Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 392 |
| ensemblid | ENSG00000175220.12 |
| hgncid | 673 |
| symbol | ARHGAP1 |
| name | Rho GTPase activating protein 1 |
| refseq_nuc | NM_004308.5 |
| refseq_prot | NP_004299.1 |
| ensembl_nuc | ENST00000311956.9 |
| ensembl_prot | ENSP00000310491.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 46677080 |
| end | 46700619 |
| strand | - |
| ver | v1.2 |
| region | chr11:46677080-46700619 |
| region5000 | chr11:46672080-46705619 |
| regionname0 | ARHGAP1_chr11_46677080_46700619 |
| regionname5000 | ARHGAP1_chr11_46672080_46705619 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 439 | 342 | 94 | 72 | 126 | 12 | 36 | 102 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | MDPLS others(434): Show |
chr11 | 46672080 | 46705619 |
| a0002 | 0/0 | 439 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | MDPLS others(434): Show |
chr11 | 46672080 | 46705619 |
| a0003 | 0/0 | 439 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | MDPLS others(434): Show |
chr11 | 46672080 | 46705619 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1317 | 304 | 61 | 69 | 125 | 12 | 36 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | ATGGA others(1312): Show |
chr11 | 46672080 | 46705619 | ||
| a0001c0002 | 0/0 | 1317 | 20 | 19 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | ATGGA others(1312): Show |
chr11 | 46672080 | 46705619 | ||
| a0001c0003 | 0/0 | 1317 | 14 | 13 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | ATGGA others(1312): Show |
chr11 | 46672080 | 46705619 | ||
| a0001c0004 | 1/0 | 1317 | 2 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | ATGGA others(1312): Show |
chr11 | 46672080 | 46705619 | ||
| a0001c0006 | 0/0 | 1317 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | ATGGA others(1312): Show |
chr11 | 46672080 | 46705619 | ||
| a0001c0007 | 0/0 | 1317 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | ATGGA others(1312): Show |
chr11 | 46672080 | 46705619 | ||
| a0002c0008 | 0/0 | 1317 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | ATGGA others(1312): Show |
chr11 | 46672080 | 46705619 | ||
| a0003c0005 | 0/0 | 1317 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | ATGGA others(1312): Show |
chr11 | 46672080 | 46705619 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3395 | 241 | 46 | 63 | 94 | 12 | 25 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0001t0002 | 0/0 | 3395 | 24 | 1 | 1 | 17 | 0 | 5 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0001t0004 | 0/0 | 3395 | 7 | 7 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0001t0005 | 0/0 | 3395 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0001t0006 | 0/0 | 3396 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3391): Show |
chr11 | 46672080 | 46705619 |
| a0001c0001t0008 | 0/0 | 3395 | 3 | 1 | 2 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0001t0009 | 0/0 | 3395 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0001t0010 | 0/0 | 3396 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3391): Show |
chr11 | 46672080 | 46705619 |
| a0001c0001t0012 | 0/0 | 3395 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0001t0013 | 0/0 | 3395 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0001t0014 | 0/0 | 3395 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0001t0015 | 0/0 | 3395 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0001t0017 | 0/0 | 3395 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0001t0019 | 0/0 | 3395 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0001t0020 | 0/0 | 3395 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0001t0021 | 0/0 | 3395 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0001t0022 | 0/0 | 3395 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0001t0023 | 0/0 | 3395 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0001t0025 | 0/0 | 3395 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0001t0026 | 0/0 | 3395 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0001t0027 | 0/0 | 3395 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0002t0001 | 0/0 | 3395 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0002t0003 | 0/0 | 3395 | 12 | 12 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0002t0007 | 0/0 | 3395 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0002t0016 | 0/0 | 3395 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0002t0018 | 0/0 | 3395 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0002t0024 | 0/0 | 3395 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0003t0001 | 0/0 | 3395 | 13 | 12 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0003t0006 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3391): Show |
chr11 | 46672080 | 46705619 |
| a0001c0004t0011 | 1/0 | 3395 | 2 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0006t0001 | 0/0 | 3395 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0001c0007t0001 | 0/0 | 3395 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0002c0008t0001 | 0/0 | 3395 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| a0003c0005t0001 | 0/0 | 3395 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | GTTCC others(3390): Show |
chr11 | 46672080 | 46705619 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 42 | 7 | 10 | 13 | 5 | 7 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0002 | 0/0 | 28 | 0 | 4 | 22 | 1 | 1 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0003 | 0/0 | 12 | 4 | 5 | 2 | 0 | 1 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0005 | 0/0 | 9 | 0 | 9 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0007 | 0/0 | 8 | 0 | 5 | 0 | 2 | 1 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0008 | 0/0 | 7 | 1 | 2 | 0 | 0 | 4 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0009 | 0/0 | 6 | 2 | 2 | 1 | 1 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0014 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0068 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0002g0010 | 0/0 | 6 | 1 | 1 | 2 | 0 | 2 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0002g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0004g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0004g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0005g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0006g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0006g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0008g0022 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0009g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0009g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0010g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0010g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0012g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0013g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0014g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0014g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0015g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0017g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0019g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0020g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0021g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0022g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0023g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0025g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0026g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0001t0027g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0002t0003g0006 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0002t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0002t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0002t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0002t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0002t0007g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0002t0007g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0002t0016g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0002t0018g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0002t0024g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0003t0001g0004 | 0/0 | 11 | 10 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0003t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0003t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0003t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0004t0011g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0004t0011g0142 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0006t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0001c0007t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0002c0008t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| a0003c0005t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | FIN | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00639 | hp1 | a0001 | c0001 | t0008 | g0022 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01106 | hp1 | a0001 | c0001 | t0008 | g0022 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01175 | hp2 | a0001 | c0007 | t0001 | g0150 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01192 | hp2 | a0001 | c0001 | t0013 | g0027 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01243 | hp1 | a0001 | c0002 | t0024 | g0077 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01256 | hp1 | a0001 | c0001 | t0026 | g0133 | AMR | CLM | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0004 | AMR | CLM | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | IBS | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | IBS | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01884 | hp2 | a0001 | c0002 | t0003 | g0080 | AFR | ACB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01891 | hp2 | a0001 | c0001 | t0009 | g0100 | AFR | ACB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01934 | hp2 | a0001 | c0001 | t0022 | g0101 | AMR | PEL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | KHV | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CDX | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02257 | hp1 | a0001 | c0001 | t0008 | g0022 | AFR | ACB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | ACB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02258 | hp2 | a0001 | c0002 | t0003 | g0148 | AFR | ACB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02451 | hp1 | a0001 | c0002 | t0018 | g0073 | AFR | ACB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02451 | hp2 | a0001 | c0004 | t0011 | g0141 | AFR | ACB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02572 | hp1 | a0001 | c0002 | t0016 | g0075 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02572 | hp2 | a0001 | c0003 | t0006 | g0078 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02602 | hp1 | a0001 | c0001 | t0025 | g0159 | SAS | PJL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0070 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02622 | hp2 | a0001 | c0002 | t0003 | g0006 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02647 | hp1 | a0001 | c0002 | t0003 | g0006 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02698 | hp1 | a0001 | c0001 | t0012 | g0037 | SAS | PJL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0071 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0006 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0102 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02818 | hp2 | a0001 | c0001 | t0017 | g0146 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02895 | hp1 | a0001 | c0002 | t0003 | g0079 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02897 | hp2 | a0001 | c0002 | t0003 | g0006 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02922 | hp1 | a0001 | c0002 | t0003 | g0006 | AFR | ESN | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02965 | hp1 | a0001 | c0002 | t0007 | g0084 | AFR | ESN | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02976 | hp1 | a0001 | c0001 | t0021 | g0109 | AFR | ESN | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0083 | AFR | ESN | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | ESN | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | ESN | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03139 | hp2 | a0001 | c0002 | t0007 | g0085 | AFR | ESN | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | MSL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03209 | hp2 | a0001 | c0002 | t0003 | g0006 | AFR | MSL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03225 | hp2 | a0001 | c0002 | t0003 | g0006 | AFR | MSL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03453 | hp1 | a0001 | c0002 | t0003 | g0006 | AFR | MSL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03492 | hp1 | a0001 | c0001 | t0012 | g0037 | SAS | PJL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0074 | AFR | ESN | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0081 | AFR | ESN | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03540 | hp1 | a0001 | c0002 | t0003 | g0006 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03710 | hp1 | a0001 | c0001 | t0020 | g0117 | SAS | PJL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03834 | hp1 | a0001 | c0001 | t0014 | g0105 | SAS | BEB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0124 | SAS | STU | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0130 | SAS | BEB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | STU | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | STU | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG04228 | hp1 | a0001 | c0001 | t0014 | g0069 | SAS | STU | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | YRI | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18522 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | YRI | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | CHB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | YRI | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18961 | hp2 | a0002 | c0008 | t0001 | g0108 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18964 | hp2 | a0001 | c0001 | t0027 | g0161 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18984 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18987 | hp1 | a0001 | c0001 | t0015 | g0032 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18989 | hp1 | a0001 | c0006 | t0001 | g0103 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18995 | hp1 | a0001 | c0001 | t0015 | g0032 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18998 | hp2 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19000 | hp1 | a0001 | c0001 | t0006 | g0043 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19000 | hp2 | a0001 | c0001 | t0006 | g0098 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19003 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19007 | hp2 | a0003 | c0005 | t0001 | g0047 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | LWK | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19043 | hp1 | a0001 | c0001 | t0023 | g0119 | AFR | LWK | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | LWK | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19054 | hp1 | a0001 | c0001 | t0006 | g0048 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19068 | hp1 | a0001 | c0001 | t0010 | g0131 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19084 | hp2 | a0001 | c0001 | t0010 | g0128 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | YRI | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ASW | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | ASW | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | GIH | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | ACB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02486 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | ACB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | ACB | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG03471 | hp2 | a0001 | c0002 | t0007 | g0076 | AFR | MSL | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | USA | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0082 | AFR | USA | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18955 | hp1 | a0001 | c0001 | t0013 | g0027 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA20300 | hp1 | a0001 | c0001 | t0019 | g0097 | AFR | USA | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | USA | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | LWK | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | LWK | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0068 | REF | REF | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| homoSapiens | grch38p0 | a0001 | c0004 | t0011 | g0142 | REF | REF | ARHGAP1_chr11_46672080_46705619 | ARHGAP1 | chr11 | 46672080 | 46705619 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:46681351 | T | C | 1 | a0002 | 1 | NA18961.hp2 | missense_variant | MODERATE | c.478A>G | p.Ile160Val | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 6/13 | 596/3395 | 478/1320 | 160/439 | chr11 | 46681351 | |||
| chr11:46695734 | G | T | 1 | a0003 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.155C>A | p.Pro52Gln | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/13 | 273/3395 | 155/1320 | 52/439 | chr11 | 46695734 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:46679712 | G | A | 1 | a0001c0006 | 1 | NA18989.hp1 | synonymous_variant | LOW | c.963C>T | p.Phe321Phe | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 11/13 | 1081/3395 | 963/1320 | 321/439 | chr11 | 46679712 | |||
| chr11:46679721 | G | A | 1 | a0001c0007 | 1 | HG01175.hp2 | synonymous_variant | LOW | c.954C>T | p.Leu318Leu | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 11/13 | 1072/3395 | 954/1320 | 318/439 | chr11 | 46679721 | |||
| chr11:46680215 | C | T | 1 | a0001c0003 | 14 | HG01261.hp1 HG02109.hp2 HG02258.hp1 others(11): Show |
synonymous_variant | LOW | c.888G>A | p.Lys296Lys | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 10/13 | 1006/3395 | 888/1320 | 296/439 | chr11 | 46680215 | |||
| chr11:46681058 | G | A | 1 | a0001c0002 | 20 | HG01243.hp1 HG01884.hp2 HG02258.hp2 others(17): Show |
synonymous_variant | LOW | c.588C>T | p.Ser196Ser | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 7/13 | 706/3395 | 588/1320 | 196/439 | chr11 | 46681058 | |||
| chr11:46681370 | T | C | 7 | a0001c0001 a0001c0002 a0001c0003 others(4): Show |
341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
synonymous_variant | LOW | c.459A>G | p.Lys153Lys | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 6/13 | 577/3395 | 459/1320 | 153/439 | chr11 | 46681370 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:46677117 | A | C | 1 | a0001c0002t0024 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1920T>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 13/13 | 1920 | chr11 | 46677117 | ||||||
| chr11:46677211 | A | G | 1 | a0001c0001t0023 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1826T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 13/13 | 1826 | chr11 | 46677211 | ||||||
| chr11:46677302 | C | T | 1 | a0001c0001t0022 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1735G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 13/13 | 1735 | chr11 | 46677302 | ||||||
| chr11:46677398 | G | T | 2 | a0001c0002t0007 a0001c0002t0018 |
4 | HG02451.hp1 HG02965.hp1 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1639C>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 13/13 | 1639 | chr11 | 46677398 | ||||||
| chr11:46677574 | G | A | 1 | a0001c0001t0008 | 3 | HG00639.hp1 HG01106.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1463C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 13/13 | 1463 | chr11 | 46677574 | ||||||
| chr11:46677607 | C | T | 1 | a0001c0001t0021 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1430G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 13/13 | 1430 | chr11 | 46677607 | ||||||
| chr11:46677677 | T | C | 33 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(30): Show |
341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
3_prime_UTR_variant | MODIFIER | c.*1360A>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 13/13 | 1360 | chr11 | 46677677 | ||||||
| chr11:46677678 | G | A | 1 | a0001c0001t0025 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1359C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 13/13 | 1359 | chr11 | 46677678 | ||||||
| chr11:46677892 | C | T | 1 | a0001c0001t0020 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1145G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 13/13 | 1145 | chr11 | 46677892 | ||||||
| chr11:46677898 | C | G | 1 | a0001c0001t0019 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1139G>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 13/13 | 1139 | chr11 | 46677898 | ||||||
| chr11:46677935 | T | C | 1 | a0001c0001t0012 | 2 | HG02698.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1102A>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 13/13 | 1102 | chr11 | 46677935 | ||||||
| chr11:46677944 | G | GA | 3 | a0001c0001t0006 a0001c0001t0010 a0001c0003t0006 |
6 | HG02572.hp2 NA19000.hp1 NA19000.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1092dupT | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 13/13 | 1092 | chr11 | 46677944 | ||||||
| chr11:46677945 | A | G | 4 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0016 others(1): Show |
17 | HG01884.hp2 HG02258.hp2 HG02451.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1092T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 13/13 | 1092 | chr11 | 46677945 | ||||||
| chr11:46678226 | A | G | 2 | a0001c0001t0002 a0001c0001t0010 |
26 | HG00609.hp2 HG00673.hp1 HG01496.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*811T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 13/13 | 811 | chr11 | 46678226 | ||||||
| chr11:46678249 | C | T | 1 | a0001c0002t0018 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*788G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 13/13 | 788 | chr11 | 46678249 | ||||||
| chr11:46678250 | G | A | 1 | a0001c0001t0005 | 5 | NA18941.hp1 NA18979.hp1 NA18984.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*787C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 13/13 | 787 | chr11 | 46678250 | ||||||
| chr11:46678269 | C | T | 1 | a0001c0001t0009 | 2 | HG01891.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*768G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 13/13 | 768 | chr11 | 46678269 | ||||||
| chr11:46678270 | G | A | 1 | a0001c0001t0013 | 2 | HG01192.hp2 NA18955.hp1 |
3_prime_UTR_variant | MODIFIER | c.*767C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 13/13 | 767 | chr11 | 46678270 | ||||||
| chr11:46678541 | T | A | 1 | a0001c0001t0014 | 2 | HG03834.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*496A>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 13/13 | 496 | chr11 | 46678541 | ||||||
| chr11:46678653 | G | C | 1 | a0001c0001t0008 | 3 | HG00639.hp1 HG01106.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*384C>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 13/13 | 384 | chr11 | 46678653 | ||||||
| chr11:46678718 | A | T | 1 | a0001c0001t0017 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*319T>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 13/13 | 319 | chr11 | 46678718 | ||||||
| chr11:46678726 | G | A | 1 | a0001c0001t0026 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*311C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 13/13 | 311 | chr11 | 46678726 | ||||||
| chr11:46678816 | G | A | 1 | a0001c0001t0015 | 2 | NA18987.hp1 NA18995.hp1 |
3_prime_UTR_variant | MODIFIER | c.*221C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 13/13 | 221 | chr11 | 46678816 | ||||||
| chr11:46678956 | G | A | 1 | a0001c0001t0027 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*81C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 13/13 | 81 | chr11 | 46678956 | ||||||
| chr11:46678997 | C | T | 1 | a0001c0002t0016 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*40G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 13/13 | 40 | chr11 | 46678997 | ||||||
| chr11:46678998 | G | A | 1 | a0001c0001t0004 | 7 | HG02559.hp2 HG02622.hp1 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*39C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 13/13 | 39 | chr11 | 46678998 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:46679305 | G | A | 1 | a0001c0001t0009g0102 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1131+60C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 12/12 | chr11 | 46679305 | |||||||
| chr11:46679558 | G | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0038 others(2): Show |
14 | HG00099.hp1 HG00738.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.1027+90C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 11/12 | chr11 | 46679558 | |||||||
| chr11:46679573 | C | T | 1 | a0001c0001t0006g0048 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1027+75G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 11/12 | chr11 | 46679573 | |||||||
| chr11:46679574 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0026g0133 |
3 | HG01256.hp1 HG01358.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1027+74C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 11/12 | chr11 | 46679574 | |||||||
| chr11:46679622 | G | T | 4 | a0001c0001t0002g0035 a0001c0001t0002g0127 a0001c0001t0002g0132 others(1): Show |
5 | NA18943.hp1 NA19003.hp2 NA19077.hp1 others(2): Show |
intron_variant | MODIFIER | c.1027+26C>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 11/12 | chr11 | 46679622 | |||||||
| chr11:46680178 | G | T | 30 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0017 others(27): Show |
70 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.898+27C>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 10/12 | chr11 | 46680178 | |||||||
| chr11:46680288 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG02886.hp2 | splice_region_variant&intron_variant | LOW | c.821-6T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 9/12 | chr11 | 46680288 | |||||||
| chr11:46680313 | G | A | 1 | a0001c0001t0020g0117 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.821-31C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 9/12 | chr11 | 46680313 | |||||||
| chr11:46680415 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.820+72G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 9/12 | chr11 | 46680415 | |||||||
| chr11:46680443 | G | T | 6 | a0001c0001t0001g0039 a0001c0001t0001g0134 a0001c0001t0004g0019 others(3): Show |
10 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.820+44C>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 9/12 | chr11 | 46680443 | |||||||
| chr11:46680610 | C | T | 30 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0017 others(27): Show |
70 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.743+30G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 8/12 | chr11 | 46680610 | |||||||
| chr11:46680827 | C | T | 2 | a0001c0002t0007g0084 a0001c0002t0007g0085 |
2 | HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.636-80G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 7/12 | chr11 | 46680827 | |||||||
| chr11:46680869 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.636-122G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 7/12 | chr11 | 46680869 | |||||||
| chr11:46680887 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.635+124C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 7/12 | chr11 | 46680887 | |||||||
| chr11:46680937 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0134 |
3 | HG02723.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.635+74G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 7/12 | chr11 | 46680937 | |||||||
| chr11:46680982 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0134 |
3 | HG02723.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.635+29G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 7/12 | chr11 | 46680982 | |||||||
| chr11:46681141 | G | A | 20 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0025 others(17): Show |
39 | HG00735.hp1 HG01070.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.537-32C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 6/12 | chr11 | 46681141 | |||||||
| chr11:46681194 | G | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0040 a0001c0001t0001g0120 others(2): Show |
8 | HG02280.hp2 HG02615.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.537-85C>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 6/12 | chr11 | 46681194 | |||||||
| chr11:46681205 | C | T | 2 | a0001c0002t0007g0084 a0001c0002t0007g0085 |
2 | HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.536+88G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 6/12 | chr11 | 46681205 | |||||||
| chr11:46681452 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0023g0119 |
2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.450-73G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 5/12 | chr11 | 46681452 | |||||||
| chr11:46681631 | A | G | 5 | a0001c0001t0001g0024 a0001c0001t0001g0040 a0001c0001t0001g0120 others(2): Show |
8 | HG02280.hp2 HG02615.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.450-252T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 5/12 | chr11 | 46681631 | |||||||
| chr11:46682270 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.318-88G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46682270 | |||||||
| chr11:46682290 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.318-108T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46682290 | |||||||
| chr11:46682556 | G | T | 69 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(66): Show |
139 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.318-374C>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46682556 | |||||||
| chr11:46682576 | C | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0144 |
2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.318-394G>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46682576 | |||||||
| chr11:46682740 | A | AGACCAG | 4 | a0001c0001t0001g0033 a0001c0001t0001g0104 a0001c0001t0001g0110 others(1): Show |
5 | HG00438.hp1 NA18947.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.318-564_318-559dup others(6): Show |
ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46682740 | |||||||
| chr11:46682889 | A | G | 26 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0025 others(23): Show |
48 | HG00673.hp1 HG00735.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.318-707T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46682889 | |||||||
| chr11:46683037 | C | CT | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(108): Show |
265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.318-856dupA | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46683037 | |||||||
| chr11:46683037 | C | CTT | 18 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0021 others(15): Show |
27 | HG00438.hp2 HG01106.hp2 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.318-857_318-856dup others(2): Show |
ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46683037 | |||||||
| chr11:46683132 | AG | A | 30 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0017 others(27): Show |
70 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.318-951delC | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46683132 | |||||||
| chr11:46683403 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.318-1221G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46683403 | |||||||
| chr11:46683496 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.318-1314T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46683496 | |||||||
| chr11:46683643 | C | CT | 3 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0051 |
7 | HG02040.hp1 HG02132.hp1 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.318-1462dupA | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46683643 | |||||||
| chr11:46683643 | CT | C | 44 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(41): Show |
82 | HG00099.hp1 HG00609.hp2 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.318-1462delA | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46683643 | |||||||
| chr11:46683686 | G | A | 2 | a0001c0001t0014g0069 a0001c0001t0014g0105 |
2 | HG03834.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.318-1504C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46683686 | |||||||
| chr11:46683932 | G | T | 1 | a0003c0005t0001g0047 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.318-1750C>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46683932 | |||||||
| chr11:46684189 | C | A | 1 | a0001c0001t0001g0106 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.318-2007G>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46684189 | |||||||
| chr11:46684268 | A | G | 1 | a0001c0001t0006g0048 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.318-2086T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46684268 | |||||||
| chr11:46684316 | G | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0144 |
2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.318-2134C>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46684316 | |||||||
| chr11:46684424 | T | A | 4 | a0001c0001t0001g0091 a0001c0001t0001g0118 a0001c0001t0001g0140 others(1): Show |
4 | HG00735.hp1 HG01257.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.318-2242A>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46684424 | |||||||
| chr11:46684432 | G | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0144 |
2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.318-2250C>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46684432 | |||||||
| chr11:46684957 | G | A | 1 | a0001c0002t0007g0084 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.318-2775C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46684957 | |||||||
| chr11:46685017 | G | T | 1 | a0001c0001t0004g0028 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.318-2835C>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46685017 | |||||||
| chr11:46685020 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.318-2838C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46685020 | |||||||
| chr11:46685087 | C | CA | 55 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(52): Show |
109 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.318-2906dupT | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46685087 | |||||||
| chr11:46685087 | C | CAA | 29 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(26): Show |
55 | HG00673.hp1 HG00735.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.318-2907_318-2906d others(4): Show |
ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46685087 | |||||||
| chr11:46685329 | C | CT | 33 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0017 others(30): Show |
73 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.317+2843dupA | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46685329 | |||||||
| chr11:46685329 | CT | C | 17 | a0001c0001t0021g0109 a0001c0002t0001g0074 a0001c0002t0001g0083 others(14): Show |
35 | HG01243.hp1 HG01261.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.317+2843delA | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46685329 | |||||||
| chr11:46685413 | C | T | 1 | a0001c0001t0006g0043 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.317+2760G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46685413 | |||||||
| chr11:46685433 | T | C | 1 | a0001c0001t0001g0060 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.317+2740A>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46685433 | |||||||
| chr11:46685487 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0095 |
4 | HG00741.hp1 HG01106.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.317+2686T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46685487 | |||||||
| chr11:46685650 | C | G | 1 | a0001c0001t0001g0094 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.317+2523G>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46685650 | |||||||
| chr11:46685676 | C | CT | 14 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0006g0048 others(11): Show |
22 | HG01243.hp1 HG01884.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.317+2496dupA | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46685676 | |||||||
| chr11:46685676 | CT | C | 35 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(32): Show |
64 | HG00735.hp1 HG01070.hp1 HG01074.hp1 others(61): Show |
intron_variant | MODIFIER | c.317+2496delA | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46685676 | |||||||
| chr11:46685878 | G | T | 1 | a0001c0001t0001g0066 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.317+2295C>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46685878 | |||||||
| chr11:46685973 | CT | C | 8 | a0001c0001t0001g0050 a0001c0001t0001g0062 a0001c0001t0001g0111 others(5): Show |
8 | HG01071.hp2 HG01169.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.317+2199delA | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46685973 | |||||||
| chr11:46686124 | A | G | 1 | a0001c0001t0001g0040 | 2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.317+2049T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46686124 | |||||||
| chr11:46686232 | C | T | 1 | a0001c0001t0012g0037 | 2 | HG02698.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.317+1941G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46686232 | |||||||
| chr11:46686457 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0023g0119 |
2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.317+1716G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46686457 | |||||||
| chr11:46686609 | C | T | 1 | a0001c0002t0001g0074 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.317+1564G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46686609 | |||||||
| chr11:46686641 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.317+1532C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46686641 | |||||||
| chr11:46686646 | C | T | 33 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(30): Show |
81 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.317+1527G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46686646 | |||||||
| chr11:46686719 | A | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0144 |
2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.317+1454T>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46686719 | |||||||
| chr11:46686760 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.317+1413C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46686760 | |||||||
| chr11:46687052 | A | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.317+1121T>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46687052 | |||||||
| chr11:46687154 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.317+1019G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46687154 | |||||||
| chr11:46687172 | C | G | 1 | a0001c0001t0002g0126 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.317+1001G>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46687172 | |||||||
| chr11:46687359 | G | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | NA18959.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.317+814C>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46687359 | |||||||
| chr11:46687409 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.317+764G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46687409 | |||||||
| chr11:46687742 | A | G | 1 | a0001c0001t0002g0125 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.317+431T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46687742 | |||||||
| chr11:46687772 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.317+401T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46687772 | |||||||
| chr11:46687942 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.317+231C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46687942 | |||||||
| chr11:46687961 | C | T | 1 | a0001c0002t0007g0084 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.317+212G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46687961 | |||||||
| chr11:46688078 | G | C | 1 | a0001c0001t0001g0036 | 2 | HG01069.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.317+95C>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46688078 | |||||||
| chr11:46688109 | C | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0120 a0001c0001t0012g0037 others(1): Show |
7 | HG02280.hp2 HG02698.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.317+64G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46688109 | |||||||
| chr11:46688134 | C | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0149 |
3 | HG02615.hp1 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.317+39G>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46688134 | |||||||
| chr11:46688147 | C | G | 1 | a0001c0001t0006g0048 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.317+26G>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 4/12 | chr11 | 46688147 | |||||||
| chr11:46688486 | A | AT | 11 | a0001c0002t0001g0074 a0001c0002t0003g0006 a0001c0002t0003g0079 others(8): Show |
19 | HG01243.hp1 HG02258.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.230-227dupA | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46688486 | |||||||
| chr11:46688561 | A | G | 17 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0038 others(14): Show |
32 | HG00099.hp1 HG00609.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.230-301T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46688561 | |||||||
| chr11:46688931 | A | C | 1 | a0001c0001t0010g0131 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.230-671T>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46688931 | |||||||
| chr11:46689081 | C | CA | 28 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0025 others(25): Show |
50 | HG00735.hp1 HG01070.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.230-822dupT | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46689081 | |||||||
| chr11:46689230 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0017g0146 |
4 | HG02280.hp2 HG02818.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.230-970G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46689230 | |||||||
| chr11:46689279 | T | C | 24 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0025 others(21): Show |
46 | HG00735.hp1 HG01070.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.230-1019A>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46689279 | |||||||
| chr11:46689353 | T | TG | 24 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0025 others(21): Show |
46 | HG00735.hp1 HG01070.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.230-1094dupC | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46689353 | |||||||
| chr11:46689442 | A | C | 2 | a0001c0001t0001g0040 a0001c0001t0001g0149 |
3 | HG02615.hp1 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.230-1182T>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46689442 | |||||||
| chr11:46689447 | A | G | 2 | a0001c0001t0002g0123 a0001c0001t0002g0124 |
2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.230-1187T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46689447 | |||||||
| chr11:46689515 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.230-1255A>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46689515 | |||||||
| chr11:46689727 | G | A | 1 | a0001c0001t0004g0071 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.230-1467C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46689727 | |||||||
| chr11:46689776 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.230-1516G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46689776 | |||||||
| chr11:46689785 | TGCCTTGG others(3450): Show |
T | 1 | a0001c0001t0001g0092 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.229+2418_230-1526d others(2): Show |
ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46689785 | |||||||
| chr11:46689803 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0012 |
6 | HG00609.hp1 HG02080.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.230-1543G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46689803 | |||||||
| chr11:46689853 | T | A | 1 | a0001c0003t0001g0004 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.230-1593A>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46689853 | |||||||
| chr11:46689940 | T | C | 1 | a0001c0001t0001g0023 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.230-1680A>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46689940 | |||||||
| chr11:46690040 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.230-1780A>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46690040 | |||||||
| chr11:46690043 | C | T | 2 | a0001c0002t0003g0006 a0001c0002t0003g0079 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.230-1783G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46690043 | |||||||
| chr11:46690094 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.230-1834G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46690094 | |||||||
| chr11:46690228 | A | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.230-1968T>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46690228 | |||||||
| chr11:46690230 | A | C | 1 | a0001c0001t0001g0122 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.230-1970T>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46690230 | |||||||
| chr11:46690304 | A | G | 53 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(50): Show |
101 | HG00735.hp1 HG01070.hp1 HG01074.hp1 others(98): Show |
intron_variant | MODIFIER | c.230-2044T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46690304 | |||||||
| chr11:46690573 | T | G | 3 | a0001c0001t0001g0091 a0001c0001t0001g0140 a0001c0001t0020g0117 |
3 | HG00735.hp1 HG01257.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.230-2313A>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46690573 | |||||||
| chr11:46690679 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.230-2419G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46690679 | |||||||
| chr11:46691451 | AT | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.230-3192delA | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46691451 | |||||||
| chr11:46691451 | ATT | A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(2): Show |
7 | HG00639.hp2 HG01123.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.230-3193_230-3192d others(4): Show |
ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46691451 | |||||||
| chr11:46691512 | C | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0041 others(10): Show |
25 | HG01070.hp1 HG01081.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.230-3252G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46691512 | |||||||
| chr11:46691521 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0129 |
6 | HG00099.hp1 HG01123.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.230-3261C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46691521 | |||||||
| chr11:46691545 | G | C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02886.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.230-3285C>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46691545 | |||||||
| chr11:46691615 | C | G | 3 | a0001c0001t0001g0024 a0001c0001t0001g0120 a0001c0001t0017g0146 |
5 | HG02280.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.230-3355G>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46691615 | |||||||
| chr11:46691638 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.230-3378C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46691638 | |||||||
| chr11:46691652 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.230-3392T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46691652 | |||||||
| chr11:46691863 | T | C | 1 | a0001c0001t0002g0130 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.230-3603A>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46691863 | |||||||
| chr11:46691961 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.229+3699T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46691961 | |||||||
| chr11:46692112 | G | C | 1 | a0001c0002t0001g0083 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.229+3548C>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46692112 | |||||||
| chr11:46692309 | C | T | 1 | a0001c0006t0001g0103 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.229+3351G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46692309 | |||||||
| chr11:46692409 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.229+3251G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46692409 | |||||||
| chr11:46692729 | T | C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(87): Show |
186 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(183): Show |
intron_variant | MODIFIER | c.229+2931A>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46692729 | |||||||
| chr11:46692791 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.229+2869C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46692791 | |||||||
| chr11:46692847 | C | G | 1 | a0001c0001t0001g0057 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.229+2813G>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46692847 | |||||||
| chr11:46692854 | AT | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(99): Show |
212 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.229+2805delA | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46692854 | |||||||
| chr11:46692909 | G | C | 2 | a0001c0001t0004g0019 a0001c0001t0004g0071 |
2 | HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.229+2751C>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46692909 | |||||||
| chr11:46692946 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.229+2714C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46692946 | |||||||
| chr11:46692952 | ACGCTATT others(9): Show |
A | 1 | a0001c0001t0002g0064 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.229+2692_229+2707d others(18): Show |
ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46692952 | |||||||
| chr11:46692977 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(157): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.229+2683A>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46692977 | |||||||
| chr11:46693133 | T | A | 1 | a0001c0001t0004g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.229+2527A>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46693133 | |||||||
| chr11:46693169 | T | G | 1 | a0001c0002t0001g0083 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.229+2491A>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46693169 | |||||||
| chr11:46693186 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.229+2474G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46693186 | |||||||
| chr11:46693407 | C | CT | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(157): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.229+2252dupA | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46693407 | |||||||
| chr11:46693713 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.229+1947C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46693713 | |||||||
| chr11:46694213 | G | T | 2 | a0001c0002t0007g0084 a0001c0002t0007g0085 |
2 | HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.229+1447C>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46694213 | |||||||
| chr11:46694292 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.229+1368C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46694292 | |||||||
| chr11:46694339 | C | A | 1 | a0001c0001t0002g0132 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.229+1321G>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46694339 | |||||||
| chr11:46694446 | C | T | 1 | a0001c0001t0023g0119 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.229+1214G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46694446 | |||||||
| chr11:46694762 | G | A | 1 | a0001c0001t0023g0119 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.229+898C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46694762 | |||||||
| chr11:46694909 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.229+751T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46694909 | |||||||
| chr11:46695146 | C | A | 1 | a0001c0001t0001g0023 | 3 | NA18973.hp1 NA19010.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.229+514G>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46695146 | |||||||
| chr11:46695191 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0120 a0001c0001t0017g0146 |
5 | HG02280.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.229+469C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46695191 | |||||||
| chr11:46695377 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0026g0133 |
3 | HG01256.hp1 HG01358.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.229+283C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46695377 | |||||||
| chr11:46695426 | A | G | 1 | a0001c0001t0001g0044 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.229+234T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46695426 | |||||||
| chr11:46695543 | A | C | 1 | a0001c0001t0001g0120 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.229+117T>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 3/12 | chr11 | 46695543 | |||||||
| chr11:46695948 | G | A | 2 | a0001c0002t0007g0084 a0001c0002t0007g0085 |
2 | HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.133+27C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 2/12 | chr11 | 46695948 | |||||||
| chr11:46696224 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0120 a0001c0001t0017g0146 |
5 | HG02280.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-68C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46696224 | |||||||
| chr11:46696331 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-49-175C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46696331 | |||||||
| chr11:46696388 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0086 |
5 | HG01109.hp2 HG03540.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-232C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46696388 | |||||||
| chr11:46696506 | C | T | 1 | a0001c0002t0018g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-49-350G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46696506 | |||||||
| chr11:46696760 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-49-604A>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46696760 | |||||||
| chr11:46696954 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0149 |
3 | HG02615.hp1 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-49-798C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46696954 | |||||||
| chr11:46697038 | A | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0149 |
3 | HG02615.hp1 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-49-882T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46697038 | |||||||
| chr11:46697067 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-49-911C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46697067 | |||||||
| chr11:46697113 | T | C | 18 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0038 others(15): Show |
34 | HG00099.hp1 HG00609.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.-49-957A>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46697113 | |||||||
| chr11:46697440 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-49-1284C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46697440 | |||||||
| chr11:46697841 | C | G | 1 | a0001c0001t0001g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-49-1685G>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46697841 | |||||||
| chr11:46697994 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-49-1838T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46697994 | |||||||
| chr11:46698447 | C | CA | 6 | a0001c0001t0001g0087 a0001c0001t0001g0135 a0001c0001t0001g0136 others(3): Show |
6 | HG01109.hp1 HG02165.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+2103dupT | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46698447 | |||||||
| chr11:46698544 | G | C | 1 | a0001c0001t0001g0138 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-50+2007C>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46698544 | |||||||
| chr11:46698607 | CA | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.-50+1943delT | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46698607 | |||||||
| chr11:46698718 | C | T | 22 | a0001c0001t0001g0013 a0001c0001t0001g0029 a0001c0001t0001g0030 others(19): Show |
45 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(42): Show |
intron_variant | MODIFIER | c.-50+1833G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46698718 | |||||||
| chr11:46699003 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-50+1548A>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699003 | |||||||
| chr11:46699129 | A | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0149 |
3 | HG02615.hp1 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-50+1422T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699129 | |||||||
| chr11:46699163 | A | T | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1388T>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699163 | |||||||
| chr11:46699164 | A | C | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1387T>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699164 | |||||||
| chr11:46699166 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1385A>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699166 | |||||||
| chr11:46699168 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1383A>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699168 | |||||||
| chr11:46699171 | G | C | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1380C>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699171 | |||||||
| chr11:46699183 | C | A | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1368G>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699183 | |||||||
| chr11:46699185 | T | A | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1366A>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699185 | |||||||
| chr11:46699186 | T | A | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1365A>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699186 | |||||||
| chr11:46699188 | T | G | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1363A>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699188 | |||||||
| chr11:46699192 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1359T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699192 | |||||||
| chr11:46699193 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1358T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699193 | |||||||
| chr11:46699194 | T | A | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1357A>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699194 | |||||||
| chr11:46699195 | C | G | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1356G>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699195 | |||||||
| chr11:46699196 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1355T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699196 | |||||||
| chr11:46699197 | C | A | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1354G>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699197 | |||||||
| chr11:46699198 | T | G | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1353A>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699198 | |||||||
| chr11:46699200 | T | A | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1351A>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699200 | |||||||
| chr11:46699201 | T | A | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1350A>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699201 | |||||||
| chr11:46699202 | T | A | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1349A>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699202 | |||||||
| chr11:46699207 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1344T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699207 | |||||||
| chr11:46699208 | C | A | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1343G>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699208 | |||||||
| chr11:46699210 | T | A | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1341A>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699210 | |||||||
| chr11:46699212 | T | A | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1339A>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699212 | |||||||
| chr11:46699213 | G | C | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1338C>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699213 | |||||||
| chr11:46699214 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1337C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699214 | |||||||
| chr11:46699218 | A | C | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1333T>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699218 | |||||||
| chr11:46699219 | T | G | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1332A>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699219 | |||||||
| chr11:46699221 | C | G | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-50+1330G>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699221 | |||||||
| chr11:46699304 | A | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0044 a0001c0001t0001g0045 |
4 | NA18961.hp1 NA18972.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50+1247T>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699304 | |||||||
| chr11:46699423 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-50+1128T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699423 | |||||||
| chr11:46699427 | G | C | 2 | a0001c0001t0001g0024 a0001c0001t0017g0146 |
4 | HG02280.hp2 HG02818.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+1124C>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699427 | |||||||
| chr11:46699456 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-50+1095C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699456 | |||||||
| chr11:46699701 | TA | T | 5 | a0001c0001t0001g0042 a0001c0001t0004g0019 a0001c0001t0004g0028 others(2): Show |
8 | HG02559.hp2 HG02622.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-50+849delT | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699701 | |||||||
| chr11:46699800 | A | G | 1 | a0001c0001t0014g0069 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-50+751T>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699800 | |||||||
| chr11:46699815 | T | C | 1 | a0001c0001t0001g0039 | 2 | HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-50+736A>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46699815 | |||||||
| chr11:46700022 | T | G | 1 | a0001c0001t0001g0151 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-50+529A>C | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46700022 | |||||||
| chr11:46700055 | A | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(31): Show |
82 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.-50+496T>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46700055 | |||||||
| chr11:46700134 | G | C | 1 | a0001c0002t0003g0148 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-50+417C>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46700134 | |||||||
| chr11:46700195 | T | C | 2 | a0001c0001t0001g0040 a0001c0001t0001g0149 |
3 | HG02615.hp1 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-50+356A>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46700195 | |||||||
| chr11:46700209 | G | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0151 a0001c0007t0001g0150 |
6 | HG00735.hp2 HG01175.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+342C>G | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46700209 | |||||||
| chr11:46700276 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0006g0043 |
5 | NA18953.hp2 NA18971.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+275G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46700276 | |||||||
| chr11:46700468 | G | A | 17 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0041 others(14): Show |
33 | HG01070.hp1 HG01081.hp2 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.-50+83C>T | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46700468 | |||||||
| chr11:46700505 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-50+46G>A | ARHGAP1 | ENSG00000175220.12 | transcript | ENST00000311956.9 | protein_coding | 1/12 | chr11 | 46700505 |