Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5742 |
| ensemblid | ENSG00000095303.17 |
| hgncid | 9604 |
| symbol | PTGS1 |
| name | prostaglandin-endoperoxide synthase 1 |
| refseq_nuc | NM_000962.4 |
| refseq_prot | NP_000953.2 |
| ensembl_nuc | ENST00000362012.7 |
| ensembl_prot | ENSP00000354612.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 122371024 |
| end | 122395703 |
| strand | + |
| ver | v1.2 |
| region | chr9:122371024-122395703 |
| region5000 | chr9:122366024-122400703 |
| regionname0 | PTGS1_chr9_122371024_122395703 |
| regionname5000 | PTGS1_chr9_122366024_122400703 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 599 | 279 | 82 | 52 | 110 | 6 | 28 | 78 | PTGS1_chr9_122366024_122400703 | PTGS1 | MSRSL others(594): Show |
chr9 | 122366024 | 122400703 |
| a0002 | 1/0 | 599 | 23 | 0 | 3 | 5 | 4 | 10 | 5 | PTGS1_chr9_122366024_122400703 | PTGS1 | MSRSL others(594): Show |
chr9 | 122366024 | 122400703 |
| a0003 | 0/0 | 599 | 16 | 13 | 2 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | MSRSL others(594): Show |
chr9 | 122366024 | 122400703 |
| a0004 | 0/0 | 599 | 5 | 0 | 5 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | MSRSL others(594): Show |
chr9 | 122366024 | 122400703 |
| a0005 | 0/0 | 599 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | MSRSL others(594): Show |
chr9 | 122366024 | 122400703 |
| a0006 | 0/0 | 599 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | MSRSL others(594): Show |
chr9 | 122366024 | 122400703 |
| a0007 | 0/0 | 599 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | MSRSL others(594): Show |
chr9 | 122366024 | 122400703 |
| a0008 | 0/0 | 599 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | MSRSL others(594): Show |
chr9 | 122366024 | 122400703 |
| a0009 | 0/0 | 599 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | MSRSL others(594): Show |
chr9 | 122366024 | 122400703 |
| a0010 | 0/0 | 599 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | MSRSL others(594): Show |
chr9 | 122366024 | 122400703 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1797 | 180 | 25 | 36 | 86 | 6 | 26 | PTGS1_chr9_122366024_122400703 | PTGS1 | ATGAG others(1792): Show |
chr9 | 122366024 | 122400703 | ||
| a0001c0002 | 0/0 | 1797 | 50 | 31 | 14 | 4 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | ATGAG others(1792): Show |
chr9 | 122366024 | 122400703 | ||
| a0001c0003 | 0/0 | 1797 | 23 | 4 | 0 | 18 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | ATGAG others(1792): Show |
chr9 | 122366024 | 122400703 | ||
| a0001c0006 | 0/0 | 1797 | 9 | 8 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | ATGAG others(1792): Show |
chr9 | 122366024 | 122400703 | ||
| a0001c0008 | 0/0 | 1797 | 7 | 7 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | ATGAG others(1792): Show |
chr9 | 122366024 | 122400703 | ||
| a0001c0011 | 0/0 | 1797 | 3 | 3 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | ATGAG others(1792): Show |
chr9 | 122366024 | 122400703 | ||
| a0001c0012 | 0/0 | 1797 | 2 | 2 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | ATGAG others(1792): Show |
chr9 | 122366024 | 122400703 | ||
| a0001c0013 | 0/0 | 1797 | 2 | 1 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | ATGAG others(1792): Show |
chr9 | 122366024 | 122400703 | ||
| a0001c0018 | 0/0 | 1797 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | ATGAG others(1792): Show |
chr9 | 122366024 | 122400703 | ||
| a0001c0019 | 0/0 | 1797 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | ATGAG others(1792): Show |
chr9 | 122366024 | 122400703 | ||
| a0001c0021 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | ATGAG others(1792): Show |
chr9 | 122366024 | 122400703 | ||
| a0002c0004 | 1/0 | 1797 | 14 | 0 | 3 | 5 | 1 | 4 | PTGS1_chr9_122366024_122400703 | PTGS1 | ATGAG others(1792): Show |
chr9 | 122366024 | 122400703 | ||
| a0002c0007 | 0/0 | 1797 | 9 | 0 | 0 | 0 | 3 | 6 | PTGS1_chr9_122366024_122400703 | PTGS1 | ATGAG others(1792): Show |
chr9 | 122366024 | 122400703 | ||
| a0003c0005 | 0/0 | 1797 | 10 | 9 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | ATGAG others(1792): Show |
chr9 | 122366024 | 122400703 | ||
| a0003c0014 | 0/0 | 1797 | 2 | 2 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | ATGAG others(1792): Show |
chr9 | 122366024 | 122400703 | ||
| a0003c0015 | 0/0 | 1797 | 2 | 0 | 1 | 0 | 1 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | ATGAG others(1792): Show |
chr9 | 122366024 | 122400703 | ||
| a0003c0024 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | ATGAG others(1792): Show |
chr9 | 122366024 | 122400703 | ||
| a0003c0025 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | ATGAG others(1792): Show |
chr9 | 122366024 | 122400703 | ||
| a0004c0009 | 0/0 | 1797 | 5 | 0 | 5 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | ATGAG others(1792): Show |
chr9 | 122366024 | 122400703 | ||
| a0005c0010 | 0/0 | 1797 | 4 | 3 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | ATGAG others(1792): Show |
chr9 | 122366024 | 122400703 | ||
| a0006c0023 | 0/0 | 1797 | 1 | 0 | 0 | 0 | 1 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | ATGAG others(1792): Show |
chr9 | 122366024 | 122400703 | ||
| a0007c0022 | 0/0 | 1797 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | ATGAG others(1792): Show |
chr9 | 122366024 | 122400703 | ||
| a0008c0016 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | ATGAG others(1792): Show |
chr9 | 122366024 | 122400703 | ||
| a0009c0017 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | ATGAG others(1792): Show |
chr9 | 122366024 | 122400703 | ||
| a0010c0020 | 0/0 | 1797 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | ATGAG others(1792): Show |
chr9 | 122366024 | 122400703 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5020 | 142 | 19 | 29 | 68 | 5 | 20 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0001t0003 | 0/0 | 5020 | 8 | 0 | 0 | 7 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0001t0004 | 0/0 | 5020 | 18 | 2 | 5 | 6 | 1 | 4 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0001t0011 | 0/0 | 5020 | 2 | 0 | 2 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0001t0012 | 0/0 | 5020 | 2 | 2 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0001t0014 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0001t0015 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0001t0017 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0001t0019 | 0/0 | 5020 | 1 | 0 | 0 | 0 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0001t0020 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0001t0023 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0001t0024 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0001t0025 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0002t0001 | 0/0 | 5020 | 26 | 18 | 5 | 2 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0002t0002 | 0/0 | 5020 | 14 | 13 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0002t0006 | 0/0 | 5020 | 9 | 0 | 8 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0002t0022 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0003t0001 | 0/0 | 5020 | 12 | 4 | 0 | 8 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0003t0003 | 0/0 | 5020 | 10 | 0 | 0 | 9 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0003t0004 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0006t0007 | 0/0 | 5020 | 4 | 4 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0006t0008 | 0/0 | 5020 | 3 | 2 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0006t0009 | 0/0 | 5020 | 2 | 2 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0008t0001 | 0/0 | 5020 | 2 | 2 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0008t0002 | 0/0 | 5020 | 5 | 5 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0011t0001 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0011t0002 | 0/0 | 5020 | 2 | 2 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0012t0005 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0012t0013 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0013t0010 | 0/0 | 5020 | 2 | 1 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0018t0001 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0019t0001 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0001c0021t0001 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0002c0004t0001 | 1/0 | 5020 | 7 | 0 | 0 | 2 | 1 | 3 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0002c0004t0003 | 0/0 | 5020 | 6 | 0 | 3 | 3 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0002c0004t0018 | 0/0 | 5020 | 1 | 0 | 0 | 0 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0002c0007t0001 | 0/0 | 5020 | 9 | 0 | 0 | 0 | 3 | 6 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0003c0005t0005 | 0/0 | 5020 | 7 | 6 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0003c0005t0007 | 0/0 | 5020 | 3 | 3 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0003c0014t0005 | 0/0 | 5020 | 2 | 2 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0003c0015t0001 | 0/0 | 5020 | 2 | 0 | 1 | 0 | 1 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0003c0024t0026 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0003c0025t0002 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0004c0009t0001 | 0/0 | 5020 | 5 | 0 | 5 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0005c0010t0002 | 0/0 | 5020 | 4 | 3 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0006c0023t0001 | 0/0 | 5020 | 1 | 0 | 0 | 0 | 1 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0007c0022t0006 | 0/0 | 5020 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0008c0016t0001 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0009c0017t0021 | 0/0 | 5020 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| a0010c0020t0016 | 0/0 | 5020 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | AGTGT others(5015): Show |
chr9 | 122366024 | 122400703 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 17 | 0 | 4 | 7 | 1 | 5 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0002 | 0/0 | 8 | 0 | 1 | 5 | 0 | 2 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0015 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0036 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0206 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0003g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0004g0001 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0004g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0004g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0011g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0011g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0012g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0014g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0015g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0017g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0019g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0020g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0023g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0024g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0001t0025g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0001g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0002g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0002g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0002g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0002g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0006g0004 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0006g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0006g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0006g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0002t0022g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0003t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0003t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0003t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0003t0003g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0003t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0003t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0003t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0003t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0003t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0003t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0003t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0006t0007g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0006t0007g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0006t0007g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0006t0008g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0006t0008g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0006t0008g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0006t0009g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0008t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0008t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0008t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0008t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0008t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0008t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0008t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0011t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0011t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0012t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0012t0013g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0013t0010g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0013t0010g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0018t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0019t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0001c0021t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0002c0004t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0002c0004t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0002c0004t0001g0109 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0002c0004t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0002c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0002c0004t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0002c0004t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0002c0004t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0002c0004t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0002c0004t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0002c0004t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0002c0004t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0002c0004t0018g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0002c0007t0001g0016 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0002c0007t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0002c0007t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0002c0007t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0002c0007t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0002c0007t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0003c0005t0005g0003 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0003c0005t0005g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0003c0005t0007g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0003c0014t0005g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0003c0014t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0003c0015t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0003c0015t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0003c0024t0026g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0003c0025t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0004c0009t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0004c0009t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0004c0009t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0004c0009t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0004c0009t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0005c0010t0002g0012 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0005c0010t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0006c0023t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0007c0022t0006g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0008c0016t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0009c0017t0021g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| a0010c0020t0016g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0216 | EUR | GBR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | FIN | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG00280 | hp2 | a0006 | c0023 | t0001 | g0153 | EUR | FIN | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | FIN | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG00323 | hp2 | a0002 | c0004 | t0001 | g0110 | EUR | FIN | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG00438 | hp1 | a0001 | c0001 | t0024 | g0086 | EAS | CHS | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG00544 | hp1 | a0001 | c0003 | t0001 | g0052 | EAS | CHS | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | CHS | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG00609 | hp1 | a0001 | c0019 | t0001 | g0002 | EAS | CHS | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG00609 | hp2 | a0001 | c0003 | t0003 | g0051 | EAS | CHS | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG00639 | hp1 | a0001 | c0006 | t0008 | g0189 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG00639 | hp2 | a0004 | c0009 | t0001 | g0193 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0107 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG00735 | hp2 | a0004 | c0009 | t0001 | g0192 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0156 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0155 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01069 | hp2 | a0004 | c0009 | t0001 | g0218 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01074 | hp2 | a0004 | c0009 | t0001 | g0194 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01081 | hp1 | a0001 | c0002 | t0006 | g0004 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01081 | hp2 | a0004 | c0009 | t0001 | g0021 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01106 | hp2 | a0002 | c0004 | t0003 | g0108 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01109 | hp1 | a0001 | c0013 | t0010 | g0131 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0064 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01243 | hp1 | a0003 | c0005 | t0005 | g0003 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0170 | AMR | CLM | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01256 | hp2 | a0001 | c0002 | t0006 | g0004 | AMR | CLM | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01258 | hp1 | a0001 | c0002 | t0006 | g0004 | AMR | CLM | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0033 | AMR | CLM | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | CLM | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0040 | AMR | CLM | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0168 | AMR | CLM | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01358 | hp1 | a0002 | c0004 | t0003 | g0112 | AMR | CLM | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01358 | hp2 | a0001 | c0002 | t0006 | g0004 | AMR | CLM | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01433 | hp2 | a0003 | c0015 | t0001 | g0074 | AMR | CLM | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01496 | hp1 | a0005 | c0010 | t0002 | g0012 | AMR | CLM | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01516 | hp1 | a0002 | c0007 | t0001 | g0121 | EUR | IBS | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01516 | hp2 | a0002 | c0007 | t0001 | g0119 | EUR | IBS | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01517 | hp1 | a0002 | c0007 | t0001 | g0120 | EUR | IBS | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01884 | hp1 | a0001 | c0001 | t0020 | g0165 | AFR | ACB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01884 | hp2 | a0003 | c0005 | t0005 | g0003 | AFR | ACB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01891 | hp1 | a0001 | c0006 | t0008 | g0188 | AFR | ACB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01928 | hp2 | a0001 | c0002 | t0006 | g0132 | AMR | PEL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0181 | AMR | PEL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | PEL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01952 | hp1 | a0001 | c0002 | t0006 | g0004 | AMR | PEL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01978 | hp1 | a0001 | c0002 | t0006 | g0140 | AMR | PEL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01981 | hp2 | a0001 | c0001 | t0011 | g0147 | AMR | PEL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01993 | hp2 | a0002 | c0004 | t0003 | g0111 | AMR | PEL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02004 | hp2 | a0007 | c0022 | t0006 | g0001 | AMR | PEL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02055 | hp1 | a0001 | c0006 | t0007 | g0186 | AFR | ACB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | ACB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | KHV | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | KHV | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02129 | hp1 | a0001 | c0003 | t0004 | g0053 | EAS | KHV | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02135 | hp2 | a0001 | c0002 | t0022 | g0141 | EAS | KHV | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02145 | hp1 | a0001 | c0006 | t0008 | g0205 | AFR | ACB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CDX | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | CDX | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0126 | AFR | ACB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02258 | hp1 | a0001 | c0011 | t0002 | g0025 | AFR | ACB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0047 | AFR | ACB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02280 | hp1 | a0003 | c0005 | t0007 | g0013 | AFR | ACB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02280 | hp2 | a0003 | c0005 | t0005 | g0003 | AFR | ACB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02300 | hp1 | a0001 | c0001 | t0011 | g0137 | AMR | PEL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02451 | hp1 | a0001 | c0001 | t0012 | g0001 | AFR | ACB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | ACB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02523 | hp1 | a0001 | c0001 | t0015 | g0150 | EAS | KHV | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0219 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02602 | hp1 | a0002 | c0007 | t0001 | g0016 | SAS | PJL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02615 | hp1 | a0001 | c0006 | t0007 | g0042 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0060 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0043 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0022 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0026 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02647 | hp2 | a0001 | c0021 | t0001 | g0063 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02683 | hp1 | a0002 | c0004 | t0018 | g0001 | SAS | PJL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02698 | hp2 | a0002 | c0007 | t0001 | g0016 | SAS | PJL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02717 | hp1 | a0001 | c0012 | t0005 | g0062 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02717 | hp2 | a0001 | c0008 | t0002 | g0209 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0200 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02723 | hp2 | a0005 | c0010 | t0002 | g0012 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0148 | SAS | PJL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02818 | hp1 | a0001 | c0008 | t0002 | g0215 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0127 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0198 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0061 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02896 | hp1 | a0003 | c0005 | t0005 | g0003 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02896 | hp2 | a0003 | c0014 | t0005 | g0072 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02897 | hp1 | a0003 | c0014 | t0005 | g0071 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0199 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02922 | hp2 | a0003 | c0005 | t0005 | g0003 | AFR | ESN | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | ESN | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02970 | hp1 | a0005 | c0010 | t0002 | g0128 | AFR | ESN | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02970 | hp2 | a0001 | c0008 | t0002 | g0213 | AFR | ESN | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03017 | hp1 | a0002 | c0004 | t0001 | g0007 | SAS | PJL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03017 | hp2 | a0002 | c0007 | t0001 | g0016 | SAS | PJL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03041 | hp1 | a0001 | c0006 | t0009 | g0035 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03041 | hp2 | a0003 | c0005 | t0007 | g0013 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03098 | hp1 | a0001 | c0008 | t0002 | g0212 | AFR | MSL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03098 | hp2 | a0003 | c0005 | t0005 | g0003 | AFR | MSL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03130 | hp1 | a0001 | c0011 | t0001 | g0185 | AFR | ESN | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03139 | hp1 | a0001 | c0006 | t0007 | g0042 | AFR | ESN | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03139 | hp2 | a0001 | c0012 | t0013 | g0048 | AFR | ESN | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0045 | AFR | ESN | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0161 | AFR | ESN | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03209 | hp1 | a0001 | c0006 | t0009 | g0035 | AFR | MSL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | MSL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03225 | hp2 | a0001 | c0001 | t0012 | g0001 | AFR | MSL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0125 | AFR | MSL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03453 | hp2 | a0001 | c0003 | t0001 | g0026 | AFR | MSL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03486 | hp1 | a0001 | c0008 | t0002 | g0210 | AFR | MSL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0043 | AFR | MSL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03491 | hp1 | a0002 | c0004 | t0001 | g0115 | SAS | PJL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03491 | hp2 | a0002 | c0007 | t0001 | g0139 | SAS | PJL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03492 | hp1 | a0002 | c0004 | t0001 | g0116 | SAS | PJL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | ESN | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03540 | hp1 | a0009 | c0017 | t0021 | g0068 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03579 | hp1 | a0001 | c0008 | t0001 | g0211 | AFR | MSL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0045 | AFR | MSL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03654 | hp2 | a0002 | c0007 | t0001 | g0029 | SAS | PJL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0142 | SAS | PJL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03688 | hp1 | a0001 | c0003 | t0003 | g0162 | SAS | STU | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03710 | hp2 | a0001 | c0001 | t0019 | g0001 | SAS | PJL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03942 | hp2 | a0002 | c0007 | t0001 | g0029 | SAS | BEB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0184 | SAS | STU | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0083 | SAS | STU | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | STU | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0069 | SAS | STU | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0022 | AFR | YRI | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | YRI | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0022 | AFR | YRI | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18906 | hp2 | a0001 | c0001 | t0023 | g0059 | AFR | YRI | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18941 | hp2 | a0001 | c0003 | t0003 | g0024 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18942 | hp1 | a0001 | c0018 | t0001 | g0173 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0122 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18944 | hp1 | a0001 | c0002 | t0006 | g0164 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18944 | hp2 | a0001 | c0003 | t0001 | g0217 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18945 | hp1 | a0002 | c0004 | t0001 | g0046 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18945 | hp2 | a0002 | c0004 | t0003 | g0113 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18947 | hp1 | a0001 | c0003 | t0003 | g0011 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18949 | hp1 | a0001 | c0003 | t0003 | g0133 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18954 | hp2 | a0001 | c0003 | t0003 | g0054 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18961 | hp1 | a0001 | c0003 | t0001 | g0030 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18963 | hp1 | a0001 | c0003 | t0001 | g0030 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18969 | hp2 | a0001 | c0003 | t0003 | g0123 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18982 | hp2 | a0002 | c0004 | t0003 | g0118 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18983 | hp1 | a0001 | c0001 | t0025 | g0101 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18988 | hp2 | a0001 | c0001 | t0014 | g0090 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18993 | hp2 | a0002 | c0004 | t0003 | g0114 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18994 | hp2 | a0001 | c0003 | t0001 | g0134 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19000 | hp1 | a0001 | c0001 | t0017 | g0006 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19004 | hp1 | a0001 | c0003 | t0003 | g0024 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19007 | hp1 | a0010 | c0020 | t0016 | g0001 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19010 | hp1 | a0001 | c0003 | t0001 | g0023 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19012 | hp1 | a0001 | c0003 | t0001 | g0023 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0136 | AFR | LWK | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19030 | hp2 | a0001 | c0006 | t0007 | g0187 | AFR | LWK | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19043 | hp1 | a0005 | c0010 | t0002 | g0012 | AFR | LWK | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0208 | AFR | LWK | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19060 | hp1 | a0001 | c0003 | t0003 | g0011 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19060 | hp2 | a0001 | c0003 | t0001 | g0023 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19066 | hp1 | a0002 | c0004 | t0001 | g0046 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19082 | hp2 | a0001 | c0003 | t0003 | g0011 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | YRI | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA19240 | hp2 | a0001 | c0013 | t0010 | g0204 | AFR | YRI | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA20129 | hp1 | a0003 | c0005 | t0007 | g0013 | AFR | ASW | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ASW | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | TSI | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA20752 | hp2 | a0003 | c0015 | t0001 | g0075 | EUR | TSI | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | GIH | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0001 | SAS | GIH | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01123 | hp1 | a0001 | c0002 | t0006 | g0004 | AMR | CLM | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02109 | hp1 | a0001 | c0011 | t0002 | g0025 | AFR | ACB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0044 | AFR | ACB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0047 | AFR | ACB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0050 | AFR | ACB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0197 | AFR | ACB | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03471 | hp1 | a0001 | c0008 | t0001 | g0214 | AFR | MSL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG03471 | hp2 | a0008 | c0016 | t0001 | g0067 | AFR | MSL | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0044 | AFR | USA | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| HG06807 | hp2 | a0003 | c0005 | t0005 | g0073 | AFR | USA | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA20300 | hp1 | a0003 | c0025 | t0002 | g0070 | AFR | USA | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | USA | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA21309 | hp1 | a0003 | c0024 | t0026 | g0076 | AFR | LWK | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | LWK | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0206 | REF | REF | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| homoSapiens | grch38p0 | a0002 | c0004 | t0001 | g0109 | REF | REF | PTGS1_chr9_122366024_122400703 | PTGS1 | chr9 | 122366024 | 122400703 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:122371200 | T | C | 9 | a0001 a0003 a0004 others(6): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
missense_variant | MODERATE | c.22T>C | p.Trp8Arg | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/11 | 83/5020 | 22/1800 | 8/599 | chr9 | 122371200 | |||
| chr9:122371228 | C | T | 1 | a0003 | 16 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(13): Show |
missense_variant | MODERATE | c.50C>T | p.Pro17Leu | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/11 | 111/5020 | 50/1800 | 17/599 | chr9 | 122371228 | |||
| chr9:122378015 | C | T | 1 | a0008 | 1 | HG03471.hp2 | missense_variant&splice_region_variant | MODERATE | c.211C>T | p.Pro71Ser | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 3/11 | 272/5020 | 211/1800 | 71/599 | chr9 | 122378015 | |||
| chr9:122378507 | C | T | 1 | a0006 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.286C>T | p.Arg96Cys | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 4/11 | 347/5020 | 286/1800 | 96/599 | chr9 | 122378507 | |||
| chr9:122381428 | A | C | 1 | a0005 | 4 | HG01496.hp1 HG02723.hp2 HG02970.hp1 others(1): Show |
missense_variant | MODERATE | c.554A>C | p.Lys185Thr | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 6/11 | 615/5020 | 554/1800 | 185/599 | chr9 | 122381428 | |||
| chr9:122381509 | C | G | 1 | a0007 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.635C>G | p.Ser212Cys | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 6/11 | 696/5020 | 635/1800 | 212/599 | chr9 | 122381509 | |||
| chr9:122381694 | C | A | 1 | a0004 | 5 | HG00639.hp2 HG00735.hp2 HG01069.hp2 others(2): Show |
missense_variant | MODERATE | c.709C>A | p.Leu237Met | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/11 | 770/5020 | 709/1800 | 237/599 | chr9 | 122381694 | |||
| chr9:122386458 | A | G | 1 | a0009 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.1022A>G | p.Lys341Arg | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/11 | 1083/5020 | 1022/1800 | 341/599 | chr9 | 122386458 | |||
| chr9:122390243 | G | A | 1 | a0010 | 1 | NA19007.hp1 | missense_variant | MODERATE | c.1342G>A | p.Val448Met | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/11 | 1403/5020 | 1342/1800 | 448/599 | chr9 | 122390243 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:122377927 | G | A | 7 | a0001c0003 a0001c0008 a0001c0011 others(4): Show |
50 | HG00544.hp1 HG00609.hp2 HG01243.hp1 others(47): Show |
synonymous_variant | LOW | c.123G>A | p.Gln41Gln | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 3/11 | 184/5020 | 123/1800 | 41/599 | chr9 | 122377927 | |||
| chr9:122378008 | C | T | 1 | a0001c0008 | 7 | HG02717.hp2 HG02818.hp1 HG02970.hp2 others(4): Show |
synonymous_variant | LOW | c.204C>T | p.Cys68Cys | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 3/11 | 265/5020 | 204/1800 | 68/599 | chr9 | 122378008 | |||
| chr9:122381513 | C | A | 13 | a0001c0002 a0001c0006 a0001c0008 others(10): Show |
104 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(101): Show |
synonymous_variant | LOW | c.639C>A | p.Gly213Gly | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 6/11 | 700/5020 | 639/1800 | 213/599 | chr9 | 122381513 | |||
| chr9:122383538 | G | A | 1 | a0001c0018 | 1 | NA18942.hp1 | synonymous_variant | LOW | c.792G>A | p.Ser264Ser | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/11 | 853/5020 | 792/1800 | 264/599 | chr9 | 122383538 | |||
| chr9:122383652 | G | A | 1 | a0001c0019 | 1 | HG00609.hp1 | synonymous_variant | LOW | c.906G>A | p.Thr302Thr | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/11 | 967/5020 | 906/1800 | 302/599 | chr9 | 122383652 | |||
| chr9:122386697 | C | T | 1 | a0003c0025 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.1261C>T | p.Leu421Leu | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/11 | 1322/5020 | 1261/1800 | 421/599 | chr9 | 122386697 | |||
| chr9:122392241 | G | A | 1 | a0001c0013 | 2 | HG01109.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.1497G>A | p.Ala499Ala | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 1558/5020 | 1497/1800 | 499/599 | chr9 | 122392241 | |||
| chr9:122392256 | T | C | 6 | a0001c0006 a0001c0012 a0001c0013 others(3): Show |
26 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(23): Show |
synonymous_variant | LOW | c.1512T>C | p.Pro504Pro | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 1573/5020 | 1512/1800 | 504/599 | chr9 | 122392256 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:122371061 | G | A | 1 | a0001c0006t0009 | 2 | HG03041.hp1 HG03209.hp1 |
5_prime_UTR_variant | MODIFIER | c.-24G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 1/11 | 24 | chr9 | 122371061 | ||||||
| chr9:122392631 | C | A | 9 | a0001c0006t0007 a0001c0006t0008 a0001c0006t0009 others(6): Show |
25 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*87C>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 87 | chr9 | 122392631 | ||||||
| chr9:122392908 | T | G | 7 | a0001c0006t0007 a0001c0006t0008 a0001c0012t0005 others(4): Show |
21 | HG00639.hp1 HG01243.hp1 HG01884.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*364T>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 364 | chr9 | 122392908 | ||||||
| chr9:122392935 | T | G | 1 | a0001c0001t0014 | 1 | NA18988.hp2 | 3_prime_UTR_variant | MODIFIER | c.*391T>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 391 | chr9 | 122392935 | ||||||
| chr9:122393034 | A | C | 15 | a0001c0002t0002 a0001c0006t0007 a0001c0006t0008 others(12): Show |
52 | HG00639.hp1 HG01109.hp1 HG01109.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*490A>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 490 | chr9 | 122393034 | ||||||
| chr9:122393045 | C | T | 1 | a0001c0001t0025 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*501C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 501 | chr9 | 122393045 | ||||||
| chr9:122393129 | A | G | 19 | a0001c0001t0003 a0001c0001t0024 a0001c0002t0002 others(16): Show |
77 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*585A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 585 | chr9 | 122393129 | ||||||
| chr9:122393130 | G | A | 1 | a0001c0001t0011 | 2 | HG01981.hp2 HG02300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*586G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 586 | chr9 | 122393130 | ||||||
| chr9:122393299 | G | A | 1 | a0003c0024t0026 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*755G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 755 | chr9 | 122393299 | ||||||
| chr9:122393329 | T | C | 1 | a0001c0006t0008 | 3 | HG00639.hp1 HG01891.hp1 HG02145.hp1 |
3_prime_UTR_variant | MODIFIER | c.*785T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 785 | chr9 | 122393329 | ||||||
| chr9:122393406 | A | G | 15 | a0001c0002t0002 a0001c0006t0007 a0001c0006t0008 others(12): Show |
52 | HG00639.hp1 HG01109.hp1 HG01109.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*862A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 862 | chr9 | 122393406 | ||||||
| chr9:122393453 | C | T | 1 | a0001c0001t0023 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*909C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 909 | chr9 | 122393453 | ||||||
| chr9:122393507 | G | T | 18 | a0001c0002t0002 a0001c0002t0006 a0001c0002t0022 others(15): Show |
63 | HG00639.hp1 HG01081.hp1 HG01109.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*963G>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 963 | chr9 | 122393507 | ||||||
| chr9:122393510 | C | G | 18 | a0001c0002t0002 a0001c0002t0006 a0001c0002t0022 others(15): Show |
63 | HG00639.hp1 HG01081.hp1 HG01109.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*966C>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 966 | chr9 | 122393510 | ||||||
| chr9:122393578 | A | G | 4 | a0001c0012t0005 a0001c0012t0013 a0003c0005t0005 others(1): Show |
11 | HG01243.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1034A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 1034 | chr9 | 122393578 | ||||||
| chr9:122393617 | G | A | 1 | a0001c0001t0024 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1073G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 1073 | chr9 | 122393617 | ||||||
| chr9:122393651 | G | C | 4 | a0001c0001t0003 a0001c0001t0024 a0001c0003t0003 others(1): Show |
25 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1107G>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 1107 | chr9 | 122393651 | ||||||
| chr9:122393700 | T | G | 1 | a0001c0001t0015 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1156T>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 1156 | chr9 | 122393700 | ||||||
| chr9:122394010 | C | T | 1 | a0009c0017t0021 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1466C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 1466 | chr9 | 122394010 | ||||||
| chr9:122394118 | C | T | 2 | a0001c0013t0010 a0009c0017t0021 |
3 | HG01109.hp1 HG03540.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1574C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 1574 | chr9 | 122394118 | ||||||
| chr9:122394119 | G | A | 1 | a0010c0020t0016 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1575G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 1575 | chr9 | 122394119 | ||||||
| chr9:122394121 | T | G | 1 | a0001c0001t0017 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1577T>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 1577 | chr9 | 122394121 | ||||||
| chr9:122394336 | G | A | 2 | a0001c0002t0022 a0002c0004t0018 |
2 | HG02135.hp2 HG02683.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1792G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 1792 | chr9 | 122394336 | ||||||
| chr9:122394919 | C | A | 3 | a0001c0001t0004 a0001c0001t0019 a0001c0003t0004 |
20 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2375C>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 2375 | chr9 | 122394919 | ||||||
| chr9:122395026 | C | T | 1 | a0001c0001t0012 | 2 | HG02451.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2482C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 2482 | chr9 | 122395026 | ||||||
| chr9:122395037 | G | A | 4 | a0001c0001t0003 a0001c0001t0024 a0001c0003t0003 others(1): Show |
25 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2493G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 2493 | chr9 | 122395037 | ||||||
| chr9:122395131 | G | A | 1 | a0001c0001t0019 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2587G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 2587 | chr9 | 122395131 | ||||||
| chr9:122395235 | C | T | 1 | a0001c0001t0020 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2691C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 2691 | chr9 | 122395235 | ||||||
| chr9:122395269 | C | T | 3 | a0001c0012t0005 a0003c0005t0005 a0003c0014t0005 |
10 | HG01243.hp1 HG01884.hp2 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2725C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 2725 | chr9 | 122395269 | ||||||
| chr9:122395355 | G | A | 1 | a0001c0001t0020 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2811G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 2811 | chr9 | 122395355 | ||||||
| chr9:122395439 | T | G | 4 | a0001c0001t0003 a0001c0001t0024 a0001c0003t0003 others(1): Show |
25 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2895T>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 11/11 | 2895 | chr9 | 122395439 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:122371436 | C | G | 1 | a0004c0009t0001g0218 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.94+164C>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122371436 | |||||||
| chr9:122371436 | C | T | 2 | a0001c0002t0001g0219 a0001c0002t0002g0047 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.94+164C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122371436 | |||||||
| chr9:122371449 | T | C | 26 | a0001c0001t0001g0049 a0001c0001t0001g0055 a0001c0001t0001g0056 others(23): Show |
33 | HG00544.hp1 HG00609.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.94+177T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122371449 | |||||||
| chr9:122371590 | A | G | 2 | a0001c0003t0001g0023 a0001c0003t0001g0217 |
4 | NA18944.hp2 NA19010.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+318A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122371590 | |||||||
| chr9:122371877 | C | T | 1 | a0001c0001t0004g0216 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.94+605C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122371877 | |||||||
| chr9:122371917 | C | T | 10 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0002t0002g0064 others(7): Show |
13 | HG01109.hp2 HG01243.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.94+645C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122371917 | |||||||
| chr9:122371962 | G | A | 1 | a0001c0003t0001g0026 | 2 | HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.94+690G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122371962 | |||||||
| chr9:122371962 | G | T | 15 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0065 others(12): Show |
19 | HG01109.hp2 HG01243.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.94+690G>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122371962 | |||||||
| chr9:122372061 | G | C | 15 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0065 others(12): Show |
19 | HG01109.hp2 HG01243.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.94+789G>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122372061 | |||||||
| chr9:122372118 | T | G | 15 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0065 others(12): Show |
19 | HG01109.hp2 HG01243.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.94+846T>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122372118 | |||||||
| chr9:122372137 | G | A | 4 | a0001c0003t0001g0060 a0001c0003t0001g0061 a0001c0012t0005g0062 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+865G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122372137 | |||||||
| chr9:122372247 | G | A | 3 | a0001c0001t0001g0049 a0001c0001t0004g0050 a0001c0012t0013g0048 |
3 | HG02559.hp1 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.94+975G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122372247 | |||||||
| chr9:122372265 | A | G | 7 | a0001c0008t0001g0211 a0001c0008t0001g0214 a0001c0008t0002g0209 others(4): Show |
7 | HG02717.hp2 HG02818.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+993A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122372265 | |||||||
| chr9:122372315 | G | A | 1 | a0009c0017t0021g0068 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.94+1043G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122372315 | |||||||
| chr9:122372369 | A | T | 23 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0065 others(20): Show |
27 | HG01109.hp2 HG01243.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.94+1097A>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122372369 | |||||||
| chr9:122372390 | G | T | 1 | a0001c0001t0001g0207 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.94+1118G>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122372390 | |||||||
| chr9:122372433 | T | C | 1 | a0001c0001t0004g0069 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.94+1161T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122372433 | |||||||
| chr9:122372676 | C | T | 1 | a0002c0004t0001g0046 | 2 | NA18945.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.94+1404C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122372676 | |||||||
| chr9:122372690 | T | C | 8 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0003t0001g0052 others(5): Show |
11 | HG00544.hp1 HG00609.hp2 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.94+1418T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122372690 | |||||||
| chr9:122372823 | GT | G | 17 | a0001c0002t0001g0208 a0001c0008t0001g0211 a0001c0008t0001g0214 others(14): Show |
24 | HG01243.hp1 HG01433.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.94+1560delT | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 122372823 | ||||||
| chr9:122372881 | G | A | 19 | a0001c0002t0001g0208 a0001c0008t0001g0211 a0001c0008t0001g0214 others(16): Show |
29 | HG01243.hp1 HG01433.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.94+1609G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122372881 | |||||||
| chr9:122372968 | TGGGAGGA others(51): Show |
T | 1 | a0003c0024t0026g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.94+1703_94+1760del others(58): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 122372968 | ||||||
| chr9:122372975 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(199): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.94+1703A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122372975 | |||||||
| chr9:122372979 | A | G | 1 | a0001c0001t0001g0002 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.94+1707A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122372979 | |||||||
| chr9:122373063 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.94+1791G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122373063 | |||||||
| chr9:122373140 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.94+1868G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122373140 | |||||||
| chr9:122373210 | T | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(35): Show |
58 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.94+1938T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122373210 | |||||||
| chr9:122373261 | G | A | 16 | a0001c0001t0001g0049 a0001c0001t0001g0057 a0001c0001t0001g0058 others(13): Show |
19 | HG01109.hp2 HG01243.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.94+1989G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122373261 | |||||||
| chr9:122373381 | A | G | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(209): Show |
310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.94+2109A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122373381 | |||||||
| chr9:122373471 | T | G | 3 | a0001c0001t0001g0049 a0001c0001t0004g0050 a0001c0012t0013g0048 |
3 | HG02559.hp1 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.94+2199T>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122373471 | |||||||
| chr9:122373512 | C | T | 36 | a0001c0001t0001g0049 a0001c0001t0001g0057 a0001c0001t0001g0058 others(33): Show |
43 | HG01109.hp2 HG01243.hp2 HG01496.hp1 others(40): Show |
intron_variant | MODIFIER | c.94+2240C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122373512 | |||||||
| chr9:122373649 | C | T | 6 | a0001c0002t0001g0219 a0001c0002t0002g0047 a0002c0007t0001g0029 others(3): Show |
8 | HG01516.hp1 HG01516.hp2 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.94+2377C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122373649 | |||||||
| chr9:122373668 | G | C | 37 | a0001c0001t0001g0049 a0001c0001t0001g0057 a0001c0001t0001g0058 others(34): Show |
44 | HG01109.hp2 HG01243.hp2 HG01496.hp1 others(41): Show |
intron_variant | MODIFIER | c.94+2396G>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122373668 | |||||||
| chr9:122373690 | G | A | 1 | a0001c0001t0004g0122 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.94+2418G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122373690 | |||||||
| chr9:122373799 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(209): Show |
310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.94+2527T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122373799 | |||||||
| chr9:122373856 | CTT | C | 37 | a0001c0001t0001g0049 a0001c0001t0001g0057 a0001c0001t0001g0058 others(34): Show |
44 | HG01109.hp2 HG01243.hp2 HG01496.hp1 others(41): Show |
intron_variant | MODIFIER | c.94+2595_94+2596del others(2): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 122373856 | ||||||
| chr9:122373909 | C | T | 37 | a0001c0001t0001g0049 a0001c0001t0001g0057 a0001c0001t0001g0058 others(34): Show |
44 | HG01109.hp2 HG01243.hp2 HG01496.hp1 others(41): Show |
intron_variant | MODIFIER | c.94+2637C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122373909 | |||||||
| chr9:122373947 | A | G | 37 | a0001c0001t0001g0049 a0001c0001t0001g0057 a0001c0001t0001g0058 others(34): Show |
44 | HG01109.hp2 HG01243.hp2 HG01496.hp1 others(41): Show |
intron_variant | MODIFIER | c.94+2675A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122373947 | |||||||
| chr9:122373962 | A | G | 37 | a0001c0001t0001g0049 a0001c0001t0001g0057 a0001c0001t0001g0058 others(34): Show |
44 | HG01109.hp2 HG01243.hp2 HG01496.hp1 others(41): Show |
intron_variant | MODIFIER | c.94+2690A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122373962 | |||||||
| chr9:122374157 | C | T | 1 | a0001c0011t0002g0025 | 2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.94+2885C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122374157 | |||||||
| chr9:122374168 | C | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(163): Show |
249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.94+2896C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122374168 | |||||||
| chr9:122374605 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(156): Show |
239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.95-3294A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122374605 | |||||||
| chr9:122374943 | A | G | 2 | a0001c0002t0001g0219 a0001c0002t0002g0047 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.95-2956A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122374943 | |||||||
| chr9:122375002 | G | A | 3 | a0001c0002t0001g0219 a0001c0003t0001g0060 a0001c0003t0001g0061 |
3 | HG02572.hp1 HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.95-2897G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122375002 | |||||||
| chr9:122375102 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.95-2797G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122375102 | |||||||
| chr9:122375136 | C | A | 3 | a0001c0011t0002g0025 a0001c0012t0005g0062 a0005c0010t0002g0012 |
6 | HG01496.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-2763C>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122375136 | |||||||
| chr9:122375200 | G | A | 1 | a0002c0004t0003g0108 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.95-2699G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122375200 | |||||||
| chr9:122375232 | T | C | 46 | a0001c0001t0001g0049 a0001c0001t0001g0057 a0001c0001t0001g0058 others(43): Show |
58 | HG00544.hp1 HG00609.hp2 HG01109.hp2 others(55): Show |
intron_variant | MODIFIER | c.95-2667T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122375232 | |||||||
| chr9:122375237 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.95-2662C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122375237 | |||||||
| chr9:122375240 | A | C | 24 | a0001c0001t0001g0049 a0001c0001t0001g0078 a0001c0001t0001g0201 others(21): Show |
30 | HG01109.hp2 HG01891.hp2 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.95-2659A>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122375240 | |||||||
| chr9:122375344 | C | A | 1 | a0001c0001t0001g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.95-2555C>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122375344 | |||||||
| chr9:122375345 | G | A | 12 | a0001c0001t0001g0078 a0001c0001t0001g0201 a0001c0001t0001g0202 others(9): Show |
16 | HG01109.hp2 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.95-2554G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122375345 | |||||||
| chr9:122375365 | T | C | 15 | a0001c0001t0001g0078 a0001c0001t0001g0201 a0001c0001t0001g0202 others(12): Show |
19 | HG01109.hp2 HG01891.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.95-2534T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122375365 | |||||||
| chr9:122375369 | G | A | 2 | a0001c0013t0010g0131 a0001c0013t0010g0204 |
2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.95-2530G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122375369 | |||||||
| chr9:122375416 | A | T | 37 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0195 others(34): Show |
46 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.95-2483A>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122375416 | |||||||
| chr9:122375948 | C | T | 1 | a0008c0016t0001g0067 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.95-1951C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122375948 | |||||||
| chr9:122375950 | T | C | 1 | a0001c0011t0001g0185 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.95-1949T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122375950 | |||||||
| chr9:122376035 | A | G | 1 | a0001c0002t0002g0064 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.95-1864A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122376035 | |||||||
| chr9:122376185 | C | T | 9 | a0001c0001t0001g0049 a0001c0008t0001g0211 a0001c0008t0001g0214 others(6): Show |
9 | HG02717.hp2 HG02818.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-1714C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122376185 | |||||||
| chr9:122376199 | T | C | 1 | a0001c0002t0001g0208 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.95-1700T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122376199 | |||||||
| chr9:122376344 | T | TTG | 46 | a0001c0001t0001g0019 a0001c0001t0001g0038 a0001c0001t0001g0039 others(43): Show |
55 | HG00408.hp1 HG00408.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.95-1511_95-1510dup others(2): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 122376344 | ||||||
| chr9:122376344 | T | TTGTG | 11 | a0001c0001t0001g0049 a0001c0001t0001g0182 a0001c0001t0001g0183 others(8): Show |
12 | HG00738.hp1 HG00738.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.95-1513_95-1510dup others(4): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 122376344 | ||||||
| chr9:122376344 | T | TTGTGTG | 3 | a0001c0001t0001g0041 a0001c0001t0001g0104 a0001c0008t0001g0214 |
4 | HG01069.hp1 HG01071.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-1515_95-1510dup others(6): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 122376344 | ||||||
| chr9:122376344 | T | TTGTGTGT others(1): Show |
8 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0003t0001g0052 others(5): Show |
8 | HG00544.hp1 HG00609.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-1517_95-1510dup others(8): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 122376344 | ||||||
| chr9:122376344 | T | TTGTGTGT others(3): Show |
1 | a0001c0003t0004g0053 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.95-1519_95-1510dup others(10): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 122376344 | ||||||
| chr9:122376344 | T | TTGTGTGT others(5): Show |
2 | a0001c0003t0003g0011 a0001c0003t0003g0024 |
5 | NA18941.hp2 NA18947.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-1521_95-1510dup others(12): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 122376344 | ||||||
| chr9:122376344 | TTG | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(77): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.95-1511_95-1510del others(2): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 122376344 | ||||||
| chr9:122376344 | TTGTG | T | 14 | a0001c0001t0001g0014 a0001c0001t0001g0081 a0001c0001t0011g0137 others(11): Show |
20 | HG00438.hp2 HG01109.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.95-1513_95-1510del others(4): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 122376344 | ||||||
| chr9:122376344 | TTGTGTG | T | 9 | a0001c0001t0001g0055 a0001c0001t0001g0080 a0001c0001t0001g0135 others(6): Show |
12 | HG01074.hp1 HG01928.hp2 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.95-1515_95-1510del others(6): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 122376344 | ||||||
| chr9:122376344 | TTGTGTGT others(1): Show |
T | 3 | a0001c0002t0001g0124 a0001c0002t0001g0125 a0005c0010t0002g0012 |
5 | HG01496.hp1 HG02723.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-1517_95-1510del others(8): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 122376344 | ||||||
| chr9:122376344 | TTGTGTGT others(11): Show |
T | 1 | a0003c0015t0001g0074 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.95-1527_95-1510del others(18): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 122376344 | ||||||
| chr9:122376344 | TTGTGTGT others(19): Show |
T | 12 | a0001c0001t0001g0078 a0001c0001t0001g0201 a0001c0001t0001g0202 others(9): Show |
16 | HG01109.hp2 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.95-1535_95-1510del others(26): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 122376344 | ||||||
| chr9:122376407 | C | T | 2 | a0001c0001t0004g0037 a0001c0001t0004g0122 |
3 | NA18942.hp2 NA18966.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.95-1492C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122376407 | |||||||
| chr9:122376416 | A | C | 88 | a0001c0001t0001g0049 a0001c0001t0001g0057 a0001c0001t0001g0058 others(85): Show |
115 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.95-1483A>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122376416 | |||||||
| chr9:122376691 | G | A | 3 | a0001c0002t0001g0197 a0001c0002t0002g0044 a0001c0002t0002g0064 |
4 | HG01109.hp2 HG02109.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-1208G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122376691 | |||||||
| chr9:122377039 | A | G | 9 | a0001c0003t0001g0052 a0001c0003t0001g0060 a0001c0003t0001g0061 others(6): Show |
12 | HG00544.hp1 HG00609.hp2 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.95-860A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122377039 | |||||||
| chr9:122377061 | T | G | 40 | a0001c0001t0001g0179 a0001c0001t0001g0190 a0001c0001t0001g0191 others(37): Show |
49 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.95-838T>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122377061 | |||||||
| chr9:122377129 | G | A | 38 | a0001c0001t0001g0179 a0001c0001t0001g0190 a0001c0001t0001g0191 others(35): Show |
46 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.95-770G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122377129 | |||||||
| chr9:122377143 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.95-756C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122377143 | |||||||
| chr9:122377224 | G | C | 4 | a0001c0006t0007g0187 a0003c0014t0005g0071 a0003c0014t0005g0072 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-675G>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122377224 | |||||||
| chr9:122377249 | A | T | 14 | a0001c0001t0001g0078 a0001c0001t0001g0201 a0001c0001t0001g0202 others(11): Show |
18 | HG01109.hp2 HG01891.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.95-650A>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122377249 | |||||||
| chr9:122377453 | G | A | 1 | a0001c0002t0002g0161 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.95-446G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122377453 | |||||||
| chr9:122377457 | C | T | 3 | a0001c0011t0002g0025 a0005c0010t0002g0012 a0005c0010t0002g0128 |
6 | HG01496.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-442C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122377457 | |||||||
| chr9:122377539 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.95-360A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122377539 | |||||||
| chr9:122377613 | C | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0176 a0001c0001t0001g0177 |
4 | HG02922.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-286C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122377613 | |||||||
| chr9:122377619 | G | A | 7 | a0001c0003t0001g0052 a0001c0003t0003g0011 a0001c0003t0003g0024 others(4): Show |
10 | HG00544.hp1 HG00609.hp2 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.95-280G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122377619 | |||||||
| chr9:122377641 | C | T | 2 | a0001c0013t0010g0131 a0001c0013t0010g0204 |
2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.95-258C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122377641 | |||||||
| chr9:122377795 | C | T | 1 | a0001c0021t0001g0063 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.95-104C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122377795 | |||||||
| chr9:122377846 | G | T | 1 | a0001c0001t0001g0177 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.95-53G>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 2/10 | chr9 | 122377846 | |||||||
| chr9:122378047 | G | A | 11 | a0001c0002t0001g0020 a0001c0006t0007g0042 a0001c0006t0007g0186 others(8): Show |
14 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.211+32G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 3/10 | chr9 | 122378047 | |||||||
| chr9:122378221 | G | A | 9 | a0001c0003t0001g0026 a0001c0003t0001g0060 a0001c0003t0001g0061 others(6): Show |
13 | HG00609.hp2 HG02622.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.211+206G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 3/10 | chr9 | 122378221 | |||||||
| chr9:122378280 | T | A | 1 | a0001c0001t0001g0082 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.212-153T>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 3/10 | chr9 | 122378280 | |||||||
| chr9:122378417 | G | C | 82 | a0001c0001t0003g0083 a0001c0001t0003g0163 a0001c0002t0001g0021 others(79): Show |
111 | HG00609.hp2 HG00639.hp1 HG00639.hp2 others(108): Show |
intron_variant | MODIFIER | c.212-16G>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 3/10 | chr9 | 122378417 | |||||||
| chr9:122378625 | T | C | 2 | a0001c0002t0001g0098 a0001c0002t0001g0138 |
2 | NA18968.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.352+52T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 4/10 | chr9 | 122378625 | |||||||
| chr9:122378960 | T | C | 14 | a0001c0001t0003g0008 a0001c0001t0003g0083 a0001c0001t0003g0084 others(11): Show |
17 | HG00438.hp1 HG00597.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.496+42T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122378960 | |||||||
| chr9:122379115 | C | T | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | NA19007.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.496+197C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122379115 | |||||||
| chr9:122379116 | A | T | 1 | a0001c0001t0025g0101 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.496+198A>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122379116 | |||||||
| chr9:122379186 | C | T | 8 | a0001c0002t0001g0098 a0001c0002t0001g0138 a0001c0002t0006g0004 others(5): Show |
14 | HG01081.hp1 HG01123.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.496+268C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122379186 | |||||||
| chr9:122379204 | G | A | 4 | a0001c0001t0003g0163 a0002c0004t0003g0113 a0002c0004t0003g0114 others(1): Show |
4 | NA18945.hp2 NA18982.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+286G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122379204 | |||||||
| chr9:122379428 | T | C | 29 | a0001c0002t0001g0017 a0001c0002t0001g0021 a0001c0002t0001g0040 others(26): Show |
36 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.496+510T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122379428 | |||||||
| chr9:122379442 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.496+524A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122379442 | |||||||
| chr9:122379503 | T | A | 1 | a0001c0002t0002g0045 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.496+585T>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122379503 | |||||||
| chr9:122379507 | G | T | 28 | a0001c0002t0001g0017 a0001c0002t0001g0021 a0001c0002t0001g0040 others(25): Show |
35 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.496+589G>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122379507 | |||||||
| chr9:122379694 | T | C | 1 | a0001c0001t0023g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.496+776T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122379694 | |||||||
| chr9:122379695 | G | A | 1 | a0001c0001t0023g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.496+777G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122379695 | |||||||
| chr9:122379798 | T | C | 1 | a0001c0001t0001g0055 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.496+880T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122379798 | |||||||
| chr9:122379812 | AT | A | 7 | a0001c0002t0002g0022 a0001c0002t0002g0045 a0001c0002t0002g0198 others(4): Show |
10 | HG02630.hp2 HG02723.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.496+900delT | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 122379812 | ||||||
| chr9:122379965 | T | G | 2 | a0005c0010t0002g0012 a0005c0010t0002g0128 |
4 | HG01496.hp1 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+1047T>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122379965 | |||||||
| chr9:122380081 | G | C | 6 | a0001c0011t0001g0185 a0001c0012t0005g0062 a0001c0012t0013g0048 others(3): Show |
13 | HG01243.hp1 HG01884.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.496+1163G>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122380081 | |||||||
| chr9:122380109 | A | G | 7 | a0001c0002t0001g0098 a0001c0002t0001g0138 a0001c0002t0006g0004 others(4): Show |
12 | HG01081.hp1 HG01123.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.496+1191A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122380109 | |||||||
| chr9:122380202 | G | A | 56 | a0001c0002t0001g0017 a0001c0002t0001g0021 a0001c0002t0001g0040 others(53): Show |
80 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.497-1169G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122380202 | |||||||
| chr9:122380280 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.497-1091A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122380280 | |||||||
| chr9:122380422 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.497-949G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122380422 | |||||||
| chr9:122380430 | A | G | 28 | a0001c0002t0001g0017 a0001c0002t0001g0021 a0001c0002t0001g0040 others(25): Show |
35 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.497-941A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122380430 | |||||||
| chr9:122380431 | C | T | 7 | a0001c0002t0001g0098 a0001c0002t0001g0138 a0001c0002t0006g0004 others(4): Show |
12 | HG01081.hp1 HG01123.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.497-940C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122380431 | |||||||
| chr9:122380464 | C | CA | 3 | a0001c0008t0002g0209 a0001c0008t0002g0210 a0001c0008t0002g0215 |
3 | HG02717.hp2 HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.497-902dupA | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 122380464 | ||||||
| chr9:122380464 | CA | C | 2 | a0005c0010t0002g0012 a0005c0010t0002g0128 |
4 | HG01496.hp1 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-902delA | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 122380464 | ||||||
| chr9:122380466 | A | AAAAT | 33 | a0001c0001t0001g0009 a0001c0001t0001g0036 a0001c0001t0001g0078 others(30): Show |
43 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.497-863_497-860dup others(4): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 122380466 | ||||||
| chr9:122380466 | A | AAAATAAA others(1): Show |
4 | a0001c0001t0003g0084 a0001c0001t0004g0069 a0001c0001t0004g0142 others(1): Show |
4 | HG02055.hp1 HG03669.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-867_497-860dup others(8): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 122380466 | ||||||
| chr9:122380466 | AAAAT | A | 23 | a0001c0001t0001g0034 a0001c0001t0001g0097 a0001c0001t0001g0157 others(20): Show |
25 | HG00741.hp1 HG00741.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.497-863_497-860del others(4): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 122380466 | ||||||
| chr9:122380466 | AAAATAAA others(1): Show |
A | 10 | a0001c0001t0001g0158 a0001c0002t0001g0219 a0001c0011t0001g0185 others(7): Show |
17 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.497-867_497-860del others(8): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 122380466 | ||||||
| chr9:122380466 | AAAATAAA others(9): Show |
A | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | HG00738.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.497-875_497-860del others(16): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 122380466 | ||||||
| chr9:122380470 | T | A | 11 | a0001c0002t0001g0043 a0001c0002t0001g0197 a0001c0002t0002g0044 others(8): Show |
14 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.497-901T>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122380470 | |||||||
| chr9:122380474 | T | A | 11 | a0001c0002t0001g0043 a0001c0002t0001g0197 a0001c0002t0002g0044 others(8): Show |
14 | HG01109.hp2 HG02109.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.497-897T>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122380474 | |||||||
| chr9:122380478 | T | A | 4 | a0001c0002t0002g0064 a0001c0008t0002g0212 a0001c0008t0002g0213 others(1): Show |
4 | HG01109.hp2 HG02818.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-893T>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122380478 | |||||||
| chr9:122380630 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.497-741G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122380630 | |||||||
| chr9:122380718 | G | T | 6 | a0001c0011t0001g0185 a0001c0012t0005g0062 a0001c0012t0013g0048 others(3): Show |
13 | HG01243.hp1 HG01884.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.497-653G>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122380718 | |||||||
| chr9:122380760 | C | A | 1 | a0001c0006t0009g0035 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.497-611C>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122380760 | |||||||
| chr9:122380782 | C | T | 71 | a0001c0002t0001g0017 a0001c0002t0001g0020 a0001c0002t0001g0021 others(68): Show |
103 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.497-589C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122380782 | |||||||
| chr9:122380868 | T | C | 73 | a0001c0002t0001g0017 a0001c0002t0001g0020 a0001c0002t0001g0021 others(70): Show |
105 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(102): Show |
intron_variant | MODIFIER | c.497-503T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122380868 | |||||||
| chr9:122381105 | C | G | 71 | a0001c0002t0001g0017 a0001c0002t0001g0020 a0001c0002t0001g0021 others(68): Show |
103 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.497-266C>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122381105 | |||||||
| chr9:122381109 | CCT | C | 3 | a0001c0003t0001g0023 a0001c0003t0001g0217 a0001c0003t0003g0133 |
5 | NA18944.hp2 NA18949.hp1 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-258_497-257del others(2): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 122381109 | ||||||
| chr9:122381169 | C | T | 1 | a0001c0006t0009g0035 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.497-202C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122381169 | |||||||
| chr9:122381177 | C | T | 2 | a0003c0014t0005g0071 a0003c0014t0005g0072 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.497-194C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122381177 | |||||||
| chr9:122381179 | T | C | 3 | a0003c0014t0005g0071 a0003c0014t0005g0072 a0003c0025t0002g0070 |
3 | HG02896.hp2 HG02897.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.497-192T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 5/10 | chr9 | 122381179 | |||||||
| chr9:122381601 | G | A | 1 | a0001c0006t0009g0035 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.678+49G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 6/10 | chr9 | 122381601 | |||||||
| chr9:122381757 | G | A | 6 | a0001c0002t0002g0022 a0001c0002t0002g0045 a0001c0002t0002g0198 others(3): Show |
9 | HG02630.hp2 HG02723.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.762+10G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | chr9 | 122381757 | |||||||
| chr9:122381760 | CA | C | 73 | a0001c0002t0001g0017 a0001c0002t0001g0020 a0001c0002t0001g0021 others(70): Show |
105 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(102): Show |
intron_variant | MODIFIER | c.762+14delA | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | chr9 | 122381760 | |||||||
| chr9:122381866 | A | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(221): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(320): Show |
intron_variant | MODIFIER | c.762+119A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | chr9 | 122381866 | |||||||
| chr9:122381882 | G | A | 1 | a0001c0002t0002g0064 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.762+135G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | chr9 | 122381882 | |||||||
| chr9:122381892 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0087 |
2 | HG00597.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.762+145G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | chr9 | 122381892 | |||||||
| chr9:122381914 | G | A | 3 | a0001c0001t0001g0065 a0001c0001t0020g0165 a0001c0021t0001g0063 |
3 | HG01884.hp1 HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.762+167G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | chr9 | 122381914 | |||||||
| chr9:122382042 | C | T | 3 | a0001c0002t0001g0219 a0001c0013t0010g0131 a0001c0013t0010g0204 |
3 | HG01109.hp1 HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.762+295C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | chr9 | 122382042 | |||||||
| chr9:122382079 | A | G | 69 | a0001c0002t0001g0017 a0001c0002t0001g0020 a0001c0002t0001g0021 others(66): Show |
98 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.762+332A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | chr9 | 122382079 | |||||||
| chr9:122382144 | G | C | 63 | a0001c0002t0001g0017 a0001c0002t0001g0020 a0001c0002t0001g0021 others(60): Show |
87 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.762+397G>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | chr9 | 122382144 | |||||||
| chr9:122382144 | G | T | 1 | a0008c0016t0001g0067 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.762+397G>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | chr9 | 122382144 | |||||||
| chr9:122382164 | C | T | 1 | a0004c0009t0001g0194 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.762+417C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | chr9 | 122382164 | |||||||
| chr9:122382491 | C | T | 10 | a0001c0001t0003g0083 a0001c0001t0003g0163 a0002c0004t0001g0115 others(7): Show |
10 | HG01106.hp2 HG01358.hp1 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.762+744C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | chr9 | 122382491 | |||||||
| chr9:122382532 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.762+785A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | chr9 | 122382532 | |||||||
| chr9:122382563 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.762+816A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | chr9 | 122382563 | |||||||
| chr9:122382640 | T | C | 7 | a0001c0002t0001g0020 a0001c0006t0007g0042 a0001c0006t0007g0186 others(4): Show |
10 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.763-869T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | chr9 | 122382640 | |||||||
| chr9:122382662 | T | C | 33 | a0001c0002t0001g0021 a0001c0002t0001g0040 a0001c0002t0001g0098 others(30): Show |
46 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.763-847T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | chr9 | 122382662 | |||||||
| chr9:122383031 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.763-478G>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | chr9 | 122383031 | |||||||
| chr9:122383050 | G | C | 82 | a0001c0001t0003g0083 a0001c0001t0003g0163 a0001c0002t0001g0017 others(79): Show |
114 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(111): Show |
intron_variant | MODIFIER | c.763-459G>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | chr9 | 122383050 | |||||||
| chr9:122383099 | T | C | 1 | a0001c0002t0001g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.763-410T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | chr9 | 122383099 | |||||||
| chr9:122383179 | TG | T | 3 | a0001c0002t0001g0219 a0001c0013t0010g0131 a0001c0013t0010g0204 |
3 | HG01109.hp1 HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.763-329delG | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | chr9 | 122383179 | |||||||
| chr9:122383180 | GT | G | 74 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0003g0083 others(71): Show |
98 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.763-316delT | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 122383180 | ||||||
| chr9:122383180 | GTT | G | 6 | a0001c0011t0001g0185 a0001c0012t0005g0062 a0001c0012t0013g0048 others(3): Show |
13 | HG01243.hp1 HG01884.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.763-317_763-316del others(2): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 122383180 | ||||||
| chr9:122383196 | GTTTTTTT others(8): Show |
G | 72 | a0001c0002t0001g0017 a0001c0002t0001g0020 a0001c0002t0001g0021 others(69): Show |
104 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(101): Show |
intron_variant | MODIFIER | c.763-295_763-281del others(15): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 122383196 | ||||||
| chr9:122383207 | CT | C | 11 | a0001c0001t0003g0083 a0001c0001t0003g0163 a0002c0004t0001g0115 others(8): Show |
11 | HG01106.hp2 HG01358.hp1 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.763-288delT | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 122383207 | ||||||
| chr9:122383228 | T | G | 1 | a0009c0017t0021g0068 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.763-281T>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | chr9 | 122383228 | |||||||
| chr9:122383322 | G | A | 3 | a0001c0002t0001g0219 a0001c0013t0010g0131 a0001c0013t0010g0204 |
3 | HG01109.hp1 HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.763-187G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | chr9 | 122383322 | |||||||
| chr9:122383338 | T | C | 1 | a0001c0002t0001g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.763-171T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | chr9 | 122383338 | |||||||
| chr9:122383340 | G | A | 74 | a0001c0002t0001g0017 a0001c0002t0001g0020 a0001c0002t0001g0021 others(71): Show |
106 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.763-169G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | chr9 | 122383340 | |||||||
| chr9:122383464 | T | C | 92 | a0001c0001t0003g0083 a0001c0001t0003g0163 a0001c0002t0001g0017 others(89): Show |
128 | HG00609.hp2 HG00639.hp1 HG00639.hp2 others(125): Show |
intron_variant | MODIFIER | c.763-45T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 7/10 | chr9 | 122383464 | |||||||
| chr9:122383818 | C | CG | 31 | a0001c0001t0001g0006 a0001c0001t0001g0027 a0001c0001t0001g0028 others(28): Show |
37 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.1009+70dupG | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 122383818 | ||||||
| chr9:122383819 | G | A | 3 | a0001c0002t0001g0219 a0001c0013t0010g0131 a0001c0013t0010g0204 |
3 | HG01109.hp1 HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1009+64G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122383819 | |||||||
| chr9:122383832 | G | A | 28 | a0001c0002t0001g0017 a0001c0002t0001g0020 a0001c0002t0001g0043 others(25): Show |
39 | HG00639.hp1 HG01109.hp2 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.1009+77G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122383832 | |||||||
| chr9:122383873 | T | C | 3 | a0001c0002t0001g0020 a0001c0002t0001g0043 a0001c0002t0002g0161 |
6 | HG02055.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1009+118T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122383873 | |||||||
| chr9:122384090 | T | C | 66 | a0001c0002t0001g0017 a0001c0002t0001g0020 a0001c0002t0001g0021 others(63): Show |
95 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.1009+335T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122384090 | |||||||
| chr9:122384100 | G | A | 9 | a0001c0003t0001g0026 a0001c0003t0001g0060 a0001c0003t0001g0061 others(6): Show |
13 | HG00609.hp2 HG02622.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.1009+345G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122384100 | |||||||
| chr9:122384167 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1009+412A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122384167 | |||||||
| chr9:122384193 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1009+438A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122384193 | |||||||
| chr9:122384199 | C | T | 20 | a0001c0002t0001g0021 a0001c0002t0001g0040 a0001c0002t0001g0107 others(17): Show |
25 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.1009+444C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122384199 | |||||||
| chr9:122384265 | G | T | 7 | a0001c0006t0007g0042 a0001c0006t0007g0186 a0001c0006t0007g0187 others(4): Show |
10 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1009+510G>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122384265 | |||||||
| chr9:122384422 | T | C | 17 | a0001c0002t0001g0020 a0001c0002t0001g0208 a0001c0006t0007g0042 others(14): Show |
28 | HG00639.hp1 HG01243.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1009+667T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122384422 | |||||||
| chr9:122384616 | C | T | 75 | a0001c0002t0001g0017 a0001c0002t0001g0020 a0001c0002t0001g0021 others(72): Show |
107 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(104): Show |
intron_variant | MODIFIER | c.1009+861C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122384616 | |||||||
| chr9:122384664 | C | T | 75 | a0001c0002t0001g0017 a0001c0002t0001g0020 a0001c0002t0001g0021 others(72): Show |
107 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(104): Show |
intron_variant | MODIFIER | c.1009+909C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122384664 | |||||||
| chr9:122384701 | T | G | 75 | a0001c0002t0001g0017 a0001c0002t0001g0020 a0001c0002t0001g0021 others(72): Show |
107 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(104): Show |
intron_variant | MODIFIER | c.1009+946T>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122384701 | |||||||
| chr9:122384826 | G | A | 15 | a0001c0003t0001g0060 a0001c0003t0001g0061 a0001c0006t0007g0042 others(12): Show |
24 | HG00639.hp1 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1009+1071G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122384826 | |||||||
| chr9:122385057 | G | A | 1 | a0001c0006t0009g0035 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1009+1302G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122385057 | |||||||
| chr9:122385170 | A | C | 75 | a0001c0002t0001g0017 a0001c0002t0001g0020 a0001c0002t0001g0021 others(72): Show |
107 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(104): Show |
intron_variant | MODIFIER | c.1010-1276A>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122385170 | |||||||
| chr9:122385183 | G | C | 75 | a0001c0002t0001g0017 a0001c0002t0001g0020 a0001c0002t0001g0021 others(72): Show |
107 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(104): Show |
intron_variant | MODIFIER | c.1010-1263G>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122385183 | |||||||
| chr9:122385250 | G | A | 1 | a0001c0006t0009g0035 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1010-1196G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122385250 | |||||||
| chr9:122385253 | T | C | 75 | a0001c0002t0001g0017 a0001c0002t0001g0020 a0001c0002t0001g0021 others(72): Show |
107 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(104): Show |
intron_variant | MODIFIER | c.1010-1193T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122385253 | |||||||
| chr9:122385258 | G | A | 1 | a0009c0017t0021g0068 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1010-1188G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122385258 | |||||||
| chr9:122385342 | G | T | 1 | a0001c0006t0009g0035 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1010-1104G>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122385342 | |||||||
| chr9:122385408 | G | A | 75 | a0001c0002t0001g0017 a0001c0002t0001g0020 a0001c0002t0001g0021 others(72): Show |
107 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(104): Show |
intron_variant | MODIFIER | c.1010-1038G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122385408 | |||||||
| chr9:122385580 | A | T | 1 | a0001c0008t0002g0213 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1010-866A>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122385580 | |||||||
| chr9:122385584 | A | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0100 |
2 | HG02165.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1010-862A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122385584 | |||||||
| chr9:122385592 | A | G | 75 | a0001c0002t0001g0017 a0001c0002t0001g0020 a0001c0002t0001g0021 others(72): Show |
107 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(104): Show |
intron_variant | MODIFIER | c.1010-854A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122385592 | |||||||
| chr9:122385612 | T | C | 24 | a0001c0002t0001g0017 a0001c0002t0001g0020 a0001c0002t0001g0043 others(21): Show |
34 | HG01109.hp2 HG01496.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.1010-834T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122385612 | |||||||
| chr9:122385641 | G | T | 51 | a0001c0002t0001g0021 a0001c0002t0001g0040 a0001c0002t0001g0098 others(48): Show |
73 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.1010-805G>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122385641 | |||||||
| chr9:122385652 | G | A | 2 | a0001c0013t0010g0131 a0001c0013t0010g0204 |
2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1010-794G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122385652 | |||||||
| chr9:122385863 | C | CG | 7 | a0001c0002t0001g0098 a0001c0002t0001g0138 a0001c0002t0006g0004 others(4): Show |
12 | HG01081.hp1 HG01123.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.1010-583_1010-582i others(3): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122385863 | |||||||
| chr9:122385920 | C | T | 1 | a0001c0002t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1010-526C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122385920 | |||||||
| chr9:122386013 | G | C | 2 | a0001c0003t0001g0030 a0001c0003t0001g0134 |
3 | NA18961.hp1 NA18963.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1010-433G>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122386013 | |||||||
| chr9:122386130 | TA | T | 81 | a0001c0001t0001g0049 a0001c0001t0001g0092 a0001c0001t0001g0157 others(78): Show |
113 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(110): Show |
intron_variant | MODIFIER | c.1010-301delA | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 122386130 | ||||||
| chr9:122386142 | A | G | 8 | a0001c0001t0003g0083 a0001c0001t0003g0163 a0002c0004t0003g0108 others(5): Show |
8 | HG01106.hp2 HG01358.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.1010-304A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122386142 | |||||||
| chr9:122386155 | A | C | 1 | a0001c0002t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1010-291A>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122386155 | |||||||
| chr9:122386264 | T | C | 2 | a0002c0007t0001g0119 a0002c0007t0001g0120 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1010-182T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122386264 | |||||||
| chr9:122386268 | G | T | 1 | a0009c0017t0021g0068 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1010-178G>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122386268 | |||||||
| chr9:122386292 | G | T | 14 | a0001c0006t0007g0042 a0001c0006t0007g0186 a0001c0006t0007g0187 others(11): Show |
23 | HG00639.hp1 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1010-154G>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122386292 | |||||||
| chr9:122386317 | A | G | 27 | a0001c0002t0001g0017 a0001c0002t0001g0020 a0001c0002t0001g0043 others(24): Show |
37 | HG01109.hp2 HG01496.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.1010-129A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122386317 | |||||||
| chr9:122386353 | A | G | 83 | a0001c0001t0003g0083 a0001c0001t0003g0163 a0001c0002t0001g0017 others(80): Show |
115 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(112): Show |
intron_variant | MODIFIER | c.1010-93A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 8/10 | chr9 | 122386353 | |||||||
| chr9:122386828 | G | A | 1 | a0001c0002t0022g0141 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1296+96G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122386828 | |||||||
| chr9:122387031 | G | A | 8 | a0001c0001t0003g0083 a0001c0001t0003g0163 a0002c0004t0003g0108 others(5): Show |
8 | HG01106.hp2 HG01358.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.1296+299G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122387031 | |||||||
| chr9:122387041 | C | T | 1 | a0001c0006t0009g0035 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1296+309C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122387041 | |||||||
| chr9:122387081 | G | A | 1 | a0001c0001t0024g0086 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1296+349G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122387081 | |||||||
| chr9:122387132 | A | G | 2 | a0004c0009t0001g0192 a0004c0009t0001g0193 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1296+400A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122387132 | |||||||
| chr9:122387223 | G | A | 1 | a0001c0001t0011g0147 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1296+491G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122387223 | |||||||
| chr9:122387270 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0175 |
3 | HG01070.hp1 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1296+538C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122387270 | |||||||
| chr9:122387396 | T | C | 2 | a0001c0001t0001g0038 a0001c0001t0001g0178 |
3 | HG02683.hp2 HG02698.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1296+664T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122387396 | |||||||
| chr9:122387405 | T | C | 8 | a0001c0001t0003g0083 a0001c0001t0003g0163 a0002c0004t0003g0108 others(5): Show |
8 | HG01106.hp2 HG01358.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.1296+673T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122387405 | |||||||
| chr9:122387679 | T | C | 67 | a0001c0001t0003g0083 a0001c0001t0003g0163 a0001c0002t0001g0017 others(64): Show |
90 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.1296+947T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122387679 | |||||||
| chr9:122387691 | A | G | 91 | a0001c0001t0003g0083 a0001c0001t0003g0163 a0001c0002t0001g0017 others(88): Show |
126 | HG00609.hp2 HG00639.hp1 HG00639.hp2 others(123): Show |
intron_variant | MODIFIER | c.1296+959A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122387691 | |||||||
| chr9:122387724 | T | G | 67 | a0001c0001t0003g0083 a0001c0001t0003g0163 a0001c0002t0001g0017 others(64): Show |
90 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.1296+992T>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122387724 | |||||||
| chr9:122387772 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1296+1040T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122387772 | |||||||
| chr9:122387794 | G | A | 11 | a0001c0006t0007g0042 a0001c0006t0007g0186 a0001c0006t0007g0187 others(8): Show |
19 | HG00639.hp1 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1296+1062G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122387794 | |||||||
| chr9:122387998 | T | C | 1 | a0001c0006t0009g0035 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1296+1266T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122387998 | |||||||
| chr9:122388074 | C | T | 1 | a0001c0006t0009g0035 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1296+1342C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122388074 | |||||||
| chr9:122388148 | G | A | 8 | a0001c0003t0001g0060 a0001c0003t0001g0061 a0001c0003t0003g0011 others(5): Show |
11 | HG00609.hp2 HG02622.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.1296+1416G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122388148 | |||||||
| chr9:122388175 | C | T | 1 | a0001c0003t0001g0026 | 2 | HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1296+1443C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122388175 | |||||||
| chr9:122388202 | T | G | 9 | a0001c0002t0001g0017 a0001c0002t0001g0124 a0001c0002t0001g0125 others(6): Show |
11 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1296+1470T>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122388202 | |||||||
| chr9:122388224 | T | A | 16 | a0001c0006t0007g0042 a0001c0006t0007g0186 a0001c0006t0007g0187 others(13): Show |
25 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1296+1492T>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122388224 | |||||||
| chr9:122388238 | G | A | 16 | a0001c0006t0007g0042 a0001c0006t0007g0186 a0001c0006t0007g0187 others(13): Show |
25 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1296+1506G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122388238 | |||||||
| chr9:122388277 | C | T | 6 | a0001c0012t0005g0062 a0001c0012t0013g0048 a0003c0005t0005g0003 others(3): Show |
11 | HG01243.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1296+1545C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122388277 | |||||||
| chr9:122388293 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0144 |
3 | HG00280.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1296+1561G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122388293 | |||||||
| chr9:122388321 | T | C | 1 | a0001c0001t0004g0148 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1296+1589T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122388321 | |||||||
| chr9:122388584 | C | G | 4 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0145 others(1): Show |
4 | HG00280.hp2 HG03669.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1297-1614C>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122388584 | |||||||
| chr9:122388609 | A | G | 62 | a0001c0001t0003g0083 a0001c0001t0003g0163 a0001c0002t0001g0017 others(59): Show |
87 | HG00609.hp2 HG00639.hp1 HG01106.hp2 others(84): Show |
intron_variant | MODIFIER | c.1297-1589A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122388609 | |||||||
| chr9:122388670 | C | T | 13 | a0001c0006t0007g0042 a0001c0006t0007g0186 a0001c0006t0007g0187 others(10): Show |
21 | HG00639.hp1 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1297-1528C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122388670 | |||||||
| chr9:122388741 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1297-1457C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122388741 | |||||||
| chr9:122388785 | CT | C | 16 | a0001c0006t0007g0042 a0001c0006t0007g0186 a0001c0006t0007g0187 others(13): Show |
25 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1297-1411delT | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 122388785 | ||||||
| chr9:122389096 | T | G | 3 | a0001c0001t0004g0155 a0001c0001t0004g0168 a0001c0001t0004g0181 |
3 | HG00741.hp2 HG01346.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.1297-1102T>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122389096 | |||||||
| chr9:122389107 | G | A | 6 | a0001c0012t0005g0062 a0001c0012t0013g0048 a0003c0005t0005g0003 others(3): Show |
11 | HG01243.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1297-1091G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122389107 | |||||||
| chr9:122389148 | CT | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(155): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.1297-1030delT | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 122389148 | ||||||
| chr9:122389148 | CTT | C | 11 | a0001c0001t0001g0166 a0001c0001t0003g0083 a0001c0001t0003g0163 others(8): Show |
11 | HG00741.hp1 HG01106.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.1297-1031_1297-103 others(6): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 122389148 | ||||||
| chr9:122389148 | CTTT | C | 8 | a0001c0003t0001g0060 a0001c0003t0001g0061 a0001c0003t0003g0011 others(5): Show |
11 | HG00609.hp2 HG02622.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.1297-1032_1297-103 others(7): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 122389148 | ||||||
| chr9:122389177 | A | G | 17 | a0001c0002t0001g0020 a0001c0006t0007g0042 a0001c0006t0007g0186 others(14): Show |
28 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1297-1021A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122389177 | |||||||
| chr9:122389203 | T | A | 1 | a0001c0001t0001g0149 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1297-995T>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122389203 | |||||||
| chr9:122389219 | T | C | 62 | a0001c0001t0003g0083 a0001c0001t0003g0163 a0001c0002t0001g0017 others(59): Show |
87 | HG00609.hp2 HG00639.hp1 HG01106.hp2 others(84): Show |
intron_variant | MODIFIER | c.1297-979T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122389219 | |||||||
| chr9:122389270 | T | C | 17 | a0001c0002t0001g0020 a0001c0006t0007g0042 a0001c0006t0007g0186 others(14): Show |
28 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1297-928T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122389270 | |||||||
| chr9:122389292 | T | A | 17 | a0001c0002t0001g0020 a0001c0006t0007g0042 a0001c0006t0007g0186 others(14): Show |
28 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1297-906T>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122389292 | |||||||
| chr9:122389292 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1297-906T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122389292 | |||||||
| chr9:122389397 | C | T | 16 | a0001c0006t0007g0042 a0001c0006t0007g0186 a0001c0006t0007g0187 others(13): Show |
25 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1297-801C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122389397 | |||||||
| chr9:122389433 | A | G | 17 | a0001c0002t0001g0020 a0001c0006t0007g0042 a0001c0006t0007g0186 others(14): Show |
28 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1297-765A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122389433 | |||||||
| chr9:122389516 | T | C | 17 | a0001c0002t0001g0020 a0001c0006t0007g0042 a0001c0006t0007g0186 others(14): Show |
28 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1297-682T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122389516 | |||||||
| chr9:122389605 | T | A | 63 | a0001c0001t0003g0083 a0001c0001t0003g0163 a0001c0002t0001g0017 others(60): Show |
88 | HG00609.hp2 HG00639.hp1 HG01106.hp2 others(85): Show |
intron_variant | MODIFIER | c.1297-593T>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122389605 | |||||||
| chr9:122389623 | C | A | 1 | a0001c0003t0003g0011 | 3 | NA18947.hp1 NA19060.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1297-575C>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122389623 | |||||||
| chr9:122389688 | T | C | 17 | a0001c0002t0001g0020 a0001c0006t0007g0042 a0001c0006t0007g0186 others(14): Show |
28 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1297-510T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122389688 | |||||||
| chr9:122389698 | T | C | 1 | a0001c0001t0015g0150 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1297-500T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122389698 | |||||||
| chr9:122389720 | T | C | 17 | a0001c0002t0001g0020 a0001c0006t0007g0042 a0001c0006t0007g0186 others(14): Show |
28 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1297-478T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122389720 | |||||||
| chr9:122389835 | T | C | 17 | a0001c0002t0001g0020 a0001c0006t0007g0042 a0001c0006t0007g0186 others(14): Show |
28 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1297-363T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122389835 | |||||||
| chr9:122389961 | A | T | 14 | a0001c0002t0001g0020 a0001c0006t0007g0042 a0001c0006t0007g0186 others(11): Show |
24 | HG00639.hp1 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1297-237A>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122389961 | |||||||
| chr9:122390019 | G | C | 17 | a0001c0002t0001g0020 a0001c0006t0007g0042 a0001c0006t0007g0186 others(14): Show |
28 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1297-179G>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122390019 | |||||||
| chr9:122390067 | T | C | 1 | a0001c0006t0009g0035 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1297-131T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 9/10 | chr9 | 122390067 | |||||||
| chr9:122390506 | G | T | 1 | a0001c0001t0001g0057 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1444+161G>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122390506 | |||||||
| chr9:122390620 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1444+275G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122390620 | |||||||
| chr9:122390669 | G | A | 6 | a0001c0001t0001g0039 a0001c0001t0001g0176 a0001c0002t0002g0161 others(3): Show |
10 | HG01496.hp1 HG02109.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1444+324G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122390669 | |||||||
| chr9:122390690 | A | G | 58 | a0001c0001t0003g0008 a0001c0001t0003g0083 a0001c0001t0003g0084 others(55): Show |
83 | HG00438.hp1 HG00597.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.1444+345A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122390690 | |||||||
| chr9:122390699 | C | T | 19 | a0001c0002t0001g0021 a0001c0002t0001g0040 a0001c0002t0001g0107 others(16): Show |
24 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.1444+354C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122390699 | |||||||
| chr9:122390713 | C | T | 6 | a0001c0002t0001g0017 a0001c0002t0001g0124 a0001c0002t0001g0125 others(3): Show |
8 | HG02257.hp1 HG02572.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1444+368C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122390713 | |||||||
| chr9:122390722 | C | A | 16 | a0001c0006t0007g0042 a0001c0006t0007g0186 a0001c0006t0007g0187 others(13): Show |
25 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1444+377C>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122390722 | |||||||
| chr9:122390850 | T | C | 2 | a0001c0002t0002g0044 a0001c0002t0002g0064 |
3 | HG01109.hp2 HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1444+505T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122390850 | |||||||
| chr9:122390875 | C | T | 3 | a0001c0001t0001g0152 a0001c0001t0001g0166 a0001c0001t0001g0174 |
3 | HG00408.hp1 NA18968.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1444+530C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122390875 | |||||||
| chr9:122390889 | A | T | 16 | a0001c0006t0007g0042 a0001c0006t0007g0186 a0001c0006t0007g0187 others(13): Show |
25 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1444+544A>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122390889 | |||||||
| chr9:122391022 | C | T | 2 | a0003c0014t0005g0071 a0003c0014t0005g0072 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1444+677C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391022 | |||||||
| chr9:122391073 | G | A | 16 | a0001c0006t0007g0042 a0001c0006t0007g0186 a0001c0006t0007g0187 others(13): Show |
25 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1444+728G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391073 | |||||||
| chr9:122391095 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1444+750C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391095 | |||||||
| chr9:122391113 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1444+768A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391113 | |||||||
| chr9:122391145 | T | C | 16 | a0001c0006t0007g0042 a0001c0006t0007g0186 a0001c0006t0007g0187 others(13): Show |
25 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1444+800T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391145 | |||||||
| chr9:122391161 | C | T | 4 | a0001c0002t0002g0161 a0001c0011t0002g0025 a0005c0010t0002g0012 others(1): Show |
7 | HG01496.hp1 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1444+816C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391161 | |||||||
| chr9:122391162 | G | A | 16 | a0001c0006t0007g0042 a0001c0006t0007g0186 a0001c0006t0007g0187 others(13): Show |
25 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1444+817G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391162 | |||||||
| chr9:122391264 | A | G | 3 | a0001c0006t0009g0035 a0001c0013t0010g0131 a0001c0013t0010g0204 |
4 | HG01109.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1444+919A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391264 | |||||||
| chr9:122391270 | A | C | 16 | a0001c0006t0007g0042 a0001c0006t0007g0186 a0001c0006t0007g0187 others(13): Show |
25 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1445-919A>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391270 | |||||||
| chr9:122391302 | A | T | 1 | a0001c0002t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1445-887A>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391302 | |||||||
| chr9:122391309 | CATATACA others(46): Show |
C | 2 | a0001c0013t0010g0131 a0001c0013t0010g0204 |
2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1445-874_1445-822d others(55): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 122391309 | ||||||
| chr9:122391313 | TAC | T | 21 | a0001c0001t0001g0041 a0001c0001t0001g0143 a0001c0001t0001g0183 others(18): Show |
30 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1445-868_1445-867d others(4): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 122391313 | ||||||
| chr9:122391315 | C | T | 14 | a0001c0006t0007g0042 a0001c0006t0007g0186 a0001c0006t0007g0187 others(11): Show |
23 | HG00639.hp1 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1445-874C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391315 | |||||||
| chr9:122391317 | C | T | 14 | a0001c0006t0007g0042 a0001c0006t0007g0186 a0001c0006t0007g0187 others(11): Show |
23 | HG00639.hp1 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1445-872C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391317 | |||||||
| chr9:122391321 | CATATATA others(48): Show |
C | 1 | a0001c0006t0009g0035 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1445-859_1445-805d others(57): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 122391321 | ||||||
| chr9:122391325 | TATATGTG others(78): Show |
T | 13 | a0001c0006t0007g0042 a0001c0006t0007g0186 a0001c0006t0007g0187 others(10): Show |
21 | HG00639.hp1 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1445-859_1445-775d others(87): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 122391325 | ||||||
| chr9:122391347 | CTATATAT others(7): Show |
C | 13 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0082 others(10): Show |
14 | HG00597.hp2 HG00738.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1445-805_1445-792d others(16): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 122391347 | ||||||
| chr9:122391347 | CTATATAT others(21): Show |
C | 1 | a0001c0001t0001g0014 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1445-819_1445-792d others(30): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 122391347 | ||||||
| chr9:122391347 | CTATATAT others(33): Show |
C | 13 | a0001c0001t0003g0008 a0001c0001t0003g0083 a0001c0001t0003g0084 others(10): Show |
16 | HG00438.hp1 HG00597.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.1445-819_1445-780d others(42): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 122391347 | ||||||
| chr9:122391358 | CAT | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0171 others(42): Show |
56 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1445-819_1445-818d others(4): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 122391358 | ||||||
| chr9:122391362 | T | TATATATA others(1): Show |
6 | a0001c0003t0003g0011 a0001c0003t0003g0024 a0001c0003t0003g0051 others(3): Show |
9 | HG00609.hp2 HG03688.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.1445-820_1445-819i others(10): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 122391362 | ||||||
| chr9:122391368 | TATAC | T | 31 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0015 others(28): Show |
47 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.1445-817_1445-814d others(6): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 122391368 | ||||||
| chr9:122391370 | T | C | 20 | a0001c0002t0001g0017 a0001c0002t0002g0022 a0001c0002t0002g0044 others(17): Show |
28 | HG01109.hp2 HG01496.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1445-819T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391370 | |||||||
| chr9:122391372 | C | T | 20 | a0001c0002t0001g0017 a0001c0002t0002g0022 a0001c0002t0002g0044 others(17): Show |
28 | HG01109.hp2 HG01496.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1445-817C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391372 | |||||||
| chr9:122391372 | CAT | C | 7 | a0001c0001t0001g0034 a0001c0001t0001g0049 a0001c0001t0001g0057 others(4): Show |
8 | HG01070.hp1 HG01071.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.1445-805_1445-804d others(4): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 122391372 | ||||||
| chr9:122391374 | T | C | 33 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0015 others(30): Show |
49 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.1445-815T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391374 | |||||||
| chr9:122391374 | TATATATA others(5): Show |
T | 1 | a0008c0016t0001g0067 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1445-779_1445-768d others(14): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 122391374 | ||||||
| chr9:122391376 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1445-813T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391376 | |||||||
| chr9:122391384 | T | C | 15 | a0001c0002t0001g0017 a0001c0002t0001g0124 a0001c0002t0001g0125 others(12): Show |
20 | HG00609.hp2 HG02257.hp1 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.1445-805T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391384 | |||||||
| chr9:122391386 | C | T | 6 | a0001c0003t0003g0011 a0001c0003t0003g0024 a0001c0003t0003g0051 others(3): Show |
9 | HG00609.hp2 HG03688.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.1445-803C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391386 | |||||||
| chr9:122391386 | CATATATA others(37): Show |
C | 19 | a0001c0002t0002g0022 a0001c0002t0002g0044 a0001c0002t0002g0045 others(16): Show |
27 | HG01109.hp2 HG01496.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1445-791_1445-748d others(46): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 122391386 | ||||||
| chr9:122391395 | A | G | 6 | a0001c0003t0003g0011 a0001c0003t0003g0024 a0001c0003t0003g0051 others(3): Show |
9 | HG00609.hp2 HG03688.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.1445-794A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391395 | |||||||
| chr9:122391396 | T | C | 3 | a0001c0006t0009g0035 a0001c0013t0010g0131 a0001c0013t0010g0204 |
4 | HG01109.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1445-793T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391396 | |||||||
| chr9:122391398 | C | T | 6 | a0001c0003t0003g0011 a0001c0003t0003g0024 a0001c0003t0003g0051 others(3): Show |
9 | HG00609.hp2 HG03688.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.1445-791C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391398 | |||||||
| chr9:122391410 | CAT | C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0002t0001g0136 others(5): Show |
12 | HG00544.hp2 HG02559.hp2 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.1445-763_1445-762d others(4): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 122391410 | ||||||
| chr9:122391410 | CATATATA others(1): Show |
C | 3 | a0001c0006t0009g0035 a0001c0013t0010g0131 a0001c0013t0010g0204 |
4 | HG01109.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1445-769_1445-762d others(10): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 122391410 | ||||||
| chr9:122391411 | A | G | 7 | a0001c0001t0001g0082 a0001c0001t0001g0087 a0001c0001t0001g0169 others(4): Show |
8 | HG00597.hp2 HG02129.hp1 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.1445-778A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391411 | |||||||
| chr9:122391412 | T | TATATATA others(3): Show |
1 | a0001c0001t0001g0036 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1445-768_1445-767i others(12): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 122391412 | ||||||
| chr9:122391412 | TATATATA others(9): Show |
T | 19 | a0001c0002t0001g0021 a0001c0002t0001g0040 a0001c0002t0001g0170 others(16): Show |
24 | HG00639.hp2 HG00735.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.1445-761_1445-746d others(18): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 122391412 | ||||||
| chr9:122391414 | TATATATA others(7): Show |
T | 2 | a0001c0002t0001g0107 a0004c0009t0001g0218 |
2 | HG00735.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1445-761_1445-748d others(16): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 122391414 | ||||||
| chr9:122391418 | T | C | 13 | a0001c0006t0007g0042 a0001c0006t0007g0186 a0001c0006t0007g0187 others(10): Show |
21 | HG00639.hp1 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1445-771T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391418 | |||||||
| chr9:122391424 | TATAC | T | 8 | a0001c0002t0001g0098 a0001c0002t0001g0138 a0001c0002t0006g0004 others(5): Show |
13 | HG01081.hp1 HG01123.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.1445-761_1445-758d others(6): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 122391424 | ||||||
| chr9:122391426 | T | C | 2 | a0001c0002t0001g0136 a0001c0002t0001g0197 |
2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1445-763T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391426 | |||||||
| chr9:122391428 | C | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(5): Show |
9 | HG00597.hp2 HG02615.hp2 HG03492.hp1 others(6): Show |
intron_variant | MODIFIER | c.1445-761C>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391428 | |||||||
| chr9:122391428 | CAT | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(145): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.1445-744_1445-743d others(4): Show |
PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 122391428 | ||||||
| chr9:122391430 | T | C | 39 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(36): Show |
59 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1445-759T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391430 | |||||||
| chr9:122391432 | T | C | 2 | a0001c0006t0008g0188 a0001c0006t0008g0205 |
2 | HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1445-757T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391432 | |||||||
| chr9:122391435 | A | G | 19 | a0001c0002t0002g0022 a0001c0002t0002g0044 a0001c0002t0002g0045 others(16): Show |
27 | HG01109.hp2 HG01496.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1445-754A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391435 | |||||||
| chr9:122391437 | A | G | 1 | a0004c0009t0001g0218 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1445-752A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391437 | |||||||
| chr9:122391573 | G | C | 3 | a0001c0002t0001g0126 a0001c0002t0001g0127 a0001c0002t0001g0129 |
3 | HG02257.hp1 HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1445-616G>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391573 | |||||||
| chr9:122391600 | T | C | 1 | a0001c0002t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1445-589T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391600 | |||||||
| chr9:122391607 | C | G | 13 | a0001c0001t0003g0008 a0001c0001t0003g0083 a0001c0001t0003g0084 others(10): Show |
16 | HG00438.hp1 HG00597.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.1445-582C>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391607 | |||||||
| chr9:122391630 | A | G | 29 | a0001c0001t0003g0008 a0001c0001t0003g0083 a0001c0001t0003g0084 others(26): Show |
41 | HG00438.hp1 HG00597.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1445-559A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391630 | |||||||
| chr9:122391637 | A | G | 13 | a0001c0006t0007g0042 a0001c0006t0007g0186 a0001c0006t0007g0187 others(10): Show |
21 | HG00639.hp1 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1445-552A>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391637 | |||||||
| chr9:122391712 | AT | A | 7 | a0001c0006t0007g0042 a0001c0006t0007g0186 a0001c0006t0007g0187 others(4): Show |
10 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1445-476delT | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391712 | |||||||
| chr9:122391715 | G | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0158 |
2 | HG03654.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1445-474G>T | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391715 | |||||||
| chr9:122391720 | C | CG | 13 | a0001c0002t0002g0044 a0001c0002t0002g0047 a0001c0002t0002g0064 others(10): Show |
18 | HG01109.hp2 HG01496.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1445-464dupG | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 122391720 | ||||||
| chr9:122391834 | G | A | 1 | a0001c0006t0009g0035 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1445-355G>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391834 | |||||||
| chr9:122391914 | G | C | 1 | a0001c0001t0001g0177 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1445-275G>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122391914 | |||||||
| chr9:122392035 | T | G | 16 | a0001c0006t0007g0042 a0001c0006t0007g0186 a0001c0006t0007g0187 others(13): Show |
25 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1445-154T>G | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122392035 | |||||||
| chr9:122392093 | T | C | 1 | a0001c0002t0001g0124 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1445-96T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122392093 | |||||||
| chr9:122392151 | T | A | 3 | a0001c0002t0001g0136 a0001c0002t0001g0197 a0001c0002t0001g0208 |
3 | HG02559.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1445-38T>A | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122392151 | |||||||
| chr9:122392160 | T | C | 16 | a0001c0006t0007g0042 a0001c0006t0007g0186 a0001c0006t0007g0187 others(13): Show |
25 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1445-29T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122392160 | |||||||
| chr9:122392176 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1445-13T>C | PTGS1 | ENSG00000095303.17 | transcript | ENST00000362012.7 | protein_coding | 10/10 | chr9 | 122392176 |