Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 145482 |
| ensemblid | ENSG00000140043.12 |
| hgncid | 20149 |
| symbol | PTGR2 |
| name | prostaglandin reductase 2 |
| refseq_nuc | NM_001146154.2 |
| refseq_prot | NP_001139626.1 |
| ensembl_nuc | ENST00000555661.6 |
| ensembl_prot | ENSP00000452280.1 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 73851831 |
| end | 73885726 |
| strand | + |
| ver | v1.2 |
| region | chr14:73851831-73885726 |
| region5000 | chr14:73846831-73890726 |
| regionname0 | PTGR2_chr14_73851831_73885726 |
| regionname5000 | PTGR2_chr14_73846831_73890726 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 351 | 418 | 93 | 78 | 183 | 18 | 44 | 139 | PTGR2_chr14_73846831_73890726 | PTGR2 | MIVQR others(346): Show |
chr14 | 73846831 | 73890726 |
| a0002 | 0/0 | 351 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | MIVQR others(346): Show |
chr14 | 73846831 | 73890726 |
| a0003 | 0/0 | 351 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | MIVQR others(346): Show |
chr14 | 73846831 | 73890726 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1053 | 218 | 42 | 33 | 102 | 10 | 31 | PTGR2_chr14_73846831_73890726 | PTGR2 | ATGAT others(1048): Show |
chr14 | 73846831 | 73890726 | ||
| a0001c0002 | 1/1 | 1053 | 200 | 51 | 45 | 81 | 8 | 13 | PTGR2_chr14_73846831_73890726 | PTGR2 | ATGAT others(1048): Show |
chr14 | 73846831 | 73890726 | ||
| a0002c0004 | 0/0 | 1053 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | ATGAT others(1048): Show |
chr14 | 73846831 | 73890726 | ||
| a0003c0003 | 0/0 | 1053 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | ATGAT others(1048): Show |
chr14 | 73846831 | 73890726 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 2765 | 85 | 5 | 9 | 59 | 2 | 10 | PTGR2_chr14_73846831_73890726 | PTGR2 | GCGCG others(2760): Show |
chr14 | 73846831 | 73890726 |
| a0001c0001t0003 | 0/0 | 2765 | 71 | 18 | 19 | 17 | 7 | 10 | PTGR2_chr14_73846831_73890726 | PTGR2 | GCGCG others(2760): Show |
chr14 | 73846831 | 73890726 |
| a0001c0001t0004 | 0/0 | 2765 | 49 | 15 | 4 | 18 | 1 | 11 | PTGR2_chr14_73846831_73890726 | PTGR2 | GCGCG others(2760): Show |
chr14 | 73846831 | 73890726 |
| a0001c0001t0008 | 0/0 | 2765 | 8 | 0 | 0 | 8 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | GCGCG others(2760): Show |
chr14 | 73846831 | 73890726 |
| a0001c0001t0011 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | GCGCG others(2760): Show |
chr14 | 73846831 | 73890726 |
| a0001c0001t0012 | 0/0 | 2765 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | GCGCG others(2760): Show |
chr14 | 73846831 | 73890726 |
| a0001c0001t0013 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | GCGCG others(2760): Show |
chr14 | 73846831 | 73890726 |
| a0001c0001t0014 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | GCGCG others(2760): Show |
chr14 | 73846831 | 73890726 |
| a0001c0001t0015 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | GCGCG others(2760): Show |
chr14 | 73846831 | 73890726 |
| a0001c0002t0001 | 1/1 | 2765 | 134 | 40 | 17 | 63 | 6 | 6 | PTGR2_chr14_73846831_73890726 | PTGR2 | GCGCG others(2760): Show |
chr14 | 73846831 | 73890726 |
| a0001c0002t0005 | 0/0 | 2765 | 41 | 0 | 22 | 11 | 2 | 6 | PTGR2_chr14_73846831_73890726 | PTGR2 | GCGCG others(2760): Show |
chr14 | 73846831 | 73890726 |
| a0001c0002t0006 | 0/0 | 2765 | 9 | 0 | 2 | 7 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | GCGCG others(2760): Show |
chr14 | 73846831 | 73890726 |
| a0001c0002t0007 | 0/0 | 2766 | 8 | 6 | 2 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | GCGCG others(2761): Show |
chr14 | 73846831 | 73890726 |
| a0001c0002t0009 | 0/0 | 2765 | 2 | 2 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | GCGCG others(2760): Show |
chr14 | 73846831 | 73890726 |
| a0001c0002t0010 | 0/0 | 2765 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | GCGCG others(2760): Show |
chr14 | 73846831 | 73890726 |
| a0001c0002t0016 | 0/0 | 2765 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | GCGCG others(2760): Show |
chr14 | 73846831 | 73890726 |
| a0001c0002t0017 | 0/0 | 2765 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | GCGCG others(2760): Show |
chr14 | 73846831 | 73890726 |
| a0001c0002t0018 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | GCGCG others(2760): Show |
chr14 | 73846831 | 73890726 |
| a0001c0002t0019 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | GCGCG others(2760): Show |
chr14 | 73846831 | 73890726 |
| a0001c0002t0020 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | GCGCG others(2760): Show |
chr14 | 73846831 | 73890726 |
| a0002c0004t0001 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | GCGCG others(2760): Show |
chr14 | 73846831 | 73890726 |
| a0003c0003t0001 | 0/0 | 2765 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | GCGCG others(2760): Show |
chr14 | 73846831 | 73890726 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0001 | 0/0 | 10 | 0 | 0 | 9 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0003 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0005 | 0/0 | 5 | 0 | 1 | 1 | 0 | 3 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0007 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0009 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0008g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0008g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0008g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0008g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0008g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0008g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0008g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0008g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0011g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0012g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0013g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0014g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0001t0015g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0020 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0257 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0002 | 0/0 | 7 | 0 | 6 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0005g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0006g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0006g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0006g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0006g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0006g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0006g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0006g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0007g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0007g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0007g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0007g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0009g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0009g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0010g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0016g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0017g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0018g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0019g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0001c0002t0020g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0002c0004t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| a0003c0003t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0100 | EUR | GBR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0051 | EUR | GBR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0109 | EUR | GBR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0132 | EUR | GBR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00280 | hp1 | a0001 | c0002 | t0005 | g0196 | EUR | FIN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0018 | EUR | FIN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00323 | hp1 | a0001 | c0002 | t0005 | g0194 | EUR | FIN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0012 | EUR | FIN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00408 | hp1 | a0001 | c0001 | t0008 | g0092 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0059 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0227 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0331 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0069 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0038 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00558 | hp2 | a0001 | c0002 | t0006 | g0004 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0260 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00621 | hp1 | a0001 | c0001 | t0008 | g0095 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0106 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00639 | hp2 | a0001 | c0002 | t0005 | g0179 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0108 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0337 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | CHS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0336 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00735 | hp2 | a0001 | c0002 | t0010 | g0143 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0111 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0065 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00741 | hp1 | a0001 | c0002 | t0005 | g0190 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0016 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0224 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0334 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0158 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01070 | hp2 | a0001 | c0002 | t0005 | g0183 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01071 | hp1 | a0001 | c0002 | t0005 | g0011 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0225 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0042 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0148 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0256 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0161 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01099 | hp1 | a0001 | c0002 | t0005 | g0002 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0145 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01106 | hp2 | a0001 | c0002 | t0005 | g0185 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0088 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01109 | hp2 | a0001 | c0002 | t0007 | g0174 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0296 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01167 | hp2 | a0001 | c0002 | t0005 | g0195 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0322 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01168 | hp2 | a0001 | c0002 | t0005 | g0002 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01169 | hp1 | a0001 | c0002 | t0005 | g0199 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0150 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0016 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0226 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0159 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01243 | hp1 | a0001 | c0002 | t0016 | g0345 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01243 | hp2 | a0001 | c0001 | t0012 | g0342 | AMR | PUR | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0140 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01256 | hp1 | a0001 | c0002 | t0005 | g0011 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0242 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01257 | hp1 | a0001 | c0002 | t0005 | g0182 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0026 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0035 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01261 | hp2 | a0001 | c0002 | t0005 | g0002 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0340 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01346 | hp2 | a0001 | c0002 | t0005 | g0203 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0103 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0339 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0116 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01496 | hp1 | a0001 | c0002 | t0007 | g0172 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0029 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0154 | EUR | IBS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0019 | EUR | IBS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0034 | EUR | IBS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0007 | EUR | IBS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0007 | EUR | IBS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0020 | EUR | IBS | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0082 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0156 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0219 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0079 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01928 | hp1 | a0001 | c0002 | t0005 | g0002 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01928 | hp2 | a0001 | c0002 | t0006 | g0280 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01934 | hp2 | a0001 | c0002 | t0005 | g0181 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01943 | hp1 | a0001 | c0002 | t0005 | g0184 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01943 | hp2 | a0001 | c0002 | t0006 | g0281 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0124 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0125 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0113 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0121 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0131 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01978 | hp2 | a0001 | c0002 | t0005 | g0192 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01981 | hp1 | a0001 | c0002 | t0005 | g0002 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0338 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01993 | hp1 | a0001 | c0002 | t0005 | g0180 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01993 | hp2 | a0001 | c0002 | t0005 | g0207 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0347 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0247 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0243 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02040 | hp2 | a0001 | c0002 | t0005 | g0002 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0330 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0341 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0223 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0236 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02083 | hp1 | a0001 | c0001 | t0008 | g0093 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0259 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02129 | hp2 | a0001 | c0002 | t0005 | g0024 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0057 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0261 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0215 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02145 | hp2 | a0001 | c0002 | t0007 | g0006 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0096 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02148 | hp2 | a0001 | c0002 | t0005 | g0011 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | CDX | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0056 | EAS | CDX | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | CDX | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02165 | hp2 | a0001 | c0002 | t0005 | g0197 | EAS | CDX | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0087 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0270 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0134 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0276 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0118 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0114 | AMR | PEL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0119 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0046 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02523 | hp2 | a0001 | c0002 | t0005 | g0201 | EAS | KHV | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0147 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0221 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0063 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02602 | hp2 | a0001 | c0002 | t0005 | g0188 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0073 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0077 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0271 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0157 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02630 | hp2 | a0001 | c0002 | t0007 | g0006 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0218 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0237 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0245 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0048 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0078 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02723 | hp1 | a0001 | c0002 | t0007 | g0171 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0086 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02735 | hp1 | a0001 | c0002 | t0005 | g0187 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0036 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0344 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02738 | hp2 | a0001 | c0002 | t0017 | g0178 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0277 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02809 | hp2 | a0001 | c0002 | t0018 | g0209 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0162 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0164 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0085 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0074 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0212 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0099 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0346 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0104 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0274 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0275 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02965 | hp2 | a0001 | c0002 | t0020 | g0216 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0084 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0055 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02976 | hp2 | a0001 | c0002 | t0007 | g0006 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03017 | hp1 | a0001 | c0002 | t0005 | g0202 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03041 | hp1 | a0001 | c0001 | t0013 | g0343 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03041 | hp2 | a0001 | c0002 | t0009 | g0176 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0284 | AFR | MSL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0149 | AFR | MSL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03130 | hp1 | a0001 | c0002 | t0009 | g0177 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03130 | hp2 | a0001 | c0001 | t0011 | g0139 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0080 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03139 | hp2 | a0002 | c0004 | t0001 | g0163 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0072 | AFR | ESN | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03209 | hp1 | a0001 | c0002 | t0007 | g0006 | AFR | MSL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0047 | AFR | MSL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0321 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0273 | AFR | MSL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | MSL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0211 | AFR | MSL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0332 | AFR | MSL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0329 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03491 | hp1 | a0001 | c0002 | t0005 | g0186 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0309 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03492 | hp1 | a0001 | c0002 | t0005 | g0024 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0213 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0160 | AFR | GWD | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0272 | AFR | MSL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03579 | hp2 | a0001 | c0001 | t0015 | g0137 | AFR | MSL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0071 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0062 | SAS | STU | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0292 | SAS | STU | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0289 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0098 | SAS | PJL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0054 | SAS | BEB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0279 | SAS | BEB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | BEB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0326 | SAS | BEB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0120 | SAS | BEB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0070 | SAS | BEB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03942 | hp2 | a0001 | c0002 | t0005 | g0204 | SAS | BEB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0325 | SAS | STU | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0058 | SAS | STU | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0217 | SAS | BEB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0146 | SAS | BEB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0122 | SAS | STU | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0076 | SAS | STU | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0068 | SAS | STU | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0327 | SAS | STU | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0019 | SAS | STU | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0067 | SAS | STU | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0142 | AFR | YRI | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0155 | AFR | YRI | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | CHB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | CHB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | CHB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0208 | AFR | YRI | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | YRI | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18940 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18941 | hp1 | a0001 | c0002 | t0006 | g0263 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18948 | hp1 | a0001 | c0001 | t0008 | g0094 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18949 | hp1 | a0001 | c0002 | t0006 | g0278 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18950 | hp1 | a0001 | c0002 | t0005 | g0206 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18954 | hp1 | a0001 | c0001 | t0008 | g0089 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18957 | hp1 | a0001 | c0002 | t0005 | g0198 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18957 | hp2 | a0001 | c0001 | t0008 | g0091 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18961 | hp1 | a0001 | c0002 | t0005 | g0189 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18962 | hp2 | a0001 | c0002 | t0005 | g0193 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0348 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18968 | hp2 | a0001 | c0002 | t0005 | g0205 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18972 | hp1 | a0001 | c0002 | t0005 | g0191 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0349 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18982 | hp2 | a0001 | c0002 | t0006 | g0012 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18993 | hp2 | a0001 | c0002 | t0006 | g0004 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18994 | hp1 | a0001 | c0002 | t0005 | g0200 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18995 | hp2 | a0003 | c0003 | t0001 | g0350 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19000 | hp1 | a0001 | c0002 | t0006 | g0269 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19030 | hp1 | a0001 | c0002 | t0019 | g0022 | AFR | LWK | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19030 | hp2 | a0001 | c0001 | t0014 | g0138 | AFR | LWK | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0064 | AFR | LWK | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0220 | AFR | LWK | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19055 | hp1 | a0001 | c0002 | t0006 | g0229 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19055 | hp2 | a0001 | c0001 | t0008 | g0135 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0264 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0351 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19090 | hp1 | a0001 | c0001 | t0008 | g0090 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19240 | hp1 | a0001 | c0002 | t0007 | g0173 | AFR | YRI | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0141 | AFR | YRI | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ASW | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | ASW | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0252 | EUR | TSI | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0022 | EUR | TSI | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0130 | EUR | TSI | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0034 | EUR | TSI | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0144 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG01123 | hp2 | a0001 | c0002 | t0005 | g0002 | AMR | CLM | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0052 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0285 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0210 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0081 | AFR | ACB | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0228 | AFR | MSL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0170 | AFR | MSL | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0222 | AFR | USA | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0066 | AFR | USA | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0151 | AFR | USA | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0129 | AFR | USA | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0214 | AFR | LWK | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0335 | AFR | LWK | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0257 | REF | REF | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0020 | REF | REF | PTGR2_chr14_73846831_73890726 | PTGR2 | chr14 | 73846831 | 73890726 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:73851942 | G | C | 1 | a0001 | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
splice_region_variant | LOW | c.-49G>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/10 | chr14 | 73851942 | |||||||
| chr14:73877114 | T | A | 1 | a0003 | 1 | NA18995.hp2 | missense_variant | MODERATE | c.465T>A | p.Asn155Lys | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/10 | 625/2765 | 465/1056 | 155/351 | chr14 | 73877114 | |||
| chr14:73880122 | C | T | 1 | a0002 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.797C>T | p.Pro266Leu | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/10 | 957/2765 | 797/1056 | 266/351 | chr14 | 73880122 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:73874094 | A | T | 1 | a0001c0001 | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
synonymous_variant | LOW | c.228A>T | p.Gly76Gly | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/10 | 388/2765 | 228/1056 | 76/351 | chr14 | 73874094 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:73851844 | C | G | 2 | a0001c0001t0004 a0001c0001t0008 |
57 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(54): Show |
5_prime_UTR_variant | MODIFIER | c.-147C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/10 | 7019 | chr14 | 73851844 | ||||||
| chr14:73851890 | T | C | 1 | a0001c0002t0010 | 1 | HG00735.hp2 | 5_prime_UTR_variant | MODIFIER | c.-101T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/10 | 6973 | chr14 | 73851890 | ||||||
| chr14:73851896 | C | T | 1 | a0001c0002t0020 | 1 | HG02965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-95C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/10 | 6967 | chr14 | 73851896 | ||||||
| chr14:73851909 | A | G | 1 | a0001c0002t0019 | 1 | NA19030.hp1 | 5_prime_UTR_variant | MODIFIER | c.-82A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/10 | 6954 | chr14 | 73851909 | ||||||
| chr14:73851911 | C | T | 1 | a0001c0002t0018 | 1 | HG02809.hp2 | 5_prime_UTR_variant | MODIFIER | c.-80C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/10 | 6952 | chr14 | 73851911 | ||||||
| chr14:73884406 | G | A | 9 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(6): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*229G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 229 | chr14 | 73884406 | ||||||
| chr14:73884446 | G | A | 1 | a0001c0001t0011 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*269G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 269 | chr14 | 73884446 | ||||||
| chr14:73884566 | G | A | 1 | a0001c0001t0012 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*389G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 389 | chr14 | 73884566 | ||||||
| chr14:73884610 | C | T | 2 | a0001c0002t0005 a0001c0002t0017 |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*433C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 433 | chr14 | 73884610 | ||||||
| chr14:73884785 | G | A | 1 | a0001c0002t0016 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*608G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 608 | chr14 | 73884785 | ||||||
| chr14:73884785 | G | C | 4 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0012 others(1): Show |
74 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*608G>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 608 | chr14 | 73884785 | ||||||
| chr14:73884843 | A | AT | 1 | a0001c0002t0007 | 8 | HG01109.hp2 HG01496.hp1 HG02145.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*667dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 668 | INFO_REALIGN_3_PRIME | chr14 | 73884843 | |||||
| chr14:73884849 | T | G | 1 | a0001c0001t0014 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*672T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 672 | chr14 | 73884849 | ||||||
| chr14:73884861 | A | G | 3 | a0001c0001t0004 a0001c0001t0014 a0001c0001t0015 |
51 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*684A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 684 | chr14 | 73884861 | ||||||
| chr14:73884940 | G | A | 1 | a0001c0002t0009 | 2 | HG03041.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*763G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 763 | chr14 | 73884940 | ||||||
| chr14:73885062 | G | C | 5 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(2): Show |
144 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*885G>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 885 | chr14 | 73885062 | ||||||
| chr14:73885088 | A | G | 6 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(3): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*911A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 911 | chr14 | 73885088 | ||||||
| chr14:73885126 | T | C | 1 | a0001c0002t0006 | 9 | HG00558.hp2 HG01928.hp2 HG01943.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*949T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 949 | chr14 | 73885126 | ||||||
| chr14:73885257 | C | G | 1 | a0001c0002t0017 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1080C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 1080 | chr14 | 73885257 | ||||||
| chr14:73885270 | C | T | 5 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(2): Show |
144 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*1093C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 1093 | chr14 | 73885270 | ||||||
| chr14:73885285 | A | G | 1 | a0001c0001t0014 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1108A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 1108 | chr14 | 73885285 | ||||||
| chr14:73885398 | A | C | 4 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0012 others(1): Show |
74 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*1221A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 1221 | chr14 | 73885398 | ||||||
| chr14:73885611 | G | T | 9 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(6): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*1434G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 10/10 | 1434 | chr14 | 73885611 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:73851961 | G | T | 5 | a0001c0002t0001g0347 a0001c0002t0001g0348 a0001c0002t0001g0349 others(2): Show |
5 | HG02015.hp1 NA18966.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+18G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73851961 | |||||||
| chr14:73851970 | G | A | 113 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(110): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.-48+27G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73851970 | |||||||
| chr14:73851982 | C | T | 2 | a0001c0002t0001g0346 a0001c0002t0016g0345 |
2 | HG01243.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-48+39C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73851982 | |||||||
| chr14:73851999 | C | T | 3 | a0001c0001t0011g0139 a0001c0001t0014g0138 a0001c0001t0015g0137 |
3 | HG03130.hp2 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-48+56C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73851999 | |||||||
| chr14:73852011 | A | G | 343 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(340): Show |
407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.-48+68A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852011 | |||||||
| chr14:73852051 | G | T | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-48+108G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852051 | |||||||
| chr14:73852082 | G | T | 2 | a0001c0002t0006g0280 a0001c0002t0006g0281 |
2 | HG01928.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.-48+139G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852082 | |||||||
| chr14:73852083 | C | G | 315 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(312): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.-48+140C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852083 | |||||||
| chr14:73852129 | G | GT | 5 | a0001c0001t0002g0344 a0001c0001t0003g0136 a0001c0001t0008g0135 others(2): Show |
5 | HG02738.hp1 HG03831.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+194dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73852129 | ||||||
| chr14:73852154 | G | A | 2 | a0001c0001t0003g0007 a0001c0001t0003g0035 |
4 | HG01261.hp1 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+211G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852154 | |||||||
| chr14:73852163 | G | A | 5 | a0001c0002t0007g0006 a0001c0002t0007g0171 a0001c0002t0007g0172 others(2): Show |
8 | HG01109.hp2 HG01496.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-48+220G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852163 | |||||||
| chr14:73852252 | T | TTGGACTC others(319): Show |
1 | a0001c0001t0004g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-48+326_-48+327ins others(326): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73852252 | ||||||
| chr14:73852281 | G | A | 5 | a0001c0002t0001g0021 a0001c0002t0001g0148 a0001c0002t0001g0149 others(2): Show |
6 | HG01074.hp2 HG01099.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.-48+338G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852281 | |||||||
| chr14:73852371 | C | T | 1 | a0001c0002t0001g0277 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-48+428C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852371 | |||||||
| chr14:73852382 | C | T | 7 | a0001c0002t0001g0270 a0001c0002t0001g0271 a0001c0002t0001g0272 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-48+439C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852382 | |||||||
| chr14:73852500 | C | T | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-48+557C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852500 | |||||||
| chr14:73852539 | T | C | 184 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(181): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.-48+596T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852539 | |||||||
| chr14:73852616 | T | G | 2 | a0001c0002t0009g0176 a0001c0002t0009g0177 |
2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-48+673T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852616 | |||||||
| chr14:73852752 | G | A | 33 | a0001c0002t0005g0002 a0001c0002t0005g0011 a0001c0002t0005g0024 others(30): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.-48+809G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852752 | |||||||
| chr14:73852752 | G | C | 15 | a0001c0002t0001g0208 a0001c0002t0001g0210 a0001c0002t0001g0211 others(12): Show |
15 | HG01243.hp1 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-48+809G>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852752 | |||||||
| chr14:73852785 | G | A | 1 | a0001c0002t0001g0214 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-48+842G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852785 | |||||||
| chr14:73852894 | C | A | 1 | a0001c0001t0002g0282 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-48+951C>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852894 | |||||||
| chr14:73852922 | T | C | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-48+979T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73852922 | |||||||
| chr14:73853018 | C | G | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-48+1075C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73853018 | |||||||
| chr14:73853028 | C | T | 45 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(42): Show |
59 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.-48+1085C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73853028 | |||||||
| chr14:73853195 | A | G | 1 | a0001c0002t0001g0010 | 3 | HG02559.hp1 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-48+1252A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73853195 | |||||||
| chr14:73853201 | A | AG | 68 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(65): Show |
85 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.-48+1260dupG | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73853201 | ||||||
| chr14:73853205 | A | G | 1 | a0001c0001t0002g0341 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-48+1262A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73853205 | |||||||
| chr14:73853286 | G | A | 180 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(177): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.-48+1343G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73853286 | |||||||
| chr14:73853348 | GT | G | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-48+1408delT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73853348 | ||||||
| chr14:73853391 | C | T | 180 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(177): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.-48+1448C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73853391 | |||||||
| chr14:73853619 | G | A | 1 | a0001c0001t0015g0137 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-48+1676G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73853619 | |||||||
| chr14:73853677 | T | G | 1 | a0001c0001t0012g0342 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-48+1734T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73853677 | |||||||
| chr14:73853689 | G | T | 15 | a0001c0002t0001g0208 a0001c0002t0001g0210 a0001c0002t0001g0211 others(12): Show |
15 | HG01243.hp1 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-48+1746G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73853689 | |||||||
| chr14:73853783 | T | TC | 61 | a0001c0002t0001g0004 a0001c0002t0001g0012 a0001c0002t0001g0013 others(58): Show |
73 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.-48+1842dupC | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73853783 | ||||||
| chr14:73853845 | T | A | 1 | a0001c0001t0004g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-48+1902T>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73853845 | |||||||
| chr14:73853896 | C | G | 1 | a0001c0001t0003g0133 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-48+1953C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73853896 | |||||||
| chr14:73853908 | G | A | 48 | a0001c0001t0004g0016 a0001c0001t0004g0036 a0001c0001t0004g0037 others(45): Show |
49 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.-48+1965G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73853908 | |||||||
| chr14:73853945 | A | G | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-48+2002A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73853945 | |||||||
| chr14:73854013 | C | A | 104 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(101): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.-48+2070C>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73854013 | |||||||
| chr14:73854013 | C | G | 1 | a0001c0001t0011g0139 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-48+2070C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73854013 | |||||||
| chr14:73854132 | C | T | 1 | a0001c0002t0001g0170 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-48+2189C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73854132 | |||||||
| chr14:73854133 | G | A | 104 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(101): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.-48+2190G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73854133 | |||||||
| chr14:73854135 | T | C | 33 | a0001c0002t0005g0002 a0001c0002t0005g0011 a0001c0002t0005g0024 others(30): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.-48+2192T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73854135 | |||||||
| chr14:73854138 | T | C | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-48+2195T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73854138 | |||||||
| chr14:73854229 | A | G | 1 | a0001c0002t0001g0147 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-48+2286A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73854229 | |||||||
| chr14:73854535 | T | A | 1 | a0001c0001t0011g0139 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-48+2592T>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73854535 | |||||||
| chr14:73854619 | G | A | 76 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(73): Show |
93 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.-48+2676G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73854619 | |||||||
| chr14:73854633 | A | G | 1 | a0001c0001t0004g0081 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-48+2690A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73854633 | |||||||
| chr14:73855350 | A | C | 182 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(179): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.-48+3407A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73855350 | |||||||
| chr14:73855350 | A | T | 1 | a0001c0001t0003g0132 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-48+3407A>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73855350 | |||||||
| chr14:73855357 | G | T | 2 | a0001c0001t0003g0008 a0001c0001t0003g0088 |
4 | HG01109.hp1 HG03195.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+3414G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73855357 | |||||||
| chr14:73855502 | A | G | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-47-3314A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73855502 | |||||||
| chr14:73855524 | G | A | 1 | a0001c0002t0001g0223 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-47-3292G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73855524 | |||||||
| chr14:73855640 | T | G | 1 | a0001c0001t0002g0283 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-47-3176T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73855640 | |||||||
| chr14:73855684 | G | A | 1 | a0001c0001t0011g0139 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-47-3132G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73855684 | |||||||
| chr14:73855970 | C | T | 1 | a0001c0002t0005g0207 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-47-2846C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73855970 | |||||||
| chr14:73856013 | G | A | 182 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(179): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.-47-2803G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73856013 | |||||||
| chr14:73856035 | G | A | 1 | a0001c0002t0007g0171 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-47-2781G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73856035 | |||||||
| chr14:73856056 | A | G | 8 | a0001c0001t0002g0034 a0001c0001t0002g0334 a0001c0001t0002g0335 others(5): Show |
9 | HG00642.hp2 HG00735.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.-47-2760A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73856056 | |||||||
| chr14:73856389 | G | A | 3 | a0001c0001t0011g0139 a0001c0001t0012g0342 a0001c0001t0013g0343 |
3 | HG01243.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-47-2427G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73856389 | |||||||
| chr14:73856409 | G | A | 1 | a0001c0002t0001g0215 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-47-2407G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73856409 | |||||||
| chr14:73856413 | A | AT | 104 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(101): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.-47-2394dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73856413 | ||||||
| chr14:73856677 | G | C | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-47-2139G>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73856677 | |||||||
| chr14:73856679 | A | G | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-47-2137A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73856679 | |||||||
| chr14:73856770 | T | G | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-47-2046T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73856770 | |||||||
| chr14:73856927 | G | A | 2 | a0001c0001t0008g0089 a0001c0001t0008g0090 |
2 | NA18954.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-47-1889G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73856927 | |||||||
| chr14:73857039 | A | T | 2 | a0001c0001t0012g0342 a0001c0001t0013g0343 |
2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-47-1777A>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857039 | |||||||
| chr14:73857092 | C | T | 1 | a0001c0001t0002g0333 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-47-1724C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857092 | |||||||
| chr14:73857238 | G | GT | 7 | a0001c0001t0002g0286 a0001c0001t0002g0287 a0001c0001t0003g0096 others(4): Show |
7 | HG02074.hp2 HG02148.hp1 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47-1564dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857238 | ||||||
| chr14:73857238 | G | GTT | 157 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(154): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-47-1565_-47-1564d others(4): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857238 | ||||||
| chr14:73857238 | G | GTTT | 21 | a0001c0001t0002g0332 a0001c0001t0003g0017 a0001c0001t0003g0083 others(18): Show |
22 | HG00621.hp1 HG01891.hp2 HG01978.hp1 others(19): Show |
intron_variant | MODIFIER | c.-47-1566_-47-1564d others(5): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857238 | ||||||
| chr14:73857281 | A | G | 1 | a0001c0001t0015g0137 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-47-1535A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857281 | |||||||
| chr14:73857554 | C | T | 104 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(101): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.-47-1262C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857554 | |||||||
| chr14:73857620 | CA | C | 197 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(194): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.-47-1186delA | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857620 | ||||||
| chr14:73857630 | A | T | 6 | a0001c0001t0002g0015 a0001c0002t0001g0152 a0001c0002t0001g0153 others(3): Show |
6 | HG01070.hp1 HG01192.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-1186A>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857630 | |||||||
| chr14:73857664 | G | GT | 19 | a0001c0002t0001g0023 a0001c0002t0001g0144 a0001c0002t0001g0145 others(16): Show |
20 | HG01106.hp1 HG01109.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.-47-1130dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857664 | ||||||
| chr14:73857664 | G | GTGTTTTT others(6): Show |
1 | a0001c0001t0002g0288 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-47-1151_-47-1150i others(15): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857664 | ||||||
| chr14:73857664 | G | GTT | 12 | a0001c0001t0002g0290 a0001c0002t0001g0025 a0001c0002t0001g0168 others(9): Show |
13 | HG02015.hp1 HG02145.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.-47-1131_-47-1130d others(4): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857664 | ||||||
| chr14:73857664 | G | GTTT | 16 | a0001c0002t0001g0210 a0001c0002t0001g0211 a0001c0002t0001g0212 others(13): Show |
16 | HG01243.hp1 HG01891.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-47-1132_-47-1130d others(5): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857664 | ||||||
| chr14:73857664 | G | GTTTTTTT others(2): Show |
25 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0008 others(22): Show |
37 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(34): Show |
intron_variant | MODIFIER | c.-47-1138_-47-1130d others(11): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857664 | ||||||
| chr14:73857664 | G | GTTTTTTT others(3): Show |
31 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0334 others(28): Show |
36 | HG00099.hp2 HG01069.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.-47-1139_-47-1130d others(12): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857664 | ||||||
| chr14:73857664 | G | GTTTTTTT others(4): Show |
50 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0031 others(47): Show |
64 | HG00408.hp1 HG00408.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.-47-1140_-47-1130d others(13): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857664 | ||||||
| chr14:73857664 | G | GTTTTTTT others(5): Show |
35 | a0001c0001t0002g0015 a0001c0001t0002g0032 a0001c0001t0002g0033 others(32): Show |
39 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.-47-1141_-47-1130d others(14): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857664 | ||||||
| chr14:73857664 | G | GTTTTTTT others(6): Show |
15 | a0001c0001t0002g0317 a0001c0001t0002g0318 a0001c0001t0002g0319 others(12): Show |
15 | HG00673.hp2 HG01168.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.-47-1142_-47-1130d others(15): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857664 | ||||||
| chr14:73857664 | G | GTTTTTTT others(7): Show |
4 | a0001c0001t0002g0327 a0001c0001t0004g0072 a0001c0001t0004g0073 others(1): Show |
4 | HG02615.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-1143_-47-1130d others(16): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857664 | ||||||
| chr14:73857664 | G | GTTTTTTT others(8): Show |
5 | a0001c0001t0002g0328 a0001c0001t0002g0329 a0001c0001t0002g0330 others(2): Show |
5 | HG00423.hp2 HG02055.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47-1144_-47-1130d others(17): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857664 | ||||||
| chr14:73857664 | GT | G | 41 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(38): Show |
50 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.-47-1130delT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857664 | ||||||
| chr14:73857666 | T | TTTTTTTT others(4): Show |
1 | a0001c0001t0002g0289 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-47-1140_-47-1139i others(13): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73857666 | ||||||
| chr14:73857700 | G | A | 76 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(73): Show |
93 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.-47-1116G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857700 | |||||||
| chr14:73857737 | C | T | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-47-1079C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857737 | |||||||
| chr14:73857804 | G | A | 1 | a0001c0002t0017g0178 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-47-1012G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857804 | |||||||
| chr14:73857814 | T | G | 235 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(232): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.-47-1002T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857814 | |||||||
| chr14:73857829 | T | C | 14 | a0001c0002t0001g0208 a0001c0002t0001g0210 a0001c0002t0001g0211 others(11): Show |
14 | HG01243.hp1 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-47-987T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857829 | |||||||
| chr14:73857862 | G | T | 4 | a0001c0002t0009g0176 a0001c0002t0009g0177 a0001c0002t0018g0209 others(1): Show |
4 | HG02809.hp2 HG02965.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-954G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857862 | |||||||
| chr14:73857933 | T | C | 1 | a0001c0001t0003g0100 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-47-883T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857933 | |||||||
| chr14:73857959 | G | A | 104 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(101): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.-47-857G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857959 | |||||||
| chr14:73857960 | C | T | 104 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(101): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.-47-856C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857960 | |||||||
| chr14:73857968 | T | C | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-47-848T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857968 | |||||||
| chr14:73857995 | A | G | 1 | a0002c0004t0001g0163 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-47-821A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73857995 | |||||||
| chr14:73858080 | T | C | 3 | a0001c0001t0011g0139 a0001c0001t0012g0342 a0001c0001t0013g0343 |
3 | HG01243.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-47-736T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73858080 | |||||||
| chr14:73858104 | G | A | 61 | a0001c0002t0001g0004 a0001c0002t0001g0012 a0001c0002t0001g0013 others(58): Show |
73 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.-47-712G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73858104 | |||||||
| chr14:73858212 | G | A | 3 | a0001c0001t0011g0139 a0001c0001t0012g0342 a0001c0001t0013g0343 |
3 | HG01243.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-47-604G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73858212 | |||||||
| chr14:73858249 | A | G | 1 | a0001c0001t0004g0079 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-47-567A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73858249 | |||||||
| chr14:73858256 | A | C | 1 | a0001c0001t0002g0340 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-47-560A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73858256 | |||||||
| chr14:73858260 | C | T | 311 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(308): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.-47-556C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73858260 | |||||||
| chr14:73858313 | GA | G | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-47-501delA | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr14 | 73858313 | ||||||
| chr14:73858338 | G | A | 1 | a0001c0002t0001g0140 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-47-478G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73858338 | |||||||
| chr14:73858446 | G | A | 2 | a0001c0001t0012g0342 a0001c0001t0013g0343 |
2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-47-370G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73858446 | |||||||
| chr14:73858548 | G | A | 104 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(101): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.-47-268G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73858548 | |||||||
| chr14:73858550 | C | A | 2 | a0001c0001t0003g0008 a0001c0001t0003g0088 |
4 | HG01109.hp1 HG03195.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47-266C>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73858550 | |||||||
| chr14:73858743 | A | G | 1 | a0001c0001t0003g0100 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-47-73A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 1/9 | chr14 | 73858743 | |||||||
| chr14:73858948 | T | G | 5 | a0001c0002t0007g0006 a0001c0002t0007g0171 a0001c0002t0007g0172 others(2): Show |
8 | HG01109.hp2 HG01496.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.37+49T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73858948 | |||||||
| chr14:73859089 | A | G | 3 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0332 |
3 | HG02109.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.37+190A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73859089 | |||||||
| chr14:73859189 | A | G | 15 | a0001c0002t0001g0208 a0001c0002t0001g0210 a0001c0002t0001g0211 others(12): Show |
15 | HG01243.hp1 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.37+290A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73859189 | |||||||
| chr14:73859190 | T | C | 2 | a0001c0001t0012g0342 a0001c0001t0013g0343 |
2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.37+291T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73859190 | |||||||
| chr14:73859331 | G | A | 2 | a0001c0001t0002g0291 a0001c0001t0002g0305 |
2 | NA18993.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.37+432G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73859331 | |||||||
| chr14:73859713 | T | A | 1 | a0001c0001t0003g0112 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.37+814T>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73859713 | |||||||
| chr14:73859748 | C | T | 1 | a0001c0002t0001g0162 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.38-791C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73859748 | |||||||
| chr14:73859784 | TA | T | 102 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(99): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.38-743delA | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 73859784 | ||||||
| chr14:73859805 | T | C | 1 | a0001c0002t0020g0216 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.38-734T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73859805 | |||||||
| chr14:73859865 | G | GT | 70 | a0001c0001t0003g0085 a0001c0002t0001g0004 a0001c0002t0001g0012 others(67): Show |
82 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.38-661dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr14 | 73859865 | ||||||
| chr14:73859873 | T | C | 1 | a0001c0001t0003g0101 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.38-666T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73859873 | |||||||
| chr14:73859906 | T | G | 15 | a0001c0002t0001g0025 a0001c0002t0001g0214 a0001c0002t0001g0215 others(12): Show |
16 | HG01891.hp1 HG02015.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.38-633T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73859906 | |||||||
| chr14:73859918 | G | A | 1 | a0001c0002t0005g0179 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.38-621G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73859918 | |||||||
| chr14:73859973 | C | T | 2 | a0001c0001t0003g0008 a0001c0001t0003g0088 |
4 | HG01109.hp1 HG03195.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-566C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73859973 | |||||||
| chr14:73860005 | C | T | 2 | a0001c0002t0005g0205 a0001c0002t0005g0206 |
2 | NA18950.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.38-534C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73860005 | |||||||
| chr14:73860021 | G | A | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.38-518G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73860021 | |||||||
| chr14:73860200 | G | T | 126 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(123): Show |
144 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.38-339G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73860200 | |||||||
| chr14:73860263 | T | C | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.38-276T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73860263 | |||||||
| chr14:73860324 | G | A | 7 | a0001c0002t0005g0011 a0001c0002t0005g0179 a0001c0002t0005g0180 others(4): Show |
9 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.38-215G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73860324 | |||||||
| chr14:73860397 | G | T | 180 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(177): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.38-142G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73860397 | |||||||
| chr14:73860495 | C | A | 3 | a0001c0001t0011g0139 a0001c0001t0012g0342 a0001c0001t0013g0343 |
3 | HG01243.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.38-44C>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 2/9 | chr14 | 73860495 | |||||||
| chr14:73860790 | A | G | 3 | a0001c0001t0011g0139 a0001c0001t0012g0342 a0001c0001t0013g0343 |
3 | HG01243.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.156+133A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73860790 | |||||||
| chr14:73860913 | A | G | 1 | a0001c0001t0004g0052 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.156+256A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73860913 | |||||||
| chr14:73860918 | A | C | 73 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(70): Show |
90 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.156+261A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73860918 | |||||||
| chr14:73861047 | G | C | 1 | a0001c0002t0001g0214 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.156+390G>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861047 | |||||||
| chr14:73861053 | C | A | 1 | a0001c0001t0002g0306 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.156+396C>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861053 | |||||||
| chr14:73861095 | C | T | 1 | a0001c0001t0003g0082 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.156+438C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861095 | |||||||
| chr14:73861208 | T | C | 1 | a0001c0002t0005g0185 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.156+551T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861208 | |||||||
| chr14:73861299 | A | G | 3 | a0001c0002t0001g0223 a0001c0002t0001g0259 a0001c0002t0001g0260 |
3 | HG00597.hp2 HG02074.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.156+642A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861299 | |||||||
| chr14:73861410 | C | T | 2 | a0001c0001t0003g0083 a0001c0001t0003g0084 |
2 | HG02486.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.156+753C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861410 | |||||||
| chr14:73861424 | T | C | 9 | a0001c0001t0003g0008 a0001c0001t0003g0017 a0001c0001t0003g0082 others(6): Show |
12 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.156+767T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861424 | |||||||
| chr14:73861439 | C | T | 2 | a0001c0001t0014g0138 a0001c0001t0015g0137 |
2 | HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.156+782C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861439 | |||||||
| chr14:73861453 | G | T | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.156+796G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861453 | |||||||
| chr14:73861609 | G | T | 1 | a0001c0001t0004g0052 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.156+952G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861609 | |||||||
| chr14:73861650 | C | T | 5 | a0001c0002t0007g0006 a0001c0002t0007g0171 a0001c0002t0007g0172 others(2): Show |
8 | HG01109.hp2 HG01496.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.156+993C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861650 | |||||||
| chr14:73861651 | G | A | 1 | a0001c0001t0003g0082 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.156+994G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861651 | |||||||
| chr14:73861706 | C | T | 3 | a0001c0001t0011g0139 a0001c0001t0012g0342 a0001c0001t0013g0343 |
3 | HG01243.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.156+1049C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861706 | |||||||
| chr14:73861883 | C | CT | 7 | a0001c0001t0002g0306 a0001c0002t0001g0169 a0001c0002t0001g0215 others(4): Show |
7 | HG02145.hp1 NA18991.hp1 NA18994.hp2 others(4): Show |
intron_variant | MODIFIER | c.156+1238dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73861883 | ||||||
| chr14:73861940 | C | T | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.156+1283C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73861940 | |||||||
| chr14:73862002 | C | T | 1 | a0001c0001t0002g0285 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.156+1345C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73862002 | |||||||
| chr14:73862096 | G | T | 73 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(70): Show |
90 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.156+1439G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73862096 | |||||||
| chr14:73862199 | G | T | 314 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(311): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.156+1542G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73862199 | |||||||
| chr14:73862202 | G | T | 293 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(290): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.156+1545G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73862202 | |||||||
| chr14:73862300 | C | T | 1 | a0001c0002t0007g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.156+1643C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73862300 | |||||||
| chr14:73862369 | G | A | 59 | a0001c0001t0003g0008 a0001c0001t0003g0017 a0001c0001t0003g0082 others(56): Show |
63 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.156+1712G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73862369 | |||||||
| chr14:73862864 | C | T | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.156+2207C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73862864 | |||||||
| chr14:73862869 | G | A | 2 | a0001c0001t0012g0342 a0001c0001t0013g0343 |
2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.156+2212G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73862869 | |||||||
| chr14:73862939 | C | T | 1 | a0001c0002t0018g0209 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.156+2282C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73862939 | |||||||
| chr14:73863078 | A | G | 76 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(73): Show |
93 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.156+2421A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73863078 | |||||||
| chr14:73863135 | A | T | 1 | a0001c0001t0015g0137 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.156+2478A>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73863135 | |||||||
| chr14:73863179 | T | A | 1 | a0001c0001t0014g0138 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.156+2522T>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73863179 | |||||||
| chr14:73863350 | C | T | 1 | a0001c0002t0018g0209 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.156+2693C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73863350 | |||||||
| chr14:73863355 | C | G | 3 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0332 |
3 | HG02109.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.156+2698C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73863355 | |||||||
| chr14:73863445 | G | A | 1 | a0001c0001t0004g0036 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.156+2788G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73863445 | |||||||
| chr14:73863475 | C | T | 3 | a0001c0001t0011g0139 a0001c0001t0012g0342 a0001c0001t0013g0343 |
3 | HG01243.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.156+2818C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73863475 | |||||||
| chr14:73863496 | A | G | 2 | a0001c0001t0002g0303 a0001c0001t0002g0304 |
2 | NA18955.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.156+2839A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73863496 | |||||||
| chr14:73863682 | T | G | 1 | a0001c0001t0014g0138 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.156+3025T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73863682 | |||||||
| chr14:73863760 | C | T | 180 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(177): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.156+3103C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73863760 | |||||||
| chr14:73863779 | C | G | 3 | a0001c0002t0001g0160 a0001c0002t0001g0161 a0001c0002t0001g0170 |
3 | HG01081.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.156+3122C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73863779 | |||||||
| chr14:73863903 | A | G | 3 | a0001c0002t0009g0176 a0001c0002t0009g0177 a0001c0002t0018g0209 |
3 | HG02809.hp2 HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.156+3246A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73863903 | |||||||
| chr14:73863907 | C | T | 3 | a0001c0001t0004g0072 a0001c0001t0004g0073 a0001c0001t0004g0074 |
3 | HG02615.hp1 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.156+3250C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73863907 | |||||||
| chr14:73864272 | G | A | 1 | a0001c0002t0005g0180 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.156+3615G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73864272 | |||||||
| chr14:73864444 | C | G | 1 | a0001c0001t0004g0078 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.156+3787C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73864444 | |||||||
| chr14:73864854 | C | T | 1 | a0002c0004t0001g0163 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.156+4197C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73864854 | |||||||
| chr14:73864919 | G | A | 3 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0332 |
3 | HG02109.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.156+4262G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73864919 | |||||||
| chr14:73864984 | G | A | 48 | a0001c0001t0004g0016 a0001c0001t0004g0036 a0001c0001t0004g0037 others(45): Show |
49 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.156+4327G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73864984 | |||||||
| chr14:73864984 | G | T | 56 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(53): Show |
73 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.156+4327G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73864984 | |||||||
| chr14:73865087 | A | T | 3 | a0001c0002t0005g0203 a0001c0002t0005g0204 a0001c0002t0017g0178 |
3 | HG01346.hp2 HG02738.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.156+4430A>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73865087 | |||||||
| chr14:73865209 | C | T | 1 | a0001c0002t0005g0202 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.156+4552C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73865209 | |||||||
| chr14:73865210 | G | A | 7 | a0001c0002t0001g0208 a0001c0002t0001g0210 a0001c0002t0001g0211 others(4): Show |
7 | HG01243.hp1 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.156+4553G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73865210 | |||||||
| chr14:73865212 | C | T | 2 | a0001c0001t0012g0342 a0001c0001t0013g0343 |
2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.156+4555C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73865212 | |||||||
| chr14:73865429 | C | T | 104 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(101): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.156+4772C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73865429 | |||||||
| chr14:73865559 | T | C | 2 | a0001c0002t0001g0214 a0001c0002t0001g0219 |
2 | HG01891.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.156+4902T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73865559 | |||||||
| chr14:73865623 | G | A | 4 | a0001c0002t0001g0022 a0001c0002t0001g0154 a0001c0002t0001g0162 others(1): Show |
4 | HG01515.hp1 HG02818.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.156+4966G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73865623 | |||||||
| chr14:73865631 | T | A | 1 | a0001c0002t0001g0227 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.156+4974T>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73865631 | |||||||
| chr14:73865725 | T | C | 3 | a0001c0002t0009g0176 a0001c0002t0009g0177 a0001c0002t0018g0209 |
3 | HG02809.hp2 HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.156+5068T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73865725 | |||||||
| chr14:73865753 | A | G | 180 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(177): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.156+5096A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73865753 | |||||||
| chr14:73865775 | C | T | 60 | a0001c0002t0001g0004 a0001c0002t0001g0012 a0001c0002t0001g0013 others(57): Show |
72 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.156+5118C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73865775 | |||||||
| chr14:73866008 | T | C | 1 | a0001c0001t0011g0139 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.156+5351T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866008 | |||||||
| chr14:73866106 | G | A | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.156+5449G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866106 | |||||||
| chr14:73866157 | A | C | 3 | a0001c0001t0011g0139 a0001c0001t0012g0342 a0001c0001t0013g0343 |
3 | HG01243.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.156+5500A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866157 | |||||||
| chr14:73866292 | C | A | 1 | a0001c0002t0001g0144 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.156+5635C>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866292 | |||||||
| chr14:73866348 | A | C | 102 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(99): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.156+5691A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866348 | |||||||
| chr14:73866361 | TCTC | T | 15 | a0001c0002t0001g0025 a0001c0002t0001g0214 a0001c0002t0001g0215 others(12): Show |
16 | HG01891.hp1 HG02015.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.156+5707_156+5709d others(5): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73866361 | ||||||
| chr14:73866383 | C | T | 1 | a0001c0002t0005g0188 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.156+5726C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866383 | |||||||
| chr14:73866395 | C | T | 1 | a0001c0002t0001g0256 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.156+5738C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866395 | |||||||
| chr14:73866695 | A | C | 45 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(42): Show |
59 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.156+6038A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866695 | |||||||
| chr14:73866725 | A | T | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.156+6068A>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866725 | |||||||
| chr14:73866816 | C | T | 2 | a0001c0001t0003g0127 a0001c0001t0003g0128 |
2 | NA19072.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.156+6159C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866816 | |||||||
| chr14:73866859 | C | T | 1 | a0001c0002t0001g0144 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.156+6202C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866859 | |||||||
| chr14:73866904 | C | T | 1 | a0001c0002t0005g0187 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.156+6247C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866904 | |||||||
| chr14:73866945 | C | T | 13 | a0001c0002t0001g0208 a0001c0002t0001g0210 a0001c0002t0001g0211 others(10): Show |
13 | HG01243.hp1 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.156+6288C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866945 | |||||||
| chr14:73866946 | G | A | 4 | a0001c0002t0001g0025 a0001c0002t0001g0220 a0001c0002t0001g0222 others(1): Show |
5 | HG02622.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.156+6289G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73866946 | |||||||
| chr14:73867013 | C | T | 61 | a0001c0002t0001g0004 a0001c0002t0001g0012 a0001c0002t0001g0013 others(58): Show |
73 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.156+6356C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73867013 | |||||||
| chr14:73867062 | C | T | 1 | a0001c0001t0004g0071 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.156+6405C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73867062 | |||||||
| chr14:73867088 | C | CA | 36 | a0001c0002t0001g0010 a0001c0002t0001g0026 a0001c0002t0001g0027 others(33): Show |
41 | HG00423.hp1 HG00621.hp2 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.156+6451dupA | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73867088 | ||||||
| chr14:73867088 | CA | C | 6 | a0001c0002t0005g0181 a0001c0002t0005g0186 a0001c0002t0005g0189 others(3): Show |
6 | HG00741.hp1 HG01934.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.156+6451delA | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73867088 | ||||||
| chr14:73867088 | CAA | C | 41 | a0001c0001t0002g0283 a0001c0001t0002g0290 a0001c0001t0002g0292 others(38): Show |
50 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.156+6450_156+6451d others(4): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73867088 | ||||||
| chr14:73867088 | CAAA | C | 72 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(69): Show |
89 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.156+6449_156+6451d others(5): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73867088 | ||||||
| chr14:73867088 | CAAAA | C | 94 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0332 others(91): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.156+6448_156+6451d others(6): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73867088 | ||||||
| chr14:73867101 | A | AAAC | 13 | a0001c0002t0001g0025 a0001c0002t0001g0214 a0001c0002t0001g0215 others(10): Show |
14 | HG01891.hp1 HG02145.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.156+6446_156+6447i others(5): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73867101 | ||||||
| chr14:73867109 | C | A | 60 | a0001c0002t0001g0004 a0001c0002t0001g0012 a0001c0002t0001g0013 others(57): Show |
72 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.156+6452C>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73867109 | |||||||
| chr14:73867117 | C | A | 3 | a0001c0001t0003g0008 a0001c0001t0003g0088 a0001c0002t0001g0239 |
5 | HG01109.hp1 HG03195.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.156+6460C>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73867117 | |||||||
| chr14:73867117 | C | CA | 34 | a0001c0001t0004g0066 a0001c0002t0005g0002 a0001c0002t0005g0011 others(31): Show |
43 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.156+6468dupA | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73867117 | ||||||
| chr14:73867190 | C | T | 1 | a0001c0001t0011g0139 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.156+6533C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73867190 | |||||||
| chr14:73867191 | A | G | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.156+6534A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73867191 | |||||||
| chr14:73867324 | T | C | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.156+6667T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73867324 | |||||||
| chr14:73867407 | G | C | 1 | a0001c0001t0004g0045 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.157-6616G>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73867407 | |||||||
| chr14:73867502 | T | TA | 7 | a0001c0002t0001g0010 a0001c0002t0001g0155 a0001c0002t0001g0156 others(4): Show |
9 | HG01081.hp2 HG01884.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.157-6511dupA | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73867502 | ||||||
| chr14:73867502 | TA | T | 33 | a0001c0002t0005g0002 a0001c0002t0005g0011 a0001c0002t0005g0024 others(30): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.157-6511delA | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73867502 | ||||||
| chr14:73867559 | A | C | 1 | a0001c0001t0014g0138 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.157-6464A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73867559 | |||||||
| chr14:73867689 | T | C | 2 | a0001c0001t0002g0293 a0001c0001t0002g0320 |
2 | NA18955.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.157-6334T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73867689 | |||||||
| chr14:73868015 | G | A | 38 | a0001c0001t0003g0113 a0001c0001t0003g0114 a0001c0001t0003g0124 others(35): Show |
47 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.157-6008G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73868015 | |||||||
| chr14:73868195 | A | G | 1 | a0001c0001t0002g0327 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.157-5828A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73868195 | |||||||
| chr14:73868246 | G | A | 15 | a0001c0002t0001g0208 a0001c0002t0001g0210 a0001c0002t0001g0211 others(12): Show |
15 | HG01243.hp1 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.157-5777G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73868246 | |||||||
| chr14:73868442 | T | A | 3 | a0001c0001t0011g0139 a0001c0001t0012g0342 a0001c0001t0013g0343 |
3 | HG01243.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.157-5581T>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73868442 | |||||||
| chr14:73868512 | A | G | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.157-5511A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73868512 | |||||||
| chr14:73868619 | C | A | 1 | a0001c0001t0011g0139 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.157-5404C>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73868619 | |||||||
| chr14:73868787 | TA | T | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.157-5224delA | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73868787 | ||||||
| chr14:73868796 | A | AG | 4 | a0001c0002t0001g0010 a0001c0002t0001g0155 a0001c0002t0001g0156 others(1): Show |
6 | HG01884.hp2 HG02559.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.157-5227_157-5226i others(3): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73868796 | |||||||
| chr14:73868936 | C | G | 2 | a0001c0002t0001g0212 a0001c0002t0001g0213 |
2 | HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.157-5087C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73868936 | |||||||
| chr14:73868981 | G | A | 1 | a0001c0001t0003g0115 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.157-5042G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73868981 | |||||||
| chr14:73869132 | G | A | 1 | a0001c0002t0001g0240 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.157-4891G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73869132 | |||||||
| chr14:73869168 | C | G | 1 | a0001c0002t0001g0215 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.157-4855C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73869168 | |||||||
| chr14:73869427 | C | T | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.157-4596C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73869427 | |||||||
| chr14:73869446 | C | T | 2 | a0001c0002t0001g0212 a0001c0002t0001g0213 |
2 | HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.157-4577C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73869446 | |||||||
| chr14:73869451 | GGTGGGAG others(19): Show |
G | 1 | a0001c0001t0008g0135 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.157-4550_157-4525d others(28): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73869451 | ||||||
| chr14:73869529 | A | G | 5 | a0001c0002t0001g0028 a0001c0002t0001g0253 a0001c0002t0001g0254 others(2): Show |
6 | NA18969.hp2 NA18975.hp1 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.157-4494A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73869529 | |||||||
| chr14:73869554 | A | G | 3 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0332 |
3 | HG02109.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.157-4469A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73869554 | |||||||
| chr14:73869573 | CA | C | 58 | a0001c0002t0001g0004 a0001c0002t0001g0012 a0001c0002t0001g0013 others(55): Show |
70 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.157-4434delA | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73869573 | ||||||
| chr14:73869807 | C | G | 1 | a0001c0002t0001g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.157-4216C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73869807 | |||||||
| chr14:73869851 | C | G | 5 | a0001c0002t0007g0006 a0001c0002t0007g0171 a0001c0002t0007g0172 others(2): Show |
8 | HG01109.hp2 HG01496.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.157-4172C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73869851 | |||||||
| chr14:73870012 | C | CAGAG | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.157-4009_157-4006d others(6): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73870012 | ||||||
| chr14:73870015 | A | G | 7 | a0001c0002t0001g0010 a0001c0002t0001g0155 a0001c0002t0001g0156 others(4): Show |
9 | HG01081.hp2 HG01884.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.157-4008A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870015 | |||||||
| chr14:73870034 | A | G | 33 | a0001c0002t0005g0002 a0001c0002t0005g0011 a0001c0002t0005g0024 others(30): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.157-3989A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870034 | |||||||
| chr14:73870062 | T | C | 1 | a0001c0001t0002g0308 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.157-3961T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870062 | |||||||
| chr14:73870114 | C | T | 1 | a0001c0002t0018g0209 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.157-3909C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870114 | |||||||
| chr14:73870120 | G | A | 76 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(73): Show |
93 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.157-3903G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870120 | |||||||
| chr14:73870167 | T | C | 1 | a0001c0002t0001g0164 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.157-3856T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870167 | |||||||
| chr14:73870193 | C | CT | 120 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(117): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.157-3812dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73870193 | ||||||
| chr14:73870193 | C | CTT | 73 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(70): Show |
90 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.157-3813_157-3812d others(4): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73870193 | ||||||
| chr14:73870193 | C | CTTT | 6 | a0001c0001t0002g0314 a0001c0001t0002g0315 a0001c0001t0002g0316 others(3): Show |
6 | HG00423.hp2 HG00621.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.157-3814_157-3812d others(5): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73870193 | ||||||
| chr14:73870193 | CT | C | 39 | a0001c0001t0011g0139 a0001c0002t0001g0347 a0001c0002t0005g0002 others(36): Show |
51 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.157-3812delT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73870193 | ||||||
| chr14:73870247 | T | C | 231 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(228): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.157-3776T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870247 | |||||||
| chr14:73870306 | A | G | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.157-3717A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870306 | |||||||
| chr14:73870325 | C | G | 5 | a0001c0002t0001g0224 a0001c0002t0001g0225 a0001c0002t0001g0226 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.157-3698C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870325 | |||||||
| chr14:73870377 | G | T | 180 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(177): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.157-3646G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870377 | |||||||
| chr14:73870435 | C | T | 1 | a0001c0002t0001g0025 | 2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.157-3588C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870435 | |||||||
| chr14:73870440 | A | G | 1 | a0001c0001t0004g0070 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.157-3583A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870440 | |||||||
| chr14:73870449 | G | T | 1 | a0001c0001t0003g0122 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.157-3574G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870449 | |||||||
| chr14:73870562 | AAATT | A | 3 | a0001c0001t0011g0139 a0001c0001t0012g0342 a0001c0001t0013g0343 |
3 | HG01243.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.157-3457_157-3454d others(6): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73870562 | ||||||
| chr14:73870801 | T | C | 2 | a0001c0001t0012g0342 a0001c0001t0013g0343 |
2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.157-3222T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870801 | |||||||
| chr14:73870870 | T | G | 1 | a0001c0001t0003g0114 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.157-3153T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73870870 | |||||||
| chr14:73871171 | G | A | 1 | a0001c0002t0001g0145 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.157-2852G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73871171 | |||||||
| chr14:73871289 | C | T | 1 | a0001c0002t0001g0222 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.157-2734C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73871289 | |||||||
| chr14:73871341 | C | CT | 24 | a0001c0001t0002g0313 a0001c0001t0002g0340 a0001c0002t0001g0022 others(21): Show |
25 | HG00597.hp1 HG01346.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.157-2656dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73871341 | ||||||
| chr14:73871341 | C | CTT | 10 | a0001c0001t0002g0291 a0001c0001t0002g0305 a0001c0002t0005g0182 others(7): Show |
10 | HG00323.hp1 HG01167.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.157-2657_157-2656d others(4): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73871341 | ||||||
| chr14:73871341 | C | CTTT | 23 | a0001c0002t0005g0002 a0001c0002t0005g0011 a0001c0002t0005g0024 others(20): Show |
32 | HG00280.hp1 HG00639.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.157-2658_157-2656d others(5): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73871341 | ||||||
| chr14:73871341 | CT | C | 43 | a0001c0001t0002g0014 a0001c0001t0002g0031 a0001c0001t0002g0282 others(40): Show |
48 | HG00323.hp2 HG01074.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.157-2656delT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73871341 | ||||||
| chr14:73871341 | CTT | C | 6 | a0001c0001t0002g0328 a0001c0001t0004g0016 a0001c0001t0004g0051 others(3): Show |
7 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.157-2657_157-2656d others(4): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73871341 | ||||||
| chr14:73871341 | CTTT | C | 41 | a0001c0001t0004g0037 a0001c0001t0004g0038 a0001c0001t0004g0040 others(38): Show |
41 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.157-2658_157-2656d others(5): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73871341 | ||||||
| chr14:73871341 | CTTTT | C | 10 | a0001c0001t0003g0009 a0001c0001t0003g0083 a0001c0001t0003g0084 others(7): Show |
12 | HG02451.hp2 HG02486.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.157-2659_157-2656d others(6): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73871341 | ||||||
| chr14:73871341 | CTTTTT | C | 46 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(43): Show |
61 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.157-2660_157-2656d others(7): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73871341 | ||||||
| chr14:73871518 | A | T | 180 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(177): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.157-2505A>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73871518 | |||||||
| chr14:73871656 | A | G | 2 | a0001c0001t0003g0018 a0001c0001t0003g0096 |
3 | HG00280.hp2 HG01255.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.157-2367A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73871656 | |||||||
| chr14:73871846 | T | A | 45 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(42): Show |
59 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.157-2177T>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73871846 | |||||||
| chr14:73872015 | C | T | 7 | a0001c0002t0005g0191 a0001c0002t0005g0193 a0001c0002t0005g0200 others(4): Show |
7 | HG02523.hp2 HG03017.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.157-2008C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73872015 | |||||||
| chr14:73872079 | C | G | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.157-1944C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73872079 | |||||||
| chr14:73872181 | G | A | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.157-1842G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73872181 | |||||||
| chr14:73872188 | A | G | 216 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(213): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.157-1835A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73872188 | |||||||
| chr14:73872447 | A | G | 1 | a0001c0001t0003g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.157-1576A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73872447 | |||||||
| chr14:73872508 | C | T | 3 | a0001c0002t0001g0160 a0001c0002t0001g0161 a0001c0002t0001g0170 |
3 | HG01081.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.157-1515C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73872508 | |||||||
| chr14:73872635 | C | T | 33 | a0001c0002t0005g0002 a0001c0002t0005g0011 a0001c0002t0005g0024 others(30): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.157-1388C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73872635 | |||||||
| chr14:73872917 | C | T | 1 | a0001c0001t0002g0302 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.157-1106C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73872917 | |||||||
| chr14:73872972 | CA | C | 14 | a0001c0001t0002g0304 a0001c0001t0002g0328 a0001c0001t0003g0088 others(11): Show |
14 | HG01109.hp1 HG01243.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.157-1037delA | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73872972 | ||||||
| chr14:73872987 | T | A | 3 | a0001c0001t0011g0139 a0001c0001t0012g0342 a0001c0001t0013g0343 |
3 | HG01243.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.157-1036T>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73872987 | |||||||
| chr14:73873035 | G | T | 3 | a0001c0001t0003g0008 a0001c0001t0003g0082 a0001c0001t0003g0088 |
5 | HG01109.hp1 HG01884.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.157-988G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73873035 | |||||||
| chr14:73873056 | A | C | 76 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(73): Show |
93 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.157-967A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73873056 | |||||||
| chr14:73873182 | C | G | 1 | a0001c0002t0006g0229 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.157-841C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73873182 | |||||||
| chr14:73873318 | AAAAG | A | 60 | a0001c0002t0001g0004 a0001c0002t0001g0012 a0001c0002t0001g0013 others(57): Show |
72 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.157-701_157-698del others(4): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73873318 | ||||||
| chr14:73873381 | A | G | 1 | a0001c0002t0005g0191 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.157-642A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73873381 | |||||||
| chr14:73873438 | G | A | 76 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(73): Show |
93 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.157-585G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73873438 | |||||||
| chr14:73873465 | CT | C | 34 | a0001c0002t0001g0168 a0001c0002t0005g0002 a0001c0002t0005g0011 others(31): Show |
43 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.157-546delT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr14 | 73873465 | ||||||
| chr14:73873473 | T | C | 61 | a0001c0002t0001g0004 a0001c0002t0001g0012 a0001c0002t0001g0013 others(58): Show |
73 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.157-550T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73873473 | |||||||
| chr14:73873528 | A | G | 5 | a0001c0002t0007g0006 a0001c0002t0007g0171 a0001c0002t0007g0172 others(2): Show |
8 | HG01109.hp2 HG01496.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.157-495A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73873528 | |||||||
| chr14:73873555 | C | T | 1 | a0001c0002t0001g0164 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.157-468C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73873555 | |||||||
| chr14:73873570 | T | C | 1 | a0001c0002t0005g0188 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.157-453T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73873570 | |||||||
| chr14:73873646 | C | T | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.157-377C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73873646 | |||||||
| chr14:73873710 | C | T | 3 | a0001c0002t0001g0234 a0001c0002t0001g0235 a0001c0002t0001g0266 |
3 | NA18966.hp2 NA19012.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.157-313C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73873710 | |||||||
| chr14:73873852 | A | G | 180 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(177): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.157-171A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73873852 | |||||||
| chr14:73873902 | G | A | 33 | a0001c0002t0005g0002 a0001c0002t0005g0011 a0001c0002t0005g0024 others(30): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.157-121G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 3/9 | chr14 | 73873902 | |||||||
| chr14:73874224 | A | G | 4 | a0001c0001t0003g0100 a0001c0001t0003g0108 a0001c0001t0003g0109 others(1): Show |
4 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+10A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73874224 | |||||||
| chr14:73874252 | G | C | 3 | a0001c0002t0005g0185 a0001c0002t0005g0190 a0001c0002t0005g0194 |
3 | HG00323.hp1 HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.348+38G>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73874252 | |||||||
| chr14:73874254 | A | G | 3 | a0001c0002t0005g0185 a0001c0002t0005g0190 a0001c0002t0005g0194 |
3 | HG00323.hp1 HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.348+40A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73874254 | |||||||
| chr14:73874331 | C | T | 1 | a0001c0001t0002g0338 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.348+117C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73874331 | |||||||
| chr14:73874384 | G | A | 1 | a0001c0001t0014g0138 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.348+170G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73874384 | |||||||
| chr14:73874421 | G | A | 127 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(124): Show |
145 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.348+207G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73874421 | |||||||
| chr14:73874425 | C | G | 33 | a0001c0002t0005g0002 a0001c0002t0005g0011 a0001c0002t0005g0024 others(30): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.348+211C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73874425 | |||||||
| chr14:73874608 | C | T | 1 | a0001c0001t0002g0282 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.348+394C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73874608 | |||||||
| chr14:73874735 | G | A | 76 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(73): Show |
93 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.348+521G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73874735 | |||||||
| chr14:73874901 | C | T | 33 | a0001c0002t0005g0002 a0001c0002t0005g0011 a0001c0002t0005g0024 others(30): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.348+687C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73874901 | |||||||
| chr14:73874982 | C | T | 4 | a0001c0002t0001g0022 a0001c0002t0001g0154 a0001c0002t0001g0162 others(1): Show |
4 | HG01515.hp1 HG02818.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+768C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73874982 | |||||||
| chr14:73874984 | G | A | 1 | a0001c0001t0015g0137 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.348+770G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73874984 | |||||||
| chr14:73874999 | T | C | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.348+785T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73874999 | |||||||
| chr14:73875008 | A | G | 1 | a0001c0002t0005g0207 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.348+794A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875008 | |||||||
| chr14:73875051 | G | A | 33 | a0001c0002t0005g0002 a0001c0002t0005g0011 a0001c0002t0005g0024 others(30): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.348+837G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875051 | |||||||
| chr14:73875090 | C | G | 3 | a0001c0002t0001g0160 a0001c0002t0001g0161 a0001c0002t0001g0170 |
3 | HG01081.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.348+876C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875090 | |||||||
| chr14:73875235 | C | G | 61 | a0001c0002t0001g0004 a0001c0002t0001g0012 a0001c0002t0001g0013 others(58): Show |
73 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.348+1021C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875235 | |||||||
| chr14:73875293 | C | T | 45 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(42): Show |
59 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.348+1079C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875293 | |||||||
| chr14:73875323 | A | G | 1 | a0001c0001t0004g0064 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.348+1109A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875323 | |||||||
| chr14:73875408 | C | T | 1 | a0001c0002t0007g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.348+1194C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875408 | |||||||
| chr14:73875453 | C | T | 70 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(67): Show |
88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.348+1239C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875453 | |||||||
| chr14:73875462 | C | A | 5 | a0001c0002t0007g0006 a0001c0002t0007g0171 a0001c0002t0007g0172 others(2): Show |
8 | HG01109.hp2 HG01496.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.348+1248C>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875462 | |||||||
| chr14:73875538 | A | G | 2 | a0001c0001t0012g0342 a0001c0001t0013g0343 |
2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.348+1324A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875538 | |||||||
| chr14:73875555 | A | C | 1 | a0001c0001t0004g0070 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.348+1341A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875555 | |||||||
| chr14:73875639 | C | T | 1 | a0001c0001t0002g0344 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.349-1359C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875639 | |||||||
| chr14:73875660 | G | T | 1 | a0001c0001t0014g0138 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.349-1338G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875660 | |||||||
| chr14:73875710 | T | C | 126 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(123): Show |
144 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.349-1288T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875710 | |||||||
| chr14:73875734 | C | T | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.349-1264C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875734 | |||||||
| chr14:73875738 | C | CT | 11 | a0001c0001t0002g0301 a0001c0002t0001g0270 a0001c0002t0001g0271 others(8): Show |
11 | HG00735.hp2 HG00741.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.349-1245dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73875738 | ||||||
| chr14:73875738 | CT | C | 61 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(58): Show |
78 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.349-1245delT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73875738 | ||||||
| chr14:73875820 | C | CT | 11 | a0001c0001t0002g0313 a0001c0001t0003g0110 a0001c0001t0003g0113 others(8): Show |
11 | HG01975.hp1 HG02602.hp1 HG03098.hp2 others(8): Show |
intron_variant | MODIFIER | c.349-1159dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73875820 | ||||||
| chr14:73875820 | C | CTT | 52 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(49): Show |
69 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.349-1160_349-1159d others(4): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73875820 | ||||||
| chr14:73875820 | CT | C | 12 | a0001c0002t0001g0220 a0001c0002t0001g0224 a0001c0002t0001g0241 others(9): Show |
15 | HG00280.hp1 HG01069.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.349-1159delT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73875820 | ||||||
| chr14:73875935 | C | T | 3 | a0001c0001t0004g0054 a0001c0001t0004g0062 a0001c0001t0004g0063 |
3 | HG02602.hp1 HG03688.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.349-1063C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875935 | |||||||
| chr14:73875939 | G | T | 1 | a0001c0001t0003g0107 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.349-1059G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73875939 | |||||||
| chr14:73876109 | G | A | 76 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(73): Show |
93 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.349-889G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73876109 | |||||||
| chr14:73876176 | G | A | 7 | a0001c0002t0001g0208 a0001c0002t0001g0210 a0001c0002t0001g0211 others(4): Show |
7 | HG01243.hp1 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.349-822G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73876176 | |||||||
| chr14:73876444 | A | C | 1 | a0001c0001t0004g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.349-554A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73876444 | |||||||
| chr14:73876483 | C | CTTTTTTT | 6 | a0001c0001t0003g0017 a0001c0001t0003g0085 a0001c0001t0003g0086 others(3): Show |
7 | HG02055.hp1 HG02257.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.349-505_349-499dup others(7): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | ||||||
| chr14:73876483 | C | CTTTTTTT others(1): Show |
45 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(42): Show |
59 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.349-506_349-499dup others(8): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | ||||||
| chr14:73876483 | C | CTTTTTTT others(2): Show |
7 | a0001c0001t0003g0009 a0001c0001t0003g0088 a0001c0001t0003g0105 others(4): Show |
9 | HG00140.hp1 HG00639.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.349-507_349-499dup others(9): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | ||||||
| chr14:73876483 | C | CTTTTTTT others(5): Show |
5 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0309 others(2): Show |
5 | HG02071.hp2 HG02109.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-510_349-499dup others(12): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | ||||||
| chr14:73876483 | C | CTTTTTTT others(6): Show |
53 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(50): Show |
69 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.349-511_349-499dup others(13): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | ||||||
| chr14:73876483 | C | CTTTTTTT others(7): Show |
17 | a0001c0001t0002g0033 a0001c0001t0002g0286 a0001c0001t0002g0287 others(14): Show |
18 | HG02055.hp2 HG02074.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.349-512_349-499dup others(14): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | ||||||
| chr14:73876483 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0002g0301 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.349-513_349-499dup others(15): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | ||||||
| chr14:73876483 | C | CTTTTTTT others(19): Show |
8 | a0001c0001t0004g0037 a0001c0001t0004g0039 a0001c0001t0004g0043 others(5): Show |
8 | HG00099.hp2 HG00738.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.349-499_349-498ins others(26): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | ||||||
| chr14:73876483 | C | CTTTTTTT others(20): Show |
13 | a0001c0001t0004g0016 a0001c0001t0004g0036 a0001c0001t0004g0038 others(10): Show |
14 | HG00408.hp2 HG00544.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.349-499_349-498ins others(27): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | ||||||
| chr14:73876483 | C | CTTTTTTT others(21): Show |
15 | a0001c0001t0004g0041 a0001c0001t0004g0042 a0001c0001t0004g0060 others(12): Show |
15 | HG01074.hp1 HG01891.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.349-499_349-498ins others(28): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | ||||||
| chr14:73876483 | C | CTTTTTTT others(23): Show |
1 | a0001c0001t0004g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.349-499_349-498ins others(30): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | ||||||
| chr14:73876483 | C | CTTTTTTT others(24): Show |
1 | a0001c0001t0004g0076 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.349-499_349-498ins others(31): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | ||||||
| chr14:73876483 | C | CTTTTTTT others(25): Show |
1 | a0001c0001t0004g0045 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.349-499_349-498ins others(32): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | ||||||
| chr14:73876483 | C | CTTTTTTT others(29): Show |
2 | a0001c0001t0004g0061 a0001c0001t0004g0075 |
2 | NA19063.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.349-499_349-498ins others(36): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | ||||||
| chr14:73876483 | C | CTTTTTTT others(30): Show |
2 | a0001c0001t0004g0044 a0001c0001t0004g0050 |
2 | NA18974.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.349-499_349-498ins others(37): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | ||||||
| chr14:73876483 | C | CTTTTTTT others(31): Show |
1 | a0001c0001t0004g0069 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.349-499_349-498ins others(38): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | ||||||
| chr14:73876483 | C | CTTTTTTT others(37): Show |
1 | a0001c0001t0004g0052 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.349-499_349-498ins others(44): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr14 | 73876483 | ||||||
| chr14:73876558 | T | G | 1 | a0001c0002t0001g0153 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.349-440T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73876558 | |||||||
| chr14:73876597 | T | G | 1 | a0001c0001t0003g0102 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.349-401T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73876597 | |||||||
| chr14:73876674 | G | A | 1 | a0001c0002t0005g0191 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.349-324G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73876674 | |||||||
| chr14:73876717 | T | C | 1 | a0001c0001t0003g0109 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.349-281T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73876717 | |||||||
| chr14:73876758 | T | A | 1 | a0001c0002t0005g0203 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.349-240T>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73876758 | |||||||
| chr14:73876840 | C | G | 1 | a0001c0001t0004g0052 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.349-158C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73876840 | |||||||
| chr14:73876908 | A | C | 1 | a0001c0001t0002g0299 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.349-90A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73876908 | |||||||
| chr14:73876909 | C | T | 33 | a0001c0002t0005g0002 a0001c0002t0005g0011 a0001c0002t0005g0024 others(30): Show |
42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.349-89C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 4/9 | chr14 | 73876909 | |||||||
| chr14:73877275 | A | C | 1 | a0001c0002t0001g0164 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.519+107A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73877275 | |||||||
| chr14:73877276 | AT | A | 48 | a0001c0001t0004g0016 a0001c0001t0004g0036 a0001c0001t0004g0037 others(45): Show |
49 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.519+118delT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 73877276 | ||||||
| chr14:73877278 | T | A | 45 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(42): Show |
59 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.519+110T>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73877278 | |||||||
| chr14:73877350 | C | T | 2 | a0001c0001t0014g0138 a0001c0001t0015g0137 |
2 | HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.519+182C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73877350 | |||||||
| chr14:73877378 | C | T | 6 | a0001c0001t0003g0017 a0001c0001t0003g0083 a0001c0001t0003g0084 others(3): Show |
7 | HG02055.hp1 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.519+210C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73877378 | |||||||
| chr14:73877409 | T | C | 1 | a0001c0001t0015g0137 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.519+241T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73877409 | |||||||
| chr14:73877492 | T | C | 1 | a0001c0001t0011g0139 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.519+324T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73877492 | |||||||
| chr14:73877573 | C | A | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.519+405C>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73877573 | |||||||
| chr14:73877587 | A | G | 15 | a0001c0002t0001g0025 a0001c0002t0001g0214 a0001c0002t0001g0215 others(12): Show |
16 | HG01891.hp1 HG02015.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.519+419A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73877587 | |||||||
| chr14:73877613 | G | GT | 40 | a0001c0001t0003g0087 a0001c0001t0011g0139 a0001c0002t0001g0010 others(37): Show |
51 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.519+457dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 73877613 | ||||||
| chr14:73877613 | G | GTT | 49 | a0001c0001t0004g0016 a0001c0001t0004g0036 a0001c0001t0004g0037 others(46): Show |
50 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.519+456_519+457dup others(2): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 73877613 | ||||||
| chr14:73877613 | G | GTTT | 73 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(70): Show |
90 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.519+455_519+457dup others(3): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 73877613 | ||||||
| chr14:73877613 | G | GTTTT | 7 | a0001c0001t0002g0284 a0001c0001t0002g0287 a0001c0001t0002g0290 others(4): Show |
7 | HG00642.hp2 HG02135.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.519+454_519+457dup others(4): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 73877613 | ||||||
| chr14:73877640 | TCTTA | T | 3 | a0001c0001t0004g0058 a0001c0001t0004g0067 a0001c0001t0004g0076 |
3 | HG04115.hp2 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.519+475_519+478del others(4): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 73877640 | ||||||
| chr14:73877912 | C | A | 2 | a0001c0002t0005g0197 a0001c0002t0005g0198 |
2 | HG02165.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.519+744C>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73877912 | |||||||
| chr14:73877971 | A | G | 57 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(54): Show |
74 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.519+803A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73877971 | |||||||
| chr14:73878019 | G | A | 1 | a0001c0001t0002g0323 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.519+851G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73878019 | |||||||
| chr14:73878048 | A | C | 1 | a0001c0002t0001g0260 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.519+880A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73878048 | |||||||
| chr14:73878260 | C | G | 2 | a0001c0002t0001g0232 a0001c0002t0001g0233 |
2 | NA18956.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.520-836C>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73878260 | |||||||
| chr14:73878282 | G | A | 1 | a0001c0001t0002g0310 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.520-814G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73878282 | |||||||
| chr14:73878351 | T | A | 1 | a0001c0002t0005g0200 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.520-745T>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73878351 | |||||||
| chr14:73878354 | ATTTAATT others(15): Show |
A | 2 | a0001c0002t0009g0176 a0001c0002t0009g0177 |
2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.520-740_520-719del others(22): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr14 | 73878354 | ||||||
| chr14:73878449 | T | G | 1 | a0001c0001t0004g0048 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.520-647T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73878449 | |||||||
| chr14:73878718 | A | T | 3 | a0001c0002t0001g0160 a0001c0002t0001g0161 a0001c0002t0001g0170 |
3 | HG01081.hp2 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.520-378A>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 5/9 | chr14 | 73878718 | |||||||
| chr14:73879488 | G | C | 10 | a0001c0002t0001g0023 a0001c0002t0001g0152 a0001c0002t0001g0153 others(7): Show |
11 | HG01070.hp1 HG01192.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.729+183G>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 6/9 | chr14 | 73879488 | |||||||
| chr14:73879591 | G | A | 2 | a0001c0001t0003g0108 a0001c0001t0003g0123 |
2 | HG00642.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.729+286G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 6/9 | chr14 | 73879591 | |||||||
| chr14:73879592 | A | G | 76 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(73): Show |
93 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.729+287A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 6/9 | chr14 | 73879592 | |||||||
| chr14:73879645 | T | TTGCGTAG others(3): Show |
216 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(213): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.729+340_729+341ins others(10): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 6/9 | chr14 | 73879645 | |||||||
| chr14:73879678 | A | G | 1 | a0001c0001t0004g0064 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.729+373A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 6/9 | chr14 | 73879678 | |||||||
| chr14:73879726 | T | C | 1 | a0001c0002t0005g0180 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.730-329T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 6/9 | chr14 | 73879726 | |||||||
| chr14:73880294 | C | T | 2 | a0001c0001t0004g0079 a0001c0001t0004g0080 |
2 | HG01891.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.851+118C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880294 | |||||||
| chr14:73880323 | A | G | 1 | a0001c0002t0001g0346 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.851+147A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880323 | |||||||
| chr14:73880339 | G | A | 4 | a0001c0001t0003g0103 a0001c0001t0003g0118 a0001c0001t0003g0121 others(1): Show |
4 | HG01358.hp1 HG01952.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.851+163G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880339 | |||||||
| chr14:73880397 | A | C | 73 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(70): Show |
90 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.851+221A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880397 | |||||||
| chr14:73880418 | CA | C | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.851+249delA | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 73880418 | ||||||
| chr14:73880587 | C | CA | 50 | a0001c0001t0002g0305 a0001c0001t0004g0016 a0001c0001t0004g0036 others(47): Show |
51 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.851+424dupA | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr14 | 73880587 | ||||||
| chr14:73880593 | A | C | 4 | a0001c0002t0005g0024 a0001c0002t0005g0186 a0001c0002t0005g0187 others(1): Show |
5 | HG02129.hp2 HG02602.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.851+417A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880593 | |||||||
| chr14:73880599 | A | AC | 53 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(50): Show |
70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.851+423_851+424ins others(1): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880599 | |||||||
| chr14:73880599 | A | C | 3 | a0001c0001t0011g0139 a0001c0001t0012g0342 a0001c0001t0013g0343 |
3 | HG01243.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.851+423A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880599 | |||||||
| chr14:73880600 | A | C | 81 | a0001c0002t0001g0004 a0001c0002t0001g0012 a0001c0002t0001g0013 others(78): Show |
96 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.851+424A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880600 | |||||||
| chr14:73880601 | C | A | 2 | a0001c0001t0004g0050 a0001c0001t0004g0066 |
2 | HG06807.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.851+425C>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880601 | |||||||
| chr14:73880639 | T | C | 1 | a0001c0001t0008g0092 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.851+463T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880639 | |||||||
| chr14:73880678 | T | C | 7 | a0001c0002t0001g0010 a0001c0002t0001g0155 a0001c0002t0001g0156 others(4): Show |
9 | HG01081.hp2 HG01884.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.851+502T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880678 | |||||||
| chr14:73880710 | A | G | 59 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(56): Show |
76 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.852-495A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880710 | |||||||
| chr14:73880736 | C | T | 113 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(110): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.852-469C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880736 | |||||||
| chr14:73880835 | C | T | 1 | a0001c0001t0003g0119 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.852-370C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880835 | |||||||
| chr14:73880851 | A | C | 190 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(187): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.852-354A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880851 | |||||||
| chr14:73880853 | G | A | 1 | a0001c0001t0003g0112 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.852-352G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73880853 | |||||||
| chr14:73881019 | T | C | 1 | a0001c0001t0003g0123 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.852-186T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 7/9 | chr14 | 73881019 | |||||||
| chr14:73881565 | A | ATTG | 231 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(228): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.939+275_939+276ins others(3): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 73881565 | ||||||
| chr14:73881728 | A | C | 1 | a0001c0002t0007g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.939+436A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | chr14 | 73881728 | |||||||
| chr14:73881772 | C | CT | 7 | a0001c0002t0001g0019 a0001c0002t0001g0144 a0001c0002t0001g0145 others(4): Show |
7 | HG01106.hp1 HG01123.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.939+509dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 73881772 | ||||||
| chr14:73881772 | CT | C | 99 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(96): Show |
118 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.939+509delT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 73881772 | ||||||
| chr14:73881772 | CTT | C | 158 | a0001c0001t0002g0033 a0001c0001t0002g0284 a0001c0001t0002g0285 others(155): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.939+508_939+509del others(2): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 73881772 | ||||||
| chr14:73881772 | CTTTTTTT others(3): Show |
C | 32 | a0001c0002t0005g0002 a0001c0002t0005g0011 a0001c0002t0005g0024 others(29): Show |
40 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.939+500_939+509del others(10): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 73881772 | ||||||
| chr14:73881772 | CTTTTTTT others(4): Show |
C | 2 | a0001c0002t0005g0011 a0001c0002t0005g0183 |
2 | HG01070.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.939+499_939+509del others(11): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 73881772 | ||||||
| chr14:73881807 | G | A | 1 | a0001c0002t0001g0150 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.939+515G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | chr14 | 73881807 | |||||||
| chr14:73881836 | T | G | 1 | a0001c0001t0004g0077 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.939+544T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | chr14 | 73881836 | |||||||
| chr14:73881860 | T | G | 181 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(178): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.940-539T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | chr14 | 73881860 | |||||||
| chr14:73881887 | A | G | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.940-512A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | chr14 | 73881887 | |||||||
| chr14:73881891 | A | C | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.940-508A>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | chr14 | 73881891 | |||||||
| chr14:73881949 | A | T | 1 | a0001c0001t0003g0035 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.940-450A>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | chr14 | 73881949 | |||||||
| chr14:73882034 | A | G | 5 | a0001c0001t0002g0033 a0001c0001t0002g0286 a0001c0001t0002g0301 others(2): Show |
6 | NA18944.hp1 NA18947.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.940-365A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | chr14 | 73882034 | |||||||
| chr14:73882055 | T | G | 1 | a0001c0002t0005g0187 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.940-344T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | chr14 | 73882055 | |||||||
| chr14:73882070 | GTGCACC | G | 1 | a0001c0002t0001g0010 | 3 | HG02559.hp1 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.940-326_940-321del others(6): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr14 | 73882070 | ||||||
| chr14:73882105 | T | G | 1 | a0001c0001t0003g0120 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.940-294T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | chr14 | 73882105 | |||||||
| chr14:73882116 | A | G | 236 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(233): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.940-283A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | chr14 | 73882116 | |||||||
| chr14:73882241 | A | G | 1 | a0001c0002t0001g0145 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.940-158A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | chr14 | 73882241 | |||||||
| chr14:73882390 | G | T | 2 | a0001c0001t0012g0342 a0001c0001t0013g0343 |
2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.940-9G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 8/9 | chr14 | 73882390 | |||||||
| chr14:73882524 | G | A | 104 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(101): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.979+86G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73882524 | |||||||
| chr14:73882566 | T | G | 1 | a0001c0002t0001g0260 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.979+128T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73882566 | |||||||
| chr14:73882610 | C | T | 183 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(180): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.979+172C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73882610 | |||||||
| chr14:73882636 | G | T | 7 | a0001c0002t0001g0208 a0001c0002t0001g0210 a0001c0002t0001g0211 others(4): Show |
7 | HG01243.hp1 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.979+198G>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73882636 | |||||||
| chr14:73882645 | C | T | 1 | a0001c0001t0002g0312 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.979+207C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73882645 | |||||||
| chr14:73882657 | C | T | 1 | a0001c0002t0001g0246 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.979+219C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73882657 | |||||||
| chr14:73882668 | T | G | 1 | a0001c0002t0001g0346 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.979+230T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73882668 | |||||||
| chr14:73882799 | CCTTTTTT others(10): Show |
C | 1 | a0001c0001t0011g0139 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.979+362_979+378del others(17): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73882799 | |||||||
| chr14:73882800 | C | CT | 44 | a0001c0002t0001g0004 a0001c0002t0001g0013 a0001c0002t0001g0020 others(41): Show |
48 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.979+400dupT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | ||||||
| chr14:73882800 | C | CTT | 14 | a0001c0002t0001g0012 a0001c0002t0001g0026 a0001c0002t0001g0208 others(11): Show |
14 | HG00280.hp1 HG00735.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.979+399_979+400dup others(2): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | ||||||
| chr14:73882800 | C | CTTT | 12 | a0001c0002t0001g0012 a0001c0002t0001g0029 a0001c0002t0001g0211 others(9): Show |
12 | HG00323.hp2 HG01167.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.979+398_979+400dup others(3): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | ||||||
| chr14:73882800 | C | CTTTT | 10 | a0001c0002t0001g0272 a0001c0002t0001g0276 a0001c0002t0005g0024 others(7): Show |
11 | HG00323.hp1 HG02129.hp2 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.979+397_979+400dup others(4): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | ||||||
| chr14:73882800 | C | CTTTTT | 7 | a0001c0002t0005g0186 a0001c0002t0005g0188 a0001c0002t0005g0191 others(4): Show |
7 | HG02523.hp2 HG02602.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.979+396_979+400dup others(5): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | ||||||
| chr14:73882800 | C | CTTTTTTT others(3): Show |
1 | a0001c0002t0001g0271 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.979+391_979+400dup others(10): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | ||||||
| chr14:73882800 | C | CTTTTTTT others(4): Show |
4 | a0001c0002t0005g0180 a0001c0002t0005g0182 a0001c0002t0005g0183 others(1): Show |
4 | HG01070.hp2 HG01257.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.979+390_979+400dup others(11): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | ||||||
| chr14:73882800 | C | CTTTTTTT others(5): Show |
4 | a0001c0002t0005g0011 a0001c0002t0005g0179 a0001c0002t0005g0181 others(1): Show |
6 | HG00639.hp2 HG01071.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.979+389_979+400dup others(12): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | ||||||
| chr14:73882800 | C | CTTTTTTT others(8): Show |
1 | a0001c0002t0005g0002 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.979+386_979+400dup others(15): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | ||||||
| chr14:73882800 | C | CTTTTTTT others(9): Show |
1 | a0001c0002t0005g0002 | 2 | HG01168.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.979+385_979+400dup others(16): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | ||||||
| chr14:73882800 | C | CTTTTTTT others(10): Show |
1 | a0001c0002t0005g0199 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.979+384_979+400dup others(17): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | ||||||
| chr14:73882800 | C | CTTTTTTT others(11): Show |
1 | a0001c0002t0005g0185 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.979+383_979+400dup others(18): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | ||||||
| chr14:73882800 | C | CTTTTTTT others(12): Show |
1 | a0001c0002t0005g0207 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.979+382_979+400dup others(19): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | ||||||
| chr14:73882800 | C | CTTTTTTT others(13): Show |
2 | a0001c0002t0005g0002 a0001c0002t0005g0192 |
3 | HG01123.hp2 HG01928.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.979+381_979+400dup others(20): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | ||||||
| chr14:73882800 | C | CTTTTTTT others(16): Show |
1 | a0001c0002t0005g0002 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.979+378_979+400dup others(23): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | ||||||
| chr14:73882800 | CT | C | 12 | a0001c0002t0001g0019 a0001c0002t0001g0141 a0001c0002t0001g0142 others(9): Show |
12 | HG01070.hp1 HG01192.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.979+400delT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | ||||||
| chr14:73882800 | CTT | C | 8 | a0001c0002t0001g0010 a0001c0002t0001g0152 a0001c0002t0001g0154 others(5): Show |
10 | HG01515.hp1 HG02559.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.979+399_979+400del others(2): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | ||||||
| chr14:73882800 | CTTT | C | 9 | a0001c0002t0001g0021 a0001c0002t0001g0022 a0001c0002t0001g0023 others(6): Show |
10 | HG01074.hp2 HG01123.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.979+398_979+400del others(3): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | ||||||
| chr14:73882800 | CTTTT | C | 10 | a0001c0002t0001g0021 a0001c0002t0001g0151 a0001c0002t0001g0153 others(7): Show |
10 | HG00741.hp1 HG01081.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.979+397_979+400del others(4): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | ||||||
| chr14:73882800 | CTTTTTTT others(3): Show |
C | 52 | a0001c0001t0002g0032 a0001c0001t0002g0282 a0001c0001t0002g0285 others(49): Show |
55 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.979+391_979+400del others(10): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | ||||||
| chr14:73882800 | CTTTTTTT others(4): Show |
C | 127 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(124): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.979+390_979+400del others(11): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | ||||||
| chr14:73882800 | CTTTTTTT others(5): Show |
C | 10 | a0001c0001t0002g0001 a0001c0001t0002g0309 a0001c0001t0002g0322 others(7): Show |
12 | HG01109.hp2 HG01168.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.979+389_979+400del others(12): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | ||||||
| chr14:73882800 | CTTTTTTT others(10): Show |
C | 1 | a0001c0002t0001g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.979+384_979+400del others(17): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | ||||||
| chr14:73882800 | CTTTTTTT others(15): Show |
C | 1 | a0001c0002t0001g0164 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.979+379_979+400del others(22): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73882800 | ||||||
| chr14:73882844 | G | A | 2 | a0001c0001t0004g0042 a0001c0001t0004g0081 |
2 | HG01074.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.979+406G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73882844 | |||||||
| chr14:73882913 | C | T | 2 | a0001c0001t0011g0139 a0001c0002t0001g0220 |
2 | HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.979+475C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73882913 | |||||||
| chr14:73882965 | C | T | 1 | a0001c0001t0015g0137 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.979+527C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73882965 | |||||||
| chr14:73883072 | C | T | 2 | a0001c0001t0014g0138 a0001c0001t0015g0137 |
2 | HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.979+634C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73883072 | |||||||
| chr14:73883178 | C | T | 1 | a0001c0001t0003g0108 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.979+740C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73883178 | |||||||
| chr14:73883180 | TCACCTC | T | 3 | a0001c0002t0001g0025 a0001c0002t0001g0222 a0001c0002t0001g0277 |
4 | HG02622.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.979+744_979+749del others(6): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883180 | ||||||
| chr14:73883188 | C | CTT | 14 | a0001c0001t0004g0037 a0001c0002t0001g0013 a0001c0002t0001g0026 others(11): Show |
17 | HG00621.hp2 HG01256.hp2 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.979+781_979+782dup others(2): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883188 | C | CTTT | 28 | a0001c0002t0001g0004 a0001c0002t0001g0012 a0001c0002t0001g0028 others(25): Show |
34 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.979+780_979+782dup others(3): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883188 | C | CTTTT | 9 | a0001c0002t0001g0027 a0001c0002t0001g0030 a0001c0002t0001g0223 others(6): Show |
11 | HG00597.hp1 HG01433.hp1 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.979+779_979+782dup others(4): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883188 | C | CTTTTT | 11 | a0001c0002t0001g0224 a0001c0002t0001g0225 a0001c0002t0001g0226 others(8): Show |
14 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.979+778_979+782dup others(5): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883188 | C | CTTTTTT | 5 | a0001c0001t0002g0014 a0001c0001t0002g0298 a0001c0001t0002g0307 others(2): Show |
7 | HG00438.hp2 HG03486.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.979+777_979+782dup others(6): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883188 | C | CTTTTTTT | 23 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0033 others(20): Show |
34 | HG00438.hp1 HG00544.hp1 HG02523.hp1 others(31): Show |
intron_variant | MODIFIER | c.979+776_979+782dup others(7): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883188 | C | CTTTTTTT others(1): Show |
28 | a0001c0001t0002g0015 a0001c0001t0002g0034 a0001c0001t0002g0289 others(25): Show |
31 | HG00408.hp1 HG00642.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.979+775_979+782dup others(8): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883188 | C | CTTTTTTT others(2): Show |
16 | a0001c0001t0002g0031 a0001c0001t0002g0285 a0001c0001t0002g0287 others(13): Show |
17 | HG00423.hp2 HG00621.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.979+774_979+782dup others(9): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883188 | C | CTTTTTTT others(3): Show |
7 | a0001c0001t0002g0299 a0001c0001t0002g0314 a0001c0001t0002g0344 others(4): Show |
7 | HG02071.hp2 HG02109.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.979+773_979+782dup others(10): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883188 | C | CTTTTTTT others(4): Show |
3 | a0001c0001t0004g0044 a0001c0001t0004g0056 a0001c0001t0004g0077 |
3 | HG02155.hp2 HG02615.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.979+772_979+782dup others(11): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883188 | C | CTTTTTTT others(5): Show |
4 | a0001c0001t0002g0292 a0001c0001t0004g0059 a0001c0001t0004g0060 others(1): Show |
4 | HG00408.hp2 HG02602.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.979+771_979+782dup others(12): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883188 | C | CTTTTTTT others(6): Show |
4 | a0001c0001t0004g0038 a0001c0001t0004g0054 a0001c0001t0004g0057 others(1): Show |
4 | HG00544.hp2 HG02132.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.979+770_979+782dup others(13): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883188 | C | CTTTTTTT others(7): Show |
2 | a0001c0001t0004g0062 a0001c0001t0004g0078 |
2 | HG02717.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.979+769_979+782dup others(14): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883188 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0004g0053 a0001c0001t0004g0081 |
2 | HG02559.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.979+768_979+782dup others(15): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883188 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0004g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.979+767_979+782dup others(16): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883188 | C | CTTTTTTT others(11): Show |
1 | a0001c0001t0004g0045 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.979+765_979+782dup others(18): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883188 | C | CTTTTTTT others(12): Show |
4 | a0001c0001t0002g0319 a0001c0001t0004g0071 a0001c0001t0004g0080 others(1): Show |
4 | HG02258.hp2 HG03139.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.979+764_979+782dup others(19): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883188 | C | CTTTTTTT others(13): Show |
4 | a0001c0001t0004g0051 a0001c0001t0004g0064 a0001c0001t0004g0065 others(1): Show |
4 | HG00099.hp2 HG00738.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.979+763_979+782dup others(20): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883188 | CT | C | 38 | a0001c0001t0004g0040 a0001c0001t0004g0041 a0001c0001t0004g0068 others(35): Show |
43 | HG00280.hp1 HG01074.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.979+782delT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883188 | CTT | C | 35 | a0001c0001t0004g0058 a0001c0001t0004g0067 a0001c0001t0004g0076 others(32): Show |
44 | HG00639.hp2 HG00741.hp1 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.979+781_979+782del others(2): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883188 | CTTT | C | 8 | a0001c0001t0002g0321 a0001c0001t0004g0016 a0001c0001t0004g0070 others(5): Show |
9 | HG00323.hp1 HG00741.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.979+780_979+782del others(3): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883188 | CTTTTTTT others(3): Show |
C | 7 | a0001c0001t0002g0288 a0001c0002t0001g0270 a0001c0002t0001g0271 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.979+773_979+782del others(10): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883188 | CTTTTTTT others(4): Show |
C | 8 | a0001c0002t0001g0208 a0001c0002t0001g0210 a0001c0002t0001g0211 others(5): Show |
8 | HG01243.hp1 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.979+772_979+782del others(11): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883188 | CTTTTTTT others(5): Show |
C | 6 | a0001c0001t0003g0008 a0001c0001t0003g0088 a0001c0001t0004g0046 others(3): Show |
8 | HG01109.hp1 HG02451.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.979+771_979+782del others(12): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883188 | CTTTTTTT others(6): Show |
C | 52 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(49): Show |
67 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.979+770_979+782del others(13): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883188 | CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0003g0105 a0001c0001t0003g0113 |
2 | HG01975.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.979+769_979+782del others(14): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883188 | CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0011g0139 a0001c0002t0001g0228 |
2 | HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.979+768_979+782del others(15): Show |
PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883188 | ||||||
| chr14:73883189 | T | C | 3 | a0001c0002t0001g0025 a0001c0002t0001g0222 a0001c0002t0001g0277 |
4 | HG02622.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.979+751T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73883189 | |||||||
| chr14:73883360 | CT | C | 182 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(179): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.980-727delT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73883360 | ||||||
| chr14:73883431 | T | C | 1 | a0001c0001t0014g0138 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.980-670T>C | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73883431 | |||||||
| chr14:73883446 | A | G | 73 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(70): Show |
90 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.980-655A>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73883446 | |||||||
| chr14:73883524 | C | T | 73 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(70): Show |
90 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.980-577C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73883524 | |||||||
| chr14:73883602 | T | G | 2 | a0001c0001t0012g0342 a0001c0001t0013g0343 |
2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.980-499T>G | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73883602 | |||||||
| chr14:73883610 | C | T | 73 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(70): Show |
90 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.980-491C>T | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73883610 | |||||||
| chr14:73883935 | G | A | 73 | a0001c0001t0002g0001 a0001c0001t0002g0014 a0001c0001t0002g0015 others(70): Show |
90 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.980-166G>A | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | chr14 | 73883935 | |||||||
| chr14:73884091 | CTT | C | 5 | a0001c0002t0007g0006 a0001c0002t0007g0171 a0001c0002t0007g0172 others(2): Show |
8 | HG01109.hp2 HG01496.hp1 HG02145.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.980-6_980-5delTT | PTGR2 | ENSG00000140043.12 | transcript | ENST00000555661.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr14 | 73884091 |