Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 171482 |
| ensemblid | ENSG00000183304.10 |
| hgncid | 18403 |
| symbol | FAM9A |
| name | family with sequence similarity 9 member A |
| refseq_nuc | NM_174951.3 |
| refseq_prot | NP_777611.1 |
| ensembl_nuc | ENST00000381003.7 |
| ensembl_prot | ENSP00000370391.3 |
| mane_status | MANE Select |
| chr | chrX |
| start | 8790795 |
| end | 8801383 |
| strand | - |
| ver | v1.2 |
| region | chrX:8790795-8801383 |
| region5000 | chrX:8785795-8806383 |
| regionname0 | FAM9A_chrX_8790795_8801383 |
| regionname5000 | FAM9A_chrX_8785795_8806383 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 332 | 283 | 64 | 53 | 127 | 11 | 26 | 100 | FAM9A_chrX_8785795_8806383 | FAM9A | MEPVG others(327): Show |
chrX | 8785795 | 8806383 |
| a0002 | 0/0 | 332 | 7 | 4 | 1 | 0 | 2 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | MEPVG others(327): Show |
chrX | 8785795 | 8806383 |
| a0003 | 0/0 | 331 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | MEPVG others(326): Show |
chrX | 8785795 | 8806383 |
| a0004 | 0/0 | 331 | 3 | 0 | 0 | 2 | 0 | 1 | 2 | FAM9A_chrX_8785795_8806383 | FAM9A | MEPVG others(326): Show |
chrX | 8785795 | 8806383 |
| a0005 | 0/0 | 326 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | MEPVG others(321): Show |
chrX | 8785795 | 8806383 |
| a0006 | 0/0 | 332 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM9A_chrX_8785795_8806383 | FAM9A | MEPVG others(327): Show |
chrX | 8785795 | 8806383 |
| a0007 | 0/0 | 332 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | MEPVG others(327): Show |
chrX | 8785795 | 8806383 |
| a0008 | 0/0 | 332 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | MEPVG others(327): Show |
chrX | 8785795 | 8806383 |
| a0009 | 0/0 | 289 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | MEPVG others(284): Show |
chrX | 8785795 | 8806383 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 996 | 274 | 58 | 52 | 127 | 11 | 24 | FAM9A_chrX_8785795_8806383 | FAM9A | ATGGA others(991): Show |
chrX | 8785795 | 8806383 | ||
| a0001c0003 | 0/0 | 996 | 7 | 6 | 1 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | ATGGA others(991): Show |
chrX | 8785795 | 8806383 | ||
| a0001c0006 | 0/0 | 996 | 2 | 0 | 0 | 0 | 0 | 2 | FAM9A_chrX_8785795_8806383 | FAM9A | ATGGA others(991): Show |
chrX | 8785795 | 8806383 | ||
| a0002c0002 | 0/0 | 996 | 7 | 4 | 1 | 0 | 2 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | ATGGA others(991): Show |
chrX | 8785795 | 8806383 | ||
| a0003c0005 | 0/0 | 993 | 3 | 0 | 3 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | ATGGA others(988): Show |
chrX | 8785795 | 8806383 | ||
| a0004c0004 | 0/0 | 993 | 3 | 0 | 0 | 2 | 0 | 1 | FAM9A_chrX_8785795_8806383 | FAM9A | ATGGA others(988): Show |
chrX | 8785795 | 8806383 | ||
| a0005c0008 | 0/0 | 978 | 2 | 0 | 0 | 2 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | ATGGA others(973): Show |
chrX | 8785795 | 8806383 | ||
| a0006c0007 | 0/0 | 996 | 2 | 0 | 0 | 2 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | ATGGA others(991): Show |
chrX | 8785795 | 8806383 | ||
| a0007c0009 | 0/0 | 996 | 1 | 1 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | ATGGA others(991): Show |
chrX | 8785795 | 8806383 | ||
| a0008c0010 | 0/0 | 996 | 1 | 1 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | ATGGA others(991): Show |
chrX | 8785795 | 8806383 | ||
| a0009c0011 | 0/0 | 905 | 1 | 0 | 0 | 0 | 0 | 1 | FAM9A_chrX_8785795_8806383 | FAM9A | GTTCA others(900): Show |
chrX | 8785795 | 8806383 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1519 | 260 | 49 | 50 | 124 | 11 | 24 | FAM9A_chrX_8785795_8806383 | FAM9A | CATTT others(1514): Show |
chrX | 8785795 | 8806383 |
| a0001c0001t0002 | 0/0 | 1519 | 11 | 9 | 2 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | CATTT others(1514): Show |
chrX | 8785795 | 8806383 |
| a0001c0001t0004 | 0/0 | 1519 | 3 | 0 | 0 | 3 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | CATTT others(1514): Show |
chrX | 8785795 | 8806383 |
| a0001c0003t0003 | 0/0 | 1519 | 7 | 6 | 1 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | CATTT others(1514): Show |
chrX | 8785795 | 8806383 |
| a0001c0006t0001 | 0/0 | 1519 | 2 | 0 | 0 | 0 | 0 | 2 | FAM9A_chrX_8785795_8806383 | FAM9A | CATTT others(1514): Show |
chrX | 8785795 | 8806383 |
| a0002c0002t0001 | 0/0 | 1519 | 7 | 4 | 1 | 0 | 2 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | CATTT others(1514): Show |
chrX | 8785795 | 8806383 |
| a0003c0005t0001 | 0/0 | 1516 | 3 | 0 | 3 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | CATTT others(1511): Show |
chrX | 8785795 | 8806383 |
| a0004c0004t0001 | 0/0 | 1516 | 3 | 0 | 0 | 2 | 0 | 1 | FAM9A_chrX_8785795_8806383 | FAM9A | CATTT others(1511): Show |
chrX | 8785795 | 8806383 |
| a0005c0008t0001 | 0/0 | 1501 | 2 | 0 | 0 | 2 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | CATTT others(1496): Show |
chrX | 8785795 | 8806383 |
| a0006c0007t0001 | 0/0 | 1519 | 2 | 0 | 0 | 2 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | CATTT others(1514): Show |
chrX | 8785795 | 8806383 |
| a0007c0009t0001 | 0/0 | 1519 | 1 | 1 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | CATTT others(1514): Show |
chrX | 8785795 | 8806383 |
| a0008c0010t0001 | 0/0 | 1519 | 1 | 1 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | CATTT others(1514): Show |
chrX | 8785795 | 8806383 |
| a0009c0011t0005 | 0/0 | 1390 | 1 | 0 | 0 | 0 | 0 | 1 | FAM9A_chrX_8785795_8806383 | FAM9A | CATTT others(1385): Show |
chrX | 8785795 | 8806383 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 89 | 13 | 12 | 46 | 4 | 13 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0002 | 0/0 | 73 | 5 | 14 | 49 | 2 | 3 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0003 | 0/0 | 13 | 0 | 3 | 10 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0004 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0005 | 0/0 | 8 | 2 | 2 | 0 | 1 | 3 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0008 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0002g0006 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0002g0017 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0001t0004g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0003t0003g0007 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0001c0006t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0002c0002t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0002c0002t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0003c0005t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0004c0004t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0004c0004t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0004c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0005c0008t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0006c0007t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0007c0009t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0008c0010t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| a0009c0011t0005g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | GBR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | FIN | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0058 | EUR | FIN | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG00741 | hp2 | a0003 | c0005 | t0001 | g0015 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01106 | hp1 | a0001 | c0003 | t0003 | g0007 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01256 | hp1 | a0003 | c0005 | t0001 | g0015 | AMR | CLM | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01361 | hp2 | a0003 | c0005 | t0001 | g0015 | AMR | CLM | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0065 | EUR | IBS | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0018 | EUR | IBS | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0018 | EUR | IBS | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01891 | hp2 | a0007 | c0009 | t0001 | g0034 | AFR | ACB | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02074 | hp1 | a0005 | c0008 | t0001 | g0023 | EAS | KHV | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | ACB | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02165 | hp2 | a0005 | c0008 | t0001 | g0023 | EAS | CDX | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02257 | hp1 | a0001 | c0003 | t0003 | g0007 | AFR | ACB | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02258 | hp1 | a0008 | c0010 | t0001 | g0047 | AFR | ACB | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02280 | hp2 | a0001 | c0003 | t0003 | g0007 | AFR | ACB | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02922 | hp2 | a0001 | c0003 | t0003 | g0007 | AFR | ESN | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03239 | hp1 | a0009 | c0011 | t0005 | g0061 | SAS | PJL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | MSL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03579 | hp1 | a0001 | c0003 | t0003 | g0007 | AFR | MSL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG04184 | hp1 | a0001 | c0006 | t0001 | g0025 | SAS | BEB | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | STU | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG04204 | hp1 | a0001 | c0006 | t0001 | g0025 | SAS | STU | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG04228 | hp1 | a0004 | c0004 | t0001 | g0051 | SAS | STU | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | YRI | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18950 | hp1 | a0006 | c0007 | t0001 | g0022 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18998 | hp1 | a0004 | c0004 | t0001 | g0036 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19068 | hp1 | a0004 | c0004 | t0001 | g0037 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19091 | hp1 | a0006 | c0007 | t0001 | g0022 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | YRI | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ASW | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02109 | hp2 | a0001 | c0003 | t0003 | g0007 | AFR | ACB | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG06807 | hp1 | a0001 | c0003 | t0003 | g0007 | AFR | USA | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0050 | REF | REF | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | FAM9A_chrX_8785795_8806383 | FAM9A | chrX | 8785795 | 8806383 |
| 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:8793680 | G | A | 1 | a0006 | 2 | NA18950.hp1 NA19091.hp1 |
missense_variant | MODERATE | c.908C>T | p.Pro303Leu | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 8/10 | 1019/1519 | 908/999 | 303/332 | chrX | 8793680 | |||
| chrX:8795139 | TCTC | T | 1 | a0004 | 3 | HG04228.hp1 NA18998.hp1 NA19068.hp1 |
disruptive_inframe_deletion | MODERATE | c.767_769delGAG | p.Gly256del | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 7/10 | 880/1519 | 767/999 | 256/332 | chrX | 8795139 | |||
| chrX:8795154 | CCTT | C | 1 | a0003 | 3 | HG00741.hp2 HG01256.hp1 HG01361.hp2 |
disruptive_inframe_deletion | MODERATE | c.752_754delAAG | p.Glu251del | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 7/10 | 865/1519 | 752/999 | 251/332 | chrX | 8795154 | |||
| chrX:8795268 | GCTGCTGC others(11): Show |
G | 1 | a0005 | 2 | HG02074.hp1 HG02165.hp2 |
disruptive_inframe_deletion | MODERATE | c.623_640delAAGCCGCA others(10): Show |
p.Glu208_Ala213del | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 7/10 | 751/1519 | 623/999 | 208/332 | chrX | 8795268 | |||
| chrX:8796316 | T | A | 1 | a0007 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.440A>T | p.Lys147Ile | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 6/10 | 551/1519 | 440/999 | 147/332 | chrX | 8796316 | |||
| chrX:8798462 | C | T | 2 | a0002 a0007 |
8 | HG01109.hp1 HG01516.hp2 HG01517.hp2 others(5): Show |
missense_variant | MODERATE | c.238G>A | p.Asp80Asn | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 4/10 | 349/1519 | 238/999 | 80/332 | chrX | 8798462 | |||
| chrX:8798977 | T | C | 1 | a0008 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.209A>G | p.Lys70Arg | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 3/10 | 320/1519 | 209/999 | 70/332 | chrX | 8798977 | |||
| chrX:8799524 | CGGCGGCC others(1108): Show |
C | 1 | a0009 | 1 | HG03239.hp1 | exon_loss_variant&splice_region_variant | HIGH | c.-38-430_92-431del | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 2/10 | chrX | 8799524 | |||||||
| chrX:8799835 | CGGGCCCT others(1108): Show |
C | 1 | a0001 | 1 | NA19084.hp2 | exon_loss_variant&splice_region_variant | HIGH | c.-39+361_91+245del | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 2/10 | chrX | 8799835 |
| 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:8791374 | G | A | 1 | a0001c0003 | 7 | HG01106.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
synonymous_variant | LOW | c.936C>T | p.Ala312Ala | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 9/10 | 1047/1519 | 936/999 | 312/332 | chrX | 8791374 | |||
| chrX:8798979 | C | T | 1 | a0001c0006 | 2 | HG04184.hp1 HG04204.hp1 |
synonymous_variant | LOW | c.207G>A | p.Ala69Ala | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 3/10 | 318/1519 | 207/999 | 69/332 | chrX | 8798979 |
| 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:8791291 | G | A | 1 | a0001c0003t0003 | 7 | HG01106.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*20C>T | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 9/10 | 20 | chrX | 8791291 | ||||||
| chrX:8791301 | A | G | 1 | a0001c0001t0002 | 11 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*10T>C | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 9/10 | 10 | chrX | 8791301 | ||||||
| chrX:8801366 | C | T | 1 | a0001c0001t0004 | 3 | NA18954.hp1 NA18963.hp2 NA19056.hp1 |
5_prime_UTR_variant | MODIFIER | c.-94G>A | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 1/10 | 1195 | chrX | 8801366 |
| 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:8791742 | C | T | 1 | a0001c0001t0001g0020 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.931-363G>A | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 8/9 | chrX | 8791742 | |||||||
| chrX:8792018 | A | C | 5 | a0001c0001t0001g0059 a0002c0002t0001g0012 a0002c0002t0001g0018 others(2): Show |
9 | HG01109.hp1 HG01243.hp1 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.931-639T>G | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 8/9 | chrX | 8792018 | |||||||
| chrX:8792083 | A | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0013 |
16 | HG00438.hp1 HG00735.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.931-704T>A | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 8/9 | chrX | 8792083 | |||||||
| chrX:8792085 | A | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0045 a0001c0001t0001g0063 |
5 | HG01884.hp2 HG02004.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.931-706T>A | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 8/9 | chrX | 8792085 | |||||||
| chrX:8792125 | A | G | 5 | a0001c0001t0001g0059 a0002c0002t0001g0012 a0002c0002t0001g0018 others(2): Show |
9 | HG01109.hp1 HG01243.hp1 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.931-746T>C | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 8/9 | chrX | 8792125 | |||||||
| chrX:8792190 | G | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0049 others(3): Show |
15 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.931-811C>G | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 8/9 | chrX | 8792190 | |||||||
| chrX:8792976 | C | T | 1 | a0001c0001t0001g0026 | 2 | NA18954.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.930+682G>A | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 8/9 | chrX | 8792976 | |||||||
| chrX:8793013 | A | T | 1 | a0001c0001t0001g0004 | 9 | HG02109.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.930+645T>A | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 8/9 | chrX | 8793013 | |||||||
| chrX:8793140 | G | C | 1 | a0002c0002t0001g0018 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.930+518C>G | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 8/9 | chrX | 8793140 | |||||||
| chrX:8793211 | T | C | 2 | a0002c0002t0001g0019 a0007c0009t0001g0034 |
3 | HG01109.hp1 HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.930+447A>G | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 8/9 | chrX | 8793211 | |||||||
| chrX:8793234 | A | G | 1 | a0001c0001t0001g0021 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.930+424T>C | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 8/9 | chrX | 8793234 | |||||||
| chrX:8793326 | A | C | 1 | a0001c0003t0003g0007 | 7 | HG01106.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.930+332T>G | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 8/9 | chrX | 8793326 | |||||||
| chrX:8793365 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.930+293G>A | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 8/9 | chrX | 8793365 | |||||||
| chrX:8793387 | C | A | 1 | a0001c0001t0001g0062 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.930+271G>T | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 8/9 | chrX | 8793387 | |||||||
| chrX:8793512 | T | G | 19 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(16): Show |
107 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.930+146A>C | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 8/9 | chrX | 8793512 | |||||||
| chrX:8793517 | C | T | 1 | a0001c0001t0001g0024 | 2 | HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.930+141G>A | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 8/9 | chrX | 8793517 | |||||||
| chrX:8793584 | G | A | 38 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(35): Show |
159 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.930+74C>T | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 8/9 | chrX | 8793584 | |||||||
| chrX:8793841 | C | T | 1 | a0001c0001t0001g0013 | 3 | HG00735.hp2 HG01081.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.832-85G>A | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 7/9 | chrX | 8793841 | |||||||
| chrX:8794036 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.832-280T>C | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 7/9 | chrX | 8794036 | |||||||
| chrX:8794214 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.832-458C>T | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 7/9 | chrX | 8794214 | |||||||
| chrX:8794748 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.831+330T>C | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 7/9 | chrX | 8794748 | |||||||
| chrX:8794800 | C | T | 1 | a0004c0004t0001g0036 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.831+278G>A | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 7/9 | chrX | 8794800 | |||||||
| chrX:8794936 | T | C | 1 | a0001c0001t0001g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.831+142A>G | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 7/9 | chrX | 8794936 | |||||||
| chrX:8794947 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.831+131G>A | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 7/9 | chrX | 8794947 | |||||||
| chrX:8794987 | C | T | 1 | a0001c0001t0001g0026 | 2 | NA18954.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.831+91G>A | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 7/9 | chrX | 8794987 | |||||||
| chrX:8795541 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.489-121A>G | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 6/9 | chrX | 8795541 | |||||||
| chrX:8796040 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.488+228C>T | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 6/9 | chrX | 8796040 | |||||||
| chrX:8796090 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.488+178T>C | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 6/9 | chrX | 8796090 | |||||||
| chrX:8796427 | G | A | 1 | a0001c0003t0003g0007 | 7 | HG01106.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.374-45C>T | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 5/9 | chrX | 8796427 | |||||||
| chrX:8796454 | G | A | 1 | a0001c0001t0001g0024 | 2 | HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.374-72C>T | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 5/9 | chrX | 8796454 | |||||||
| chrX:8796616 | T | C | 1 | a0001c0001t0001g0020 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.374-234A>G | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 5/9 | chrX | 8796616 | |||||||
| chrX:8796641 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.374-259A>G | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 5/9 | chrX | 8796641 | |||||||
| chrX:8796700 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.374-318A>G | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 5/9 | chrX | 8796700 | |||||||
| chrX:8796736 | A | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0030 |
5 | HG02080.hp1 HG03017.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.374-354T>A | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 5/9 | chrX | 8796736 | |||||||
| chrX:8796922 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.374-540C>T | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 5/9 | chrX | 8796922 | |||||||
| chrX:8796935 | T | C | 2 | a0002c0002t0001g0012 a0002c0002t0001g0018 |
3 | HG01516.hp2 HG01517.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.374-553A>G | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 5/9 | chrX | 8796935 | |||||||
| chrX:8797016 | C | T | 2 | a0002c0002t0001g0019 a0007c0009t0001g0034 |
3 | HG01109.hp1 HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.374-634G>A | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 5/9 | chrX | 8797016 | |||||||
| chrX:8797128 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.374-746A>G | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 5/9 | chrX | 8797128 | |||||||
| chrX:8797274 | G | A | 1 | a0001c0003t0003g0007 | 7 | HG01106.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.373+876C>T | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 5/9 | chrX | 8797274 | |||||||
| chrX:8797711 | A | G | 1 | a0001c0001t0001g0035 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.373+439T>C | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 5/9 | chrX | 8797711 | |||||||
| chrX:8797728 | C | A | 2 | a0002c0002t0001g0019 a0007c0009t0001g0034 |
3 | HG01109.hp1 HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.373+422G>T | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 5/9 | chrX | 8797728 | |||||||
| chrX:8797936 | T | C | 1 | a0001c0001t0001g0009 | 6 | NA18995.hp1 NA19003.hp1 NA19012.hp1 others(3): Show |
intron_variant | MODIFIER | c.373+214A>G | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 5/9 | chrX | 8797936 | |||||||
| chrX:8798250 | T | C | 23 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(20): Show |
120 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.342-69A>G | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 4/9 | chrX | 8798250 | |||||||
| chrX:8798504 | C | A | 1 | a0001c0001t0001g0057 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.221-25G>T | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 3/9 | chrX | 8798504 | |||||||
| chrX:8798873 | T | C | 1 | a0001c0001t0001g0027 | 2 | HG02523.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.220+93A>G | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 3/9 | chrX | 8798873 | |||||||
| chrX:8798900 | C | A | 2 | a0001c0001t0002g0006 a0001c0001t0002g0017 |
11 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+66G>T | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 3/9 | chrX | 8798900 | |||||||
| chrX:8798902 | A | G | 5 | a0001c0001t0001g0004 a0002c0002t0001g0012 a0002c0002t0001g0018 others(2): Show |
17 | HG01109.hp1 HG01516.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.220+64T>C | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 3/9 | chrX | 8798902 | |||||||
| chrX:8798925 | G | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
6 | HG01884.hp2 HG02004.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+41C>G | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 3/9 | chrX | 8798925 | |||||||
| chrX:8799175 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.92-81C>T | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 2/9 | chrX | 8799175 | |||||||
| chrX:8799180 | G | A | 1 | a0001c0001t0001g0024 | 2 | HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.92-86C>T | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 2/9 | chrX | 8799180 | |||||||
| chrX:8799186 | G | T | 1 | a0001c0001t0001g0048 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.92-92C>A | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 2/9 | chrX | 8799186 | |||||||
| chrX:8799271 | C | T | 1 | a0001c0001t0001g0004 | 9 | HG02109.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.92-177G>A | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 2/9 | chrX | 8799271 | |||||||
| chrX:8799274 | C | G | 35 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(32): Show |
154 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.92-180G>C | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 2/9 | chrX | 8799274 | |||||||
| chrX:8799313 | C | G | 1 | a0001c0001t0001g0033 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.92-219G>C | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 2/9 | chrX | 8799313 | |||||||
| chrX:8799314 | A | C | 1 | a0001c0001t0001g0033 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.92-220T>G | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 2/9 | chrX | 8799314 | |||||||
| chrX:8799315 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.92-221G>A | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 2/9 | chrX | 8799315 | |||||||
| chrX:8799316 | C | G | 1 | a0001c0001t0001g0033 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.92-222G>C | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 2/9 | chrX | 8799316 | |||||||
| chrX:8799349 | C | A | 1 | a0001c0001t0001g0059 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.92-255G>T | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 2/9 | chrX | 8799349 | |||||||
| chrX:8799523 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.92-429G>T | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 2/9 | chrX | 8799523 | |||||||
| chrX:8799542 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0035 |
2 | HG02129.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.92-448C>T | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 2/9 | chrX | 8799542 | |||||||
| chrX:8799630 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.91+451G>A | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 2/9 | chrX | 8799630 | |||||||
| chrX:8799696 | A | G | 3 | a0001c0001t0001g0002 a0004c0004t0001g0036 a0004c0004t0001g0037 |
3 | NA18998.hp1 NA19068.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.91+385T>C | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 2/9 | chrX | 8799696 | |||||||
| chrX:8799706 | C | T | 2 | a0004c0004t0001g0036 a0004c0004t0001g0037 |
2 | NA18998.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.91+375G>A | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 2/9 | chrX | 8799706 | |||||||
| chrX:8799719 | C | A | 2 | a0004c0004t0001g0036 a0004c0004t0001g0037 |
2 | NA18998.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.91+362G>T | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 2/9 | chrX | 8799719 | |||||||
| chrX:8799749 | C | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(17): Show |
108 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.91+332G>A | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 2/9 | chrX | 8799749 | |||||||
| chrX:8799758 | A | C | 3 | a0001c0001t0001g0014 a0004c0004t0001g0036 a0004c0004t0001g0037 |
3 | HG02965.hp1 NA18998.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.91+323T>G | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 2/9 | chrX | 8799758 | |||||||
| chrX:8799798 | C | A | 2 | a0004c0004t0001g0036 a0004c0004t0001g0037 |
2 | NA18998.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.91+283G>T | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 2/9 | chrX | 8799798 | |||||||
| chrX:8799813 | C | G | 2 | a0004c0004t0001g0036 a0004c0004t0001g0037 |
2 | NA18998.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.91+268G>C | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 2/9 | chrX | 8799813 | |||||||
| chrX:8799824 | C | G | 2 | a0004c0004t0001g0036 a0004c0004t0001g0037 |
2 | NA18998.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.91+257G>C | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 2/9 | chrX | 8799824 | |||||||
| chrX:8799831 | A | C | 35 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(32): Show |
154 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.91+250T>G | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 2/9 | chrX | 8799831 | |||||||
| chrX:8799835 | C | T | 2 | a0004c0004t0001g0036 a0004c0004t0001g0037 |
2 | NA18998.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.91+246G>A | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 2/9 | chrX | 8799835 | |||||||
| chrX:8800039 | C | T | 1 | a0001c0001t0001g0024 | 2 | HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.91+42G>A | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 2/9 | chrX | 8800039 | |||||||
| chrX:8800373 | G | C | 3 | a0001c0001t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 |
4 | HG00544.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38-164C>G | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 1/9 | chrX | 8800373 | |||||||
| chrX:8800531 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-38-322A>G | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 1/9 | chrX | 8800531 | |||||||
| chrX:8800559 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-38-350C>T | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 1/9 | chrX | 8800559 | |||||||
| chrX:8800623 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-38-414T>C | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 1/9 | chrX | 8800623 | |||||||
| chrX:8800639 | G | C | 1 | a0001c0001t0001g0001 | 2 | HG01261.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.-38-430C>G | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 1/9 | chrX | 8800639 | |||||||
| chrX:8800679 | C | A | 1 | a0001c0001t0001g0062 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-38-470G>T | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 1/9 | chrX | 8800679 | |||||||
| chrX:8800770 | TCCCCTGC others(3): Show |
T | 1 | a0001c0001t0001g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-39+531_-39+540del others(10): Show |
FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 1/9 | chrX | 8800770 | |||||||
| chrX:8800873 | C | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0063 a0001c0001t0002g0006 others(1): Show |
15 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-39+438G>T | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 1/9 | chrX | 8800873 | |||||||
| chrX:8800913 | A | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0030 a0001c0001t0001g0031 others(2): Show |
17 | HG00642.hp1 HG01106.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-39+398T>G | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 1/9 | chrX | 8800913 | |||||||
| chrX:8800928 | G | C | 1 | a0001c0001t0001g0063 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-39+383C>G | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 1/9 | chrX | 8800928 | |||||||
| chrX:8800950 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-39+361A>G | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 1/9 | chrX | 8800950 | |||||||
| chrX:8800978 | C | A | 1 | a0001c0001t0001g0065 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-39+333G>T | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 1/9 | chrX | 8800978 | |||||||
| chrX:8801128 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-39+183G>A | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 1/9 | chrX | 8801128 | |||||||
| chrX:8801138 | G | A | 1 | a0001c0001t0002g0017 | 3 | HG01167.hp1 HG01169.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-39+173C>T | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 1/9 | chrX | 8801138 | |||||||
| chrX:8801278 | C | G | 1 | a0001c0001t0001g0028 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-39+33G>C | FAM9A | ENSG00000183304.10 | transcript | ENST00000381003.7 | protein_coding | 1/9 | chrX | 8801278 |