72735137 | |||||||
| chr11:72735419 | C | T | 83 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(80): Show |
89 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.-127-2822G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72735419 | |||||||
| chr11:72735460 | G | A | 83 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(80): Show |
89 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.-127-2863C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72735460 | |||||||
| chr11:72735471 | C | G | 56 | a0001c0001t0001g0039 a0001c0001t0001g0046 a0001c0002t0001g0005 others(53): Show |
61 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.-127-2874G>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72735471 | |||||||
| chr11:72735526 | G | A | 4 | a0001c0001t0001g0120 a0005c0010t0002g0301 a0005c0010t0002g0302 others(1): Show |
4 | HG02148.hp2 NA18973.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.-127-2929C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72735526 | |||||||
| chr11:72735629 | T | C | 13 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0016 others(10): Show |
17 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.-127-3032A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72735629 | |||||||
| chr11:72735686 | A | C | 82 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(79): Show |
88 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.-127-3089T>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72735686 | |||||||
| chr11:72735817 | G | A | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG02818.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-127-3220C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72735817 | |||||||
| chr11:72735881 | C | T | 6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(3): Show |
6 | HG02451.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-127-3284G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72735881 | |||||||
| chr11:72735913 | A | G | 127 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(124): Show |
133 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.-127-3316T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72735913 | |||||||
| chr11:72735962 | C | T | 1 | a0001c0006t0001g0218 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-127-3365G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72735962 | |||||||
| chr11:72736238 | C | T | 6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(3): Show |
6 | HG02451.hp2 HG02976.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-127-3641G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72736238 | |||||||
| chr11:72736239 | C | CT | 59 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
62 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.-127-3643dupA | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72736239 | |||||||
| chr11:72736239 | C | CTT | 84 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(81): Show |
90 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.-127-3644_-127-364 others(6): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72736239 | |||||||
| chr11:72736239 | CT | C | 14 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 others(11): Show |
14 | HG02258.hp1 HG02615.hp1 HG02735.hp2 others(11): Show |
intron_variant | MODIFIER | c.-127-3643delA | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72736239 | |||||||
| chr11:72736268 | G | C | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG02818.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-127-3671C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72736268 | |||||||
| chr11:72736339 | C | T | 2 | a0001c0001t0001g0110 a0001c0004t0001g0248 |
2 | HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-127-3742G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72736339 | |||||||
| chr11:72736360 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-127-3763G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72736360 | |||||||
| chr11:72736375 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-127-3778C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72736375 | |||||||
| chr11:72736423 | T | C | 1 | a0003c0005t0001g0216 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-127-3826A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72736423 | |||||||
| chr11:72736484 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02896.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-127-3887G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72736484 | |||||||
| chr11:72736636 | C | T | 2 | a0001c0001t0002g0305 a0001c0001t0002g0306 |
2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-127-4039G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72736636 | |||||||
| chr11:72736810 | G | A | 2 | a0001c0004t0001g0048 a0001c0004t0001g0049 |
2 | HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-127-4213C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72736810 | |||||||
| chr11:72737126 | G | T | 1 | a0001c0001t0001g0110 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-127-4529C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72737126 | |||||||
| chr11:72737211 | C | T | 76 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(73): Show |
82 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.-127-4614G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72737211 | |||||||
| chr11:72737327 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-127-4730C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72737327 | |||||||
| chr11:72737340 | A | C | 82 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(79): Show |
88 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.-127-4743T>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72737340 | |||||||
| chr11:72737513 | C | G | 76 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(73): Show |
82 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.-127-4916G>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72737513 | |||||||
| chr11:72737573 | A | G | 1 | a0002c0003t0001g0062 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-127-4976T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72737573 | |||||||
| chr11:72737628 | CT | C | 25 | a0001c0001t0001g0007 a0001c0001t0001g0078 a0001c0001t0001g0093 others(22): Show |
26 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.-127-5032delA | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72737628 | |||||||
| chr11:72737822 | C | T | 1 | a0001c0001t0002g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-127-5225G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72737822 | |||||||
| chr11:72738204 | T | C | 177 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(174): Show |
184 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.-127-5607A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72738204 | |||||||
| chr11:72738443 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-127-5846A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72738443 | |||||||
| chr11:72738529 | G | T | 1 | a0001c0001t0001g0162 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-127-5932C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72738529 | |||||||
| chr11:72738671 | G | A | 76 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(73): Show |
82 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.-127-6074C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72738671 | |||||||
| chr11:72738682 | A | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
6 | HG02257.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-127-6085T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72738682 | |||||||
| chr11:72738724 | G | A | 2 | a0001c0001t0003g0024 a0001c0001t0003g0025 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-127-6127C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72738724 | |||||||
| chr11:72738932 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-127-6335C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72738932 | |||||||
| chr11:72738942 | C | T | 1 | a0001c0001t0001g0249 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-127-6345G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72738942 | |||||||
| chr11:72739046 | T | A | 3 | a0001c0002t0001g0016 a0001c0002t0001g0217 a0001c0002t0001g0240 |
4 | HG00642.hp1 HG01496.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-127-6449A>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72739046 | |||||||
| chr11:72739173 | G | A | 76 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(73): Show |
82 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.-127-6576C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72739173 | |||||||
| chr11:72739181 | T | C | 82 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(79): Show |
88 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.-127-6584A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72739181 | |||||||
| chr11:72739340 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-127-6743A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72739340 | |||||||
| chr11:72739433 | G | A | 7 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(4): Show |
7 | HG02451.hp2 HG02976.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-127-6836C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72739433 | |||||||
| chr11:72739455 | T | A | 7 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(4): Show |
7 | HG02451.hp2 HG02976.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-127-6858A>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72739455 | |||||||
| chr11:72739573 | G | A | 1 | a0001c0002t0001g0192 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-127-6976C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72739573 | |||||||
| chr11:72739679 | C | T | 76 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(73): Show |
82 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.-127-7082G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72739679 | |||||||
| chr11:72739730 | C | T | 76 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(73): Show |
82 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.-127-7133G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72739730 | |||||||
| chr11:72739896 | T | A | 75 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(72): Show |
81 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.-127-7299A>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72739896 | |||||||
| chr11:72739925 | C | T | 82 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(79): Show |
88 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.-127-7328G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72739925 | |||||||
| chr11:72739934 | G | A | 1 | a0001c0004t0001g0248 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-127-7337C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72739934 | |||||||
| chr11:72739944 | T | G | 7 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(4): Show |
7 | HG02451.hp2 HG02976.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-127-7347A>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72739944 | |||||||
| chr11:72739959 | T | C | 82 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(79): Show |
88 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.-127-7362A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72739959 | |||||||
| chr11:72739992 | C | T | 1 | a0001c0002t0001g0040 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-127-7395G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72739992 | |||||||
| chr11:72740194 | G | A | 83 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(80): Show |
89 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.-127-7597C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72740194 | |||||||
| chr11:72740335 | C | T | 89 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(86): Show |
95 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.-127-7738G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72740335 | |||||||
| chr11:72740675 | C | T | 2 | a0001c0035t0001g0269 a0019c0021t0001g0268 |
2 | NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-127-8078G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72740675 | |||||||
| chr11:72740814 | G | A | 1 | a0001c0006t0001g0218 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-127-8217C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72740814 | |||||||
| chr11:72740896 | A | C | 89 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(86): Show |
95 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.-127-8299T>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72740896 | |||||||
| chr11:72741066 | T | TCTGGCCC others(12): Show |
82 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(79): Show |
88 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.-127-8488_-127-847 others(23): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72741066 | |||||||
| chr11:72741193 | C | T | 1 | a0019c0021t0001g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-127-8596G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72741193 | |||||||
| chr11:72741436 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-127-8839C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72741436 | |||||||
| chr11:72741600 | A | G | 97 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(94): Show |
103 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.-127-9003T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72741600 | |||||||
| chr11:72741631 | C | T | 7 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(4): Show |
7 | HG02451.hp2 HG02976.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-127-9034G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72741631 | |||||||
| chr11:72741676 | G | A | 2 | a0001c0001t0001g0107 a0002c0003t0001g0282 |
2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-127-9079C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72741676 | |||||||
| chr11:72741810 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-127-9213G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72741810 | |||||||
| chr11:72741925 | G | T | 96 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(93): Show |
102 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.-127-9328C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72741925 | |||||||
| chr11:72742050 | A | G | 96 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(93): Show |
102 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.-127-9453T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72742050 | |||||||
| chr11:72742117 | C | A | 1 | a0001c0004t0001g0061 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-127-9520G>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72742117 | |||||||
| chr11:72742264 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-127-9667C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72742264 | |||||||
| chr11:72742270 | C | A | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG02735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-127-9673G>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72742270 | |||||||
| chr11:72742294 | G | A | 1 | a0002c0025t0001g0278 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-127-9697C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72742294 | |||||||
| chr11:72742521 | G | C | 2 | a0002c0003t0001g0283 a0002c0003t0001g0284 |
2 | HG02723.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-128+9807C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72742521 | |||||||
| chr11:72742551 | G | A | 94 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(91): Show |
100 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.-128+9777C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72742551 | |||||||
| chr11:72742601 | C | G | 7 | a0001c0008t0001g0287 a0001c0008t0001g0288 a0001c0008t0001g0290 others(4): Show |
7 | HG01074.hp1 HG01884.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-128+9727G>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72742601 | |||||||
| chr11:72742693 | A | G | 264 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(261): Show |
278 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.-128+9635T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72742693 | |||||||
| chr11:72742805 | G | A | 95 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(92): Show |
101 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.-128+9523C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72742805 | |||||||
| chr11:72742835 | C | T | 2 | a0002c0003t0001g0277 a0002c0025t0001g0278 |
2 | HG02486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-128+9493G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72742835 | |||||||
| chr11:72742998 | C | T | 7 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(4): Show |
7 | HG02451.hp2 HG02976.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-128+9330G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72742998 | |||||||
| chr11:72743215 | C | A | 96 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(93): Show |
102 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.-128+9113G>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72743215 | |||||||
| chr11:72743225 | A | T | 5 | a0001c0001t0001g0197 a0001c0001t0001g0222 a0001c0001t0001g0223 others(2): Show |
5 | HG00733.hp1 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.-128+9103T>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72743225 | |||||||
| chr11:72743307 | T | C | 2 | a0001c0004t0001g0156 a0011c0033t0001g0155 |
2 | HG02080.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.-128+9021A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72743307 | |||||||
| chr11:72743337 | C | T | 1 | a0001c0008t0001g0288 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-128+8991G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72743337 | |||||||
| chr11:72743367 | C | T | 1 | a0001c0001t0002g0305 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-128+8961G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72743367 | |||||||
| chr11:72743404 | C | G | 1 | a0001c0001t0001g0168 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-128+8924G>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72743404 | |||||||
| chr11:72743437 | C | T | 14 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(11): Show |
14 | HG01074.hp1 HG01884.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-128+8891G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72743437 | |||||||
| chr11:72743450 | G | C | 7 | a0001c0008t0001g0287 a0001c0008t0001g0288 a0001c0008t0001g0290 others(4): Show |
7 | HG01074.hp1 HG01884.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-128+8878C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72743450 | |||||||
| chr11:72743501 | T | C | 14 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(11): Show |
14 | HG01074.hp1 HG01884.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-128+8827A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72743501 | |||||||
| chr11:72743574 | T | C | 14 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(11): Show |
14 | HG01074.hp1 HG01884.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-128+8754A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72743574 | |||||||
| chr11:72743700 | C | T | 1 | a0014c0036t0001g0294 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-128+8628G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72743700 | |||||||
| chr11:72743711 | C | T | 1 | a0001c0004t0001g0126 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-128+8617G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72743711 | |||||||
| chr11:72743722 | G | A | 14 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(11): Show |
14 | HG01074.hp1 HG01884.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-128+8606C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72743722 | |||||||
| chr11:72743780 | T | A | 14 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(11): Show |
14 | HG01074.hp1 HG01884.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-128+8548A>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72743780 | |||||||
| chr11:72743909 | C | T | 1 | a0003c0005t0001g0030 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-128+8419G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72743909 | |||||||
| chr11:72743932 | C | T | 1 | a0001c0008t0001g0287 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-128+8396G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72743932 | |||||||
| chr11:72743989 | C | T | 95 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(92): Show |
101 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.-128+8339G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72743989 | |||||||
| chr11:72744004 | G | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-128+8324C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72744004 | |||||||
| chr11:72744107 | C | T | 95 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(92): Show |
101 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.-128+8221G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72744107 | |||||||
| chr11:72744140 | ATGTCACC others(15): Show |
A | 7 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(4): Show |
7 | HG02451.hp2 HG02976.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-128+8166_-128+818 others(26): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72744140 | |||||||
| chr11:72744162 | G | C | 90 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(87): Show |
96 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.-128+8166C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72744162 | |||||||
| chr11:72744191 | A | G | 1 | a0014c0036t0001g0294 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-128+8137T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72744191 | |||||||
| chr11:72744463 | C | T | 23 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(20): Show |
24 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.-128+7865G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72744463 | |||||||
| chr11:72744467 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-128+7861C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72744467 | |||||||
| chr11:72744491 | C | A | 1 | a0001c0001t0001g0125 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-128+7837G>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72744491 | |||||||
| chr11:72744600 | G | A | 88 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(85): Show |
94 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.-128+7728C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72744600 | |||||||
| chr11:72744637 | C | T | 7 | a0001c0008t0001g0287 a0001c0008t0001g0288 a0001c0008t0001g0290 others(4): Show |
7 | HG01074.hp1 HG01884.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-128+7691G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72744637 | |||||||
| chr11:72744708 | T | C | 1 | a0001c0002t0001g0193 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-128+7620A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72744708 | |||||||
| chr11:72744823 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0104 a0001c0001t0001g0105 others(1): Show |
5 | HG02257.hp2 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-128+7505C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72744823 | |||||||
| chr11:72744840 | C | T | 22 | a0002c0003t0002g0022 a0002c0003t0002g0304 a0002c0003t0002g0308 others(19): Show |
23 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.-128+7488G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72744840 | |||||||
| chr11:72744884 | C | A | 1 | a0002c0003t0001g0219 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-128+7444G>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72744884 | |||||||
| chr11:72744924 | G | C | 1 | a0001c0001t0001g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-128+7404C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72744924 | |||||||
| chr11:72744972 | G | T | 1 | a0001c0001t0002g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-128+7356C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72744972 | |||||||
| chr11:72744987 | G | A | 1 | a0001c0002t0001g0040 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-128+7341C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72744987 | |||||||
| chr11:72745020 | G | A | 7 | a0001c0008t0001g0287 a0001c0008t0001g0288 a0001c0008t0001g0290 others(4): Show |
7 | HG01074.hp1 HG01884.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-128+7308C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72745020 | |||||||
| chr11:72745173 | A | C | 105 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(102): Show |
112 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.-128+7155T>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72745173 | |||||||
| chr11:72745182 | C | CT | 98 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0082 others(95): Show |
103 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.-128+7145dupA | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72745182 | |||||||
| chr11:72745182 | C | CTT | 19 | a0001c0001t0001g0046 a0001c0001t0001g0251 a0001c0001t0002g0306 others(16): Show |
20 | HG00735.hp2 HG01243.hp2 HG02155.hp1 others(17): Show |
intron_variant | MODIFIER | c.-128+7144_-128+714 others(6): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72745182 | |||||||
| chr11:72745182 | CT | C | 20 | a0001c0001t0001g0011 a0001c0001t0001g0104 a0001c0001t0001g0105 others(17): Show |
21 | HG01069.hp1 HG01123.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.-128+7145delA | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72745182 | |||||||
| chr11:72745261 | T | C | 1 | a0002c0003t0001g0241 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-128+7067A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72745261 | |||||||
| chr11:72745302 | C | T | 2 | a0001c0004t0001g0048 a0001c0004t0001g0049 |
2 | HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-128+7026G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72745302 | |||||||
| chr11:72745346 | G | A | 2 | a0002c0003t0001g0220 a0009c0026t0001g0242 |
2 | HG02027.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.-128+6982C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72745346 | |||||||
| chr11:72745355 | A | AT | 54 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0120 others(51): Show |
55 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.-128+6972dupA | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72745355 | |||||||
| chr11:72745355 | AT | A | 79 | a0001c0001t0001g0039 a0001c0001t0001g0104 a0001c0001t0001g0105 others(76): Show |
85 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.-128+6972delA | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72745355 | |||||||
| chr11:72745394 | C | T | 1 | a0002c0003t0001g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-128+6934G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72745394 | |||||||
| chr11:72745452 | C | T | 3 | a0001c0001t0001g0106 a0001c0001t0001g0109 a0001c0001t0001g0110 |
3 | HG02922.hp2 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-128+6876G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72745452 | |||||||
| chr11:72745456 | G | A | 104 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(101): Show |
111 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.-128+6872C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72745456 | |||||||
| chr11:72745486 | G | A | 7 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0295 others(4): Show |
7 | HG02451.hp2 HG02976.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-128+6842C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72745486 | |||||||
| chr11:72745616 | ATGGAGTA others(5): Show |
A | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0002c0003t0001g0244 others(1): Show |
4 | HG01069.hp1 HG01168.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.-128+6700_-128+671 others(16): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72745616 | |||||||
| chr11:72745665 | G | C | 54 | a0001c0001t0001g0039 a0001c0001t0001g0046 a0001c0002t0001g0005 others(51): Show |
59 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-128+6663C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72745665 | |||||||
| chr11:72745817 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-128+6511C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72745817 | |||||||
| chr11:72745855 | G | A | 21 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0027 others(18): Show |
23 | HG00558.hp1 HG01993.hp1 HG02293.hp1 others(20): Show |
intron_variant | MODIFIER | c.-128+6473C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72745855 | |||||||
| chr11:72746166 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-128+6162G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72746166 | |||||||
| chr11:72746442 | C | T | 23 | a0001c0002t0002g0307 a0002c0003t0002g0022 a0002c0003t0002g0304 others(20): Show |
24 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.-128+5886G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72746442 | |||||||
| chr11:72746486 | C | T | 105 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(102): Show |
112 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.-128+5842G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72746486 | |||||||
| chr11:72746519 | C | T | 1 | a0003c0005t0001g0108 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-128+5809G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72746519 | |||||||
| chr11:72746681 | C | A | 1 | a0001c0001t0002g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-128+5647G>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72746681 | |||||||
| chr11:72746749 | G | T | 2 | a0001c0002t0001g0041 a0001c0002t0001g0042 |
2 | NA18948.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.-128+5579C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72746749 | |||||||
| chr11:72746811 | A | C | 1 | a0001c0001t0001g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-128+5517T>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72746811 | |||||||
| chr11:72746963 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-128+5365G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72746963 | |||||||
| chr11:72746993 | G | A | 1 | a0001c0001t0001g0039 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-128+5335C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72746993 | |||||||
| chr11:72747059 | G | T | 7 | a0001c0008t0001g0287 a0001c0008t0001g0288 a0001c0008t0001g0290 others(4): Show |
7 | HG01074.hp1 HG01884.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-128+5269C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72747059 | |||||||
| chr11:72747151 | A | G | 120 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(117): Show |
127 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.-128+5177T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72747151 | |||||||
| chr11:72747316 | G | A | 83 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(80): Show |
89 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.-128+5012C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72747316 | |||||||
| chr11:72747430 | A | G | 1 | a0001c0001t0002g0321 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-128+4898T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72747430 | |||||||
| chr11:72747538 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-128+4790G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72747538 | |||||||
| chr11:72747574 | C | T | 12 | a0001c0001t0001g0039 a0001c0004t0001g0034 a0001c0004t0001g0036 others(9): Show |
13 | HG00597.hp2 HG00621.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.-128+4754G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72747574 | |||||||
| chr11:72747722 | T | C | 1 | a0003c0005t0001g0267 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-128+4606A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72747722 | |||||||
| chr11:72747815 | C | T | 1 | a0002c0003t0001g0196 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-128+4513G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72747815 | |||||||
| chr11:72747887 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-128+4441C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72747887 | |||||||
| chr11:72748293 | G | A | 1 | a0001c0001t0002g0306 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-128+4035C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72748293 | |||||||
| chr11:72748303 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-128+4025G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72748303 | |||||||
| chr11:72748306 | G | T | 2 | a0002c0012t0001g0285 a0002c0012t0001g0286 |
2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-128+4022C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72748306 | |||||||
| chr11:72748322 | T | C | 8 | a0001c0002t0001g0246 a0001c0008t0001g0287 a0001c0008t0001g0288 others(5): Show |
8 | HG01074.hp1 HG01884.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.-128+4006A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72748322 | |||||||
| chr11:72748483 | A | G | 264 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(261): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.-128+3845T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72748483 | |||||||
| chr11:72748519 | C | CA | 64 | a0001c0001t0001g0007 a0001c0001t0001g0077 a0001c0001t0001g0078 others(61): Show |
66 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.-128+3808dupT | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72748519 | |||||||
| chr11:72748651 | C | T | 28 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0292 others(25): Show |
29 | HG01074.hp1 HG01884.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.-128+3677G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72748651 | |||||||
| chr11:72748830 | TG | T | 25 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(22): Show |
26 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.-128+3497delC | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72748830 | |||||||
| chr11:72748900 | T | C | 3 | a0001c0001t0001g0015 a0001c0001t0007g0300 a0002c0003t0001g0195 |
4 | HG01243.hp1 HG03195.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-128+3428A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72748900 | |||||||
| chr11:72749110 | G | A | 56 | a0001c0001t0001g0110 a0001c0001t0001g0197 a0001c0001t0001g0222 others(53): Show |
58 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.-128+3218C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72749110 | |||||||
| chr11:72749353 | A | C | 25 | a0001c0001t0002g0305 a0001c0001t0002g0306 a0001c0002t0002g0307 others(22): Show |
26 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.-128+2975T>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72749353 | |||||||
| chr11:72749405 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-128+2923T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72749405 | |||||||
| chr11:72749468 | AGGCTGTT others(4): Show |
A | 1 | a0001c0001t0001g0247 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-128+2849_-128+285 others(15): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72749468 | |||||||
| chr11:72749649 | T | C | 26 | a0001c0001t0002g0305 a0001c0001t0002g0306 a0001c0001t0002g0321 others(23): Show |
27 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.-128+2679A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72749649 | |||||||
| chr11:72749710 | C | T | 26 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(23): Show |
27 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.-128+2618G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72749710 | |||||||
| chr11:72749717 | A | T | 23 | a0001c0002t0002g0307 a0002c0003t0002g0022 a0002c0003t0002g0304 others(20): Show |
24 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.-128+2611T>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72749717 | |||||||
| chr11:72749804 | C | A | 1 | a0001c0004t0001g0248 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-128+2524G>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72749804 | |||||||
| chr11:72749862 | C | T | 61 | a0001c0001t0001g0039 a0001c0001t0001g0046 a0001c0001t0001g0077 others(58): Show |
66 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.-128+2466G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72749862 | |||||||
| chr11:72749885 | A | AT | 26 | a0001c0001t0002g0305 a0001c0001t0002g0306 a0001c0001t0002g0321 others(23): Show |
27 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.-128+2442_-128+244 others(5): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72749885 | |||||||
| chr11:72750218 | C | G | 1 | a0010c0014t0001g0117 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-128+2110G>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72750218 | |||||||
| chr11:72750456 | G | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0114 a0001c0001t0001g0115 others(1): Show |
5 | HG00738.hp1 HG01081.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-128+1872C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72750456 | |||||||
| chr11:72750462 | C | T | 2 | a0001c0001t0002g0305 a0001c0001t0002g0306 |
2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-128+1866G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72750462 | |||||||
| chr11:72750511 | C | T | 1 | a0001c0002t0001g0113 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-128+1817G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72750511 | |||||||
| chr11:72750746 | G | A | 1 | a0014c0036t0001g0294 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-128+1582C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72750746 | |||||||
| chr11:72750767 | A | AG | 27 | a0001c0001t0002g0305 a0001c0001t0002g0306 a0001c0001t0002g0321 others(24): Show |
28 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.-128+1560_-128+156 others(5): Show |
ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72750767 | |||||||
| chr11:72750898 | G | A | 1 | a0006c0011t0001g0112 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-128+1430C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72750898 | |||||||
| chr11:72750899 | T | G | 1 | a0006c0011t0001g0112 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-128+1429A>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72750899 | |||||||
| chr11:72750900 | C | T | 1 | a0006c0011t0001g0112 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-128+1428G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72750900 | |||||||
| chr11:72751013 | G | C | 9 | a0002c0003t0002g0304 a0002c0003t0002g0322 a0002c0003t0002g0323 others(6): Show |
9 | HG00544.hp2 HG00558.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.-128+1315C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72751013 | |||||||
| chr11:72751180 | G | A | 1 | a0001c0001t0003g0026 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-128+1148C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72751180 | |||||||
| chr11:72751271 | C | T | 303 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(300): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.-128+1057G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72751271 | |||||||
| chr11:72751330 | T | C | 146 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(143): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.-128+998A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72751330 | |||||||
| chr11:72751559 | A | C | 1 | a0002c0003t0002g0304 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-128+769T>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72751559 | |||||||
| chr11:72751560 | G | T | 1 | a0002c0003t0002g0304 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-128+768C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72751560 | |||||||
| chr11:72751562 | G | T | 1 | a0002c0003t0002g0304 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-128+766C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72751562 | |||||||
| chr11:72751563 | T | A | 1 | a0002c0003t0002g0304 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-128+765A>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72751563 | |||||||
| chr11:72751566 | A | T | 1 | a0002c0003t0002g0304 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-128+762T>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72751566 | |||||||
| chr11:72751568 | T | G | 1 | a0002c0003t0002g0304 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-128+760A>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72751568 | |||||||
| chr11:72751569 | C | T | 1 | a0002c0003t0002g0304 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-128+759G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72751569 | |||||||
| chr11:72751570 | C | G | 1 | a0002c0003t0002g0304 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-128+758G>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72751570 | |||||||
| chr11:72751571 | T | A | 1 | a0002c0003t0002g0304 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-128+757A>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72751571 | |||||||
| chr11:72751573 | C | G | 1 | a0002c0003t0002g0304 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-128+755G>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72751573 | |||||||
| chr11:72751574 | C | T | 1 | a0002c0003t0002g0304 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-128+754G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72751574 | |||||||
| chr11:72751575 | G | T | 1 | a0002c0003t0002g0304 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-128+753C>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72751575 | |||||||
| chr11:72751589 | A | G | 118 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0046 others(115): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.-128+739T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72751589 | |||||||
| chr11:72751648 | A | G | 2 | a0001c0002t0001g0027 a0001c0002t0001g0028 |
2 | NA18951.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.-128+680T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72751648 | |||||||
| chr11:72751703 | G | A | 4 | a0001c0001t0003g0024 a0001c0001t0003g0025 a0001c0001t0003g0026 others(1): Show |
4 | HG01168.hp1 HG01169.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.-128+625C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72751703 | |||||||
| chr11:72751791 | C | T | 3 | a0005c0010t0002g0301 a0005c0010t0002g0302 a0005c0010t0002g0303 |
3 | NA18973.hp1 NA18977.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-128+537G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72751791 | |||||||
| chr11:72751824 | T | C | 2 | a0001c0001t0001g0295 a0001c0001t0001g0296 |
2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-128+504A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72751824 | |||||||
| chr11:72752185 | C | A | 3 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0034t0001g0299 |
3 | NA18973.hp2 NA18987.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.-128+143G>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72752185 |