Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1450 | 249 | 63 | 56 | 94 | 8 | 27 | 72 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0002 | 0/0 | 1450 | 68 | 24 | 15 | 19 | 2 | 8 | 11 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0003 | 0/0 | 1450 | 14 | 0 | 3 | 11 | 0 | 0 | 6 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0004 | 0/0 | 1450 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0005 | 0/0 | 1450 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0006 | 0/0 | 1450 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0007 | 0/0 | 1450 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0008 | 0/0 | 1450 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0009 | 0/0 | 1450 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0010 | 0/1 | 1450 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0011 | 0/0 | 1450 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0012 | 0/0 | 1450 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0013 | 0/0 | 1450 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0014 | 0/0 | 1450 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0015 | 0/0 | 1450 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0016 | 0/0 | 1450 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0017 | 0/0 | 1450 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0018 | 0/0 | 1450 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0019 | 0/0 | 1450 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0020 | 0/0 | 1450 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0021 | 0/0 | 1450 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 4353 | 109 | 51 | 18 | 29 | 2 | 8 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0002 | 0/0 | 4353 | 84 | 2 | 29 | 36 | 6 | 11 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0003 | 0/0 | 4353 | 64 | 21 | 14 | 19 | 2 | 8 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0004 | 0/0 | 4353 | 32 | 6 | 5 | 15 | 0 | 6 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0005 | 0/0 | 4353 | 14 | 0 | 3 | 11 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0006 | 0/0 | 4353 | 7 | 0 | 0 | 7 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0007 | 0/0 | 4353 | 6 | 0 | 1 | 5 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0008 | 0/0 | 4353 | 4 | 3 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0009 | 0/0 | 4353 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0010 | 0/0 | 4353 | 3 | 0 | 0 | 3 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0011 | 0/0 | 4353 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0012 | 0/0 | 4353 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0013 | 0/0 | 4353 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0014 | 0/0 | 4353 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0015 | 0/0 | 4353 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0016 | 0/1 | 4353 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0017 | 0/0 | 4353 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0018 | 0/0 | 4353 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0019 | 0/0 | 4353 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0020 | 0/0 | 4353 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0021 | 0/0 | 4353 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0022 | 0/0 | 4353 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0023 | 0/0 | 4353 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0024 | 0/0 | 4353 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0025 | 0/0 | 4353 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0026 | 0/0 | 4353 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0027 | 0/0 | 4353 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0028 | 0/0 | 4353 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0029 | 0/0 | 4353 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0030 | 0/0 | 4353 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0031 | 0/0 | 4353 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0032 | 0/0 | 4353 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0033 | 0/0 | 4353 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0034 | 0/0 | 4353 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0035 | 0/0 | 4353 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| c0036 | 0/0 | 4353 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 804 | 315 | 87 | 64 | 124 | 8 | 30 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| t0002 | 0/0 | 804 | 31 | 4 | 8 | 9 | 2 | 8 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| t0003 | 0/0 | 804 | 4 | 1 | 3 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| t0004 | 0/0 | 804 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| t0005 | 0/0 | 804 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| t0006 | 0/0 | 804 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| t0007 | 0/0 | 804 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0003 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0270 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 4353 | 109 | 51 | 18 | 29 | 2 | 8 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0002 | 0/0 | 4353 | 84 | 2 | 29 | 36 | 6 | 11 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0004 | 0/0 | 4353 | 32 | 6 | 5 | 15 | 0 | 6 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0006 | 0/0 | 4353 | 7 | 0 | 0 | 7 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0007 | 0/0 | 4353 | 6 | 0 | 1 | 5 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0008 | 0/0 | 4353 | 4 | 3 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0013 | 0/0 | 4353 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0019 | 0/0 | 4353 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0024 | 0/0 | 4353 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0028 | 0/0 | 4353 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0030 | 0/0 | 4353 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0034 | 0/0 | 4353 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0035 | 0/0 | 4353 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0002c0003 | 0/0 | 4353 | 64 | 21 | 14 | 19 | 2 | 8 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0002c0012 | 0/0 | 4353 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0002c0020 | 0/0 | 4353 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0002c0025 | 0/0 | 4353 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0003c0005 | 0/0 | 4353 | 14 | 0 | 3 | 11 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0004c0009 | 0/0 | 4353 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0005c0010 | 0/0 | 4353 | 3 | 0 | 0 | 3 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0006c0011 | 0/0 | 4353 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0007c0014 | 0/0 | 4353 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0008c0036 | 0/0 | 4353 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0009c0033 | 0/0 | 4353 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0010c0016 | 0/1 | 4353 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0011c0017 | 0/0 | 4353 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0012c0031 | 0/0 | 4353 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0013c0027 | 0/0 | 4353 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0014c0021 | 0/0 | 4353 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0015c0022 | 0/0 | 4353 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0016c0026 | 0/0 | 4353 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0017c0023 | 0/0 | 4353 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0018c0029 | 0/0 | 4353 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0019c0018 | 0/0 | 4353 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0020c0032 | 0/0 | 4353 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0021c0015 | 0/0 | 4353 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | 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 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0001t0002 | 0/0 | 5156 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0001t0003 | 0/0 | 5156 | 3 | 1 | 2 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0001t0004 | 0/0 | 5156 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0001t0007 | 0/0 | 5156 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0002t0001 | 0/0 | 5156 | 83 | 2 | 29 | 36 | 6 | 10 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0002t0002 | 0/0 | 5156 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0004t0001 | 0/0 | 5156 | 31 | 6 | 5 | 14 | 0 | 6 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0004t0006 | 0/0 | 5156 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0006t0001 | 0/0 | 5156 | 7 | 0 | 0 | 7 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0007t0001 | 0/0 | 5156 | 6 | 0 | 1 | 5 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0008t0001 | 0/0 | 5156 | 4 | 3 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0013t0001 | 0/0 | 5156 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0019t0001 | 0/0 | 5156 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0024t0001 | 0/0 | 5156 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0028t0003 | 0/0 | 5156 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0030t0001 | 0/0 | 5156 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0034t0001 | 0/0 | 5156 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0001c0035t0001 | 0/0 | 5156 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0002c0003t0001 | 0/0 | 5156 | 43 | 21 | 7 | 13 | 0 | 2 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0002c0003t0002 | 0/0 | 5156 | 21 | 0 | 7 | 6 | 2 | 6 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0002c0012t0001 | 0/0 | 5156 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0002c0020t0002 | 0/0 | 5156 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0002c0025t0001 | 0/0 | 5156 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0003c0005t0001 | 0/0 | 5156 | 14 | 0 | 3 | 11 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0004c0009t0001 | 0/0 | 5156 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0005c0010t0002 | 0/0 | 5156 | 3 | 0 | 0 | 3 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0006c0011t0001 | 0/0 | 5156 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0007c0014t0001 | 0/0 | 5156 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0008c0036t0001 | 0/0 | 5156 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0009c0033t0001 | 0/0 | 5156 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0010c0016t0001 | 0/1 | 5156 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0011c0017t0001 | 0/0 | 5156 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0012c0031t0001 | 0/0 | 5156 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0013c0027t0001 | 0/0 | 5156 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0014c0021t0001 | 0/0 | 5156 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0015c0022t0002 | 0/0 | 5156 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0016c0026t0001 | 0/0 | 5156 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0017c0023t0001 | 0/0 | 5156 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0018c0029t0005 | 0/0 | 5156 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0019c0018t0002 | 0/0 | 5156 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0020c0032t0001 | 0/0 | 5156 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| a0021c0015t0001 | 0/0 | 5156 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | copy fasta | chr11 | 72680069 | 72757408 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0076 | 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 |
| a0001c0001t0001g0081 | 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 |
| a0001c0001t0001g0088 | 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 |
| a0001c0001t0001g0101 | 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 |
| a0001c0001t0001g0108 | 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 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 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 |
| 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 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0148 | 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 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0256 | 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 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0270 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0276 | 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 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0001t0007g0303 | 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 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0060 | 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 |
| a0001c0002t0001g0064 | 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 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0072 | 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 |
| a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0206 | 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 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0218 | 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 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0255 | 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 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0263 | 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 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0002t0002g0310 | 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 |
| a0001c0004t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0004t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0001c0004t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0004t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0006t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0006t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0006t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0006t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0006t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0006t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0006t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0007t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0007t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0007t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0007t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0007t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0008t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0008t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0013t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0019t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0024t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0028t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0030t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0034t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0001c0035t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0086 | 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 |
| a0002c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0192 | 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 |
| a0002c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0205 | 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 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0002c0003t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0002c0003t0001g0222 | 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 |
| a0002c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0273 | 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 |
| 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 |
| a0002c0003t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0002c0003t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0002c0003t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0003t0002g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0012t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0012t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0020t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0002c0025t0001g0281 | 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 |
| a0003c0005t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0003c0005t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0003c0005t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 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 |
| a0003c0005t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0003c0005t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0003c0005t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0003c0005t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0003c0005t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0003c0005t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0004c0009t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0004c0009t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0005c0010t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0005c0010t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0005c0010t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0006c0011t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0006c0011t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0007c0014t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0008c0036t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0009c0033t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0010c0016t0001g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0011c0017t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0012c0031t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0013c0027t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0014c0021t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0015c0022t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0016c0026t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0017c0023t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0018c0029t0005g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0019c0018t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0020c0032t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| a0021c0015t0001g0040 | 0/0 | 1 | 1 | 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 | g0037 | EUR | GBR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00099 | hp2 | a0002 | c0003 | t0002 | g0320 | EUR | GBR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0126 | EUR | GBR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00140 | hp2 | a0002 | c0003 | t0002 | g0019 | EUR | GBR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00438 | hp2 | a0002 | c0003 | t0001 | g0200 | EAS | CHS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00544 | hp1 | a0001 | c0004 | t0001 | g0050 | EAS | CHS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00544 | hp2 | a0002 | c0003 | t0002 | g0331 | EAS | CHS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00558 | hp1 | a0001 | c0007 | t0001 | g0069 | EAS | CHS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00558 | hp2 | a0002 | c0003 | t0002 | g0330 | EAS | CHS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00597 | hp1 | a0002 | c0003 | t0001 | g0210 | EAS | CHS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00597 | hp2 | a0001 | c0004 | t0001 | g0032 | EAS | CHS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00621 | hp1 | a0001 | c0004 | t0001 | g0033 | EAS | CHS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00621 | hp2 | a0001 | c0006 | t0001 | g0119 | EAS | CHS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0179 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0186 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0218 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0190 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0263 | EAS | CHS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0017 | 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 | g0047 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0188 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0176 | 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 | g0160 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0174 | 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 | g0233 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01074 | hp1 | a0001 | c0008 | t0001 | g0291 | 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 | g0007 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0178 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01099 | hp1 | a0001 | c0004 | t0001 | g0052 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0203 | 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 | g0209 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0226 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01167 | hp2 | a0001 | c0004 | t0001 | g0048 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01168 | hp2 | a0002 | c0003 | t0001 | g0245 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0225 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01175 | hp1 | a0018 | c0029 | t0005 | g0053 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01175 | hp2 | a0003 | c0005 | t0001 | g0217 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01243 | hp2 | a0002 | c0003 | t0002 | g0321 | AMR | PUR | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0170 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01255 | hp2 | a0002 | c0003 | t0002 | g0316 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01258 | hp1 | a0002 | c0003 | t0002 | g0314 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0202 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01346 | hp1 | a0002 | c0003 | t0002 | g0312 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01346 | hp2 | a0001 | c0024 | t0001 | g0187 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01358 | hp1 | a0003 | c0005 | t0001 | g0027 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0171 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0182 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01361 | hp2 | a0001 | c0004 | t0001 | g0168 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01433 | hp1 | a0002 | c0020 | t0002 | g0322 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01433 | hp2 | a0001 | c0028 | t0003 | g0020 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01496 | hp1 | a0002 | c0003 | t0002 | g0318 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0173 | EUR | IBS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0014 | EUR | IBS | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01884 | hp1 | a0001 | c0008 | t0001 | g0290 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01891 | hp1 | a0002 | c0003 | t0001 | g0018 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01891 | hp2 | a0002 | c0003 | t0001 | g0211 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01928 | hp1 | a0002 | c0003 | t0001 | g0015 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01928 | hp2 | a0002 | c0003 | t0001 | g0133 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01934 | hp2 | a0002 | c0003 | t0002 | g0315 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01943 | hp1 | a0003 | c0005 | t0001 | g0035 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01952 | hp1 | a0002 | c0003 | t0002 | g0326 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01975 | hp2 | a0002 | c0003 | t0001 | g0215 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01978 | hp2 | a0002 | c0003 | t0001 | g0015 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01993 | hp1 | a0001 | c0007 | t0001 | g0067 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0181 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0247 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02027 | hp2 | a0016 | c0026 | t0001 | g0243 | 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 | g0183 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02056 | hp2 | a0007 | c0014 | t0001 | g0115 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02071 | hp1 | a0002 | c0003 | t0001 | g0242 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0262 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02074 | hp2 | a0001 | c0004 | t0001 | g0044 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02080 | hp1 | a0001 | c0004 | t0001 | g0154 | 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 | g0237 | 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 | g0031 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02132 | hp2 | a0002 | c0003 | t0002 | g0329 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0264 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02145 | hp1 | a0002 | c0003 | t0001 | g0279 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02148 | hp1 | a0001 | c0004 | t0001 | g0163 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02155 | hp1 | a0003 | c0005 | t0001 | g0026 | EAS | CDX | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02155 | hp2 | a0009 | c0033 | t0001 | g0153 | EAS | CDX | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0121 | 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 | g0023 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02258 | hp1 | a0004 | c0009 | t0001 | g0278 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02258 | hp2 | a0002 | c0003 | t0001 | g0086 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02293 | hp1 | a0002 | c0003 | t0001 | g0059 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0172 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02523 | hp1 | a0003 | c0005 | t0001 | g0269 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02523 | hp2 | a0002 | c0003 | t0001 | g0221 | EAS | KHV | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02572 | hp2 | a0001 | c0004 | t0001 | g0083 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02602 | hp1 | a0002 | c0003 | t0001 | g0246 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02602 | hp2 | a0017 | c0023 | t0001 | g0164 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02615 | hp1 | a0004 | c0009 | t0001 | g0277 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02615 | hp2 | a0021 | c0015 | t0001 | g0040 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02622 | hp2 | a0001 | c0004 | t0001 | g0085 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0309 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02630 | hp2 | a0001 | c0004 | t0001 | g0100 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02723 | hp1 | a0002 | c0003 | t0001 | g0286 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0308 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0201 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02738 | hp2 | a0001 | c0004 | t0001 | g0049 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02886 | hp1 | a0002 | c0003 | t0001 | g0282 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02886 | hp2 | a0002 | c0012 | t0001 | g0288 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02895 | hp1 | a0008 | c0036 | t0001 | g0297 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0227 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02965 | hp1 | a0002 | c0003 | t0001 | g0285 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02970 | hp1 | a0002 | c0003 | t0001 | g0292 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02976 | hp1 | a0004 | c0009 | t0001 | g0274 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03017 | hp1 | a0002 | c0003 | t0002 | g0317 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03017 | hp2 | a0011 | c0017 | t0001 | g0231 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03041 | hp1 | a0002 | c0003 | t0001 | g0287 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0324 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0155 | 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 | g0192 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03209 | hp2 | a0001 | c0004 | t0001 | g0041 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03225 | hp2 | a0002 | c0012 | t0001 | g0289 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0303 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03486 | hp1 | a0002 | c0003 | t0001 | g0284 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0011 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0240 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0189 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0011 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03516 | hp1 | a0002 | c0003 | t0001 | g0212 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03540 | hp1 | a0002 | c0003 | t0001 | g0075 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0078 | AFR | GWD | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03579 | hp2 | a0002 | c0003 | t0001 | g0283 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0191 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03654 | hp2 | a0015 | c0022 | t0002 | g0313 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03688 | hp1 | a0002 | c0003 | t0002 | g0019 | 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 | g0045 | SAS | BEB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03831 | hp2 | a0002 | c0003 | t0002 | g0332 | SAS | BEB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03834 | hp1 | a0001 | c0004 | t0001 | g0051 | SAS | BEB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0310 | 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 | g0180 | SAS | BEB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03942 | hp2 | a0001 | c0019 | t0001 | g0177 | SAS | BEB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG04115 | hp1 | a0001 | c0004 | t0001 | g0058 | SAS | STU | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG04115 | hp2 | a0002 | c0003 | t0002 | g0323 | SAS | STU | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0165 | SAS | BEB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG04199 | hp1 | a0001 | c0013 | t0001 | g0169 | SAS | STU | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG04199 | hp2 | a0002 | c0003 | t0002 | g0311 | SAS | STU | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG04204 | hp1 | a0002 | c0003 | t0002 | g0328 | SAS | STU | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0204 | SAS | STU | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | YRI | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | YRI | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18612 | hp1 | a0001 | c0006 | t0001 | g0146 | EAS | CHB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18612 | hp2 | a0002 | c0003 | t0001 | g0228 | EAS | CHB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18906 | hp1 | a0001 | c0035 | t0001 | g0272 | AFR | YRI | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | YRI | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18940 | hp1 | a0001 | c0004 | t0001 | g0042 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18940 | hp2 | a0002 | c0003 | t0002 | g0307 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18944 | hp1 | a0001 | c0006 | t0001 | g0139 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18944 | hp2 | a0001 | c0030 | t0001 | g0216 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18948 | hp1 | a0006 | c0011 | t0001 | g0149 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0039 | 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 | g0012 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18954 | hp2 | a0003 | c0005 | t0001 | g0125 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18959 | hp1 | a0001 | c0004 | t0001 | g0056 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18960 | hp1 | a0003 | c0005 | t0001 | g0244 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18960 | hp2 | a0002 | c0003 | t0001 | g0229 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18963 | hp1 | a0001 | c0006 | t0001 | g0062 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18965 | hp2 | a0020 | c0032 | t0001 | g0268 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18966 | hp1 | a0001 | c0007 | t0001 | g0068 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18966 | hp2 | a0001 | c0004 | t0001 | g0057 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18967 | hp2 | a0003 | c0005 | t0001 | g0029 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18968 | hp1 | a0002 | c0003 | t0002 | g0327 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18969 | hp2 | a0002 | c0003 | t0001 | g0208 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18971 | hp1 | a0001 | c0004 | t0001 | g0130 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18973 | hp1 | a0005 | c0010 | t0002 | g0305 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18977 | hp2 | a0005 | c0010 | t0002 | g0304 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18980 | hp2 | a0002 | c0003 | t0001 | g0134 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18981 | hp1 | a0003 | c0005 | t0001 | g0030 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18981 | hp2 | a0002 | c0003 | t0001 | g0205 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18987 | hp1 | a0001 | c0034 | t0001 | g0302 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18987 | hp2 | a0002 | c0003 | t0002 | g0325 | 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 | g0008 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18991 | hp1 | a0006 | c0011 | t0001 | g0110 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18992 | hp1 | a0003 | c0005 | t0001 | g0107 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18993 | hp1 | a0001 | c0007 | t0001 | g0080 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18994 | hp2 | a0013 | c0027 | t0001 | g0143 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18995 | hp1 | a0005 | c0010 | t0002 | g0306 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18995 | hp2 | a0002 | c0003 | t0001 | g0199 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18998 | hp2 | a0001 | c0006 | t0001 | g0219 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18999 | hp1 | a0002 | c0003 | t0001 | g0222 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19000 | hp1 | a0001 | c0004 | t0001 | g0124 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19003 | hp1 | a0001 | c0007 | t0001 | g0065 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19010 | hp1 | a0001 | c0006 | t0001 | g0120 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19010 | hp2 | a0002 | c0003 | t0001 | g0220 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19030 | hp1 | a0014 | c0021 | t0001 | g0271 | AFR | LWK | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19030 | hp2 | a0001 | c0008 | t0001 | g0294 | AFR | LWK | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | LWK | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19043 | hp2 | a0002 | c0003 | t0001 | g0079 | AFR | LWK | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19055 | hp2 | a0001 | c0004 | t0006 | g0055 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19056 | hp1 | a0002 | c0003 | t0001 | g0207 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19066 | hp1 | a0003 | c0005 | t0001 | g0028 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19077 | hp1 | a0001 | c0007 | t0001 | g0061 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19077 | hp2 | a0001 | c0004 | t0001 | g0257 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19090 | hp1 | a0001 | c0006 | t0001 | g0152 | 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 | g0129 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19240 | hp1 | a0002 | c0003 | t0001 | g0087 | AFR | YRI | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA19240 | hp2 | a0001 | c0008 | t0001 | g0293 | AFR | YRI | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA20129 | hp1 | a0019 | c0018 | t0002 | g0319 | AFR | ASW | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ASW | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0175 | EUR | TSI | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0234 | EUR | TSI | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0238 | EUR | TSI | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0241 | EUR | TSI | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA20905 | hp1 | a0001 | c0004 | t0001 | g0054 | SAS | GIH | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA20905 | hp2 | a0001 | c0004 | t0001 | g0046 | SAS | GIH | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0239 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG01123 | hp2 | a0012 | c0031 | t0001 | g0034 | AMR | CLM | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02486 | hp1 | a0002 | c0003 | t0001 | g0280 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02486 | hp2 | a0002 | c0003 | t0001 | g0273 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0111 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0084 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | USA | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| HG06807 | hp2 | a0002 | c0003 | t0001 | g0018 | AFR | USA | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA20300 | hp1 | a0002 | c0025 | t0001 | g0281 | AFR | USA | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | USA | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA21309 | hp1 | a0002 | c0003 | t0001 | g0117 | AFR | LWK | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| NA21309 | hp2 | a0001 | c0004 | t0001 | g0249 | AFR | LWK | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| homoSapiens_chm13v2 | hp1 | a0010 | c0016 | t0001 | g0197 | REF | REF | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0270 | REF | REF | ARAP1_chr11_72680069_72757408 | ARAP1 | chr11 | 72680069 | 72757408 |
| 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 | a0003a0012a0016 | 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 | a0017 | 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 | 6 | a0002a0010a0011others(3): Show | 73 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(70): 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 | a0015 | 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 | a0018 | 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 | a0014 | 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 | a0013 | 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 | a0019 | 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 | a0012 | 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 | a0011 | 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 | a0020 | 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 | ||
| chr11:72710530
|
C | T | 1 | a0010 | 1 | homoSapiens_chm13v2.hp1 | missense_variant | MODERATE | c.1271G>A | p.Arg424Gln | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 10/35 | 1479/5156 | 1271/4353 | 424/1450 | chr11 | 72710530 | ||
| chr11:72710537
|
G | A | 1 | a0009 | 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 | a0021 | 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 | a0008 | 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 | a0007 | 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 |
| 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 | a0001c0002a0001c0007a0001c0013others(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 | a0013c0027 | 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 | a0001c0019a0002c0020 | 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 | a0001c0004a0001c0007a0003c0005others(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 |
| 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 | a0018c0029t0005 | 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 | a0001c0001t0003a0001c0028t0003 | 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 | a0001c0001t0003a0001c0028t0003 | 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 | a0001c0001t0002a0001c0002t0002a0002c0003t0002others(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 |
| 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 | a0001c0001t0001g0088a0002c0003t0001g0284a0002c0003t0001g0286others(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 | 131 | a0001c0001t0001g0006a0001c0001t0001g0076a0001c0001t0001g0088others(128): 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 | 131 | a0001c0001t0001g0006a0001c0001t0001g0076a0001c0001t0001g0088others(128): 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 | 75 | a0001c0001t0001g0010a0001c0001t0001g0077a0001c0001t0001g0081others(72): 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 | a0001c0004t0001g0163 | 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 | a0001c0002t0001g0173 | 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 | a0001c0002t0001g0002a0001c0002t0001g0011a0001c0002t0001g0012others(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 | a0001c0001t0001g0105 | 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 | a0001c0004t0001g0051 | 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 | a0001c0002t0001g0214 | 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 | a0001c0001t0001g0098 | 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 | a0001c0001t0001g0112 | 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 | a0001c0002t0001g0189 | 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0106 | 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 | a0001c0004t0001g0041a0001c0004t0001g0083a0001c0004t0001g0084others(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 | 189 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0076others(186): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.4071-270delA | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 31/34 | chr11 | 72688007 | ||||||
| chr11:72688010
|
T | G | 75 | a0001c0001t0001g0010a0001c0001t0001g0077a0001c0001t0001g0081others(72): 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 | a0001c0001t0003g0021a0001c0001t0003g0022 | 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 | 130 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0076others(127): 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 | a0001c0004t0001g0041a0001c0004t0001g0083a0001c0004t0001g0084others(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 | 126 | a0001c0001t0001g0006a0001c0001t0001g0076a0001c0001t0001g0088others(123): 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 | a0002c0003t0001g0086a0002c0003t0001g0087a0002c0003t0001g0192others(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 | 59 | a0001c0001t0001g0109a0001c0001t0001g0132a0001c0001t0001g0147others(56): Show | 60 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(57): 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 | a0001c0002t0001g0190 | 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 | a0001c0006t0001g0120 | 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 | 128 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0076others(125): 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0002g0324 | 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 | a0001c0001t0001g0091 | 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 | 70 | a0001c0001t0001g0010a0001c0001t0001g0077a0001c0001t0001g0081others(67): 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 | a0001c0001t0001g0099a0001c0001t0001g0296 | 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 | a0001c0001t0001g0077a0001c0001t0001g0156 | 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 | a0001c0001t0001g0006a0001c0001t0001g0092a0001c0001t0001g0093others(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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0105a0001c0001t0001g0184 | 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 | a0002c0003t0002g0314 | 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 | a0001c0001t0001g0008a0001c0001t0001g0162a0001c0002t0001g0167 | 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 | a0001c0006t0001g0062a0001c0006t0001g0139 | 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 | a0001c0001t0001g0076a0001c0001t0001g0298a0001c0001t0001g0299others(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 | 129 | a0001c0001t0001g0006a0001c0001t0001g0076a0001c0001t0001g0088others(126): 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 | a0005c0010t0002g0304a0005c0010t0002g0305a0005c0010t0002g0306 | 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 | a0001c0001t0001g0105a0001c0001t0001g0184 | 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 | a0001c0001t0001g0142 | 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 | a0001c0001t0001g0092 | 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 | 127 | a0001c0001t0001g0006a0001c0001t0001g0076a0001c0001t0001g0088others(124): 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 | a0001c0001t0001g0105a0001c0001t0001g0184 | 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 | a0001c0001t0001g0094 | 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 | 125 | a0001c0001t0001g0006a0001c0001t0001g0076a0001c0001t0001g0088others(122): 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 | a0001c0002t0001g0204 | 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 | a0001c0002t0001g0002a0001c0002t0001g0174a0001c0002t0001g0175others(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 | a0001c0001t0001g0252 | 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 | 101 | a0001c0001t0001g0010a0001c0001t0001g0077a0001c0001t0001g0095others(98): Show | 105 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(102): 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 | a0001c0002t0001g0037 | 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 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0076others(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 | a0001c0001t0001g0151a0001c0001t0001g0238 | 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 | a0001c0001t0001g0116 | 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 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0109others(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 | a0001c0001t0001g0007a0001c0001t0001g0112a0001c0001t0001g0113 | 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 | a0008c0036t0001g0297a0014c0021t0001g0271 | 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 | 69 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0088others(66): 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 | a0001c0004t0001g0045a0001c0004t0001g0046 | 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 | 19 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0088others(16): 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 | a0001c0002t0001g0167a0001c0002t0001g0213a0001c0030t0001g0216 | 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 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0161others(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 | a0006c0011t0001g0110a0006c0011t0001g0149 | 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 | a0003c0005t0001g0028a0003c0005t0001g0029a0003c0005t0001g0030 | 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 | a0001c0001t0001g0295a0001c0001t0001g0296 | 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 | 241 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0076others(238): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): 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 | a0001c0001t0001g0157 | 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 | 267 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0043others(264): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): 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 | a0001c0001t0001g0077a0001c0001t0001g0156 | 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 | 267 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0043others(264): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): 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 | a0001c0001t0003g0023 | 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 | a0001c0024t0001g0187 | 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 | a0001c0001t0001g0296 | 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 | 168 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0076others(165): 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 | 82 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(79): 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 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0088others(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 | a0014c0021t0001g0271 | 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 | 267 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0043others(264): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): 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 | a0008c0036t0001g0297 | 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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0043a0001c0001t0001g0103a0001c0001t0001g0104others(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 | a0002c0003t0002g0317 | 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 | 37 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0017others(34): 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 | 268 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0043others(265): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): 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 | a0001c0001t0002g0324 | 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 | 238 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0077others(235): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): 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 | a0001c0001t0001g0232 | 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 | a0001c0004t0001g0047 | 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 | a0001c0004t0001g0033 | 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 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0077others(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 | 72 | a0001c0001t0001g0159a0001c0001t0001g0160a0002c0003t0001g0015others(69): Show | 75 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(72): 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 | a0001c0001t0001g0043a0001c0001t0001g0103a0001c0001t0001g0104others(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 | 88 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(85): 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 | a0001c0008t0001g0290a0001c0008t0001g0291a0001c0008t0001g0293others(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 | a0016c0026t0001g0243 | 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 | a0009c0033t0001g0153 | 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 | 166 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0077others(163): 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 | 166 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0077others(163): 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 | a0001c0001t0004g0078 | 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 | a0001c0001t0001g0295a0001c0001t0001g0296 | 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 | a0001c0001t0001g0233 | 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 | a0002c0003t0002g0329 | 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 | a0001c0001t0002g0324 | 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 | a0001c0001t0001g0295a0001c0001t0001g0296 | 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 | a0002c0012t0001g0289 | 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 | 166 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0077others(163): 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 | a0001c0035t0001g0272 | 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 | 166 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0077others(163): 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 | a0001c0001t0003g0021 | 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 | a0001c0001t0003g0021 | 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 | 166 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0077others(163): 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 | a0001c0001t0001g0184 | 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 | a0001c0002t0001g0191 | 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 | a0001c0001t0003g0021 | 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 | 166 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0077others(163): 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 | a0001c0001t0003g0021 | 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 | 268 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0043others(265): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.3166+144G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 22/34 | chr11 | 72696839 | ||||||
| chr11:72696896
|
C | T | 17 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0088others(14): 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 | 166 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0077others(163): 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 | a0001c0001t0001g0184a0001c0004t0001g0001a0001c0004t0001g0032others(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 | a0001c0001t0003g0021 | 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 | a0001c0004t0001g0041a0001c0004t0001g0083a0001c0004t0001g0084others(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 | a0001c0002t0001g0230 | 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 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0002g0324 | 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 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0077others(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 | a0001c0002t0001g0014a0001c0002t0001g0201a0001c0002t0001g0202others(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 | a0001c0001t0001g0006a0001c0001t0001g0092a0001c0001t0001g0093others(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 | a0002c0012t0001g0289a0003c0005t0001g0217 | 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 | 70 | a0002c0003t0001g0015a0002c0003t0001g0018a0002c0003t0001g0059others(67): Show | 73 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2542-38G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 18/34 | chr11 | 72698144 | ||||||
| chr11:72698215
|
C | T | 166 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0077others(163): 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 | a0002c0003t0001g0280 | 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 | a0001c0002t0001g0122a0001c0002t0001g0135a0001c0002t0001g0136others(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 | a0001c0002t0001g0126 | 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 | a0002c0003t0001g0209 | 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 | a0001c0008t0001g0290a0001c0008t0001g0291a0001c0008t0001g0293others(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 | 166 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0077others(163): 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 | a0003c0005t0001g0217 | 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 | a0001c0007t0001g0061a0001c0007t0001g0065a0001c0007t0001g0068others(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 | a0001c0001t0001g0105a0001c0001t0001g0106 | 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 | a0001c0001t0001g0105a0001c0001t0001g0106 | 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 | a0002c0003t0001g0222 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0275a0001c0001t0001g0276a0004c0009t0001g0274others(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 | a0001c0001t0001g0105a0001c0001t0001g0106 | 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 | a0001c0001t0001g0156 | 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 | a0001c0004t0001g0054 | 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 | a0001c0002t0001g0267 | 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 | 166 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0077others(163): 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 | 82 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(79): 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 | a0001c0001t0001g0295a0001c0001t0001g0296 | 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 | a0008c0036t0001g0297 | 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 | 156 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0077others(153): 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 | a0001c0001t0001g0103a0001c0001t0001g0104 | 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 | 72 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(69): 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 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0300others(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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0295a0001c0001t0001g0296 | 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 | 166 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0077others(163): 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 | a0002c0003t0001g0086a0002c0003t0001g0087a0002c0003t0001g0195 | 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 | a0001c0002t0001g0189 | 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 | a0001c0001t0001g0009a0001c0001t0001g0116a0001c0001t0001g0118others(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 | 166 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0077others(163): 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 | 166 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0077others(163): 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 | 166 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0077others(163): 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 | a0001c0008t0001g0294 | 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 | a0002c0003t0001g0211 | 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 | a0002c0003t0001g0286a0002c0003t0001g0287 | 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 | a0001c0004t0001g0048 | 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 | 69 | a0002c0003t0001g0015a0002c0003t0001g0018a0002c0003t0001g0059others(66): Show | 72 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.2167+266G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 15/34 | chr11 | 72702639 | ||||||
| chr11:72702774
|
C | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 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 | a0001c0001t0001g0043a0001c0001t0001g0103a0001c0001t0001g0104others(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 | 158 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0077others(155): 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 | 38 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0017others(35): 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 | a0001c0004t0001g0050 | 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 | a0001c0001t0001g0010a0001c0001t0001g0299 | 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 | a0001c0001t0001g0298 | 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 | 108 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0092others(105): Show | 113 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.1993-330delC | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 14/34 | chr11 | 72703408 | ||||||
| chr11:72703410
|
G | A | 1 | a0002c0025t0001g0281 | 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 | 40 | a0001c0001t0001g0184a0001c0002t0001g0005a0001c0002t0001g0016others(37): 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 | a0001c0002t0001g0002a0001c0002t0001g0013a0001c0002t0001g0037others(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 | a0001c0002t0001g0003a0001c0002t0001g0011a0001c0002t0001g0170others(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 | a0001c0004t0001g0032a0001c0004t0001g0041a0001c0004t0001g0044others(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 | a0001c0004t0001g0048a0001c0004t0001g0049a0001c0004t0001g0051others(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 | a0001c0004t0001g0001a0001c0004t0001g0033a0001c0004t0001g0042others(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 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0088others(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 | a0001c0004t0006g0055 | 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 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0088others(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 | a0001c0007t0001g0061a0001c0007t0001g0065a0001c0007t0001g0068others(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 | a0001c0001t0002g0324 | 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 | a0001c0004t0001g0154a0009c0033t0001g0153 | 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 | a0001c0001t0001g0184 | 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 | a0001c0004t0001g0048 | 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 | a0001c0004t0001g0249 | 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 | 91 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0088others(88): 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 | 157 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0077others(154): 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 | a0008c0036t0001g0297a0014c0021t0001g0271 | 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 | a0002c0003t0001g0220 | 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 | a0001c0001t0001g0252a0001c0001t0001g0265 | 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 | a0001c0002t0001g0237 | 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 | 157 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0077others(154): 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 | a0001c0004t0001g0001a0001c0004t0001g0032a0001c0004t0001g0033others(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 | a0001c0004t0001g0001a0001c0004t0001g0032a0001c0004t0001g0033others(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 | a0001c0004t0001g0057 | 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 | a0001c0006t0001g0219 | 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 | a0001c0001t0001g0010a0001c0001t0001g0161a0001c0001t0001g0275others(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 | 80 | a0001c0001t0001g0043a0001c0002t0001g0014a0001c0002t0001g0201others(77): Show | 84 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.1809+118C>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 13/34 | chr11 | 72705687 | ||||||
| chr11:72705688
|
G | T | 80 | a0001c0001t0001g0043a0001c0002t0001g0014a0001c0002t0001g0201others(77): Show | 84 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(81): 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 | a0001c0004t0001g0044 | 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 | a0001c0001t0001g0105 | 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 | 72 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(69): 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 | a0001c0001t0001g0252a0001c0001t0001g0265 | 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 | a0001c0004t0001g0130 | 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 | a0001c0004t0001g0083 | 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 | a0002c0003t0001g0087a0002c0003t0001g0195 | 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 | a0001c0002t0001g0225a0001c0002t0001g0226 | 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 | a0002c0003t0002g0323 | 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0145 | 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 | a0001c0002t0001g0191 | 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 | a0003c0005t0001g0028a0003c0005t0001g0029a0003c0005t0001g0030 | 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 | a0002c0003t0001g0086a0002c0003t0001g0087a0002c0003t0001g0195 | 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 | a0006c0011t0001g0149 | 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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0077others(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 | a0021c0015t0001g0040 | 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 | a0001c0002t0001g0213 | 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 | a0002c0003t0001g0117 | 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 | a0004c0009t0001g0274a0004c0009t0001g0277a0004c0009t0001g0278 | 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 | a0001c0001t0001g0108 | 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 | a0002c0003t0001g0133a0002c0003t0001g0199a0002c0003t0001g0205others(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 | a0002c0003t0002g0326 | 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 | 80 | a0001c0002t0001g0002a0001c0002t0001g0003a0001c0002t0001g0005others(77): 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 | 270 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0043others(267): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): 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 | a0002c0003t0001g0018a0002c0003t0001g0273a0002c0003t0001g0279others(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 | a0001c0002t0001g0264 | 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 | a0002c0003t0001g0279 | 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 | a0001c0002t0001g0201a0001c0002t0001g0202a0001c0002t0001g0203others(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 | a0001c0001t0001g0223a0001c0001t0001g0224 | 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 | a0001c0001t0001g0082a0001c0001t0001g0093a0001c0001t0001g0118others(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 | a0001c0001t0001g0252 | 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 | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 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 | a0002c0003t0002g0332 | 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 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0103a0001c0001t0001g0104 | 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 | a0011c0017t0001g0231 | 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 | a0001c0001t0001g0105a0001c0001t0001g0106 | 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 | a0001c0001t0001g0092 | 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 | a0001c0008t0001g0290a0001c0008t0001g0291a0001c0008t0001g0293others(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 | 31 | a0001c0002t0001g0014a0001c0002t0001g0201a0001c0002t0001g0202others(28): Show | 33 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(30): 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 | a0001c0004t0001g0001a0001c0004t0001g0032a0001c0004t0001g0033others(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 | 13 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0088others(10): 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 | a0001c0001t0001g0252 | 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 | a0008c0036t0001g0297a0014c0021t0001g0271 | 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 | 15 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0088others(12): 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 | a0014c0021t0001g0271 | 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 | a0001c0001t0002g0324 | 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 | 81 | a0001c0001t0001g0043a0001c0001t0001g0094a0001c0001t0001g0098others(78): Show | 84 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.1023-196dupA | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 7/34 | chr11 | 72711694 | ||||||
| chr11:72711694
|
C | CTT | 88 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0076others(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 | 92 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0089others(89): 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 | a0001c0008t0001g0290a0001c0008t0001g0291a0001c0008t0001g0293others(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 | a0002c0003t0002g0312 | 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 | a0001c0001t0001g0184 | 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 | 268 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0043others(265): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): 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 | a0002c0003t0001g0286a0002c0003t0001g0287 | 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 | a0001c0004t0001g0001a0001c0004t0001g0032a0001c0004t0001g0033others(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 | a0001c0002t0001g0261 | 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 | a0008c0036t0001g0297a0014c0021t0001g0271 | 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 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0077others(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 | a0001c0001t0001g0184 | 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 | a0002c0003t0001g0117 | 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 | a0001c0001t0001g0301 | 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 | a0001c0001t0001g0010a0001c0001t0001g0076a0001c0001t0001g0077others(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 | a0002c0003t0001g0200 | 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 | a0008c0036t0001g0297 | 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 | a0001c0001t0001g0006a0001c0001t0001g0092a0001c0001t0001g0093others(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 | a0001c0006t0001g0152 | 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 | a0001c0001t0002g0308a0001c0001t0002g0309 | 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 | a0002c0012t0001g0288a0002c0012t0001g0289 | 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 | a0020c0032t0001g0268 | 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 | a0002c0003t0001g0192 | 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 | a0003c0005t0001g0028 | 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 | a0001c0028t0003g0020 | 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 | 253 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(250): Show | 267 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(264): 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 | a0016c0026t0001g0243 | 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 | a0001c0001t0001g0101a0001c0001t0001g0105a0001c0004t0001g0051others(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 | a0001c0001t0001g0043a0001c0001t0001g0103a0001c0001t0001g0104others(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 | a0002c0003t0001g0280 | 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 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(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 | a0001c0002t0001g0111 | 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 | a0001c0001t0001g0108a0002c0003t0002g0328a0014c0021t0001g0271 | 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 | a0001c0002t0001g0237 | 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 | a0001c0001t0001g0108a0001c0002t0001g0237a0002c0003t0002g0328others(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 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0250others(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 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(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 | a0001c0002t0001g0206a0002c0003t0001g0207a0002c0003t0001g0228others(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 | a0002c0025t0001g0281 | 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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | a0001c0001t0002g0309 | 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 | a0020c0032t0001g0268 | 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 | a0001c0002t0002g0310 | 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 | a0001c0001t0001g0010a0001c0001t0001g0103a0001c0001t0001g0104others(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 | a0020c0032t0001g0268 | 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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0108 | 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 | 269 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(266): Show | 283 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(280): Show |
intron_variant | MODIFIER | c.510-1044dupC | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72715364 | ||||||
| chr11:72715570
|
C | CT | 135 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(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 | 51 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0088others(48): Show | 52 | HG00597.hp1 HG00642.hp1 HG01099.hp2 others(49): 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 | a0001c0001t0001g0077a0001c0001t0001g0102a0001c0001t0001g0157others(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 | a0002c0012t0001g0289 | 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 | a0001c0002t0001g0204 | 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 | a0001c0001t0001g0106a0001c0001t0001g0295a0001c0001t0001g0296 | 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 | a0001c0001t0002g0309 | 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 | a0002c0003t0001g0292 | 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 | 157 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0036others(154): 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 | a0002c0003t0001g0192 | 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 | 83 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0082others(80): 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 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0096others(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 | a0001c0001t0001g0108a0001c0001t0001g0113a0001c0001t0001g0114others(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 | a0001c0002t0001g0173a0002c0003t0002g0019a0002c0003t0002g0307others(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 | a0020c0032t0001g0268 | 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 | a0002c0003t0002g0019a0002c0003t0002g0316a0002c0003t0002g0318others(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 | a0001c0004t0001g0163a0001c0004t0001g0168 | 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 | a0002c0003t0002g0317 | 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 | a0001c0001t0001g0106 | 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 | a0001c0002t0001g0111a0001c0002t0001g0172a0001c0002t0001g0181others(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 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0097others(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 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0101others(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 | a0001c0001t0001g0006a0001c0001t0001g0092a0001c0001t0001g0093others(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 | a0001c0001t0001g0010a0001c0001t0001g0103a0001c0001t0001g0104others(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 | a0001c0001t0001g0295a0001c0001t0001g0296 | 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 | a0002c0003t0001g0280 | 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 | a0001c0001t0001g0159a0001c0001t0001g0160 | 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 | a0001c0001t0001g0106 | 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 | a0002c0003t0001g0075a0002c0003t0001g0280 | 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 | a0001c0004t0001g0249 | 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 | a0002c0003t0001g0075a0002c0003t0001g0280 | 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 | a0002c0003t0001g0018a0002c0003t0001g0273a0002c0003t0001g0283 | 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 | a0002c0003t0001g0292 | 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 | a0001c0004t0001g0045a0001c0004t0001g0046 | 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 | 137 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(134): 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 | a0001c0001t0001g0043 | 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 | a0002c0003t0002g0328 | 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 | a0001c0008t0001g0294 | 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 | a0005c0010t0002g0305 | 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 | a0001c0001t0002g0308a0001c0001t0002g0309a0002c0003t0002g0019others(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 | a0001c0001t0002g0308a0001c0001t0002g0309a0002c0003t0002g0019others(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 | a0001c0002t0001g0002a0001c0002t0001g0174a0001c0002t0001g0175others(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 | a0001c0001t0001g0104 | 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 | a0002c0003t0002g0329a0002c0003t0002g0330a0002c0003t0002g0331 | 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 | a0001c0008t0001g0290a0001c0008t0001g0291a0001c0008t0001g0293others(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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | a0001c0034t0001g0302 | 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 | a0001c0002t0001g0003a0001c0002t0001g0013a0001c0002t0001g0186others(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 | 256 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(253): Show | 268 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(265): 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 | a0001c0002t0001g0173 | 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 | 118 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(115): 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 | a0001c0001t0001g0006a0001c0001t0001g0092a0001c0001t0001g0093others(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 | a0002c0003t0001g0075a0002c0003t0001g0280a0002c0025t0001g0281 | 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 | a0001c0002t0001g0206a0001c0002t0001g0230a0002c0003t0001g0207others(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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | a0001c0004t0001g0154 | 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 | a0002c0003t0001g0284 | 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 | a0001c0001t0001g0251 | 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 | a0001c0004t0006g0055 | 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 | a0001c0001t0002g0308a0001c0001t0002g0309a0002c0003t0002g0019others(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 | a0002c0003t0002g0019a0002c0003t0002g0307a0002c0003t0002g0311others(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 | a0001c0001t0002g0308a0001c0001t0002g0309 | 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 | a0001c0001t0001g0010a0001c0001t0001g0103a0001c0001t0001g0104others(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 | a0003c0005t0001g0027 | 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 | 93 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(90): 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 | a0001c0001t0002g0308a0001c0001t0002g0309a0002c0003t0002g0019others(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 | a0001c0002t0001g0182 | 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 | 86 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(83): 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 | a0001c0002t0001g0126 | 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 | a0001c0002t0001g0017a0001c0002t0001g0267 | 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 | a0001c0001t0002g0308 | 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 | a0001c0004t0001g0249 | 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 | 117 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(114): 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 | 264 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(261): Show | 277 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(274): Show |
intron_variant | MODIFIER | c.509+3594A>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72723026 | ||||||
| chr11:72723073
|
C | T | 101 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(98): Show | 105 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.509+3547G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72723073 | ||||||
| chr11:72723327
|
A | G | 264 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(261): Show | 277 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(274): 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 | a0002c0003t0001g0018a0002c0003t0001g0273 | 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 | a0001c0004t0001g0057 | 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0159a0001c0001t0001g0160 | 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 | a0002c0003t0001g0199a0002c0003t0001g0205 | 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 | a0001c0002t0001g0012a0001c0002t0001g0183 | 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 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0155a0001c0001t0001g0156 | 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 | 77 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(74): 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 | a0001c0001t0001g0128 | 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 | a0001c0001t0001g0250a0001c0001t0001g0253a0001c0001t0001g0256others(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 | 107 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(104): 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 | 107 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(104): 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 | a0001c0001t0002g0308a0001c0001t0002g0309a0001c0002t0001g0186others(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 | 80 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(77): 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 | a0001c0002t0001g0038a0001c0002t0001g0039 | 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 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0088others(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 | a0001c0001t0001g0108a0007c0014t0001g0115 | 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 | 61 | a0001c0001t0001g0036a0001c0001t0001g0043a0001c0002t0001g0005others(58): 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 | a0001c0001t0001g0233 | 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 | a0001c0001t0001g0131a0001c0001t0001g0150 | 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 | a0001c0004t0001g0083a0001c0004t0001g0084a0001c0004t0001g0085others(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 | a0001c0001t0001g0158 | 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 | a0001c0008t0001g0290a0001c0008t0001g0291a0001c0008t0001g0293others(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 | a0001c0001t0001g0105 | 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 | 77 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(74): 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 | 125 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(122): Show | 131 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.509+267C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72726353 | ||||||
| chr11:72726405
|
G | A | 1 | a0010c0016t0001g0197 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.509+215C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 3/34 | chr11 | 72726405 | ||||||
| chr11:72726427
|
C | T | 1 | a0001c0001t0002g0324 | 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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | a0002c0003t0001g0059 | 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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | a0001c0002t0001g0060a0001c0002t0001g0064 | 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 | a0001c0002t0001g0063a0001c0002t0001g0074 | 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 | a0001c0001t0001g0295a0001c0001t0001g0296 | 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 | a0001c0001t0001g0105 | 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 | a0002c0003t0002g0317 | 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 | a0001c0004t0001g0168 | 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 | a0001c0002t0001g0122 | 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 | a0001c0001t0002g0309 | 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 | a0001c0002t0001g0011a0001c0002t0001g0189 | 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 | a0002c0025t0001g0281 | 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 | a0001c0001t0001g0295a0001c0001t0001g0296 | 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 | a0001c0001t0001g0105a0001c0004t0001g0249 | 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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0233 | 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 | a0002c0003t0001g0018a0002c0003t0001g0273a0002c0003t0001g0279others(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 | a0001c0002t0001g0165 | 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 | 77 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(74): 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 | 57 | a0001c0001t0001g0036a0001c0001t0001g0043a0001c0002t0001g0005others(54): 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0002g0308a0001c0001t0002g0309 | 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 | a0007c0014t0001g0115 | 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 | a0001c0002t0001g0111 | 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 | a0003c0005t0001g0125 | 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 | a0001c0001t0002g0324 | 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 | a0001c0001t0001g0236 | 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 | 78 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(75): 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 | a0001c0001t0001g0121a0001c0001t0001g0127a0001c0001t0001g0129 | 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 | 249 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(246): Show | 261 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(258): Show |
intron_variant | MODIFIER | c.-45+2591delT | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72729923 | ||||||
| chr11:72730274
|
C | T | 4 | a0001c0001t0001g0036a0003c0005t0001g0028a0003c0005t0001g0029others(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 | a0004c0009t0001g0278 | 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 | 256 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(253): Show | 268 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(265): Show |
intron_variant | MODIFIER | c.-45+2129A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 2/34 | chr11 | 72730386 | ||||||
| chr11:72730450
|
G | A | 84 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(81): 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 | a0001c0004t0001g0249 | 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 | a0006c0011t0001g0149 | 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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | a0001c0002t0001g0255 | 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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | a0001c0004t0001g0249 | 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 | a0001c0004t0001g0001a0001c0004t0001g0042a0001c0004t0001g0056others(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 | a0002c0003t0001g0079 | 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 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0109 | 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 | a0001c0001t0002g0324 | 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 | a0001c0001t0001g0105 | 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 | 57 | a0001c0001t0001g0036a0001c0001t0001g0043a0001c0002t0001g0005others(54): 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 | a0001c0001t0001g0118 | 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 | a0001c0001t0002g0324 | 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 | a0002c0003t0001g0228 | 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 | a0002c0003t0001g0220 | 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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | 78 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(75): 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 | 116 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(113): 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 | 84 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(81): 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 | a0001c0002t0001g0167 | 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 | 105 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(102): 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 | a0002c0003t0001g0242 | 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 | 84 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(81): 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 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0109others(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 | 84 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(81): 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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | 84 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(81): 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 | a0001c0001t0001g0101a0001c0004t0001g0083a0001c0004t0001g0084others(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 | a0001c0004t0001g0249 | 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 | 78 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(75): 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 | 84 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(81): 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 | a0001c0001t0001g0091 | 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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | a0001c0004t0001g0130 | 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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0185others(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 | 76 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(73): 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 | a0001c0001t0001g0010a0001c0001t0001g0103a0001c0001t0001g0104others(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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | a0002c0003t0001g0018a0002c0003t0001g0075a0002c0003t0001g0273others(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 | a0001c0001t0001g0127 | 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 | 46 | a0001c0001t0001g0198a0001c0001t0001g0223a0001c0001t0001g0224others(43): Show | 47 | HG00438.hp2 HG00597.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.-127-2540G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72735137 | ||||||
| chr11:72735419
|
C | T | 84 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(81): 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 | 84 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(81): 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 | 57 | a0001c0001t0001g0036a0001c0001t0001g0043a0001c0002t0001g0005others(54): 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 | a0001c0001t0001g0118a0005c0010t0002g0304a0005c0010t0002g0305others(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 | a0001c0002t0001g0003a0001c0002t0001g0013a0001c0002t0001g0014others(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 | 83 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(80): 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 | a0001c0001t0001g0295a0001c0001t0001g0296 | 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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | 128 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(125): Show | 134 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(131): 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 | a0001c0006t0001g0219 | 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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(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 | 85 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(82): 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 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(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 | a0001c0001t0001g0295a0001c0001t0001g0296 | 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 | a0001c0001t0001g0109a0001c0004t0001g0249 | 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 | a0001c0001t0001g0103a0001c0001t0001g0104 | 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 | a0001c0001t0001g0043 | 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 | a0003c0005t0001g0217 | 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 | a0001c0001t0001g0092a0001c0001t0001g0093 | 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 | a0001c0001t0002g0308a0001c0001t0002g0309 | 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 | a0001c0004t0001g0045a0001c0004t0001g0046 | 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 | a0001c0001t0001g0109 | 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 | 77 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(74): 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 | a0001c0001t0001g0098 | 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 | 83 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(80): 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 | 77 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(74): 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 | a0002c0003t0001g0059 | 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 | a0001c0001t0001g0006a0001c0001t0001g0077a0001c0001t0001g0092others(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 | a0001c0001t0002g0324 | 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 | 178 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(175): Show | 185 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(182): 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 | a0001c0001t0001g0109 | 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 | a0001c0001t0001g0160 | 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 | 77 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(74): 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 | a0001c0001t0001g0010a0001c0001t0001g0103a0001c0001t0001g0104others(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 | a0001c0001t0003g0021a0001c0001t0003g0022 | 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 | a0001c0001t0001g0151 | 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 | a0001c0001t0001g0250 | 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 | a0001c0002t0001g0014a0001c0002t0001g0218a0001c0002t0001g0241 | 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 | 77 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(74): 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 | 83 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(80): 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 | a0001c0001t0001g0295 | 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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | a0001c0002t0001g0190 | 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 | 77 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(74): 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 | 77 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(74): 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 | ||||||
| chr11:72739755
|
T | C | 1 | a0010c0016t0001g0197 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-127-7158A>G | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72739755 | ||||||
| chr11:72739896
|
T | A | 76 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(73): 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 | 83 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(80): 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 | a0001c0004t0001g0249 | 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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | 83 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(80): 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 | a0001c0002t0001g0037 | 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 | 84 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(81): 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 | 90 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(87): 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 | a0001c0035t0001g0272a0014c0021t0001g0271 | 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 | a0001c0006t0001g0219 | 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 | 90 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(87): 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 |
83 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(80): 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 | a0014c0021t0001g0271 | 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 | a0001c0001t0001g0105 | 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 | 98 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(95): 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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | a0001c0001t0001g0106a0002c0003t0001g0285 | 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 | a0001c0001t0001g0088 | 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 | 97 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(94): 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 | 97 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(94): 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 | a0001c0004t0001g0058 | 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 | a0001c0001t0001g0166 | 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 | a0001c0001t0001g0235a0001c0001t0001g0236 | 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 | a0002c0025t0001g0281 | 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 | a0002c0003t0001g0286a0002c0003t0001g0287 | 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 | 95 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(92): 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 | a0001c0008t0001g0290a0001c0008t0001g0291a0001c0008t0001g0293others(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 | 266 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(263): Show | 279 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.-128+9635T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72742693 | ||||||
| chr11:72742805
|
G | A | 96 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(93): 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 | a0002c0003t0001g0280a0002c0025t0001g0281 | 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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | 97 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(94): 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 | a0001c0001t0001g0198a0001c0001t0001g0223a0001c0001t0001g0224others(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 | a0001c0004t0001g0154a0009c0033t0001g0153 | 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 | a0001c0008t0001g0291 | 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 | a0001c0001t0002g0308 | 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 | a0001c0001t0001g0166 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-128+8924G>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72743404 | ||||||
| chr11:72743420
|
A | G | 331 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(328): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.-128+8908T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72743420 | ||||||
| chr11:72743437
|
C | T | 14 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | a0001c0008t0001g0290a0001c0008t0001g0291a0001c0008t0001g0293others(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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | a0008c0036t0001g0297 | 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 | a0001c0004t0001g0124 | 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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | a0003c0005t0001g0027 | 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 | a0001c0008t0001g0290 | 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 | 96 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(93): 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 | a0001c0001t0001g0155a0001c0001t0001g0156 | 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 | 96 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(93): 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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | 91 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(88): 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 | a0008c0036t0001g0297 | 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 | a0001c0001t0001g0006a0001c0001t0001g0081a0001c0001t0001g0082others(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 | a0001c0001t0001g0109 | 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 | a0001c0001t0001g0123 | 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 | 89 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(86): 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 | a0001c0008t0001g0290a0001c0008t0001g0291a0001c0008t0001g0293others(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 | a0001c0002t0001g0191 | 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 | a0001c0001t0001g0010a0001c0001t0001g0103a0001c0001t0001g0104others(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 | a0002c0003t0002g0019a0002c0003t0002g0307a0002c0003t0002g0311others(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 | a0002c0003t0001g0220 | 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 | a0001c0001t0001g0108 | 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 | a0001c0001t0002g0324 | 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 | a0001c0002t0001g0037 | 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 | a0001c0008t0001g0290a0001c0008t0001g0291a0001c0008t0001g0293others(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 | 106 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(103): 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 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0081others(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 | a0001c0001t0001g0043a0001c0001t0001g0252a0001c0001t0002g0309others(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 | a0001c0001t0001g0010a0001c0001t0001g0103a0001c0001t0001g0104others(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 | a0002c0003t0001g0242 | 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 | a0001c0004t0001g0045a0001c0004t0001g0046 | 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 | a0002c0003t0001g0221a0016c0026t0001g0243 | 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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0118others(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 | 81 | a0001c0001t0001g0036a0001c0001t0001g0103a0001c0001t0001g0104others(78): Show | 86 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.-128+6972delA | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72745355 | ||||||
| chr11:72745394
|
C | T | 1 | a0002c0003t0001g0117 | 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 | a0001c0001t0001g0105a0001c0001t0001g0108a0001c0001t0001g0109 | 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 | 105 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(102): 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 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0298others(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 | a0001c0001t0001g0159a0001c0001t0001g0160a0002c0003t0001g0245others(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 | 55 | a0001c0001t0001g0036a0001c0001t0001g0043a0001c0002t0001g0005others(52): 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 | a0001c0001t0001g0248 | 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 | 22 | a0001c0002t0001g0005a0001c0002t0001g0024a0001c0002t0001g0025others(19): 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 | a0001c0001t0001g0198 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-128+6162G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72746166 | ||||||
| chr11:72746363
|
C | T | 1 | a0010c0016t0001g0197 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-128+5965G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72746363 | ||||||
| chr11:72746442
|
C | T | 23 | a0001c0002t0002g0310a0002c0003t0002g0019a0002c0003t0002g0307others(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 | ||||||
| chr11:72746484
|
C | T | 1 | a0010c0016t0001g0197 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-128+5844G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72746484 | ||||||
| chr11:72746486
|
C | T | 106 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(103): 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 | a0003c0005t0001g0107 | 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 | a0001c0001t0002g0324 | 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 | a0001c0002t0001g0038a0001c0002t0001g0039 | 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 | a0001c0001t0001g0108 | 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 | a0001c0001t0001g0248 | 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 | a0001c0001t0001g0036 | 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 | a0001c0008t0001g0290a0001c0008t0001g0291a0001c0008t0001g0293others(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 | 121 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(118): 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 | 84 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(81): 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 | a0001c0001t0002g0324 | 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 | a0001c0001t0001g0109 | 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 | a0001c0001t0001g0036a0001c0004t0001g0032a0001c0004t0001g0033others(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 | a0003c0005t0001g0269 | 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 | a0001c0001t0001g0162 | 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 | a0001c0001t0002g0309 | 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 | a0001c0001t0001g0116 | 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 | a0002c0012t0001g0288a0002c0012t0001g0289 | 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 | a0001c0002t0001g0247a0001c0008t0001g0290a0001c0008t0001g0291others(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 | 266 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(263): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): 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 | a0001c0001t0001g0006a0001c0001t0001g0076a0001c0001t0001g0077others(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 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0295others(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 | a0001c0001t0001g0006a0001c0001t0001g0081a0001c0001t0001g0082others(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 | 4 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0007g0303others(1): Show | 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 | 57 | a0001c0001t0001g0109a0001c0001t0001g0198a0001c0001t0001g0223others(54): Show | 59 | HG00438.hp2 HG00597.hp1 HG00642.hp1 others(56): 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 | a0001c0001t0002g0308a0001c0001t0002g0309a0001c0002t0002g0310others(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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0248 | 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 | a0001c0001t0002g0308a0001c0001t0002g0309a0001c0001t0002g0324others(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 | a0001c0001t0001g0006a0001c0001t0001g0081a0001c0001t0001g0082others(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 | a0001c0002t0002g0310a0002c0003t0002g0019a0002c0003t0002g0307others(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 | a0001c0004t0001g0249 | 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 | 62 | a0001c0001t0001g0036a0001c0001t0001g0043a0001c0001t0001g0076others(59): 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 | a0001c0001t0002g0308a0001c0001t0002g0309a0001c0001t0002g0324others(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 | a0007c0014t0001g0115 | 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 | a0001c0001t0001g0007a0001c0001t0001g0112a0001c0001t0001g0113others(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 | a0001c0001t0002g0308a0001c0001t0002g0309 | 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 | a0001c0002t0001g0111 | 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 | a0008c0036t0001g0297 | 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 | a0001c0001t0002g0308a0001c0001t0002g0309a0001c0001t0002g0324others(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 | a0006c0011t0001g0110 | 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 | a0006c0011t0001g0110 | 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 | a0006c0011t0001g0110 | 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 | a0002c0003t0002g0307a0002c0003t0002g0325a0002c0003t0002g0326others(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 | a0001c0001t0003g0023 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-128+1148C>T | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72751180 | ||||||
| chr11:72751200
|
A | G | 331 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(328): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.-128+1128T>C | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72751200 | ||||||
| chr11:72751271
|
C | T | 306 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(303): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.-128+1057G>A | ARAP1 | ENSG00000186635.16 | transcript | ENST00000393609.8 | protein_coding | 1/34 | chr11 | 72751271 | ||||||
| chr11:72751330
|
T | C | 147 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(144): 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 | a0002c0003t0002g0307 | 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 | a0002c0003t0002g0307 | 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 | a0002c0003t0002g0307 | 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 | a0002c0003t0002g0307 | 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 | a0002c0003t0002g0307 | 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 | a0002c0003t0002g0307 | 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 | a0002c0003t0002g0307 | 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 | a0002c0003t0002g0307 | 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 | a0002c0003t0002g0307 | 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 | a0002c0003t0002g0307 | 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 | a0002c0003t0002g0307 | 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 | a0002c0003t0002g0307 | 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 | 119 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0043others(116): 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 | a0001c0002t0001g0024a0001c0002t0001g0025 | 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 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0023others(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 | a0005c0010t0002g0304a0005c0010t0002g0305a0005c0010t0002g0306 | 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 | a0001c0001t0001g0298a0001c0001t0001g0299 | 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 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0034t0001g0302 | 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 |