Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 414 |
| ensemblid | ENSG00000006756.16 |
| hgncid | 717 |
| symbol | ARSD |
| name | arylsulfatase D |
| refseq_nuc | NM_001669.4 |
| refseq_prot | NP_001660.2 |
| ensembl_nuc | ENST00000381154.6 |
| ensembl_prot | ENSP00000370546.1 |
| mane_status | MANE Select |
| chr | chrX |
| start | 2903972 |
| end | 2929339 |
| strand | - |
| ver | v1.2 |
| region | chrX:2903972-2929339 |
| region5000 | chrX:2898972-2934339 |
| regionname0 | ARSD_chrX_2903972_2929339 |
| regionname5000 | ARSD_chrX_2898972_2934339 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 593 | 131 | 38 | 34 | 43 | 6 | 9 | 33 | ARSD_chrX_2898972_2934339 | ARSD | MRSAA others(588): Show |
chrX | 2898972 | 2934339 |
| a0002 | 1/0 | 593 | 119 | 22 | 17 | 51 | 6 | 22 | 41 | ARSD_chrX_2898972_2934339 | ARSD | MRSAA others(588): Show |
chrX | 2898972 | 2934339 |
| a0003 | 0/0 | 593 | 67 | 12 | 5 | 48 | 1 | 1 | 39 | ARSD_chrX_2898972_2934339 | ARSD | MRSAA others(588): Show |
chrX | 2898972 | 2934339 |
| a0004 | 0/0 | 593 | 19 | 5 | 1 | 13 | 0 | 0 | 9 | ARSD_chrX_2898972_2934339 | ARSD | MRSAA others(588): Show |
chrX | 2898972 | 2934339 |
| a0005 | 0/0 | 593 | 4 | 2 | 2 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | MRSAA others(588): Show |
chrX | 2898972 | 2934339 |
| a0006 | 0/0 | 593 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ARSD_chrX_2898972_2934339 | ARSD | MRSAA others(588): Show |
chrX | 2898972 | 2934339 |
| a0007 | 0/0 | 593 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | MRSAA others(588): Show |
chrX | 2898972 | 2934339 |
| a0008 | 0/0 | 593 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | MRSAA others(588): Show |
chrX | 2898972 | 2934339 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1779 | 120 | 31 | 33 | 40 | 6 | 9 | ARSD_chrX_2898972_2934339 | ARSD | ATGCG others(1774): Show |
chrX | 2898972 | 2934339 | ||
| a0001c0006 | 0/0 | 1779 | 8 | 7 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ATGCG others(1774): Show |
chrX | 2898972 | 2934339 | ||
| a0001c0009 | 0/0 | 1779 | 3 | 0 | 0 | 3 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ATGCG others(1774): Show |
chrX | 2898972 | 2934339 | ||
| a0002c0002 | 1/0 | 1779 | 100 | 9 | 13 | 49 | 6 | 22 | ARSD_chrX_2898972_2934339 | ARSD | ATGCG others(1774): Show |
chrX | 2898972 | 2934339 | ||
| a0002c0005 | 0/0 | 1779 | 15 | 11 | 4 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ATGCG others(1774): Show |
chrX | 2898972 | 2934339 | ||
| a0002c0010 | 0/0 | 1779 | 2 | 2 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ATGCG others(1774): Show |
chrX | 2898972 | 2934339 | ||
| a0002c0013 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ATGCG others(1774): Show |
chrX | 2898972 | 2934339 | ||
| a0002c0015 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ATGCG others(1774): Show |
chrX | 2898972 | 2934339 | ||
| a0003c0003 | 0/0 | 1779 | 57 | 4 | 4 | 47 | 1 | 1 | ARSD_chrX_2898972_2934339 | ARSD | ATGCG others(1774): Show |
chrX | 2898972 | 2934339 | ||
| a0003c0007 | 0/0 | 1779 | 7 | 6 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ATGCG others(1774): Show |
chrX | 2898972 | 2934339 | ||
| a0003c0014 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ATGCG others(1774): Show |
chrX | 2898972 | 2934339 | ||
| a0003c0017 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ATGCG others(1774): Show |
chrX | 2898972 | 2934339 | ||
| a0003c0018 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ATGCG others(1774): Show |
chrX | 2898972 | 2934339 | ||
| a0004c0004 | 0/0 | 1779 | 18 | 4 | 1 | 13 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ATGCG others(1774): Show |
chrX | 2898972 | 2934339 | ||
| a0004c0012 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ATGCG others(1774): Show |
chrX | 2898972 | 2934339 | ||
| a0005c0008 | 0/0 | 1779 | 3 | 1 | 2 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ATGCG others(1774): Show |
chrX | 2898972 | 2934339 | ||
| a0005c0019 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ATGCG others(1774): Show |
chrX | 2898972 | 2934339 | ||
| a0006c0011 | 0/0 | 1779 | 2 | 0 | 0 | 2 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ATGCG others(1774): Show |
chrX | 2898972 | 2934339 | ||
| a0007c0016 | 0/0 | 1779 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ATGCG others(1774): Show |
chrX | 2898972 | 2934339 | ||
| a0008c0020 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ATGCG others(1774): Show |
chrX | 2898972 | 2934339 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5145 | 71 | 21 | 20 | 22 | 3 | 5 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5140): Show |
chrX | 2898972 | 2934339 |
| a0001c0001t0002 | 0/0 | 5145 | 3 | 0 | 0 | 3 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5140): Show |
chrX | 2898972 | 2934339 |
| a0001c0001t0004 | 0/0 | 5138 | 18 | 3 | 7 | 5 | 1 | 2 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5133): Show |
chrX | 2898972 | 2934339 |
| a0001c0001t0006 | 0/0 | 5144 | 9 | 2 | 2 | 2 | 2 | 1 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5139): Show |
chrX | 2898972 | 2934339 |
| a0001c0001t0007 | 0/0 | 5146 | 4 | 0 | 2 | 2 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5141): Show |
chrX | 2898972 | 2934339 |
| a0001c0001t0009 | 0/0 | 5138 | 2 | 0 | 0 | 2 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5133): Show |
chrX | 2898972 | 2934339 |
| a0001c0001t0010 | 0/0 | 5144 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5139): Show |
chrX | 2898972 | 2934339 |
| a0001c0001t0011 | 0/0 | 5144 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5139): Show |
chrX | 2898972 | 2934339 |
| a0001c0001t0013 | 0/0 | 5144 | 4 | 4 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5139): Show |
chrX | 2898972 | 2934339 |
| a0001c0001t0014 | 0/0 | 5144 | 2 | 0 | 1 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5139): Show |
chrX | 2898972 | 2934339 |
| a0001c0001t0018 | 0/1 | 5138 | 2 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5133): Show |
chrX | 2898972 | 2934339 |
| a0001c0001t0029 | 0/0 | 5144 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5139): Show |
chrX | 2898972 | 2934339 |
| a0001c0001t0030 | 0/0 | 5145 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5140): Show |
chrX | 2898972 | 2934339 |
| a0001c0001t0031 | 0/0 | 5138 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5133): Show |
chrX | 2898972 | 2934339 |
| a0001c0006t0008 | 0/0 | 5144 | 5 | 5 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5139): Show |
chrX | 2898972 | 2934339 |
| a0001c0006t0017 | 0/0 | 5145 | 3 | 2 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5140): Show |
chrX | 2898972 | 2934339 |
| a0001c0009t0009 | 0/0 | 5138 | 3 | 0 | 0 | 3 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5133): Show |
chrX | 2898972 | 2934339 |
| a0002c0002t0001 | 1/0 | 5145 | 35 | 4 | 3 | 12 | 0 | 15 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5140): Show |
chrX | 2898972 | 2934339 |
| a0002c0002t0002 | 0/0 | 5145 | 31 | 0 | 5 | 21 | 0 | 5 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5140): Show |
chrX | 2898972 | 2934339 |
| a0002c0002t0004 | 0/0 | 5138 | 6 | 0 | 2 | 1 | 3 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5133): Show |
chrX | 2898972 | 2934339 |
| a0002c0002t0006 | 0/0 | 5144 | 3 | 1 | 0 | 1 | 1 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5139): Show |
chrX | 2898972 | 2934339 |
| a0002c0002t0007 | 0/0 | 5146 | 3 | 0 | 1 | 1 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5141): Show |
chrX | 2898972 | 2934339 |
| a0002c0002t0009 | 0/0 | 5138 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5133): Show |
chrX | 2898972 | 2934339 |
| a0002c0002t0010 | 0/0 | 5144 | 2 | 1 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5139): Show |
chrX | 2898972 | 2934339 |
| a0002c0002t0011 | 0/0 | 5144 | 3 | 0 | 1 | 2 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5139): Show |
chrX | 2898972 | 2934339 |
| a0002c0002t0014 | 0/0 | 5144 | 2 | 0 | 0 | 1 | 1 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5139): Show |
chrX | 2898972 | 2934339 |
| a0002c0002t0016 | 0/0 | 5145 | 3 | 3 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5140): Show |
chrX | 2898972 | 2934339 |
| a0002c0002t0018 | 0/0 | 5138 | 1 | 0 | 0 | 0 | 1 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5133): Show |
chrX | 2898972 | 2934339 |
| a0002c0002t0019 | 0/0 | 5145 | 3 | 0 | 0 | 3 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5140): Show |
chrX | 2898972 | 2934339 |
| a0002c0002t0022 | 0/0 | 5145 | 2 | 0 | 0 | 2 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5140): Show |
chrX | 2898972 | 2934339 |
| a0002c0002t0027 | 0/0 | 5145 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5140): Show |
chrX | 2898972 | 2934339 |
| a0002c0002t0032 | 0/0 | 5144 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5139): Show |
chrX | 2898972 | 2934339 |
| a0002c0002t0037 | 0/0 | 5146 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5141): Show |
chrX | 2898972 | 2934339 |
| a0002c0002t0038 | 0/0 | 5145 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5140): Show |
chrX | 2898972 | 2934339 |
| a0002c0002t0039 | 0/0 | 5145 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5140): Show |
chrX | 2898972 | 2934339 |
| a0002c0005t0001 | 0/0 | 5145 | 11 | 8 | 3 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5140): Show |
chrX | 2898972 | 2934339 |
| a0002c0005t0006 | 0/0 | 5144 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5139): Show |
chrX | 2898972 | 2934339 |
| a0002c0005t0021 | 0/0 | 5143 | 2 | 1 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5138): Show |
chrX | 2898972 | 2934339 |
| a0002c0005t0028 | 0/0 | 5145 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5140): Show |
chrX | 2898972 | 2934339 |
| a0002c0010t0008 | 0/0 | 5144 | 2 | 2 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5139): Show |
chrX | 2898972 | 2934339 |
| a0002c0013t0010 | 0/0 | 5144 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5139): Show |
chrX | 2898972 | 2934339 |
| a0002c0015t0009 | 0/0 | 5138 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5133): Show |
chrX | 2898972 | 2934339 |
| a0003c0003t0001 | 0/0 | 5145 | 4 | 1 | 2 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5140): Show |
chrX | 2898972 | 2934339 |
| a0003c0003t0002 | 0/0 | 5145 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5140): Show |
chrX | 2898972 | 2934339 |
| a0003c0003t0003 | 0/0 | 5147 | 31 | 0 | 0 | 31 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5142): Show |
chrX | 2898972 | 2934339 |
| a0003c0003t0005 | 0/0 | 5147 | 8 | 2 | 0 | 4 | 1 | 1 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5142): Show |
chrX | 2898972 | 2934339 |
| a0003c0003t0010 | 0/0 | 5144 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5139): Show |
chrX | 2898972 | 2934339 |
| a0003c0003t0011 | 0/0 | 5144 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5139): Show |
chrX | 2898972 | 2934339 |
| a0003c0003t0012 | 0/0 | 5146 | 4 | 0 | 0 | 4 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5141): Show |
chrX | 2898972 | 2934339 |
| a0003c0003t0015 | 0/0 | 5148 | 2 | 0 | 0 | 2 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5143): Show |
chrX | 2898972 | 2934339 |
| a0003c0003t0023 | 0/0 | 5146 | 2 | 1 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5141): Show |
chrX | 2898972 | 2934339 |
| a0003c0003t0035 | 0/0 | 5147 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5142): Show |
chrX | 2898972 | 2934339 |
| a0003c0003t0036 | 0/0 | 5143 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5138): Show |
chrX | 2898972 | 2934339 |
| a0003c0003t0040 | 0/0 | 5148 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5143): Show |
chrX | 2898972 | 2934339 |
| a0003c0007t0003 | 0/0 | 5147 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5142): Show |
chrX | 2898972 | 2934339 |
| a0003c0007t0005 | 0/0 | 5147 | 6 | 5 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5142): Show |
chrX | 2898972 | 2934339 |
| a0003c0014t0005 | 0/0 | 5147 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5142): Show |
chrX | 2898972 | 2934339 |
| a0003c0017t0034 | 0/0 | 5148 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5143): Show |
chrX | 2898972 | 2934339 |
| a0003c0018t0012 | 0/0 | 5146 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5141): Show |
chrX | 2898972 | 2934339 |
| a0004c0004t0002 | 0/0 | 5145 | 2 | 0 | 1 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5140): Show |
chrX | 2898972 | 2934339 |
| a0004c0004t0003 | 0/0 | 5147 | 5 | 0 | 0 | 5 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5142): Show |
chrX | 2898972 | 2934339 |
| a0004c0004t0005 | 0/0 | 5147 | 8 | 3 | 0 | 5 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5142): Show |
chrX | 2898972 | 2934339 |
| a0004c0004t0015 | 0/0 | 5148 | 2 | 0 | 0 | 2 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5143): Show |
chrX | 2898972 | 2934339 |
| a0004c0004t0033 | 0/0 | 5148 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5143): Show |
chrX | 2898972 | 2934339 |
| a0004c0012t0005 | 0/0 | 5147 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5142): Show |
chrX | 2898972 | 2934339 |
| a0005c0008t0020 | 0/0 | 5144 | 2 | 1 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5139): Show |
chrX | 2898972 | 2934339 |
| a0005c0008t0026 | 0/0 | 5142 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5137): Show |
chrX | 2898972 | 2934339 |
| a0005c0019t0025 | 0/0 | 5143 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5138): Show |
chrX | 2898972 | 2934339 |
| a0006c0011t0001 | 0/0 | 5145 | 2 | 0 | 0 | 2 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5140): Show |
chrX | 2898972 | 2934339 |
| a0007c0016t0001 | 0/0 | 5145 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5140): Show |
chrX | 2898972 | 2934339 |
| a0008c0020t0024 | 0/0 | 5145 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | ACTAG others(5140): Show |
chrX | 2898972 | 2934339 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0004g0011 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0004g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0004g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0006g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0006g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0006g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0006g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0006g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0006g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0006g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0007g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0007g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0007g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0007g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0009g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0009g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0010g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0011g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0013g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0013g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0013g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0013g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0014g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0014g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0018g0140 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0018g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0029g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0030g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0001t0031g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0006t0008g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0006t0008g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0006t0008g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0006t0008g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0006t0008g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0006t0017g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0006t0017g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0006t0017g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0009t0009g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0009t0009g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0001c0009t0009g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0136 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0004g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0004g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0004g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0006g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0007g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0007g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0007g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0009g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0010g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0010g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0011g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0011g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0011g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0014g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0014g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0016g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0016g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0016g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0018g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0019g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0019g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0019g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0022g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0022g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0027g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0032g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0037g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0038g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0002t0039g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0005t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0005t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0005t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0005t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0005t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0005t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0005t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0005t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0005t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0005t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0005t0006g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0005t0021g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0005t0021g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0005t0028g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0010t0008g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0010t0008g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0013t0010g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0002c0015t0009g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0003g0001 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0005g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0005g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0010g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0011g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0012g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0012g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0012g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0012g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0015g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0015g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0023g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0023g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0035g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0036g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0003t0040g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0007t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0007t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0007t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0007t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0007t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0007t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0007t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0014t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0017t0034g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0003c0018t0012g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0004c0004t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0004c0004t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0004c0004t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0004c0004t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0004c0004t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0004c0004t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0004c0004t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0004c0004t0005g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0004c0004t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0004c0004t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0004c0004t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0004c0004t0005g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0004c0004t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0004c0004t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0004c0004t0015g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0004c0004t0015g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0004c0004t0033g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0004c0012t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0005c0008t0020g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0005c0008t0026g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0005c0019t0025g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0006c0011t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0007c0016t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| a0008c0020t0024g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0006 | g0067 | EUR | GBR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00099 | hp2 | a0001 | c0001 | t0006 | g0088 | EUR | GBR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00140 | hp1 | a0002 | c0002 | t0004 | g0049 | EUR | GBR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | FIN | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00323 | hp1 | a0002 | c0002 | t0014 | g0027 | EUR | FIN | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00323 | hp2 | a0002 | c0002 | t0006 | g0051 | EUR | FIN | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00408 | hp1 | a0003 | c0018 | t0012 | g0297 | EAS | CHS | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00408 | hp2 | a0001 | c0001 | t0009 | g0292 | EAS | CHS | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0015 | EAS | CHS | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00438 | hp2 | a0002 | c0002 | t0019 | g0276 | EAS | CHS | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00544 | hp1 | a0003 | c0003 | t0003 | g0282 | EAS | CHS | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00544 | hp2 | a0002 | c0002 | t0004 | g0074 | EAS | CHS | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00558 | hp1 | a0003 | c0003 | t0012 | g0233 | EAS | CHS | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00558 | hp2 | a0003 | c0003 | t0001 | g0073 | EAS | CHS | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | CHS | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00597 | hp2 | a0004 | c0004 | t0003 | g0285 | EAS | CHS | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00609 | hp1 | a0003 | c0003 | t0003 | g0020 | EAS | CHS | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | CHS | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0160 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0156 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0296 | EAS | CHS | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00733 | hp2 | a0002 | c0002 | t0007 | g0026 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00735 | hp2 | a0002 | c0002 | t0004 | g0185 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0279 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0179 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01070 | hp1 | a0001 | c0001 | t0006 | g0161 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01070 | hp2 | a0005 | c0008 | t0026 | g0032 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01071 | hp2 | a0005 | c0008 | t0020 | g0006 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01074 | hp1 | a0002 | c0005 | t0021 | g0077 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01081 | hp2 | a0001 | c0001 | t0007 | g0200 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0072 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01109 | hp1 | a0001 | c0006 | t0017 | g0226 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0119 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01168 | hp1 | a0002 | c0002 | t0004 | g0047 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01168 | hp2 | a0001 | c0001 | t0018 | g0164 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01192 | hp1 | a0001 | c0001 | t0007 | g0202 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01243 | hp1 | a0003 | c0007 | t0005 | g0147 | AMR | PUR | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01255 | hp1 | a0003 | c0003 | t0001 | g0053 | AMR | CLM | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01257 | hp1 | a0002 | c0002 | t0010 | g0245 | AMR | CLM | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01257 | hp2 | a0003 | c0003 | t0011 | g0237 | AMR | CLM | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01258 | hp1 | a0003 | c0003 | t0002 | g0235 | AMR | CLM | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0165 | AMR | CLM | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | CLM | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0017 | AMR | CLM | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0138 | AMR | CLM | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01496 | hp1 | a0002 | c0005 | t0001 | g0029 | AMR | CLM | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01516 | hp1 | a0002 | c0002 | t0004 | g0061 | EUR | IBS | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01516 | hp2 | a0002 | c0002 | t0018 | g0063 | EUR | IBS | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01517 | hp2 | a0002 | c0002 | t0004 | g0052 | EUR | IBS | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01884 | hp2 | a0004 | c0012 | t0005 | g0127 | AFR | ACB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01891 | hp1 | a0003 | c0007 | t0005 | g0144 | AFR | ACB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01891 | hp2 | a0003 | c0003 | t0001 | g0221 | AFR | ACB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01934 | hp1 | a0004 | c0004 | t0002 | g0264 | AMR | PEL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01943 | hp1 | a0001 | c0001 | t0006 | g0142 | AMR | PEL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01975 | hp2 | a0001 | c0001 | t0014 | g0100 | AMR | PEL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01981 | hp2 | a0003 | c0003 | t0001 | g0035 | AMR | PEL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01993 | hp1 | a0007 | c0016 | t0001 | g0148 | AMR | PEL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01993 | hp2 | a0002 | c0002 | t0011 | g0234 | AMR | PEL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0187 | AMR | PEL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0201 | EAS | KHV | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02027 | hp1 | a0001 | c0001 | t0009 | g0307 | EAS | KHV | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0305 | EAS | KHV | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0283 | EAS | KHV | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02074 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | KHV | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | KHV | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02080 | hp2 | a0003 | c0003 | t0003 | g0303 | EAS | KHV | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02083 | hp1 | a0004 | c0004 | t0005 | g0095 | EAS | KHV | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02129 | hp1 | a0002 | c0002 | t0019 | g0288 | EAS | KHV | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02132 | hp1 | a0004 | c0004 | t0005 | g0086 | EAS | KHV | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02135 | hp1 | a0003 | c0003 | t0035 | g0039 | EAS | KHV | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02145 | hp1 | a0001 | c0001 | t0029 | g0143 | AFR | ACB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02155 | hp1 | a0002 | c0002 | t0032 | g0115 | EAS | CDX | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0308 | EAS | CDX | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02165 | hp1 | a0004 | c0004 | t0003 | g0291 | EAS | CDX | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0239 | EAS | CDX | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02257 | hp1 | a0002 | c0002 | t0016 | g0097 | AFR | ACB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0090 | AFR | ACB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02258 | hp1 | a0003 | c0007 | t0005 | g0023 | AFR | ACB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0246 | AMR | PEL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02280 | hp1 | a0008 | c0020 | t0024 | g0113 | AFR | ACB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02280 | hp2 | a0001 | c0001 | t0013 | g0167 | AFR | ACB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02293 | hp1 | a0002 | c0005 | t0001 | g0005 | AMR | PEL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02451 | hp2 | a0002 | c0005 | t0001 | g0184 | AFR | ACB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0122 | AFR | GWD | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0056 | SAS | PJL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02615 | hp1 | a0004 | c0004 | t0005 | g0107 | AFR | GWD | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0111 | AFR | GWD | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02622 | hp1 | a0002 | c0010 | t0008 | g0033 | AFR | GWD | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0193 | AFR | GWD | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02647 | hp1 | a0002 | c0005 | t0001 | g0081 | AFR | GWD | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0249 | SAS | PJL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02683 | hp2 | a0001 | c0001 | t0006 | g0117 | SAS | PJL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0118 | AFR | GWD | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02723 | hp2 | a0002 | c0005 | t0001 | g0212 | AFR | GWD | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0182 | SAS | PJL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02809 | hp2 | a0002 | c0002 | t0016 | g0220 | AFR | GWD | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02886 | hp2 | a0002 | c0005 | t0001 | g0194 | AFR | GWD | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02895 | hp1 | a0002 | c0002 | t0006 | g0082 | AFR | GWD | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0083 | AFR | GWD | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02922 | hp2 | a0003 | c0003 | t0023 | g0108 | AFR | ESN | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02965 | hp1 | a0005 | c0008 | t0020 | g0006 | AFR | ESN | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02976 | hp1 | a0002 | c0002 | t0010 | g0229 | AFR | ESN | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02976 | hp2 | a0004 | c0004 | t0033 | g0152 | AFR | ESN | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0250 | SAS | PJL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03041 | hp1 | a0002 | c0005 | t0001 | g0110 | AFR | GWD | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03098 | hp1 | a0001 | c0001 | t0013 | g0208 | AFR | MSL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03130 | hp1 | a0002 | c0005 | t0021 | g0211 | AFR | ESN | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03139 | hp1 | a0001 | c0006 | t0008 | g0092 | AFR | ESN | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03195 | hp1 | a0002 | c0005 | t0028 | g0191 | AFR | ESN | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03195 | hp2 | a0004 | c0004 | t0005 | g0225 | AFR | ESN | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03209 | hp1 | a0002 | c0010 | t0008 | g0034 | AFR | MSL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0070 | SAS | PJL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0028 | SAS | PJL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03453 | hp2 | a0003 | c0003 | t0005 | g0112 | AFR | MSL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03486 | hp1 | a0001 | c0006 | t0008 | g0223 | AFR | MSL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0183 | SAS | PJL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03491 | hp1 | a0003 | c0003 | t0005 | g0071 | SAS | PJL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0057 | SAS | PJL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03516 | hp1 | a0001 | c0006 | t0017 | g0217 | AFR | ESN | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0159 | AFR | GWD | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03540 | hp2 | a0001 | c0001 | t0013 | g0219 | AFR | GWD | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03579 | hp1 | a0003 | c0017 | t0034 | g0206 | AFR | MSL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0251 | SAS | PJL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0066 | SAS | PJL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0139 | SAS | STU | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0085 | SAS | PJL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03704 | hp2 | a0001 | c0001 | t0030 | g0075 | SAS | PJL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0069 | SAS | PJL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0141 | SAS | BEB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0277 | SAS | BEB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0059 | SAS | BEB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0116 | SAS | BEB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | STU | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0048 | SAS | BEB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0022 | SAS | BEB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0263 | SAS | STU | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG04204 | hp1 | a0002 | c0002 | t0027 | g0060 | SAS | STU | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG04228 | hp1 | a0002 | c0002 | t0007 | g0054 | SAS | STU | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18522 | hp1 | a0002 | c0005 | t0006 | g0214 | AFR | YRI | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18612 | hp1 | a0003 | c0003 | t0003 | g0294 | EAS | CHB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18747 | hp1 | a0001 | c0001 | t0011 | g0290 | EAS | CHB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18906 | hp1 | a0002 | c0005 | t0001 | g0213 | AFR | YRI | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18906 | hp2 | a0001 | c0006 | t0008 | g0224 | AFR | YRI | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0287 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0269 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18941 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18941 | hp2 | a0002 | c0002 | t0037 | g0236 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18942 | hp1 | a0002 | c0002 | t0014 | g0105 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18942 | hp2 | a0002 | c0013 | t0010 | g0267 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18946 | hp1 | a0004 | c0004 | t0005 | g0128 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18946 | hp2 | a0003 | c0003 | t0005 | g0080 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18947 | hp1 | a0003 | c0003 | t0003 | g0301 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0255 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18948 | hp1 | a0003 | c0003 | t0012 | g0273 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18949 | hp2 | a0001 | c0001 | t0031 | g0176 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18950 | hp1 | a0002 | c0002 | t0006 | g0150 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0243 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0266 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18952 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0265 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18954 | hp2 | a0001 | c0009 | t0009 | g0230 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18956 | hp1 | a0002 | c0002 | t0038 | g0241 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18956 | hp2 | a0002 | c0002 | t0002 | g0242 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18959 | hp1 | a0001 | c0001 | t0010 | g0310 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18961 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18963 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18965 | hp1 | a0003 | c0003 | t0005 | g0104 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18967 | hp1 | a0003 | c0003 | t0003 | g0256 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18968 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18969 | hp1 | a0003 | c0003 | t0012 | g0271 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18969 | hp2 | a0001 | c0001 | t0006 | g0166 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18970 | hp1 | a0006 | c0011 | t0001 | g0009 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0300 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18972 | hp1 | a0004 | c0004 | t0015 | g0133 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18973 | hp1 | a0004 | c0004 | t0005 | g0014 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18974 | hp1 | a0003 | c0003 | t0040 | g0274 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18975 | hp1 | a0003 | c0003 | t0003 | g0257 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18975 | hp2 | a0004 | c0004 | t0002 | g0254 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18977 | hp1 | a0003 | c0003 | t0003 | g0268 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18979 | hp1 | a0002 | c0002 | t0007 | g0055 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0298 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18980 | hp1 | a0003 | c0003 | t0012 | g0280 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18980 | hp2 | a0002 | c0015 | t0009 | g0240 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18982 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18983 | hp1 | a0002 | c0002 | t0022 | g0098 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18984 | hp1 | a0003 | c0003 | t0015 | g0038 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18986 | hp1 | a0001 | c0001 | t0006 | g0197 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18987 | hp1 | a0003 | c0003 | t0003 | g0302 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18987 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18989 | hp1 | a0003 | c0003 | t0003 | g0275 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18990 | hp1 | a0006 | c0011 | t0001 | g0009 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18991 | hp2 | a0003 | c0003 | t0003 | g0293 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18993 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18997 | hp1 | a0004 | c0004 | t0005 | g0014 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18997 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18998 | hp1 | a0001 | c0001 | t0007 | g0204 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19000 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19001 | hp1 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19002 | hp1 | a0003 | c0003 | t0023 | g0103 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19004 | hp1 | a0003 | c0003 | t0003 | g0309 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19005 | hp1 | a0004 | c0004 | t0003 | g0286 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19006 | hp1 | a0001 | c0009 | t0009 | g0259 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19007 | hp1 | a0002 | c0002 | t0011 | g0270 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19010 | hp1 | a0002 | c0002 | t0019 | g0260 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19030 | hp1 | a0001 | c0006 | t0008 | g0094 | AFR | LWK | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19030 | hp2 | a0004 | c0004 | t0005 | g0151 | AFR | LWK | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19043 | hp1 | a0002 | c0005 | t0001 | g0215 | AFR | LWK | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19055 | hp1 | a0003 | c0003 | t0015 | g0102 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19056 | hp1 | a0003 | c0003 | t0003 | g0272 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19057 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0299 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19060 | hp1 | a0003 | c0003 | t0005 | g0043 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19062 | hp1 | a0003 | c0003 | t0003 | g0295 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19063 | hp1 | a0003 | c0003 | t0003 | g0304 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0247 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19065 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19066 | hp1 | a0004 | c0004 | t0003 | g0261 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19067 | hp1 | a0003 | c0003 | t0036 | g0281 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19068 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19070 | hp1 | a0003 | c0003 | t0003 | g0244 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19074 | hp1 | a0002 | c0002 | t0022 | g0099 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19074 | hp2 | a0001 | c0001 | t0014 | g0064 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19075 | hp1 | a0003 | c0003 | t0010 | g0252 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19076 | hp1 | a0001 | c0001 | t0007 | g0137 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19077 | hp1 | a0003 | c0003 | t0003 | g0228 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19078 | hp2 | a0004 | c0004 | t0015 | g0135 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19080 | hp2 | a0002 | c0002 | t0039 | g0278 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19084 | hp1 | a0003 | c0003 | t0003 | g0289 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0284 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19087 | hp1 | a0002 | c0002 | t0009 | g0253 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19087 | hp2 | a0002 | c0002 | t0011 | g0248 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19088 | hp1 | a0003 | c0003 | t0003 | g0020 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19090 | hp1 | a0004 | c0004 | t0003 | g0262 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19090 | hp2 | a0003 | c0003 | t0005 | g0037 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19091 | hp1 | a0001 | c0009 | t0009 | g0231 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19240 | hp1 | a0003 | c0007 | t0003 | g0232 | AFR | YRI | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA19240 | hp2 | a0003 | c0003 | t0005 | g0216 | AFR | YRI | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA20129 | hp1 | a0001 | c0006 | t0017 | g0227 | AFR | ASW | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA20129 | hp2 | a0002 | c0002 | t0016 | g0209 | AFR | ASW | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0017 | EUR | TSI | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA20805 | hp1 | a0003 | c0003 | t0005 | g0196 | EUR | TSI | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0011 | SAS | GIH | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG01123 | hp2 | a0002 | c0005 | t0001 | g0005 | AMR | CLM | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02109 | hp2 | a0003 | c0007 | t0005 | g0036 | AFR | ACB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02486 | hp1 | a0002 | c0005 | t0001 | g0149 | AFR | ACB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG02559 | hp2 | a0003 | c0007 | t0005 | g0146 | AFR | ACB | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG03471 | hp1 | a0005 | c0019 | t0025 | g0210 | AFR | MSL | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG06807 | hp1 | a0003 | c0007 | t0005 | g0145 | AFR | USA | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0042 | AFR | USA | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA20300 | hp1 | a0001 | c0001 | t0013 | g0222 | AFR | USA | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA20300 | hp2 | a0001 | c0006 | t0008 | g0093 | AFR | USA | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA21309 | hp1 | a0003 | c0014 | t0005 | g0125 | AFR | LWK | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0186 | AFR | LWK | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0018 | g0140 | REF | REF | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0136 | REF | REF | ARSD_chrX_2898972_2934339 | ARSD | chrX | 2898972 | 2934339 |
| 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:2907362 | A | G | 5 | a0003 a0004 a0005 others(2): Show |
92 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(89): Show |
missense_variant | MODERATE | c.1691T>C | p.Met564Thr | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 1755/5145 | 1691/1782 | 564/593 | chrX | 2907362 | |||
| chrX:2907471 | G | A | 1 | a0007 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.1582C>T | p.Pro528Ser | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 1646/5145 | 1582/1782 | 528/593 | chrX | 2907471 | |||
| chrX:2907555 | C | T | 2 | a0005 a0008 |
5 | HG01070.hp2 HG01071.hp2 HG02280.hp1 others(2): Show |
missense_variant | MODERATE | c.1498G>A | p.Val500Ile | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 1562/5145 | 1498/1782 | 500/593 | chrX | 2907555 | |||
| chrX:2909889 | C | T | 2 | a0005 a0008 |
5 | HG01070.hp2 HG01071.hp2 HG02280.hp1 others(2): Show |
missense_variant | MODERATE | c.1226G>A | p.Gly409Glu | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/10 | 1290/5145 | 1226/1782 | 409/593 | chrX | 2909889 | |||
| chrX:2917883 | G | C | 1 | a0006 | 2 | NA18970.hp1 NA18990.hp1 |
missense_variant | MODERATE | c.784C>G | p.His262Asp | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/10 | 848/5145 | 784/1782 | 262/593 | chrX | 2917883 | |||
| chrX:2917996 | G | C | 4 | a0001 a0004 a0006 others(1): Show |
152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
missense_variant | MODERATE | c.671C>G | p.Ser224Cys | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/10 | 735/5145 | 671/1782 | 224/593 | chrX | 2917996 |
| 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:2907322 | G | A | 3 | a0005c0008 a0005c0019 a0008c0020 |
5 | HG01070.hp2 HG01071.hp2 HG02280.hp1 others(2): Show |
synonymous_variant | LOW | c.1731C>T | p.Cys577Cys | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 1795/5145 | 1731/1782 | 577/593 | chrX | 2907322 | |||
| chrX:2907463 | G | A | 2 | a0001c0009 a0002c0015 |
4 | NA18954.hp2 NA18980.hp2 NA19006.hp1 others(1): Show |
synonymous_variant | LOW | c.1590C>T | p.Thr530Thr | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 1654/5145 | 1590/1782 | 530/593 | chrX | 2907463 | |||
| chrX:2907577 | C | G | 1 | a0003c0017 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.1476G>C | p.Ala492Ala | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 1540/5145 | 1476/1782 | 492/593 | chrX | 2907577 | |||
| chrX:2907586 | G | A | 1 | a0003c0017 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.1467C>T | p.Pro489Pro | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 1531/5145 | 1467/1782 | 489/593 | chrX | 2907586 | |||
| chrX:2909936 | G | A | 1 | a0003c0018 | 1 | HG00408.hp1 | synonymous_variant | LOW | c.1179C>T | p.Pro393Pro | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/10 | 1243/5145 | 1179/1782 | 393/593 | chrX | 2909936 | |||
| chrX:2910759 | T | C | 2 | a0001c0006 a0002c0010 |
10 | HG01109.hp1 HG02622.hp1 HG03139.hp1 others(7): Show |
synonymous_variant | LOW | c.1035A>G | p.Leu345Leu | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 7/10 | 1099/5145 | 1035/1782 | 345/593 | chrX | 2910759 | |||
| chrX:2915620 | T | C | 3 | a0002c0005 a0003c0007 a0005c0019 |
23 | HG01074.hp1 HG01123.hp2 HG01243.hp1 others(20): Show |
synonymous_variant | LOW | c.936A>G | p.Ala312Ala | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/10 | 1000/5145 | 936/1782 | 312/593 | chrX | 2915620 | |||
| chrX:2918043 | C | G | 1 | a0003c0014 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.624G>C | p.Ala208Ala | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/10 | 688/5145 | 624/1782 | 208/593 | chrX | 2918043 | |||
| chrX:2920611 | G | T | 1 | a0002c0013 | 1 | NA18942.hp2 | synonymous_variant | LOW | c.429C>A | p.Thr143Thr | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/10 | 493/5145 | 429/1782 | 143/593 | chrX | 2920611 | |||
| chrX:2925666 | C | T | 1 | a0004c0012 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.144G>A | p.Ala48Ala | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/10 | 208/5145 | 144/1782 | 48/593 | chrX | 2925666 |
| 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:2903980 | T | C | 1 | a0003c0017t0034 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3291A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 3291 | chrX | 2903980 | ||||||
| chrX:2904212 | C | T | 27 | a0001c0001t0013 a0001c0001t0029 a0001c0006t0008 others(24): Show |
97 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*3059G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 3059 | chrX | 2904212 | ||||||
| chrX:2904560 | G | T | 27 | a0001c0001t0013 a0001c0001t0029 a0001c0006t0008 others(24): Show |
97 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*2711C>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 2711 | chrX | 2904560 | ||||||
| chrX:2904903 | CT | C | 27 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0029 others(24): Show |
87 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*2367delA | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 2367 | chrX | 2904903 | ||||||
| chrX:2904903 | CTT | C | 4 | a0003c0003t0012 a0003c0003t0023 a0003c0018t0012 others(1): Show |
8 | HG00408.hp1 HG00558.hp1 HG01070.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2366_*2367delAA | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 2366 | chrX | 2904903 | ||||||
| chrX:2905017 | C | T | 1 | a0002c0002t0016 | 3 | HG02257.hp1 HG02809.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2254G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 2254 | chrX | 2905017 | ||||||
| chrX:2905258 | C | T | 3 | a0001c0006t0008 a0001c0006t0017 a0002c0010t0008 |
10 | HG01109.hp1 HG02622.hp1 HG03139.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2013G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 2013 | chrX | 2905258 | ||||||
| chrX:2905337 | A | G | 1 | a0002c0005t0028 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1934T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 1934 | chrX | 2905337 | ||||||
| chrX:2905361 | C | T | 2 | a0001c0001t0018 a0002c0002t0018 |
2 | HG01168.hp2 HG01516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1910G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 1910 | chrX | 2905361 | ||||||
| chrX:2905438 | A | G | 4 | a0001c0001t0029 a0005c0008t0020 a0005c0008t0026 others(1): Show |
5 | HG01070.hp2 HG01071.hp2 HG02145.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1833T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 1833 | chrX | 2905438 | ||||||
| chrX:2905544 | C | T | 26 | a0001c0001t0013 a0001c0001t0029 a0001c0006t0008 others(23): Show |
96 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*1727G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 1727 | chrX | 2905544 | ||||||
| chrX:2905617 | T | A | 18 | a0003c0003t0003 a0003c0003t0005 a0003c0003t0012 others(15): Show |
77 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1654A>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 1654 | chrX | 2905617 | ||||||
| chrX:2905642 | T | G | 26 | a0001c0001t0013 a0001c0001t0029 a0001c0006t0008 others(23): Show |
96 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*1629A>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 1629 | chrX | 2905642 | ||||||
| chrX:2905713 | C | T | 1 | a0002c0002t0027 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1558G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 1558 | chrX | 2905713 | ||||||
| chrX:2905857 | T | C | 4 | a0001c0001t0029 a0005c0008t0020 a0005c0008t0026 others(1): Show |
5 | HG01070.hp2 HG01071.hp2 HG02145.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1414A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 1414 | chrX | 2905857 | ||||||
| chrX:2906084 | G | A | 1 | a0001c0001t0030 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1187C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 1187 | chrX | 2906084 | ||||||
| chrX:2906110 | C | T | 1 | a0002c0002t0039 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1161G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 1161 | chrX | 2906110 | ||||||
| chrX:2906134 | G | A | 1 | a0001c0001t0031 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1137C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 1137 | chrX | 2906134 | ||||||
| chrX:2906136 | A | AT | 4 | a0001c0001t0007 a0002c0002t0007 a0002c0002t0037 others(1): Show |
9 | HG00733.hp2 HG01081.hp2 HG01192.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1134dupA | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 1134 | chrX | 2906136 | ||||||
| chrX:2906136 | AT | A | 25 | a0001c0001t0006 a0001c0001t0011 a0001c0001t0013 others(22): Show |
103 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*1134delA | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 1134 | chrX | 2906136 | ||||||
| chrX:2906136 | ATTTTTTT | A | 9 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0018 others(6): Show |
34 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1128_*1134delAAAA others(3): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 1128 | chrX | 2906136 | ||||||
| chrX:2906169 | A | G | 16 | a0003c0003t0003 a0003c0003t0005 a0003c0003t0012 others(13): Show |
75 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1102T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 1102 | chrX | 2906169 | ||||||
| chrX:2906287 | G | A | 1 | a0003c0003t0035 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*984C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 984 | chrX | 2906287 | ||||||
| chrX:2906722 | G | A | 3 | a0002c0002t0019 a0002c0002t0022 a0002c0002t0032 |
6 | HG00438.hp2 HG02129.hp1 HG02155.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*549C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 549 | chrX | 2906722 | ||||||
| chrX:2906744 | C | G | 4 | a0005c0008t0020 a0005c0008t0026 a0005c0019t0025 others(1): Show |
5 | HG01070.hp2 HG01071.hp2 HG02280.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*527G>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 527 | chrX | 2906744 | ||||||
| chrX:2907001 | T | C | 16 | a0003c0003t0003 a0003c0003t0005 a0003c0003t0012 others(13): Show |
75 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*270A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 270 | chrX | 2907001 | ||||||
| chrX:2907042 | G | A | 1 | a0001c0001t0013 | 4 | HG02280.hp2 HG03098.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*229C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 229 | chrX | 2907042 | ||||||
| chrX:2907093 | A | G | 23 | a0001c0001t0013 a0003c0003t0003 a0003c0003t0005 others(20): Show |
86 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*178T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 178 | chrX | 2907093 | ||||||
| chrX:2907116 | C | CAAAA | 17 | a0003c0003t0003 a0003c0003t0005 a0003c0003t0012 others(14): Show |
76 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*151_*154dupTTTT | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 154 | chrX | 2907116 | ||||||
| chrX:2907123 | G | A | 3 | a0001c0006t0008 a0001c0006t0017 a0002c0010t0008 |
10 | HG01109.hp1 HG02622.hp1 HG03139.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*148C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 10/10 | 148 | chrX | 2907123 | ||||||
| chrX:2929329 | G | A | 26 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0010 others(23): Show |
104 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(101): Show |
5_prime_UTR_variant | MODIFIER | c.-54C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/10 | 54 | chrX | 2929329 |
| 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:2907713 | T | A | 63 | a0003c0003t0003g0001 a0003c0003t0003g0020 a0003c0003t0003g0228 others(60): Show |
76 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.1421-81A>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 9/9 | chrX | 2907713 | |||||||
| chrX:2907737 | G | A | 63 | a0003c0003t0003g0001 a0003c0003t0003g0020 a0003c0003t0003g0228 others(60): Show |
76 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.1421-105C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 9/9 | chrX | 2907737 | |||||||
| chrX:2907756 | C | T | 1 | a0002c0002t0014g0027 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1421-124G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 9/9 | chrX | 2907756 | |||||||
| chrX:2907762 | A | G | 1 | a0002c0002t0002g0247 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1421-130T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 9/9 | chrX | 2907762 | |||||||
| chrX:2907822 | G | C | 1 | a0003c0017t0034g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1421-190C>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 9/9 | chrX | 2907822 | |||||||
| chrX:2907886 | G | A | 62 | a0003c0003t0003g0001 a0003c0003t0003g0020 a0003c0003t0003g0228 others(59): Show |
75 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.1421-254C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 9/9 | chrX | 2907886 | |||||||
| chrX:2908129 | G | A | 69 | a0002c0002t0001g0116 a0002c0002t0002g0299 a0002c0002t0002g0300 others(66): Show |
83 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.1421-497C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 9/9 | chrX | 2908129 | |||||||
| chrX:2908132 | CATCT | C | 4 | a0001c0001t0013g0167 a0001c0001t0013g0208 a0001c0001t0013g0219 others(1): Show |
4 | HG02280.hp2 HG03098.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1421-504_1421-501d others(6): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 9/9 | chrX | 2908132 | |||||||
| chrX:2908198 | T | C | 67 | a0002c0002t0001g0116 a0002c0002t0002g0299 a0002c0002t0002g0300 others(64): Show |
80 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.1420+523A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 9/9 | chrX | 2908198 | |||||||
| chrX:2908231 | T | TTATCTAT others(5): Show |
1 | a0003c0017t0034g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1420+478_1420+489d others(14): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 9/9 | chrX | 2908231 | |||||||
| chrX:2908231 | T | TTATCTAT others(21): Show |
2 | a0005c0008t0020g0006 a0005c0008t0026g0032 |
3 | HG01070.hp2 HG01071.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1420+489_1420+490i others(30): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 9/9 | chrX | 2908231 | |||||||
| chrX:2908231 | T | TTATCTAT others(25): Show |
1 | a0005c0019t0025g0210 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1420+489_1420+490i others(34): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 9/9 | chrX | 2908231 | |||||||
| chrX:2908238 | T | TCTATCTA others(21): Show |
1 | a0008c0020t0024g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1420+482_1420+483i others(30): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 9/9 | chrX | 2908238 | |||||||
| chrX:2908252 | A | G | 72 | a0001c0001t0001g0030 a0001c0001t0001g0045 a0001c0001t0001g0046 others(69): Show |
77 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.1420+469T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 9/9 | chrX | 2908252 | |||||||
| chrX:2908382 | T | C | 1 | a0003c0017t0034g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1420+339A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 9/9 | chrX | 2908382 | |||||||
| chrX:2908534 | T | C | 1 | a0001c0001t0011g0290 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1420+187A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 9/9 | chrX | 2908534 | |||||||
| chrX:2908534 | T | TC | 21 | a0001c0001t0001g0114 a0001c0001t0001g0172 a0001c0001t0001g0177 others(18): Show |
21 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(18): Show |
intron_variant | MODIFIER | c.1420+186dupG | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 9/9 | chrX | 2908534 | |||||||
| chrX:2908534 | T | TCC | 35 | a0001c0001t0001g0030 a0001c0001t0001g0045 a0001c0001t0001g0158 others(32): Show |
39 | HG00099.hp1 HG00597.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1420+185_1420+186d others(4): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 9/9 | chrX | 2908534 | |||||||
| chrX:2908535 | C | CT | 68 | a0002c0002t0001g0116 a0002c0002t0002g0299 a0002c0002t0002g0300 others(65): Show |
81 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1420+185_1420+186i others(3): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 9/9 | chrX | 2908535 | |||||||
| chrX:2908535 | C | CTCT | 4 | a0005c0008t0020g0006 a0005c0008t0026g0032 a0005c0019t0025g0210 others(1): Show |
5 | HG01070.hp2 HG01071.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1420+185_1420+186i others(5): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 9/9 | chrX | 2908535 | |||||||
| chrX:2908541 | C | T | 5 | a0003c0017t0034g0206 a0005c0008t0020g0006 a0005c0008t0026g0032 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1420+180G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 9/9 | chrX | 2908541 | |||||||
| chrX:2908605 | T | TCCAC | 4 | a0005c0008t0020g0006 a0005c0008t0026g0032 a0005c0019t0025g0210 others(1): Show |
5 | HG01070.hp2 HG01071.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1420+112_1420+115d others(6): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 9/9 | chrX | 2908605 | |||||||
| chrX:2908966 | T | A | 1 | a0001c0001t0004g0165 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1299-124A>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/9 | chrX | 2908966 | |||||||
| chrX:2909080 | G | GCA | 13 | a0001c0001t0001g0084 a0001c0001t0001g0195 a0001c0001t0029g0143 others(10): Show |
13 | HG00280.hp1 HG01109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1299-240_1299-239d others(4): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/9 | chrX | 2909080 | |||||||
| chrX:2909080 | G | GCACA | 5 | a0003c0003t0012g0271 a0003c0003t0012g0273 a0003c0003t0012g0280 others(2): Show |
5 | HG03579.hp1 NA18948.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.1299-242_1299-239d others(6): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/9 | chrX | 2909080 | |||||||
| chrX:2909080 | G | GCACACA | 4 | a0005c0008t0020g0006 a0005c0008t0026g0032 a0005c0019t0025g0210 others(1): Show |
5 | HG01070.hp2 HG01071.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1299-244_1299-239d others(8): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/9 | chrX | 2909080 | |||||||
| chrX:2909080 | G | GCACACAC others(1): Show |
4 | a0002c0002t0001g0116 a0002c0002t0002g0305 a0002c0005t0021g0077 others(1): Show |
4 | HG01074.hp1 HG02056.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1299-246_1299-239d others(10): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/9 | chrX | 2909080 | |||||||
| chrX:2909080 | G | GCACACAC others(3): Show |
53 | a0002c0002t0002g0299 a0002c0002t0002g0300 a0003c0003t0003g0001 others(50): Show |
66 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.1299-248_1299-239d others(12): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/9 | chrX | 2909080 | |||||||
| chrX:2909080 | G | GCACACAC others(5): Show |
2 | a0004c0004t0015g0133 a0004c0004t0015g0135 |
2 | NA18972.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1299-250_1299-239d others(14): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/9 | chrX | 2909080 | |||||||
| chrX:2909193 | CT | C | 5 | a0004c0004t0003g0286 a0005c0008t0020g0006 a0005c0008t0026g0032 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1299-352delA | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/9 | chrX | 2909193 | |||||||
| chrX:2909308 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1299-466G>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/9 | chrX | 2909308 | |||||||
| chrX:2909327 | A | G | 1 | a0003c0007t0003g0232 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1299-485T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/9 | chrX | 2909327 | |||||||
| chrX:2909330 | G | A | 53 | a0001c0001t0001g0030 a0001c0001t0001g0045 a0001c0001t0001g0046 others(50): Show |
58 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1298+487C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/9 | chrX | 2909330 | |||||||
| chrX:2909360 | G | A | 63 | a0002c0002t0001g0116 a0002c0002t0002g0299 a0002c0002t0002g0300 others(60): Show |
76 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.1298+457C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/9 | chrX | 2909360 | |||||||
| chrX:2909431 | G | A | 1 | a0002c0002t0001g0070 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1298+386C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/9 | chrX | 2909431 | |||||||
| chrX:2909524 | A | G | 2 | a0002c0002t0002g0266 a0002c0002t0002g0284 |
2 | NA18951.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1298+293T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/9 | chrX | 2909524 | |||||||
| chrX:2909551 | G | A | 1 | a0003c0017t0034g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1298+266C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/9 | chrX | 2909551 | |||||||
| chrX:2909552 | C | T | 1 | a0003c0017t0034g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1298+265G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/9 | chrX | 2909552 | |||||||
| chrX:2909554 | C | G | 1 | a0003c0017t0034g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1298+263G>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/9 | chrX | 2909554 | |||||||
| chrX:2909639 | A | G | 63 | a0002c0002t0001g0116 a0002c0002t0002g0299 a0002c0002t0002g0300 others(60): Show |
76 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.1298+178T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/9 | chrX | 2909639 | |||||||
| chrX:2909669 | G | A | 3 | a0001c0001t0001g0132 a0002c0002t0002g0247 a0002c0002t0002g0298 |
3 | HG00423.hp2 NA18979.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1298+148C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/9 | chrX | 2909669 | |||||||
| chrX:2909683 | C | CA | 16 | a0001c0001t0001g0109 a0001c0001t0001g0153 a0001c0001t0001g0175 others(13): Show |
16 | HG00597.hp1 HG00741.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.1298+133dupT | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/9 | chrX | 2909683 | |||||||
| chrX:2909683 | CA | C | 61 | a0001c0001t0001g0003 a0001c0001t0001g0155 a0001c0001t0001g0157 others(58): Show |
76 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.1298+133delT | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/9 | chrX | 2909683 | |||||||
| chrX:2909683 | CAA | C | 7 | a0002c0002t0002g0299 a0003c0003t0003g0272 a0003c0003t0005g0104 others(4): Show |
7 | HG02615.hp1 HG02922.hp2 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1298+132_1298+133d others(4): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/9 | chrX | 2909683 | |||||||
| chrX:2909719 | CA | C | 5 | a0003c0017t0034g0206 a0005c0008t0020g0006 a0005c0008t0026g0032 others(2): Show |
6 | HG01070.hp2 HG01071.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1298+97delT | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/9 | chrX | 2909719 | |||||||
| chrX:2909753 | T | TA | 68 | a0001c0001t0001g0124 a0001c0001t0001g0129 a0001c0001t0001g0130 others(65): Show |
82 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.1298+63dupT | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/9 | chrX | 2909753 | |||||||
| chrX:2909778 | A | T | 2 | a0002c0005t0021g0077 a0002c0005t0021g0211 |
2 | HG01074.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1298+39T>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 8/9 | chrX | 2909778 | |||||||
| chrX:2910011 | C | T | 1 | a0002c0002t0002g0308 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1136-32G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 7/9 | chrX | 2910011 | |||||||
| chrX:2910064 | G | A | 1 | a0003c0003t0003g0302 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1136-85C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 7/9 | chrX | 2910064 | |||||||
| chrX:2910081 | C | T | 23 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0040 others(20): Show |
26 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.1136-102G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 7/9 | chrX | 2910081 | |||||||
| chrX:2910212 | G | A | 1 | a0002c0005t0021g0211 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1136-233C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 7/9 | chrX | 2910212 | |||||||
| chrX:2910316 | T | TTAA | 143 | a0001c0001t0001g0030 a0001c0001t0001g0045 a0001c0001t0001g0046 others(140): Show |
162 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.1136-338_1136-337i others(5): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 7/9 | chrX | 2910316 | |||||||
| chrX:2910344 | TTTAAAAT others(1): Show |
T | 4 | a0001c0001t0001g0030 a0001c0001t0014g0100 a0002c0005t0001g0005 others(1): Show |
5 | HG01123.hp2 HG01496.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1135+307_1135+314d others(10): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 7/9 | chrX | 2910344 | |||||||
| chrX:2910367 | A | C | 1 | a0003c0014t0005g0125 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1135+292T>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 7/9 | chrX | 2910367 | |||||||
| chrX:2910530 | C | T | 3 | a0002c0002t0016g0097 a0002c0002t0016g0209 a0002c0002t0016g0220 |
3 | HG02257.hp1 HG02809.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1135+129G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 7/9 | chrX | 2910530 | |||||||
| chrX:2911151 | C | G | 1 | a0004c0004t0033g0152 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1001-358G>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2911151 | |||||||
| chrX:2911580 | G | A | 60 | a0002c0002t0001g0116 a0002c0002t0002g0299 a0002c0002t0002g0300 others(57): Show |
73 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1001-787C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2911580 | |||||||
| chrX:2911669 | C | CA | 8 | a0001c0001t0001g0046 a0001c0001t0001g0076 a0001c0001t0001g0177 others(5): Show |
8 | HG02559.hp2 HG02738.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1001-877dupT | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2911669 | |||||||
| chrX:2911684 | AAG | A | 60 | a0002c0002t0001g0116 a0002c0002t0002g0299 a0002c0002t0002g0300 others(57): Show |
73 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.1001-893_1001-892d others(4): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2911684 | |||||||
| chrX:2911687 | A | G | 62 | a0002c0002t0001g0116 a0002c0002t0002g0299 a0002c0002t0002g0300 others(59): Show |
75 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.1001-894T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2911687 | |||||||
| chrX:2911697 | C | A | 1 | a0003c0017t0034g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1001-904G>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2911697 | |||||||
| chrX:2911735 | T | A | 62 | a0002c0002t0001g0116 a0002c0002t0002g0299 a0002c0002t0002g0300 others(59): Show |
75 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.1001-942A>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2911735 | |||||||
| chrX:2911962 | C | G | 63 | a0002c0002t0001g0116 a0002c0002t0002g0296 a0002c0002t0002g0299 others(60): Show |
76 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.1001-1169G>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2911962 | |||||||
| chrX:2912050 | G | C | 19 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0155 others(16): Show |
20 | HG01070.hp2 HG01071.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.1001-1257C>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2912050 | |||||||
| chrX:2912050 | G | T | 70 | a0001c0001t0001g0030 a0001c0001t0001g0045 a0001c0001t0001g0046 others(67): Show |
75 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1001-1257C>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2912050 | |||||||
| chrX:2912227 | G | A | 1 | a0001c0001t0006g0166 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1001-1434C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2912227 | |||||||
| chrX:2912250 | T | C | 153 | a0001c0001t0001g0030 a0001c0001t0001g0045 a0001c0001t0001g0046 others(150): Show |
171 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.1001-1457A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2912250 | |||||||
| chrX:2912311 | A | C | 1 | a0001c0001t0031g0176 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1001-1518T>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2912311 | |||||||
| chrX:2912312 | C | T | 1 | a0001c0001t0031g0176 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1001-1519G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2912312 | |||||||
| chrX:2912313 | T | C | 1 | a0001c0001t0031g0176 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1001-1520A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2912313 | |||||||
| chrX:2912319 | A | G | 1 | a0004c0004t0005g0151 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1001-1526T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2912319 | |||||||
| chrX:2912525 | G | T | 1 | a0003c0007t0003g0232 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1001-1732C>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2912525 | |||||||
| chrX:2912593 | C | G | 57 | a0002c0002t0001g0116 a0002c0002t0002g0296 a0002c0002t0002g0299 others(54): Show |
70 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1001-1800G>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2912593 | |||||||
| chrX:2912780 | A | G | 15 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0155 others(12): Show |
15 | HG01261.hp1 HG02280.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1001-1987T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2912780 | |||||||
| chrX:2912974 | G | A | 1 | a0005c0019t0025g0210 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1001-2181C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2912974 | |||||||
| chrX:2913259 | C | G | 4 | a0002c0005t0001g0213 a0002c0005t0001g0215 a0002c0005t0006g0214 others(1): Show |
4 | HG03195.hp1 NA18522.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000+2297G>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2913259 | |||||||
| chrX:2913399 | T | C | 7 | a0001c0001t0001g0124 a0001c0001t0001g0153 a0002c0005t0001g0213 others(4): Show |
7 | HG02109.hp1 HG03195.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1000+2157A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2913399 | |||||||
| chrX:2913450 | A | C | 1 | a0001c0001t0001g0163 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1000+2106T>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2913450 | |||||||
| chrX:2913506 | G | A | 1 | a0003c0014t0005g0125 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1000+2050C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2913506 | |||||||
| chrX:2913519 | G | A | 4 | a0001c0001t0001g0123 a0003c0003t0005g0080 a0003c0014t0005g0125 others(1): Show |
4 | HG01884.hp2 HG02630.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000+2037C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2913519 | |||||||
| chrX:2913540 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1000+2016G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2913540 | |||||||
| chrX:2913541 | G | A | 1 | a0003c0014t0005g0125 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1000+2015C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2913541 | |||||||
| chrX:2913645 | G | C | 7 | a0002c0005t0001g0149 a0003c0007t0005g0144 a0003c0007t0005g0145 others(4): Show |
8 | HG01070.hp2 HG01071.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1000+1911C>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2913645 | |||||||
| chrX:2913716 | T | C | 1 | a0003c0003t0023g0103 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1000+1840A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2913716 | |||||||
| chrX:2913746 | G | C | 10 | a0002c0002t0001g0008 a0002c0002t0001g0021 a0002c0002t0001g0041 others(7): Show |
11 | HG00323.hp1 HG00597.hp1 NA18941.hp2 others(8): Show |
intron_variant | MODIFIER | c.1000+1810C>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2913746 | |||||||
| chrX:2913796 | G | A | 1 | a0001c0001t0013g0208 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1000+1760C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2913796 | |||||||
| chrX:2913803 | G | C | 1 | a0002c0002t0001g0183 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1000+1753C>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2913803 | |||||||
| chrX:2913881 | G | A | 11 | a0002c0002t0016g0209 a0002c0005t0001g0194 a0002c0005t0001g0213 others(8): Show |
11 | HG02622.hp1 HG02886.hp2 HG03195.hp1 others(8): Show |
intron_variant | MODIFIER | c.1000+1675C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2913881 | |||||||
| chrX:2913908 | G | C | 5 | a0002c0002t0007g0026 a0003c0003t0023g0108 a0004c0004t0005g0151 others(2): Show |
6 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000+1648C>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2913908 | |||||||
| chrX:2913960 | A | G | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(146): Show |
163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1000+1596T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2913960 | |||||||
| chrX:2914224 | G | A | 1 | a0001c0001t0004g0179 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1000+1332C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2914224 | |||||||
| chrX:2914235 | C | CT | 80 | a0001c0001t0007g0137 a0002c0002t0001g0022 a0002c0002t0001g0072 others(77): Show |
96 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1000+1320dupA | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2914235 | |||||||
| chrX:2914256 | G | C | 2 | a0001c0001t0002g0306 a0001c0001t0009g0307 |
2 | HG02027.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1000+1300C>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2914256 | |||||||
| chrX:2914326 | G | A | 1 | a0001c0001t0031g0176 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1000+1230C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2914326 | |||||||
| chrX:2914357 | G | A | 3 | a0002c0002t0001g0083 a0002c0002t0006g0082 a0003c0003t0001g0221 |
3 | HG01891.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1000+1199C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2914357 | |||||||
| chrX:2914418 | T | TG | 18 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0002c0002t0001g0021 others(15): Show |
18 | HG00544.hp2 HG00597.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.1000+1137dupC | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2914418 | |||||||
| chrX:2914418 | TG | T | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(115): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1000+1137delC | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2914418 | |||||||
| chrX:2914418 | TGGG | T | 78 | a0002c0002t0001g0022 a0002c0002t0001g0072 a0002c0002t0001g0079 others(75): Show |
94 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1000+1135_1000+113 others(7): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2914418 | |||||||
| chrX:2914421 | G | C | 2 | a0001c0001t0001g0124 a0001c0001t0001g0153 |
2 | HG02109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1000+1135C>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2914421 | |||||||
| chrX:2914422 | G | C | 1 | a0001c0001t0001g0169 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1000+1134C>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2914422 | |||||||
| chrX:2914423 | G | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0177 |
2 | NA18945.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1000+1133C>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2914423 | |||||||
| chrX:2914432 | G | A | 1 | a0003c0003t0023g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1000+1124C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2914432 | |||||||
| chrX:2914510 | G | A | 1 | a0003c0014t0005g0125 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1000+1046C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2914510 | |||||||
| chrX:2914698 | C | T | 76 | a0002c0002t0001g0022 a0002c0002t0001g0072 a0002c0002t0001g0079 others(73): Show |
92 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1000+858G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2914698 | |||||||
| chrX:2914701 | G | C | 257 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(254): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1000+855C>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2914701 | |||||||
| chrX:2914999 | C | T | 1 | a0001c0009t0009g0230 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1000+557G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2914999 | |||||||
| chrX:2915099 | C | G | 85 | a0002c0002t0001g0022 a0002c0002t0001g0042 a0002c0002t0001g0048 others(82): Show |
101 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1000+457G>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2915099 | |||||||
| chrX:2915177 | C | T | 1 | a0004c0004t0005g0107 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1000+379G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2915177 | |||||||
| chrX:2915236 | C | G | 1 | a0003c0003t0023g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1000+320G>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2915236 | |||||||
| chrX:2915257 | C | T | 80 | a0002c0002t0001g0022 a0002c0002t0001g0042 a0002c0002t0001g0048 others(77): Show |
96 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1000+299G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2915257 | |||||||
| chrX:2915279 | C | G | 81 | a0002c0002t0001g0022 a0002c0002t0001g0042 a0002c0002t0001g0048 others(78): Show |
97 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1000+277G>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2915279 | |||||||
| chrX:2915311 | C | T | 80 | a0002c0002t0001g0022 a0002c0002t0001g0042 a0002c0002t0001g0048 others(77): Show |
96 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1000+245G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2915311 | |||||||
| chrX:2915445 | G | A | 2 | a0002c0005t0001g0005 a0002c0005t0001g0029 |
3 | HG01123.hp2 HG01496.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1000+111C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2915445 | |||||||
| chrX:2915465 | G | C | 258 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(255): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1000+91C>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2915465 | |||||||
| chrX:2915495 | A | T | 2 | a0001c0001t0002g0306 a0001c0001t0009g0307 |
2 | HG02027.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1000+61T>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2915495 | |||||||
| chrX:2915511 | C | G | 2 | a0001c0001t0004g0011 a0001c0001t0004g0101 |
3 | NA18957.hp1 NA19001.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1000+45G>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2915511 | |||||||
| chrX:2915514 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1000+42C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 6/9 | chrX | 2915514 | |||||||
| chrX:2915815 | T | C | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(251): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.864-123A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2915815 | |||||||
| chrX:2915885 | A | C | 24 | a0002c0002t0001g0111 a0002c0005t0001g0005 a0002c0005t0001g0029 others(21): Show |
25 | HG01074.hp1 HG01123.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.864-193T>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2915885 | |||||||
| chrX:2915950 | G | A | 1 | a0002c0002t0001g0069 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.864-258C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2915950 | |||||||
| chrX:2916029 | G | A | 2 | a0003c0003t0012g0271 a0003c0003t0012g0280 |
2 | NA18969.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.864-337C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2916029 | |||||||
| chrX:2916032 | C | T | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(247): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.864-340G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2916032 | |||||||
| chrX:2916060 | A | G | 12 | a0002c0002t0001g0111 a0002c0005t0001g0149 a0002c0005t0001g0194 others(9): Show |
12 | HG01891.hp1 HG02486.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.864-368T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2916060 | |||||||
| chrX:2916131 | C | CA | 77 | a0001c0001t0031g0176 a0002c0002t0001g0021 a0002c0002t0001g0022 others(74): Show |
93 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.864-440dupT | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2916131 | |||||||
| chrX:2916131 | C | CAA | 11 | a0001c0001t0001g0068 a0001c0001t0001g0087 a0001c0001t0001g0180 others(8): Show |
11 | HG01070.hp1 HG01081.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.864-441_864-440dup others(2): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2916131 | |||||||
| chrX:2916131 | C | CAAA | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(131): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.864-442_864-440dup others(3): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2916131 | |||||||
| chrX:2916131 | C | CAAAA | 12 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0114 others(9): Show |
12 | HG01256.hp1 HG01496.hp2 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.864-443_864-440dup others(4): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2916131 | |||||||
| chrX:2916131 | CA | C | 22 | a0002c0002t0001g0111 a0002c0005t0001g0005 a0002c0005t0001g0029 others(19): Show |
23 | HG01074.hp1 HG01123.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.864-440delT | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2916131 | |||||||
| chrX:2916189 | A | G | 4 | a0001c0001t0004g0017 a0001c0001t0004g0159 a0001c0001t0004g0160 others(1): Show |
5 | HG00639.hp2 HG01358.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.864-497T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2916189 | |||||||
| chrX:2916360 | G | T | 24 | a0001c0001t0001g0030 a0002c0002t0001g0111 a0002c0005t0001g0005 others(21): Show |
25 | HG01074.hp1 HG01123.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.864-668C>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2916360 | |||||||
| chrX:2916369 | G | T | 23 | a0002c0002t0001g0111 a0002c0005t0001g0005 a0002c0005t0001g0029 others(20): Show |
24 | HG01074.hp1 HG01123.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.864-677C>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2916369 | |||||||
| chrX:2916375 | G | A | 12 | a0002c0002t0001g0111 a0002c0005t0001g0149 a0002c0005t0001g0194 others(9): Show |
12 | HG01891.hp1 HG02486.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.864-683C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2916375 | |||||||
| chrX:2916414 | C | T | 85 | a0002c0002t0001g0022 a0002c0002t0001g0042 a0002c0002t0001g0048 others(82): Show |
101 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.864-722G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2916414 | |||||||
| chrX:2916489 | G | C | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(256): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.864-797C>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2916489 | |||||||
| chrX:2916527 | G | A | 1 | a0002c0002t0001g0050 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.864-835C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2916527 | |||||||
| chrX:2916682 | C | T | 85 | a0002c0002t0001g0022 a0002c0002t0001g0042 a0002c0002t0001g0048 others(82): Show |
101 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.864-990G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2916682 | |||||||
| chrX:2916799 | C | T | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(256): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.863+1005G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2916799 | |||||||
| chrX:2917066 | CA | C | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(205): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.863+737delT | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2917066 | |||||||
| chrX:2917066 | CAA | C | 21 | a0001c0001t0004g0078 a0001c0001t0007g0137 a0001c0001t0007g0200 others(18): Show |
21 | HG00408.hp1 HG00673.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.863+736_863+737del others(2): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2917066 | |||||||
| chrX:2917087 | AT | A | 13 | a0001c0001t0001g0030 a0002c0002t0002g0284 a0002c0005t0001g0005 others(10): Show |
14 | HG01074.hp1 HG01123.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.863+716delA | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2917087 | |||||||
| chrX:2917088 | T | A | 1 | a0003c0007t0005g0036 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.863+716A>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2917088 | |||||||
| chrX:2917282 | C | T | 4 | a0001c0001t0001g0109 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
4 | HG00741.hp2 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.863+522G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2917282 | |||||||
| chrX:2917430 | T | G | 6 | a0002c0002t0001g0118 a0002c0002t0010g0229 a0002c0002t0016g0209 others(3): Show |
6 | HG02622.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.863+374A>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2917430 | |||||||
| chrX:2917454 | G | C | 12 | a0002c0002t0001g0111 a0002c0005t0001g0149 a0002c0005t0001g0194 others(9): Show |
12 | HG01891.hp1 HG02486.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.863+350C>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2917454 | |||||||
| chrX:2917542 | T | C | 5 | a0002c0002t0001g0118 a0002c0002t0010g0229 a0002c0002t0016g0209 others(2): Show |
5 | HG02622.hp1 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.863+262A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2917542 | |||||||
| chrX:2917565 | C | T | 1 | a0002c0002t0002g0298 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.863+239G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2917565 | |||||||
| chrX:2917638 | T | A | 1 | a0002c0002t0010g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.863+166A>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2917638 | |||||||
| chrX:2917648 | A | C | 2 | a0002c0010t0008g0033 a0002c0010t0008g0034 |
2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.863+156T>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2917648 | |||||||
| chrX:2917753 | G | A | 24 | a0002c0002t0001g0111 a0002c0005t0001g0005 a0002c0005t0001g0029 others(21): Show |
25 | HG01074.hp1 HG01123.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.863+51C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2917753 | |||||||
| chrX:2917754 | A | G | 12 | a0002c0002t0001g0111 a0002c0005t0001g0149 a0002c0005t0001g0194 others(9): Show |
12 | HG01891.hp1 HG02486.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.863+50T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 5/9 | chrX | 2917754 | |||||||
| chrX:2918241 | A | C | 2 | a0002c0002t0002g0242 a0002c0002t0002g0243 |
2 | NA18950.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.440-14T>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2918241 | |||||||
| chrX:2918360 | A | G | 2 | a0002c0002t0002g0019 a0002c0002t0011g0270 |
3 | NA18955.hp1 NA18994.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.440-133T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2918360 | |||||||
| chrX:2918472 | C | G | 4 | a0002c0002t0001g0118 a0002c0002t0016g0209 a0002c0010t0008g0033 others(1): Show |
4 | HG02622.hp1 HG02723.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.440-245G>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2918472 | |||||||
| chrX:2918532 | C | T | 1 | a0002c0002t0032g0115 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.440-305G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2918532 | |||||||
| chrX:2918567 | G | A | 1 | a0003c0003t0005g0216 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.440-340C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2918567 | |||||||
| chrX:2918619 | A | G | 3 | a0003c0003t0023g0108 a0005c0008t0020g0006 a0005c0008t0026g0032 |
4 | HG01070.hp2 HG01071.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.440-392T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2918619 | |||||||
| chrX:2918664 | T | C | 5 | a0001c0001t0002g0306 a0001c0001t0004g0011 a0001c0001t0004g0078 others(2): Show |
6 | HG02027.hp1 HG02080.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.440-437A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2918664 | |||||||
| chrX:2918689 | G | C | 1 | a0002c0002t0001g0183 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.440-462C>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2918689 | |||||||
| chrX:2918695 | A | C | 3 | a0001c0001t0001g0030 a0002c0005t0001g0005 a0002c0005t0001g0029 |
4 | HG01123.hp2 HG01496.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.440-468T>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2918695 | |||||||
| chrX:2918695 | A | G | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(233): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.440-468T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2918695 | |||||||
| chrX:2918696 | T | C | 239 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(236): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.440-469A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2918696 | |||||||
| chrX:2918704 | C | T | 1 | a0001c0001t0009g0292 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.440-477G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2918704 | |||||||
| chrX:2918705 | A | G | 2 | a0005c0008t0020g0006 a0005c0008t0026g0032 |
3 | HG01070.hp2 HG01071.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.440-478T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2918705 | |||||||
| chrX:2918726 | C | G | 3 | a0003c0003t0023g0108 a0005c0008t0020g0006 a0005c0008t0026g0032 |
4 | HG01070.hp2 HG01071.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.440-499G>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2918726 | |||||||
| chrX:2918746 | C | T | 251 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(248): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.440-519G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2918746 | |||||||
| chrX:2918809 | T | C | 5 | a0002c0002t0001g0118 a0002c0002t0010g0229 a0002c0002t0016g0209 others(2): Show |
5 | HG02622.hp1 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.440-582A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2918809 | |||||||
| chrX:2918933 | C | G | 1 | a0001c0001t0001g0158 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.440-706G>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2918933 | |||||||
| chrX:2918957 | T | C | 3 | a0002c0002t0001g0083 a0002c0002t0006g0082 a0003c0003t0001g0221 |
3 | HG01891.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.440-730A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2918957 | |||||||
| chrX:2918993 | T | A | 2 | a0002c0002t0002g0255 a0002c0002t0002g0287 |
2 | NA18939.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.440-766A>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2918993 | |||||||
| chrX:2919218 | G | GTCC | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(256): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.440-994_440-992dup others(3): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2919218 | |||||||
| chrX:2919250 | A | G | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(256): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.440-1023T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2919250 | |||||||
| chrX:2919317 | G | A | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(128): Show |
144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.440-1090C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2919317 | |||||||
| chrX:2919396 | G | A | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(128): Show |
144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.440-1169C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2919396 | |||||||
| chrX:2919415 | A | C | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(256): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.439+1186T>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2919415 | |||||||
| chrX:2919469 | C | T | 1 | a0003c0003t0023g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.439+1132G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2919469 | |||||||
| chrX:2919627 | A | G | 1 | a0003c0003t0005g0216 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.439+974T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2919627 | |||||||
| chrX:2919700 | T | C | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(244): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.439+901A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2919700 | |||||||
| chrX:2919813 | G | C | 246 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(243): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.439+788C>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2919813 | |||||||
| chrX:2919814 | TTGTTGAA others(4): Show |
T | 246 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(243): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.439+776_439+786del others(11): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2919814 | |||||||
| chrX:2919979 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.439+622T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2919979 | |||||||
| chrX:2920034 | C | T | 1 | a0001c0006t0008g0223 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.439+567G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2920034 | |||||||
| chrX:2920147 | AGAGAAGG others(9): Show |
A | 1 | a0003c0003t0005g0104 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.439+438_439+453del others(16): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2920147 | |||||||
| chrX:2920219 | A | G | 2 | a0001c0001t0001g0124 a0001c0001t0001g0153 |
2 | HG02109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.439+382T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2920219 | |||||||
| chrX:2920381 | T | A | 2 | a0005c0008t0020g0006 a0005c0008t0026g0032 |
3 | HG01070.hp2 HG01071.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.439+220A>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2920381 | |||||||
| chrX:2920416 | A | T | 4 | a0002c0002t0002g0269 a0003c0003t0003g0268 a0003c0003t0005g0104 others(1): Show |
4 | NA18940.hp1 NA18965.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+185T>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2920416 | |||||||
| chrX:2920515 | C | T | 11 | a0002c0002t0001g0111 a0002c0005t0001g0194 a0002c0005t0001g0213 others(8): Show |
11 | HG01891.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.439+86G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 4/9 | chrX | 2920515 | |||||||
| chrX:2920798 | T | C | 2 | a0005c0008t0020g0006 a0005c0008t0026g0032 |
3 | HG01070.hp2 HG01071.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.317-75A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 3/9 | chrX | 2920798 | |||||||
| chrX:2920983 | T | C | 91 | a0002c0002t0001g0022 a0002c0002t0001g0042 a0002c0002t0001g0048 others(88): Show |
107 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.317-260A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 3/9 | chrX | 2920983 | |||||||
| chrX:2921437 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.316+466C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 3/9 | chrX | 2921437 | |||||||
| chrX:2921529 | G | A | 1 | a0002c0002t0019g0288 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.316+374C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 3/9 | chrX | 2921529 | |||||||
| chrX:2921577 | A | G | 2 | a0002c0002t0010g0229 a0008c0020t0024g0113 |
2 | HG02280.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.316+326T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 3/9 | chrX | 2921577 | |||||||
| chrX:2921789 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.316+114C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 3/9 | chrX | 2921789 | |||||||
| chrX:2922057 | G | A | 11 | a0002c0002t0001g0111 a0002c0005t0001g0194 a0002c0005t0001g0213 others(8): Show |
11 | HG01891.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.195-33C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2922057 | |||||||
| chrX:2922213 | A | ATC | 3 | a0001c0001t0001g0129 a0001c0001t0001g0195 a0001c0001t0004g0156 |
3 | HG00280.hp1 HG00642.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.195-191_195-190dup others(2): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2922213 | |||||||
| chrX:2922236 | T | A | 5 | a0002c0002t0001g0111 a0003c0003t0005g0112 a0003c0007t0005g0144 others(2): Show |
5 | HG01891.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.195-212A>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2922236 | |||||||
| chrX:2922238 | A | T | 1 | a0002c0002t0002g0266 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.195-214T>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2922238 | |||||||
| chrX:2922391 | G | A | 1 | a0002c0002t0016g0209 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.195-367C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2922391 | |||||||
| chrX:2922556 | C | T | 1 | a0001c0001t0001g0016 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.195-532G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2922556 | |||||||
| chrX:2922640 | A | G | 11 | a0002c0002t0001g0111 a0002c0005t0001g0194 a0002c0005t0001g0213 others(8): Show |
11 | HG01891.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.195-616T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2922640 | |||||||
| chrX:2922757 | G | C | 1 | a0003c0003t0003g0289 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.195-733C>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2922757 | |||||||
| chrX:2922779 | A | G | 6 | a0002c0005t0001g0194 a0002c0005t0001g0213 a0002c0005t0001g0215 others(3): Show |
6 | HG02886.hp2 HG03195.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.195-755T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2922779 | |||||||
| chrX:2922782 | A | G | 258 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(255): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.195-758T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2922782 | |||||||
| chrX:2922842 | C | CA | 10 | a0001c0001t0001g0178 a0002c0002t0001g0059 a0002c0002t0001g0062 others(7): Show |
10 | HG01175.hp1 HG01257.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.195-819dupT | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2922842 | |||||||
| chrX:2922842 | CA | C | 12 | a0001c0006t0008g0093 a0002c0002t0001g0050 a0002c0002t0001g0070 others(9): Show |
12 | HG01891.hp2 HG01993.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.195-819delT | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2922842 | |||||||
| chrX:2922842 | CAA | C | 29 | a0001c0001t0001g0024 a0001c0001t0001g0068 a0001c0001t0001g0109 others(26): Show |
30 | HG00741.hp1 HG00741.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.195-820_195-819del others(2): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2922842 | |||||||
| chrX:2922842 | CAAA | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(90): Show |
105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.195-821_195-819del others(3): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2922842 | |||||||
| chrX:2922842 | CAAAA | C | 20 | a0001c0001t0001g0045 a0001c0001t0001g0120 a0001c0001t0001g0124 others(17): Show |
21 | HG01243.hp1 HG01496.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.195-822_195-819del others(4): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2922842 | |||||||
| chrX:2922842 | CAAAAA | C | 7 | a0002c0005t0001g0213 a0002c0005t0001g0215 a0002c0005t0006g0214 others(4): Show |
7 | HG01074.hp1 HG01891.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.195-823_195-819del others(5): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2922842 | |||||||
| chrX:2922842 | CAAAAAAA others(14): Show |
C | 93 | a0001c0001t0002g0306 a0001c0001t0004g0011 a0001c0001t0004g0078 others(90): Show |
110 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.195-839_195-819del others(21): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2922842 | |||||||
| chrX:2922865 | A | G | 1 | a0002c0002t0002g0265 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.195-841T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2922865 | |||||||
| chrX:2922868 | A | G | 1 | a0008c0020t0024g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.195-844T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2922868 | |||||||
| chrX:2922877 | A | G | 1 | a0004c0004t0033g0152 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.195-853T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2922877 | |||||||
| chrX:2922882 | AAAAG | A | 14 | a0001c0001t0001g0030 a0001c0001t0006g0067 a0002c0005t0001g0005 others(11): Show |
15 | HG00099.hp1 HG01074.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.195-862_195-859del others(4): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2922882 | |||||||
| chrX:2922902 | GAA | G | 11 | a0002c0002t0001g0111 a0002c0005t0001g0194 a0002c0005t0001g0213 others(8): Show |
11 | HG01891.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.195-880_195-879del others(2): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2922902 | |||||||
| chrX:2922973 | CGTGAGGC others(8): Show |
C | 93 | a0001c0001t0002g0306 a0001c0001t0004g0011 a0001c0001t0004g0078 others(90): Show |
110 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.195-964_195-950del others(15): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2922973 | |||||||
| chrX:2923237 | G | A | 2 | a0004c0004t0005g0086 a0004c0004t0005g0095 |
2 | HG02083.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.195-1213C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2923237 | |||||||
| chrX:2923248 | T | G | 4 | a0003c0003t0023g0108 a0003c0017t0034g0206 a0005c0008t0020g0006 others(1): Show |
5 | HG01070.hp2 HG01071.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.195-1224A>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2923248 | |||||||
| chrX:2923884 | C | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(123): Show |
138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.194+1732G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2923884 | |||||||
| chrX:2923903 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(126): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.194+1713A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2923903 | |||||||
| chrX:2924039 | T | C | 1 | a0002c0002t0002g0247 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.194+1577A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2924039 | |||||||
| chrX:2924126 | G | A | 5 | a0002c0005t0001g0213 a0002c0005t0001g0215 a0002c0005t0006g0214 others(2): Show |
5 | HG03195.hp1 HG03471.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.194+1490C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2924126 | |||||||
| chrX:2924156 | C | G | 6 | a0002c0005t0001g0194 a0002c0005t0001g0213 a0002c0005t0001g0215 others(3): Show |
6 | HG02886.hp2 HG03195.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.194+1460G>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2924156 | |||||||
| chrX:2924455 | G | A | 1 | a0004c0004t0003g0291 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.194+1161C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2924455 | |||||||
| chrX:2924460 | C | A | 10 | a0001c0001t0013g0222 a0001c0006t0017g0217 a0002c0002t0001g0042 others(7): Show |
10 | HG02257.hp1 HG02809.hp2 HG03195.hp1 others(7): Show |
intron_variant | MODIFIER | c.194+1156G>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2924460 | |||||||
| chrX:2924479 | A | G | 6 | a0001c0001t0029g0143 a0002c0002t0001g0083 a0002c0002t0006g0082 others(3): Show |
6 | HG01891.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.194+1137T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2924479 | |||||||
| chrX:2924497 | C | G | 1 | a0004c0004t0005g0086 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.194+1119G>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2924497 | |||||||
| chrX:2924556 | G | A | 2 | a0002c0002t0001g0111 a0003c0003t0005g0112 |
2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.194+1060C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2924556 | |||||||
| chrX:2924812 | G | A | 93 | a0001c0001t0002g0306 a0001c0001t0004g0011 a0001c0001t0004g0078 others(90): Show |
110 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.194+804C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2924812 | |||||||
| chrX:2924906 | C | T | 1 | a0001c0001t0006g0142 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.194+710G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2924906 | |||||||
| chrX:2925032 | A | T | 4 | a0002c0005t0001g0213 a0002c0005t0001g0215 a0002c0005t0006g0214 others(1): Show |
4 | HG03195.hp1 NA18522.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.194+584T>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2925032 | |||||||
| chrX:2925098 | T | C | 231 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(228): Show |
261 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.194+518A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2925098 | |||||||
| chrX:2925211 | A | G | 97 | a0001c0001t0002g0306 a0001c0001t0004g0011 a0001c0001t0004g0078 others(94): Show |
114 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.194+405T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2925211 | |||||||
| chrX:2925311 | G | A | 3 | a0002c0002t0001g0118 a0002c0010t0008g0033 a0002c0010t0008g0034 |
3 | HG02622.hp1 HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.194+305C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2925311 | |||||||
| chrX:2925388 | C | T | 31 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0120 others(28): Show |
32 | HG01074.hp1 HG01109.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.194+228G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2925388 | |||||||
| chrX:2925403 | T | A | 1 | a0001c0001t0004g0179 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.194+213A>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2925403 | |||||||
| chrX:2925568 | C | T | 2 | a0002c0002t0001g0111 a0003c0003t0005g0112 |
2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.194+48G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 2/9 | chrX | 2925568 | |||||||
| chrX:2925777 | A | G | 85 | a0001c0001t0002g0306 a0001c0001t0004g0011 a0001c0001t0004g0078 others(82): Show |
102 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.45-12T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2925777 | |||||||
| chrX:2925838 | C | T | 21 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0120 others(18): Show |
22 | HG01123.hp2 HG01261.hp1 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.45-73G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2925838 | |||||||
| chrX:2925874 | C | T | 1 | a0002c0002t0001g0138 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.45-109G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2925874 | |||||||
| chrX:2925975 | G | A | 1 | a0003c0003t0003g0293 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.45-210C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2925975 | |||||||
| chrX:2926531 | T | C | 5 | a0002c0002t0002g0239 a0002c0002t0002g0242 a0002c0002t0002g0243 others(2): Show |
5 | HG02165.hp2 NA18950.hp2 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-766A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2926531 | |||||||
| chrX:2926617 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02698.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.45-852C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2926617 | |||||||
| chrX:2926673 | C | T | 2 | a0004c0004t0003g0261 a0004c0004t0003g0262 |
2 | NA19066.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.45-908G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2926673 | |||||||
| chrX:2926739 | C | T | 1 | a0002c0002t0019g0260 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.45-974G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2926739 | |||||||
| chrX:2926849 | G | C | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.45-1084C>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2926849 | |||||||
| chrX:2926979 | C | T | 3 | a0001c0001t0001g0203 a0001c0001t0001g0205 a0001c0001t0007g0204 |
3 | NA18968.hp1 NA18998.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.45-1214G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2926979 | |||||||
| chrX:2927021 | C | T | 33 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0120 others(30): Show |
34 | HG01074.hp1 HG01123.hp2 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.45-1256G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2927021 | |||||||
| chrX:2927023 | C | G | 33 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0120 others(30): Show |
34 | HG01074.hp1 HG01123.hp2 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.45-1258G>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2927023 | |||||||
| chrX:2927162 | T | C | 4 | a0002c0005t0001g0213 a0002c0005t0001g0215 a0002c0005t0006g0214 others(1): Show |
4 | HG03195.hp1 NA18522.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-1397A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2927162 | |||||||
| chrX:2927212 | G | C | 33 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0120 others(30): Show |
34 | HG01074.hp1 HG01123.hp2 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.45-1447C>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2927212 | |||||||
| chrX:2927240 | C | CT | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(207): Show |
240 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.45-1476dupA | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2927240 | |||||||
| chrX:2927240 | C | CTT | 30 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0031 others(27): Show |
31 | HG01074.hp1 HG01123.hp2 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.45-1477_45-1476dup others(2): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2927240 | |||||||
| chrX:2927251 | A | T | 24 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0120 others(21): Show |
25 | HG01074.hp1 HG01123.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.45-1486T>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2927251 | |||||||
| chrX:2927366 | T | C | 33 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0120 others(30): Show |
34 | HG01074.hp1 HG01123.hp2 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.45-1601A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2927366 | |||||||
| chrX:2927377 | A | G | 4 | a0001c0001t0013g0222 a0001c0006t0017g0217 a0002c0002t0001g0083 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-1612T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2927377 | |||||||
| chrX:2927476 | A | G | 37 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0120 others(34): Show |
38 | HG01074.hp1 HG01123.hp2 HG01261.hp1 others(35): Show |
intron_variant | MODIFIER | c.45-1711T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2927476 | |||||||
| chrX:2927809 | C | CA | 39 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0120 others(36): Show |
40 | HG01074.hp1 HG01123.hp2 HG01261.hp1 others(37): Show |
intron_variant | MODIFIER | c.44+1422dupT | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2927809 | |||||||
| chrX:2927812 | C | G | 1 | a0002c0005t0021g0077 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.44+1420G>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2927812 | |||||||
| chrX:2927829 | C | T | 13 | a0001c0001t0013g0222 a0001c0006t0017g0217 a0002c0002t0001g0042 others(10): Show |
13 | HG02622.hp1 HG02723.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.44+1403G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2927829 | |||||||
| chrX:2927975 | A | C | 2 | a0001c0001t0013g0222 a0001c0006t0017g0217 |
2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.44+1257T>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2927975 | |||||||
| chrX:2927980 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0004g0186 a0002c0002t0004g0185 |
4 | HG00735.hp2 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.44+1252C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2927980 | |||||||
| chrX:2928023 | T | C | 93 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0126 others(90): Show |
110 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.44+1209A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2928023 | |||||||
| chrX:2928163 | C | G | 1 | a0002c0005t0001g0194 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.44+1069G>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2928163 | |||||||
| chrX:2928289 | C | T | 2 | a0002c0002t0001g0083 a0002c0002t0006g0082 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.44+943G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2928289 | |||||||
| chrX:2928294 | A | T | 2 | a0001c0001t0001g0218 a0003c0003t0005g0216 |
2 | HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.44+938T>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2928294 | |||||||
| chrX:2928301 | G | T | 17 | a0001c0001t0001g0218 a0001c0001t0013g0222 a0001c0006t0008g0223 others(14): Show |
18 | HG01070.hp2 HG01071.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.44+931C>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2928301 | |||||||
| chrX:2928341 | G | A | 20 | a0001c0001t0001g0218 a0001c0001t0013g0222 a0001c0006t0008g0223 others(17): Show |
21 | HG01070.hp2 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.44+891C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2928341 | |||||||
| chrX:2928497 | C | CCGGGGGG others(34): Show |
1 | a0002c0002t0001g0044 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.44+694_44+734dupCC others(39): Show |
ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2928497 | |||||||
| chrX:2928603 | G | A | 2 | a0002c0010t0008g0033 a0002c0010t0008g0034 |
2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.44+629C>T | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2928603 | |||||||
| chrX:2928624 | G | C | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(105): Show |
118 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.44+608C>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2928624 | |||||||
| chrX:2928661 | A | G | 94 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(91): Show |
101 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.44+571T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2928661 | |||||||
| chrX:2928672 | T | TG | 83 | a0001c0001t0001g0192 a0001c0001t0002g0258 a0001c0001t0002g0306 others(80): Show |
98 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.44+559dupC | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2928672 | |||||||
| chrX:2928672 | TG | T | 55 | a0001c0001t0001g0013 a0001c0001t0001g0045 a0001c0001t0001g0046 others(52): Show |
59 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.44+559delC | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2928672 | |||||||
| chrX:2928801 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.44+431G>A | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2928801 | |||||||
| chrX:2928976 | T | C | 177 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0045 others(174): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.44+256A>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2928976 | |||||||
| chrX:2929092 | A | G | 198 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0013 others(195): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.44+140T>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2929092 | |||||||
| chrX:2929116 | C | G | 160 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0031 others(157): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.44+116G>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2929116 | |||||||
| chrX:2929123 | T | G | 8 | a0001c0001t0001g0218 a0001c0001t0013g0219 a0001c0006t0017g0217 others(5): Show |
8 | HG02809.hp1 HG02809.hp2 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.44+109A>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2929123 | |||||||
| chrX:2929147 | G | C | 7 | a0001c0001t0013g0222 a0001c0006t0008g0223 a0001c0006t0008g0224 others(4): Show |
7 | HG01109.hp1 HG01891.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.44+85C>G | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2929147 | |||||||
| chrX:2929160 | C | G | 1 | a0002c0002t0007g0026 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.44+72G>C | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2929160 | |||||||
| chrX:2929170 | A | AC | 6 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0002c0002t0001g0021 others(3): Show |
6 | HG01496.hp2 HG01978.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.44+61dupG | ARSD | ENSG00000006756.16 | transcript | ENST00000381154.6 | protein_coding | 1/9 | chrX | 2929170 |