Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 54540 |
|---|---|
| ensemblid | ENSG00000146067.17 |
| hgncid | 25524 |
| symbol | FAM193B |
| name | family with sequence similarity 193 member B |
| refseq_nuc | NM_001190946.3 |
| refseq_prot | NP_001177875.1 |
| ensembl_nuc | ENST00000514747.6 |
| ensembl_prot | ENSP00000422131.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 177519789 |
| end | 177554563 |
| strand | - |
| ver | v1.2 |
| region | chr5:177519789-177554563 |
| region5000 | chr5:177514789-177559563 |
| regionname0 | FAM193B_chr5_177519789_177554563 |
| regionname5000 | FAM193B_chr5_177514789_177559563 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 822 | 350 | 71 | 66 | 164 | 12 | 36 | 125 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0002 | 1/0 | 822 | 5 | 4 | 0 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0003 | 0/0 | 822 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0004 | 0/0 | 822 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0005 | 0/0 | 822 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0006 | 0/0 | 822 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0007 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0008 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0009 | 0/0 | 822 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0010 | 0/0 | 822 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0011 | 0/0 | 822 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2469 | 343 | 70 | 66 | 161 | 12 | 33 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| c0002 | 1/0 | 2469 | 5 | 4 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| c0003 | 0/0 | 2469 | 4 | 4 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| c0004 | 0/0 | 2469 | 3 | 3 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| c0005 | 0/0 | 2469 | 2 | 0 | 0 | 0 | 0 | 2 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| c0006 | 0/0 | 2469 | 2 | 0 | 2 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| c0007 | 0/0 | 2469 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| c0008 | 0/0 | 2469 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| c0009 | 0/0 | 2469 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| c0010 | 0/0 | 2469 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| c0011 | 0/0 | 2469 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| c0012 | 0/0 | 2469 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| c0013 | 0/0 | 2469 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| c0014 | 0/0 | 2469 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| c0015 | 0/0 | 2469 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| c0016 | 0/0 | 2469 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| c0017 | 0/0 | 2469 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 498 | 88 | 8 | 21 | 43 | 5 | 11 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0002 | 0/0 | 498 | 58 | 0 | 11 | 44 | 0 | 3 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0003 | 0/0 | 504 | 25 | 10 | 11 | 4 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0004 | 0/0 | 510 | 15 | 1 | 0 | 14 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0005 | 0/0 | 516 | 12 | 2 | 2 | 8 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0006 | 0/0 | 510 | 11 | 0 | 5 | 2 | 1 | 3 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0007 | 0/0 | 519 | 11 | 0 | 2 | 7 | 0 | 2 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0008 | 0/0 | 495 | 7 | 6 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0009 | 0/0 | 507 | 7 | 6 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0010 | 0/0 | 495 | 6 | 0 | 5 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0011 | 0/0 | 501 | 6 | 3 | 2 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0012 | 0/0 | 504 | 6 | 5 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0013 | 0/0 | 507 | 6 | 5 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0014 | 0/0 | 513 | 6 | 1 | 0 | 1 | 0 | 4 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0015 | 0/0 | 522 | 6 | 3 | 0 | 3 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0016 | 0/0 | 501 | 5 | 3 | 2 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0017 | 0/0 | 510 | 5 | 3 | 0 | 1 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0018 | 0/0 | 513 | 5 | 0 | 1 | 4 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0019 | 0/0 | 513 | 5 | 0 | 1 | 2 | 0 | 2 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0020 | 0/0 | 534 | 5 | 3 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0021 | 0/0 | 501 | 4 | 4 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0022 | 0/0 | 507 | 4 | 1 | 0 | 0 | 2 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0023 | 0/0 | 525 | 4 | 1 | 0 | 2 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0024 | 0/0 | 498 | 3 | 1 | 0 | 1 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0025 | 0/1 | 501 | 3 | 0 | 1 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0026 | 0/0 | 516 | 3 | 0 | 0 | 3 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0027 | 0/0 | 525 | 3 | 0 | 0 | 2 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0028 | 0/0 | 528 | 3 | 1 | 0 | 1 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0029 | 0/0 | 537 | 3 | 1 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0030 | 1/0 | 499 | 3 | 2 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0031 | 0/0 | 493 | 3 | 3 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0032 | 0/0 | 489 | 2 | 1 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0033 | 0/0 | 495 | 2 | 0 | 0 | 0 | 1 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0034 | 0/0 | 519 | 2 | 2 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0035 | 0/0 | 522 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0036 | 0/0 | 522 | 2 | 0 | 0 | 1 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0037 | 0/0 | 531 | 2 | 0 | 0 | 1 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0038 | 0/0 | 552 | 2 | 0 | 0 | 1 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0039 | 0/0 | 498 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0040 | 0/0 | 498 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0041 | 0/0 | 501 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0042 | 0/0 | 504 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0043 | 0/0 | 504 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0044 | 0/0 | 516 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0045 | 0/0 | 519 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0046 | 0/0 | 519 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0047 | 0/0 | 525 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0048 | 0/0 | 531 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0049 | 0/0 | 531 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0050 | 0/0 | 534 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0051 | 0/0 | 537 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0052 | 0/0 | 540 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0053 | 0/0 | 543 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0054 | 0/0 | 543 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0055 | 0/0 | 546 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0056 | 0/0 | 546 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0057 | 0/0 | 552 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0058 | 0/0 | 555 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0059 | 0/0 | 564 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0060 | 0/0 | 567 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0061 | 0/0 | 582 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0062 | 0/0 | 499 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| t0063 | 0/0 | 507 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0002 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0004 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0005 | 0/0 | 5 | 1 | 2 | 0 | 1 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0006 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0011 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0012 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0013 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0014 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0017 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0020 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0037 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0039 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0040 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0125 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0272 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2469 | 343 | 70 | 66 | 161 | 12 | 33 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0005 | 0/0 | 2469 | 2 | 0 | 0 | 0 | 0 | 2 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0007 | 0/0 | 2469 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0009 | 0/0 | 2469 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0010 | 0/0 | 2469 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0011 | 0/0 | 2469 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0014 | 0/0 | 2469 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0002c0002 | 1/0 | 2469 | 5 | 4 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0003c0003 | 0/0 | 2469 | 4 | 4 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0004c0004 | 0/0 | 2469 | 3 | 3 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0005c0006 | 0/0 | 2469 | 2 | 0 | 2 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0006c0015 | 0/0 | 2469 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0007c0012 | 0/0 | 2469 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0008c0013 | 0/0 | 2469 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0009c0016 | 0/0 | 2469 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0010c0017 | 0/0 | 2469 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0011c0008 | 0/0 | 2469 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2966 | 85 | 8 | 21 | 40 | 5 | 11 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0002 | 0/0 | 2966 | 56 | 0 | 9 | 44 | 0 | 3 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0003 | 0/0 | 2972 | 24 | 10 | 10 | 4 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0004 | 0/0 | 2978 | 15 | 1 | 0 | 14 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0005 | 0/0 | 2984 | 12 | 2 | 2 | 8 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0006 | 0/0 | 2978 | 10 | 0 | 5 | 2 | 1 | 2 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0007 | 0/0 | 2987 | 11 | 0 | 2 | 7 | 0 | 2 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0008 | 0/0 | 2963 | 7 | 6 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0009 | 0/0 | 2975 | 6 | 5 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0010 | 0/0 | 2963 | 5 | 0 | 4 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0011 | 0/0 | 2969 | 6 | 3 | 2 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0012 | 0/0 | 2972 | 6 | 5 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0013 | 0/0 | 2975 | 6 | 5 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0014 | 0/0 | 2981 | 6 | 1 | 0 | 1 | 0 | 4 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0015 | 0/0 | 2990 | 5 | 2 | 0 | 3 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0016 | 0/0 | 2969 | 5 | 3 | 2 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0017 | 0/0 | 2978 | 5 | 3 | 0 | 1 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0018 | 0/0 | 2981 | 4 | 0 | 1 | 3 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0019 | 0/0 | 2981 | 4 | 0 | 1 | 2 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0020 | 0/0 | 3002 | 2 | 1 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0022 | 0/0 | 2975 | 3 | 1 | 0 | 0 | 2 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0023 | 0/0 | 2993 | 4 | 1 | 0 | 2 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0024 | 0/0 | 2966 | 3 | 1 | 0 | 1 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0025 | 0/1 | 2969 | 3 | 0 | 1 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0026 | 0/0 | 2984 | 3 | 0 | 0 | 3 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0027 | 0/0 | 2993 | 3 | 0 | 0 | 2 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0028 | 0/0 | 2996 | 3 | 1 | 0 | 1 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0029 | 0/0 | 3005 | 3 | 1 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0032 | 0/0 | 2957 | 2 | 1 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0033 | 0/0 | 2963 | 2 | 0 | 0 | 0 | 1 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0034 | 0/0 | 2987 | 2 | 2 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0035 | 0/0 | 2990 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0036 | 0/0 | 2990 | 2 | 0 | 0 | 1 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0037 | 0/0 | 2999 | 2 | 0 | 0 | 1 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0038 | 0/0 | 3020 | 2 | 0 | 0 | 1 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0039 | 0/0 | 2966 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0040 | 0/0 | 2966 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0041 | 0/0 | 2969 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0042 | 0/0 | 2972 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0043 | 0/0 | 2972 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0044 | 0/0 | 2984 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0045 | 0/0 | 2987 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0047 | 0/0 | 2993 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0048 | 0/0 | 2999 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0049 | 0/0 | 2999 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0050 | 0/0 | 3002 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0051 | 0/0 | 3005 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0052 | 0/0 | 3008 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0053 | 0/0 | 3011 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0054 | 0/0 | 3011 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0055 | 0/0 | 3014 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0056 | 0/0 | 3014 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0057 | 0/0 | 3020 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0058 | 0/0 | 3023 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0059 | 0/0 | 3032 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0060 | 0/0 | 3035 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0061 | 0/0 | 3050 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0062 | 0/0 | 2967 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0001t0063 | 0/0 | 2975 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0005t0006 | 0/0 | 2978 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0005t0022 | 0/0 | 2975 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0007t0001 | 0/0 | 2966 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0009t0001 | 0/0 | 2966 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0010t0019 | 0/0 | 2981 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0011t0001 | 0/0 | 2966 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0001c0014t0046 | 0/0 | 2987 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0002c0002t0030 | 1/0 | 2967 | 2 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0002c0002t0031 | 0/0 | 2961 | 3 | 3 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0003c0003t0021 | 0/0 | 2969 | 4 | 4 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0004c0004t0015 | 0/0 | 2990 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0004c0004t0020 | 0/0 | 3002 | 2 | 2 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0005c0006t0002 | 0/0 | 2966 | 2 | 0 | 2 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0006c0015t0030 | 0/0 | 2967 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0007c0012t0018 | 0/0 | 2981 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0008c0013t0020 | 0/0 | 3002 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0009c0016t0010 | 0/0 | 2963 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0010c0017t0003 | 0/0 | 2972 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| a0011c0008t0009 | 0/0 | 2975 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | copy fasta | chr5 | 177514789 | 177559563 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0005 | 0/0 | 5 | 1 | 2 | 0 | 1 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0001 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0004 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0006 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0004g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0005g0013 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0005g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0006g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0006g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0006g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0006g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0006g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0006g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0006g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0006g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0006g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0007g0014 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0007g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0007g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0007g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0007g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0007g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0007g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0008g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0008g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0008g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0009g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0009g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0009g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0009g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0009g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0009g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0010g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0010g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0010g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0010g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0011g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0011g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0011g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0011g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0011g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0011g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0012g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0012g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0012g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0012g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0012g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0012g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0013g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0013g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0013g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0013g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0013g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0014g0020 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0014g0037 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0014g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0015g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0015g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0015g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0015g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0015g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0016g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0016g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0016g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0016g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0016g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0017g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0017g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0017g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0017g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0017g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0018g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0018g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0018g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0019g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0019g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0019g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0019g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0020g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0020g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0022g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0022g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0022g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0023g0040 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0023g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0023g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0024g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0024g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0024g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0025g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0025g0125 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0025g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0026g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0026g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0026g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0027g0039 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0027g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0028g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0028g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0028g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0029g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0029g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0029g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0032g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0032g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0033g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0033g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0034g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0034g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0035g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0035g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0036g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0036g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0037g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0037g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0038g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0038g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0039g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0040g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0041g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0042g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0043g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0044g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0045g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0047g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0048g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0049g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0050g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0051g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0052g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0053g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0054g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0055g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0056g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0057g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0058g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0059g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0060g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0061g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0062g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0001t0063g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0005t0006g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0005t0022g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0007t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0009t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0010t0019g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0011t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0001c0014t0046g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0002c0002t0030g0272 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0002c0002t0030g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0002c0002t0031g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0002c0002t0031g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0003c0003t0021g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0003c0003t0021g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0004c0004t0015g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0004c0004t0020g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0004c0004t0020g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0005c0006t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0005c0006t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0006c0015t0030g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0007c0012t0018g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0008c0013t0020g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0009c0016t0010g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0010c0017t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| a0011c0008t0009g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0043 | g0150 | EUR | GBR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00099 | hp2 | a0001 | c0001 | t0033 | g0045 | EUR | GBR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | GBR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00140 | hp2 | a0001 | c0001 | t0037 | g0248 | EUR | GBR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00408 | hp1 | a0001 | c0001 | t0023 | g0040 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00408 | hp2 | a0001 | c0001 | t0017 | g0181 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00423 | hp1 | a0001 | c0001 | t0061 | g0270 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00438 | hp2 | a0001 | c0001 | t0015 | g0237 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00558 | hp1 | a0001 | c0001 | t0011 | g0132 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00558 | hp2 | a0001 | c0001 | t0015 | g0236 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00609 | hp2 | a0001 | c0001 | t0023 | g0241 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0149 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0013 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00673 | hp1 | a0001 | c0001 | t0005 | g0210 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | CHS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00735 | hp1 | a0001 | c0001 | t0006 | g0187 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00738 | hp2 | a0001 | c0001 | t0006 | g0035 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00741 | hp1 | a0001 | c0001 | t0018 | g0206 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0156 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0158 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01081 | hp1 | a0001 | c0001 | t0013 | g0168 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01081 | hp2 | a0005 | c0006 | t0002 | g0058 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01106 | hp1 | a0010 | c0017 | t0003 | g0146 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01106 | hp2 | a0001 | c0001 | t0010 | g0021 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0142 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01167 | hp1 | a0001 | c0001 | t0010 | g0044 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01175 | hp2 | a0001 | c0001 | t0052 | g0259 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01243 | hp1 | a0001 | c0001 | t0008 | g0051 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01243 | hp2 | a0001 | c0001 | t0012 | g0139 | AMR | PUR | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0213 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01258 | hp1 | a0001 | c0001 | t0006 | g0186 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01261 | hp2 | a0001 | c0001 | t0016 | g0135 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0157 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01346 | hp2 | a0001 | c0001 | t0053 | g0260 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01496 | hp1 | a0001 | c0001 | t0006 | g0197 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01496 | hp2 | a0001 | c0001 | t0007 | g0014 | AMR | CLM | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01516 | hp2 | a0001 | c0001 | t0022 | g0170 | EUR | IBS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01517 | hp2 | a0001 | c0001 | t0022 | g0167 | EUR | IBS | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01884 | hp1 | a0001 | c0001 | t0040 | g0080 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01884 | hp2 | a0001 | c0001 | t0017 | g0188 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01891 | hp1 | a0001 | c0001 | t0011 | g0128 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01891 | hp2 | a0001 | c0001 | t0013 | g0166 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01928 | hp1 | a0001 | c0001 | t0010 | g0021 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01928 | hp2 | a0001 | c0001 | t0025 | g0126 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01934 | hp1 | a0005 | c0006 | t0002 | g0057 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01934 | hp2 | a0001 | c0001 | t0009 | g0164 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01943 | hp1 | a0001 | c0001 | t0007 | g0014 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01978 | hp1 | a0001 | c0001 | t0011 | g0131 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01978 | hp2 | a0009 | c0016 | t0010 | g0047 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01981 | hp2 | a0001 | c0001 | t0016 | g0134 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG01993 | hp2 | a0001 | c0001 | t0010 | g0048 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02004 | hp1 | a0001 | c0001 | t0006 | g0035 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02027 | hp1 | a0001 | c0001 | t0054 | g0261 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02040 | hp2 | a0001 | c0001 | t0010 | g0049 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02055 | hp1 | a0002 | c0002 | t0031 | g0041 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02071 | hp1 | a0008 | c0013 | t0020 | g0253 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02129 | hp1 | a0001 | c0001 | t0015 | g0235 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02132 | hp1 | a0001 | c0001 | t0007 | g0224 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02135 | hp2 | a0001 | c0001 | t0019 | g0202 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02145 | hp2 | a0001 | c0001 | t0012 | g0159 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02148 | hp2 | a0001 | c0001 | t0011 | g0133 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02165 | hp1 | a0001 | c0001 | t0055 | g0262 | EAS | CDX | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0196 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02257 | hp2 | a0001 | c0001 | t0024 | g0115 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0053 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02258 | hp2 | a0001 | c0001 | t0023 | g0240 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02280 | hp1 | a0001 | c0001 | t0022 | g0165 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02280 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02300 | hp1 | a0001 | c0001 | t0019 | g0200 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02451 | hp1 | a0001 | c0001 | t0013 | g0169 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02451 | hp2 | a0001 | c0001 | t0012 | g0160 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02572 | hp1 | a0004 | c0004 | t0015 | g0228 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02572 | hp2 | a0001 | c0001 | t0020 | g0254 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02615 | hp2 | a0001 | c0001 | t0056 | g0263 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02622 | hp1 | a0001 | c0001 | t0016 | g0127 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02622 | hp2 | a0002 | c0002 | t0031 | g0275 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02630 | hp1 | a0003 | c0003 | t0021 | g0018 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02630 | hp2 | a0006 | c0015 | t0030 | g0273 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02647 | hp1 | a0001 | c0001 | t0034 | g0219 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02647 | hp2 | a0001 | c0001 | t0012 | g0152 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02698 | hp1 | a0001 | c0001 | t0049 | g0245 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0143 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02717 | hp2 | a0003 | c0003 | t0021 | g0018 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02723 | hp1 | a0001 | c0001 | t0011 | g0130 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02723 | hp2 | a0001 | c0001 | t0014 | g0037 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02735 | hp1 | a0001 | c0001 | t0027 | g0039 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0171 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0154 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02818 | hp1 | a0001 | c0001 | t0015 | g0232 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02818 | hp2 | a0001 | c0001 | t0044 | g0218 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02886 | hp1 | a0003 | c0003 | t0021 | g0018 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02886 | hp2 | a0011 | c0008 | t0009 | g0162 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02895 | hp1 | a0001 | c0001 | t0008 | g0054 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02895 | hp2 | a0001 | c0001 | t0058 | g0267 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02896 | hp1 | a0001 | c0001 | t0017 | g0180 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02896 | hp2 | a0004 | c0004 | t0020 | g0250 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02897 | hp1 | a0001 | c0001 | t0008 | g0052 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02897 | hp2 | a0004 | c0004 | t0020 | g0249 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | ESN | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | ESN | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02965 | hp1 | a0001 | c0001 | t0013 | g0034 | AFR | ESN | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02965 | hp2 | a0002 | c0002 | t0031 | g0041 | AFR | ESN | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02970 | hp1 | a0001 | c0001 | t0015 | g0233 | AFR | ESN | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02970 | hp2 | a0001 | c0001 | t0012 | g0153 | AFR | ESN | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02976 | hp1 | a0001 | c0001 | t0034 | g0220 | AFR | ESN | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02976 | hp2 | a0001 | c0001 | t0016 | g0123 | AFR | ESN | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03041 | hp2 | a0001 | c0001 | t0011 | g0129 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0172 | AFR | MSL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03130 | hp1 | a0003 | c0003 | t0021 | g0137 | AFR | ESN | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | ESN | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03139 | hp1 | a0001 | c0001 | t0017 | g0184 | AFR | ESN | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03139 | hp2 | a0001 | c0001 | t0008 | g0050 | AFR | ESN | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | MSL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0151 | AFR | MSL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03453 | hp1 | a0001 | c0014 | t0046 | g0227 | AFR | MSL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0173 | AFR | MSL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03486 | hp1 | a0001 | c0001 | t0029 | g0258 | AFR | MSL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0163 | AFR | MSL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03490 | hp2 | a0001 | c0001 | t0017 | g0177 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03491 | hp2 | a0001 | c0001 | t0033 | g0046 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0214 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03540 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | GWD | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03654 | hp1 | a0001 | c0001 | t0019 | g0199 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03669 | hp1 | a0001 | c0001 | t0028 | g0243 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03688 | hp1 | a0001 | c0001 | t0006 | g0185 | SAS | STU | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0066 | SAS | STU | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03704 | hp1 | a0001 | c0001 | t0006 | g0183 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03704 | hp2 | a0001 | c0001 | t0014 | g0020 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03710 | hp2 | a0001 | c0001 | t0007 | g0222 | SAS | PJL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03834 | hp2 | a0001 | c0001 | t0014 | g0020 | SAS | BEB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03942 | hp2 | a0001 | c0001 | t0007 | g0225 | SAS | BEB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG04115 | hp2 | a0001 | c0001 | t0014 | g0020 | SAS | STU | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG04184 | hp1 | a0001 | c0001 | t0025 | g0124 | SAS | BEB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG04184 | hp2 | a0001 | c0001 | t0014 | g0205 | SAS | BEB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG04199 | hp1 | a0001 | c0010 | t0019 | g0201 | SAS | STU | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG04199 | hp2 | a0001 | c0001 | t0036 | g0231 | SAS | STU | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG04204 | hp1 | a0001 | c0001 | t0038 | g0265 | SAS | STU | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG04204 | hp2 | a0001 | c0005 | t0022 | g0161 | SAS | STU | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | STU | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG04228 | hp2 | a0001 | c0001 | t0024 | g0077 | SAS | STU | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | YRI | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18612 | hp2 | a0001 | c0001 | t0020 | g0252 | EAS | CHB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18747 | hp2 | a0001 | c0001 | t0006 | g0179 | EAS | CHB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0141 | AFR | YRI | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18942 | hp1 | a0007 | c0012 | t0018 | g0198 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18943 | hp1 | a0001 | c0011 | t0001 | g0109 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18944 | hp1 | a0001 | c0001 | t0027 | g0039 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18945 | hp1 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0192 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18946 | hp1 | a0001 | c0001 | t0007 | g0226 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18946 | hp2 | a0001 | c0001 | t0005 | g0207 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18947 | hp1 | a0001 | c0001 | t0028 | g0244 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18949 | hp1 | a0001 | c0009 | t0001 | g0092 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18949 | hp2 | a0001 | c0001 | t0019 | g0203 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18951 | hp2 | a0001 | c0001 | t0006 | g0178 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18952 | hp2 | a0001 | c0001 | t0007 | g0038 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18957 | hp2 | a0001 | c0001 | t0039 | g0055 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18959 | hp1 | a0001 | c0001 | t0014 | g0037 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18964 | hp2 | a0001 | c0001 | t0005 | g0217 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0191 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18968 | hp2 | a0001 | c0001 | t0051 | g0255 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18969 | hp1 | a0001 | c0001 | t0029 | g0257 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18970 | hp2 | a0001 | c0001 | t0018 | g0036 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18971 | hp1 | a0001 | c0001 | t0035 | g0234 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18973 | hp2 | a0001 | c0001 | t0007 | g0223 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18974 | hp2 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18977 | hp1 | a0001 | c0001 | t0036 | g0229 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18979 | hp2 | a0001 | c0001 | t0035 | g0230 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18980 | hp2 | a0001 | c0001 | t0007 | g0014 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18982 | hp2 | a0001 | c0001 | t0063 | g0276 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18984 | hp1 | a0001 | c0001 | t0026 | g0209 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18984 | hp2 | a0001 | c0001 | t0018 | g0036 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18985 | hp2 | a0001 | c0001 | t0005 | g0211 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18989 | hp1 | a0001 | c0001 | t0060 | g0269 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18992 | hp1 | a0001 | c0001 | t0018 | g0204 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA18999 | hp2 | a0001 | c0001 | t0029 | g0256 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0189 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0212 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19010 | hp2 | a0001 | c0001 | t0027 | g0238 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19011 | hp1 | a0001 | c0001 | t0007 | g0038 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19011 | hp2 | a0001 | c0001 | t0032 | g0042 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19043 | hp1 | a0002 | c0002 | t0030 | g0274 | AFR | LWK | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19043 | hp2 | a0001 | c0001 | t0016 | g0136 | AFR | LWK | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19055 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19056 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19057 | hp2 | a0001 | c0001 | t0062 | g0271 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19058 | hp1 | a0001 | c0001 | t0042 | g0138 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19058 | hp2 | a0001 | c0001 | t0038 | g0264 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19060 | hp2 | a0001 | c0007 | t0001 | g0076 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19062 | hp1 | a0001 | c0001 | t0050 | g0251 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19068 | hp1 | a0001 | c0001 | t0026 | g0208 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19075 | hp2 | a0001 | c0001 | t0004 | g0193 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19079 | hp1 | a0001 | c0001 | t0041 | g0122 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19079 | hp2 | a0001 | c0001 | t0026 | g0215 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19081 | hp2 | a0001 | c0001 | t0057 | g0266 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19083 | hp2 | a0001 | c0001 | t0037 | g0247 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19086 | hp2 | a0001 | c0001 | t0007 | g0014 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19087 | hp1 | a0001 | c0001 | t0024 | g0078 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19088 | hp1 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19240 | hp1 | a0001 | c0001 | t0047 | g0239 | AFR | YRI | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0174 | AFR | YRI | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | TSI | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | TSI | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA20805 | hp1 | a0001 | c0001 | t0006 | g0182 | EUR | TSI | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA20805 | hp2 | a0001 | c0001 | t0023 | g0040 | EUR | TSI | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA20905 | hp1 | a0001 | c0001 | t0045 | g0221 | SAS | GIH | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA20905 | hp2 | a0001 | c0005 | t0006 | g0176 | SAS | GIH | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02109 | hp1 | a0001 | c0001 | t0013 | g0175 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02109 | hp2 | a0001 | c0001 | t0059 | g0268 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0216 | AFR | ACB | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG03471 | hp2 | a0001 | c0001 | t0028 | g0242 | AFR | MSL | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG06807 | hp1 | a0001 | c0001 | t0048 | g0246 | AFR | USA | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| HG06807 | hp2 | a0001 | c0001 | t0012 | g0140 | AFR | USA | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA20300 | hp1 | a0001 | c0001 | t0032 | g0043 | AFR | USA | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| NA20300 | hp2 | a0001 | c0001 | t0013 | g0034 | AFR | USA | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0025 | g0125 | REF | REF | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0030 | g0272 | REF | REF | FAM193B_chr5_177514789_177559563 | FAM193B | chr5 | 177514789 | 177559563 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:177524275
|
A | G | 8 | a0001a0004a0005others(5): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
missense_variant | MODERATE | c.2206T>C | p.Ser736Pro | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 6/9 | 2311/2968 | 2206/2469 | 736/822 | chr5 | 177524275 | ||
| chr5:177524629
|
G | A | 1 | a0007 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.1852C>T | p.Pro618Ser | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 6/9 | 1957/2968 | 1852/2469 | 618/822 | chr5 | 177524629 | ||
| chr5:177524706
|
T | C | 1 | a0008 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.1775A>G | p.Asn592Ser | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 6/9 | 1880/2968 | 1775/2469 | 592/822 | chr5 | 177524706 | ||
| chr5:177524712
|
A | G | 1 | a0003 | 4 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
missense_variant | MODERATE | c.1769T>C | p.Val590Ala | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 6/9 | 1874/2968 | 1769/2469 | 590/822 | chr5 | 177524712 | ||
| chr5:177524715
|
G | T | 1 | a0004 | 3 | HG02572.hp1 HG02896.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.1766C>A | p.Thr589Asn | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 6/9 | 1871/2968 | 1766/2469 | 589/822 | chr5 | 177524715 | ||
| chr5:177524913
|
G | A | 1 | a0005 | 2 | HG01081.hp2 HG01934.hp1 |
missense_variant | MODERATE | c.1568C>T | p.Ser523Phe | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 6/9 | 1673/2968 | 1568/2469 | 523/822 | chr5 | 177524913 | ||
| chr5:177525177
|
T | G | 1 | a0006 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.1304A>C | p.Glu435Ala | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 6/9 | 1409/2968 | 1304/2469 | 435/822 | chr5 | 177525177 | ||
| chr5:177536530
|
G | A | 1 | a0009 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.904C>T | p.His302Tyr | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/9 | 1009/2968 | 904/2469 | 302/822 | chr5 | 177536530 | ||
| chr5:177539137
|
G | C | 1 | a0010 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.221C>G | p.Ala74Gly | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 2/9 | 326/2968 | 221/2469 | 74/822 | chr5 | 177539137 | ||
| chr5:177554281
|
C | T | 1 | a0011 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.178G>A | p.Asp60Asn | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 283/2968 | 178/2469 | 60/822 | chr5 | 177554281 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:177523962
|
A | G | 1 | a0001c0011 | 1 | NA18943.hp1 | synonymous_variant | LOW | c.2367T>C | p.Phe789Phe | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/9 | 2472/2968 | 2367/2469 | 789/822 | chr5 | 177523962 | ||
| chr5:177524993
|
G | A | 1 | a0001c0014 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1488C>T | p.Ser496Ser | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 6/9 | 1593/2968 | 1488/2469 | 496/822 | chr5 | 177524993 | ||
| chr5:177525107
|
C | T | 1 | a0001c0010 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.1374G>A | p.Glu458Glu | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 6/9 | 1479/2968 | 1374/2469 | 458/822 | chr5 | 177525107 | ||
| chr5:177536636
|
G | T | 1 | a0001c0009 | 1 | NA18949.hp1 | synonymous_variant | LOW | c.798C>A | p.Pro266Pro | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/9 | 903/2968 | 798/2469 | 266/822 | chr5 | 177536636 | ||
| chr5:177554315
|
C | T | 1 | a0001c0005 | 2 | HG04204.hp2 NA20905.hp2 |
synonymous_variant | LOW | c.144G>A | p.Ala48Ala | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 249/2968 | 144/2469 | 48/822 | chr5 | 177554315 | ||
| chr5:177554369
|
C | T | 1 | a0001c0007 | 1 | NA19060.hp2 | synonymous_variant | LOW | c.90G>A | p.Glu30Glu | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 195/2968 | 90/2469 | 30/822 | chr5 | 177554369 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:177519961
|
G | A | 1 | a0001c0014t0046 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*222C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 9/9 | 2014 | chr5 | 177519961 | |||||
| chr5:177520069
|
G | A | 1 | a0003c0003t0021 | 4 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*114C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 9/9 | 1906 | chr5 | 177520069 | |||||
| chr5:177520088
|
C | T | 1 | a0001c0001t0040 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*95G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 9/9 | 1887 | chr5 | 177520088 | |||||
| chr5:177520106
|
G | A | 20 | a0001c0001t0005a0001c0001t0006a0001c0001t0019others(17): Show | 55 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*77C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 9/9 | 1869 | chr5 | 177520106 | |||||
| chr5:177520152
|
C | T | 47 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(44): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*31G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 9/9 | 1823 | chr5 | 177520152 | |||||
| chr5:177554468
|
C | T | 6 | a0001c0001t0002a0001c0001t0039a0001c0001t0041others(3): Show | 62 | HG00544.hp1 HG00609.hp1 HG00673.hp2 others(59): Show |
5_prime_UTR_variant | MODIFIER | c.-10G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 10 | chr5 | 177554468 | |||||
| chr5:177554489
|
A | ACGCCG | 5 | a0001c0001t0003a0001c0001t0012a0001c0001t0042others(2): Show | 33 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(30): Show |
5_prime_UTR_variant | MODIFIER | c.-36_-32dupCGGCG | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | |||||
| chr5:177554489
|
A | ACGCCGCG others(1): Show |
6 | a0001c0001t0009a0001c0001t0013a0001c0001t0022others(3): Show | 18 | HG01081.hp1 HG01516.hp2 HG01517.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGCGGCG | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | |||||
| chr5:177554489
|
A | ACGCCGCG others(4): Show |
4 | a0001c0001t0004a0001c0001t0006a0001c0001t0017others(1): Show | 31 | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(28): Show |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGCG others(3): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | |||||
| chr5:177554489
|
A | ACGCCGCG others(7): Show |
5 | a0001c0001t0014a0001c0001t0018a0001c0001t0019others(2): Show | 16 | HG00741.hp1 HG02135.hp2 HG02300.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(6): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | |||||
| chr5:177554489
|
A | ACGCCGCG others(10): Show |
3 | a0001c0001t0005a0001c0001t0026a0001c0001t0044 | 16 | HG00639.hp2 HG00673.hp1 HG01255.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(9): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | |||||
| chr5:177554489
|
A | ACGCCGCG others(13): Show |
4 | a0001c0001t0007a0001c0001t0034a0001c0001t0045others(1): Show | 15 | HG01496.hp2 HG01943.hp1 HG02132.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(12): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | |||||
| chr5:177554489
|
A | ACGCCGCG others(16): Show |
4 | a0001c0001t0015a0001c0001t0035a0001c0001t0036others(1): Show | 10 | HG00438.hp2 HG00558.hp2 HG02129.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(15): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | |||||
| chr5:177554489
|
A | ACGCCGCG others(19): Show |
3 | a0001c0001t0023a0001c0001t0027a0001c0001t0047 | 8 | HG00408.hp1 HG00609.hp2 HG02258.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(18): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | |||||
| chr5:177554489
|
A | ACGCCGCG others(22): Show |
1 | a0001c0001t0028 | 3 | HG03471.hp2 HG03669.hp1 NA18947.hp1 |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(21): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | |||||
| chr5:177554489
|
A | ACGCCGCG others(25): Show |
3 | a0001c0001t0037a0001c0001t0048a0001c0001t0049 | 4 | HG00140.hp2 HG02698.hp1 HG06807.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(24): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | |||||
| chr5:177554489
|
A | ACGCCGCG others(28): Show |
4 | a0001c0001t0020a0001c0001t0050a0004c0004t0020others(1): Show | 6 | HG02071.hp1 HG02572.hp2 HG02896.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(27): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | |||||
| chr5:177554489
|
A | ACGCCGCG others(31): Show |
2 | a0001c0001t0029a0001c0001t0051 | 4 | HG03486.hp1 NA18968.hp2 NA18969.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(30): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | |||||
| chr5:177554489
|
A | ACGCCGCG others(34): Show |
1 | a0001c0001t0052 | 1 | HG01175.hp2 | 5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(33): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | |||||
| chr5:177554489
|
A | ACGCCGCG others(37): Show |
2 | a0001c0001t0053a0001c0001t0054 | 2 | HG01346.hp2 HG02027.hp1 |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(36): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | |||||
| chr5:177554489
|
A | ACGCCGCG others(40): Show |
2 | a0001c0001t0055a0001c0001t0056 | 2 | HG02165.hp1 HG02615.hp2 |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(39): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | |||||
| chr5:177554489
|
A | ACGCCGCG others(46): Show |
2 | a0001c0001t0038a0001c0001t0057 | 3 | HG04204.hp1 NA19058.hp2 NA19081.hp2 |
5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(45): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | |||||
| chr5:177554489
|
A | ACGCCGCG others(49): Show |
1 | a0001c0001t0058 | 1 | HG02895.hp2 | 5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(48): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | |||||
| chr5:177554489
|
A | ACGCCGCG others(58): Show |
1 | a0001c0001t0059 | 1 | HG02109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(57): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | |||||
| chr5:177554489
|
A | ACGCCGCG others(61): Show |
1 | a0001c0001t0060 | 1 | NA18989.hp1 | 5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(60): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | |||||
| chr5:177554489
|
A | ACGCCGCG others(76): Show |
1 | a0001c0001t0061 | 1 | HG00423.hp1 | 5_prime_UTR_variant | MODIFIER | c.-32_-31insGCGGCGGC others(75): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | |||||
| chr5:177554489
|
ACGCCGC | A | 1 | a0002c0002t0031 | 3 | HG02055.hp1 HG02622.hp2 HG02965.hp2 |
5_prime_UTR_variant | MODIFIER | c.-37_-32delGCGGCG | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 32 | chr5 | 177554489 | |||||
| chr5:177554492
|
C | CCG | 5 | a0001c0001t0011a0001c0001t0016a0001c0001t0025others(2): Show | 19 | HG00558.hp1 HG01261.hp2 HG01891.hp1 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-36_-35dupCG | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 35 | chr5 | 177554492 | |||||
| chr5:177554494
|
GC | G | 9 | a0001c0001t0001a0001c0001t0002a0001c0001t0024others(6): Show | 151 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(148): Show |
5_prime_UTR_variant | MODIFIER | c.-37delG | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 37 | chr5 | 177554494 | |||||
| chr5:177554494
|
GCCGC | G | 4 | a0001c0001t0008a0001c0001t0010a0001c0001t0033others(1): Show | 15 | HG00099.hp2 HG01106.hp2 HG01167.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-40_-37delGCGG | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 37 | chr5 | 177554494 | |||||
| chr5:177554494
|
GCCGCCGC others(3): Show |
G | 1 | a0001c0001t0032 | 2 | NA19011.hp2 NA20300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-46_-37delGCGGCGGC others(2): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 37 | chr5 | 177554494 | |||||
| chr5:177554532
|
T | C | 1 | a0001c0001t0063 | 1 | NA18982.hp2 | 5_prime_UTR_variant | MODIFIER | c.-74A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/9 | 74 | chr5 | 177554532 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:177520194
|
AAAAG | A | 4 | a0002c0002t0030g0274a0002c0002t0031g0041a0002c0002t0031g0275others(1): Show | 5 | HG02055.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.*2-17_*2-14delCTTT | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177520194 | ||||||
| chr5:177520298
|
T | C | 7 | a0001c0001t0008g0022a0001c0001t0008g0050a0001c0001t0008g0051others(4): Show | 8 | HG01243.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.*2-117A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177520298 | ||||||
| chr5:177520365
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.*2-184C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177520365 | ||||||
| chr5:177520403
|
G | T | 273 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(270): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.*2-222C>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177520403 | ||||||
| chr5:177520507
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0097 | 2 | HG01099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.*2-326G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177520507 | ||||||
| chr5:177520599
|
G | A | 1 | a0001c0001t0019g0200 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.*2-418C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177520599 | ||||||
| chr5:177521120
|
G | T | 62 | a0001c0001t0004g0003a0001c0001t0004g0189a0001c0001t0004g0190others(59): Show | 76 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.*1+854C>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177521120 | ||||||
| chr5:177521170
|
G | A | 2 | a0001c0001t0006g0182a0001c0001t0006g0197 | 2 | HG01496.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.*1+804C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177521170 | ||||||
| chr5:177521257
|
A | G | 1 | a0001c0001t0063g0276 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.*1+717T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177521257 | ||||||
| chr5:177521518
|
T | C | 1 | a0001c0001t0011g0129 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.*1+456A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177521518 | ||||||
| chr5:177521533
|
G | A | 1 | a0001c0001t0010g0044 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.*1+441C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177521533 | ||||||
| chr5:177521567
|
G | A | 1 | a0001c0001t0024g0115 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.*1+407C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177521567 | ||||||
| chr5:177521715
|
T | G | 62 | a0001c0001t0004g0003a0001c0001t0004g0189a0001c0001t0004g0190others(59): Show | 76 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.*1+259A>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177521715 | ||||||
| chr5:177521716
|
T | C | 83 | a0001c0001t0003g0019a0001c0001t0003g0033a0001c0001t0003g0141others(80): Show | 92 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.*1+258A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177521716 | ||||||
| chr5:177521746
|
G | A | 1 | a0001c0001t0002g0062 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.*1+228C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177521746 | ||||||
| chr5:177521776
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.*1+198C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177521776 | ||||||
| chr5:177521788
|
A | C | 1 | a0001c0001t0008g0053 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.*1+186T>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177521788 | ||||||
| chr5:177521820
|
T | A | 275 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(272): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.*1+154A>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 8/8 | chr5 | 177521820 | ||||||
| chr5:177522321
|
T | C | 83 | a0001c0001t0003g0019a0001c0001t0003g0033a0001c0001t0003g0141others(80): Show | 92 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.2373-250A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177522321 | ||||||
| chr5:177522351
|
G | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(106): Show | 173 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.2373-280C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177522351 | ||||||
| chr5:177522475
|
G | C | 1 | a0001c0001t0003g0142 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2373-404C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177522475 | ||||||
| chr5:177522497
|
T | A | 1 | a0001c0001t0001g0032 | 2 | HG01069.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.2373-426A>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177522497 | ||||||
| chr5:177522610
|
G | T | 109 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(106): Show | 173 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.2373-539C>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177522610 | ||||||
| chr5:177522679
|
A | G | 4 | a0001c0001t0015g0232a0001c0001t0023g0240a0001c0001t0028g0242others(1): Show | 4 | HG02258.hp2 HG02818.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2373-608T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177522679 | ||||||
| chr5:177522887
|
G | T | 1 | a0001c0001t0032g0042 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2373-816C>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177522887 | ||||||
| chr5:177523095
|
G | A | 2 | a0003c0003t0021g0018a0003c0003t0021g0137 | 4 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2372+862C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177523095 | ||||||
| chr5:177523171
|
T | C | 1 | a0001c0001t0041g0122 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2372+786A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177523171 | ||||||
| chr5:177523251
|
C | T | 1 | a0001c0001t0040g0080 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2372+706G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177523251 | ||||||
| chr5:177523291
|
C | T | 1 | a0001c0001t0040g0080 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2372+666G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177523291 | ||||||
| chr5:177523326
|
CATT | C | 3 | a0001c0001t0012g0139a0001c0001t0012g0140a0001c0001t0016g0123 | 3 | HG01243.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2372+628_2372+630d others(5): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177523326 | ||||||
| chr5:177523413
|
C | T | 11 | a0001c0001t0001g0011a0001c0001t0001g0094a0001c0001t0001g0101others(8): Show | 14 | HG00423.hp2 HG01175.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.2372+544G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177523413 | ||||||
| chr5:177523638
|
T | C | 1 | a0001c0001t0053g0260 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2372+319A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177523638 | ||||||
| chr5:177523793
|
A | G | 275 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(272): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.2372+164T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177523793 | ||||||
| chr5:177523822
|
G | C | 63 | a0001c0001t0004g0003a0001c0001t0004g0189a0001c0001t0004g0190others(60): Show | 77 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.2372+135C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177523822 | ||||||
| chr5:177523878
|
T | C | 275 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(272): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.2372+79A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 7/8 | chr5 | 177523878 | ||||||
| chr5:177525215
|
C | T | 1 | a0001c0001t0029g0258 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1276-10G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177525215 | ||||||
| chr5:177525342
|
C | G | 1 | a0006c0015t0030g0273 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1276-137G>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177525342 | ||||||
| chr5:177525431
|
C | T | 1 | a0001c0001t0008g0050 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1276-226G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177525431 | ||||||
| chr5:177525639
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0018g0206 | 2 | HG00140.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.1276-434C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177525639 | ||||||
| chr5:177525697
|
G | A | 5 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0016g0127others(2): Show | 5 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1276-492C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177525697 | ||||||
| chr5:177525823
|
C | T | 1 | a0001c0001t0010g0048 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1276-618G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177525823 | ||||||
| chr5:177525918
|
C | T | 193 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(190): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1276-713G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177525918 | ||||||
| chr5:177525951
|
C | G | 1 | a0001c0001t0001g0010 | 4 | HG02145.hp1 HG02559.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1276-746G>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177525951 | ||||||
| chr5:177526017
|
G | A | 191 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(188): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1276-812C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177526017 | ||||||
| chr5:177526130
|
C | T | 1 | a0001c0001t0003g0145 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1276-925G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177526130 | ||||||
| chr5:177526131
|
G | A | 5 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0016g0127others(2): Show | 5 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1276-926C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177526131 | ||||||
| chr5:177526293
|
C | T | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(268): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.1276-1088G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177526293 | ||||||
| chr5:177526414
|
C | T | 7 | a0001c0001t0008g0022a0001c0001t0008g0050a0001c0001t0008g0051others(4): Show | 8 | HG01243.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1276-1209G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177526414 | ||||||
| chr5:177526465
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1276-1260G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177526465 | ||||||
| chr5:177526524
|
T | C | 2 | a0001c0001t0011g0131a0001c0001t0011g0133 | 2 | HG01978.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1276-1319A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177526524 | ||||||
| chr5:177526813
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1276-1608T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177526813 | ||||||
| chr5:177526851
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0081 | 5 | HG02055.hp2 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1276-1646A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177526851 | ||||||
| chr5:177526906
|
C | A | 6 | a0001c0001t0009g0163a0001c0001t0009g0164a0004c0004t0015g0228others(3): Show | 6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1276-1701G>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177526906 | ||||||
| chr5:177526924
|
A | G | 4 | a0001c0001t0001g0015a0001c0001t0001g0084a0001c0001t0001g0086others(1): Show | 6 | NA18952.hp1 NA18961.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.1276-1719T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177526924 | ||||||
| chr5:177527121
|
G | GC | 63 | a0001c0001t0004g0003a0001c0001t0004g0189a0001c0001t0004g0190others(60): Show | 77 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1276-1917dupG | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177527121 | ||||||
| chr5:177527240
|
T | C | 1 | a0001c0001t0001g0029 | 2 | NA18954.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1276-2035A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177527240 | ||||||
| chr5:177527416
|
C | T | 3 | a0001c0001t0011g0131a0001c0001t0011g0133a0001c0001t0053g0260 | 3 | HG01346.hp2 HG01978.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1276-2211G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177527416 | ||||||
| chr5:177527647
|
G | A | 1 | a0001c0001t0007g0222 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1276-2442C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177527647 | ||||||
| chr5:177527749
|
A | G | 275 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(272): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1276-2544T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177527749 | ||||||
| chr5:177527790
|
T | G | 273 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(270): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.1276-2585A>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177527790 | ||||||
| chr5:177527828
|
T | C | 5 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0060others(2): Show | 11 | NA18939.hp2 NA18942.hp2 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.1276-2623A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177527828 | ||||||
| chr5:177527926
|
C | A | 1 | a0002c0002t0031g0275 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1276-2721G>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177527926 | ||||||
| chr5:177528085
|
C | T | 1 | a0001c0001t0033g0046 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1276-2880G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177528085 | ||||||
| chr5:177528155
|
A | T | 5 | a0001c0001t0005g0212a0001c0001t0005g0213a0001c0001t0022g0165others(2): Show | 5 | HG01255.hp2 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1276-2950T>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177528155 | ||||||
| chr5:177528201
|
G | A | 1 | a0001c0001t0002g0025 | 2 | NA18962.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1276-2996C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177528201 | ||||||
| chr5:177528223
|
C | T | 2 | a0001c0001t0025g0124a0001c0001t0025g0125 | 2 | HG04184.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1276-3018G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177528223 | ||||||
| chr5:177528227
|
A | G | 275 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(272): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1276-3022T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177528227 | ||||||
| chr5:177528475
|
G | A | 1 | a0001c0001t0002g0061 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1276-3270C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177528475 | ||||||
| chr5:177528531
|
GGTCAAGA others(7): Show |
G | 1 | a0001c0001t0018g0204 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1276-3340_1276-332 others(18): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177528531 | ||||||
| chr5:177528597
|
T | A | 78 | a0001c0001t0003g0019a0001c0001t0003g0033a0001c0001t0003g0141others(75): Show | 87 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.1276-3392A>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177528597 | ||||||
| chr5:177528717
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1276-3512C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177528717 | ||||||
| chr5:177528794
|
TGA | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0032 | 5 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1276-3591_1276-359 others(6): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177528794 | ||||||
| chr5:177528840
|
C | T | 1 | a0001c0001t0002g0068 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1275+3603G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177528840 | ||||||
| chr5:177529034
|
C | G | 3 | a0001c0001t0001g0111a0001c0001t0013g0034a0001c0001t0017g0188 | 4 | HG01884.hp2 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1275+3409G>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177529034 | ||||||
| chr5:177529083
|
A | T | 1 | a0001c0001t0002g0063 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1275+3360T>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177529083 | ||||||
| chr5:177529090
|
G | A | 2 | a0001c0001t0002g0073a0001c0001t0011g0129 | 2 | HG01099.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1275+3353C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177529090 | ||||||
| chr5:177529131
|
G | T | 1 | a0001c0001t0007g0224 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1275+3312C>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177529131 | ||||||
| chr5:177529225
|
C | T | 41 | a0001c0001t0004g0003a0001c0001t0004g0189a0001c0001t0004g0190others(38): Show | 55 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.1275+3218G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177529225 | ||||||
| chr5:177529506
|
G | T | 2 | a0002c0002t0031g0041a0002c0002t0031g0275 | 3 | HG02055.hp1 HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1275+2937C>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177529506 | ||||||
| chr5:177529547
|
G | A | 6 | a0001c0001t0009g0163a0001c0001t0009g0164a0004c0004t0015g0228others(3): Show | 6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1275+2896C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177529547 | ||||||
| chr5:177529598
|
G | C | 3 | a0001c0001t0003g0006a0001c0001t0003g0156a0001c0001t0003g0158 | 7 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1275+2845C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177529598 | ||||||
| chr5:177530125
|
T | C | 63 | a0001c0001t0004g0003a0001c0001t0004g0189a0001c0001t0004g0190others(60): Show | 77 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.1275+2318A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177530125 | ||||||
| chr5:177530429
|
A | T | 1 | a0001c0001t0002g0072 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1275+2014T>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177530429 | ||||||
| chr5:177530534
|
C | T | 1 | a0001c0001t0003g0151 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1275+1909G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177530534 | ||||||
| chr5:177530791
|
C | T | 6 | a0001c0001t0024g0077a0001c0001t0033g0046a0001c0001t0049g0245others(3): Show | 6 | HG02698.hp1 HG03491.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.1275+1652G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177530791 | ||||||
| chr5:177531106
|
T | C | 1 | a0003c0003t0021g0137 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1275+1337A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177531106 | ||||||
| chr5:177531167
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1275+1276C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177531167 | ||||||
| chr5:177531396
|
G | A | 38 | a0001c0001t0001g0079a0001c0001t0002g0001a0001c0001t0002g0004others(35): Show | 66 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1275+1047C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177531396 | ||||||
| chr5:177531612
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1275+831C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177531612 | ||||||
| chr5:177531613
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1275+830G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177531613 | ||||||
| chr5:177531807
|
A | G | 5 | a0001c0001t0015g0232a0001c0001t0015g0233a0001c0001t0023g0240others(2): Show | 5 | HG02258.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1275+636T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177531807 | ||||||
| chr5:177531935
|
C | T | 3 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0067 | 5 | HG00544.hp1 HG00673.hp2 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.1275+508G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177531935 | ||||||
| chr5:177532024
|
T | C | 8 | a0001c0001t0004g0196a0001c0001t0009g0172a0001c0001t0009g0173others(5): Show | 8 | HG01261.hp2 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1275+419A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177532024 | ||||||
| chr5:177532031
|
G | A | 1 | a0002c0002t0030g0274 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1275+412C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177532031 | ||||||
| chr5:177532054
|
C | T | 10 | a0001c0001t0003g0019a0001c0001t0003g0147a0001c0001t0003g0148others(7): Show | 12 | HG01891.hp2 HG02451.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1275+389G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177532054 | ||||||
| chr5:177532295
|
T | G | 113 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(110): Show | 177 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.1275+148A>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 5/8 | chr5 | 177532295 | ||||||
| chr5:177532711
|
C | T | 1 | a0001c0001t0005g0212 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1077-70G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177532711 | ||||||
| chr5:177533295
|
C | T | 1 | a0001c0001t0023g0241 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1077-654G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177533295 | ||||||
| chr5:177533306
|
A | AT | 9 | a0001c0001t0005g0211a0001c0001t0009g0172a0001c0001t0012g0159others(6): Show | 9 | HG00099.hp1 HG00558.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1077-666dupA | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177533306 | ||||||
| chr5:177533449
|
C | T | 1 | a0001c0001t0022g0165 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1077-808G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177533449 | ||||||
| chr5:177533450
|
G | A | 113 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(110): Show | 177 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.1077-809C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177533450 | ||||||
| chr5:177533495
|
T | C | 6 | a0001c0001t0009g0163a0001c0001t0009g0164a0004c0004t0015g0228others(3): Show | 6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077-854A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177533495 | ||||||
| chr5:177533646
|
T | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(110): Show | 177 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.1077-1005A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177533646 | ||||||
| chr5:177533942
|
G | A | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(268): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.1077-1301C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177533942 | ||||||
| chr5:177534046
|
T | C | 2 | a0001c0001t0003g0148a0001c0001t0005g0207 | 2 | HG02922.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.1077-1405A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177534046 | ||||||
| chr5:177534067
|
G | T | 1 | a0001c0001t0002g0063 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1077-1426C>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177534067 | ||||||
| chr5:177534165
|
C | T | 1 | a0001c0001t0054g0261 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1077-1524G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177534165 | ||||||
| chr5:177534187
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1077-1546A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177534187 | ||||||
| chr5:177534192
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0081 | 5 | HG02055.hp2 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1077-1551G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177534192 | ||||||
| chr5:177534248
|
G | T | 1 | a0001c0001t0001g0094 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1077-1607C>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177534248 | ||||||
| chr5:177534291
|
A | AT | 190 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(187): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1077-1651dupA | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177534291 | ||||||
| chr5:177534291
|
A | ATT | 10 | a0001c0001t0001g0083a0001c0001t0001g0093a0001c0001t0001g0101others(7): Show | 13 | HG00673.hp1 HG03831.hp2 HG03942.hp1 others(10): Show |
intron_variant | MODIFIER | c.1077-1652_1077-165 others(6): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177534291 | ||||||
| chr5:177534316
|
G | A | 1 | a0001c0001t0003g0149 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1077-1675C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177534316 | ||||||
| chr5:177534624
|
A | T | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1076+1734T>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177534624 | ||||||
| chr5:177534686
|
C | T | 1 | a0001c0001t0003g0145 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1076+1672G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177534686 | ||||||
| chr5:177534688
|
G | T | 1 | a0001c0001t0003g0145 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1076+1670C>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177534688 | ||||||
| chr5:177534944
|
T | G | 1 | a0001c0001t0013g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1076+1414A>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177534944 | ||||||
| chr5:177535303
|
G | A | 1 | a0001c0001t0003g0154 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1076+1055C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177535303 | ||||||
| chr5:177535306
|
G | T | 1 | a0001c0001t0010g0044 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1076+1052C>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177535306 | ||||||
| chr5:177535328
|
G | A | 1 | a0001c0001t0002g0065 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1076+1030C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177535328 | ||||||
| chr5:177535387
|
T | C | 1 | a0001c0001t0017g0188 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1076+971A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177535387 | ||||||
| chr5:177535395
|
T | C | 6 | a0001c0001t0017g0177a0001c0001t0033g0046a0001c0001t0049g0245others(3): Show | 6 | HG02698.hp1 HG03490.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.1076+963A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177535395 | ||||||
| chr5:177535651
|
C | A | 2 | a0002c0002t0031g0041a0002c0002t0031g0275 | 3 | HG02055.hp1 HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1076+707G>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177535651 | ||||||
| chr5:177535753
|
C | T | 7 | a0001c0001t0008g0022a0001c0001t0008g0050a0001c0001t0008g0051others(4): Show | 8 | HG01243.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1076+605G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177535753 | ||||||
| chr5:177535759
|
G | T | 2 | a0001c0001t0003g0151a0001c0001t0010g0044 | 2 | HG01167.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1076+599C>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177535759 | ||||||
| chr5:177535779
|
T | C | 1 | a0001c0001t0006g0183 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1076+579A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177535779 | ||||||
| chr5:177535921
|
AT | A | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(268): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.1076+436delA | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177535921 | ||||||
| chr5:177536100
|
G | C | 1 | a0001c0001t0001g0101 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1076+258C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177536100 | ||||||
| chr5:177536173
|
A | G | 4 | a0002c0002t0030g0274a0002c0002t0031g0041a0002c0002t0031g0275others(1): Show | 5 | HG02055.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1076+185T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177536173 | ||||||
| chr5:177536332
|
G | C | 41 | a0001c0001t0004g0003a0001c0001t0004g0189a0001c0001t0004g0190others(38): Show | 55 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.1076+26C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177536332 | ||||||
| chr5:177536348
|
G | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(190): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1076+10C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 4/8 | chr5 | 177536348 | ||||||
| chr5:177536873
|
C | G | 1 | a0001c0001t0002g0067 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.689-128G>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 3/8 | chr5 | 177536873 | ||||||
| chr5:177536994
|
G | A | 3 | a0002c0002t0030g0274a0002c0002t0031g0041a0002c0002t0031g0275 | 4 | HG02055.hp1 HG02622.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.689-249C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 3/8 | chr5 | 177536994 | ||||||
| chr5:177537046
|
T | G | 3 | a0001c0001t0003g0149a0001c0001t0013g0168a0010c0017t0003g0146 | 3 | HG00639.hp1 HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.689-301A>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 3/8 | chr5 | 177537046 | ||||||
| chr5:177537133
|
C | A | 1 | a0001c0001t0006g0185 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.689-388G>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 3/8 | chr5 | 177537133 | ||||||
| chr5:177537410
|
A | G | 1 | a0001c0001t0010g0048 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.688+463T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 3/8 | chr5 | 177537410 | ||||||
| chr5:177537540
|
G | A | 3 | a0002c0002t0030g0274a0002c0002t0031g0041a0002c0002t0031g0275 | 4 | HG02055.hp1 HG02622.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+333C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 3/8 | chr5 | 177537540 | ||||||
| chr5:177538160
|
G | A | 1 | a0001c0001t0043g0150 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.454-53C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 2/8 | chr5 | 177538160 | ||||||
| chr5:177538168
|
G | A | 1 | a0001c0001t0037g0248 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.454-61C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 2/8 | chr5 | 177538168 | ||||||
| chr5:177538292
|
C | T | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(268): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.454-185G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 2/8 | chr5 | 177538292 | ||||||
| chr5:177538372
|
G | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0119a0001c0001t0001g0121 | 5 | HG01517.hp1 HG01981.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.454-265C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 2/8 | chr5 | 177538372 | ||||||
| chr5:177538398
|
T | C | 2 | a0001c0001t0001g0108a0001c0007t0001g0076 | 2 | NA19057.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.454-291A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 2/8 | chr5 | 177538398 | ||||||
| chr5:177538440
|
G | C | 1 | a0001c0001t0023g0240 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.454-333C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 2/8 | chr5 | 177538440 | ||||||
| chr5:177539236
|
C | T | 1 | a0001c0001t0003g0142 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.211-89G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177539236 | ||||||
| chr5:177539500
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.211-353A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177539500 | ||||||
| chr5:177539622
|
T | C | 69 | a0001c0001t0004g0003a0001c0001t0004g0189a0001c0001t0004g0190others(66): Show | 84 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.211-475A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177539622 | ||||||
| chr5:177539662
|
G | A | 1 | a0001c0001t0002g0066 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.211-515C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177539662 | ||||||
| chr5:177539768
|
C | T | 1 | a0001c0001t0011g0132 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.211-621G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177539768 | ||||||
| chr5:177539978
|
CTTTTT | C | 8 | a0001c0001t0004g0196a0001c0001t0009g0172a0001c0001t0009g0173others(5): Show | 8 | HG01261.hp2 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.211-836_211-832del others(5): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177539978 | ||||||
| chr5:177540238
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.211-1091G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177540238 | ||||||
| chr5:177540276
|
C | T | 2 | a0003c0003t0021g0018a0003c0003t0021g0137 | 4 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-1129G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177540276 | ||||||
| chr5:177540306
|
C | CA | 14 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0102others(11): Show | 15 | HG00423.hp2 HG00673.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.211-1160dupT | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177540306 | ||||||
| chr5:177540306
|
CA | C | 142 | a0001c0001t0001g0010a0001c0001t0001g0118a0001c0001t0002g0060others(139): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.211-1160delT | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177540306 | ||||||
| chr5:177540335
|
A | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(110): Show | 177 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.211-1188T>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177540335 | ||||||
| chr5:177540337
|
A | G | 1 | a0001c0001t0011g0131 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.211-1190T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177540337 | ||||||
| chr5:177540478
|
G | T | 4 | a0002c0002t0030g0274a0002c0002t0031g0041a0002c0002t0031g0275others(1): Show | 5 | HG02055.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.211-1331C>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177540478 | ||||||
| chr5:177540661
|
G | C | 192 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(189): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.211-1514C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177540661 | ||||||
| chr5:177540736
|
T | C | 1 | a0001c0001t0016g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.211-1589A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177540736 | ||||||
| chr5:177540864
|
C | T | 2 | a0001c0001t0014g0020a0001c0001t0014g0205 | 4 | HG03704.hp2 HG03834.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-1717G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177540864 | ||||||
| chr5:177541156
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0081 | 5 | HG02055.hp2 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.211-2009T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177541156 | ||||||
| chr5:177541395
|
C | A | 1 | a0001c0001t0003g0142 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.211-2248G>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177541395 | ||||||
| chr5:177541442
|
G | A | 1 | a0001c0001t0003g0151 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.211-2295C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177541442 | ||||||
| chr5:177541445
|
G | A | 2 | a0003c0003t0021g0018a0003c0003t0021g0137 | 4 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-2298C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177541445 | ||||||
| chr5:177541520
|
G | A | 2 | a0001c0001t0002g0004a0001c0001t0002g0069 | 6 | HG01192.hp1 HG01255.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.211-2373C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177541520 | ||||||
| chr5:177541539
|
C | T | 60 | a0001c0001t0004g0003a0001c0001t0004g0189a0001c0001t0004g0190others(57): Show | 74 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.211-2392G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177541539 | ||||||
| chr5:177541652
|
C | T | 194 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(191): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.211-2505G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177541652 | ||||||
| chr5:177541654
|
C | T | 2 | a0003c0003t0021g0018a0003c0003t0021g0137 | 4 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-2507G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177541654 | ||||||
| chr5:177541698
|
C | T | 35 | a0001c0001t0001g0079a0001c0001t0002g0001a0001c0001t0002g0004others(32): Show | 63 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.211-2551G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177541698 | ||||||
| chr5:177541742
|
A | G | 1 | a0001c0001t0007g0223 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.211-2595T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177541742 | ||||||
| chr5:177541989
|
T | C | 194 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(191): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.211-2842A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177541989 | ||||||
| chr5:177542092
|
C | T | 1 | a0001c0001t0004g0191 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.211-2945G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177542092 | ||||||
| chr5:177542214
|
T | C | 1 | a0001c0001t0002g0073 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.211-3067A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177542214 | ||||||
| chr5:177542271
|
T | C | 3 | a0001c0001t0006g0178a0001c0001t0019g0202a0001c0001t0027g0238 | 3 | HG02135.hp2 NA18951.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.211-3124A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177542271 | ||||||
| chr5:177542298
|
G | C | 1 | a0001c0001t0001g0088 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.211-3151C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177542298 | ||||||
| chr5:177542299
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.211-3152G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177542299 | ||||||
| chr5:177542624
|
G | A | 80 | a0001c0001t0001g0010a0001c0001t0001g0081a0001c0001t0003g0019others(77): Show | 92 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.211-3477C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177542624 | ||||||
| chr5:177542733
|
C | G | 5 | a0001c0001t0015g0232a0001c0001t0015g0233a0001c0001t0023g0240others(2): Show | 5 | HG02258.hp2 HG02818.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.211-3586G>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177542733 | ||||||
| chr5:177542734
|
G | A | 6 | a0001c0001t0009g0163a0001c0001t0009g0164a0004c0004t0015g0228others(3): Show | 6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-3587C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177542734 | ||||||
| chr5:177542793
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0032others(1): Show | 10 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-3646C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177542793 | ||||||
| chr5:177542823
|
C | T | 1 | a0001c0001t0004g0196 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.211-3676G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177542823 | ||||||
| chr5:177542925
|
T | C | 1 | a0001c0001t0009g0174 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.211-3778A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177542925 | ||||||
| chr5:177542942
|
A | G | 6 | a0001c0001t0009g0163a0001c0001t0009g0164a0004c0004t0015g0228others(3): Show | 6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-3795T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177542942 | ||||||
| chr5:177542995
|
T | C | 1 | a0001c0001t0007g0225 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.211-3848A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177542995 | ||||||
| chr5:177543241
|
C | T | 1 | a0006c0015t0030g0273 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.211-4094G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177543241 | ||||||
| chr5:177543304
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.211-4157G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177543304 | ||||||
| chr5:177543434
|
T | C | 194 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(191): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.211-4287A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177543434 | ||||||
| chr5:177543801
|
C | T | 1 | a0001c0001t0015g0233 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.211-4654G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177543801 | ||||||
| chr5:177543802
|
G | A | 78 | a0001c0001t0003g0019a0001c0001t0003g0033a0001c0001t0003g0141others(75): Show | 87 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.211-4655C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177543802 | ||||||
| chr5:177543854
|
G | A | 1 | a0001c0001t0015g0235 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.211-4707C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177543854 | ||||||
| chr5:177544072
|
G | C | 192 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(189): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.211-4925C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177544072 | ||||||
| chr5:177544144
|
T | G | 2 | a0001c0001t0001g0091a0001c0001t0001g0104 | 2 | HG02132.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.211-4997A>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177544144 | ||||||
| chr5:177544633
|
T | TG | 43 | a0001c0001t0001g0079a0001c0001t0001g0088a0001c0001t0002g0001others(40): Show | 71 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.211-5487dupC | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177544633 | ||||||
| chr5:177544752
|
AC | A | 3 | a0001c0001t0012g0139a0001c0001t0012g0140a0001c0001t0016g0123 | 3 | HG01243.hp2 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.211-5606delG | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177544752 | ||||||
| chr5:177544951
|
G | A | 1 | a0001c0001t0001g0010 | 4 | HG02145.hp1 HG02559.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-5804C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177544951 | ||||||
| chr5:177545020
|
T | C | 1 | a0001c0001t0008g0051 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.211-5873A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545020 | ||||||
| chr5:177545042
|
A | C | 1 | a0001c0001t0001g0082 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.211-5895T>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545042 | ||||||
| chr5:177545074
|
C | T | 1 | a0010c0017t0003g0146 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.211-5927G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545074 | ||||||
| chr5:177545146
|
C | T | 41 | a0001c0001t0004g0003a0001c0001t0004g0189a0001c0001t0004g0190others(38): Show | 55 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.211-5999G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545146 | ||||||
| chr5:177545200
|
C | T | 7 | a0001c0001t0008g0022a0001c0001t0008g0050a0001c0001t0008g0051others(4): Show | 8 | HG01243.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-6053G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545200 | ||||||
| chr5:177545258
|
G | A | 192 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(189): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.211-6111C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545258 | ||||||
| chr5:177545400
|
A | G | 1 | a0001c0001t0004g0189 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.211-6253T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545400 | ||||||
| chr5:177545404
|
T | G | 1 | a0001c0001t0004g0189 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.211-6257A>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545404 | ||||||
| chr5:177545486
|
T | A | 1 | a0001c0001t0013g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.211-6339A>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545486 | ||||||
| chr5:177545583
|
C | T | 2 | a0005c0006t0002g0057a0005c0006t0002g0058 | 2 | HG01081.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.211-6436G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545583 | ||||||
| chr5:177545619
|
C | T | 192 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(189): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.211-6472G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545619 | ||||||
| chr5:177545658
|
C | CAA | 50 | a0001c0001t0004g0003a0001c0001t0004g0190a0001c0001t0004g0191others(47): Show | 64 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.211-6513_211-6512d others(4): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545658 | ||||||
| chr5:177545658
|
C | CAAA | 8 | a0001c0001t0004g0196a0001c0001t0009g0172a0001c0001t0009g0173others(5): Show | 8 | HG02145.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-6514_211-6512d others(5): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545658 | ||||||
| chr5:177545658
|
CA | C | 182 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(179): Show | 249 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.211-6512delT | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545658 | ||||||
| chr5:177545658
|
CAA | C | 10 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(7): Show | 10 | HG00741.hp2 HG02132.hp2 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-6513_211-6512d others(4): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545658 | ||||||
| chr5:177545898
|
C | T | 1 | a0001c0001t0002g0023 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.211-6751G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177545898 | ||||||
| chr5:177546010
|
C | CGTGTT | 6 | a0001c0001t0009g0163a0001c0001t0009g0164a0004c0004t0015g0228others(3): Show | 6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-6864_211-6863i others(7): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177546010 | ||||||
| chr5:177546150
|
G | A | 203 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(200): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.211-7003C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177546150 | ||||||
| chr5:177546196
|
A | G | 7 | a0001c0001t0008g0022a0001c0001t0008g0050a0001c0001t0008g0051others(4): Show | 8 | HG01243.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-7049T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177546196 | ||||||
| chr5:177546358
|
G | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0110 | 2 | HG01975.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.211-7211C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177546358 | ||||||
| chr5:177546422
|
G | A | 4 | a0001c0001t0015g0232a0001c0001t0023g0240a0001c0001t0028g0242others(1): Show | 4 | HG02258.hp2 HG02818.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-7275C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177546422 | ||||||
| chr5:177546791
|
G | C | 4 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0044g0218others(1): Show | 4 | HG02615.hp2 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.210+7458C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177546791 | ||||||
| chr5:177546910
|
G | A | 21 | a0001c0001t0001g0010a0001c0001t0001g0081a0001c0001t0004g0196others(18): Show | 24 | HG01243.hp2 HG01261.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.210+7339C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177546910 | ||||||
| chr5:177546948
|
G | A | 1 | a0001c0001t0047g0239 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.210+7301C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177546948 | ||||||
| chr5:177546959
|
C | T | 1 | a0001c0001t0004g0196 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.210+7290G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177546959 | ||||||
| chr5:177547006
|
C | T | 2 | a0001c0001t0012g0152a0001c0001t0012g0153 | 2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.210+7243G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547006 | ||||||
| chr5:177547018
|
T | C | 194 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(191): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.210+7231A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547018 | ||||||
| chr5:177547119
|
A | G | 3 | a0001c0001t0003g0141a0001c0001t0003g0142a0001c0001t0003g0143 | 3 | HG01109.hp2 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.210+7130T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547119 | ||||||
| chr5:177547277
|
A | AATTT | 6 | a0001c0001t0009g0163a0001c0001t0009g0164a0004c0004t0015g0228others(3): Show | 6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+6968_210+6971d others(6): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547277 | ||||||
| chr5:177547286
|
C | A | 6 | a0001c0001t0009g0163a0001c0001t0009g0164a0004c0004t0015g0228others(3): Show | 6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+6963G>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547286 | ||||||
| chr5:177547286
|
C | CTTTTTT | 8 | a0001c0001t0001g0030a0001c0001t0001g0107a0001c0001t0001g0108others(5): Show | 9 | HG01069.hp1 HG01099.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.210+6957_210+6962d others(8): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547286 | ||||||
| chr5:177547286
|
C | CTTTTTTT | 88 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(85): Show | 150 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.210+6956_210+6962d others(9): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547286 | ||||||
| chr5:177547286
|
C | CTTTTTTT others(1): Show |
14 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(11): Show | 14 | HG01081.hp2 HG01258.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.210+6955_210+6962d others(10): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547286 | ||||||
| chr5:177547286
|
C | CTTTTTTT others(2): Show |
90 | a0001c0001t0001g0111a0001c0001t0003g0019a0001c0001t0003g0033others(87): Show | 100 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.210+6954_210+6962d others(11): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547286 | ||||||
| chr5:177547286
|
C | CTTTTTTT others(3): Show |
51 | a0001c0001t0003g0141a0001c0001t0003g0142a0001c0001t0003g0144others(48): Show | 66 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.210+6953_210+6962d others(12): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547286 | ||||||
| chr5:177547286
|
C | CTTTTTTT others(4): Show |
13 | a0001c0001t0001g0010a0001c0001t0001g0081a0001c0001t0004g0190others(10): Show | 18 | HG01175.hp2 HG01261.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.210+6952_210+6962d others(13): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547286 | ||||||
| chr5:177547286
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0004g0189 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.210+6951_210+6962d others(14): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547286 | ||||||
| chr5:177547290
|
T | A | 6 | a0001c0001t0009g0163a0001c0001t0009g0164a0004c0004t0015g0228others(3): Show | 6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+6959A>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547290 | ||||||
| chr5:177547378
|
G | A | 6 | a0001c0001t0009g0163a0001c0001t0009g0164a0004c0004t0015g0228others(3): Show | 6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+6871C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547378 | ||||||
| chr5:177547496
|
G | C | 63 | a0001c0001t0004g0003a0001c0001t0004g0189a0001c0001t0004g0190others(60): Show | 77 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.210+6753C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547496 | ||||||
| chr5:177547526
|
C | T | 2 | a0001c0005t0006g0176a0001c0005t0022g0161 | 2 | HG04204.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.210+6723G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547526 | ||||||
| chr5:177547527
|
T | G | 275 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(272): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.210+6722A>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547527 | ||||||
| chr5:177547530
|
C | T | 4 | a0001c0001t0026g0208a0001c0001t0026g0209a0001c0001t0050g0251others(1): Show | 4 | NA18942.hp1 NA18984.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+6719G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547530 | ||||||
| chr5:177547579
|
C | T | 109 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(106): Show | 173 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.210+6670G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547579 | ||||||
| chr5:177547680
|
C | T | 6 | a0001c0001t0009g0163a0001c0001t0009g0164a0004c0004t0015g0228others(3): Show | 6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+6569G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547680 | ||||||
| chr5:177547966
|
G | GCA | 63 | a0001c0001t0004g0003a0001c0001t0004g0189a0001c0001t0004g0190others(60): Show | 77 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.210+6281_210+6282d others(4): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177547966 | ||||||
| chr5:177548022
|
C | G | 1 | a0001c0001t0026g0208 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.210+6227G>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177548022 | ||||||
| chr5:177548139
|
C | G | 83 | a0001c0001t0003g0019a0001c0001t0003g0033a0001c0001t0003g0141others(80): Show | 92 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.210+6110G>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177548139 | ||||||
| chr5:177548243
|
T | C | 1 | a0001c0001t0005g0216 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.210+6006A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177548243 | ||||||
| chr5:177548358
|
G | GT | 6 | a0001c0001t0009g0163a0001c0001t0009g0164a0004c0004t0015g0228others(3): Show | 6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+5890dupA | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177548358 | ||||||
| chr5:177548692
|
A | G | 191 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(188): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.210+5557T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177548692 | ||||||
| chr5:177548918
|
G | C | 1 | a0001c0001t0009g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.210+5331C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177548918 | ||||||
| chr5:177548967
|
CCTTT | C | 4 | a0002c0002t0030g0274a0002c0002t0031g0041a0002c0002t0031g0275others(1): Show | 5 | HG02055.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+5278_210+5281d others(6): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177548967 | ||||||
| chr5:177548990
|
C | G | 3 | a0001c0001t0003g0141a0001c0001t0003g0142a0001c0001t0003g0143 | 3 | HG01109.hp2 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.210+5259G>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177548990 | ||||||
| chr5:177549134
|
A | C | 1 | a0005c0006t0002g0057 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.210+5115T>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549134 | ||||||
| chr5:177549187
|
CT | C | 11 | a0001c0001t0008g0022a0001c0001t0008g0051a0001c0001t0008g0052others(8): Show | 12 | HG00140.hp2 HG01243.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.210+5061delA | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549187 | ||||||
| chr5:177549187
|
CTT | C | 180 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(177): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.210+5060_210+5061d others(4): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549187 | ||||||
| chr5:177549187
|
CTTT | C | 11 | a0001c0001t0001g0031a0001c0001t0001g0110a0001c0001t0001g0118others(8): Show | 12 | HG01074.hp1 HG01168.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.210+5059_210+5061d others(5): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549187 | ||||||
| chr5:177549187
|
CTTTTT | C | 6 | a0001c0001t0006g0187a0001c0001t0009g0163a0001c0001t0009g0164others(3): Show | 6 | HG00735.hp1 HG01934.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.210+5057_210+5061d others(7): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549187 | ||||||
| chr5:177549192
|
T | C | 3 | a0001c0014t0046g0227a0003c0003t0021g0018a0003c0003t0021g0137 | 5 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.210+5057A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549192 | ||||||
| chr5:177549193
|
T | C | 1 | a0001c0001t0001g0119 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.210+5056A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549193 | ||||||
| chr5:177549194
|
T | C | 1 | a0001c0001t0002g0009 | 4 | NA18957.hp1 NA18990.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+5055A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549194 | ||||||
| chr5:177549195
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.210+5054A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549195 | ||||||
| chr5:177549338
|
G | A | 1 | a0001c0001t0059g0268 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.210+4911C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549338 | ||||||
| chr5:177549342
|
G | A | 1 | a0001c0001t0015g0233 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.210+4907C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549342 | ||||||
| chr5:177549596
|
A | G | 1 | a0001c0001t0005g0207 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.210+4653T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549596 | ||||||
| chr5:177549636
|
C | T | 1 | a0001c0001t0001g0028 | 2 | HG02071.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.210+4613G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549636 | ||||||
| chr5:177549867
|
TTATTA | T | 193 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(190): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.210+4377_210+4381d others(7): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177549867 | ||||||
| chr5:177550051
|
G | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(190): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.210+4198C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550051 | ||||||
| chr5:177550096
|
C | G | 1 | a0001c0001t0015g0235 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.210+4153G>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550096 | ||||||
| chr5:177550132
|
T | C | 1 | a0001c0014t0046g0227 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.210+4117A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550132 | ||||||
| chr5:177550154
|
T | TAA | 7 | a0001c0001t0008g0022a0001c0001t0008g0050a0001c0001t0008g0051others(4): Show | 8 | HG01243.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.210+4093_210+4094d others(4): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550154 | ||||||
| chr5:177550202
|
G | A | 1 | a0001c0001t0002g0027 | 2 | HG02040.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.210+4047C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550202 | ||||||
| chr5:177550296
|
C | T | 1 | a0001c0001t0007g0223 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.210+3953G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550296 | ||||||
| chr5:177550447
|
C | A | 1 | a0001c0001t0001g0121 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.210+3802G>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550447 | ||||||
| chr5:177550496
|
C | T | 1 | a0001c0001t0008g0050 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.210+3753G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550496 | ||||||
| chr5:177550564
|
A | G | 1 | a0001c0001t0007g0222 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.210+3685T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550564 | ||||||
| chr5:177550610
|
C | A | 49 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0015others(46): Show | 72 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.210+3639G>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550610 | ||||||
| chr5:177550850
|
G | A | 4 | a0001c0001t0010g0021a0001c0001t0010g0048a0001c0001t0010g0049others(1): Show | 5 | HG01106.hp2 HG01928.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+3399C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550850 | ||||||
| chr5:177550862
|
C | T | 2 | a0003c0003t0021g0018a0003c0003t0021g0137 | 4 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+3387G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550862 | ||||||
| chr5:177550865
|
T | C | 6 | a0001c0001t0009g0163a0001c0001t0009g0164a0004c0004t0015g0228others(3): Show | 6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+3384A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550865 | ||||||
| chr5:177550979
|
AC | A | 4 | a0002c0002t0030g0274a0002c0002t0031g0041a0002c0002t0031g0275others(1): Show | 5 | HG02055.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+3269delG | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550979 | ||||||
| chr5:177550982
|
C | T | 4 | a0002c0002t0030g0274a0002c0002t0031g0041a0002c0002t0031g0275others(1): Show | 5 | HG02055.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+3267G>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177550982 | ||||||
| chr5:177551001
|
A | AT | 83 | a0001c0001t0002g0056a0001c0001t0003g0019a0001c0001t0003g0033others(80): Show | 92 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.210+3247dupA | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551001 | ||||||
| chr5:177551028
|
TCTCA | T | 6 | a0001c0001t0009g0163a0001c0001t0009g0164a0004c0004t0015g0228others(3): Show | 6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+3217_210+3220d others(6): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551028 | ||||||
| chr5:177551048
|
T | A | 1 | a0001c0001t0029g0256 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.210+3201A>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551048 | ||||||
| chr5:177551108
|
T | A | 1 | a0001c0001t0029g0256 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.210+3141A>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551108 | ||||||
| chr5:177551109
|
A | C | 1 | a0001c0001t0029g0256 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.210+3140T>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551109 | ||||||
| chr5:177551151
|
G | GTCAGAGA others(7): Show |
1 | a0001c0001t0029g0256 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.210+3097_210+3098i others(16): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551151 | ||||||
| chr5:177551152
|
G | T | 1 | a0001c0001t0029g0256 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.210+3097C>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551152 | ||||||
| chr5:177551172
|
G | A | 2 | a0001c0001t0010g0048a0001c0001t0010g0049 | 2 | HG01993.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.210+3077C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551172 | ||||||
| chr5:177551257
|
C | CAGTT | 6 | a0001c0001t0009g0163a0001c0001t0009g0164a0004c0004t0015g0228others(3): Show | 6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+2988_210+2991d others(6): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551257 | ||||||
| chr5:177551269
|
AT | A | 264 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(261): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.210+2979delA | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551269 | ||||||
| chr5:177551269
|
ATT | A | 7 | a0001c0001t0008g0022a0001c0001t0008g0050a0001c0001t0008g0051others(4): Show | 8 | HG01243.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.210+2978_210+2979d others(4): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551269 | ||||||
| chr5:177551277
|
T | G | 5 | a0001c0001t0009g0163a0001c0001t0009g0164a0001c0001t0012g0139others(2): Show | 5 | HG01243.hp2 HG01934.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+2972A>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551277 | ||||||
| chr5:177551284
|
T | C | 1 | a0001c0001t0028g0244 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.210+2965A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551284 | ||||||
| chr5:177551405
|
A | T | 1 | a0001c0014t0046g0227 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.210+2844T>A | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551405 | ||||||
| chr5:177551966
|
G | A | 41 | a0001c0001t0004g0003a0001c0001t0004g0189a0001c0001t0004g0190others(38): Show | 55 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.210+2283C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551966 | ||||||
| chr5:177551993
|
G | A | 4 | a0002c0002t0030g0274a0002c0002t0031g0041a0002c0002t0031g0275others(1): Show | 5 | HG02055.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+2256C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177551993 | ||||||
| chr5:177552222
|
T | C | 8 | a0001c0001t0004g0196a0001c0001t0009g0172a0001c0001t0009g0173others(5): Show | 8 | HG01261.hp2 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.210+2027A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177552222 | ||||||
| chr5:177552331
|
T | C | 6 | a0001c0001t0009g0163a0001c0001t0009g0164a0004c0004t0015g0228others(3): Show | 6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+1918A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177552331 | ||||||
| chr5:177552382
|
C | G | 4 | a0002c0002t0030g0274a0002c0002t0031g0041a0002c0002t0031g0275others(1): Show | 5 | HG02055.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+1867G>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177552382 | ||||||
| chr5:177552427
|
A | G | 1 | a0001c0005t0022g0161 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.210+1822T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177552427 | ||||||
| chr5:177553003
|
T | C | 7 | a0001c0001t0008g0022a0001c0001t0008g0050a0001c0001t0008g0051others(4): Show | 8 | HG01243.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.210+1246A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177553003 | ||||||
| chr5:177553025
|
T | C | 4 | a0002c0002t0030g0274a0002c0002t0031g0041a0002c0002t0031g0275others(1): Show | 5 | HG02055.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+1224A>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177553025 | ||||||
| chr5:177553307
|
G | C | 2 | a0003c0003t0021g0018a0003c0003t0021g0137 | 4 | HG02630.hp1 HG02717.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+942C>G | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177553307 | ||||||
| chr5:177553473
|
T | G | 1 | a0001c0014t0046g0227 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.210+776A>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177553473 | ||||||
| chr5:177553650
|
A | G | 6 | a0001c0001t0009g0163a0001c0001t0009g0164a0004c0004t0015g0228others(3): Show | 6 | HG01934.hp2 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+599T>C | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177553650 | ||||||
| chr5:177553808
|
G | A | 1 | a0001c0001t0013g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.210+441C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177553808 | ||||||
| chr5:177553903
|
G | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0016others(15): Show | 30 | HG00140.hp1 HG00735.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.210+346C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177553903 | ||||||
| chr5:177553955
|
G | GCCCAGT | 4 | a0001c0001t0012g0139a0001c0001t0012g0140a0001c0001t0016g0123others(1): Show | 4 | HG01243.hp2 HG02698.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.210+288_210+293dup others(6): Show |
FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177553955 | ||||||
| chr5:177554178
|
G | A | 1 | a0001c0001t0041g0122 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.210+71C>T | FAM193B | ENSG00000146067.17 | transcript | ENST00000514747.6 | protein_coding | 1/8 | chr5 | 177554178 |