Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 22949 |
| ensemblid | ENSG00000106853.20 |
| hgncid | 18429 |
| symbol | PTGR1 |
| name | prostaglandin reductase 1 |
| refseq_nuc | NM_001146108.2 |
| refseq_prot | NP_001139580.1 |
| ensembl_nuc | ENST00000407693.7 |
| ensembl_prot | ENSP00000385763.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 111562567 |
| end | 111599647 |
| strand | - |
| ver | v1.2 |
| region | chr9:111562567-111599647 |
| region5000 | chr9:111557567-111604647 |
| regionname0 | PTGR1_chr9_111562567_111599647 |
| regionname5000 | PTGR1_chr9_111557567_111604647 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 329 | 237 | 52 | 38 | 108 | 7 | 31 | 84 | PTGR1_chr9_111557567_111604647 | PTGR1 | MVRTK others(324): Show |
chr9 | 111557567 | 111604647 |
| a0002 | 1/0 | 329 | 166 | 40 | 36 | 71 | 7 | 11 | 59 | PTGR1_chr9_111557567_111604647 | PTGR1 | MVRTK others(324): Show |
chr9 | 111557567 | 111604647 |
| a0003 | 0/0 | 329 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | MVRTK others(324): Show |
chr9 | 111557567 | 111604647 |
| a0004 | 0/0 | 329 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | MVRTK others(324): Show |
chr9 | 111557567 | 111604647 |
| a0005 | 0/0 | 329 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | MVRTK others(324): Show |
chr9 | 111557567 | 111604647 |
| a0006 | 0/0 | 329 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | MVCTK others(324): Show |
chr9 | 111557567 | 111604647 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 987 | 237 | 52 | 38 | 108 | 7 | 31 | PTGR1_chr9_111557567_111604647 | PTGR1 | ATGGT others(982): Show |
chr9 | 111557567 | 111604647 | ||
| a0002c0002 | 1/0 | 987 | 165 | 40 | 35 | 71 | 7 | 11 | PTGR1_chr9_111557567_111604647 | PTGR1 | ATGGT others(982): Show |
chr9 | 111557567 | 111604647 | ||
| a0002c0004 | 0/0 | 987 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | ATGGT others(982): Show |
chr9 | 111557567 | 111604647 | ||
| a0003c0003 | 0/0 | 987 | 2 | 0 | 0 | 0 | 0 | 2 | PTGR1_chr9_111557567_111604647 | PTGR1 | ATGGT others(982): Show |
chr9 | 111557567 | 111604647 | ||
| a0004c0006 | 0/0 | 987 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | ATGGT others(982): Show |
chr9 | 111557567 | 111604647 | ||
| a0005c0005 | 0/0 | 987 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | ATGGT others(982): Show |
chr9 | 111557567 | 111604647 | ||
| a0006c0007 | 0/0 | 987 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | ATGGT others(982): Show |
chr9 | 111557567 | 111604647 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1599 | 131 | 29 | 20 | 69 | 2 | 11 | PTGR1_chr9_111557567_111604647 | PTGR1 | GCAGT others(1594): Show |
chr9 | 111557567 | 111604647 |
| a0001c0001t0002 | 0/1 | 1599 | 94 | 23 | 18 | 28 | 5 | 19 | PTGR1_chr9_111557567_111604647 | PTGR1 | GCAGT others(1594): Show |
chr9 | 111557567 | 111604647 |
| a0001c0001t0003 | 0/0 | 1599 | 12 | 0 | 0 | 11 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | GCAGT others(1594): Show |
chr9 | 111557567 | 111604647 |
| a0002c0002t0001 | 1/0 | 1599 | 107 | 7 | 26 | 57 | 6 | 10 | PTGR1_chr9_111557567_111604647 | PTGR1 | GCAGT others(1594): Show |
chr9 | 111557567 | 111604647 |
| a0002c0002t0002 | 0/0 | 1599 | 46 | 33 | 9 | 2 | 1 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | GCAGT others(1594): Show |
chr9 | 111557567 | 111604647 |
| a0002c0002t0003 | 0/0 | 1599 | 7 | 0 | 0 | 7 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | GCAGT others(1594): Show |
chr9 | 111557567 | 111604647 |
| a0002c0002t0004 | 0/0 | 1599 | 5 | 0 | 0 | 5 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | GCAGT others(1594): Show |
chr9 | 111557567 | 111604647 |
| a0002c0004t0001 | 0/0 | 1599 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | GCAGT others(1594): Show |
chr9 | 111557567 | 111604647 |
| a0003c0003t0002 | 0/0 | 1599 | 2 | 0 | 0 | 0 | 0 | 2 | PTGR1_chr9_111557567_111604647 | PTGR1 | GCAGT others(1594): Show |
chr9 | 111557567 | 111604647 |
| a0004c0006t0001 | 0/0 | 1599 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | GCAGT others(1594): Show |
chr9 | 111557567 | 111604647 |
| a0005c0005t0001 | 0/0 | 1599 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | GCAGT others(1594): Show |
chr9 | 111557567 | 111604647 |
| a0006c0007t0001 | 0/0 | 1599 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | GCAGT others(1594): Show |
chr9 | 111557567 | 111604647 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0005 | 0/1 | 3 | 0 | 2 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0001 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0216 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0002t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0002c0004t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0003c0003t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0004c0006t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0005c0005t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| a0006c0007t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0103 | EUR | GBR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0189 | EUR | GBR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0276 | EUR | GBR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0019 | EUR | GBR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0129 | EUR | FIN | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0253 | EUR | FIN | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | CHS | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | CHS | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | CHS | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | CHS | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0278 | EAS | CHS | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | CHS | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | CHS | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | CHS | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | CHS | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0282 | EAS | CHS | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0210 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0127 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0341 | EAS | CHS | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | CHS | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0192 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0148 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0171 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0142 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0218 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0137 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01099 | hp2 | a0002 | c0004 | t0001 | g0149 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0240 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0166 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0238 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0343 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0026 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0224 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0243 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0309 | AMR | PUR | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0038 | AMR | CLM | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0191 | AMR | CLM | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | CLM | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0353 | AMR | CLM | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0021 | AMR | CLM | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0344 | AMR | CLM | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | CLM | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0136 | AMR | CLM | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0145 | AMR | CLM | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0021 | AMR | CLM | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0336 | AMR | CLM | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0019 | AMR | CLM | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0173 | AMR | CLM | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0170 | AMR | CLM | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0106 | EUR | IBS | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0139 | EUR | IBS | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0168 | EUR | IBS | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0112 | EUR | IBS | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0223 | AFR | ACB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01891 | hp2 | a0002 | c0002 | t0002 | g0244 | AFR | ACB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0131 | AMR | PEL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0161 | AMR | PEL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0206 | AMR | PEL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0277 | AMR | PEL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0134 | AMR | PEL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0132 | AMR | PEL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0326 | EAS | KHV | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | KHV | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0290 | EAS | KHV | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | KHV | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0227 | AFR | ACB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0169 | AFR | ACB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | KHV | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02071 | hp2 | a0004 | c0006 | t0001 | g0355 | EAS | KHV | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0247 | EAS | KHV | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | KHV | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | KHV | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | KHV | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0285 | EAS | KHV | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0229 | AFR | ACB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CDX | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02155 | hp2 | a0005 | c0005 | t0001 | g0183 | EAS | CDX | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0133 | AMR | PEL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02280 | hp1 | a0002 | c0002 | t0002 | g0193 | AFR | ACB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0124 | AMR | PEL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PEL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02451 | hp2 | a0002 | c0002 | t0002 | g0219 | AFR | ACB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | KHV | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | KHV | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0230 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0015 | SAS | PJL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0255 | SAS | PJL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0228 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0313 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02622 | hp2 | a0002 | c0002 | t0002 | g0222 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0217 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0199 | SAS | PJL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | PJL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0242 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02723 | hp1 | a0002 | c0002 | t0002 | g0027 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0246 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0207 | SAS | PJL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0317 | SAS | PJL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0314 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0306 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0122 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02896 | hp2 | a0002 | c0002 | t0002 | g0197 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0123 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0356 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0225 | AFR | ESN | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | ESN | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | ESN | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0308 | AFR | ESN | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | ESN | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0196 | AFR | ESN | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0357 | SAS | PJL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0307 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03098 | hp1 | a0002 | c0002 | t0002 | g0201 | AFR | MSL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0202 | AFR | MSL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0220 | AFR | ESN | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0024 | AFR | ESN | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03195 | hp1 | a0002 | c0002 | t0002 | g0039 | AFR | ESN | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0024 | AFR | ESN | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | MSL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | MSL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0254 | SAS | PJL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0221 | AFR | MSL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0310 | AFR | MSL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03486 | hp2 | a0002 | c0002 | t0002 | g0241 | AFR | MSL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0345 | SAS | PJL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0350 | SAS | PJL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0181 | SAS | PJL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0180 | SAS | PJL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0340 | SAS | PJL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03516 | hp1 | a0002 | c0002 | t0002 | g0025 | AFR | ESN | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0040 | AFR | GWD | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0311 | AFR | MSL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | MSL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0349 | SAS | PJL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0289 | SAS | PJL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0321 | SAS | PJL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0232 | SAS | PJL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03688 | hp1 | a0003 | c0003 | t0002 | g0030 | SAS | STU | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0198 | SAS | STU | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0327 | SAS | PJL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0162 | SAS | PJL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0184 | SAS | BEB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0188 | SAS | BEB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0231 | SAS | BEB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0284 | SAS | BEB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0281 | SAS | BEB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0330 | SAS | BEB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0252 | SAS | STU | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0272 | SAS | STU | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0190 | SAS | STU | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0274 | SAS | STU | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG04228 | hp1 | a0003 | c0003 | t0002 | g0030 | SAS | STU | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0187 | SAS | STU | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | CHB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | YRI | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0245 | AFR | YRI | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0147 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18949 | hp2 | a0002 | c0002 | t0003 | g0146 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18952 | hp1 | a0002 | c0002 | t0003 | g0022 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18952 | hp2 | a0002 | c0002 | t0004 | g0135 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18956 | hp1 | a0002 | c0002 | t0003 | g0177 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0302 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18970 | hp1 | a0002 | c0002 | t0004 | g0163 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18979 | hp1 | a0002 | c0002 | t0004 | g0205 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0130 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18987 | hp2 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18993 | hp2 | a0002 | c0002 | t0003 | g0214 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19010 | hp2 | a0002 | c0002 | t0003 | g0140 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | LWK | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | LWK | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | LWK | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19043 | hp2 | a0002 | c0002 | t0002 | g0026 | AFR | LWK | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19063 | hp2 | a0006 | c0007 | t0001 | g0226 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19077 | hp1 | a0002 | c0002 | t0003 | g0022 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19078 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19081 | hp1 | a0002 | c0002 | t0003 | g0141 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19084 | hp2 | a0002 | c0002 | t0004 | g0165 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19091 | hp2 | a0002 | c0002 | t0004 | g0164 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | YRI | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0200 | AFR | YRI | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | ASW | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ASW | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0015 | EUR | TSI | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0182 | EUR | TSI | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | GIH | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0118 | SAS | GIH | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0186 | AMR | CLM | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0195 | AFR | ACB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | ACB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0185 | AFR | ACB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | ACB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG02559 | hp2 | a0002 | c0002 | t0002 | g0027 | AFR | ACB | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0358 | AFR | MSL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG03471 | hp2 | a0002 | c0002 | t0002 | g0025 | AFR | MSL | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | USA | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0175 | AFR | USA | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0359 | AFR | USA | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | USA | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | LWK | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | LWK | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0005 | REF | REF | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0216 | REF | REF | PTGR1_chr9_111557567_111604647 | PTGR1 | chr9 | 111557567 | 111604647 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:111563135 | T | C | 1 | a0004 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.976A>G | p.Ile326Val | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 10/10 | 1031/1599 | 976/990 | 326/329 | chr9 | 111563135 | |||
| chr9:111570204 | G | A | 1 | a0003 | 2 | HG03688.hp1 HG04228.hp1 |
missense_variant | MODERATE | c.766C>T | p.Pro256Ser | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/10 | 821/1599 | 766/990 | 256/329 | chr9 | 111570204 | |||
| chr9:111592962 | T | C | 1 | a0005 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.173A>G | p.Lys58Arg | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/10 | 228/1599 | 173/990 | 58/329 | chr9 | 111592962 | |||
| chr9:111597344 | C | A | 3 | a0001 a0003 a0004 |
239 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(236): Show |
missense_variant | MODERATE | c.79G>T | p.Ala27Ser | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/10 | 134/1599 | 79/990 | 27/329 | chr9 | 111597344 | |||
| chr9:111597416 | G | A | 1 | a0006 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.7C>T | p.Arg3Cys | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/10 | 62/1599 | 7/990 | 3/329 | chr9 | 111597416 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:111570172 | G | T | 1 | a0002c0004 | 1 | HG01099.hp2 | synonymous_variant | LOW | c.798C>A | p.Arg266Arg | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/10 | 853/1599 | 798/990 | 266/329 | chr9 | 111570172 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:111562668 | A | G | 5 | a0001c0001t0002 a0001c0001t0003 a0002c0002t0002 others(2): Show |
160 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*453T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 10/10 | 453 | chr9 | 111562668 | ||||||
| chr9:111562842 | T | C | 3 | a0001c0001t0003 a0002c0002t0003 a0002c0002t0004 |
24 | HG00558.hp1 HG00621.hp2 HG02027.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*279A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 10/10 | 279 | chr9 | 111562842 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:111563451 | G | A | 1 | a0002c0002t0002g0197 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.880-220C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111563451 | |||||||
| chr9:111563467 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0085 |
2 | HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.880-236G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111563467 | |||||||
| chr9:111563509 | C | CT | 20 | a0001c0001t0001g0300 a0001c0001t0002g0077 a0001c0001t0002g0078 others(17): Show |
22 | HG00099.hp1 HG01074.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.880-279dupA | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111563509 | |||||||
| chr9:111563513 | T | C | 1 | a0001c0001t0001g0057 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.880-282A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111563513 | |||||||
| chr9:111563539 | T | C | 19 | a0001c0001t0002g0077 a0001c0001t0002g0078 a0001c0001t0002g0102 others(16): Show |
21 | HG00099.hp1 HG01074.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.880-308A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111563539 | |||||||
| chr9:111563569 | G | C | 19 | a0001c0001t0002g0077 a0001c0001t0002g0078 a0001c0001t0002g0102 others(16): Show |
21 | HG00099.hp1 HG01074.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.880-338C>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111563569 | |||||||
| chr9:111563639 | G | A | 1 | a0001c0001t0002g0103 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.880-408C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111563639 | |||||||
| chr9:111563733 | C | T | 44 | a0001c0001t0001g0280 a0001c0001t0002g0029 a0001c0001t0002g0031 others(41): Show |
49 | HG00558.hp1 HG00621.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.880-502G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111563733 | |||||||
| chr9:111563741 | C | T | 2 | a0001c0001t0002g0340 a0001c0001t0002g0345 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.880-510G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111563741 | |||||||
| chr9:111563760 | C | T | 15 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(12): Show |
19 | HG00738.hp2 HG01074.hp2 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.880-529G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111563760 | |||||||
| chr9:111563995 | T | C | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(249): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.880-764A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111563995 | |||||||
| chr9:111564133 | G | A | 3 | a0001c0001t0002g0032 a0001c0001t0002g0281 a0002c0002t0002g0145 |
4 | HG01167.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.880-902C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111564133 | |||||||
| chr9:111564225 | T | G | 64 | a0001c0001t0001g0280 a0001c0001t0002g0029 a0001c0001t0002g0031 others(61): Show |
69 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.880-994A>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111564225 | |||||||
| chr9:111564267 | A | G | 19 | a0001c0001t0002g0077 a0001c0001t0002g0078 a0001c0001t0002g0102 others(16): Show |
21 | HG00099.hp1 HG01074.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.880-1036T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111564267 | |||||||
| chr9:111564277 | T | TTTA | 62 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0043 others(59): Show |
65 | HG00099.hp2 HG00544.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.880-1049_880-1047d others(5): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111564277 | |||||||
| chr9:111564277 | T | TTTATTA | 9 | a0001c0001t0001g0117 a0001c0001t0001g0323 a0001c0001t0001g0328 others(6): Show |
9 | HG01256.hp2 HG01258.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.880-1052_880-1047d others(8): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111564277 | |||||||
| chr9:111564277 | TTTA | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0036 others(101): Show |
120 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.880-1049_880-1047d others(5): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111564277 | |||||||
| chr9:111564277 | TTTATTA | T | 26 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(23): Show |
33 | HG00597.hp1 HG00738.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.880-1052_880-1047d others(8): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111564277 | |||||||
| chr9:111564277 | TTTATTAT others(2): Show |
T | 14 | a0001c0001t0001g0093 a0001c0001t0001g0303 a0001c0001t0001g0304 others(11): Show |
14 | HG02080.hp2 HG02280.hp1 HG02895.hp2 others(11): Show |
intron_variant | MODIFIER | c.880-1055_880-1047d others(11): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111564277 | |||||||
| chr9:111564277 | TTTATTAT others(5): Show |
T | 1 | a0001c0001t0002g0094 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.880-1058_880-1047d others(14): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111564277 | |||||||
| chr9:111564277 | TTTATTAT others(8): Show |
T | 16 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0063 others(13): Show |
18 | HG01192.hp1 HG01243.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.880-1061_880-1047d others(17): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111564277 | |||||||
| chr9:111564323 | T | C | 1 | a0001c0001t0001g0342 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.880-1092A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111564323 | |||||||
| chr9:111564548 | C | T | 1 | a0001c0001t0002g0236 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.880-1317G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111564548 | |||||||
| chr9:111564588 | G | A | 1 | a0002c0002t0001g0017 | 2 | NA18939.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.880-1357C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111564588 | |||||||
| chr9:111564647 | T | C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(95): Show |
114 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.880-1416A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111564647 | |||||||
| chr9:111564894 | C | T | 1 | a0001c0001t0002g0109 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.880-1663G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111564894 | |||||||
| chr9:111564969 | C | T | 1 | a0002c0002t0001g0155 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.880-1738G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111564969 | |||||||
| chr9:111565078 | C | T | 8 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0063 others(5): Show |
8 | HG01891.hp1 HG02015.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.880-1847G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111565078 | |||||||
| chr9:111565134 | A | G | 1 | a0001c0001t0001g0325 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.880-1903T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111565134 | |||||||
| chr9:111565160 | C | G | 1 | a0001c0001t0001g0089 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.880-1929G>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111565160 | |||||||
| chr9:111565268 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.880-2037A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111565268 | |||||||
| chr9:111565511 | T | C | 17 | a0001c0001t0002g0051 a0001c0001t0002g0062 a0001c0001t0002g0070 others(14): Show |
17 | HG01261.hp2 HG01884.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.880-2280A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111565511 | |||||||
| chr9:111565724 | T | C | 65 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(62): Show |
78 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.880-2493A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111565724 | |||||||
| chr9:111565777 | A | C | 17 | a0001c0001t0001g0034 a0001c0001t0001g0080 a0001c0001t0001g0081 others(14): Show |
18 | HG01081.hp2 HG01255.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.880-2546T>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111565777 | |||||||
| chr9:111565912 | C | T | 1 | a0001c0001t0002g0094 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.880-2681G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111565912 | |||||||
| chr9:111565938 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.880-2707C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111565938 | |||||||
| chr9:111566042 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.880-2811A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111566042 | |||||||
| chr9:111566143 | C | T | 1 | a0002c0002t0002g0184 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.880-2912G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111566143 | |||||||
| chr9:111566193 | C | A | 19 | a0001c0001t0002g0077 a0001c0001t0002g0078 a0001c0001t0002g0102 others(16): Show |
21 | HG00099.hp1 HG01074.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.880-2962G>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111566193 | |||||||
| chr9:111566204 | A | AAAAT | 8 | a0002c0002t0002g0122 a0002c0002t0002g0123 a0002c0002t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02280.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.880-2977_880-2974d others(6): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111566204 | |||||||
| chr9:111566204 | AAAATAAA others(5): Show |
A | 1 | a0001c0001t0001g0069 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.880-2985_880-2974d others(14): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111566204 | |||||||
| chr9:111566208 | T | A | 19 | a0001c0001t0002g0077 a0001c0001t0002g0078 a0001c0001t0002g0102 others(16): Show |
21 | HG00099.hp1 HG01074.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.880-2977A>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111566208 | |||||||
| chr9:111566655 | T | C | 19 | a0001c0001t0002g0077 a0001c0001t0002g0078 a0001c0001t0002g0102 others(16): Show |
21 | HG00099.hp1 HG01074.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.880-3424A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111566655 | |||||||
| chr9:111566683 | T | G | 7 | a0002c0002t0002g0026 a0002c0002t0002g0027 a0002c0002t0002g0241 others(4): Show |
9 | HG01192.hp1 HG01243.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.879+3408A>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111566683 | |||||||
| chr9:111566735 | G | A | 37 | a0001c0001t0001g0013 a0001c0001t0001g0115 a0001c0001t0001g0265 others(34): Show |
40 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.879+3356C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111566735 | |||||||
| chr9:111566845 | A | T | 1 | a0001c0001t0002g0110 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.879+3246T>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111566845 | |||||||
| chr9:111566925 | A | G | 2 | a0002c0002t0001g0007 a0002c0002t0001g0185 |
4 | HG01884.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.879+3166T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111566925 | |||||||
| chr9:111566932 | C | CA | 4 | a0001c0001t0001g0330 a0001c0001t0002g0252 a0001c0001t0003g0249 others(1): Show |
4 | HG03942.hp1 HG04199.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.879+3158dupT | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111566932 | |||||||
| chr9:111566962 | G | A | 7 | a0002c0002t0002g0122 a0002c0002t0002g0123 a0002c0002t0002g0193 others(4): Show |
7 | HG02280.hp1 HG02895.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+3129C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111566962 | |||||||
| chr9:111566976 | C | A | 4 | a0002c0002t0002g0019 a0002c0002t0002g0169 a0002c0002t0002g0238 others(1): Show |
5 | HG00140.hp2 HG01106.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+3115G>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111566976 | |||||||
| chr9:111567081 | C | CA | 10 | a0001c0001t0001g0067 a0001c0001t0001g0295 a0001c0001t0001g0298 others(7): Show |
10 | HG01175.hp2 HG01255.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.879+3009dupT | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111567081 | |||||||
| chr9:111567104 | C | G | 19 | a0001c0001t0002g0077 a0001c0001t0002g0078 a0001c0001t0002g0102 others(16): Show |
21 | HG00099.hp1 HG01074.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.879+2987G>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111567104 | |||||||
| chr9:111567104 | C | T | 31 | a0001c0001t0001g0004 a0001c0001t0001g0093 a0001c0001t0001g0312 others(28): Show |
33 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.879+2987G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111567104 | |||||||
| chr9:111567111 | C | T | 2 | a0001c0001t0002g0344 a0001c0001t0002g0353 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.879+2980G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111567111 | |||||||
| chr9:111567112 | G | A | 1 | a0001c0001t0002g0313 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.879+2979C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111567112 | |||||||
| chr9:111567290 | C | T | 1 | a0001c0001t0001g0319 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.879+2801G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111567290 | |||||||
| chr9:111567307 | C | T | 1 | a0001c0001t0001g0251 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.879+2784G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111567307 | |||||||
| chr9:111567336 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0028 |
4 | HG00738.hp2 HG01074.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+2755G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111567336 | |||||||
| chr9:111567363 | T | C | 4 | a0002c0002t0001g0162 a0002c0002t0001g0186 a0002c0002t0001g0190 others(1): Show |
4 | HG01123.hp1 HG01255.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.879+2728A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111567363 | |||||||
| chr9:111567475 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG01515.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.879+2616C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111567475 | |||||||
| chr9:111567488 | C | T | 1 | a0001c0001t0002g0258 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.879+2603G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111567488 | |||||||
| chr9:111567566 | A | T | 2 | a0001c0001t0002g0062 a0001c0001t0002g0095 |
2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.879+2525T>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111567566 | |||||||
| chr9:111567568 | TA | T | 17 | a0001c0001t0001g0034 a0001c0001t0001g0080 a0001c0001t0001g0081 others(14): Show |
18 | HG01081.hp2 HG01255.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.879+2522delT | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111567568 | |||||||
| chr9:111567736 | C | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0293 others(8): Show |
15 | HG02080.hp2 HG02135.hp1 NA18955.hp1 others(12): Show |
intron_variant | MODIFIER | c.879+2355G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111567736 | |||||||
| chr9:111567796 | C | A | 5 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0090 others(2): Show |
5 | HG02109.hp1 HG02886.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+2295G>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111567796 | |||||||
| chr9:111567934 | G | A | 5 | a0001c0001t0001g0045 a0002c0002t0001g0016 a0002c0002t0001g0017 others(2): Show |
7 | NA18939.hp1 NA18941.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+2157C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111567934 | |||||||
| chr9:111568067 | G | A | 98 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(95): Show |
114 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.879+2024C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111568067 | |||||||
| chr9:111568210 | G | A | 1 | a0002c0002t0004g0165 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.879+1881C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111568210 | |||||||
| chr9:111568325 | T | C | 83 | a0001c0001t0001g0280 a0001c0001t0002g0029 a0001c0001t0002g0031 others(80): Show |
90 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.879+1766A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111568325 | |||||||
| chr9:111568396 | A | C | 50 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0033 others(47): Show |
59 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.879+1695T>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111568396 | |||||||
| chr9:111568403 | G | A | 19 | a0001c0001t0002g0077 a0001c0001t0002g0078 a0001c0001t0002g0102 others(16): Show |
21 | HG00099.hp1 HG01074.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.879+1688C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111568403 | |||||||
| chr9:111568683 | G | A | 1 | a0001c0001t0001g0296 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.879+1408C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111568683 | |||||||
| chr9:111568691 | T | C | 212 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(209): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.879+1400A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111568691 | |||||||
| chr9:111568704 | C | T | 40 | a0001c0001t0001g0013 a0001c0001t0001g0115 a0001c0001t0001g0265 others(37): Show |
43 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(40): Show |
intron_variant | MODIFIER | c.879+1387G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111568704 | |||||||
| chr9:111568871 | G | A | 1 | a0002c0002t0001g0189 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.879+1220C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111568871 | |||||||
| chr9:111568872 | G | A | 1 | a0002c0002t0001g0189 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.879+1219C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111568872 | |||||||
| chr9:111568937 | A | G | 1 | a0004c0006t0001g0355 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.879+1154T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111568937 | |||||||
| chr9:111568964 | C | T | 1 | a0001c0001t0002g0272 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.879+1127G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111568964 | |||||||
| chr9:111569049 | G | A | 1 | a0001c0001t0002g0234 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.879+1042C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111569049 | |||||||
| chr9:111569211 | C | T | 4 | a0001c0001t0002g0261 a0001c0001t0002g0264 a0001c0001t0002g0267 others(1): Show |
4 | NA18943.hp2 NA18971.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+880G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111569211 | |||||||
| chr9:111569218 | A | T | 19 | a0001c0001t0002g0077 a0001c0001t0002g0078 a0001c0001t0002g0102 others(16): Show |
21 | HG00099.hp1 HG01074.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.879+873T>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111569218 | |||||||
| chr9:111569505 | C | T | 37 | a0001c0001t0001g0013 a0001c0001t0001g0115 a0001c0001t0001g0265 others(34): Show |
40 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.879+586G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111569505 | |||||||
| chr9:111569707 | G | A | 8 | a0001c0001t0002g0311 a0002c0002t0002g0026 a0002c0002t0002g0027 others(5): Show |
10 | HG01192.hp1 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.879+384C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111569707 | |||||||
| chr9:111569988 | G | A | 4 | a0002c0002t0001g0021 a0002c0002t0001g0124 a0002c0002t0001g0134 others(1): Show |
5 | HG01099.hp2 HG01257.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+103C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 9/9 | chr9 | 111569988 | |||||||
| chr9:111570309 | T | C | 1 | a0002c0002t0001g0174 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.761-100A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111570309 | |||||||
| chr9:111570485 | T | C | 216 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(213): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.761-276A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111570485 | |||||||
| chr9:111570493 | T | C | 3 | a0002c0002t0002g0025 a0002c0002t0002g0224 a0002c0002t0002g0225 |
4 | HG01192.hp2 HG02922.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.761-284A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111570493 | |||||||
| chr9:111570498 | C | T | 2 | a0001c0001t0001g0312 a0001c0001t0002g0314 |
2 | HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.761-289G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111570498 | |||||||
| chr9:111570599 | G | A | 40 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(37): Show |
45 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.761-390C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111570599 | |||||||
| chr9:111570695 | C | T | 2 | a0002c0002t0001g0014 a0002c0002t0001g0148 |
3 | HG00735.hp2 HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.761-486G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111570695 | |||||||
| chr9:111570703 | C | T | 1 | a0001c0001t0002g0314 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.761-494G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111570703 | |||||||
| chr9:111570848 | A | G | 64 | a0001c0001t0001g0280 a0001c0001t0002g0029 a0001c0001t0002g0031 others(61): Show |
69 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.761-639T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111570848 | |||||||
| chr9:111570884 | C | A | 7 | a0001c0001t0002g0062 a0001c0001t0002g0095 a0001c0001t0002g0096 others(4): Show |
7 | HG02559.hp1 HG02818.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.761-675G>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111570884 | |||||||
| chr9:111571012 | C | A | 63 | a0001c0001t0001g0280 a0001c0001t0002g0029 a0001c0001t0002g0031 others(60): Show |
68 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.761-803G>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111571012 | |||||||
| chr9:111571015 | C | G | 63 | a0001c0001t0001g0280 a0001c0001t0002g0029 a0001c0001t0002g0031 others(60): Show |
68 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.761-806G>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111571015 | |||||||
| chr9:111571016 | T | A | 63 | a0001c0001t0001g0280 a0001c0001t0002g0029 a0001c0001t0002g0031 others(60): Show |
68 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.761-807A>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111571016 | |||||||
| chr9:111571017 | GCTAGAAG others(561): Show |
G | 63 | a0001c0001t0001g0280 a0001c0001t0002g0029 a0001c0001t0002g0031 others(60): Show |
68 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.761-1376_761-809de others(1): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111571017 | |||||||
| chr9:111571047 | T | A | 4 | a0002c0002t0001g0170 a0002c0002t0002g0137 a0002c0002t0002g0171 others(1): Show |
4 | HG00738.hp1 HG01099.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.761-838A>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111571047 | |||||||
| chr9:111571055 | T | C | 4 | a0002c0002t0001g0170 a0002c0002t0002g0137 a0002c0002t0002g0171 others(1): Show |
4 | HG00738.hp1 HG01099.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.761-846A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111571055 | |||||||
| chr9:111571229 | T | C | 1 | a0001c0001t0002g0079 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.761-1020A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111571229 | |||||||
| chr9:111571254 | A | G | 2 | a0002c0002t0001g0167 a0002c0002t0001g0213 |
2 | NA18950.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.761-1045T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111571254 | |||||||
| chr9:111571480 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.761-1271A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111571480 | |||||||
| chr9:111571485 | G | A | 3 | a0001c0001t0002g0306 a0001c0001t0002g0309 a0001c0001t0002g0310 |
3 | HG01243.hp2 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.761-1276C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111571485 | |||||||
| chr9:111571543 | A | G | 16 | a0001c0001t0002g0077 a0001c0001t0002g0078 a0001c0001t0002g0102 others(13): Show |
17 | HG00099.hp1 HG01074.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.761-1334T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111571543 | |||||||
| chr9:111571572 | G | A | 3 | a0001c0001t0002g0306 a0001c0001t0002g0309 a0001c0001t0002g0310 |
3 | HG01243.hp2 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.761-1363C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111571572 | |||||||
| chr9:111571591 | CCTCCGCC others(5): Show |
C | 63 | a0001c0001t0001g0280 a0001c0001t0002g0029 a0001c0001t0002g0031 others(60): Show |
68 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.761-1394_761-1383d others(14): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111571591 | |||||||
| chr9:111571656 | TTTTGTTT others(1): Show |
T | 37 | a0001c0001t0001g0013 a0001c0001t0001g0115 a0001c0001t0001g0265 others(34): Show |
40 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.761-1455_761-1448d others(10): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111571656 | |||||||
| chr9:111571785 | T | G | 19 | a0001c0001t0002g0077 a0001c0001t0002g0078 a0001c0001t0002g0102 others(16): Show |
21 | HG00099.hp1 HG01074.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.761-1576A>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111571785 | |||||||
| chr9:111571929 | C | T | 2 | a0002c0002t0001g0198 a0002c0002t0001g0199 |
2 | HG02698.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.761-1720G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111571929 | |||||||
| chr9:111572170 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.761-1961C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111572170 | |||||||
| chr9:111572174 | A | G | 1 | a0002c0002t0001g0170 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.761-1965T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111572174 | |||||||
| chr9:111572352 | T | C | 1 | a0002c0002t0002g0184 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.761-2143A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111572352 | |||||||
| chr9:111572370 | A | G | 253 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(250): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.761-2161T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111572370 | |||||||
| chr9:111572450 | C | T | 1 | a0001c0001t0002g0313 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.761-2241G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111572450 | |||||||
| chr9:111572569 | G | A | 4 | a0002c0002t0001g0132 a0002c0002t0001g0133 a0002c0002t0001g0161 others(1): Show |
4 | HG01070.hp2 HG01952.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.760+2165C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111572569 | |||||||
| chr9:111572635 | T | C | 19 | a0001c0001t0002g0077 a0001c0001t0002g0078 a0001c0001t0002g0102 others(16): Show |
21 | HG00099.hp1 HG01074.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.760+2099A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111572635 | |||||||
| chr9:111572756 | C | CA | 59 | a0001c0001t0001g0013 a0001c0001t0001g0052 a0001c0001t0001g0053 others(56): Show |
62 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.760+1977dupT | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111572756 | |||||||
| chr9:111572756 | C | CAA | 53 | a0001c0001t0001g0087 a0001c0001t0001g0280 a0001c0001t0002g0029 others(50): Show |
58 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.760+1976_760+1977d others(4): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111572756 | |||||||
| chr9:111572756 | C | CAAA | 13 | a0001c0001t0002g0259 a0001c0001t0002g0264 a0001c0001t0002g0274 others(10): Show |
13 | HG00621.hp2 HG01346.hp2 HG04204.hp2 others(10): Show |
intron_variant | MODIFIER | c.760+1975_760+1977d others(5): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111572756 | |||||||
| chr9:111572756 | CA | C | 15 | a0001c0001t0002g0077 a0001c0001t0002g0078 a0002c0002t0001g0179 others(12): Show |
16 | HG01192.hp2 HG02055.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.760+1977delT | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111572756 | |||||||
| chr9:111572756 | CAAAAAAA | C | 64 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(61): Show |
77 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.760+1971_760+1977d others(9): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111572756 | |||||||
| chr9:111572759 | A | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0055 others(7): Show |
11 | HG01358.hp2 HG01928.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.760+1975T>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111572759 | |||||||
| chr9:111572772 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0002g0262 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.760+1961_760+1962i others(22): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111572772 | |||||||
| chr9:111572791 | A | T | 1 | a0002c0002t0001g0206 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.760+1943T>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111572791 | |||||||
| chr9:111572845 | A | C | 1 | a0001c0001t0002g0083 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.760+1889T>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111572845 | |||||||
| chr9:111572938 | A | T | 64 | a0001c0001t0001g0280 a0001c0001t0002g0029 a0001c0001t0002g0031 others(61): Show |
69 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.760+1796T>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111572938 | |||||||
| chr9:111573030 | T | C | 4 | a0001c0001t0001g0004 a0001c0001t0001g0093 a0001c0001t0002g0083 others(1): Show |
6 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.760+1704A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111573030 | |||||||
| chr9:111573065 | G | C | 15 | a0001c0001t0002g0077 a0001c0001t0002g0078 a0001c0001t0002g0102 others(12): Show |
15 | HG00099.hp1 HG01074.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.760+1669C>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111573065 | |||||||
| chr9:111573084 | A | C | 5 | a0001c0001t0001g0043 a0001c0001t0001g0089 a0001c0001t0001g0091 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.760+1650T>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111573084 | |||||||
| chr9:111573224 | T | A | 1 | a0002c0002t0001g0192 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.760+1510A>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111573224 | |||||||
| chr9:111573265 | G | A | 4 | a0002c0002t0001g0132 a0002c0002t0001g0133 a0002c0002t0001g0161 others(1): Show |
4 | HG01070.hp2 HG01952.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.760+1469C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111573265 | |||||||
| chr9:111573283 | GA | G | 19 | a0001c0001t0001g0312 a0001c0001t0002g0051 a0001c0001t0002g0062 others(16): Show |
19 | HG01261.hp2 HG01884.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.760+1450delT | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111573283 | |||||||
| chr9:111573566 | G | A | 1 | a0002c0002t0001g0125 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.760+1168C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111573566 | |||||||
| chr9:111573584 | G | C | 18 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0252 others(15): Show |
19 | HG00140.hp2 HG00738.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.760+1150C>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111573584 | |||||||
| chr9:111573593 | C | T | 65 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(62): Show |
78 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.760+1141G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111573593 | |||||||
| chr9:111573605 | G | A | 40 | a0001c0001t0001g0013 a0001c0001t0001g0115 a0001c0001t0001g0265 others(37): Show |
43 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(40): Show |
intron_variant | MODIFIER | c.760+1129C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111573605 | |||||||
| chr9:111573843 | C | T | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(249): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.760+891G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111573843 | |||||||
| chr9:111573988 | G | C | 1 | a0002c0002t0001g0151 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.760+746C>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111573988 | |||||||
| chr9:111574359 | T | C | 19 | a0001c0001t0002g0077 a0001c0001t0002g0078 a0001c0001t0002g0102 others(16): Show |
21 | HG00099.hp1 HG01074.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.760+375A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111574359 | |||||||
| chr9:111574406 | G | A | 1 | a0001c0001t0002g0313 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.760+328C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111574406 | |||||||
| chr9:111574418 | C | T | 63 | a0001c0001t0001g0280 a0001c0001t0002g0029 a0001c0001t0002g0031 others(60): Show |
68 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.760+316G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111574418 | |||||||
| chr9:111574480 | C | A | 1 | a0002c0002t0003g0146 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.760+254G>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111574480 | |||||||
| chr9:111574604 | T | TA | 72 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0063 others(69): Show |
79 | HG00280.hp2 HG00544.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.760+129dupT | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111574604 | |||||||
| chr9:111574614 | A | G | 19 | a0001c0001t0002g0077 a0001c0001t0002g0078 a0001c0001t0002g0102 others(16): Show |
21 | HG00099.hp1 HG01074.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.760+120T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | 111574614 | |||||||
| chr9:111574943 | G | A | 19 | a0001c0001t0002g0077 a0001c0001t0002g0078 a0001c0001t0002g0102 others(16): Show |
21 | HG00099.hp1 HG01074.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.652-101C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111574943 | |||||||
| chr9:111575009 | A | G | 1 | a0002c0002t0001g0188 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.652-167T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111575009 | |||||||
| chr9:111575018 | C | T | 12 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(9): Show |
12 | HG01081.hp2 HG01255.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.652-176G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111575018 | |||||||
| chr9:111575126 | T | C | 258 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(255): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.652-284A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111575126 | |||||||
| chr9:111575133 | T | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0049 a0001c0001t0001g0054 others(5): Show |
9 | HG02155.hp1 HG02523.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.652-291A>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111575133 | |||||||
| chr9:111575231 | G | T | 4 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0099 others(1): Show |
4 | HG02145.hp2 HG02257.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.652-389C>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111575231 | |||||||
| chr9:111575356 | C | A | 1 | a0002c0002t0002g0147 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.652-514G>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111575356 | |||||||
| chr9:111575823 | T | C | 41 | a0001c0001t0001g0013 a0001c0001t0001g0115 a0001c0001t0001g0265 others(38): Show |
44 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.652-981A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111575823 | |||||||
| chr9:111575990 | C | CA | 20 | a0001c0001t0002g0077 a0001c0001t0002g0078 a0001c0001t0002g0102 others(17): Show |
22 | HG00099.hp1 HG01074.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.652-1149dupT | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111575990 | |||||||
| chr9:111576444 | T | C | 2 | a0001c0001t0001g0312 a0001c0001t0002g0314 |
2 | HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.652-1602A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111576444 | |||||||
| chr9:111576533 | A | G | 1 | a0002c0002t0001g0207 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.652-1691T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111576533 | |||||||
| chr9:111576566 | G | C | 7 | a0002c0002t0002g0026 a0002c0002t0002g0027 a0002c0002t0002g0241 others(4): Show |
9 | HG01192.hp1 HG01243.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.652-1724C>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111576566 | |||||||
| chr9:111576612 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.652-1770A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111576612 | |||||||
| chr9:111576775 | A | G | 1 | a0001c0001t0001g0012 | 2 | HG00738.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.652-1933T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111576775 | |||||||
| chr9:111577026 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.651+1770C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111577026 | |||||||
| chr9:111577090 | C | CA | 22 | a0001c0001t0001g0004 a0001c0001t0001g0093 a0001c0001t0002g0051 others(19): Show |
24 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.651+1705dupT | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111577090 | |||||||
| chr9:111577171 | A | G | 1 | a0002c0002t0003g0177 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.651+1625T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111577171 | |||||||
| chr9:111577197 | G | A | 63 | a0001c0001t0001g0280 a0001c0001t0002g0029 a0001c0001t0002g0031 others(60): Show |
68 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.651+1599C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111577197 | |||||||
| chr9:111577359 | G | A | 63 | a0001c0001t0001g0280 a0001c0001t0002g0029 a0001c0001t0002g0031 others(60): Show |
68 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.651+1437C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111577359 | |||||||
| chr9:111577435 | T | C | 1 | a0002c0002t0001g0133 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.651+1361A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111577435 | |||||||
| chr9:111577534 | A | T | 19 | a0001c0001t0002g0077 a0001c0001t0002g0078 a0001c0001t0002g0102 others(16): Show |
21 | HG00099.hp1 HG01074.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.651+1262T>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111577534 | |||||||
| chr9:111577556 | C | A | 3 | a0001c0001t0001g0323 a0001c0001t0001g0328 a0001c0001t0001g0356 |
3 | HG02896.hp1 HG02897.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.651+1240G>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111577556 | |||||||
| chr9:111577623 | T | C | 1 | a0001c0001t0002g0255 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.651+1173A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111577623 | |||||||
| chr9:111577660 | C | A | 1 | a0002c0002t0001g0161 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.651+1136G>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111577660 | |||||||
| chr9:111577674 | A | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0091 |
2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.651+1122T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111577674 | |||||||
| chr9:111577758 | T | C | 31 | a0001c0001t0001g0004 a0001c0001t0001g0093 a0001c0001t0001g0312 others(28): Show |
33 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.651+1038A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111577758 | |||||||
| chr9:111577759 | T | C | 1 | a0001c0001t0002g0083 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.651+1037A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111577759 | |||||||
| chr9:111577899 | T | G | 17 | a0001c0001t0002g0051 a0001c0001t0002g0062 a0001c0001t0002g0070 others(14): Show |
17 | HG01261.hp2 HG01884.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.651+897A>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111577899 | |||||||
| chr9:111577962 | G | C | 63 | a0001c0001t0001g0280 a0001c0001t0002g0029 a0001c0001t0002g0031 others(60): Show |
68 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.651+834C>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111577962 | |||||||
| chr9:111577983 | TAATGAGT others(4): Show |
T | 1 | a0001c0001t0002g0268 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.651+802_651+812del others(11): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111577983 | |||||||
| chr9:111578000 | T | G | 1 | a0001c0001t0002g0268 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.651+796A>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578000 | |||||||
| chr9:111578000 | T | TG | 61 | a0001c0001t0001g0280 a0001c0001t0001g0342 a0001c0001t0002g0029 others(58): Show |
66 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.651+795dupC | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578000 | |||||||
| chr9:111578053 | G | T | 1 | a0001c0001t0001g0093 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.651+743C>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578053 | |||||||
| chr9:111578075 | C | T | 2 | a0001c0001t0001g0312 a0001c0001t0002g0314 |
2 | HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.651+721G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578075 | |||||||
| chr9:111578076 | G | A | 7 | a0002c0002t0002g0026 a0002c0002t0002g0027 a0002c0002t0002g0241 others(4): Show |
9 | HG01192.hp1 HG01243.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.651+720C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578076 | |||||||
| chr9:111578107 | G | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0093 a0001c0001t0002g0083 others(9): Show |
14 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.651+689C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578107 | |||||||
| chr9:111578119 | A | C | 1 | a0001c0001t0001g0093 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.651+677T>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578119 | |||||||
| chr9:111578131 | A | T | 1 | a0002c0002t0001g0178 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.651+665T>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578131 | |||||||
| chr9:111578139 | C | G | 19 | a0001c0001t0002g0077 a0001c0001t0002g0078 a0001c0001t0002g0102 others(16): Show |
21 | HG00099.hp1 HG01074.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.651+657G>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578139 | |||||||
| chr9:111578141 | T | A | 1 | a0001c0001t0002g0116 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.651+655A>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578141 | |||||||
| chr9:111578238 | T | C | 1 | a0002c0002t0001g0215 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.651+558A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578238 | |||||||
| chr9:111578269 | G | A | 1 | a0001c0001t0001g0273 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.651+527C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578269 | |||||||
| chr9:111578312 | C | T | 7 | a0002c0002t0002g0122 a0002c0002t0002g0123 a0002c0002t0002g0193 others(4): Show |
7 | HG02280.hp1 HG02895.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.651+484G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578312 | |||||||
| chr9:111578316 | T | TTATTTCT others(3163): Show |
1 | a0001c0001t0002g0264 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.651+479_651+480ins others(3170): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578316 | |||||||
| chr9:111578316 | T | TTATTTCT others(2623): Show |
1 | a0001c0001t0002g0338 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.651+479_651+480ins others(2630): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578316 | |||||||
| chr9:111578316 | T | TTATTTCT others(2960): Show |
1 | a0001c0001t0002g0269 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.651+479_651+480ins others(2967): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578316 | |||||||
| chr9:111578316 | T | TTATTTCT others(3100): Show |
1 | a0001c0001t0002g0267 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.651+479_651+480ins others(3107): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578316 | |||||||
| chr9:111578316 | T | TTATTTCT others(3138): Show |
1 | a0001c0001t0002g0286 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.651+479_651+480ins others(3145): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578316 | |||||||
| chr9:111578316 | T | TTATTTCT others(3117): Show |
1 | a0001c0001t0002g0261 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.651+479_651+480ins others(3124): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578316 | |||||||
| chr9:111578316 | T | TTATTTCT others(3141): Show |
1 | a0001c0001t0002g0050 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.651+479_651+480ins others(3148): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578316 | |||||||
| chr9:111578316 | T | TTATTTCT others(3235): Show |
1 | a0001c0001t0002g0329 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.651+479_651+480ins others(3242): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578316 | |||||||
| chr9:111578316 | T | TTATTTCT others(3153): Show |
1 | a0001c0001t0002g0268 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.651+479_651+480ins others(3160): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578316 | |||||||
| chr9:111578316 | T | TTATTTCT others(3219): Show |
1 | a0001c0001t0002g0326 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.651+479_651+480ins others(3226): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578316 | |||||||
| chr9:111578316 | T | TTATTTCT others(3243): Show |
1 | a0001c0001t0002g0263 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.651+479_651+480ins others(3250): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578316 | |||||||
| chr9:111578316 | T | TTATTTCT others(3166): Show |
1 | a0001c0001t0002g0262 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.651+479_651+480ins others(3173): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578316 | |||||||
| chr9:111578316 | T | TTATTTCT others(3070): Show |
1 | a0001c0001t0002g0253 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.651+479_651+480ins others(3077): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578316 | |||||||
| chr9:111578316 | T | TTATTTCT others(3178): Show |
1 | a0001c0001t0002g0341 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.651+479_651+480ins others(3185): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578316 | |||||||
| chr9:111578316 | T | TTATTTCT others(3488): Show |
1 | a0001c0001t0002g0335 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.651+479_651+480ins others(3495): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578316 | |||||||
| chr9:111578316 | T | TTATTTCT others(3024): Show |
1 | a0001c0001t0002g0064 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.651+479_651+480ins others(3031): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578316 | |||||||
| chr9:111578316 | T | TTATTTCT others(3044): Show |
1 | a0001c0001t0002g0260 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.651+479_651+480ins others(3051): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578316 | |||||||
| chr9:111578316 | T | TTATTTCT others(3275): Show |
1 | a0002c0002t0002g0147 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.651+479_651+480ins others(3282): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578316 | |||||||
| chr9:111578316 | T | TTATTTCT others(2907): Show |
1 | a0001c0001t0002g0320 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.651+479_651+480ins others(2914): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578316 | |||||||
| chr9:111578332 | T | C | 8 | a0002c0002t0002g0122 a0002c0002t0002g0123 a0002c0002t0002g0193 others(5): Show |
8 | HG02109.hp2 HG02280.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.651+464A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578332 | |||||||
| chr9:111578584 | A | G | 101 | a0001c0001t0001g0280 a0001c0001t0001g0312 a0001c0001t0002g0029 others(98): Show |
108 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.651+212T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578584 | |||||||
| chr9:111578591 | G | A | 3 | a0001c0001t0002g0306 a0001c0001t0002g0309 a0001c0001t0002g0310 |
3 | HG01243.hp2 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.651+205C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578591 | |||||||
| chr9:111578612 | C | T | 63 | a0001c0001t0001g0280 a0001c0001t0002g0029 a0001c0001t0002g0031 others(60): Show |
68 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.651+184G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578612 | |||||||
| chr9:111578713 | C | G | 6 | a0001c0001t0002g0005 a0001c0001t0002g0106 a0001c0001t0002g0107 others(3): Show |
7 | HG00642.hp1 HG01106.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.651+83G>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578713 | |||||||
| chr9:111578753 | T | C | 12 | a0001c0001t0001g0004 a0001c0001t0001g0093 a0001c0001t0002g0083 others(9): Show |
14 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.651+43A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | 111578753 | |||||||
| chr9:111578960 | A | G | 52 | a0001c0001t0001g0280 a0001c0001t0002g0029 a0001c0001t0002g0031 others(49): Show |
56 | HG00280.hp2 HG00558.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.496-9T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111578960 | |||||||
| chr9:111579096 | C | T | 82 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(79): Show |
93 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.496-145G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111579096 | |||||||
| chr9:111579122 | C | A | 3 | a0001c0001t0001g0063 a0001c0001t0001g0068 a0001c0001t0002g0062 |
3 | HG02965.hp2 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.496-171G>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111579122 | |||||||
| chr9:111579164 | A | C | 45 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(42): Show |
49 | HG00738.hp2 HG01074.hp2 HG01261.hp2 others(46): Show |
intron_variant | MODIFIER | c.496-213T>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111579164 | |||||||
| chr9:111579495 | C | A | 34 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0037 others(31): Show |
38 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.496-544G>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111579495 | |||||||
| chr9:111579551 | C | T | 3 | a0002c0002t0002g0025 a0002c0002t0002g0224 a0002c0002t0002g0225 |
4 | HG01192.hp2 HG02922.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.496-600G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111579551 | |||||||
| chr9:111579691 | C | T | 22 | a0001c0001t0001g0013 a0001c0001t0001g0115 a0001c0001t0001g0117 others(19): Show |
24 | HG00408.hp2 HG00642.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.496-740G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111579691 | |||||||
| chr9:111579793 | T | C | 1 | a0001c0001t0002g0119 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.496-842A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111579793 | |||||||
| chr9:111579798 | G | A | 3 | a0002c0002t0001g0136 a0002c0002t0001g0139 a0002c0002t0001g0168 |
3 | HG01346.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.496-847C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111579798 | |||||||
| chr9:111579866 | G | A | 5 | a0002c0002t0002g0019 a0002c0002t0002g0169 a0002c0002t0002g0175 others(2): Show |
6 | HG00140.hp2 HG01106.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.496-915C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111579866 | |||||||
| chr9:111580026 | C | T | 1 | a0001c0001t0001g0343 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.496-1075G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111580026 | |||||||
| chr9:111580098 | A | G | 105 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(102): Show |
113 | HG00099.hp1 HG00408.hp2 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.496-1147T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111580098 | |||||||
| chr9:111580166 | A | G | 2 | a0001c0001t0001g0034 a0001c0001t0002g0313 |
3 | HG02615.hp2 HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.496-1215T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111580166 | |||||||
| chr9:111580233 | G | A | 1 | a0002c0002t0001g0154 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.496-1282C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111580233 | |||||||
| chr9:111580389 | A | C | 37 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(34): Show |
41 | HG00738.hp2 HG01074.hp2 HG01358.hp2 others(38): Show |
intron_variant | MODIFIER | c.496-1438T>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111580389 | |||||||
| chr9:111580436 | C | T | 2 | a0001c0001t0001g0359 a0001c0001t0002g0098 |
2 | HG01261.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.496-1485G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111580436 | |||||||
| chr9:111580482 | G | A | 36 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(33): Show |
38 | HG00408.hp2 HG00642.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.496-1531C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111580482 | |||||||
| chr9:111580485 | G | A | 37 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(34): Show |
41 | HG00738.hp2 HG01074.hp2 HG01358.hp2 others(38): Show |
intron_variant | MODIFIER | c.496-1534C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111580485 | |||||||
| chr9:111580668 | T | C | 44 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0256 others(41): Show |
51 | HG00140.hp1 HG00558.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.496-1717A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111580668 | |||||||
| chr9:111580679 | T | C | 342 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(339): Show |
389 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.496-1728A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111580679 | |||||||
| chr9:111580680 | G | A | 34 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(31): Show |
39 | HG00408.hp2 HG00642.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.496-1729C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111580680 | |||||||
| chr9:111580709 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.496-1758G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111580709 | |||||||
| chr9:111580713 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.496-1762G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111580713 | |||||||
| chr9:111580755 | C | CA | 99 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(96): Show |
107 | HG00099.hp1 HG00408.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.496-1805dupT | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111580755 | |||||||
| chr9:111580861 | C | T | 103 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(100): Show |
111 | HG00099.hp1 HG00408.hp2 HG00642.hp1 others(108): Show |
intron_variant | MODIFIER | c.496-1910G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111580861 | |||||||
| chr9:111580894 | G | C | 1 | a0001c0001t0001g0330 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.496-1943C>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111580894 | |||||||
| chr9:111581096 | G | T | 70 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(67): Show |
76 | HG00408.hp2 HG00642.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.496-2145C>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111581096 | |||||||
| chr9:111581354 | G | A | 49 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(46): Show |
54 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.495+2118C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111581354 | |||||||
| chr9:111581503 | C | A | 103 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(100): Show |
111 | HG00099.hp1 HG00408.hp2 HG00642.hp1 others(108): Show |
intron_variant | MODIFIER | c.495+1969G>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111581503 | |||||||
| chr9:111581558 | C | T | 1 | a0002c0002t0001g0159 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.495+1914G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111581558 | |||||||
| chr9:111581957 | C | T | 250 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(247): Show |
277 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.495+1515G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111581957 | |||||||
| chr9:111582123 | G | A | 28 | a0001c0001t0001g0004 a0001c0001t0001g0080 a0001c0001t0001g0081 others(25): Show |
30 | HG00099.hp1 HG00741.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.495+1349C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111582123 | |||||||
| chr9:111582210 | CTG | C | 75 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(72): Show |
81 | HG00408.hp2 HG00642.hp1 HG00738.hp2 others(78): Show |
intron_variant | MODIFIER | c.495+1260_495+1261d others(4): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111582210 | |||||||
| chr9:111582328 | C | A | 1 | a0001c0001t0002g0236 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.495+1144G>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111582328 | |||||||
| chr9:111582524 | T | TATA | 103 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(100): Show |
111 | HG00099.hp1 HG00408.hp2 HG00642.hp1 others(108): Show |
intron_variant | MODIFIER | c.495+947_495+948ins others(3): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111582524 | |||||||
| chr9:111582533 | A | T | 37 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(34): Show |
41 | HG00738.hp2 HG01074.hp2 HG01358.hp2 others(38): Show |
intron_variant | MODIFIER | c.495+939T>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111582533 | |||||||
| chr9:111582581 | G | A | 1 | a0002c0002t0001g0158 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.495+891C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111582581 | |||||||
| chr9:111582821 | T | G | 5 | a0002c0002t0001g0131 a0002c0002t0001g0132 a0002c0002t0001g0133 others(2): Show |
5 | HG01070.hp2 HG01928.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.495+651A>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111582821 | |||||||
| chr9:111582825 | A | C | 4 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(1): Show |
4 | HG02559.hp1 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+647T>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111582825 | |||||||
| chr9:111582948 | A | G | 76 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(73): Show |
82 | HG00408.hp2 HG00642.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.495+524T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111582948 | |||||||
| chr9:111582990 | C | A | 1 | a0002c0002t0001g0155 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.495+482G>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111582990 | |||||||
| chr9:111583165 | A | G | 6 | a0002c0002t0001g0020 a0002c0002t0001g0188 a0002c0002t0001g0215 others(3): Show |
7 | HG00408.hp1 HG00438.hp2 HG00673.hp2 others(4): Show |
intron_variant | MODIFIER | c.495+307T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111583165 | |||||||
| chr9:111583305 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0002g0313 |
3 | HG02615.hp2 HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.495+167G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111583305 | |||||||
| chr9:111583430 | T | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0068 a0001c0001t0002g0062 |
3 | HG02965.hp2 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.495+42A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 6/9 | chr9 | 111583430 | |||||||
| chr9:111583650 | A | G | 1 | a0002c0002t0002g0196 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.378-61T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 5/9 | chr9 | 111583650 | |||||||
| chr9:111583761 | C | T | 8 | a0001c0001t0001g0101 a0001c0001t0002g0077 a0001c0001t0002g0078 others(5): Show |
8 | HG00099.hp1 HG01074.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.378-172G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 5/9 | chr9 | 111583761 | |||||||
| chr9:111583772 | G | A | 8 | a0001c0001t0001g0101 a0001c0001t0002g0077 a0001c0001t0002g0078 others(5): Show |
8 | HG00099.hp1 HG01074.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.378-183C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 5/9 | chr9 | 111583772 | |||||||
| chr9:111583891 | G | T | 3 | a0001c0001t0001g0034 a0001c0001t0001g0312 a0001c0001t0002g0313 |
4 | HG02615.hp2 HG02630.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.378-302C>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 5/9 | chr9 | 111583891 | |||||||
| chr9:111583892 | G | A | 2 | a0001c0001t0001g0359 a0001c0001t0002g0098 |
2 | HG01261.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.378-303C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 5/9 | chr9 | 111583892 | |||||||
| chr9:111584096 | G | A | 7 | a0002c0002t0001g0136 a0002c0002t0001g0139 a0002c0002t0001g0168 others(4): Show |
7 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.378-507C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 5/9 | chr9 | 111584096 | |||||||
| chr9:111584182 | G | T | 4 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(1): Show |
4 | HG02559.hp1 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.378-593C>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 5/9 | chr9 | 111584182 | |||||||
| chr9:111584272 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.378-683C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 5/9 | chr9 | 111584272 | |||||||
| chr9:111584381 | C | G | 24 | a0001c0001t0001g0013 a0001c0001t0001g0115 a0001c0001t0001g0117 others(21): Show |
26 | HG00408.hp2 HG00642.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.378-792G>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 5/9 | chr9 | 111584381 | |||||||
| chr9:111584535 | A | C | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
206 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.378-946T>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 5/9 | chr9 | 111584535 | |||||||
| chr9:111584547 | TG | T | 4 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(1): Show |
4 | HG02559.hp1 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.378-959delC | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 5/9 | chr9 | 111584547 | |||||||
| chr9:111584737 | A | C | 3 | a0002c0002t0001g0038 a0002c0002t0001g0040 a0002c0002t0002g0039 |
3 | HG01255.hp1 HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.378-1148T>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 5/9 | chr9 | 111584737 | |||||||
| chr9:111584989 | C | A | 1 | a0001c0001t0001g0336 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.377+1009G>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 5/9 | chr9 | 111584989 | |||||||
| chr9:111585040 | A | G | 18 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0042 others(15): Show |
20 | HG01358.hp2 HG01928.hp1 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.377+958T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 5/9 | chr9 | 111585040 | |||||||
| chr9:111585058 | A | G | 1 | a0002c0002t0001g0124 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.377+940T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 5/9 | chr9 | 111585058 | |||||||
| chr9:111585121 | T | C | 18 | a0001c0001t0001g0004 a0001c0001t0001g0080 a0001c0001t0001g0081 others(15): Show |
20 | HG00741.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.377+877A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 5/9 | chr9 | 111585121 | |||||||
| chr9:111585160 | G | A | 1 | a0002c0002t0001g0156 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.377+838C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 5/9 | chr9 | 111585160 | |||||||
| chr9:111585269 | G | A | 1 | a0002c0002t0001g0120 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.377+729C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 5/9 | chr9 | 111585269 | |||||||
| chr9:111585311 | C | A | 50 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(47): Show |
55 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.377+687G>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 5/9 | chr9 | 111585311 | |||||||
| chr9:111585494 | A | G | 103 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(100): Show |
112 | HG00099.hp1 HG00408.hp2 HG00642.hp1 others(109): Show |
intron_variant | MODIFIER | c.377+504T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 5/9 | chr9 | 111585494 | |||||||
| chr9:111585702 | C | T | 1 | a0002c0002t0001g0157 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.377+296G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 5/9 | chr9 | 111585702 | |||||||
| chr9:111585839 | T | C | 8 | a0002c0002t0001g0246 a0002c0002t0002g0026 a0002c0002t0002g0027 others(5): Show |
10 | HG01192.hp1 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.377+159A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 5/9 | chr9 | 111585839 | |||||||
| chr9:111585913 | C | T | 64 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0033 others(61): Show |
73 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.377+85G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 5/9 | chr9 | 111585913 | |||||||
| chr9:111586233 | G | A | 103 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(100): Show |
112 | HG00099.hp1 HG00408.hp2 HG00642.hp1 others(109): Show |
intron_variant | MODIFIER | c.210-68C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111586233 | |||||||
| chr9:111586284 | G | A | 65 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0033 others(62): Show |
74 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.210-119C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111586284 | |||||||
| chr9:111586337 | C | T | 76 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(73): Show |
83 | HG00408.hp2 HG00642.hp1 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.210-172G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111586337 | |||||||
| chr9:111586408 | C | T | 1 | a0001c0001t0001g0325 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.210-243G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111586408 | |||||||
| chr9:111586518 | T | C | 3 | a0002c0002t0001g0038 a0002c0002t0001g0040 a0002c0002t0002g0039 |
3 | HG01255.hp1 HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.210-353A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111586518 | |||||||
| chr9:111586565 | T | C | 65 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0033 others(62): Show |
74 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.210-400A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111586565 | |||||||
| chr9:111586580 | G | C | 168 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(165): Show |
186 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.210-415C>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111586580 | |||||||
| chr9:111586726 | T | A | 8 | a0001c0001t0001g0265 a0001c0001t0002g0029 a0001c0001t0002g0258 others(5): Show |
9 | NA18943.hp2 NA18944.hp2 NA18946.hp1 others(6): Show |
intron_variant | MODIFIER | c.210-561A>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111586726 | |||||||
| chr9:111586782 | A | ACT | 11 | a0001c0001t0001g0042 a0001c0001t0001g0058 a0001c0001t0001g0059 others(8): Show |
11 | HG01978.hp2 HG02055.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.210-619_210-618dup others(2): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111586782 | |||||||
| chr9:111586782 | A | ACTCT | 36 | a0001c0001t0001g0008 a0001c0001t0001g0034 a0001c0001t0001g0035 others(33): Show |
42 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.210-621_210-618dup others(4): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111586782 | |||||||
| chr9:111586799 | C | A | 10 | a0001c0001t0001g0028 a0001c0001t0001g0257 a0001c0001t0001g0266 others(7): Show |
11 | HG01515.hp1 HG01516.hp1 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.210-634G>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111586799 | |||||||
| chr9:111586801 | C | A | 20 | a0001c0001t0001g0028 a0001c0001t0001g0251 a0001c0001t0001g0257 others(17): Show |
22 | HG00280.hp2 HG01070.hp2 HG01515.hp1 others(19): Show |
intron_variant | MODIFIER | c.210-636G>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111586801 | |||||||
| chr9:111586803 | C | A | 39 | a0001c0001t0001g0028 a0001c0001t0001g0088 a0001c0001t0001g0251 others(36): Show |
44 | HG00280.hp2 HG01070.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.210-638G>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111586803 | |||||||
| chr9:111586803 | C | CTA | 4 | a0001c0001t0002g0284 a0002c0002t0002g0193 a0002c0002t0002g0196 others(1): Show |
4 | HG02280.hp1 HG02896.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.210-640_210-639dup others(2): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111586803 | |||||||
| chr9:111586803 | C | CTATA | 3 | a0001c0001t0001g0337 a0001c0001t0002g0344 a0001c0001t0002g0353 |
3 | HG01256.hp2 HG01258.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.210-642_210-639dup others(4): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111586803 | |||||||
| chr9:111586803 | C | CTCTA | 13 | a0001c0001t0001g0312 a0001c0001t0001g0317 a0001c0001t0001g0319 others(10): Show |
13 | HG00597.hp2 HG00639.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.210-639_210-638ins others(4): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111586803 | |||||||
| chr9:111586803 | CTA | C | 7 | a0001c0001t0001g0101 a0001c0001t0002g0077 a0001c0001t0002g0078 others(4): Show |
7 | HG01074.hp1 HG02622.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.210-640_210-639del others(2): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111586803 | |||||||
| chr9:111586805 | A | C | 160 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(157): Show |
176 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.210-640T>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111586805 | |||||||
| chr9:111586807 | A | C | 52 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(49): Show |
56 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.210-642T>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111586807 | |||||||
| chr9:111586809 | A | C | 23 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(20): Show |
26 | HG00738.hp2 HG01074.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.210-644T>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111586809 | |||||||
| chr9:111586811 | A | C | 1 | a0001c0001t0001g0055 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.210-646T>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111586811 | |||||||
| chr9:111586826 | CT | C | 51 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(48): Show |
56 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.210-662delA | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111586826 | |||||||
| chr9:111586831 | T | C | 37 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(34): Show |
41 | HG00738.hp2 HG01074.hp2 HG01358.hp2 others(38): Show |
intron_variant | MODIFIER | c.210-666A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111586831 | |||||||
| chr9:111586970 | A | C | 5 | a0002c0002t0004g0135 a0002c0002t0004g0163 a0002c0002t0004g0164 others(2): Show |
5 | NA18952.hp2 NA18970.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.210-805T>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111586970 | |||||||
| chr9:111587079 | T | C | 2 | a0002c0002t0001g0159 a0002c0002t0001g0160 |
2 | NA18951.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.210-914A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111587079 | |||||||
| chr9:111587097 | A | G | 230 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(227): Show |
255 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.210-932T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111587097 | |||||||
| chr9:111587455 | T | G | 65 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0033 others(62): Show |
74 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.210-1290A>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111587455 | |||||||
| chr9:111587544 | C | T | 1 | a0002c0002t0001g0134 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.210-1379G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111587544 | |||||||
| chr9:111587596 | C | T | 103 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(100): Show |
112 | HG00099.hp1 HG00408.hp2 HG00642.hp1 others(109): Show |
intron_variant | MODIFIER | c.210-1431G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111587596 | |||||||
| chr9:111587608 | C | T | 103 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(100): Show |
112 | HG00099.hp1 HG00408.hp2 HG00642.hp1 others(109): Show |
intron_variant | MODIFIER | c.210-1443G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111587608 | |||||||
| chr9:111587969 | T | G | 13 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0256 others(10): Show |
17 | HG02080.hp2 HG02135.hp1 NA18955.hp1 others(14): Show |
intron_variant | MODIFIER | c.210-1804A>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111587969 | |||||||
| chr9:111588013 | T | TTTTC | 216 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(213): Show |
239 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.210-1852_210-1849d others(6): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111588013 | |||||||
| chr9:111588100 | A | G | 2 | a0002c0002t0001g0007 a0002c0002t0001g0185 |
4 | HG01884.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.210-1935T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111588100 | |||||||
| chr9:111588140 | TGAGTAGC others(7): Show |
T | 1 | a0001c0001t0003g0290 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.210-1989_210-1976d others(16): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111588140 | |||||||
| chr9:111588196 | A | AT | 67 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0043 others(64): Show |
71 | HG00099.hp1 HG00408.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.210-2032dupA | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111588196 | |||||||
| chr9:111588196 | A | ATT | 36 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(33): Show |
40 | HG00738.hp2 HG01074.hp2 HG01358.hp2 others(37): Show |
intron_variant | MODIFIER | c.210-2033_210-2032d others(4): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111588196 | |||||||
| chr9:111588196 | AT | A | 53 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(50): Show |
58 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.210-2032delA | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111588196 | |||||||
| chr9:111588257 | C | T | 103 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(100): Show |
112 | HG00099.hp1 HG00408.hp2 HG00642.hp1 others(109): Show |
intron_variant | MODIFIER | c.210-2092G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111588257 | |||||||
| chr9:111588283 | G | A | 3 | a0002c0002t0001g0038 a0002c0002t0001g0040 a0002c0002t0002g0039 |
3 | HG01255.hp1 HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.210-2118C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111588283 | |||||||
| chr9:111588302 | T | C | 2 | a0002c0002t0001g0190 a0002c0002t0001g0191 |
2 | HG01255.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.210-2137A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111588302 | |||||||
| chr9:111588319 | C | G | 23 | a0002c0002t0001g0221 a0002c0002t0002g0024 a0002c0002t0002g0025 others(20): Show |
25 | HG01192.hp2 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.210-2154G>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111588319 | |||||||
| chr9:111588359 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.210-2194G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111588359 | |||||||
| chr9:111588522 | C | A | 2 | a0001c0001t0002g0269 a0001c0001t0002g0286 |
2 | NA18944.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.210-2357G>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111588522 | |||||||
| chr9:111588568 | C | T | 1 | a0001c0001t0002g0255 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.210-2403G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111588568 | |||||||
| chr9:111588582 | A | G | 1 | a0001c0001t0002g0083 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.210-2417T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111588582 | |||||||
| chr9:111588682 | C | T | 4 | a0001c0001t0001g0035 a0001c0001t0001g0300 a0001c0001t0001g0346 others(1): Show |
5 | HG00544.hp2 NA18946.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.210-2517G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111588682 | |||||||
| chr9:111588861 | C | T | 24 | a0001c0001t0001g0013 a0001c0001t0001g0115 a0001c0001t0001g0117 others(21): Show |
26 | HG00408.hp2 HG00642.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.210-2696G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111588861 | |||||||
| chr9:111589070 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.210-2905C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111589070 | |||||||
| chr9:111589081 | C | T | 7 | a0002c0002t0002g0122 a0002c0002t0002g0123 a0002c0002t0002g0193 others(4): Show |
7 | HG02280.hp1 HG02895.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.210-2916G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111589081 | |||||||
| chr9:111589202 | G | A | 3 | a0001c0001t0001g0117 a0001c0001t0002g0110 a0001c0001t0002g0111 |
3 | HG01123.hp2 HG03490.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.210-3037C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111589202 | |||||||
| chr9:111589390 | T | C | 1 | a0001c0001t0002g0094 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.210-3225A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111589390 | |||||||
| chr9:111589468 | G | C | 1 | a0001c0001t0001g0271 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.210-3303C>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111589468 | |||||||
| chr9:111589469 | C | G | 1 | a0001c0001t0001g0271 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.210-3304G>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111589469 | |||||||
| chr9:111589550 | G | C | 220 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(217): Show |
243 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.209+3376C>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111589550 | |||||||
| chr9:111589582 | T | C | 8 | a0002c0002t0001g0246 a0002c0002t0002g0026 a0002c0002t0002g0027 others(5): Show |
10 | HG01192.hp1 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.209+3344A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111589582 | |||||||
| chr9:111589642 | C | CT | 8 | a0002c0002t0001g0038 a0002c0002t0001g0040 a0002c0002t0001g0131 others(5): Show |
8 | HG01070.hp2 HG01255.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.209+3283dupA | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111589642 | |||||||
| chr9:111589642 | CT | C | 33 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(30): Show |
35 | HG00408.hp2 HG00642.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.209+3283delA | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111589642 | |||||||
| chr9:111589764 | A | AG | 21 | a0001c0001t0001g0028 a0001c0001t0001g0251 a0001c0001t0001g0257 others(18): Show |
23 | HG00280.hp2 HG01515.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.209+3161dupC | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111589764 | |||||||
| chr9:111589877 | C | G | 1 | a0001c0001t0001g0271 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.209+3049G>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111589877 | |||||||
| chr9:111589878 | G | C | 1 | a0001c0001t0001g0271 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.209+3048C>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111589878 | |||||||
| chr9:111590195 | G | A | 25 | a0002c0002t0001g0182 a0002c0002t0001g0192 a0002c0002t0001g0221 others(22): Show |
27 | HG00735.hp1 HG01192.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.209+2731C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111590195 | |||||||
| chr9:111590207 | T | C | 8 | a0002c0002t0001g0246 a0002c0002t0002g0026 a0002c0002t0002g0027 others(5): Show |
10 | HG01192.hp1 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.209+2719A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111590207 | |||||||
| chr9:111590311 | T | C | 8 | a0002c0002t0001g0246 a0002c0002t0002g0026 a0002c0002t0002g0027 others(5): Show |
10 | HG01192.hp1 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.209+2615A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111590311 | |||||||
| chr9:111590312 | G | A | 32 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(29): Show |
34 | HG00408.hp2 HG00642.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.209+2614C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111590312 | |||||||
| chr9:111590343 | T | C | 1 | a0001c0001t0002g0248 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.209+2583A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111590343 | |||||||
| chr9:111590347 | G | A | 172 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(169): Show |
190 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.209+2579C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111590347 | |||||||
| chr9:111590462 | A | G | 169 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(166): Show |
187 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.209+2464T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111590462 | |||||||
| chr9:111590529 | C | T | 251 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(248): Show |
278 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.209+2397G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111590529 | |||||||
| chr9:111590547 | T | C | 1 | a0002c0002t0001g0212 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.209+2379A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111590547 | |||||||
| chr9:111590707 | A | C | 2 | a0001c0001t0001g0359 a0001c0001t0002g0098 |
2 | HG01261.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.209+2219T>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111590707 | |||||||
| chr9:111590907 | G | C | 38 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(35): Show |
42 | HG00544.hp1 HG00738.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.209+2019C>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111590907 | |||||||
| chr9:111590918 | T | C | 21 | a0001c0001t0001g0028 a0001c0001t0001g0251 a0001c0001t0001g0257 others(18): Show |
23 | HG00280.hp2 HG01515.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.209+2008A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111590918 | |||||||
| chr9:111590963 | T | TAGAA | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(249): Show |
279 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.209+1962_209+1963i others(6): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111590963 | |||||||
| chr9:111591066 | C | T | 3 | a0002c0002t0001g0038 a0002c0002t0001g0040 a0002c0002t0002g0039 |
3 | HG01255.hp1 HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.209+1860G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111591066 | |||||||
| chr9:111591082 | G | A | 2 | a0002c0002t0001g0180 a0002c0002t0001g0181 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.209+1844C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111591082 | |||||||
| chr9:111591148 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.209+1778C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111591148 | |||||||
| chr9:111591238 | G | A | 3 | a0001c0001t0002g0029 a0001c0001t0002g0258 a0001c0001t0002g0270 |
4 | NA18946.hp1 NA18990.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.209+1688C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111591238 | |||||||
| chr9:111591254 | G | A | 2 | a0001c0001t0002g0077 a0001c0001t0002g0078 |
2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.209+1672C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111591254 | |||||||
| chr9:111591293 | G | A | 7 | a0001c0001t0002g0005 a0001c0001t0002g0106 a0001c0001t0002g0107 others(4): Show |
8 | HG00642.hp1 HG01106.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.209+1633C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111591293 | |||||||
| chr9:111591295 | C | T | 1 | a0002c0002t0002g0026 | 2 | HG01192.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.209+1631G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111591295 | |||||||
| chr9:111591341 | A | C | 3 | a0001c0001t0001g0034 a0001c0001t0001g0312 a0001c0001t0002g0313 |
4 | HG02615.hp2 HG02630.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.209+1585T>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111591341 | |||||||
| chr9:111591370 | C | CT | 6 | a0002c0002t0001g0120 a0002c0002t0001g0129 a0002c0002t0002g0130 others(3): Show |
6 | HG00280.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.209+1555dupA | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111591370 | |||||||
| chr9:111591370 | CT | C | 38 | a0001c0001t0001g0034 a0001c0001t0001g0080 a0001c0001t0001g0081 others(35): Show |
39 | HG00099.hp1 HG01074.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.209+1555delA | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111591370 | |||||||
| chr9:111591375 | T | C | 64 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0033 others(61): Show |
73 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.209+1551A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111591375 | |||||||
| chr9:111591376 | T | C | 2 | a0001c0001t0001g0271 a0001c0001t0002g0119 |
2 | HG03017.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.209+1550A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111591376 | |||||||
| chr9:111591495 | G | A | 49 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(46): Show |
54 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.209+1431C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111591495 | |||||||
| chr9:111591590 | G | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0003g0290 |
3 | HG02027.hp2 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.209+1336C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111591590 | |||||||
| chr9:111591610 | A | T | 221 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(218): Show |
244 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.209+1316T>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111591610 | |||||||
| chr9:111591708 | T | C | 2 | a0002c0002t0001g0182 a0002c0002t0001g0192 |
2 | HG00735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.209+1218A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111591708 | |||||||
| chr9:111591755 | T | C | 38 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(35): Show |
42 | HG00544.hp1 HG00738.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.209+1171A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111591755 | |||||||
| chr9:111591813 | C | T | 30 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(27): Show |
34 | HG00544.hp1 HG00738.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.209+1113G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111591813 | |||||||
| chr9:111591814 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.209+1112C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111591814 | |||||||
| chr9:111591904 | G | A | 3 | a0002c0002t0001g0038 a0002c0002t0001g0040 a0002c0002t0002g0039 |
3 | HG01255.hp1 HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.209+1022C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111591904 | |||||||
| chr9:111592032 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.209+894G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111592032 | |||||||
| chr9:111592217 | G | C | 62 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0033 others(59): Show |
71 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.209+709C>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111592217 | |||||||
| chr9:111592238 | C | G | 1 | a0001c0001t0001g0293 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.209+688G>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111592238 | |||||||
| chr9:111592470 | A | C | 18 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0042 others(15): Show |
20 | HG01358.hp2 HG01928.hp1 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.209+456T>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111592470 | |||||||
| chr9:111592490 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.209+436G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111592490 | |||||||
| chr9:111592509 | G | A | 1 | a0002c0002t0001g0199 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.209+417C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111592509 | |||||||
| chr9:111592538 | C | T | 1 | a0002c0002t0001g0128 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.209+388G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111592538 | |||||||
| chr9:111592594 | G | A | 22 | a0002c0002t0001g0221 a0002c0002t0002g0024 a0002c0002t0002g0025 others(19): Show |
24 | HG01192.hp2 HG01884.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.209+332C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111592594 | |||||||
| chr9:111592607 | A | G | 1 | a0002c0002t0001g0127 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.209+319T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111592607 | |||||||
| chr9:111592610 | AAG | A | 8 | a0002c0002t0001g0246 a0002c0002t0002g0026 a0002c0002t0002g0027 others(5): Show |
10 | HG01192.hp1 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.209+314_209+315del others(2): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111592610 | |||||||
| chr9:111592751 | C | T | 1 | a0001c0001t0002g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.209+175G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 4/9 | chr9 | 111592751 | |||||||
| chr9:111592986 | C | CAAA | 4 | a0002c0002t0001g0246 a0002c0002t0002g0026 a0002c0002t0002g0027 others(1): Show |
6 | HG01192.hp1 HG02559.hp2 HG02723.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.153-7_153-5dupTTT | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 3/9 | chr9 | 111592986 | |||||||
| chr9:111592986 | CA | C | 82 | a0001c0001t0001g0048 a0001c0001t0001g0065 a0001c0001t0001g0066 others(79): Show |
88 | HG00140.hp2 HG00408.hp1 HG00621.hp1 others(85): Show |
splice_region_variant&intron_variant | LOW | c.153-5delT | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 3/9 | chr9 | 111592986 | |||||||
| chr9:111592986 | CAA | C | 179 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(176): Show |
211 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(208): Show |
splice_region_variant&intron_variant | LOW | c.153-6_153-5delTT | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 3/9 | chr9 | 111592986 | |||||||
| chr9:111592986 | CAAA | C | 27 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0257 others(24): Show |
31 | HG00280.hp2 HG00741.hp2 HG01070.hp1 others(28): Show |
splice_region_variant&intron_variant | LOW | c.153-7_153-5delTTT | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 3/9 | chr9 | 111592986 | |||||||
| chr9:111592986 | CAAAA | C | 7 | a0001c0001t0001g0034 a0001c0001t0001g0312 a0001c0001t0002g0095 others(4): Show |
8 | HG01255.hp1 HG02559.hp1 HG02630.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.153-8_153-5delTTTT | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 3/9 | chr9 | 111592986 | |||||||
| chr9:111592986 | CAAAAAAA others(4): Show |
C | 7 | a0001c0001t0001g0013 a0001c0001t0001g0115 a0001c0001t0002g0306 others(4): Show |
8 | HG00408.hp2 HG01243.hp2 HG02132.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.153-15_153-5delTTT others(8): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 3/9 | chr9 | 111592986 | |||||||
| chr9:111592986 | CAAAAAAA others(5): Show |
C | 23 | a0001c0001t0001g0117 a0001c0001t0001g0237 a0001c0001t0002g0005 others(20): Show |
24 | HG00642.hp1 HG01081.hp1 HG01106.hp2 others(21): Show |
splice_region_variant&intron_variant | LOW | c.153-16_153-5delTTT others(9): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 3/9 | chr9 | 111592986 | |||||||
| chr9:111593103 | A | G | 7 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(4): Show |
7 | HG01081.hp2 HG01891.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.153-121T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 3/9 | chr9 | 111593103 | |||||||
| chr9:111593296 | T | C | 1 | a0002c0002t0001g0246 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.153-314A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 3/9 | chr9 | 111593296 | |||||||
| chr9:111593573 | T | C | 4 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(1): Show |
4 | HG02559.hp1 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-591A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 3/9 | chr9 | 111593573 | |||||||
| chr9:111593644 | T | C | 2 | a0001c0001t0002g0259 a0001c0001t0002g0301 |
2 | NA18966.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.152+578A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 3/9 | chr9 | 111593644 | |||||||
| chr9:111593918 | AG | A | 104 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(101): Show |
113 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.152+303delC | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 3/9 | chr9 | 111593918 | |||||||
| chr9:111593994 | G | C | 61 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0033 others(58): Show |
70 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.152+228C>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 3/9 | chr9 | 111593994 | |||||||
| chr9:111594087 | T | C | 219 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(216): Show |
242 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.152+135A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 3/9 | chr9 | 111594087 | |||||||
| chr9:111594196 | A | G | 2 | a0001c0001t0002g0259 a0001c0001t0002g0301 |
2 | NA18966.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.152+26T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 3/9 | chr9 | 111594196 | |||||||
| chr9:111594323 | T | C | 4 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0097 others(1): Show |
4 | HG02559.hp1 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-56A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111594323 | |||||||
| chr9:111594379 | C | T | 213 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(210): Show |
235 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.107-112G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111594379 | |||||||
| chr9:111594416 | G | T | 2 | a0001c0001t0002g0107 a0001c0001t0002g0108 |
2 | HG01109.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.107-149C>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111594416 | |||||||
| chr9:111594423 | C | T | 1 | a0002c0002t0002g0217 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.107-156G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111594423 | |||||||
| chr9:111594458 | T | C | 61 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0033 others(58): Show |
70 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.107-191A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111594458 | |||||||
| chr9:111594513 | C | T | 1 | a0001c0001t0002g0083 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.107-246G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111594513 | |||||||
| chr9:111594546 | A | ATCC | 23 | a0001c0001t0001g0004 a0001c0001t0001g0080 a0001c0001t0001g0084 others(20): Show |
25 | HG00099.hp1 HG00741.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.107-280_107-279ins others(3): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111594546 | |||||||
| chr9:111594546 | A | ATCCT | 4 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0101 others(1): Show |
4 | HG02738.hp2 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-280_107-279ins others(4): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111594546 | |||||||
| chr9:111594549 | C | CT | 10 | a0001c0001t0001g0053 a0001c0001t0001g0257 a0001c0001t0001g0293 others(7): Show |
10 | HG01255.hp1 HG03041.hp1 HG03195.hp1 others(7): Show |
intron_variant | MODIFIER | c.107-283dupA | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111594549 | |||||||
| chr9:111594549 | C | CTT | 122 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(119): Show |
133 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.107-284_107-283dup others(2): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111594549 | |||||||
| chr9:111594549 | C | T | 27 | a0001c0001t0001g0004 a0001c0001t0001g0080 a0001c0001t0001g0081 others(24): Show |
29 | HG00099.hp1 HG00741.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.107-282G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111594549 | |||||||
| chr9:111594742 | C | T | 7 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0052 others(4): Show |
7 | HG02015.hp2 HG02717.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.107-475G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111594742 | |||||||
| chr9:111594830 | G | A | 2 | a0001c0001t0003g0291 a0001c0001t0003g0292 |
2 | NA18961.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.107-563C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111594830 | |||||||
| chr9:111594851 | C | CT | 72 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0033 others(69): Show |
82 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.107-585dupA | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111594851 | |||||||
| chr9:111594851 | C | CTT | 47 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(44): Show |
52 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.107-586_107-585dup others(2): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111594851 | |||||||
| chr9:111594851 | CT | C | 66 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(63): Show |
72 | HG00544.hp1 HG00738.hp2 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.107-585delA | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111594851 | |||||||
| chr9:111594874 | A | C | 1 | a0001c0001t0001g0318 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.107-607T>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111594874 | |||||||
| chr9:111594879 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.107-612A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111594879 | |||||||
| chr9:111595379 | T | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0028 others(112): Show |
130 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.107-1112A>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111595379 | |||||||
| chr9:111595441 | C | T | 2 | a0002c0002t0002g0122 a0002c0002t0002g0123 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.107-1174G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111595441 | |||||||
| chr9:111595662 | C | A | 10 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0256 others(7): Show |
14 | HG02135.hp1 NA18955.hp1 NA18960.hp1 others(11): Show |
intron_variant | MODIFIER | c.107-1395G>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111595662 | |||||||
| chr9:111595672 | C | T | 115 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0028 others(112): Show |
130 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.107-1405G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111595672 | |||||||
| chr9:111595933 | G | A | 1 | a0002c0002t0002g0202 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.106+1384C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111595933 | |||||||
| chr9:111595960 | C | T | 1 | a0001c0001t0001g0321 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.106+1357G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111595960 | |||||||
| chr9:111595997 | A | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
6 | HG02040.hp1 HG02074.hp1 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.106+1320T>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111595997 | |||||||
| chr9:111596084 | A | G | 1 | a0002c0002t0001g0121 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.106+1233T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111596084 | |||||||
| chr9:111596123 | G | T | 1 | a0002c0002t0001g0120 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.106+1194C>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111596123 | |||||||
| chr9:111596473 | G | A | 2 | a0001c0001t0001g0359 a0001c0001t0002g0098 |
2 | HG01261.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.106+844C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111596473 | |||||||
| chr9:111596490 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.106+827G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111596490 | |||||||
| chr9:111596587 | C | T | 8 | a0001c0001t0001g0101 a0001c0001t0002g0077 a0001c0001t0002g0078 others(5): Show |
8 | HG00099.hp1 HG01074.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.106+730G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111596587 | |||||||
| chr9:111596596 | C | CA | 82 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0033 others(79): Show |
93 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.106+720dupT | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111596596 | |||||||
| chr9:111596615 | G | T | 1 | a0002c0002t0001g0247 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.106+702C>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111596615 | |||||||
| chr9:111596711 | G | A | 1 | a0001c0001t0002g0255 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.106+606C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111596711 | |||||||
| chr9:111596797 | C | T | 1 | a0001c0001t0002g0248 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.106+520G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111596797 | |||||||
| chr9:111596837 | G | T | 1 | a0001c0001t0002g0320 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.106+480C>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111596837 | |||||||
| chr9:111596877 | A | C | 1 | a0001c0001t0002g0255 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.106+440T>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111596877 | |||||||
| chr9:111596899 | C | A | 1 | a0001c0001t0001g0349 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.106+418G>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111596899 | |||||||
| chr9:111596905 | C | A | 2 | a0001c0001t0001g0317 a0001c0001t0001g0350 |
2 | HG02738.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.106+412G>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111596905 | |||||||
| chr9:111596926 | C | CA | 50 | a0001c0001t0001g0008 a0001c0001t0001g0034 a0001c0001t0001g0035 others(47): Show |
56 | HG00558.hp2 HG00597.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.106+390dupT | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111596926 | |||||||
| chr9:111596926 | C | CAA | 90 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(87): Show |
97 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.106+389_106+390dup others(2): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111596926 | |||||||
| chr9:111596926 | C | CAAA | 6 | a0001c0001t0001g0012 a0001c0001t0001g0075 a0001c0001t0001g0076 others(3): Show |
7 | HG00738.hp2 HG01074.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.106+388_106+390dup others(3): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111596926 | |||||||
| chr9:111596926 | C | CAAAA | 17 | a0001c0001t0001g0101 a0001c0001t0002g0077 a0001c0001t0002g0102 others(14): Show |
19 | HG00099.hp1 HG01074.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.106+387_106+390dup others(4): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111596926 | |||||||
| chr9:111596926 | CA | C | 108 | a0001c0001t0001g0028 a0001c0001t0002g0248 a0001c0001t0002g0252 others(105): Show |
128 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.106+390delT | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 2/9 | chr9 | 111596926 | |||||||
| chr9:111597876 | C | T | 1 | a0001c0001t0001g0251 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-10-444G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 1/9 | chr9 | 111597876 | |||||||
| chr9:111597909 | T | C | 4 | a0002c0002t0002g0227 a0002c0002t0002g0228 a0002c0002t0002g0229 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-477A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 1/9 | chr9 | 111597909 | |||||||
| chr9:111597921 | C | G | 216 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(213): Show |
239 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.-10-489G>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 1/9 | chr9 | 111597921 | |||||||
| chr9:111597994 | GT | G | 63 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0033 others(60): Show |
72 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.-10-563delA | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 1/9 | chr9 | 111597994 | |||||||
| chr9:111597994 | GTT | G | 101 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(98): Show |
110 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.-10-564_-10-563del others(2): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 1/9 | chr9 | 111597994 | |||||||
| chr9:111598006 | T | A | 2 | a0001c0001t0001g0305 a0001c0001t0001g0357 |
2 | HG02080.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.-10-574A>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 1/9 | chr9 | 111598006 | |||||||
| chr9:111598007 | T | A | 46 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(43): Show |
51 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.-10-575A>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 1/9 | chr9 | 111598007 | |||||||
| chr9:111598008 | T | A | 53 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(50): Show |
58 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-10-576A>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 1/9 | chr9 | 111598008 | |||||||
| chr9:111598387 | T | G | 3 | a0002c0002t0001g0038 a0002c0002t0001g0040 a0002c0002t0002g0039 |
3 | HG01255.hp1 HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-10-955A>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 1/9 | chr9 | 111598387 | |||||||
| chr9:111598495 | A | T | 17 | a0001c0001t0001g0013 a0001c0001t0001g0115 a0001c0001t0001g0117 others(14): Show |
19 | HG00408.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-10-1063T>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 1/9 | chr9 | 111598495 | |||||||
| chr9:111598561 | C | G | 1 | a0001c0001t0001g0004 | 3 | HG00741.hp2 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-11+1042G>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 1/9 | chr9 | 111598561 | |||||||
| chr9:111598665 | T | G | 8 | a0002c0002t0001g0246 a0002c0002t0002g0026 a0002c0002t0002g0027 others(5): Show |
10 | HG01192.hp1 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-11+938A>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 1/9 | chr9 | 111598665 | |||||||
| chr9:111598666 | T | G | 1 | a0002c0002t0001g0247 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-11+937A>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 1/9 | chr9 | 111598666 | |||||||
| chr9:111598754 | C | T | 1 | a0001c0001t0002g0105 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-11+849G>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 1/9 | chr9 | 111598754 | |||||||
| chr9:111598772 | G | T | 5 | a0001c0001t0002g0306 a0001c0001t0002g0307 a0001c0001t0002g0308 others(2): Show |
5 | HG01243.hp2 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+831C>A | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 1/9 | chr9 | 111598772 | |||||||
| chr9:111598799 | G | A | 30 | a0001c0001t0001g0004 a0001c0001t0001g0080 a0001c0001t0001g0081 others(27): Show |
32 | HG00099.hp1 HG00741.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.-11+804C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 1/9 | chr9 | 111598799 | |||||||
| chr9:111598836 | G | GT | 76 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(73): Show |
82 | HG00099.hp1 HG00544.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.-11+766dupA | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 1/9 | chr9 | 111598836 | |||||||
| chr9:111599075 | C | A | 3 | a0002c0002t0001g0038 a0002c0002t0001g0040 a0002c0002t0002g0039 |
3 | HG01255.hp1 HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-11+528G>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 1/9 | chr9 | 111599075 | |||||||
| chr9:111599137 | A | G | 195 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(192): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.-11+466T>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 1/9 | chr9 | 111599137 | |||||||
| chr9:111599141 | T | C | 65 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0033 others(62): Show |
74 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.-11+462A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 1/9 | chr9 | 111599141 | |||||||
| chr9:111599186 | C | G | 1 | a0002c0002t0001g0041 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-11+417G>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 1/9 | chr9 | 111599186 | |||||||
| chr9:111599375 | C | G | 3 | a0002c0002t0001g0038 a0002c0002t0001g0040 a0002c0002t0002g0039 |
3 | HG01255.hp1 HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-11+228G>C | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 1/9 | chr9 | 111599375 | |||||||
| chr9:111599379 | G | C | 53 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0036 others(50): Show |
58 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.-11+224C>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 1/9 | chr9 | 111599379 | |||||||
| chr9:111599427 | G | C | 51 | a0001c0001t0001g0008 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
57 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.-11+176C>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 1/9 | chr9 | 111599427 | |||||||
| chr9:111599475 | T | C | 1 | a0001c0001t0002g0358 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-11+128A>G | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 1/9 | chr9 | 111599475 | |||||||
| chr9:111599487 | G | A | 1 | a0001c0001t0001g0359 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-11+116C>T | PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 1/9 | chr9 | 111599487 |