Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5034 |
| ensemblid | ENSG00000185624.16 |
| hgncid | 8548 |
| symbol | P4HB |
| name | prolyl 4-hydroxylase subunit beta |
| refseq_nuc | NM_000918.4 |
| refseq_prot | NP_000909.2 |
| ensembl_nuc | ENST00000331483.9 |
| ensembl_prot | ENSP00000327801.4 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 81843166 |
| end | 81860535 |
| strand | - |
| ver | v1.2 |
| region | chr17:81843166-81860535 |
| region5000 | chr17:81838166-81865535 |
| regionname0 | P4HB_chr17_81843166_81860535 |
| regionname5000 | P4HB_chr17_81838166_81865535 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 508 | 373 | 91 | 82 | 150 | 12 | 36 | 114 | P4HB_chr17_81838166_81865535 | P4HB | MLRRA others(503): Show |
chr17 | 81838166 | 81865535 |
| a0002 | 0/0 | 508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | MLRRA others(503): Show |
chr17 | 81838166 | 81865535 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1524 | 243 | 53 | 51 | 95 | 9 | 33 | P4HB_chr17_81838166_81865535 | P4HB | ATGCT others(1519): Show |
chr17 | 81838166 | 81865535 | ||
| a0001c0002 | 0/0 | 1524 | 72 | 28 | 8 | 34 | 0 | 2 | P4HB_chr17_81838166_81865535 | P4HB | ATGCT others(1519): Show |
chr17 | 81838166 | 81865535 | ||
| a0001c0003 | 0/0 | 1524 | 51 | 4 | 23 | 20 | 3 | 1 | P4HB_chr17_81838166_81865535 | P4HB | ATGCT others(1519): Show |
chr17 | 81838166 | 81865535 | ||
| a0001c0004 | 0/0 | 1524 | 3 | 3 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | ATGCT others(1519): Show |
chr17 | 81838166 | 81865535 | ||
| a0001c0005 | 0/0 | 1524 | 2 | 2 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | ATGCT others(1519): Show |
chr17 | 81838166 | 81865535 | ||
| a0001c0006 | 0/0 | 1524 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | ATGCT others(1519): Show |
chr17 | 81838166 | 81865535 | ||
| a0001c0007 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | ATGCT others(1519): Show |
chr17 | 81838166 | 81865535 | ||
| a0002c0008 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | ATGCT others(1519): Show |
chr17 | 81838166 | 81865535 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2437 | 219 | 46 | 43 | 90 | 9 | 29 | P4HB_chr17_81838166_81865535 | P4HB | GCTCT others(2432): Show |
chr17 | 81838166 | 81865535 |
| a0001c0001t0004 | 0/0 | 2437 | 7 | 6 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | GCTCT others(2432): Show |
chr17 | 81838166 | 81865535 |
| a0001c0001t0005 | 0/0 | 2437 | 7 | 0 | 4 | 0 | 0 | 3 | P4HB_chr17_81838166_81865535 | P4HB | GCTCT others(2432): Show |
chr17 | 81838166 | 81865535 |
| a0001c0001t0006 | 0/0 | 2438 | 3 | 0 | 2 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | GCTCT others(2433): Show |
chr17 | 81838166 | 81865535 |
| a0001c0001t0007 | 0/0 | 2437 | 2 | 1 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | GCTCT others(2432): Show |
chr17 | 81838166 | 81865535 |
| a0001c0001t0008 | 0/0 | 2437 | 2 | 0 | 0 | 2 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | GCTCT others(2432): Show |
chr17 | 81838166 | 81865535 |
| a0001c0001t0010 | 0/0 | 2437 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | GCTCT others(2432): Show |
chr17 | 81838166 | 81865535 |
| a0001c0001t0011 | 0/0 | 2437 | 1 | 0 | 0 | 0 | 0 | 1 | P4HB_chr17_81838166_81865535 | P4HB | GCTCT others(2432): Show |
chr17 | 81838166 | 81865535 |
| a0001c0001t0012 | 0/0 | 2437 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | GCTCT others(2432): Show |
chr17 | 81838166 | 81865535 |
| a0001c0002t0001 | 0/0 | 2437 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | GCTCT others(2432): Show |
chr17 | 81838166 | 81865535 |
| a0001c0002t0002 | 0/0 | 2437 | 50 | 8 | 7 | 33 | 0 | 2 | P4HB_chr17_81838166_81865535 | P4HB | GCTCT others(2432): Show |
chr17 | 81838166 | 81865535 |
| a0001c0002t0004 | 0/0 | 2437 | 18 | 18 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | GCTCT others(2432): Show |
chr17 | 81838166 | 81865535 |
| a0001c0002t0013 | 0/0 | 2438 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | GCTCT others(2433): Show |
chr17 | 81838166 | 81865535 |
| a0001c0002t0014 | 0/0 | 2438 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | GCTCT others(2433): Show |
chr17 | 81838166 | 81865535 |
| a0001c0002t0015 | 0/0 | 2437 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | GCTCT others(2432): Show |
chr17 | 81838166 | 81865535 |
| a0001c0003t0003 | 0/0 | 2437 | 48 | 4 | 23 | 17 | 3 | 1 | P4HB_chr17_81838166_81865535 | P4HB | GCTCT others(2432): Show |
chr17 | 81838166 | 81865535 |
| a0001c0003t0009 | 0/0 | 2438 | 2 | 0 | 0 | 2 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | GCTCT others(2433): Show |
chr17 | 81838166 | 81865535 |
| a0001c0003t0016 | 0/0 | 2437 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | GCTCT others(2432): Show |
chr17 | 81838166 | 81865535 |
| a0001c0004t0004 | 0/0 | 2437 | 3 | 3 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | GCTCT others(2432): Show |
chr17 | 81838166 | 81865535 |
| a0001c0005t0004 | 0/0 | 2437 | 2 | 2 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | GCTCT others(2432): Show |
chr17 | 81838166 | 81865535 |
| a0001c0006t0004 | 0/0 | 2437 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | GCTCT others(2432): Show |
chr17 | 81838166 | 81865535 |
| a0001c0007t0004 | 0/0 | 2437 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | GCTCT others(2432): Show |
chr17 | 81838166 | 81865535 |
| a0002c0008t0001 | 0/0 | 2437 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | GCTCT others(2432): Show |
chr17 | 81838166 | 81865535 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 30 | 2 | 7 | 11 | 4 | 5 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0004 | 0/0 | 9 | 0 | 0 | 8 | 1 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0005 | 0/0 | 8 | 0 | 3 | 1 | 0 | 4 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0006 | 0/0 | 8 | 2 | 3 | 0 | 1 | 2 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0008 | 0/0 | 7 | 3 | 3 | 0 | 0 | 1 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0010 | 0/0 | 6 | 3 | 1 | 2 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0012 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0039 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0042 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0004g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0005g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0005g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0005g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0005g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0006g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0006g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0006g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0007g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0007g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0008g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0008g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0010g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0011g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0001t0012g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0002g0003 | 0/0 | 13 | 0 | 3 | 8 | 0 | 2 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0002g0011 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0002g0013 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0002g0014 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0004g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0004g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0013g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0014g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0002t0015g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0003t0003g0002 | 0/0 | 16 | 2 | 9 | 5 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0003t0003g0009 | 0/0 | 7 | 1 | 2 | 2 | 2 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0003t0003g0026 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0003t0003g0027 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0003t0003g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0003t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0003t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0003t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0003t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0003t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0003t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0003t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0003t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0003t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0003t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0003t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0003t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0003t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0003t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0003t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0003t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0003t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0003t0009g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0003t0009g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0003t0016g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0004t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0004t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0004t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0005t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0005t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0006t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0001c0007t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| a0002c0008t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0119 | EUR | FIN | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00423 | hp1 | a0001 | c0002 | t0014 | g0174 | EAS | CHS | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00423 | hp2 | a0001 | c0001 | t0010 | g0090 | EAS | CHS | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0031 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00642 | hp2 | a0001 | c0001 | t0005 | g0038 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00741 | hp1 | a0001 | c0003 | t0003 | g0002 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG00741 | hp2 | a0001 | c0003 | t0003 | g0002 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01069 | hp1 | a0001 | c0003 | t0003 | g0155 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01069 | hp2 | a0001 | c0003 | t0003 | g0002 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01070 | hp2 | a0001 | c0003 | t0003 | g0002 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01071 | hp1 | a0001 | c0003 | t0003 | g0154 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01071 | hp2 | a0001 | c0003 | t0003 | g0002 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01106 | hp2 | a0001 | c0003 | t0003 | g0002 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01109 | hp2 | a0001 | c0001 | t0006 | g0093 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0081 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0031 | AMR | PUR | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01255 | hp1 | a0001 | c0001 | t0007 | g0108 | AMR | CLM | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01256 | hp2 | a0001 | c0003 | t0003 | g0152 | AMR | CLM | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01257 | hp1 | a0001 | c0003 | t0003 | g0002 | AMR | CLM | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01258 | hp2 | a0001 | c0003 | t0003 | g0151 | AMR | CLM | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01261 | hp2 | a0001 | c0002 | t0015 | g0189 | AMR | CLM | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01346 | hp1 | a0001 | c0003 | t0003 | g0153 | AMR | CLM | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01346 | hp2 | a0001 | c0003 | t0003 | g0009 | AMR | CLM | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01361 | hp1 | a0001 | c0003 | t0003 | g0158 | AMR | CLM | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01361 | hp2 | a0001 | c0001 | t0006 | g0088 | AMR | CLM | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01433 | hp1 | a0001 | c0003 | t0003 | g0141 | AMR | CLM | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01496 | hp1 | a0001 | c0003 | t0003 | g0002 | AMR | CLM | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01516 | hp2 | a0001 | c0003 | t0003 | g0009 | EUR | IBS | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01517 | hp1 | a0001 | c0003 | t0003 | g0009 | EUR | IBS | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0014 | AFR | ACB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0045 | AFR | ACB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01891 | hp2 | a0001 | c0002 | t0013 | g0198 | AFR | ACB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01934 | hp1 | a0001 | c0003 | t0003 | g0009 | AMR | PEL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01934 | hp2 | a0001 | c0003 | t0003 | g0149 | AMR | PEL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01943 | hp1 | a0001 | c0003 | t0003 | g0150 | AMR | PEL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0167 | AMR | PEL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0013 | AMR | PEL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0166 | AMR | PEL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01975 | hp1 | a0001 | c0003 | t0003 | g0026 | AMR | PEL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01978 | hp2 | a0001 | c0003 | t0003 | g0027 | AMR | PEL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01981 | hp1 | a0001 | c0003 | t0003 | g0002 | AMR | PEL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02027 | hp1 | a0001 | c0001 | t0008 | g0131 | EAS | KHV | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0175 | EAS | KHV | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02055 | hp1 | a0001 | c0005 | t0004 | g0194 | AFR | ACB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02071 | hp1 | a0001 | c0001 | t0008 | g0123 | EAS | KHV | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | KHV | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02132 | hp2 | a0001 | c0003 | t0003 | g0160 | EAS | KHV | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0013 | AMR | PEL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CDX | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02165 | hp2 | a0001 | c0006 | t0004 | g0142 | EAS | CDX | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02257 | hp1 | a0001 | c0003 | t0003 | g0002 | AFR | ACB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0102 | AFR | ACB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | ACB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02300 | hp2 | a0001 | c0003 | t0003 | g0148 | AMR | PEL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02451 | hp2 | a0001 | c0003 | t0003 | g0002 | AFR | ACB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0178 | EAS | KHV | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0076 | SAS | PJL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02615 | hp2 | a0001 | c0004 | t0004 | g0164 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0190 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0191 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0038 | SAS | PJL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02717 | hp2 | a0001 | c0002 | t0004 | g0048 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0180 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02735 | hp2 | a0001 | c0001 | t0011 | g0063 | SAS | PJL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02895 | hp1 | a0001 | c0002 | t0004 | g0203 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02895 | hp2 | a0001 | c0002 | t0004 | g0028 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02897 | hp1 | a0001 | c0002 | t0004 | g0196 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02922 | hp1 | a0002 | c0008 | t0001 | g0138 | AFR | ESN | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0176 | AFR | ESN | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02976 | hp2 | a0001 | c0002 | t0004 | g0195 | AFR | ESN | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03041 | hp1 | a0001 | c0002 | t0004 | g0202 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | MSL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | ESN | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0184 | AFR | ESN | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03209 | hp1 | a0001 | c0002 | t0004 | g0199 | AFR | MSL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03453 | hp1 | a0001 | c0002 | t0004 | g0188 | AFR | MSL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03486 | hp1 | a0001 | c0005 | t0004 | g0200 | AFR | MSL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03486 | hp2 | a0001 | c0002 | t0004 | g0163 | AFR | MSL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03516 | hp1 | a0001 | c0002 | t0004 | g0186 | AFR | ESN | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0192 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03540 | hp2 | a0001 | c0004 | t0004 | g0165 | AFR | GWD | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03579 | hp1 | a0001 | c0002 | t0004 | g0028 | AFR | MSL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03669 | hp1 | a0001 | c0001 | t0005 | g0072 | SAS | PJL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | BEB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | STU | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | STU | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG04199 | hp1 | a0001 | c0003 | t0003 | g0026 | SAS | STU | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | STU | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | STU | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | STU | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0045 | AFR | YRI | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | YRI | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18747 | hp1 | a0001 | c0003 | t0003 | g0044 | EAS | CHB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18906 | hp1 | a0001 | c0002 | t0004 | g0204 | AFR | YRI | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | YRI | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18943 | hp1 | a0001 | c0003 | t0003 | g0027 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18951 | hp1 | a0001 | c0003 | t0003 | g0026 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18954 | hp2 | a0001 | c0003 | t0003 | g0002 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18959 | hp1 | a0001 | c0003 | t0003 | g0044 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18959 | hp2 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18964 | hp1 | a0001 | c0003 | t0003 | g0002 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18968 | hp2 | a0001 | c0003 | t0003 | g0009 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0179 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18977 | hp1 | a0001 | c0003 | t0009 | g0156 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18978 | hp2 | a0001 | c0003 | t0003 | g0159 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18979 | hp2 | a0001 | c0001 | t0012 | g0096 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18980 | hp1 | a0001 | c0003 | t0003 | g0002 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18985 | hp2 | a0001 | c0003 | t0009 | g0157 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0172 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18990 | hp2 | a0001 | c0003 | t0003 | g0002 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18992 | hp1 | a0001 | c0003 | t0003 | g0143 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18992 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18998 | hp1 | a0001 | c0003 | t0016 | g0205 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19000 | hp1 | a0001 | c0003 | t0003 | g0027 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19001 | hp2 | a0001 | c0003 | t0003 | g0146 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19030 | hp1 | a0001 | c0002 | t0004 | g0201 | AFR | LWK | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0117 | AFR | LWK | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | LWK | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19043 | hp2 | a0001 | c0007 | t0004 | g0193 | AFR | LWK | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19055 | hp2 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19062 | hp2 | a0001 | c0003 | t0003 | g0144 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19063 | hp2 | a0001 | c0003 | t0003 | g0002 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19066 | hp2 | a0001 | c0003 | t0003 | g0009 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19083 | hp1 | a0001 | c0001 | t0006 | g0098 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0177 | AFR | ASW | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA20129 | hp2 | a0001 | c0003 | t0003 | g0145 | AFR | ASW | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA20752 | hp1 | a0001 | c0003 | t0003 | g0147 | EUR | TSI | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | GIH | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | GIH | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02109 | hp1 | a0001 | c0002 | t0004 | g0197 | AFR | ACB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02486 | hp2 | a0001 | c0003 | t0003 | g0009 | AFR | ACB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02559 | hp1 | a0001 | c0002 | t0004 | g0187 | AFR | ACB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG02559 | hp2 | a0001 | c0002 | t0004 | g0162 | AFR | ACB | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| HG03471 | hp2 | a0001 | c0004 | t0004 | g0161 | AFR | MSL | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA20300 | hp1 | a0001 | c0002 | t0004 | g0048 | AFR | USA | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | LWK | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| NA21309 | hp2 | a0001 | c0002 | t0004 | g0028 | AFR | LWK | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0042 | REF | REF | P4HB_chr17_81838166_81865535 | P4HB | chr17 | 81838166 | 81865535 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:81859252 | T | C | 1 | a0002 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.281A>G | p.Tyr94Cys | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/11 | 345/2437 | 281/1527 | 94/508 | chr17 | 81859252 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:81844021 | A | G | 1 | a0001c0007 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.1518T>C | p.Asp506Asp | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 11/11 | 1582/2437 | 1518/1527 | 506/508 | chr17 | 81844021 | |||
| chr17:81845216 | G | A | 1 | a0001c0005 | 2 | HG02055.hp1 HG03486.hp1 |
synonymous_variant | LOW | c.1374C>T | p.Asn458Asn | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 10/11 | 1438/2437 | 1374/1527 | 458/508 | chr17 | 81845216 | |||
| chr17:81845225 | A | G | 4 | a0001c0002 a0001c0003 a0001c0005 others(1): Show |
126 | HG00423.hp1 HG00639.hp1 HG00741.hp1 others(123): Show |
synonymous_variant | LOW | c.1365T>C | p.Ile455Ile | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 10/11 | 1429/2437 | 1365/1527 | 455/508 | chr17 | 81845225 | |||
| chr17:81847258 | G | A | 1 | a0001c0003 | 51 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(48): Show |
synonymous_variant | LOW | c.714C>T | p.Ile238Ile | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 5/11 | 778/2437 | 714/1527 | 238/508 | chr17 | 81847258 | |||
| chr17:81859230 | G | A | 1 | a0001c0004 | 3 | HG02615.hp2 HG03471.hp2 HG03540.hp2 |
synonymous_variant | LOW | c.303C>T | p.Thr101Thr | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/11 | 367/2437 | 303/1527 | 101/508 | chr17 | 81859230 | |||
| chr17:81860384 | G | T | 2 | a0001c0003 a0001c0006 |
52 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(49): Show |
synonymous_variant | LOW | c.88C>A | p.Arg30Arg | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 1/11 | 152/2437 | 88/1527 | 30/508 | chr17 | 81860384 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:81843346 | A | G | 1 | a0001c0001t0007 | 2 | HG01255.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*666T>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 11/11 | 666 | chr17 | 81843346 | ||||||
| chr17:81843357 | G | A | 1 | a0001c0001t0008 | 2 | HG02027.hp1 HG02071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*655C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 11/11 | 655 | chr17 | 81843357 | ||||||
| chr17:81843412 | C | A | 5 | a0001c0002t0002 a0001c0002t0014 a0001c0003t0003 others(2): Show |
102 | HG00423.hp1 HG00639.hp1 HG00741.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*600G>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 11/11 | 600 | chr17 | 81843412 | ||||||
| chr17:81843524 | C | T | 1 | a0001c0001t0010 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*488G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 11/11 | 488 | chr17 | 81843524 | ||||||
| chr17:81843531 | C | CG | 4 | a0001c0001t0006 a0001c0002t0013 a0001c0002t0014 others(1): Show |
7 | HG00423.hp1 HG01109.hp2 HG01361.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*480dupC | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 11/11 | 480 | chr17 | 81843531 | ||||||
| chr17:81843717 | G | A | 1 | a0001c0001t0011 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*295C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 11/11 | 295 | chr17 | 81843717 | ||||||
| chr17:81843795 | T | G | 2 | a0001c0002t0002 a0001c0002t0014 |
51 | HG00423.hp1 HG00639.hp1 HG01884.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*217A>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 11/11 | 217 | chr17 | 81843795 | ||||||
| chr17:81843859 | G | A | 1 | a0001c0001t0012 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*153C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 11/11 | 153 | chr17 | 81843859 | ||||||
| chr17:81843929 | G | C | 1 | a0001c0002t0015 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*83C>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 11/11 | 83 | chr17 | 81843929 | ||||||
| chr17:81843951 | G | A | 1 | a0001c0001t0005 | 7 | HG00642.hp1 HG00642.hp2 HG01167.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*61C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 11/11 | 61 | chr17 | 81843951 | ||||||
| chr17:81860484 | T | G | 13 | a0001c0001t0004 a0001c0002t0002 a0001c0002t0004 others(10): Show |
136 | HG00423.hp1 HG00639.hp1 HG00741.hp1 others(133): Show |
5_prime_UTR_variant | MODIFIER | c.-13A>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 1/11 | 13 | chr17 | 81860484 | ||||||
| chr17:81860504 | G | A | 1 | a0001c0003t0016 | 1 | NA18998.hp1 | 5_prime_UTR_variant | MODIFIER | c.-33C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 1/11 | 33 | chr17 | 81860504 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:81844101 | C | T | 24 | a0001c0002t0002g0003 a0001c0002t0002g0011 a0001c0002t0002g0013 others(21): Show |
51 | HG00423.hp1 HG00639.hp1 HG01884.hp2 others(48): Show |
intron_variant | MODIFIER | c.1447-9G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 10/10 | chr17 | 81844101 | |||||||
| chr17:81844178 | C | T | 2 | a0001c0001t0008g0123 a0001c0001t0008g0131 |
2 | HG02027.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.1447-86G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 10/10 | chr17 | 81844178 | |||||||
| chr17:81844179 | G | A | 15 | a0001c0001t0001g0112 a0001c0002t0004g0028 a0001c0002t0004g0048 others(12): Show |
18 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1447-87C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 10/10 | chr17 | 81844179 | |||||||
| chr17:81844249 | C | CACCTGGA others(26): Show |
1 | a0001c0003t0009g0157 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1447-158_1447-157i others(35): Show |
P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 10/10 | chr17 | 81844249 | |||||||
| chr17:81844251 | CAG | C | 51 | a0001c0002t0002g0003 a0001c0002t0002g0011 a0001c0002t0002g0013 others(48): Show |
104 | HG00423.hp1 HG00639.hp1 HG00741.hp1 others(101): Show |
intron_variant | MODIFIER | c.1447-161_1447-160d others(4): Show |
P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 10/10 | chr17 | 81844251 | |||||||
| chr17:81844253 | G | C | 1 | a0001c0003t0009g0157 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1447-161C>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 10/10 | chr17 | 81844253 | |||||||
| chr17:81844255 | G | A | 3 | a0001c0001t0001g0106 a0001c0001t0001g0109 a0001c0001t0001g0110 |
3 | HG02258.hp1 HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1447-163C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 10/10 | chr17 | 81844255 | |||||||
| chr17:81844386 | G | A | 2 | a0001c0003t0003g0143 a0001c0003t0003g0146 |
2 | NA18992.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1447-294C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 10/10 | chr17 | 81844386 | |||||||
| chr17:81844395 | C | T | 3 | a0001c0002t0004g0186 a0001c0002t0004g0187 a0001c0002t0015g0189 |
3 | HG01261.hp2 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1447-303G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 10/10 | chr17 | 81844395 | |||||||
| chr17:81844418 | C | T | 4 | a0001c0002t0004g0186 a0001c0002t0004g0187 a0001c0002t0004g0188 others(1): Show |
4 | HG01261.hp2 HG02559.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1447-326G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 10/10 | chr17 | 81844418 | |||||||
| chr17:81844550 | C | T | 8 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0030 others(5): Show |
13 | HG01074.hp1 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1447-458G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 10/10 | chr17 | 81844550 | |||||||
| chr17:81844579 | A | G | 62 | a0001c0002t0002g0003 a0001c0002t0002g0011 a0001c0002t0002g0013 others(59): Show |
114 | HG00423.hp1 HG00639.hp1 HG00741.hp1 others(111): Show |
intron_variant | MODIFIER | c.1447-487T>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 10/10 | chr17 | 81844579 | |||||||
| chr17:81844673 | G | A | 3 | a0001c0002t0004g0162 a0001c0002t0004g0163 a0001c0002t0004g0204 |
3 | HG02559.hp2 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1446+471C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 10/10 | chr17 | 81844673 | |||||||
| chr17:81844707 | G | C | 24 | a0001c0002t0002g0003 a0001c0002t0002g0011 a0001c0002t0002g0013 others(21): Show |
51 | HG00423.hp1 HG00639.hp1 HG01884.hp2 others(48): Show |
intron_variant | MODIFIER | c.1446+437C>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 10/10 | chr17 | 81844707 | |||||||
| chr17:81844749 | C | T | 1 | a0001c0002t0004g0204 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1446+395G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 10/10 | chr17 | 81844749 | |||||||
| chr17:81844924 | G | A | 1 | a0001c0001t0001g0040 | 2 | HG01070.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.1446+220C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 10/10 | chr17 | 81844924 | |||||||
| chr17:81845050 | C | G | 1 | a0001c0001t0001g0073 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1446+94G>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 10/10 | chr17 | 81845050 | |||||||
| chr17:81845068 | G | C | 1 | a0001c0001t0004g0045 | 2 | HG01891.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1446+76C>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 10/10 | chr17 | 81845068 | |||||||
| chr17:81845074 | A | C | 11 | a0001c0002t0004g0028 a0001c0002t0004g0048 a0001c0002t0004g0195 others(8): Show |
14 | HG01891.hp2 HG02055.hp1 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.1446+70T>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 10/10 | chr17 | 81845074 | |||||||
| chr17:81845486 | G | A | 1 | a0001c0001t0004g0180 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1359+75C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 9/10 | chr17 | 81845486 | |||||||
| chr17:81845525 | G | C | 2 | a0001c0002t0002g0172 a0001c0002t0002g0185 |
2 | NA18990.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1359+36C>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 9/10 | chr17 | 81845525 | |||||||
| chr17:81845551 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1359+10C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 9/10 | chr17 | 81845551 | |||||||
| chr17:81845557 | G | A | 25 | a0001c0003t0003g0002 a0001c0003t0003g0009 a0001c0003t0003g0026 others(22): Show |
51 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(48): Show |
splice_region_variant&intron_variant | LOW | c.1359+4C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 9/10 | chr17 | 81845557 | |||||||
| chr17:81845805 | G | C | 1 | a0001c0001t0001g0135 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1178-63C>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 8/10 | chr17 | 81845805 | |||||||
| chr17:81845810 | C | G | 1 | a0001c0001t0012g0096 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1177+61G>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 8/10 | chr17 | 81845810 | |||||||
| chr17:81846074 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1057-83C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 7/10 | chr17 | 81846074 | |||||||
| chr17:81846113 | G | A | 13 | a0001c0002t0004g0028 a0001c0002t0004g0048 a0001c0002t0004g0195 others(10): Show |
16 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1057-122C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 7/10 | chr17 | 81846113 | |||||||
| chr17:81846213 | T | G | 1 | a0001c0002t0004g0195 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1056+216A>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 7/10 | chr17 | 81846213 | |||||||
| chr17:81846659 | C | T | 1 | a0001c0001t0001g0021 | 3 | HG02809.hp2 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.856-30G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 6/10 | chr17 | 81846659 | |||||||
| chr17:81846724 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.856-95A>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 6/10 | chr17 | 81846724 | |||||||
| chr17:81846839 | C | T | 1 | a0001c0002t0015g0189 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.855+108G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 6/10 | chr17 | 81846839 | |||||||
| chr17:81846840 | G | A | 1 | a0001c0002t0004g0186 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.855+107C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 6/10 | chr17 | 81846840 | |||||||
| chr17:81846845 | A | G | 73 | a0001c0001t0004g0045 a0001c0002t0002g0003 a0001c0002t0002g0011 others(70): Show |
130 | HG00423.hp1 HG00639.hp1 HG00741.hp1 others(127): Show |
intron_variant | MODIFIER | c.855+102T>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 6/10 | chr17 | 81846845 | |||||||
| chr17:81846922 | C | T | 2 | a0001c0001t0005g0072 a0001c0001t0005g0076 |
2 | HG02602.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.855+25G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 6/10 | chr17 | 81846922 | |||||||
| chr17:81847127 | A | G | 65 | a0001c0002t0002g0003 a0001c0002t0002g0011 a0001c0002t0002g0013 others(62): Show |
121 | HG00423.hp1 HG00639.hp1 HG00741.hp1 others(118): Show |
intron_variant | MODIFIER | c.730-55T>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 5/10 | chr17 | 81847127 | |||||||
| chr17:81847137 | T | C | 16 | a0001c0002t0004g0028 a0001c0002t0004g0048 a0001c0002t0004g0162 others(13): Show |
19 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.730-65A>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 5/10 | chr17 | 81847137 | |||||||
| chr17:81847161 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.729+82G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 5/10 | chr17 | 81847161 | |||||||
| chr17:81847490 | T | A | 1 | a0001c0002t0002g0175 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.625-143A>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81847490 | |||||||
| chr17:81847493 | A | G | 24 | a0001c0002t0002g0003 a0001c0002t0002g0011 a0001c0002t0002g0013 others(21): Show |
51 | HG00423.hp1 HG00639.hp1 HG01884.hp2 others(48): Show |
intron_variant | MODIFIER | c.625-146T>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81847493 | |||||||
| chr17:81847536 | G | A | 1 | a0001c0001t0007g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.625-189C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81847536 | |||||||
| chr17:81847640 | C | A | 2 | a0001c0002t0004g0162 a0001c0002t0004g0163 |
2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.625-293G>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81847640 | |||||||
| chr17:81847646 | C | A | 1 | a0001c0002t0004g0163 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.625-299G>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81847646 | |||||||
| chr17:81847855 | T | C | 1 | a0001c0002t0004g0204 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.625-508A>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81847855 | |||||||
| chr17:81847871 | G | C | 2 | a0001c0002t0004g0162 a0001c0002t0004g0163 |
2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.625-524C>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81847871 | |||||||
| chr17:81847905 | C | CT | 15 | a0001c0001t0001g0037 a0001c0001t0001g0053 a0001c0001t0001g0075 others(12): Show |
16 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.625-559dupA | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81847905 | |||||||
| chr17:81847990 | C | T | 3 | a0001c0002t0004g0162 a0001c0002t0004g0163 a0001c0002t0004g0204 |
3 | HG02559.hp2 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.625-643G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81847990 | |||||||
| chr17:81848027 | C | T | 13 | a0001c0002t0004g0028 a0001c0002t0004g0048 a0001c0002t0004g0195 others(10): Show |
16 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.625-680G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81848027 | |||||||
| chr17:81848192 | G | A | 4 | a0001c0002t0004g0188 a0001c0004t0004g0161 a0001c0004t0004g0164 others(1): Show |
4 | HG02615.hp2 HG03453.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.625-845C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81848192 | |||||||
| chr17:81848261 | G | A | 3 | a0001c0002t0004g0162 a0001c0002t0004g0163 a0001c0002t0004g0204 |
3 | HG02559.hp2 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.625-914C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81848261 | |||||||
| chr17:81848272 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.625-925G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81848272 | |||||||
| chr17:81848650 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0121 |
6 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.625-1303G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81848650 | |||||||
| chr17:81848677 | G | A | 1 | a0001c0007t0004g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.625-1330C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81848677 | |||||||
| chr17:81848709 | C | G | 2 | a0001c0002t0002g0172 a0001c0002t0002g0185 |
2 | NA18990.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.625-1362G>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81848709 | |||||||
| chr17:81848714 | C | G | 26 | a0001c0001t0004g0166 a0001c0003t0003g0002 a0001c0003t0003g0009 others(23): Show |
52 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.625-1367G>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81848714 | |||||||
| chr17:81848724 | G | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0129 |
2 | NA19074.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.625-1377C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81848724 | |||||||
| chr17:81848736 | C | CA | 50 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(47): Show |
77 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.625-1390dupT | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81848736 | |||||||
| chr17:81848736 | C | CAA | 13 | a0001c0001t0001g0054 a0001c0001t0001g0060 a0001c0001t0001g0083 others(10): Show |
14 | HG00597.hp2 HG01175.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.625-1391_625-1390d others(4): Show |
P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81848736 | |||||||
| chr17:81848736 | CA | C | 27 | a0001c0001t0001g0052 a0001c0001t0001g0071 a0001c0001t0001g0134 others(24): Show |
49 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.625-1390delT | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81848736 | |||||||
| chr17:81848736 | CAA | C | 18 | a0001c0002t0002g0003 a0001c0002t0002g0011 a0001c0002t0002g0014 others(15): Show |
41 | HG00423.hp1 HG00639.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.625-1391_625-1390d others(4): Show |
P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81848736 | |||||||
| chr17:81848919 | A | G | 8 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0030 others(5): Show |
13 | HG01074.hp1 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.625-1572T>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81848919 | |||||||
| chr17:81848939 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0077 |
3 | HG03239.hp2 HG03654.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.625-1592C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81848939 | |||||||
| chr17:81849466 | A | C | 1 | a0001c0002t0002g0191 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.625-2119T>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81849466 | |||||||
| chr17:81849510 | AAAAT | A | 3 | a0001c0002t0004g0162 a0001c0002t0004g0163 a0001c0002t0004g0204 |
3 | HG02559.hp2 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.625-2167_625-2164d others(6): Show |
P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81849510 | |||||||
| chr17:81849593 | G | A | 13 | a0001c0002t0004g0028 a0001c0002t0004g0048 a0001c0002t0004g0195 others(10): Show |
16 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.625-2246C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81849593 | |||||||
| chr17:81849826 | A | AT | 4 | a0001c0002t0002g0014 a0001c0002t0002g0190 a0001c0002t0002g0191 others(1): Show |
8 | HG01884.hp2 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.625-2480dupA | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81849826 | |||||||
| chr17:81849830 | A | AT | 20 | a0001c0002t0002g0003 a0001c0002t0002g0011 a0001c0002t0002g0013 others(17): Show |
43 | HG00423.hp1 HG00639.hp1 HG01943.hp2 others(40): Show |
intron_variant | MODIFIER | c.625-2484dupA | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81849830 | |||||||
| chr17:81849830 | A | T | 49 | a0001c0001t0004g0166 a0001c0002t0002g0014 a0001c0002t0002g0190 others(46): Show |
82 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(79): Show |
intron_variant | MODIFIER | c.625-2483T>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81849830 | |||||||
| chr17:81849864 | G | T | 1 | a0001c0002t0002g0190 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.625-2517C>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81849864 | |||||||
| chr17:81849875 | T | A | 24 | a0001c0002t0002g0003 a0001c0002t0002g0011 a0001c0002t0002g0013 others(21): Show |
51 | HG00423.hp1 HG00639.hp1 HG01884.hp2 others(48): Show |
intron_variant | MODIFIER | c.625-2528A>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81849875 | |||||||
| chr17:81849896 | C | T | 1 | a0001c0002t0002g0171 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.625-2549G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81849896 | |||||||
| chr17:81849921 | G | A | 3 | a0001c0002t0004g0162 a0001c0002t0004g0163 a0001c0002t0004g0204 |
3 | HG02559.hp2 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.625-2574C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81849921 | |||||||
| chr17:81849933 | T | C | 3 | a0001c0002t0004g0162 a0001c0002t0004g0163 a0001c0002t0004g0204 |
3 | HG02559.hp2 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.625-2586A>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81849933 | |||||||
| chr17:81849947 | C | A | 1 | a0001c0002t0002g0173 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.625-2600G>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81849947 | |||||||
| chr17:81849956 | T | G | 1 | a0001c0001t0001g0092 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.625-2609A>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81849956 | |||||||
| chr17:81849985 | G | A | 1 | a0001c0001t0004g0184 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.625-2638C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81849985 | |||||||
| chr17:81850154 | C | T | 17 | a0001c0002t0004g0028 a0001c0002t0004g0048 a0001c0002t0004g0162 others(14): Show |
20 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.625-2807G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81850154 | |||||||
| chr17:81850264 | C | G | 1 | a0001c0002t0002g0192 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.625-2917G>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81850264 | |||||||
| chr17:81850280 | G | A | 24 | a0001c0002t0002g0003 a0001c0002t0002g0011 a0001c0002t0002g0013 others(21): Show |
51 | HG00423.hp1 HG00639.hp1 HG01884.hp2 others(48): Show |
intron_variant | MODIFIER | c.625-2933C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81850280 | |||||||
| chr17:81850281 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.625-2934G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81850281 | |||||||
| chr17:81850415 | T | C | 66 | a0001c0001t0004g0166 a0001c0002t0002g0003 a0001c0002t0002g0011 others(63): Show |
122 | HG00423.hp1 HG00639.hp1 HG00741.hp1 others(119): Show |
intron_variant | MODIFIER | c.625-3068A>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81850415 | |||||||
| chr17:81850511 | CTT | C | 18 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0002t0004g0028 others(15): Show |
21 | HG00733.hp1 HG01261.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.625-3166_625-3165d others(4): Show |
P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81850511 | |||||||
| chr17:81850541 | G | A | 2 | a0001c0002t0004g0162 a0001c0002t0004g0163 |
2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.625-3194C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81850541 | |||||||
| chr17:81850575 | T | C | 16 | a0001c0002t0004g0028 a0001c0002t0004g0048 a0001c0002t0004g0162 others(13): Show |
19 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.625-3228A>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81850575 | |||||||
| chr17:81850646 | G | C | 2 | a0001c0003t0003g0147 a0001c0003t0003g0158 |
2 | HG01361.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.625-3299C>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81850646 | |||||||
| chr17:81850767 | G | A | 16 | a0001c0002t0004g0028 a0001c0002t0004g0048 a0001c0002t0004g0162 others(13): Show |
19 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.625-3420C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81850767 | |||||||
| chr17:81850801 | T | A | 2 | a0001c0002t0004g0162 a0001c0002t0004g0163 |
2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.625-3454A>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81850801 | |||||||
| chr17:81850933 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.625-3586C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81850933 | |||||||
| chr17:81850952 | G | C | 1 | a0001c0007t0004g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.625-3605C>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81850952 | |||||||
| chr17:81850970 | C | T | 4 | a0001c0002t0004g0186 a0001c0002t0004g0187 a0001c0002t0004g0188 others(1): Show |
4 | HG01261.hp2 HG02559.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-3623G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81850970 | |||||||
| chr17:81851079 | C | T | 4 | a0001c0002t0004g0186 a0001c0002t0004g0187 a0001c0002t0004g0188 others(1): Show |
4 | HG01261.hp2 HG02559.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.625-3732G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81851079 | |||||||
| chr17:81851120 | C | T | 4 | a0001c0001t0004g0045 a0001c0004t0004g0161 a0001c0004t0004g0164 others(1): Show |
5 | HG01891.hp1 HG02615.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.625-3773G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81851120 | |||||||
| chr17:81851172 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.625-3825G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81851172 | |||||||
| chr17:81851225 | C | T | 26 | a0001c0001t0004g0166 a0001c0003t0003g0002 a0001c0003t0003g0009 others(23): Show |
52 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.625-3878G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81851225 | |||||||
| chr17:81851226 | G | A | 1 | a0001c0002t0004g0188 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.625-3879C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81851226 | |||||||
| chr17:81851270 | G | A | 26 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(23): Show |
52 | HG00323.hp2 HG00408.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.624+3872C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81851270 | |||||||
| chr17:81851319 | A | G | 16 | a0001c0002t0004g0028 a0001c0002t0004g0048 a0001c0002t0004g0162 others(13): Show |
19 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.624+3823T>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81851319 | |||||||
| chr17:81851439 | C | T | 1 | a0001c0003t0003g0145 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.624+3703G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81851439 | |||||||
| chr17:81851918 | C | G | 3 | a0001c0002t0004g0186 a0001c0002t0004g0187 a0001c0002t0015g0189 |
3 | HG01261.hp2 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.624+3224G>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81851918 | |||||||
| chr17:81851934 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.624+3208T>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81851934 | |||||||
| chr17:81852038 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.624+3104G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81852038 | |||||||
| chr17:81852152 | C | T | 1 | a0002c0008t0001g0138 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.624+2990G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81852152 | |||||||
| chr17:81852196 | G | C | 2 | a0001c0001t0004g0176 a0001c0001t0004g0177 |
2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.624+2946C>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81852196 | |||||||
| chr17:81852210 | A | G | 69 | a0001c0001t0001g0058 a0001c0001t0001g0105 a0001c0001t0001g0106 others(66): Show |
125 | HG00423.hp1 HG00639.hp1 HG00741.hp1 others(122): Show |
intron_variant | MODIFIER | c.624+2932T>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81852210 | |||||||
| chr17:81852279 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.624+2863G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81852279 | |||||||
| chr17:81852430 | T | G | 1 | a0001c0003t0003g0148 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.624+2712A>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81852430 | |||||||
| chr17:81852440 | G | C | 3 | a0001c0002t0004g0186 a0001c0002t0004g0187 a0001c0002t0015g0189 |
3 | HG01261.hp2 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.624+2702C>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81852440 | |||||||
| chr17:81852452 | C | G | 3 | a0001c0004t0004g0161 a0001c0004t0004g0164 a0001c0004t0004g0165 |
3 | HG02615.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.624+2690G>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81852452 | |||||||
| chr17:81852520 | C | T | 1 | a0001c0001t0007g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.624+2622G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81852520 | |||||||
| chr17:81852587 | A | G | 66 | a0001c0001t0004g0166 a0001c0002t0002g0003 a0001c0002t0002g0011 others(63): Show |
122 | HG00423.hp1 HG00639.hp1 HG00741.hp1 others(119): Show |
intron_variant | MODIFIER | c.624+2555T>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81852587 | |||||||
| chr17:81852766 | A | G | 66 | a0001c0001t0004g0166 a0001c0002t0002g0003 a0001c0002t0002g0011 others(63): Show |
122 | HG00423.hp1 HG00639.hp1 HG00741.hp1 others(119): Show |
intron_variant | MODIFIER | c.624+2376T>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81852766 | |||||||
| chr17:81852781 | A | G | 1 | a0001c0002t0004g0187 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.624+2361T>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81852781 | |||||||
| chr17:81852987 | C | A | 5 | a0001c0002t0002g0011 a0001c0002t0002g0169 a0001c0002t0002g0170 others(2): Show |
10 | HG00423.hp1 HG00639.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.624+2155G>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81852987 | |||||||
| chr17:81853061 | C | T | 1 | a0001c0002t0002g0170 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.624+2081G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81853061 | |||||||
| chr17:81853177 | A | G | 1 | a0001c0002t0004g0186 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.624+1965T>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81853177 | |||||||
| chr17:81853211 | C | T | 3 | a0001c0002t0004g0162 a0001c0002t0004g0163 a0001c0002t0004g0204 |
3 | HG02559.hp2 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.624+1931G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81853211 | |||||||
| chr17:81853256 | G | A | 4 | a0001c0001t0004g0045 a0001c0004t0004g0161 a0001c0004t0004g0164 others(1): Show |
5 | HG01891.hp1 HG02615.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.624+1886C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81853256 | |||||||
| chr17:81853269 | G | A | 1 | a0001c0001t0006g0093 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.624+1873C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81853269 | |||||||
| chr17:81853467 | G | A | 3 | a0001c0002t0004g0162 a0001c0002t0004g0163 a0001c0002t0004g0204 |
3 | HG02559.hp2 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.624+1675C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81853467 | |||||||
| chr17:81853470 | A | G | 39 | a0001c0001t0004g0166 a0001c0002t0004g0028 a0001c0002t0004g0048 others(36): Show |
68 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.624+1672T>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81853470 | |||||||
| chr17:81853490 | CGTGAACC others(2): Show |
C | 4 | a0001c0002t0004g0028 a0001c0002t0004g0199 a0001c0002t0004g0201 others(1): Show |
6 | HG02895.hp2 HG03041.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+1643_624+1651d others(11): Show |
P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81853490 | |||||||
| chr17:81853491 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.624+1651C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81853491 | |||||||
| chr17:81853657 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.624+1485C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81853657 | |||||||
| chr17:81853714 | C | T | 1 | a0001c0003t0003g0145 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.624+1428G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81853714 | |||||||
| chr17:81853771 | T | C | 1 | a0001c0003t0009g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.624+1371A>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81853771 | |||||||
| chr17:81853888 | C | T | 2 | a0001c0001t0001g0112 a0001c0002t0004g0188 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.624+1254G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81853888 | |||||||
| chr17:81854159 | G | A | 1 | a0001c0002t0002g0192 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.624+983C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81854159 | |||||||
| chr17:81854323 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.624+819C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81854323 | |||||||
| chr17:81854419 | G | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0134 |
2 | NA18952.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.624+723C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81854419 | |||||||
| chr17:81854459 | T | C | 1 | a0001c0002t0004g0187 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.624+683A>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81854459 | |||||||
| chr17:81854543 | C | CA | 8 | a0001c0001t0001g0033 a0001c0001t0001g0049 a0001c0001t0004g0045 others(5): Show |
12 | HG00735.hp1 HG01358.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.624+598dupT | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81854543 | |||||||
| chr17:81854575 | G | A | 1 | a0001c0001t0001g0041 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.624+567C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81854575 | |||||||
| chr17:81854752 | G | C | 1 | a0001c0001t0001g0086 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.624+390C>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81854752 | |||||||
| chr17:81854833 | C | CTCTG | 16 | a0001c0002t0004g0028 a0001c0002t0004g0048 a0001c0002t0004g0162 others(13): Show |
19 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.624+308_624+309ins others(4): Show |
P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81854833 | |||||||
| chr17:81854885 | G | GA | 18 | a0001c0001t0001g0034 a0001c0001t0001g0078 a0001c0001t0001g0079 others(15): Show |
22 | HG01358.hp1 HG01433.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.624+256dupT | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81854885 | |||||||
| chr17:81854885 | GA | G | 7 | a0001c0002t0002g0046 a0001c0002t0002g0167 a0001c0002t0002g0169 others(4): Show |
8 | HG01943.hp2 HG02559.hp2 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.624+256delT | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81854885 | |||||||
| chr17:81854900 | G | C | 1 | a0001c0001t0001g0065 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.624+242C>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81854900 | |||||||
| chr17:81854952 | A | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(201): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.624+190T>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81854952 | |||||||
| chr17:81854999 | C | A | 3 | a0001c0002t0002g0014 a0001c0002t0002g0190 a0001c0002t0002g0191 |
7 | HG01884.hp2 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.624+143G>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81854999 | |||||||
| chr17:81855024 | A | G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG00733.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.624+118T>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81855024 | |||||||
| chr17:81855036 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.624+106G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81855036 | |||||||
| chr17:81855048 | G | A | 16 | a0001c0002t0004g0028 a0001c0002t0004g0048 a0001c0002t0004g0162 others(13): Show |
19 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.624+94C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 4/10 | chr17 | 81855048 | |||||||
| chr17:81855419 | G | C | 2 | a0001c0001t0004g0176 a0001c0001t0004g0177 |
2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.486+34C>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 3/10 | chr17 | 81855419 | |||||||
| chr17:81855428 | A | G | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0140 |
3 | HG02698.hp2 HG04184.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.486+25T>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 3/10 | chr17 | 81855428 | |||||||
| chr17:81855646 | G | A | 3 | a0001c0002t0004g0162 a0001c0002t0004g0163 a0001c0002t0004g0204 |
3 | HG02559.hp2 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.353-60C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81855646 | |||||||
| chr17:81855704 | T | A | 1 | a0001c0002t0002g0178 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.353-118A>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81855704 | |||||||
| chr17:81855898 | C | A | 2 | a0001c0003t0003g0149 a0001c0003t0003g0150 |
2 | HG01934.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.353-312G>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81855898 | |||||||
| chr17:81855978 | C | T | 1 | a0001c0001t0006g0098 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.353-392G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81855978 | |||||||
| chr17:81856070 | C | T | 3 | a0001c0002t0004g0162 a0001c0002t0004g0163 a0001c0002t0004g0204 |
3 | HG02559.hp2 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.353-484G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81856070 | |||||||
| chr17:81856071 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.353-485C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81856071 | |||||||
| chr17:81856334 | C | CT | 7 | a0001c0001t0001g0055 a0001c0001t0001g0058 a0001c0001t0001g0101 others(4): Show |
7 | HG03139.hp2 HG03516.hp1 HG04199.hp2 others(4): Show |
intron_variant | MODIFIER | c.353-749dupA | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81856334 | |||||||
| chr17:81856334 | CT | C | 58 | a0001c0001t0001g0030 a0001c0001t0001g0059 a0001c0001t0001g0060 others(55): Show |
90 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(87): Show |
intron_variant | MODIFIER | c.353-749delA | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81856334 | |||||||
| chr17:81856430 | C | T | 2 | a0001c0001t0001g0036 a0001c0002t0004g0188 |
3 | HG02965.hp1 HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.353-844G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81856430 | |||||||
| chr17:81856463 | G | A | 2 | a0001c0003t0003g0151 a0001c0003t0003g0152 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.353-877C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81856463 | |||||||
| chr17:81856487 | G | C | 3 | a0001c0002t0002g0014 a0001c0002t0002g0190 a0001c0002t0002g0191 |
7 | HG01884.hp2 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.353-901C>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81856487 | |||||||
| chr17:81856589 | C | T | 1 | a0001c0001t0011g0063 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.353-1003G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81856589 | |||||||
| chr17:81856601 | G | C | 1 | a0001c0002t0002g0192 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.353-1015C>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81856601 | |||||||
| chr17:81856647 | C | CT | 6 | a0001c0001t0001g0056 a0001c0001t0001g0062 a0001c0001t0001g0116 others(3): Show |
6 | HG02074.hp1 HG02523.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.353-1062dupA | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81856647 | |||||||
| chr17:81856647 | CT | C | 23 | a0001c0001t0001g0082 a0001c0002t0002g0182 a0001c0002t0002g0183 others(20): Show |
26 | HG01069.hp1 HG01256.hp2 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.353-1062delA | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81856647 | |||||||
| chr17:81856650 | T | C | 2 | a0001c0002t0004g0188 a0001c0003t0003g0153 |
2 | HG01346.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.353-1064A>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81856650 | |||||||
| chr17:81856670 | CG | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0083 a0001c0001t0001g0085 |
5 | HG00597.hp1 NA18952.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.353-1085delC | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81856670 | |||||||
| chr17:81856717 | C | T | 51 | a0001c0001t0004g0166 a0001c0002t0002g0014 a0001c0002t0002g0190 others(48): Show |
84 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(81): Show |
intron_variant | MODIFIER | c.353-1131G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81856717 | |||||||
| chr17:81856860 | G | C | 27 | a0001c0001t0004g0166 a0001c0003t0003g0002 a0001c0003t0003g0009 others(24): Show |
53 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.353-1274C>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81856860 | |||||||
| chr17:81856891 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.353-1305C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81856891 | |||||||
| chr17:81856911 | G | A | 3 | a0001c0004t0004g0161 a0001c0004t0004g0164 a0001c0004t0004g0165 |
3 | HG02615.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.353-1325C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81856911 | |||||||
| chr17:81857112 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.353-1526C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81857112 | |||||||
| chr17:81857241 | A | G | 16 | a0001c0002t0004g0028 a0001c0002t0004g0048 a0001c0002t0004g0162 others(13): Show |
19 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.353-1655T>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81857241 | |||||||
| chr17:81857305 | G | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0055 others(6): Show |
17 | HG00609.hp2 HG02074.hp2 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.353-1719C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81857305 | |||||||
| chr17:81857458 | C | A | 2 | a0001c0003t0003g0154 a0001c0003t0003g0155 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.352+1723G>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81857458 | |||||||
| chr17:81857579 | C | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0104 |
2 | HG04228.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.352+1602G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81857579 | |||||||
| chr17:81857617 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.352+1564G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81857617 | |||||||
| chr17:81857640 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.352+1541G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81857640 | |||||||
| chr17:81857662 | G | A | 13 | a0001c0002t0004g0028 a0001c0002t0004g0048 a0001c0002t0004g0195 others(10): Show |
16 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.352+1519C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81857662 | |||||||
| chr17:81857704 | A | G | 3 | a0001c0002t0004g0186 a0001c0002t0004g0187 a0001c0002t0015g0189 |
3 | HG01261.hp2 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.352+1477T>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81857704 | |||||||
| chr17:81857820 | C | T | 1 | a0001c0007t0004g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.352+1361G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81857820 | |||||||
| chr17:81857874 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.352+1307G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81857874 | |||||||
| chr17:81857986 | A | G | 1 | a0002c0008t0001g0138 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.352+1195T>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81857986 | |||||||
| chr17:81858024 | C | T | 27 | a0001c0001t0004g0166 a0001c0003t0003g0002 a0001c0003t0003g0009 others(24): Show |
53 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.352+1157G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81858024 | |||||||
| chr17:81858047 | G | T | 3 | a0001c0002t0004g0162 a0001c0002t0004g0163 a0001c0002t0004g0204 |
3 | HG02559.hp2 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.352+1134C>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81858047 | |||||||
| chr17:81858065 | C | T | 27 | a0001c0001t0004g0166 a0001c0003t0003g0002 a0001c0003t0003g0009 others(24): Show |
53 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.352+1116G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81858065 | |||||||
| chr17:81858093 | GAA | G | 3 | a0001c0002t0004g0186 a0001c0002t0004g0187 a0001c0002t0015g0189 |
3 | HG01261.hp2 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.352+1086_352+1087d others(4): Show |
P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81858093 | |||||||
| chr17:81858226 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.352+955G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81858226 | |||||||
| chr17:81858238 | C | CTTCAGCC others(3): Show |
50 | a0001c0001t0004g0166 a0001c0002t0002g0014 a0001c0002t0002g0190 others(47): Show |
83 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.352+942_352+943ins others(10): Show |
P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81858238 | |||||||
| chr17:81858247 | G | C | 1 | a0001c0005t0004g0200 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.352+934C>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81858247 | |||||||
| chr17:81858257 | C | CA | 35 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0017 others(32): Show |
53 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.352+923dupT | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81858257 | |||||||
| chr17:81858257 | C | CAA | 11 | a0001c0001t0001g0016 a0001c0001t0001g0099 a0001c0001t0001g0100 others(8): Show |
14 | HG01261.hp2 HG02027.hp1 HG03704.hp2 others(11): Show |
intron_variant | MODIFIER | c.352+922_352+923dup others(2): Show |
P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81858257 | |||||||
| chr17:81858257 | CA | C | 33 | a0001c0001t0001g0024 a0001c0001t0001g0056 a0001c0001t0001g0057 others(30): Show |
59 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.352+923delT | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81858257 | |||||||
| chr17:81858257 | CAA | C | 14 | a0001c0002t0002g0014 a0001c0002t0002g0190 a0001c0002t0002g0191 others(11): Show |
21 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.352+922_352+923del others(2): Show |
P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81858257 | |||||||
| chr17:81858257 | CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0004g0204 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.352+914_352+923del others(10): Show |
P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81858257 | |||||||
| chr17:81858417 | A | G | 1 | a0001c0001t0001g0055 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.352+764T>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81858417 | |||||||
| chr17:81858497 | T | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0135 others(2): Show |
9 | HG01884.hp1 HG02109.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.352+684A>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81858497 | |||||||
| chr17:81858590 | C | T | 8 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0030 others(5): Show |
13 | HG01074.hp1 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.352+591G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81858590 | |||||||
| chr17:81858803 | G | A | 25 | a0001c0003t0003g0002 a0001c0003t0003g0009 a0001c0003t0003g0026 others(22): Show |
51 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.352+378C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81858803 | |||||||
| chr17:81859050 | C | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(67): Show |
133 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.352+131G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81859050 | |||||||
| chr17:81859129 | G | A | 29 | a0001c0002t0002g0014 a0001c0002t0002g0190 a0001c0002t0002g0191 others(26): Show |
59 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.352+52C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81859129 | |||||||
| chr17:81859134 | G | A | 1 | a0001c0003t0003g0160 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.352+47C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 2/10 | chr17 | 81859134 | |||||||
| chr17:81859440 | TG | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0050 |
6 | HG00621.hp1 NA18942.hp1 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.146-54delC | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 1/10 | chr17 | 81859440 | |||||||
| chr17:81859448 | C | T | 13 | a0001c0002t0004g0028 a0001c0002t0004g0048 a0001c0002t0004g0195 others(10): Show |
16 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.146-61G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 1/10 | chr17 | 81859448 | |||||||
| chr17:81859459 | C | T | 1 | a0001c0004t0004g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.146-72G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 1/10 | chr17 | 81859459 | |||||||
| chr17:81859590 | A | G | 1 | a0001c0003t0003g0141 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.146-203T>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 1/10 | chr17 | 81859590 | |||||||
| chr17:81859612 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.146-225G>A | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 1/10 | chr17 | 81859612 | |||||||
| chr17:81859774 | A | G | 54 | a0001c0001t0004g0045 a0001c0002t0002g0014 a0001c0002t0002g0190 others(51): Show |
88 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(85): Show |
intron_variant | MODIFIER | c.146-387T>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 1/10 | chr17 | 81859774 | |||||||
| chr17:81859974 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.145+353C>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 1/10 | chr17 | 81859974 | |||||||
| chr17:81860176 | T | G | 48 | a0001c0002t0002g0014 a0001c0002t0002g0190 a0001c0002t0002g0191 others(45): Show |
81 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(78): Show |
intron_variant | MODIFIER | c.145+151A>C | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 1/10 | chr17 | 81860176 | |||||||
| chr17:81860197 | C | A | 1 | a0001c0001t0001g0140 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.145+130G>T | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 1/10 | chr17 | 81860197 | |||||||
| chr17:81860283 | T | C | 40 | a0001c0002t0004g0028 a0001c0002t0004g0048 a0001c0002t0004g0195 others(37): Show |
69 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.145+44A>G | P4HB | ENSG00000185624.16 | transcript | ENST00000331483.9 | protein_coding | 1/10 | chr17 | 81860283 |