Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 415 |
| ensemblid | ENSG00000157399.17 |
| hgncid | 719 |
| symbol | ARSL |
| name | arylsulfatase L |
| refseq_nuc | NM_000047.3 |
| refseq_prot | NP_000038.2 |
| ensembl_nuc | ENST00000381134.9 |
| ensembl_prot | ENSP00000370526.3 |
| mane_status | MANE Select |
| chr | chrX |
| start | 2934521 |
| end | 2964341 |
| strand | - |
| ver | v1.2 |
| region | chrX:2934521-2964341 |
| region5000 | chrX:2929521-2969341 |
| regionname0 | ARSL_chrX_2934521_2964341 |
| regionname5000 | ARSL_chrX_2929521_2969341 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 589 | 192 | 6 | 32 | 117 | 11 | 25 | 95 | ARSL_chrX_2929521_2969341 | ARSL | MLHLH others(584): Show |
chrX | 2929521 | 2969341 |
| a0002 | 1/0 | 589 | 104 | 52 | 25 | 19 | 2 | 5 | 15 | ARSL_chrX_2929521_2969341 | ARSL | MLHLH others(584): Show |
chrX | 2929521 | 2969341 |
| a0003 | 0/0 | 589 | 12 | 10 | 2 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | MLHLH others(584): Show |
chrX | 2929521 | 2969341 |
| a0004 | 0/0 | 589 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | MLHLH others(584): Show |
chrX | 2929521 | 2969341 |
| a0005 | 0/0 | 589 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | ARSL_chrX_2929521_2969341 | ARSL | MLHLH others(584): Show |
chrX | 2929521 | 2969341 |
| a0006 | 0/0 | 589 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | ARSL_chrX_2929521_2969341 | ARSL | MLHLH others(584): Show |
chrX | 2929521 | 2969341 |
| a0007 | 0/0 | 589 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | MLHLH others(584): Show |
chrX | 2929521 | 2969341 |
| a0008 | 0/0 | 589 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | MLHLH others(584): Show |
chrX | 2929521 | 2969341 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1767 | 172 | 4 | 21 | 116 | 8 | 22 | ARSL_chrX_2929521_2969341 | ARSL | ATGTT others(1762): Show |
chrX | 2929521 | 2969341 | ||
| a0001c0007 | 0/0 | 1767 | 9 | 0 | 7 | 0 | 0 | 2 | ARSL_chrX_2929521_2969341 | ARSL | ATGTT others(1762): Show |
chrX | 2929521 | 2969341 | ||
| a0001c0009 | 0/0 | 1767 | 5 | 0 | 2 | 0 | 2 | 1 | ARSL_chrX_2929521_2969341 | ARSL | ATGTT others(1762): Show |
chrX | 2929521 | 2969341 | ||
| a0001c0010 | 0/0 | 1767 | 3 | 1 | 1 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | ATGTT others(1762): Show |
chrX | 2929521 | 2969341 | ||
| a0001c0014 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | ATGTT others(1762): Show |
chrX | 2929521 | 2969341 | ||
| a0001c0015 | 0/0 | 1767 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | ATGTT others(1762): Show |
chrX | 2929521 | 2969341 | ||
| a0001c0020 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | ATGTT others(1762): Show |
chrX | 2929521 | 2969341 | ||
| a0002c0002 | 1/0 | 1767 | 74 | 30 | 19 | 18 | 1 | 5 | ARSL_chrX_2929521_2969341 | ARSL | ATGTT others(1762): Show |
chrX | 2929521 | 2969341 | ||
| a0002c0003 | 0/0 | 1767 | 14 | 12 | 2 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | ATGTT others(1762): Show |
chrX | 2929521 | 2969341 | ||
| a0002c0004 | 0/0 | 1767 | 11 | 10 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | ATGTT others(1762): Show |
chrX | 2929521 | 2969341 | ||
| a0002c0012 | 0/0 | 1767 | 2 | 0 | 2 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | ATGTT others(1762): Show |
chrX | 2929521 | 2969341 | ||
| a0002c0016 | 0/0 | 1767 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | ATGTT others(1762): Show |
chrX | 2929521 | 2969341 | ||
| a0002c0017 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | ATGTT others(1762): Show |
chrX | 2929521 | 2969341 | ||
| a0002c0018 | 0/0 | 1767 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | ATGTT others(1762): Show |
chrX | 2929521 | 2969341 | ||
| a0003c0005 | 0/0 | 1767 | 10 | 8 | 2 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | ATGTT others(1762): Show |
chrX | 2929521 | 2969341 | ||
| a0003c0013 | 0/0 | 1767 | 2 | 2 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | ATGTT others(1762): Show |
chrX | 2929521 | 2969341 | ||
| a0004c0006 | 0/0 | 1767 | 9 | 9 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | ATGTT others(1762): Show |
chrX | 2929521 | 2969341 | ||
| a0005c0008 | 0/0 | 1767 | 6 | 0 | 0 | 6 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | ATGTT others(1762): Show |
chrX | 2929521 | 2969341 | ||
| a0006c0011 | 0/0 | 1767 | 3 | 0 | 0 | 3 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | ATGTT others(1762): Show |
chrX | 2929521 | 2969341 | ||
| a0007c0021 | 0/0 | 1767 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | ATGTT others(1762): Show |
chrX | 2929521 | 2969341 | ||
| a0008c0019 | 0/0 | 1767 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | ATGTT others(1762): Show |
chrX | 2929521 | 2969341 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2219 | 169 | 3 | 21 | 115 | 7 | 22 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0001c0001t0002 | 0/0 | 2219 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTCAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0001c0001t0006 | 0/0 | 2219 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0001c0001t0009 | 0/0 | 2219 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0001c0007t0001 | 0/0 | 2219 | 8 | 0 | 7 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0001c0007t0006 | 0/0 | 2219 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0001c0009t0001 | 0/0 | 2219 | 5 | 0 | 2 | 0 | 2 | 1 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0001c0010t0001 | 0/0 | 2219 | 3 | 1 | 1 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0001c0014t0001 | 0/0 | 2219 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0001c0015t0001 | 0/0 | 2219 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0001c0020t0001 | 0/0 | 2219 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0002c0002t0001 | 1/0 | 2219 | 39 | 10 | 14 | 8 | 1 | 5 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0002c0002t0002 | 0/0 | 2219 | 13 | 12 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTCAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0002c0002t0003 | 0/0 | 2219 | 18 | 5 | 3 | 10 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0002c0002t0004 | 0/0 | 2219 | 3 | 2 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTCAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0002c0002t0008 | 0/0 | 2219 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTCAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0002c0003t0001 | 0/0 | 2219 | 5 | 4 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0002c0003t0002 | 0/0 | 2219 | 9 | 8 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTCAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0002c0004t0001 | 0/0 | 2219 | 3 | 3 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0002c0004t0002 | 0/0 | 2219 | 3 | 2 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTCAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0002c0004t0005 | 0/0 | 2219 | 4 | 4 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0002c0004t0007 | 0/0 | 2219 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTCAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0002c0012t0002 | 0/0 | 2219 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTCAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0002c0012t0003 | 0/0 | 2219 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0002c0016t0003 | 0/0 | 2219 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0002c0017t0001 | 0/0 | 2219 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0002c0018t0001 | 0/0 | 2219 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0003c0005t0001 | 0/0 | 2219 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0003c0005t0002 | 0/0 | 2219 | 5 | 3 | 2 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTCAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0003c0005t0003 | 0/0 | 2219 | 2 | 2 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0003c0005t0004 | 0/0 | 2219 | 2 | 2 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTCAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0003c0013t0001 | 0/0 | 2219 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0003c0013t0002 | 0/0 | 2219 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTCAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0004c0006t0001 | 0/0 | 2219 | 2 | 2 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0004c0006t0002 | 0/0 | 2219 | 7 | 7 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTCAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0005c0008t0001 | 0/0 | 2219 | 5 | 0 | 0 | 5 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0005c0008t0003 | 0/0 | 2219 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0006c0011t0001 | 0/0 | 2219 | 3 | 0 | 0 | 3 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0007c0021t0001 | 0/0 | 2219 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| a0008c0019t0001 | 0/0 | 2219 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | GTTAA others(2214): Show |
chrX | 2929521 | 2969341 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0284 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0006g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0001t0009g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0007t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0007t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0007t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0007t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0007t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0007t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0007t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0007t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0007t0006g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0009t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0009t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0009t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0009t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0009t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0010t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0010t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0010t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0014t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0015t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0001c0020t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0115 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0004g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0002t0008g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0003t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0003t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0003t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0003t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0003t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0003t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0003t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0003t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0003t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0003t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0003t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0003t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0004t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0004t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0004t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0004t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0004t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0004t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0004t0005g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0004t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0004t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0004t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0004t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0012t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0012t0003g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0016t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0017t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0002c0018t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0003c0005t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0003c0005t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0003c0005t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0003c0005t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0003c0005t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0003c0005t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0003c0005t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0003c0005t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0003c0005t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0003c0005t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0003c0013t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0003c0013t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0004c0006t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0004c0006t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0004c0006t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0004c0006t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0004c0006t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0004c0006t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0004c0006t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0004c0006t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0005c0008t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0005c0008t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0005c0008t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0005c0008t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0005c0008t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0005c0008t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0006c0011t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0006c0011t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0006c0011t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0007c0021t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| a0008c0019t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0018 | t0001 | g0168 | EUR | GBR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG00099 | hp2 | a0001 | c0010 | t0001 | g0134 | EUR | GBR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG00140 | hp1 | a0001 | c0009 | t0001 | g0204 | EUR | GBR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0198 | EUR | FIN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0116 | EUR | FIN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0174 | EUR | FIN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | CHS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0093 | EAS | CHS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG00423 | hp2 | a0002 | c0017 | t0001 | g0141 | EAS | CHS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG00597 | hp2 | a0002 | c0002 | t0003 | g0247 | EAS | CHS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0162 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG00642 | hp1 | a0001 | c0015 | t0001 | g0160 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG00733 | hp1 | a0002 | c0004 | t0002 | g0028 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0157 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG00741 | hp2 | a0002 | c0003 | t0001 | g0206 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01070 | hp1 | a0003 | c0005 | t0002 | g0026 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01071 | hp2 | a0003 | c0005 | t0002 | g0025 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0147 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01099 | hp1 | a0001 | c0007 | t0001 | g0291 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0148 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01109 | hp1 | a0002 | c0003 | t0002 | g0043 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0276 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01168 | hp2 | a0001 | c0009 | t0001 | g0104 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01169 | hp1 | a0001 | c0009 | t0001 | g0196 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01175 | hp1 | a0002 | c0012 | t0002 | g0036 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0021 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01256 | hp1 | a0001 | c0007 | t0001 | g0307 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01261 | hp1 | a0002 | c0002 | t0004 | g0017 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0270 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0265 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0294 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0159 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01496 | hp1 | a0002 | c0016 | t0003 | g0313 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01516 | hp1 | a0001 | c0009 | t0001 | g0105 | EUR | IBS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0191 | EUR | IBS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0190 | EUR | IBS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01884 | hp1 | a0004 | c0006 | t0001 | g0243 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0244 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01891 | hp1 | a0002 | c0003 | t0002 | g0044 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0210 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0271 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01943 | hp1 | a0001 | c0007 | t0001 | g0305 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01952 | hp1 | a0001 | c0007 | t0001 | g0306 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01981 | hp1 | a0002 | c0012 | t0003 | g0310 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01981 | hp2 | a0002 | c0002 | t0003 | g0226 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01993 | hp2 | a0001 | c0007 | t0001 | g0309 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02004 | hp1 | a0001 | c0007 | t0001 | g0293 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0260 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02129 | hp1 | a0006 | c0011 | t0001 | g0217 | EAS | KHV | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02145 | hp1 | a0002 | c0003 | t0001 | g0208 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CDX | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CDX | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CDX | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02165 | hp2 | a0001 | c0014 | t0001 | g0200 | EAS | CDX | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02257 | hp1 | a0003 | c0005 | t0003 | g0212 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02257 | hp2 | a0001 | c0010 | t0001 | g0255 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0183 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02273 | hp2 | a0001 | c0007 | t0001 | g0311 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02280 | hp1 | a0003 | c0005 | t0001 | g0080 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02280 | hp2 | a0004 | c0006 | t0002 | g0004 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0315 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02293 | hp2 | a0002 | c0002 | t0003 | g0262 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02451 | hp1 | a0002 | c0003 | t0002 | g0012 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02451 | hp2 | a0004 | c0006 | t0002 | g0027 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02572 | hp1 | a0002 | c0002 | t0003 | g0235 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02615 | hp1 | a0002 | c0002 | t0003 | g0145 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02615 | hp2 | a0003 | c0013 | t0002 | g0038 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02622 | hp1 | a0002 | c0004 | t0005 | g0118 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0209 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0019 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02630 | hp2 | a0002 | c0002 | t0003 | g0232 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02647 | hp1 | a0003 | c0005 | t0002 | g0053 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0173 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02723 | hp1 | a0004 | c0006 | t0002 | g0045 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02723 | hp2 | a0002 | c0002 | t0002 | g0034 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02809 | hp1 | a0004 | c0006 | t0002 | g0004 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02809 | hp2 | a0002 | c0003 | t0001 | g0213 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0124 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0020 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02895 | hp1 | a0002 | c0002 | t0004 | g0041 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02896 | hp1 | a0002 | c0003 | t0002 | g0052 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02896 | hp2 | a0002 | c0004 | t0005 | g0110 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02897 | hp1 | a0002 | c0003 | t0002 | g0051 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02897 | hp2 | a0002 | c0002 | t0004 | g0031 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02922 | hp1 | a0002 | c0002 | t0003 | g0175 | AFR | ESN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02922 | hp2 | a0002 | c0002 | t0002 | g0039 | AFR | ESN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02965 | hp1 | a0003 | c0005 | t0002 | g0030 | AFR | ESN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0146 | AFR | ESN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02976 | hp2 | a0002 | c0004 | t0001 | g0112 | AFR | ESN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03041 | hp1 | a0002 | c0004 | t0002 | g0042 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03041 | hp2 | a0003 | c0005 | t0002 | g0035 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03098 | hp1 | a0002 | c0003 | t0001 | g0240 | AFR | MSL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03130 | hp1 | a0004 | c0006 | t0002 | g0033 | AFR | ESN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03139 | hp1 | a0003 | c0005 | t0004 | g0054 | AFR | ESN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03195 | hp1 | a0002 | c0003 | t0002 | g0050 | AFR | ESN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03209 | hp1 | a0002 | c0004 | t0007 | g0013 | AFR | MSL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03225 | hp1 | a0007 | c0021 | t0001 | g0096 | AFR | MSL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0139 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03453 | hp1 | a0003 | c0013 | t0001 | g0296 | AFR | MSL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03453 | hp2 | a0001 | c0020 | t0001 | g0131 | AFR | MSL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03486 | hp1 | a0002 | c0004 | t0001 | g0242 | AFR | MSL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03486 | hp2 | a0002 | c0003 | t0002 | g0040 | AFR | MSL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03516 | hp1 | a0004 | c0006 | t0002 | g0046 | AFR | ESN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | ESN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0241 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03540 | hp2 | a0004 | c0006 | t0001 | g0281 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03579 | hp1 | a0002 | c0002 | t0008 | g0015 | AFR | MSL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0279 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | STU | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03704 | hp1 | a0001 | c0007 | t0006 | g0256 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0301 | SAS | BEB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03942 | hp1 | a0001 | c0007 | t0001 | g0068 | SAS | BEB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0071 | SAS | STU | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | BEB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG04184 | hp2 | a0001 | c0009 | t0001 | g0277 | SAS | BEB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | STU | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | STU | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | STU | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0130 | AFR | YRI | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CHB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18906 | hp1 | a0002 | c0004 | t0001 | g0285 | AFR | YRI | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18906 | hp2 | a0002 | c0003 | t0002 | g0023 | AFR | YRI | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18949 | hp2 | a0002 | c0002 | t0003 | g0065 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18951 | hp1 | a0002 | c0002 | t0003 | g0246 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18954 | hp1 | a0002 | c0002 | t0003 | g0251 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18962 | hp1 | a0005 | c0008 | t0001 | g0061 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18963 | hp1 | a0005 | c0008 | t0001 | g0127 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18964 | hp1 | a0005 | c0008 | t0001 | g0060 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18973 | hp2 | a0002 | c0002 | t0003 | g0092 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18979 | hp2 | a0002 | c0002 | t0003 | g0252 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18991 | hp2 | a0005 | c0008 | t0001 | g0218 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18999 | hp2 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19000 | hp1 | a0006 | c0011 | t0001 | g0067 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19004 | hp1 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0234 | AFR | LWK | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19030 | hp2 | a0003 | c0005 | t0004 | g0022 | AFR | LWK | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19043 | hp1 | a0002 | c0004 | t0002 | g0032 | AFR | LWK | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19055 | hp1 | a0008 | c0019 | t0001 | g0245 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19063 | hp1 | a0006 | c0011 | t0001 | g0298 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19064 | hp1 | a0005 | c0008 | t0001 | g0128 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19066 | hp1 | a0002 | c0002 | t0003 | g0070 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19067 | hp1 | a0001 | c0001 | t0009 | g0239 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19078 | hp2 | a0005 | c0008 | t0003 | g0126 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19090 | hp2 | a0002 | c0002 | t0003 | g0109 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0018 | AFR | YRI | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | YRI | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0029 | AFR | ASW | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA20129 | hp2 | a0002 | c0003 | t0002 | g0024 | AFR | ASW | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0282 | EUR | TSI | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0199 | EUR | TSI | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0156 | SAS | GIH | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01123 | hp1 | a0001 | c0010 | t0001 | g0308 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG01123 | hp2 | a0002 | c0002 | t0003 | g0312 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02109 | hp1 | a0002 | c0002 | t0003 | g0079 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0016 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0047 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02559 | hp1 | a0002 | c0004 | t0005 | g0129 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG02559 | hp2 | a0002 | c0002 | t0002 | g0014 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG03471 | hp1 | a0004 | c0006 | t0002 | g0048 | AFR | MSL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | USA | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| HG06807 | hp2 | a0002 | c0004 | t0005 | g0177 | AFR | USA | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA20300 | hp1 | a0003 | c0005 | t0003 | g0211 | AFR | USA | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA20300 | hp2 | a0002 | c0003 | t0001 | g0205 | AFR | USA | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0049 | AFR | LWK | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0284 | REF | REF | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0115 | REF | REF | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
| 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:2938114 | C | T | 2 | a0001 a0006 |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
missense_variant | MODERATE | c.1270G>A | p.Gly424Ser | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/11 | 1408/2219 | 1270/1770 | 424/589 | chrX | 2938114 | |||
| chrX:2949383 | G | C | 2 | a0006 a0008 |
4 | HG02129.hp1 NA19000.hp1 NA19055.hp1 others(1): Show |
missense_variant | MODERATE | c.775C>G | p.His259Asp | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/11 | 913/2219 | 775/1770 | 259/589 | chrX | 2949383 | |||
| chrX:2949610 | C | T | 1 | a0004 | 9 | HG01884.hp1 HG02280.hp2 HG02451.hp2 others(6): Show |
missense_variant | MODERATE | c.548G>A | p.Arg183His | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/11 | 686/2219 | 548/1770 | 183/589 | chrX | 2949610 | |||
| chrX:2955503 | C | T | 1 | a0005 | 6 | NA18962.hp1 NA18963.hp1 NA18964.hp1 others(3): Show |
missense_variant | MODERATE | c.220G>A | p.Val74Met | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/11 | 358/2219 | 220/1770 | 74/589 | chrX | 2955503 | |||
| chrX:2958302 | T | C | 1 | a0003 | 12 | HG01070.hp1 HG01071.hp2 HG02257.hp1 others(9): Show |
missense_variant | MODERATE | c.157A>G | p.Ile53Val | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/11 | 295/2219 | 157/1770 | 53/589 | chrX | 2958302 | |||
| chrX:2958374 | C | A | 1 | a0007 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.85G>T | p.Ala29Ser | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/11 | 223/2219 | 85/1770 | 29/589 | chrX | 2958374 |
| 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:2934874 | C | T | 1 | a0001c0009 | 5 | HG00140.hp1 HG01168.hp2 HG01169.hp1 others(2): Show |
synonymous_variant | LOW | c.1728G>A | p.Pro576Pro | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 11/11 | 1866/2219 | 1728/1770 | 576/589 | chrX | 2934874 | |||
| chrX:2934910 | G | A | 8 | a0001c0001 a0001c0007 a0001c0009 others(5): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
synonymous_variant | LOW | c.1692C>T | p.Asn564Asn | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 11/11 | 1830/2219 | 1692/1770 | 564/589 | chrX | 2934910 | |||
| chrX:2936767 | G | A | 1 | a0002c0017 | 1 | HG00423.hp2 | synonymous_variant | LOW | c.1386C>T | p.His462His | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/11 | 1524/2219 | 1386/1770 | 462/589 | chrX | 2936767 | |||
| chrX:2943135 | C | T | 1 | a0001c0014 | 1 | HG02165.hp2 | synonymous_variant | LOW | c.1056G>A | p.Ser352Ser | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/11 | 1194/2219 | 1056/1770 | 352/589 | chrX | 2943135 | |||
| chrX:2946092 | G | A | 1 | a0002c0018 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.897C>T | p.His299His | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/11 | 1035/2219 | 897/1770 | 299/589 | chrX | 2946092 | |||
| chrX:2949372 | C | T | 2 | a0001c0007 a0002c0012 |
11 | HG01099.hp1 HG01175.hp1 HG01256.hp1 others(8): Show |
synonymous_variant | LOW | c.786G>A | p.Thr262Thr | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/11 | 924/2219 | 786/1770 | 262/589 | chrX | 2949372 | |||
| chrX:2949609 | G | A | 3 | a0001c0020 a0002c0004 a0003c0013 |
14 | HG00733.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
synonymous_variant | LOW | c.549C>T | p.Arg183Arg | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/11 | 687/2219 | 549/1770 | 183/589 | chrX | 2949609 | |||
| chrX:2949663 | A | G | 1 | a0001c0010 | 3 | HG00099.hp2 HG01123.hp1 HG02257.hp2 |
synonymous_variant | LOW | c.495T>C | p.His165His | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/11 | 633/2219 | 495/1770 | 165/589 | chrX | 2949663 | |||
| chrX:2958381 | T | C | 3 | a0002c0003 a0003c0005 a0007c0021 |
25 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(22): Show |
synonymous_variant | LOW | c.78A>G | p.Ala26Ala | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/11 | 216/2219 | 78/1770 | 26/589 | chrX | 2958381 |
| 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:2934558 | C | G | 7 | a0002c0002t0003 a0002c0002t0004 a0002c0012t0003 others(4): Show |
28 | HG00597.hp2 HG01123.hp2 HG01261.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*274G>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 11/11 | 274 | chrX | 2934558 | ||||||
| chrX:2934561 | C | T | 7 | a0002c0002t0003 a0002c0002t0004 a0002c0012t0003 others(4): Show |
28 | HG00597.hp2 HG01123.hp2 HG01261.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*271G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 11/11 | 271 | chrX | 2934561 | ||||||
| chrX:2934567 | C | T | 1 | a0002c0002t0008 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*265G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 11/11 | 265 | chrX | 2934567 | ||||||
| chrX:2934651 | T | A | 1 | a0001c0001t0009 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*181A>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 11/11 | 181 | chrX | 2934651 | ||||||
| chrX:2934665 | A | G | 2 | a0002c0004t0005 a0002c0004t0007 |
5 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*167T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 11/11 | 167 | chrX | 2934665 | ||||||
| chrX:2934746 | G | A | 2 | a0001c0001t0006 a0001c0007t0006 |
2 | HG00323.hp1 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*86C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 11/11 | 86 | chrX | 2934746 | ||||||
| chrX:2964339 | A | G | 12 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0004 others(9): Show |
47 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(44): Show |
5_prime_UTR_variant | MODIFIER | c.-136T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/11 | 3939 | chrX | 2964339 |
| 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:2935242 | G | A | 4 | a0002c0002t0001g0156 a0002c0002t0001g0265 a0002c0002t0001g0282 others(1): Show |
4 | HG00099.hp1 HG01358.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.1412-52C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2935242 | |||||||
| chrX:2935552 | C | T | 6 | a0002c0004t0001g0112 a0003c0005t0002g0025 a0003c0005t0002g0026 others(3): Show |
6 | HG01070.hp1 HG01071.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1412-362G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2935552 | |||||||
| chrX:2935667 | TTTTTC | T | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(171): Show |
184 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1412-482_1412-478d others(7): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2935667 | |||||||
| chrX:2935683 | TTTTC | T | 13 | a0001c0001t0001g0082 a0001c0001t0001g0086 a0001c0001t0001g0102 others(10): Show |
13 | HG00673.hp1 HG02027.hp1 HG03710.hp1 others(10): Show |
intron_variant | MODIFIER | c.1412-497_1412-494d others(6): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2935683 | |||||||
| chrX:2935686 | TCTTTTC | T | 6 | a0001c0001t0001g0062 a0001c0001t0001g0095 a0001c0001t0001g0122 others(3): Show |
6 | HG02015.hp1 NA18959.hp1 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.1412-502_1412-497d others(8): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2935686 | |||||||
| chrX:2935692 | C | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(209): Show |
223 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1412-502G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2935692 | |||||||
| chrX:2935692 | CT | C | 8 | a0002c0002t0001g0209 a0002c0002t0001g0276 a0002c0002t0002g0016 others(5): Show |
8 | HG01168.hp1 HG02109.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1412-503delA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2935692 | |||||||
| chrX:2935696 | T | C | 1 | a0002c0017t0001g0141 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1412-506A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2935696 | |||||||
| chrX:2935707 | T | A | 44 | a0001c0001t0001g0198 a0002c0002t0001g0210 a0002c0002t0002g0018 others(41): Show |
46 | HG00280.hp1 HG00597.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.1412-517A>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2935707 | |||||||
| chrX:2935732 | C | T | 2 | a0003c0013t0001g0296 a0003c0013t0002g0038 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1412-542G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2935732 | |||||||
| chrX:2935824 | T | C | 1 | a0002c0003t0001g0213 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1412-634A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2935824 | |||||||
| chrX:2935826 | C | T | 5 | a0001c0001t0001g0055 a0001c0001t0001g0180 a0001c0001t0001g0236 others(2): Show |
5 | HG02165.hp1 NA18950.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.1412-636G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2935826 | |||||||
| chrX:2936128 | G | T | 1 | a0002c0002t0002g0018 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1411+614C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2936128 | |||||||
| chrX:2936175 | A | T | 1 | a0001c0001t0001g0164 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1411+567T>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2936175 | |||||||
| chrX:2936303 | C | G | 1 | a0002c0004t0002g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1411+439G>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2936303 | |||||||
| chrX:2936621 | C | T | 1 | a0002c0002t0002g0016 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1411+121G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2936621 | |||||||
| chrX:2936908 | C | T | 2 | a0002c0003t0001g0213 a0002c0004t0002g0028 |
2 | HG00733.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1290-45G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2936908 | |||||||
| chrX:2936994 | G | T | 1 | a0001c0001t0001g0153 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1290-131C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2936994 | |||||||
| chrX:2937130 | G | A | 4 | a0003c0005t0003g0211 a0003c0005t0003g0212 a0003c0005t0004g0022 others(1): Show |
4 | HG02257.hp1 HG03139.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1290-267C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2937130 | |||||||
| chrX:2937134 | G | C | 34 | a0002c0002t0003g0006 a0002c0002t0003g0065 a0002c0002t0003g0070 others(31): Show |
35 | HG00597.hp2 HG00733.hp1 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.1290-271C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2937134 | |||||||
| chrX:2937158 | T | C | 32 | a0002c0002t0003g0006 a0002c0002t0003g0065 a0002c0002t0003g0070 others(29): Show |
33 | HG00597.hp2 HG01123.hp2 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.1290-295A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2937158 | |||||||
| chrX:2937164 | C | A | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0179 |
3 | NA18983.hp1 NA18985.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1290-301G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2937164 | |||||||
| chrX:2937326 | G | A | 1 | a0002c0003t0001g0213 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1290-463C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2937326 | |||||||
| chrX:2937348 | C | T | 1 | a0002c0003t0001g0208 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1290-485G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2937348 | |||||||
| chrX:2937485 | T | C | 5 | a0002c0004t0005g0110 a0002c0004t0005g0118 a0002c0004t0005g0129 others(2): Show |
5 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1289+610A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2937485 | |||||||
| chrX:2937640 | T | C | 3 | a0002c0002t0002g0049 a0003c0013t0001g0296 a0003c0013t0002g0038 |
3 | HG02615.hp2 HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1289+455A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2937640 | |||||||
| chrX:2937797 | T | G | 9 | a0002c0003t0001g0205 a0002c0003t0002g0023 a0002c0003t0002g0024 others(6): Show |
9 | HG01109.hp1 HG01891.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1289+298A>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2937797 | |||||||
| chrX:2937825 | T | C | 3 | a0002c0002t0001g0209 a0002c0002t0002g0047 a0002c0003t0001g0240 |
3 | HG02486.hp1 HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1289+270A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2937825 | |||||||
| chrX:2937877 | G | C | 1 | a0001c0001t0001g0140 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1289+218C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2937877 | |||||||
| chrX:2938380 | T | TTC | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(195): Show |
207 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1127-125_1127-124d others(4): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2938380 | |||||||
| chrX:2938382 | C | T | 2 | a0002c0002t0001g0209 a0002c0002t0002g0047 |
2 | HG02486.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1127-125G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2938382 | |||||||
| chrX:2938574 | C | T | 3 | a0001c0001t0001g0091 a0001c0001t0001g0214 a0002c0002t0003g0235 |
3 | HG02572.hp1 NA18949.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1127-317G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2938574 | |||||||
| chrX:2938938 | C | T | 1 | a0002c0003t0001g0213 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1127-681G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2938938 | |||||||
| chrX:2939025 | A | G | 1 | a0002c0003t0001g0213 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1127-768T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939025 | |||||||
| chrX:2939088 | G | C | 3 | a0002c0002t0001g0130 a0002c0004t0001g0285 a0002c0004t0002g0032 |
3 | NA18522.hp1 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1127-831C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939088 | |||||||
| chrX:2939259 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1127-1002G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939259 | |||||||
| chrX:2939316 | C | G | 2 | a0002c0003t0001g0206 a0004c0006t0002g0004 |
3 | HG00741.hp2 HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1127-1059G>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939316 | |||||||
| chrX:2939317 | C | T | 6 | a0002c0002t0001g0210 a0002c0002t0002g0019 a0002c0002t0002g0020 others(3): Show |
6 | HG00733.hp1 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1127-1060G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939317 | |||||||
| chrX:2939324 | G | A | 15 | a0002c0002t0003g0006 a0002c0002t0003g0065 a0002c0002t0003g0070 others(12): Show |
16 | HG00597.hp2 HG01123.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.1127-1067C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939324 | |||||||
| chrX:2939416 | C | T | 3 | a0002c0004t0002g0028 a0003c0013t0001g0296 a0003c0013t0002g0038 |
3 | HG00733.hp1 HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1127-1159G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939416 | |||||||
| chrX:2939549 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1127-1292C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939549 | |||||||
| chrX:2939583 | C | T | 27 | a0002c0002t0003g0006 a0002c0002t0003g0065 a0002c0002t0003g0070 others(24): Show |
28 | HG00597.hp2 HG01123.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.1127-1326G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939583 | |||||||
| chrX:2939636 | A | G | 8 | a0002c0003t0001g0206 a0002c0003t0001g0240 a0002c0004t0005g0110 others(5): Show |
9 | HG00741.hp2 HG02280.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1127-1379T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939636 | |||||||
| chrX:2939772 | C | A | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(232): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1127-1515G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939772 | |||||||
| chrX:2939813 | T | A | 3 | a0002c0002t0001g0130 a0002c0004t0001g0285 a0002c0004t0002g0032 |
3 | NA18522.hp1 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1127-1556A>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939813 | |||||||
| chrX:2939864 | C | CT | 11 | a0001c0001t0001g0125 a0001c0001t0001g0172 a0002c0002t0001g0124 others(8): Show |
11 | HG00423.hp2 HG01106.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.1127-1608dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939864 | |||||||
| chrX:2939864 | CT | C | 48 | a0001c0001t0001g0063 a0001c0001t0001g0086 a0001c0001t0001g0123 others(45): Show |
50 | HG00140.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.1127-1608delA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939864 | |||||||
| chrX:2939864 | CTT | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(154): Show |
166 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1127-1609_1127-160 others(6): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939864 | |||||||
| chrX:2939864 | CTTT | C | 15 | a0001c0001t0001g0062 a0001c0001t0001g0101 a0001c0001t0001g0121 others(12): Show |
15 | HG01081.hp1 HG01169.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.1127-1610_1127-160 others(7): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939864 | |||||||
| chrX:2939913 | C | A | 1 | a0001c0001t0001g0216 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1127-1656G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939913 | |||||||
| chrX:2939914 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1127-1657T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939914 | |||||||
| chrX:2940025 | G | A | 1 | a0002c0004t0002g0028 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1127-1768C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940025 | |||||||
| chrX:2940042 | A | T | 1 | a0001c0001t0001g0189 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1127-1785T>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940042 | |||||||
| chrX:2940092 | T | G | 27 | a0002c0002t0003g0006 a0002c0002t0003g0065 a0002c0002t0003g0070 others(24): Show |
28 | HG00597.hp2 HG01123.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.1127-1835A>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940092 | |||||||
| chrX:2940100 | T | G | 1 | a0002c0017t0001g0141 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1127-1843A>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940100 | |||||||
| chrX:2940135 | T | C | 1 | a0004c0006t0002g0033 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1127-1878A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940135 | |||||||
| chrX:2940157 | T | A | 1 | a0002c0003t0001g0240 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1127-1900A>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940157 | |||||||
| chrX:2940159 | C | T | 1 | a0002c0003t0001g0240 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1127-1902G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940159 | |||||||
| chrX:2940562 | G | T | 2 | a0001c0001t0006g0116 a0001c0007t0006g0256 |
2 | HG00323.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1127-2305C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940562 | |||||||
| chrX:2940655 | A | G | 8 | a0002c0003t0001g0206 a0002c0003t0001g0240 a0002c0004t0005g0110 others(5): Show |
9 | HG00741.hp2 HG02280.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1127-2398T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940655 | |||||||
| chrX:2940672 | CCTG | C | 27 | a0002c0002t0003g0006 a0002c0002t0003g0065 a0002c0002t0003g0070 others(24): Show |
28 | HG00597.hp2 HG01123.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.1126+2390_1126+239 others(7): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940672 | |||||||
| chrX:2940890 | C | T | 6 | a0002c0004t0001g0112 a0003c0005t0002g0025 a0003c0005t0002g0026 others(3): Show |
6 | HG01070.hp1 HG01071.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1126+2175G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940890 | |||||||
| chrX:2940947 | A | C | 3 | a0002c0002t0001g0130 a0002c0004t0001g0285 a0002c0004t0002g0032 |
3 | NA18522.hp1 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1126+2118T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940947 | |||||||
| chrX:2940988 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1126+2077C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940988 | |||||||
| chrX:2941247 | CT | C | 38 | a0001c0001t0001g0172 a0002c0002t0001g0130 a0002c0002t0001g0209 others(35): Show |
39 | HG00597.hp2 HG01123.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.1126+1817delA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941247 | |||||||
| chrX:2941247 | CTTTTTTT others(3): Show |
C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(181): Show |
193 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1126+1808_1126+181 others(14): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941247 | |||||||
| chrX:2941247 | CTTTTTTT others(4): Show |
C | 5 | a0001c0001t0001g0221 a0001c0001t0001g0254 a0001c0001t0001g0273 others(2): Show |
5 | HG00408.hp1 HG01169.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1126+1807_1126+181 others(15): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941247 | |||||||
| chrX:2941253 | T | C | 1 | a0002c0003t0001g0213 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1126+1812A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941253 | |||||||
| chrX:2941401 | C | T | 27 | a0002c0002t0003g0006 a0002c0002t0003g0065 a0002c0002t0003g0070 others(24): Show |
28 | HG00597.hp2 HG01123.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.1126+1664G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941401 | |||||||
| chrX:2941411 | C | T | 1 | a0002c0002t0001g0148 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1126+1654G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941411 | |||||||
| chrX:2941412 | A | C | 1 | a0001c0001t0001g0216 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+1653T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941412 | |||||||
| chrX:2941420 | A | T | 2 | a0002c0002t0001g0209 a0002c0002t0002g0047 |
2 | HG02486.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1126+1645T>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941420 | |||||||
| chrX:2941460 | G | T | 1 | a0001c0001t0001g0248 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+1605C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941460 | |||||||
| chrX:2941461 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1126+1604C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941461 | |||||||
| chrX:2941551 | G | A | 28 | a0002c0002t0003g0006 a0002c0002t0003g0065 a0002c0002t0003g0070 others(25): Show |
29 | HG00597.hp2 HG00733.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.1126+1514C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941551 | |||||||
| chrX:2941619 | C | A | 1 | a0002c0004t0001g0242 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1126+1446G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941619 | |||||||
| chrX:2941761 | A | C | 1 | a0001c0001t0001g0273 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1126+1304T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941761 | |||||||
| chrX:2941763 | C | A | 1 | a0001c0001t0001g0273 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1126+1302G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941763 | |||||||
| chrX:2941798 | C | T | 5 | a0002c0002t0001g0210 a0002c0002t0002g0019 a0002c0002t0002g0020 others(2): Show |
5 | HG01891.hp2 HG02145.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1126+1267G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941798 | |||||||
| chrX:2941838 | C | T | 5 | a0002c0002t0001g0210 a0002c0002t0002g0019 a0002c0002t0002g0020 others(2): Show |
5 | HG01891.hp2 HG02145.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1126+1227G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941838 | |||||||
| chrX:2941950 | A | C | 1 | a0001c0001t0001g0248 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+1115T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941950 | |||||||
| chrX:2941951 | C | A | 1 | a0001c0001t0001g0248 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+1114G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941951 | |||||||
| chrX:2941952 | A | C | 1 | a0001c0001t0001g0248 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+1113T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941952 | |||||||
| chrX:2942066 | G | T | 1 | a0002c0002t0002g0018 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1126+999C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942066 | |||||||
| chrX:2942145 | A | G | 1 | a0002c0002t0002g0049 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1126+920T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942145 | |||||||
| chrX:2942160 | C | G | 1 | a0002c0003t0001g0240 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1126+905G>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942160 | |||||||
| chrX:2942266 | A | C | 1 | a0001c0001t0001g0248 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+799T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942266 | |||||||
| chrX:2942352 | C | T | 2 | a0003c0013t0001g0296 a0003c0013t0002g0038 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1126+713G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942352 | |||||||
| chrX:2942395 | G | T | 3 | a0002c0002t0001g0130 a0002c0004t0001g0285 a0002c0004t0002g0032 |
3 | NA18522.hp1 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1126+670C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942395 | |||||||
| chrX:2942401 | T | C | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(235): Show |
249 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.1126+664A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942401 | |||||||
| chrX:2942416 | T | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(240): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1126+649A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942416 | |||||||
| chrX:2942480 | C | T | 27 | a0002c0002t0003g0006 a0002c0002t0003g0065 a0002c0002t0003g0070 others(24): Show |
28 | HG00597.hp2 HG01123.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.1126+585G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942480 | |||||||
| chrX:2943317 | G | T | 5 | a0001c0001t0001g0055 a0001c0001t0001g0180 a0001c0001t0001g0236 others(2): Show |
5 | HG02165.hp1 NA18950.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.992-118C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943317 | |||||||
| chrX:2943319 | A | C | 5 | a0001c0001t0001g0055 a0001c0001t0001g0180 a0001c0001t0001g0236 others(2): Show |
5 | HG02165.hp1 NA18950.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.992-120T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943319 | |||||||
| chrX:2943420 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.992-221T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943420 | |||||||
| chrX:2943423 | A | C | 27 | a0002c0002t0003g0006 a0002c0002t0003g0065 a0002c0002t0003g0070 others(24): Show |
28 | HG00597.hp2 HG01123.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.992-224T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943423 | |||||||
| chrX:2943453 | G | A | 1 | a0001c0014t0001g0200 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.992-254C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943453 | |||||||
| chrX:2943515 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.992-316C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943515 | |||||||
| chrX:2943516 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.992-317T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943516 | |||||||
| chrX:2943603 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.992-404C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943603 | |||||||
| chrX:2943666 | C | T | 2 | a0002c0002t0002g0018 a0002c0004t0002g0028 |
2 | HG00733.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.992-467G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943666 | |||||||
| chrX:2943698 | C | T | 2 | a0002c0002t0002g0018 a0002c0004t0002g0028 |
2 | HG00733.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.992-499G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943698 | |||||||
| chrX:2943706 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.992-507G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943706 | |||||||
| chrX:2943741 | C | CA | 10 | a0001c0001t0001g0085 a0001c0001t0001g0191 a0001c0007t0001g0068 others(7): Show |
10 | HG01516.hp2 HG01981.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.992-543dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943741 | |||||||
| chrX:2943741 | CA | C | 142 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(139): Show |
147 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.992-543delT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943741 | |||||||
| chrX:2943741 | CAA | C | 35 | a0001c0001t0001g0059 a0001c0001t0001g0062 a0001c0001t0001g0064 others(32): Show |
35 | HG00323.hp1 HG00673.hp1 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.992-544_992-543del others(2): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943741 | |||||||
| chrX:2943793 | G | GAGA | 3 | a0002c0002t0001g0130 a0002c0004t0001g0285 a0002c0004t0002g0032 |
3 | NA18522.hp1 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.992-597_992-595dup others(3): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943793 | |||||||
| chrX:2943815 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.992-616T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943815 | |||||||
| chrX:2944035 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.992-836G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944035 | |||||||
| chrX:2944178 | A | G | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0179 |
3 | NA18983.hp1 NA18985.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.992-979T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944178 | |||||||
| chrX:2944186 | T | G | 24 | a0002c0002t0003g0006 a0002c0002t0003g0065 a0002c0002t0003g0070 others(21): Show |
25 | HG00597.hp2 HG01261.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.992-987A>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944186 | |||||||
| chrX:2944193 | T | C | 11 | a0001c0001t0001g0074 a0001c0001t0001g0081 a0001c0001t0001g0098 others(8): Show |
11 | HG01175.hp2 HG01496.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.992-994A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944193 | |||||||
| chrX:2944194 | C | G | 11 | a0001c0001t0001g0074 a0001c0001t0001g0081 a0001c0001t0001g0098 others(8): Show |
11 | HG01175.hp2 HG01496.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.992-995G>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944194 | |||||||
| chrX:2944200 | A | C | 6 | a0002c0004t0001g0112 a0002c0004t0005g0110 a0002c0004t0005g0118 others(3): Show |
6 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.992-1001T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944200 | |||||||
| chrX:2944223 | A | T | 1 | a0004c0006t0001g0281 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.992-1024T>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944223 | |||||||
| chrX:2944226 | C | T | 20 | a0001c0001t0001g0172 a0002c0002t0001g0124 a0002c0002t0001g0130 others(17): Show |
20 | HG00733.hp1 HG01884.hp1 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.992-1027G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944226 | |||||||
| chrX:2944230 | C | T | 2 | a0002c0002t0001g0209 a0002c0002t0002g0047 |
2 | HG02486.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.992-1031G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944230 | |||||||
| chrX:2944238 | A | G | 5 | a0003c0005t0002g0025 a0003c0005t0002g0026 a0003c0005t0002g0030 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.992-1039T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944238 | |||||||
| chrX:2944252 | G | A | 1 | a0002c0002t0003g0247 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.992-1053C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944252 | |||||||
| chrX:2944262 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.992-1063A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944262 | |||||||
| chrX:2944266 | C | T | 2 | a0002c0002t0001g0169 a0002c0002t0001g0184 |
2 | NA18972.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.992-1067G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944266 | |||||||
| chrX:2944267 | A | C | 5 | a0001c0001t0001g0055 a0001c0001t0001g0180 a0001c0001t0001g0236 others(2): Show |
5 | HG02165.hp1 NA18950.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.992-1068T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944267 | |||||||
| chrX:2944274 | T | A | 5 | a0003c0005t0002g0025 a0003c0005t0002g0026 a0003c0005t0002g0030 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.992-1075A>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944274 | |||||||
| chrX:2944296 | G | A | 4 | a0001c0001t0001g0066 a0001c0001t0001g0248 a0001c0001t0001g0249 others(1): Show |
4 | NA18946.hp2 NA18954.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.992-1097C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944296 | |||||||
| chrX:2944314 | C | T | 2 | a0002c0002t0001g0057 a0002c0002t0001g0058 |
2 | NA18986.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.992-1115G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944314 | |||||||
| chrX:2944315 | A | G | 4 | a0001c0001t0001g0108 a0002c0002t0001g0057 a0002c0002t0001g0058 others(1): Show |
4 | HG00639.hp2 HG01074.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.992-1116T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944315 | |||||||
| chrX:2944323 | G | A | 8 | a0001c0001t0001g0172 a0002c0004t0002g0042 a0004c0006t0001g0243 others(5): Show |
8 | HG01884.hp1 HG02015.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.992-1124C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944323 | |||||||
| chrX:2944326 | T | C | 6 | a0004c0006t0001g0243 a0004c0006t0002g0027 a0004c0006t0002g0033 others(3): Show |
6 | HG01884.hp1 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.992-1127A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944326 | |||||||
| chrX:2944335 | A | T | 10 | a0002c0002t0002g0049 a0002c0003t0001g0240 a0003c0013t0001g0296 others(7): Show |
10 | HG01884.hp1 HG02451.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.992-1136T>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944335 | |||||||
| chrX:2944346 | C | A | 1 | a0004c0006t0001g0243 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.992-1147G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944346 | |||||||
| chrX:2944347 | C | G | 1 | a0004c0006t0001g0243 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.992-1148G>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944347 | |||||||
| chrX:2944432 | C | T | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0195 |
3 | HG02040.hp1 HG02083.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.992-1233G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944432 | |||||||
| chrX:2944433 | A | G | 6 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0195 others(3): Show |
6 | HG02040.hp1 HG02083.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.992-1234T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944433 | |||||||
| chrX:2944453 | C | CA | 8 | a0001c0001t0001g0091 a0001c0001t0001g0101 a0001c0001t0001g0120 others(5): Show |
8 | HG02486.hp1 HG02622.hp2 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.992-1255dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944453 | |||||||
| chrX:2944463 | AC | A | 14 | a0001c0001t0001g0172 a0002c0002t0001g0130 a0002c0002t0002g0018 others(11): Show |
14 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.992-1265delG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944463 | |||||||
| chrX:2944466 | A | C | 5 | a0002c0004t0005g0110 a0002c0004t0005g0118 a0002c0004t0005g0129 others(2): Show |
5 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.992-1267T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944466 | |||||||
| chrX:2944473 | CA | C | 14 | a0001c0001t0001g0122 a0001c0001t0001g0133 a0001c0001t0001g0223 others(11): Show |
14 | HG00738.hp1 HG01884.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.992-1275delT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944473 | |||||||
| chrX:2944473 | CAA | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(161): Show |
173 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.992-1276_992-1275d others(4): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944473 | |||||||
| chrX:2944475 | A | C | 1 | a0001c0001t0001g0267 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.992-1276T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944475 | |||||||
| chrX:2944477 | A | C | 5 | a0002c0002t0001g0130 a0002c0004t0001g0112 a0002c0004t0001g0285 others(2): Show |
5 | HG00733.hp1 HG02976.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.992-1278T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944477 | |||||||
| chrX:2944482 | A | C | 49 | a0001c0001t0001g0172 a0002c0002t0001g0130 a0002c0002t0001g0210 others(46): Show |
51 | HG00597.hp2 HG00733.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.992-1283T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944482 | |||||||
| chrX:2944508 | G | GTC | 5 | a0002c0004t0005g0110 a0002c0004t0005g0118 a0002c0004t0005g0129 others(2): Show |
5 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.992-1310_992-1309i others(4): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944508 | |||||||
| chrX:2944509 | C | A | 5 | a0002c0004t0005g0110 a0002c0004t0005g0118 a0002c0004t0005g0129 others(2): Show |
5 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.992-1310G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944509 | |||||||
| chrX:2944509 | C | CCA | 3 | a0002c0002t0001g0146 a0002c0002t0001g0183 a0002c0002t0002g0021 |
3 | HG01243.hp1 HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.992-1312_992-1311d others(4): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944509 | |||||||
| chrX:2944568 | A | AT | 7 | a0002c0004t0005g0110 a0002c0004t0005g0118 a0002c0004t0005g0129 others(4): Show |
7 | HG02559.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.992-1370dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944568 | |||||||
| chrX:2944594 | A | AC | 6 | a0001c0001t0001g0120 a0001c0001t0001g0197 a0001c0001t0001g0273 others(3): Show |
6 | HG01243.hp1 HG01361.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.992-1396dupG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944594 | |||||||
| chrX:2944680 | T | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(171): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.991+1318A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944680 | |||||||
| chrX:2944808 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.991+1190C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944808 | |||||||
| chrX:2944873 | G | A | 5 | a0003c0005t0002g0025 a0003c0005t0002g0026 a0003c0005t0002g0030 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.991+1125C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944873 | |||||||
| chrX:2944916 | A | G | 2 | a0002c0002t0003g0312 a0002c0016t0003g0313 |
2 | HG01123.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.991+1082T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944916 | |||||||
| chrX:2944961 | GGAA | G | 6 | a0004c0006t0001g0243 a0004c0006t0002g0027 a0004c0006t0002g0033 others(3): Show |
6 | HG01884.hp1 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.991+1034_991+1036d others(5): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944961 | |||||||
| chrX:2945005 | T | TAAGAAG | 3 | a0002c0002t0001g0209 a0002c0002t0002g0047 a0002c0003t0001g0240 |
3 | HG02486.hp1 HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.991+987_991+992dup others(6): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945005 | |||||||
| chrX:2945011 | G | C | 1 | a0002c0002t0001g0290 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.991+987C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945011 | |||||||
| chrX:2945107 | G | C | 1 | a0002c0002t0001g0290 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.991+891C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945107 | |||||||
| chrX:2945211 | C | G | 5 | a0002c0004t0005g0110 a0002c0004t0005g0118 a0002c0004t0005g0129 others(2): Show |
5 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.991+787G>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945211 | |||||||
| chrX:2945248 | G | A | 2 | a0003c0013t0001g0296 a0003c0013t0002g0038 |
2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.991+750C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945248 | |||||||
| chrX:2945433 | T | C | 7 | a0003c0005t0002g0025 a0003c0005t0002g0026 a0003c0005t0002g0030 others(4): Show |
7 | HG01070.hp1 HG01071.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.991+565A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945433 | |||||||
| chrX:2945502 | T | C | 2 | a0002c0002t0001g0124 a0002c0003t0002g0012 |
2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.991+496A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945502 | |||||||
| chrX:2945537 | C | T | 3 | a0002c0002t0001g0146 a0002c0002t0001g0183 a0002c0002t0002g0021 |
3 | HG01243.hp1 HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.991+461G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945537 | |||||||
| chrX:2945608 | T | C | 5 | a0003c0005t0002g0025 a0003c0005t0002g0026 a0003c0005t0002g0030 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.991+390A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945608 | |||||||
| chrX:2945686 | A | G | 1 | a0002c0003t0001g0206 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.991+312T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945686 | |||||||
| chrX:2945805 | G | A | 5 | a0003c0005t0002g0025 a0003c0005t0002g0026 a0003c0005t0002g0030 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.991+193C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945805 | |||||||
| chrX:2946322 | C | CT | 16 | a0001c0001t0001g0091 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
16 | HG01175.hp2 HG02145.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.855-189dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946322 | |||||||
| chrX:2946322 | CT | C | 23 | a0001c0001t0001g0073 a0001c0001t0001g0165 a0001c0001t0001g0186 others(20): Show |
23 | HG00733.hp1 HG01069.hp1 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.855-189delA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946322 | |||||||
| chrX:2946322 | CTTTTTTT | C | 6 | a0002c0002t0001g0124 a0002c0002t0001g0271 a0002c0003t0002g0012 others(3): Show |
7 | HG01884.hp1 HG01928.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.855-195_855-189del others(7): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946322 | |||||||
| chrX:2946322 | CTTTTTTT others(1): Show |
C | 11 | a0001c0001t0001g0273 a0001c0014t0001g0200 a0001c0015t0001g0160 others(8): Show |
11 | HG00642.hp1 HG01433.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.855-196_855-189del others(8): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946322 | |||||||
| chrX:2946322 | CTTTTTTT others(2): Show |
C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(68): Show |
77 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.855-197_855-189del others(9): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946322 | |||||||
| chrX:2946322 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0287 a0001c0001t0001g0302 |
2 | HG01169.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.855-198_855-189del others(10): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946322 | |||||||
| chrX:2946322 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0006g0116 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.855-200_855-189del others(12): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946322 | |||||||
| chrX:2946496 | GC | G | 2 | a0002c0002t0002g0003 a0002c0002t0002g0014 |
3 | HG02055.hp1 HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.855-363delG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946496 | |||||||
| chrX:2946505 | A | AT | 53 | a0001c0001t0001g0063 a0001c0001t0001g0066 a0001c0001t0001g0069 others(50): Show |
54 | HG00408.hp1 HG00741.hp2 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.855-372dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946505 | |||||||
| chrX:2946505 | A | ATT | 6 | a0001c0001t0001g0170 a0001c0001t0001g0186 a0002c0003t0002g0012 others(3): Show |
6 | HG02451.hp1 HG02451.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.855-373_855-372dup others(2): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946505 | |||||||
| chrX:2946505 | AT | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(85): Show |
93 | HG00140.hp1 HG00323.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.855-372delA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946505 | |||||||
| chrX:2946505 | ATTTTTTT others(8): Show |
A | 1 | a0001c0001t0001g0295 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.855-386_855-372del others(15): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946505 | |||||||
| chrX:2946580 | C | T | 1 | a0001c0009t0001g0277 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.855-446G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946580 | |||||||
| chrX:2946599 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.855-465G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946599 | |||||||
| chrX:2946750 | A | G | 5 | a0002c0002t0001g0244 a0002c0002t0002g0003 a0002c0002t0002g0014 others(2): Show |
6 | HG01884.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.855-616T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946750 | |||||||
| chrX:2946827 | A | C | 2 | a0001c0001t0001g0084 a0001c0001t0001g0220 |
2 | NA18970.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.855-693T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946827 | |||||||
| chrX:2946969 | A | G | 4 | a0003c0005t0003g0211 a0003c0005t0003g0212 a0003c0005t0004g0022 others(1): Show |
4 | HG02257.hp1 HG03139.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.855-835T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946969 | |||||||
| chrX:2947039 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.855-905G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2947039 | |||||||
| chrX:2947040 | G | A | 3 | a0002c0002t0002g0049 a0002c0003t0001g0213 a0002c0003t0001g0240 |
3 | HG02809.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.855-906C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2947040 | |||||||
| chrX:2947124 | C | T | 3 | a0002c0002t0002g0029 a0002c0002t0004g0031 a0002c0002t0004g0041 |
3 | HG02895.hp1 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.855-990G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2947124 | |||||||
| chrX:2947141 | G | A | 2 | a0001c0001t0001g0155 a0002c0002t0001g0279 |
2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.855-1007C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2947141 | |||||||
| chrX:2947243 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.855-1109C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2947243 | |||||||
| chrX:2947255 | G | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(122): Show |
133 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.855-1121C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2947255 | |||||||
| chrX:2947815 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.854+1489C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2947815 | |||||||
| chrX:2947889 | A | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(118): Show |
128 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.854+1415T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2947889 | |||||||
| chrX:2948191 | G | T | 1 | a0001c0001t0001g0185 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.854+1113C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2948191 | |||||||
| chrX:2948341 | G | C | 3 | a0002c0002t0002g0029 a0002c0002t0004g0031 a0002c0002t0004g0041 |
3 | HG02895.hp1 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.854+963C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2948341 | |||||||
| chrX:2948371 | C | CT | 7 | a0001c0001t0001g0248 a0002c0002t0001g0124 a0002c0002t0003g0079 others(4): Show |
7 | HG01261.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.854+932dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2948371 | |||||||
| chrX:2948615 | C | T | 3 | a0002c0002t0002g0049 a0002c0003t0001g0213 a0002c0003t0001g0240 |
3 | HG02809.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.854+689G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2948615 | |||||||
| chrX:2948739 | C | T | 2 | a0002c0004t0001g0285 a0002c0004t0002g0032 |
2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.854+565G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2948739 | |||||||
| chrX:2948853 | T | C | 1 | a0002c0003t0002g0012 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.854+451A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2948853 | |||||||
| chrX:2948898 | C | T | 2 | a0002c0002t0002g0003 a0002c0002t0002g0014 |
3 | HG02055.hp1 HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.854+406G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2948898 | |||||||
| chrX:2948989 | C | T | 2 | a0002c0004t0001g0112 a0002c0004t0002g0042 |
2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.854+315G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2948989 | |||||||
| chrX:2949001 | C | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(90): Show |
100 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.854+303G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2949001 | |||||||
| chrX:2949138 | C | T | 6 | a0001c0020t0001g0131 a0002c0004t0005g0110 a0002c0004t0005g0118 others(3): Show |
6 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.854+166G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2949138 | |||||||
| chrX:2949224 | C | A | 8 | a0002c0002t0003g0006 a0002c0002t0003g0065 a0002c0002t0003g0092 others(5): Show |
9 | HG00597.hp2 NA18949.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.854+80G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2949224 | |||||||
| chrX:2950133 | G | A | 3 | a0001c0001t0001g0194 a0001c0001t0001g0303 a0001c0001t0001g0304 |
3 | NA18964.hp2 NA19064.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.431-406C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2950133 | |||||||
| chrX:2950167 | T | C | 1 | a0002c0003t0002g0012 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.431-440A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2950167 | |||||||
| chrX:2950398 | T | C | 7 | a0001c0020t0001g0131 a0002c0004t0001g0242 a0002c0004t0005g0110 others(4): Show |
7 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.431-671A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2950398 | |||||||
| chrX:2950443 | C | T | 2 | a0002c0002t0001g0169 a0002c0002t0001g0184 |
2 | NA18972.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.431-716G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2950443 | |||||||
| chrX:2950513 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(107): Show |
116 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.431-786T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2950513 | |||||||
| chrX:2950832 | GACACAGA others(6): Show |
G | 1 | a0001c0001t0001g0264 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.431-1118_431-1106d others(15): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2950832 | |||||||
| chrX:2950880 | TC | T | 8 | a0002c0002t0003g0006 a0002c0002t0003g0065 a0002c0002t0003g0092 others(5): Show |
9 | HG00597.hp2 NA18949.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.431-1154delG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2950880 | |||||||
| chrX:2951104 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.431-1377G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951104 | |||||||
| chrX:2951321 | C | T | 8 | a0002c0002t0003g0006 a0002c0002t0003g0065 a0002c0002t0003g0092 others(5): Show |
9 | HG00597.hp2 NA18949.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.431-1594G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951321 | |||||||
| chrX:2951598 | G | T | 3 | a0002c0003t0001g0208 a0002c0003t0001g0213 a0002c0003t0001g0240 |
3 | HG02145.hp1 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.430+1545C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951598 | |||||||
| chrX:2951614 | C | CA | 16 | a0001c0001t0001g0078 a0001c0001t0001g0091 a0001c0001t0001g0122 others(13): Show |
16 | HG01106.hp1 HG01175.hp2 HG03834.hp1 others(13): Show |
intron_variant | MODIFIER | c.430+1528dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951614 | |||||||
| chrX:2951614 | CA | C | 7 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0303 others(4): Show |
7 | HG01070.hp1 HG01071.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+1528delT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951614 | |||||||
| chrX:2951614 | CAA | C | 41 | a0001c0020t0001g0131 a0002c0002t0002g0029 a0002c0002t0004g0031 others(38): Show |
42 | HG00741.hp2 HG01109.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.430+1527_430+1528d others(4): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951614 | |||||||
| chrX:2951624 | A | G | 1 | a0002c0002t0001g0271 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.430+1519T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951624 | |||||||
| chrX:2951800 | TA | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(67): Show |
76 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.430+1342delT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951800 | |||||||
| chrX:2951850 | G | A | 25 | a0001c0001t0001g0056 a0001c0001t0001g0064 a0001c0001t0001g0066 others(22): Show |
26 | HG01081.hp2 HG01192.hp1 HG02056.hp1 others(23): Show |
intron_variant | MODIFIER | c.430+1293C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951850 | |||||||
| chrX:2951874 | G | GT | 15 | a0001c0001t0001g0082 a0001c0001t0001g0086 a0001c0001t0001g0101 others(12): Show |
15 | HG00735.hp2 HG01175.hp2 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.430+1268dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951874 | |||||||
| chrX:2951874 | G | GTT | 7 | a0002c0003t0001g0206 a0002c0003t0002g0023 a0002c0003t0002g0024 others(4): Show |
7 | HG00741.hp2 HG01891.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+1267_430+1268d others(4): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951874 | |||||||
| chrX:2951874 | GT | G | 20 | a0001c0001t0001g0250 a0001c0020t0001g0131 a0002c0004t0001g0112 others(17): Show |
21 | HG01884.hp1 HG02280.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.430+1268delA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951874 | |||||||
| chrX:2951874 | GTTTTTTT | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(74): Show |
84 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.430+1262_430+1268d others(9): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951874 | |||||||
| chrX:2951905 | C | G | 87 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(84): Show |
90 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.430+1238G>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951905 | |||||||
| chrX:2951990 | T | TA | 16 | a0001c0020t0001g0131 a0002c0002t0002g0029 a0002c0002t0004g0031 others(13): Show |
16 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.430+1152dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951990 | |||||||
| chrX:2952117 | G | C | 1 | a0001c0001t0001g0153 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.430+1026C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2952117 | |||||||
| chrX:2952272 | C | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(120): Show |
131 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.430+871G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2952272 | |||||||
| chrX:2952347 | C | G | 21 | a0001c0020t0001g0131 a0002c0002t0002g0029 a0002c0002t0004g0031 others(18): Show |
21 | HG01070.hp1 HG01071.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.430+796G>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2952347 | |||||||
| chrX:2952412 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0174 a0001c0001t0001g0192 others(4): Show |
8 | HG00323.hp2 HG00639.hp1 HG00733.hp2 others(5): Show |
intron_variant | MODIFIER | c.430+731G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2952412 | |||||||
| chrX:2952502 | G | A | 11 | a0001c0001t0001g0064 a0001c0001t0001g0091 a0001c0001t0001g0102 others(8): Show |
12 | HG01081.hp2 HG01192.hp1 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.430+641C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2952502 | |||||||
| chrX:2952517 | C | T | 1 | a0001c0001t0001g0253 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.430+626G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2952517 | |||||||
| chrX:2952669 | G | A | 1 | a0004c0006t0001g0243 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.430+474C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2952669 | |||||||
| chrX:2952676 | G | T | 1 | a0001c0001t0001g0248 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.430+467C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2952676 | |||||||
| chrX:2952970 | G | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(86): Show |
96 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.430+173C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2952970 | |||||||
| chrX:2953005 | A | G | 3 | a0002c0002t0002g0029 a0002c0002t0004g0031 a0002c0002t0004g0041 |
3 | HG02895.hp1 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.430+138T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2953005 | |||||||
| chrX:2953135 | G | A | 8 | a0002c0002t0003g0006 a0002c0002t0003g0065 a0002c0002t0003g0092 others(5): Show |
9 | HG00597.hp2 NA18949.hp2 NA18951.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.430+8C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2953135 | |||||||
| chrX:2953411 | C | T | 3 | a0002c0003t0001g0208 a0002c0003t0001g0213 a0002c0003t0001g0240 |
3 | HG02145.hp1 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.308-146G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2953411 | |||||||
| chrX:2953433 | G | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(64): Show |
73 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.308-168C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2953433 | |||||||
| chrX:2953490 | T | C | 20 | a0002c0003t0001g0205 a0002c0003t0001g0206 a0002c0003t0001g0208 others(17): Show |
21 | HG00741.hp2 HG01109.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.308-225A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2953490 | |||||||
| chrX:2953716 | C | T | 7 | a0004c0006t0001g0243 a0004c0006t0002g0004 a0004c0006t0002g0027 others(4): Show |
8 | HG01884.hp1 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.308-451G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2953716 | |||||||
| chrX:2953899 | T | G | 1 | a0001c0009t0001g0105 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.308-634A>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2953899 | |||||||
| chrX:2954125 | C | A | 1 | a0007c0021t0001g0096 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.308-860G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2954125 | |||||||
| chrX:2954556 | A | T | 1 | a0001c0001t0001g0164 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.307+860T>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2954556 | |||||||
| chrX:2954586 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.307+830C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2954586 | |||||||
| chrX:2954628 | G | GTATTAT | 10 | a0002c0003t0001g0208 a0002c0003t0001g0213 a0002c0003t0001g0240 others(7): Show |
11 | HG01884.hp1 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.307+782_307+787dup others(6): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2954628 | |||||||
| chrX:2954628 | G | GTATTATT others(2): Show |
10 | a0002c0003t0001g0205 a0002c0003t0001g0206 a0002c0003t0002g0023 others(7): Show |
10 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.307+779_307+787dup others(9): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2954628 | |||||||
| chrX:2954726 | G | C | 15 | a0001c0001t0001g0063 a0001c0001t0001g0103 a0001c0001t0001g0158 others(12): Show |
15 | HG00099.hp1 HG00642.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.307+690C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2954726 | |||||||
| chrX:2954738 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.307+678G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2954738 | |||||||
| chrX:2954932 | G | A | 1 | a0001c0020t0001g0131 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.307+484C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2954932 | |||||||
| chrX:2955207 | G | A | 7 | a0001c0001t0001g0161 a0001c0001t0001g0197 a0003c0005t0002g0025 others(4): Show |
7 | HG01070.hp1 HG01071.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.307+209C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2955207 | |||||||
| chrX:2955272 | A | C | 35 | a0001c0020t0001g0131 a0002c0002t0001g0130 a0002c0002t0002g0029 others(32): Show |
36 | HG00597.hp2 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.307+144T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2955272 | |||||||
| chrX:2955315 | T | G | 3 | a0002c0003t0001g0208 a0002c0003t0001g0213 a0002c0003t0001g0240 |
3 | HG02145.hp1 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.307+101A>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2955315 | |||||||
| chrX:2955597 | T | C | 1 | a0001c0001t0002g0037 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.186-60A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2955597 | |||||||
| chrX:2955804 | C | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(59): Show |
68 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.186-267G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2955804 | |||||||
| chrX:2955857 | T | C | 4 | a0001c0009t0001g0104 a0001c0009t0001g0105 a0001c0009t0001g0196 others(1): Show |
4 | HG00140.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-320A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2955857 | |||||||
| chrX:2955939 | G | C | 22 | a0002c0002t0002g0047 a0002c0003t0001g0205 a0002c0003t0001g0206 others(19): Show |
23 | HG00741.hp2 HG01109.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.186-402C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2955939 | |||||||
| chrX:2956045 | T | C | 10 | a0002c0003t0001g0205 a0002c0003t0001g0206 a0002c0003t0002g0023 others(7): Show |
10 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.186-508A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2956045 | |||||||
| chrX:2956106 | G | A | 22 | a0002c0002t0002g0047 a0002c0003t0001g0208 a0002c0003t0001g0213 others(19): Show |
23 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.186-569C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2956106 | |||||||
| chrX:2956355 | C | T | 9 | a0002c0003t0001g0205 a0002c0003t0002g0023 a0002c0003t0002g0024 others(6): Show |
9 | HG01109.hp1 HG01891.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.186-818G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2956355 | |||||||
| chrX:2956413 | T | C | 14 | a0002c0003t0001g0205 a0002c0003t0001g0206 a0002c0003t0001g0208 others(11): Show |
14 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.186-876A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2956413 | |||||||
| chrX:2956788 | C | T | 14 | a0002c0003t0001g0205 a0002c0003t0001g0208 a0002c0003t0001g0213 others(11): Show |
14 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.186-1251G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2956788 | |||||||
| chrX:2956804 | G | T | 15 | a0002c0003t0001g0205 a0002c0003t0001g0206 a0002c0003t0001g0208 others(12): Show |
15 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.186-1267C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2956804 | |||||||
| chrX:2956937 | A | T | 1 | a0001c0001t0001g0125 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.185+1337T>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2956937 | |||||||
| chrX:2956971 | C | T | 1 | a0002c0002t0001g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.185+1303G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2956971 | |||||||
| chrX:2956987 | T | C | 13 | a0002c0002t0002g0047 a0003c0005t0002g0025 a0003c0005t0002g0026 others(10): Show |
14 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.185+1287A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2956987 | |||||||
| chrX:2956988 | G | A | 13 | a0002c0002t0002g0047 a0003c0005t0002g0025 a0003c0005t0002g0026 others(10): Show |
14 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.185+1286C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2956988 | |||||||
| chrX:2956997 | A | T | 13 | a0002c0002t0002g0047 a0003c0005t0002g0025 a0003c0005t0002g0026 others(10): Show |
14 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.185+1277T>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2956997 | |||||||
| chrX:2957003 | C | CTTG | 13 | a0002c0002t0002g0047 a0003c0005t0002g0025 a0003c0005t0002g0026 others(10): Show |
14 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.185+1270_185+1271i others(5): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957003 | |||||||
| chrX:2957028 | T | C | 10 | a0002c0003t0001g0205 a0002c0003t0001g0206 a0002c0003t0002g0023 others(7): Show |
10 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.185+1246A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957028 | |||||||
| chrX:2957048 | C | T | 3 | a0006c0011t0001g0067 a0006c0011t0001g0217 a0006c0011t0001g0298 |
3 | HG02129.hp1 NA19000.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.185+1226G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957048 | |||||||
| chrX:2957076 | C | T | 1 | a0001c0001t0001g0253 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.185+1198G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957076 | |||||||
| chrX:2957093 | C | T | 1 | a0002c0003t0002g0012 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.185+1181G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957093 | |||||||
| chrX:2957145 | C | T | 1 | a0002c0002t0002g0049 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.185+1129G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957145 | |||||||
| chrX:2957215 | C | T | 15 | a0002c0003t0001g0205 a0002c0003t0001g0206 a0002c0003t0001g0208 others(12): Show |
15 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.185+1059G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957215 | |||||||
| chrX:2957220 | C | CAAA | 7 | a0002c0002t0002g0047 a0003c0005t0002g0030 a0004c0006t0001g0243 others(4): Show |
8 | HG01884.hp1 HG02280.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+1051_185+1053d others(5): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957220 | |||||||
| chrX:2957220 | C | CAAAA | 7 | a0002c0003t0002g0023 a0003c0005t0002g0025 a0003c0005t0002g0026 others(4): Show |
7 | HG01070.hp1 HG01071.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+1050_185+1053d others(6): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957220 | |||||||
| chrX:2957220 | C | CAAAAA | 10 | a0002c0003t0001g0205 a0002c0003t0001g0206 a0002c0003t0001g0208 others(7): Show |
10 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.185+1049_185+1053d others(7): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957220 | |||||||
| chrX:2957462 | A | T | 1 | a0001c0001t0001g0164 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.185+812T>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957462 | |||||||
| chrX:2957632 | C | T | 1 | a0002c0002t0001g0315 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.185+642G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957632 | |||||||
| chrX:2957688 | A | G | 2 | a0002c0002t0002g0018 a0002c0004t0002g0028 |
2 | HG00733.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.185+586T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957688 | |||||||
| chrX:2957708 | C | CA | 24 | a0001c0001t0001g0164 a0001c0001t0001g0263 a0001c0001t0001g0264 others(21): Show |
26 | HG00597.hp2 HG01361.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.185+565dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957708 | |||||||
| chrX:2957708 | C | CAA | 7 | a0002c0002t0002g0018 a0002c0004t0002g0028 a0003c0005t0002g0025 others(4): Show |
7 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+564_185+565dup others(2): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957708 | |||||||
| chrX:2957708 | C | CAAA | 11 | a0002c0003t0001g0205 a0002c0003t0001g0206 a0002c0003t0002g0012 others(8): Show |
11 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.185+563_185+565dup others(3): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957708 | |||||||
| chrX:2957727 | A | G | 1 | a0001c0001t0001g0170 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.185+547T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957727 | |||||||
| chrX:2957944 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.185+330G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957944 | |||||||
| chrX:2958149 | C | A | 10 | a0002c0003t0001g0205 a0002c0003t0001g0206 a0002c0003t0002g0023 others(7): Show |
10 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.185+125G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2958149 | |||||||
| chrX:2958173 | T | C | 2 | a0001c0001t0001g0188 a0001c0001t0001g0197 |
2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.185+101A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2958173 | |||||||
| chrX:2958238 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.185+36A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2958238 | |||||||
| chrX:2958461 | G | A | 16 | a0002c0002t0002g0047 a0002c0002t0003g0006 a0002c0002t0003g0065 others(13): Show |
18 | HG00597.hp2 HG01884.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.24-26C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2958461 | |||||||
| chrX:2958641 | G | T | 4 | a0002c0003t0001g0208 a0002c0003t0001g0213 a0002c0003t0001g0240 others(1): Show |
4 | HG02145.hp1 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.24-206C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2958641 | |||||||
| chrX:2958642 | G | T | 25 | a0002c0003t0001g0205 a0002c0003t0001g0206 a0002c0003t0001g0208 others(22): Show |
25 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.24-207C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2958642 | |||||||
| chrX:2958647 | T | C | 3 | a0001c0001t0001g0165 a0001c0001t0001g0286 a0002c0003t0002g0044 |
3 | HG01891.hp1 HG04184.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.24-212A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2958647 | |||||||
| chrX:2958848 | G | A | 1 | a0002c0002t0002g0016 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.24-413C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2958848 | |||||||
| chrX:2959031 | A | C | 1 | a0001c0001t0001g0123 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.24-596T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2959031 | |||||||
| chrX:2959409 | G | A | 1 | a0002c0003t0002g0012 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.23+969C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2959409 | |||||||
| chrX:2959447 | C | A | 5 | a0003c0005t0001g0080 a0003c0005t0003g0211 a0003c0005t0003g0212 others(2): Show |
5 | HG02257.hp1 HG02280.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.23+931G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2959447 | |||||||
| chrX:2959691 | C | T | 11 | a0002c0002t0001g0209 a0002c0002t0002g0047 a0002c0002t0004g0031 others(8): Show |
12 | HG01884.hp1 HG02280.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.23+687G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2959691 | |||||||
| chrX:2959758 | C | G | 8 | a0001c0001t0001g0055 a0001c0001t0001g0064 a0001c0001t0001g0091 others(5): Show |
8 | HG02155.hp2 HG02165.hp1 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.23+620G>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2959758 | |||||||
| chrX:2959794 | G | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(54): Show |
62 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.23+584C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2959794 | |||||||
| chrX:2959835 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(109): Show |
120 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.23+543A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2959835 | |||||||
| chrX:2959941 | G | GAGAA | 17 | a0001c0001t0001g0077 a0002c0002t0002g0047 a0002c0002t0003g0006 others(14): Show |
19 | HG00597.hp2 HG01884.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.23+433_23+436dupTT others(2): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2959941 | |||||||
| chrX:2959941 | GAGAA | G | 22 | a0001c0007t0001g0307 a0002c0002t0002g0003 a0002c0002t0002g0014 others(19): Show |
23 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.23+433_23+436delTT others(2): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2959941 | |||||||
| chrX:2959941 | GAGAAAGA others(9): Show |
G | 1 | a0001c0001t0001g0188 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.23+421_23+436delTT others(14): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2959941 | |||||||
| chrX:2960014 | A | C | 1 | a0001c0001t0001g0102 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.23+364T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960014 | |||||||
| chrX:2960025 | T | G | 4 | a0003c0005t0003g0211 a0003c0005t0003g0212 a0003c0005t0004g0022 others(1): Show |
4 | HG02257.hp1 HG03139.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.23+353A>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960025 | |||||||
| chrX:2960030 | G | T | 3 | a0003c0005t0002g0025 a0003c0005t0002g0026 a0003c0005t0002g0030 |
3 | HG01070.hp1 HG01071.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.23+348C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960030 | |||||||
| chrX:2960035 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.23+343G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960035 | |||||||
| chrX:2960040 | C | T | 6 | a0001c0001t0001g0074 a0001c0001t0001g0170 a0001c0001t0001g0171 others(3): Show |
6 | HG01175.hp2 HG01496.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.23+338G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960040 | |||||||
| chrX:2960085 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.23+293G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960085 | |||||||
| chrX:2960118 | A | C | 1 | a0002c0003t0002g0023 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.23+260T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960118 | |||||||
| chrX:2960121 | T | G | 7 | a0002c0002t0002g0003 a0002c0002t0002g0014 a0003c0005t0002g0025 others(4): Show |
8 | HG01070.hp1 HG01071.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.23+257A>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960121 | |||||||
| chrX:2960130 | G | A | 7 | a0002c0002t0002g0003 a0002c0002t0002g0014 a0003c0005t0002g0025 others(4): Show |
8 | HG01070.hp1 HG01071.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.23+248C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960130 | |||||||
| chrX:2960131 | T | C | 7 | a0002c0002t0002g0003 a0002c0002t0002g0014 a0003c0005t0002g0025 others(4): Show |
8 | HG01070.hp1 HG01071.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.23+247A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960131 | |||||||
| chrX:2960135 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0059 others(93): Show |
101 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.23+243C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960135 | |||||||
| chrX:2960137 | C | T | 2 | a0002c0002t0002g0029 a0002c0004t0001g0285 |
2 | NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.23+241G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960137 | |||||||
| chrX:2960138 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0059 others(111): Show |
120 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.23+240T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960138 | |||||||
| chrX:2960138 | A | T | 1 | a0001c0001t0001g0117 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.23+240T>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960138 | |||||||
| chrX:2960139 | G | T | 2 | a0002c0002t0001g0265 a0002c0018t0001g0168 |
2 | HG00099.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.23+239C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960139 | |||||||
| chrX:2960141 | C | T | 2 | a0002c0002t0001g0265 a0002c0018t0001g0168 |
2 | HG00099.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.23+237G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960141 | |||||||
| chrX:2960144 | C | T | 1 | a0001c0007t0001g0306 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.23+234G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960144 | |||||||
| chrX:2960149 | G | A | 2 | a0002c0002t0001g0265 a0002c0018t0001g0168 |
2 | HG00099.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.23+229C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960149 | |||||||
| chrX:2960159 | C | T | 7 | a0001c0001t0001g0076 a0001c0001t0001g0187 a0001c0001t0001g0230 others(4): Show |
7 | NA18957.hp1 NA18969.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.23+219G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960159 | |||||||
| chrX:2960184 | G | C | 2 | a0002c0002t0001g0169 a0002c0002t0001g0184 |
2 | NA18972.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.23+194C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960184 | |||||||
| chrX:2960185 | T | C | 11 | a0001c0001t0001g0074 a0001c0001t0001g0087 a0001c0001t0001g0098 others(8): Show |
11 | HG01175.hp2 HG01258.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.23+193A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960185 | |||||||
| chrX:2960193 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(88): Show |
98 | HG00140.hp1 HG00323.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.23+185G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960193 | |||||||
| chrX:2960215 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(61): Show |
69 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.23+163C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960215 | |||||||
| chrX:2960221 | A | G | 1 | a0001c0001t0001g0215 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.23+157T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960221 | |||||||
| chrX:2960240 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.23+138C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960240 | |||||||
| chrX:2960247 | C | T | 1 | a0001c0001t0006g0116 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.23+131G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960247 | |||||||
| chrX:2960255 | T | C | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(305): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.23+123A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960255 | |||||||
| chrX:2960263 | C | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(95): Show |
105 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.23+115G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960263 | |||||||
| chrX:2960268 | C | CA | 39 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0075 others(36): Show |
41 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.23+109dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960268 | |||||||
| chrX:2960268 | C | CAA | 48 | a0001c0001t0001g0001 a0001c0001t0001g0059 a0001c0001t0001g0076 others(45): Show |
50 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.23+108_23+109dupTT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960268 | |||||||
| chrX:2960268 | C | CAAA | 16 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0078 others(13): Show |
19 | HG00140.hp1 HG00408.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.23+107_23+109dupTT others(1): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960268 | |||||||
| chrX:2960268 | CA | C | 18 | a0001c0001t0001g0066 a0001c0001t0001g0098 a0001c0001t0001g0099 others(15): Show |
18 | HG01943.hp1 HG01993.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.23+109delT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960268 | |||||||
| chrX:2960268 | CAAAAAA | C | 9 | a0002c0003t0001g0205 a0002c0003t0002g0023 a0002c0003t0002g0024 others(6): Show |
9 | HG01109.hp1 HG01891.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.23+104_23+109delTT others(4): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960268 | |||||||
| chrX:2960268 | CAAAAAAA | C | 18 | a0001c0001t0001g0108 a0002c0002t0001g0209 a0002c0002t0002g0047 others(15): Show |
20 | HG00597.hp2 HG00639.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.23+103_23+109delTT others(5): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960268 | |||||||
| chrX:2960268 | CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0001g0081 a0001c0001t0001g0102 a0001c0001t0001g0107 |
3 | NA18948.hp1 NA19002.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.23+99_23+109delTTT others(8): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960268 | |||||||
| chrX:2960320 | G | GAGAA | 11 | a0001c0001t0001g0207 a0002c0003t0001g0205 a0002c0003t0001g0206 others(8): Show |
11 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.23+54_23+57dupTTCT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960320 | |||||||
| chrX:2960320 | G | GAGAAAGA others(1): Show |
5 | a0002c0003t0001g0208 a0002c0003t0001g0213 a0002c0003t0001g0240 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.23+50_23+57dupTTCT others(4): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960320 | |||||||
| chrX:2960516 | C | G | 4 | a0001c0001t0001g0055 a0001c0001t0001g0064 a0001c0001t0001g0091 others(1): Show |
4 | HG02165.hp1 NA18949.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-96G>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2960516 | |||||||
| chrX:2960519 | G | A | 1 | a0002c0004t0001g0242 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-20-99C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2960519 | |||||||
| chrX:2960520 | T | G | 1 | a0003c0013t0001g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-20-100A>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2960520 | |||||||
| chrX:2960704 | T | C | 10 | a0002c0002t0001g0209 a0002c0002t0001g0210 a0002c0002t0003g0079 others(7): Show |
10 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-20-284A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2960704 | |||||||
| chrX:2960882 | G | C | 1 | a0003c0005t0004g0054 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-20-462C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2960882 | |||||||
| chrX:2960883 | A | G | 1 | a0008c0019t0001g0245 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-20-463T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2960883 | |||||||
| chrX:2960905 | T | C | 7 | a0001c0001t0001g0059 a0002c0002t0002g0047 a0003c0005t0004g0022 others(4): Show |
7 | HG02451.hp2 HG02486.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20-485A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2960905 | |||||||
| chrX:2960996 | AT | A | 13 | a0002c0002t0002g0039 a0002c0002t0002g0047 a0002c0003t0002g0040 others(10): Show |
13 | HG01109.hp1 HG01891.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-20-577delA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2960996 | |||||||
| chrX:2961253 | G | C | 4 | a0002c0002t0001g0241 a0002c0002t0001g0244 a0002c0004t0001g0242 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-833C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2961253 | |||||||
| chrX:2961256 | C | A | 1 | a0001c0001t0001g0280 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-20-836G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2961256 | |||||||
| chrX:2961394 | T | C | 29 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(26): Show |
29 | HG00408.hp1 HG00597.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.-20-974A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2961394 | |||||||
| chrX:2961533 | C | A | 8 | a0002c0002t0002g0018 a0002c0002t0002g0021 a0002c0002t0003g0232 others(5): Show |
8 | HG01243.hp1 HG02630.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.-20-1113G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2961533 | |||||||
| chrX:2961695 | A | G | 8 | a0002c0002t0001g0234 a0002c0002t0002g0034 a0002c0002t0003g0235 others(5): Show |
8 | HG02572.hp1 HG02723.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-20-1275T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2961695 | |||||||
| chrX:2961708 | T | C | 1 | a0002c0002t0001g0233 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-20-1288A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2961708 | |||||||
| chrX:2961827 | A | T | 1 | a0002c0002t0001g0106 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-20-1407T>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2961827 | |||||||
| chrX:2961858 | G | GT | 18 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0091 others(15): Show |
19 | HG00733.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.-20-1439dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2961858 | |||||||
| chrX:2961858 | GT | G | 12 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 others(9): Show |
12 | HG01070.hp2 HG02572.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.-20-1439delA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2961858 | |||||||
| chrX:2961865 | T | G | 5 | a0001c0001t0002g0037 a0002c0002t0002g0039 a0002c0003t0002g0040 others(2): Show |
5 | HG02615.hp2 HG02922.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-1445A>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2961865 | |||||||
| chrX:2961871 | T | C | 3 | a0001c0001t0001g0090 a0001c0001t0009g0239 a0002c0002t0003g0006 |
4 | NA18988.hp1 NA18999.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-1451A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2961871 | |||||||
| chrX:2961891 | A | AT | 4 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(1): Show |
4 | HG00438.hp2 NA18955.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-1472dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2961891 | |||||||
| chrX:2962154 | A | T | 1 | a0001c0001t0001g0097 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-20-1734T>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962154 | |||||||
| chrX:2962181 | C | A | 5 | a0001c0001t0002g0037 a0002c0002t0002g0039 a0002c0003t0002g0040 others(2): Show |
5 | HG02615.hp2 HG02922.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-1761G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962181 | |||||||
| chrX:2962417 | G | A | 1 | a0003c0005t0002g0035 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-21+1807C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962417 | |||||||
| chrX:2962454 | G | A | 15 | a0002c0002t0001g0241 a0002c0002t0001g0244 a0002c0002t0002g0021 others(12): Show |
15 | HG01070.hp1 HG01071.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.-21+1770C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962454 | |||||||
| chrX:2962476 | C | T | 1 | a0002c0003t0002g0012 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-21+1748G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962476 | |||||||
| chrX:2962481 | T | C | 8 | a0002c0002t0002g0047 a0002c0003t0002g0043 a0002c0003t0002g0044 others(5): Show |
8 | HG01109.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-21+1743A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962481 | |||||||
| chrX:2962525 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-21+1699A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962525 | |||||||
| chrX:2962629 | A | T | 8 | a0002c0002t0002g0047 a0002c0003t0002g0043 a0002c0003t0002g0044 others(5): Show |
8 | HG01109.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-21+1595T>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962629 | |||||||
| chrX:2962721 | A | G | 11 | a0001c0001t0002g0037 a0002c0002t0002g0019 a0002c0002t0002g0020 others(8): Show |
11 | HG02615.hp2 HG02630.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.-21+1503T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962721 | |||||||
| chrX:2962735 | C | T | 15 | a0002c0002t0002g0003 a0002c0002t0002g0014 a0002c0002t0002g0016 others(12): Show |
16 | HG01070.hp1 HG01071.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.-21+1489G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962735 | |||||||
| chrX:2962736 | A | G | 40 | a0001c0001t0002g0037 a0002c0002t0002g0003 a0002c0002t0002g0014 others(37): Show |
42 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.-21+1488T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962736 | |||||||
| chrX:2962751 | A | C | 2 | a0002c0003t0002g0023 a0002c0003t0002g0024 |
2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-21+1473T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962751 | |||||||
| chrX:2962835 | GAT | G | 14 | a0002c0002t0001g0244 a0002c0002t0002g0021 a0002c0002t0002g0034 others(11): Show |
14 | HG01070.hp1 HG01071.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-21+1387_-21+1388d others(4): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962835 | |||||||
| chrX:2962853 | T | C | 52 | a0001c0001t0001g0010 a0001c0001t0001g0094 a0001c0001t0001g0095 others(49): Show |
54 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-21+1371A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962853 | |||||||
| chrX:2962987 | C | T | 2 | a0002c0003t0002g0023 a0002c0003t0002g0024 |
2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-21+1237G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962987 | |||||||
| chrX:2963063 | C | T | 6 | a0002c0002t0002g0021 a0002c0003t0002g0023 a0002c0003t0002g0024 others(3): Show |
6 | HG01070.hp1 HG01071.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21+1161G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963063 | |||||||
| chrX:2963119 | G | A | 4 | a0001c0001t0001g0283 a0002c0002t0001g0011 a0002c0002t0001g0282 others(1): Show |
5 | HG01081.hp1 HG01081.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21+1105C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963119 | |||||||
| chrX:2963135 | G | A | 1 | a0002c0004t0001g0285 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-21+1089C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963135 | |||||||
| chrX:2963159 | T | G | 8 | a0002c0002t0002g0019 a0002c0002t0002g0020 a0002c0002t0002g0021 others(5): Show |
8 | HG01070.hp1 HG01071.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.-21+1065A>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963159 | |||||||
| chrX:2963166 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-21+1058C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963166 | |||||||
| chrX:2963201 | T | C | 13 | a0002c0002t0002g0047 a0002c0002t0002g0049 a0002c0003t0002g0043 others(10): Show |
13 | HG01109.hp1 HG01891.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-21+1023A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963201 | |||||||
| chrX:2963287 | A | G | 1 | a0003c0005t0002g0035 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-21+937T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963287 | |||||||
| chrX:2963424 | C | T | 1 | a0005c0008t0001g0060 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-21+800G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963424 | |||||||
| chrX:2963430 | C | A | 44 | a0001c0001t0002g0037 a0002c0002t0002g0003 a0002c0002t0002g0014 others(41): Show |
46 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.-21+794G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963430 | |||||||
| chrX:2963476 | T | C | 6 | a0002c0002t0002g0021 a0002c0003t0002g0023 a0002c0003t0002g0024 others(3): Show |
6 | HG01070.hp1 HG01071.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21+748A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963476 | |||||||
| chrX:2963533 | C | CT | 40 | a0001c0001t0001g0005 a0001c0001t0001g0062 a0001c0001t0001g0063 others(37): Show |
42 | HG00423.hp1 HG00597.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.-21+690dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963533 | |||||||
| chrX:2963533 | CT | C | 27 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0289 others(24): Show |
28 | HG00733.hp1 HG01069.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.-21+690delA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963533 | |||||||
| chrX:2963533 | CTT | C | 20 | a0001c0001t0002g0037 a0002c0002t0002g0039 a0002c0002t0002g0047 others(17): Show |
20 | HG01109.hp1 HG01175.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.-21+689_-21+690del others(2): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963533 | |||||||
| chrX:2963533 | CTTT | C | 8 | a0002c0002t0002g0003 a0002c0002t0002g0014 a0002c0002t0002g0016 others(5): Show |
9 | HG01261.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-21+688_-21+690del others(3): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963533 | |||||||
| chrX:2963603 | C | T | 8 | a0002c0002t0002g0003 a0002c0002t0002g0014 a0002c0002t0002g0016 others(5): Show |
9 | HG01261.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-21+621G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963603 | |||||||
| chrX:2963608 | A | G | 2 | a0005c0008t0001g0060 a0005c0008t0001g0061 |
2 | NA18962.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.-21+616T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963608 | |||||||
| chrX:2963709 | G | T | 1 | a0001c0001t0001g0059 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-21+515C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963709 | |||||||
| chrX:2963978 | T | C | 11 | a0001c0001t0001g0314 a0001c0007t0001g0305 a0001c0007t0001g0306 others(8): Show |
11 | HG01123.hp1 HG01123.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.-21+246A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963978 | |||||||
| chrX:2964041 | C | T | 2 | a0002c0002t0001g0057 a0002c0002t0001g0058 |
2 | NA18986.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.-21+183G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2964041 | |||||||
| chrX:2964105 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-21+119T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2964105 | |||||||
| chrX:2964203 | A | C | 1 | a0001c0001t0001g0055 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-21+21T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2964203 |