| geneid | 7454 |
|---|---|
| ensemblid | ENSG00000015285.12 |
| hgncid | 12731 |
| symbol | WAS |
| name | WASP actin nucleation promoting factor |
| refseq_nuc | NM_000377.3 |
| refseq_prot | NP_000368.1 |
| ensembl_nuc | ENST00000376701.5 |
| ensembl_prot | ENSP00000365891.4 |
| mane_status | MANE Select |
| chr | chrX |
| start | 48683799 |
| end | 48691427 |
| strand | + |
| ver | v1.2 |
| region | chrX:48683799-48691427 |
| region5000 | chrX:48678799-48696427 |
| regionname0 | WAS_chrX_48683799_48691427 |
| regionname5000 | WAS_chrX_48678799_48696427 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 502 | 259 | 73 | 51 | 98 | 11 | 24 | 74 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0002 | 0/0 | 502 | 6 | 0 | 0 | 6 | 0 | 0 | 2 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0003 | 0/0 | 334 | 3 | 0 | 0 | 2 | 0 | 1 | 2 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0004 | 0/0 | 259 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0005 | 0/0 | 493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0006 | 0/0 | 493 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0007 | 0/0 | 493 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0008 | 0/0 | 334 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0009 | 0/0 | 502 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1509 | 257 | 72 | 51 | 98 | 11 | 23 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| c0002 | 0/0 | 1509 | 6 | 0 | 0 | 6 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| c0003 | 0/0 | 1510 | 3 | 0 | 0 | 2 | 0 | 1 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| c0004 | 0/0 | 1509 | 1 | 0 | 1 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| c0005 | 0/0 | 1508 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| c0006 | 0/0 | 1510 | 1 | 0 | 0 | 0 | 0 | 1 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| c0007 | 0/0 | 1509 | 1 | 1 | 0 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| c0008 | 0/0 | 1510 | 1 | 1 | 0 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| c0009 | 0/0 | 1510 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| c0010 | 0/0 | 1509 | 1 | 0 | 0 | 0 | 0 | 1 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| c0011 | 0/0 | 1511 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 321 | 273 | 74 | 51 | 109 | 11 | 26 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| t0002 | 0/0 | 321 | 1 | 0 | 1 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 144 | 22 | 28 | 71 | 6 | 17 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| g0002 | 0/0 | 73 | 31 | 14 | 17 | 4 | 7 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| g0003 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| g0004 | 0/0 | 9 | 8 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| g0005 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| g0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| g0007 | 0/1 | 3 | 0 | 0 | 0 | 1 | 1 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| g0011 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1509 | 257 | 72 | 51 | 98 | 11 | 23 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0001c0007 | 0/0 | 1509 | 1 | 1 | 0 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0001c0010 | 0/0 | 1509 | 1 | 0 | 0 | 0 | 0 | 1 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0002c0002 | 0/0 | 1509 | 6 | 0 | 0 | 6 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0003c0003 | 0/0 | 1510 | 3 | 0 | 0 | 2 | 0 | 1 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0004c0005 | 0/0 | 1508 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0005c0008 | 0/0 | 1510 | 1 | 1 | 0 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0006c0009 | 0/0 | 1510 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0007c0006 | 0/0 | 1510 | 1 | 0 | 0 | 0 | 0 | 1 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0008c0011 | 0/0 | 1511 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0009c0004 | 0/0 | 1509 | 1 | 0 | 1 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1829 | 256 | 72 | 50 | 98 | 11 | 23 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0001c0001t0002 | 0/0 | 1829 | 1 | 0 | 1 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0001c0007t0001 | 0/0 | 1829 | 1 | 1 | 0 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0001c0010t0001 | 0/0 | 1829 | 1 | 0 | 0 | 0 | 0 | 1 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0002c0002t0001 | 0/0 | 1829 | 6 | 0 | 0 | 6 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0003c0003t0001 | 0/0 | 1830 | 3 | 0 | 0 | 2 | 0 | 1 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0004c0005t0001 | 0/0 | 1828 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0005c0008t0001 | 0/0 | 1830 | 1 | 1 | 0 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0006c0009t0001 | 0/0 | 1830 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0007c0006t0001 | 0/0 | 1830 | 1 | 0 | 0 | 0 | 0 | 1 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0008c0011t0001 | 0/0 | 1831 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| a0009c0004t0001 | 0/0 | 1829 | 1 | 0 | 1 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | copy fasta | chrX | 48678799 | 48696427 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 136 | 22 | 28 | 64 | 6 | 16 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0001c0001t0001g0002 | 0/0 | 67 | 30 | 12 | 16 | 4 | 5 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0001c0001t0001g0003 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0001c0001t0001g0004 | 0/0 | 8 | 7 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0001c0001t0001g0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0001c0001t0001g0007 | 0/1 | 3 | 0 | 0 | 0 | 1 | 1 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0001c0001t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0001c0001t0001g0011 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0001c0007t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0001c0010t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0002c0002t0001g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0003c0003t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0003c0003t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0003c0003t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0004c0005t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0005c0008t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0006c0009t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0007c0006t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0008c0011t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| a0009c0004t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01243 | hp1 | a0009 | c0004 | t0001 | g0002 | AMR | PUR | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02055 | hp1 | a0005 | c0008 | t0001 | g0004 | AFR | ACB | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02071 | hp1 | a0006 | c0009 | t0001 | g0002 | EAS | KHV | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02809 | hp2 | a0001 | c0007 | t0001 | g0002 | AFR | GWD | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03688 | hp1 | a0003 | c0003 | t0001 | g0002 | SAS | STU | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03831 | hp2 | a0007 | c0006 | t0001 | g0001 | SAS | BEB | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03834 | hp1 | a0001 | c0010 | t0001 | g0002 | SAS | BEB | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18940 | hp1 | a0004 | c0005 | t0001 | g0020 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18956 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19067 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19076 | hp1 | a0008 | c0011 | t0001 | g0012 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | USA | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0007 | REF | REF | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0011 | REF | REF | WAS_chrX_48678799_48696427 | WAS | chrX | 48678799 | 48696427 |
| 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:48683983
|
T | G | 1 | a0009 | 1 | HG01243.hp1 | missense_variant&splice_region_variant | MODERATE | c.130T>G | p.Leu44Val | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 1/12 | 185/1829 | 130/1509 | 44/502 | chrX | 48683983 | ||
| chrX:48685815
|
AG | A | 1 | a0004 | 1 | NA18940.hp1 | frameshift_variant | HIGH | c.444delG | p.Asn149fs | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 4/12 | 499/1829 | 444/1509 | 148/502 | INFO_REALIGN_3_PRIME | chrX | 48685815 | |
| chrX:48688673
|
G | GC | 1 | a0008 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.950dupC | p.Pro318fs | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 10/12 | 1006/1829 | 951/1509 | 317/502 | INFO_REALIGN_3_PRIME | chrX | 48688673 | |
| chrX:48688723
|
T | TG | 1 | a0003 | 3 | HG03688.hp1 NA18956.hp2 NA19067.hp1 |
frameshift_variant | HIGH | c.1001dupG | p.Asn335fs | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 10/12 | 1057/1829 | 1002/1509 | 334/502 | INFO_REALIGN_3_PRIME | chrX | 48688723 | |
| chrX:48688838
|
A | AC | 1 | a0007 | 1 | HG03831.hp2 | frameshift_variant | HIGH | c.1115dupC | p.Pro373fs | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 10/12 | 1171/1829 | 1116/1509 | 372/502 | INFO_REALIGN_3_PRIME | chrX | 48688838 | |
| chrX:48688916
|
A | AC | 1 | a0005 | 1 | HG02055.hp1 | frameshift_variant | HIGH | c.1190dupC | p.Pro398fs | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 10/12 | 1246/1829 | 1191/1509 | 397/502 | INFO_REALIGN_3_PRIME | chrX | 48688916 | |
| chrX:48688931
|
A | AC | 1 | a0006 | 1 | HG02071.hp1 | frameshift_variant | HIGH | c.1205dupC | p.Pro403fs | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 10/12 | 1261/1829 | 1206/1509 | 402/502 | INFO_REALIGN_3_PRIME | chrX | 48688931 | |
| chrX:48688931
|
A | ACC | 1 | a0008 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1204_1205dupCC | p.Pro403fs | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 10/12 | 1261/1829 | 1206/1509 | 402/502 | INFO_REALIGN_3_PRIME | chrX | 48688931 | |
| chrX:48689004
|
GC | G | 1 | a0008 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1280delC | p.Pro427fs | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 10/12 | 1335/1829 | 1280/1509 | 427/502 | INFO_REALIGN_3_PRIME | chrX | 48689004 | |
| chrX:48689359
|
C | T | 1 | a0002 | 6 | HG00621.hp1 HG00673.hp1 HG02040.hp1 others(3): Show |
missense_variant | MODERATE | c.1378C>T | p.Pro460Ser | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 11/12 | 1433/1829 | 1378/1509 | 460/502 | chrX | 48689359 |
| 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:48688919
|
G | A | 1 | a0001c0007 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.1191G>A | p.Pro397Pro | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 10/12 | 1246/1829 | 1191/1509 | 397/502 | chrX | 48688919 | ||
| chrX:48689027
|
G | A | 1 | a0001c0010 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.1299G>A | p.Ala433Ala | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 10/12 | 1354/1829 | 1299/1509 | 433/502 | chrX | 48689027 |
| 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:48691274
|
C | A | 1 | a0001c0001t0002 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*112C>A | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 12/12 | 112 | chrX | 48691274 |
| 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:48684129
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.132+144C>T | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 1/11 | chrX | 48684129 | ||||||
| chrX:48684427
|
A | AC | 2 | a0001c0001t0001g0010a0001c0001t0001g0022 | 3 | HG01123.hp1 HG02717.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.273+11dupC | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 48684427 | |||||
| chrX:48684427
|
A | ACC | 3 | a0001c0001t0001g0003a0001c0001t0001g0023a0003c0003t0001g0003 | 13 | HG00544.hp2 NA18747.hp1 NA18944.hp1 others(10): Show |
intron_variant | MODIFIER | c.273+10_273+11dupCC | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 48684427 | |||||
| chrX:48684610
|
A | C | 1 | a0001c0001t0001g0021 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.273+187A>C | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 2/11 | chrX | 48684610 | ||||||
| chrX:48684957
|
C | T | 1 | a0001c0001t0001g0005 | 7 | HG00639.hp1 HG01256.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.273+534C>T | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 2/11 | chrX | 48684957 | ||||||
| chrX:48686261
|
A | G | 33 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(30): Show | 270 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.559+127A>G | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 6/11 | chrX | 48686261 | ||||||
| chrX:48686514
|
TA | T | 1 | a0004c0005t0001g0020 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.560-264delA | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chrX | 48686514 | |||||
| chrX:48686606
|
A | G | 1 | a0001c0001t0001g0010 | 2 | HG01123.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.560-175A>G | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 6/11 | chrX | 48686606 | ||||||
| chrX:48687280
|
G | GA | 1 | a0008c0011t0001g0012 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.734+326dupA | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 48687280 | |||||
| chrX:48687286
|
A | AG | 1 | a0004c0005t0001g0020 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.734+333dupG | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 48687286 | |||||
| chrX:48687358
|
TG | T | 1 | a0004c0005t0001g0020 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.734+406delG | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 48687358 | |||||
| chrX:48687483
|
G | A | 1 | a0004c0005t0001g0020 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.734+528G>A | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 7/11 | chrX | 48687483 | ||||||
| chrX:48687509
|
TG | T | 1 | a0008c0011t0001g0012 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.735-543delG | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 48687509 | |||||
| chrX:48687564
|
CA | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0009 | 8 | HG01081.hp1 HG02109.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.735-489delA | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 7/11 | chrX | 48687564 | ||||||
| chrX:48687580
|
TG | T | 1 | a0008c0011t0001g0012 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.735-472delG | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 48687580 | |||||
| chrX:48687789
|
A | AG | 1 | a0008c0011t0001g0012 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.735-264dupG | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 48687789 | |||||
| chrX:48687848
|
A | AG | 1 | a0004c0005t0001g0020 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.735-203dupG | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 48687848 | |||||
| chrX:48687967
|
TG | T | 1 | a0008c0011t0001g0012 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.735-84delG | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 48687967 | |||||
| chrX:48688219
|
T | TG | 1 | a0004c0005t0001g0020 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.778-79dupG | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chrX | 48688219 | |||||
| chrX:48688282
|
C | CT | 1 | a0004c0005t0001g0020 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.778-13dupT | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chrX | 48688282 | |||||
| chrX:48689702
|
T | C | 14 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(11): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1453+268T>C | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 11/11 | chrX | 48689702 | ||||||
| chrX:48689717
|
C | CG | 34 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(31): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1453+285dupG | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 48689717 | |||||
| chrX:48689752
|
T | TC | 1 | a0008c0011t0001g0012 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1453+318_1453+319i others(3): Show |
WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 11/11 | chrX | 48689752 | ||||||
| chrX:48689789
|
G | T | 1 | a0001c0001t0001g0019 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1453+355G>T | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 11/11 | chrX | 48689789 | ||||||
| chrX:48689831
|
T | TA | 1 | a0008c0011t0001g0012 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1453+402dupA | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 48689831 | |||||
| chrX:48689844
|
C | CA | 1 | a0001c0001t0001g0008 | 2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1453+417dupA | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 48689844 | |||||
| chrX:48689849
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1453+415A>G | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 11/11 | chrX | 48689849 | ||||||
| chrX:48689868
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1453+434G>A | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 11/11 | chrX | 48689868 | ||||||
| chrX:48689996
|
C | CA | 2 | a0001c0001t0001g0004a0005c0008t0001g0004 | 9 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1453+576dupA | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 48689996 | |||||
| chrX:48689996
|
CA | C | 1 | a0008c0011t0001g0012 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1453+576delA | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 48689996 | |||||
| chrX:48690129
|
TA | T | 1 | a0001c0001t0001g0016 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1453+701delA | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 48690129 | |||||
| chrX:48690200
|
G | C | 1 | a0001c0001t0001g0008 | 2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1453+766G>C | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 11/11 | chrX | 48690200 | ||||||
| chrX:48690300
|
G | GT | 1 | a0001c0001t0001g0015 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1454-800dupT | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 48690300 | |||||
| chrX:48690576
|
G | GA | 1 | a0001c0001t0001g0013 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1454-530dupA | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 48690576 | |||||
| chrX:48690577
|
A | AT | 14 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(11): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1454-520dupT | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 48690577 | |||||
| chrX:48690595
|
G | GCT | 1 | a0008c0011t0001g0012 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1454-512_1454-511i others(4): Show |
WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 11/11 | chrX | 48690595 | ||||||
| chrX:48690596
|
A | T | 1 | a0008c0011t0001g0012 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1454-511A>T | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 11/11 | chrX | 48690596 | ||||||
| chrX:48690597
|
C | G | 1 | a0008c0011t0001g0012 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1454-510C>G | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 11/11 | chrX | 48690597 | ||||||
| chrX:48690598
|
G | A | 1 | a0008c0011t0001g0012 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1454-509G>A | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 11/11 | chrX | 48690598 | ||||||
| chrX:48690729
|
C | T | 1 | a0001c0001t0001g0009 | 2 | HG01081.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1454-378C>T | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 11/11 | chrX | 48690729 | ||||||
| chrX:48690995
|
GC | G | 1 | a0008c0011t0001g0012 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1454-109delC | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 48690995 | |||||
| chrX:48691072
|
C | T | 1 | a0001c0001t0001g0014 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1454-35C>T | WAS | ENSG00000015285.12 | transcript | ENST00000376701.5 | protein_coding | 11/11 | chrX | 48691072 |