Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 393 |
| ensemblid | ENSG00000089820.17 |
| hgncid | 674 |
| symbol | ARHGAP4 |
| name | Rho GTPase activating protein 4 |
| refseq_nuc | NM_001666.5 |
| refseq_prot | NP_001657.3 |
| ensembl_nuc | ENST00000350060.10 |
| ensembl_prot | ENSP00000203786.8 |
| mane_status | MANE Select |
| chr | chrX |
| start | 153907378 |
| end | 153926264 |
| strand | - |
| ver | v1.2 |
| region | chrX:153907378-153926264 |
| region5000 | chrX:153902378-153931264 |
| regionname0 | ARHGAP4_chrX_153907378_153926264 |
| regionname5000 | ARHGAP4_chrX_153902378_153931264 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 946 | 292 | 72 | 48 | 132 | 11 | 27 | 99 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | MAAHG others(941): Show |
chrX | 153902378 | 153931264 |
| a0002 | 0/0 | 946 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | MAAHG others(941): Show |
chrX | 153902378 | 153931264 |
| a0003 | 0/0 | 946 | 5 | 0 | 1 | 0 | 0 | 4 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | MAAHG others(941): Show |
chrX | 153902378 | 153931264 |
| a0004 | 0/0 | 946 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | MAAHG others(941): Show |
chrX | 153902378 | 153931264 |
| a0005 | 0/0 | 946 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | MAAHG others(941): Show |
chrX | 153902378 | 153931264 |
| a0006 | 0/0 | 946 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | MAAHG others(941): Show |
chrX | 153902378 | 153931264 |
| a0007 | 0/0 | 946 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | MAAHG others(941): Show |
chrX | 153902378 | 153931264 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2838 | 191 | 52 | 29 | 89 | 4 | 17 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | ATGGC others(2833): Show |
chrX | 153902378 | 153931264 | ||
| a0001c0002 | 1/1 | 2838 | 76 | 4 | 17 | 38 | 6 | 9 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | ATGGC others(2833): Show |
chrX | 153902378 | 153931264 | ||
| a0001c0003 | 0/0 | 2838 | 11 | 11 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | ATGGC others(2833): Show |
chrX | 153902378 | 153931264 | ||
| a0001c0006 | 0/0 | 2838 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | ATGGC others(2833): Show |
chrX | 153902378 | 153931264 | ||
| a0001c0007 | 0/0 | 2838 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | ATGGC others(2833): Show |
chrX | 153902378 | 153931264 | ||
| a0001c0008 | 0/0 | 2838 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | ATGGC others(2833): Show |
chrX | 153902378 | 153931264 | ||
| a0001c0009 | 0/0 | 2838 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | ATGGC others(2833): Show |
chrX | 153902378 | 153931264 | ||
| a0001c0014 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | ATGGC others(2833): Show |
chrX | 153902378 | 153931264 | ||
| a0001c0015 | 0/0 | 2838 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | ATGGC others(2833): Show |
chrX | 153902378 | 153931264 | ||
| a0001c0016 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | ATGGC others(2833): Show |
chrX | 153902378 | 153931264 | ||
| a0001c0017 | 0/0 | 2838 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | ATGGC others(2833): Show |
chrX | 153902378 | 153931264 | ||
| a0002c0004 | 0/0 | 2838 | 6 | 5 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | ATGGC others(2833): Show |
chrX | 153902378 | 153931264 | ||
| a0003c0005 | 0/0 | 2838 | 5 | 0 | 1 | 0 | 0 | 4 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | ATGGC others(2833): Show |
chrX | 153902378 | 153931264 | ||
| a0004c0010 | 0/0 | 2838 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | ATGGC others(2833): Show |
chrX | 153902378 | 153931264 | ||
| a0005c0013 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | ATGGC others(2833): Show |
chrX | 153902378 | 153931264 | ||
| a0006c0011 | 0/0 | 2838 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | ATGGC others(2833): Show |
chrX | 153902378 | 153931264 | ||
| a0007c0012 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | ATGGC others(2833): Show |
chrX | 153902378 | 153931264 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3254 | 189 | 50 | 29 | 89 | 4 | 17 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | GCCGG others(3249): Show |
chrX | 153902378 | 153931264 |
| a0001c0001t0003 | 0/0 | 3254 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | GCCGG others(3249): Show |
chrX | 153902378 | 153931264 |
| a0001c0002t0001 | 1/1 | 3254 | 76 | 4 | 17 | 38 | 6 | 9 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | GCCGG others(3249): Show |
chrX | 153902378 | 153931264 |
| a0001c0003t0001 | 0/0 | 3254 | 11 | 11 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | GCCGG others(3249): Show |
chrX | 153902378 | 153931264 |
| a0001c0006t0002 | 0/0 | 3254 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | GCCGG others(3249): Show |
chrX | 153902378 | 153931264 |
| a0001c0007t0004 | 0/0 | 3254 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | GCCGG others(3249): Show |
chrX | 153902378 | 153931264 |
| a0001c0008t0001 | 0/0 | 3254 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | GCCGG others(3249): Show |
chrX | 153902378 | 153931264 |
| a0001c0009t0001 | 0/0 | 3254 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | GCCGG others(3249): Show |
chrX | 153902378 | 153931264 |
| a0001c0014t0001 | 0/0 | 3254 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | GCCGG others(3249): Show |
chrX | 153902378 | 153931264 |
| a0001c0015t0001 | 0/0 | 3254 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | GCCGG others(3249): Show |
chrX | 153902378 | 153931264 |
| a0001c0016t0001 | 0/0 | 3254 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | GCCGG others(3249): Show |
chrX | 153902378 | 153931264 |
| a0001c0017t0001 | 0/0 | 3254 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | GCCGG others(3249): Show |
chrX | 153902378 | 153931264 |
| a0002c0004t0001 | 0/0 | 3254 | 6 | 5 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | GCCGG others(3249): Show |
chrX | 153902378 | 153931264 |
| a0003c0005t0001 | 0/0 | 3254 | 5 | 0 | 1 | 0 | 0 | 4 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | GCCGG others(3249): Show |
chrX | 153902378 | 153931264 |
| a0004c0010t0001 | 0/0 | 3254 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | GCCGG others(3249): Show |
chrX | 153902378 | 153931264 |
| a0005c0013t0001 | 0/0 | 3254 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | GCCGG others(3249): Show |
chrX | 153902378 | 153931264 |
| a0006c0011t0001 | 0/0 | 3254 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | GCCGG others(3249): Show |
chrX | 153902378 | 153931264 |
| a0007c0012t0001 | 0/0 | 3254 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | GCCGG others(3249): Show |
chrX | 153902378 | 153931264 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 47 | 2 | 9 | 32 | 0 | 4 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0004 | 0/0 | 8 | 0 | 3 | 3 | 0 | 2 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0008 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0011 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 1 | 3 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0024 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0002 | 1/0 | 13 | 0 | 1 | 8 | 0 | 3 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0003 | 0/0 | 9 | 1 | 5 | 0 | 2 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0005 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0006 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0108 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0003t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0003t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0003t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0003t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0006t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0006t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0007t0004g0036 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0008t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0008t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0009t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0014t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0015t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0016t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0001c0017t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0002c0004t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0002c0004t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0002c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0002c0004t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0002c0004t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0003c0005t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0003c0005t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0003c0005t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0004c0010t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0004c0010t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0005c0013t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0006c0011t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| a0007c0012t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | FIN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0136 | EUR | FIN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0137 | EUR | FIN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00673 | hp1 | a0001 | c0006 | t0002 | g0017 | EAS | CHS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00735 | hp2 | a0001 | c0007 | t0004 | g0036 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00741 | hp1 | a0003 | c0005 | t0001 | g0079 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0103 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0104 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01099 | hp1 | a0002 | c0004 | t0001 | g0140 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0130 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0035 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0120 | AMR | CLM | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0139 | AMR | CLM | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0034 | AMR | CLM | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01516 | hp1 | a0001 | c0007 | t0004 | g0036 | EUR | IBS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0003 | EUR | IBS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0003 | EUR | IBS | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01884 | hp1 | a0002 | c0004 | t0001 | g0040 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01891 | hp2 | a0005 | c0013 | t0001 | g0148 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0035 | AMR | PEL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02004 | hp2 | a0001 | c0017 | t0001 | g0101 | AMR | PEL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02015 | hp1 | a0001 | c0014 | t0001 | g0122 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | CDX | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02257 | hp1 | a0001 | c0016 | t0001 | g0058 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | KHV | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0063 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0070 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0038 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02738 | hp1 | a0003 | c0005 | t0001 | g0031 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0154 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0041 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0012 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0041 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02976 | hp2 | a0001 | c0008 | t0001 | g0095 | AFR | ESN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | MSL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03130 | hp1 | a0002 | c0004 | t0001 | g0142 | AFR | ESN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03209 | hp1 | a0001 | c0003 | t0001 | g0015 | AFR | MSL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03225 | hp1 | a0002 | c0004 | t0001 | g0040 | AFR | MSL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03239 | hp2 | a0003 | c0005 | t0001 | g0030 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03486 | hp1 | a0001 | c0008 | t0001 | g0062 | AFR | MSL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0125 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | ESN | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03540 | hp1 | a0002 | c0004 | t0001 | g0155 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0015 | AFR | GWD | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0069 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03704 | hp1 | a0003 | c0005 | t0001 | g0030 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | BEB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0003 | SAS | STU | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG04184 | hp1 | a0003 | c0005 | t0001 | g0031 | SAS | BEB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0006 | SAS | STU | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG04204 | hp1 | a0006 | c0011 | t0001 | g0126 | SAS | STU | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | STU | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0015 | AFR | YRI | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18612 | hp1 | a0001 | c0006 | t0002 | g0017 | EAS | CHB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | YRI | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18993 | hp1 | a0007 | c0012 | t0001 | g0078 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18998 | hp2 | a0004 | c0010 | t0001 | g0112 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19010 | hp1 | a0004 | c0010 | t0001 | g0121 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19030 | hp2 | a0001 | c0009 | t0001 | g0026 | AFR | LWK | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19066 | hp1 | a0001 | c0006 | t0002 | g0017 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19077 | hp1 | a0001 | c0006 | t0002 | g0054 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ASW | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA20129 | hp2 | a0001 | c0009 | t0001 | g0026 | AFR | ASW | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0138 | EUR | TSI | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0134 | EUR | TSI | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA20905 | hp1 | a0001 | c0015 | t0001 | g0124 | SAS | GIH | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0015 | AFR | MSL | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | USA | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | USA | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA20300 | hp2 | a0002 | c0004 | t0001 | g0141 | AFR | USA | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0152 | AFR | LWK | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0108 | REF | REF | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0002 | REF | REF | ARHGAP4_chrX_153902378_153931264 | ARHGAP4 | chrX | 153902378 | 153931264 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:153907829 | C | T | 1 | a0004 | 2 | NA18998.hp2 NA19010.hp1 |
missense_variant | MODERATE | c.2741G>A | p.Arg914His | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 22/22 | 2803/3254 | 2741/2841 | 914/946 | chrX | 153907829 | |||
| chrX:153909841 | C | A | 1 | a0003 | 5 | HG00741.hp1 HG02738.hp1 HG03239.hp2 others(2): Show |
missense_variant | MODERATE | c.2314G>T | p.Val772Leu | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 19/22 | 2376/3254 | 2314/2841 | 772/946 | chrX | 153909841 | |||
| chrX:153909852 | C | T | 1 | a0007 | 1 | NA18993.hp1 | missense_variant | MODERATE | c.2303G>A | p.Arg768Gln | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 19/22 | 2365/3254 | 2303/2841 | 768/946 | chrX | 153909852 | |||
| chrX:153910596 | G | A | 1 | a0005 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.1832C>T | p.Ala611Val | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 16/22 | 1894/3254 | 1832/2841 | 611/946 | chrX | 153910596 | |||
| chrX:153913444 | C | T | 1 | a0006 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.1291G>A | p.Gly431Ser | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 9/22 | 1353/3254 | 1291/2841 | 431/946 | chrX | 153913444 | |||
| chrX:153921489 | G | A | 1 | a0002 | 6 | HG01099.hp1 HG01884.hp1 HG03130.hp1 others(3): Show |
missense_variant | MODERATE | c.311C>T | p.Ala104Val | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 3/22 | 373/3254 | 311/2841 | 104/946 | chrX | 153921489 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:153909514 | G | A | 1 | a0001c0008 | 2 | HG02976.hp2 HG03486.hp1 |
synonymous_variant | LOW | c.2436C>T | p.Gly812Gly | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 20/22 | 2498/3254 | 2436/2841 | 812/946 | chrX | 153909514 | |||
| chrX:153910034 | G | A | 1 | a0001c0014 | 1 | HG02015.hp1 | synonymous_variant | LOW | c.2208C>T | p.Ala736Ala | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 18/22 | 2270/3254 | 2208/2841 | 736/946 | chrX | 153910034 | |||
| chrX:153910296 | C | T | 1 | a0001c0006 | 4 | HG00673.hp1 NA18612.hp1 NA19066.hp1 others(1): Show |
synonymous_variant | LOW | c.2031G>A | p.Gln677Gln | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 17/22 | 2093/3254 | 2031/2841 | 677/946 | chrX | 153910296 | |||
| chrX:153910347 | G | A | 1 | a0001c0009 | 2 | NA19030.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.1980C>T | p.Phe660Phe | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 17/22 | 2042/3254 | 1980/2841 | 660/946 | chrX | 153910347 | |||
| chrX:153910547 | C | T | 2 | a0001c0003 a0001c0016 |
12 | HG02257.hp1 HG02615.hp1 HG02647.hp1 others(9): Show |
synonymous_variant | LOW | c.1881G>A | p.Pro627Pro | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 16/22 | 1943/3254 | 1881/2841 | 627/946 | chrX | 153910547 | |||
| chrX:153910800 | A | G | 12 | a0001c0001 a0001c0003 a0001c0006 others(9): Show |
226 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(223): Show |
synonymous_variant | LOW | c.1716T>C | p.His572His | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 15/22 | 1778/3254 | 1716/2841 | 572/946 | chrX | 153910800 | |||
| chrX:153910830 | C | T | 1 | a0001c0007 | 2 | HG00735.hp2 HG01516.hp1 |
synonymous_variant | LOW | c.1686G>A | p.Glu562Glu | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 15/22 | 1748/3254 | 1686/2841 | 562/946 | chrX | 153910830 | |||
| chrX:153913865 | G | A | 1 | a0001c0015 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.1047C>T | p.Cys349Cys | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 8/22 | 1109/3254 | 1047/2841 | 349/946 | chrX | 153913865 | |||
| chrX:153921458 | G | A | 1 | a0001c0016 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.342C>T | p.Ser114Ser | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 3/22 | 404/3254 | 342/2841 | 114/946 | chrX | 153921458 | |||
| chrX:153921790 | G | A | 1 | a0001c0017 | 1 | HG02004.hp2 | synonymous_variant | LOW | c.87C>T | p.Ser29Ser | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 2/22 | 149/3254 | 87/2841 | 29/946 | chrX | 153921790 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:153907407 | G | A | 1 | a0001c0006t0002 | 4 | HG00673.hp1 NA18612.hp1 NA19066.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*322C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 22/22 | 322 | chrX | 153907407 | ||||||
| chrX:153907505 | T | A | 1 | a0001c0007t0004 | 2 | HG00735.hp2 HG01516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*224A>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 22/22 | 224 | chrX | 153907505 | ||||||
| chrX:153907544 | C | T | 1 | a0001c0001t0003 | 2 | HG02622.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*185G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 22/22 | 185 | chrX | 153907544 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:153908160 | T | C | 4 | a0001c0001t0001g0061 a0001c0001t0001g0153 a0001c0008t0001g0062 others(1): Show |
4 | HG01884.hp2 HG02976.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2608-198A>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908160 | |||||||
| chrX:153908188 | G | A | 1 | a0001c0002t0001g0117 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2608-226C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908188 | |||||||
| chrX:153908199 | C | A | 1 | a0001c0002t0001g0139 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2608-237G>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908199 | |||||||
| chrX:153908298 | C | A | 1 | a0001c0001t0001g0065 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2608-336G>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908298 | |||||||
| chrX:153908361 | G | A | 2 | a0001c0006t0002g0017 a0001c0006t0002g0054 |
4 | HG00673.hp1 NA18612.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.2608-399C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908361 | |||||||
| chrX:153908476 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2608-514G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908476 | |||||||
| chrX:153908521 | T | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(91): Show |
188 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.2607+549A>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908521 | |||||||
| chrX:153908563 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2607+507G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908563 | |||||||
| chrX:153908986 | C | T | 1 | a0001c0001t0003g0152 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2607+84G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 21/21 | chrX | 153908986 | |||||||
| chrX:153909305 | C | G | 3 | a0001c0001t0001g0061 a0001c0008t0001g0062 a0001c0008t0001g0095 |
3 | HG01884.hp2 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2508-136G>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 20/21 | chrX | 153909305 | |||||||
| chrX:153909398 | A | G | 3 | a0001c0001t0001g0149 a0001c0009t0001g0026 a0002c0004t0001g0141 |
4 | HG02965.hp1 NA19030.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.2507+45T>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 20/21 | chrX | 153909398 | |||||||
| chrX:153909552 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2415-17G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 19/21 | chrX | 153909552 | |||||||
| chrX:153909957 | G | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0045 a0001c0001t0001g0061 others(5): Show |
12 | HG01884.hp2 HG02280.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.2231-33C>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 18/21 | chrX | 153909957 | |||||||
| chrX:153910132 | G | C | 32 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(29): Show |
46 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.2156+39C>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 17/21 | chrX | 153910132 | |||||||
| chrX:153910416 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1923-12G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 16/21 | chrX | 153910416 | |||||||
| chrX:153910439 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1923-35C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 16/21 | chrX | 153910439 | |||||||
| chrX:153911010 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1604-11T>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 13/21 | chrX | 153911010 | |||||||
| chrX:153911107 | G | A | 1 | a0001c0002t0001g0138 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1603+22C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 13/21 | chrX | 153911107 | |||||||
| chrX:153911202 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1543-13C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153911202 | |||||||
| chrX:153911252 | C | CT | 29 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(26): Show |
40 | HG00140.hp1 HG01168.hp2 HG01169.hp2 others(37): Show |
intron_variant | MODIFIER | c.1543-64dupA | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153911252 | |||||||
| chrX:153911252 | CT | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(44): Show |
120 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.1543-64delA | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153911252 | |||||||
| chrX:153911252 | CTT | C | 5 | a0001c0001t0001g0018 a0001c0001t0001g0086 a0001c0001t0001g0090 others(2): Show |
7 | HG01928.hp1 HG02622.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.1543-65_1543-64del others(2): Show |
ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153911252 | |||||||
| chrX:153911505 | T | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(86): Show |
190 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1543-316A>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153911505 | |||||||
| chrX:153911858 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG01243.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1543-669A>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153911858 | |||||||
| chrX:153911930 | A | AG | 97 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(94): Show |
202 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.1543-742_1543-741i others(3): Show |
ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153911930 | |||||||
| chrX:153911930 | A | G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0052 a0001c0001t0001g0146 |
3 | HG01168.hp2 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1543-741T>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153911930 | |||||||
| chrX:153911934 | G | A | 3 | a0001c0001t0001g0049 a0001c0001t0001g0149 a0001c0009t0001g0026 |
4 | HG02109.hp2 HG02965.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1543-745C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153911934 | |||||||
| chrX:153912141 | T | C | 2 | a0001c0001t0001g0097 a0005c0013t0001g0148 |
2 | HG01891.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1542+559A>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153912141 | |||||||
| chrX:153912211 | G | A | 1 | a0001c0017t0001g0101 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1542+489C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153912211 | |||||||
| chrX:153912478 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1542+222T>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153912478 | |||||||
| chrX:153912519 | C | T | 1 | a0001c0002t0001g0071 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1542+181G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153912519 | |||||||
| chrX:153912528 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1542+172A>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153912528 | |||||||
| chrX:153912610 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1542+90A>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 12/21 | chrX | 153912610 | |||||||
| chrX:153912969 | G | A | 1 | a0001c0002t0001g0109 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1439+55C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 11/21 | chrX | 153912969 | |||||||
| chrX:153912986 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1439+38C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 11/21 | chrX | 153912986 | |||||||
| chrX:153912992 | TC | T | 5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0052 others(2): Show |
5 | HG01099.hp1 HG01243.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1439+31delG | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 11/21 | chrX | 153912992 | |||||||
| chrX:153912994 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1439+30C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 11/21 | chrX | 153912994 | |||||||
| chrX:153912999 | G | A | 2 | a0001c0001t0001g0021 a0001c0008t0001g0095 |
4 | HG02109.hp1 HG02258.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1439+25C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 11/21 | chrX | 153912999 | |||||||
| chrX:153913936 | A | G | 1 | a0005c0013t0001g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1033-57T>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153913936 | |||||||
| chrX:153913961 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1033-82G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153913961 | |||||||
| chrX:153914069 | T | C | 1 | a0001c0002t0001g0075 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1033-190A>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153914069 | |||||||
| chrX:153914076 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1033-197G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153914076 | |||||||
| chrX:153914266 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1033-387C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153914266 | |||||||
| chrX:153914482 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(121): Show |
236 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.1033-603T>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153914482 | |||||||
| chrX:153914590 | G | A | 1 | a0001c0002t0001g0137 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1033-711C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153914590 | |||||||
| chrX:153914794 | G | A | 1 | a0001c0002t0001g0076 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1033-915C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153914794 | |||||||
| chrX:153914892 | A | T | 1 | a0001c0001t0001g0097 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1033-1013T>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153914892 | |||||||
| chrX:153914950 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG01243.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1033-1071T>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153914950 | |||||||
| chrX:153915066 | T | C | 19 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0043 others(16): Show |
26 | HG00673.hp1 HG01361.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.1033-1187A>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153915066 | |||||||
| chrX:153915119 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1033-1240C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153915119 | |||||||
| chrX:153915164 | A | C | 1 | a0001c0001t0001g0097 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1033-1285T>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153915164 | |||||||
| chrX:153915184 | G | A | 13 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0028 others(10): Show |
24 | HG00642.hp1 HG02055.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.1033-1305C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153915184 | |||||||
| chrX:153915214 | G | C | 1 | a0005c0013t0001g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1033-1335C>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153915214 | |||||||
| chrX:153915214 | G | T | 5 | a0001c0001t0001g0118 a0001c0002t0001g0009 a0001c0002t0001g0109 others(2): Show |
9 | HG02027.hp1 NA18975.hp1 NA18989.hp1 others(6): Show |
intron_variant | MODIFIER | c.1033-1335C>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153915214 | |||||||
| chrX:153915301 | T | C | 14 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0019 others(11): Show |
25 | HG00140.hp1 HG00597.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.1033-1422A>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153915301 | |||||||
| chrX:153916820 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1032+2012C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153916820 | |||||||
| chrX:153917109 | A | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(108): Show |
220 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(217): Show |
intron_variant | MODIFIER | c.1032+1723T>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153917109 | |||||||
| chrX:153917207 | G | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(77): Show |
174 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.1032+1625C>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153917207 | |||||||
| chrX:153917522 | G | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0145 |
2 | HG01175.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1032+1310C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153917522 | |||||||
| chrX:153917768 | A | C | 1 | a0001c0001t0001g0067 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1032+1064T>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153917768 | |||||||
| chrX:153917863 | T | C | 1 | a0001c0001t0001g0028 | 2 | HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1032+969A>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153917863 | |||||||
| chrX:153917945 | A | C | 1 | a0001c0001t0001g0131 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1032+887T>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153917945 | |||||||
| chrX:153918231 | T | G | 1 | a0001c0001t0001g0129 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1032+601A>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153918231 | |||||||
| chrX:153918251 | G | A | 1 | a0001c0002t0001g0130 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1032+581C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153918251 | |||||||
| chrX:153918576 | T | C | 1 | a0005c0013t0001g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1032+256A>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153918576 | |||||||
| chrX:153918583 | A | G | 6 | a0001c0001t0001g0061 a0001c0001t0001g0131 a0001c0001t0001g0153 others(3): Show |
7 | HG01884.hp2 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1032+249T>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153918583 | |||||||
| chrX:153918654 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1032+178G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153918654 | |||||||
| chrX:153918730 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1032+102C>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | 153918730 | |||||||
| chrX:153919061 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA18971.hp1 | splice_region_variant&intron_variant | LOW | c.811-8C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 6/21 | chrX | 153919061 | |||||||
| chrX:153919302 | G | C | 1 | a0001c0003t0001g0041 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.682-19C>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 5/21 | chrX | 153919302 | |||||||
| chrX:153919362 | G | A | 11 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0039 others(8): Show |
18 | HG02145.hp1 HG02280.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.682-79C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 5/21 | chrX | 153919362 | |||||||
| chrX:153919791 | T | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(66): Show |
152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.682-508A>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 5/21 | chrX | 153919791 | |||||||
| chrX:153919792 | A | AT | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(67): Show |
152 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.682-510dupA | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 5/21 | chrX | 153919792 | |||||||
| chrX:153919798 | T | A | 3 | a0001c0001t0001g0049 a0001c0001t0001g0153 a0001c0009t0001g0026 |
4 | HG02109.hp2 HG03453.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-515A>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 5/21 | chrX | 153919798 | |||||||
| chrX:153919947 | C | T | 1 | a0001c0002t0001g0109 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.682-664G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 5/21 | chrX | 153919947 | |||||||
| chrX:153919948 | G | A | 7 | a0001c0001t0001g0135 a0001c0002t0001g0003 a0001c0002t0001g0027 others(4): Show |
16 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.682-665C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 5/21 | chrX | 153919948 | |||||||
| chrX:153920192 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG01243.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.681+434G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 5/21 | chrX | 153920192 | |||||||
| chrX:153920362 | G | A | 1 | a0001c0002t0001g0138 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.681+264C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 5/21 | chrX | 153920362 | |||||||
| chrX:153921207 | G | A | 1 | a0001c0002t0001g0139 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.436-48C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 3/21 | chrX | 153921207 | |||||||
| chrX:153921250 | G | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | NA18947.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.436-91C>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 3/21 | chrX | 153921250 | |||||||
| chrX:153921296 | C | G | 1 | a0001c0001t0001g0051 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.435+69G>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 3/21 | chrX | 153921296 | |||||||
| chrX:153921911 | G | A | 1 | a0001c0002t0001g0143 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.68-102C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153921911 | |||||||
| chrX:153922019 | G | A | 1 | a0001c0001t0001g0033 | 2 | HG01952.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.68-210C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153922019 | |||||||
| chrX:153922245 | C | T | 13 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0045 others(10): Show |
19 | HG00642.hp1 HG00673.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.68-436G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153922245 | |||||||
| chrX:153922349 | C | G | 5 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
9 | HG01934.hp1 HG02818.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-540G>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153922349 | |||||||
| chrX:153922752 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.68-943A>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153922752 | |||||||
| chrX:153922762 | C | G | 1 | a0001c0002t0001g0107 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.68-953G>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153922762 | |||||||
| chrX:153922867 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.68-1058C>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153922867 | |||||||
| chrX:153923062 | C | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0047 others(3): Show |
9 | HG00597.hp2 HG01261.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-1253G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923062 | |||||||
| chrX:153923234 | C | T | 1 | a0005c0013t0001g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.68-1425G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923234 | |||||||
| chrX:153923271 | C | T | 13 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0045 others(10): Show |
19 | HG00642.hp1 HG00673.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.68-1462G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923271 | |||||||
| chrX:153923305 | C | T | 2 | a0001c0002t0001g0103 a0001c0002t0001g0104 |
2 | HG00741.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.68-1496G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923305 | |||||||
| chrX:153923870 | C | T | 13 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0045 others(10): Show |
19 | HG00642.hp1 HG00673.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.68-2061G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923870 | |||||||
| chrX:153923977 | C | T | 1 | a0001c0002t0001g0102 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.67+2159G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153923977 | |||||||
| chrX:153924021 | C | T | 2 | a0001c0001t0001g0049 a0001c0009t0001g0026 |
3 | HG02109.hp2 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.67+2115G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153924021 | |||||||
| chrX:153924293 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.67+1843C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153924293 | |||||||
| chrX:153924366 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(79): Show |
176 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.67+1770G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153924366 | |||||||
| chrX:153924400 | G | A | 1 | a0005c0013t0001g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.67+1736C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153924400 | |||||||
| chrX:153924420 | T | G | 1 | a0005c0013t0001g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.67+1716A>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153924420 | |||||||
| chrX:153924919 | A | G | 1 | a0001c0002t0001g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.67+1217T>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153924919 | |||||||
| chrX:153925252 | A | AATGATGT others(33): Show |
1 | a0001c0001t0001g0050 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.67+844_67+883dupGA others(38): Show |
ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153925252 | |||||||
| chrX:153925713 | C | G | 2 | a0001c0001t0001g0049 a0001c0009t0001g0026 |
3 | HG02109.hp2 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.67+423G>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153925713 | |||||||
| chrX:153925787 | T | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
10 | HG02280.hp1 HG02572.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.67+349A>G | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153925787 | |||||||
| chrX:153925814 | G | A | 1 | a0001c0001t0001g0025 | 3 | HG02083.hp1 NA18939.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.67+322C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153925814 | |||||||
| chrX:153925839 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0047 a0001c0001t0001g0048 |
5 | HG01261.hp1 HG02293.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+297G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153925839 | |||||||
| chrX:153925893 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG01243.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.67+243C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153925893 | |||||||
| chrX:153925898 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG01243.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.67+238T>C | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153925898 | |||||||
| chrX:153925903 | G | A | 1 | a0001c0003t0001g0154 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.67+233C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153925903 | |||||||
| chrX:153925992 | G | A | 1 | a0002c0004t0001g0155 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.67+144C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153925992 | |||||||
| chrX:153926119 | G | A | 5 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
9 | HG01934.hp1 HG02818.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+17C>T | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153926119 | |||||||
| chrX:153926129 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 |
3 | HG02451.hp1 HG02976.hp1 HG03041.hp1 |
splice_region_variant&intron_variant | LOW | c.67+7G>A | ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | 153926129 |