Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5737 |
| ensemblid | ENSG00000122420.10 |
| hgncid | 9600 |
| symbol | PTGFR |
| name | prostaglandin F receptor |
| refseq_nuc | NM_000959.4 |
| refseq_prot | NP_000950.1 |
| ensembl_nuc | ENST00000370757.8 |
| ensembl_prot | ENSP00000359793.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 78490974 |
| end | 78540701 |
| strand | + |
| ver | v1.2 |
| region | chr1:78490974-78540701 |
| region5000 | chr1:78485974-78545701 |
| regionname0 | PTGFR_chr1_78490974_78540701 |
| regionname5000 | PTGFR_chr1_78485974_78545701 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 359 | 375 | 89 | 68 | 161 | 14 | 41 | 122 | PTGFR_chr1_78485974_78545701 | PTGFR | MSMNN others(354): Show |
chr1 | 78485974 | 78545701 |
| a0002 | 0/0 | 359 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | PTGFR_chr1_78485974_78545701 | PTGFR | MSMNN others(354): Show |
chr1 | 78485974 | 78545701 |
| a0003 | 0/0 | 359 | 4 | 0 | 0 | 1 | 0 | 3 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | MSMNN others(354): Show |
chr1 | 78485974 | 78545701 |
| a0004 | 0/0 | 359 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | MSMNN others(354): Show |
chr1 | 78485974 | 78545701 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1077 | 351 | 72 | 64 | 161 | 13 | 39 | PTGFR_chr1_78485974_78545701 | PTGFR | ATGTC others(1072): Show |
chr1 | 78485974 | 78545701 | ||
| a0001c0002 | 0/0 | 1077 | 16 | 16 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ATGTC others(1072): Show |
chr1 | 78485974 | 78545701 | ||
| a0001c0003 | 0/0 | 1077 | 8 | 1 | 4 | 0 | 1 | 2 | PTGFR_chr1_78485974_78545701 | PTGFR | ATGTC others(1072): Show |
chr1 | 78485974 | 78545701 | ||
| a0002c0004 | 0/0 | 1077 | 6 | 0 | 0 | 6 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ATGTC others(1072): Show |
chr1 | 78485974 | 78545701 | ||
| a0003c0005 | 0/0 | 1077 | 4 | 0 | 0 | 1 | 0 | 3 | PTGFR_chr1_78485974_78545701 | PTGFR | ATGTC others(1072): Show |
chr1 | 78485974 | 78545701 | ||
| a0004c0006 | 0/0 | 1077 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ATGTC others(1072): Show |
chr1 | 78485974 | 78545701 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5429 | 247 | 31 | 48 | 125 | 8 | 33 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5424): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0002 | 0/0 | 5428 | 25 | 16 | 6 | 2 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5423): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0003 | 0/0 | 5429 | 26 | 0 | 0 | 26 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5424): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0004 | 0/0 | 5435 | 12 | 3 | 7 | 0 | 0 | 2 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5430): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0005 | 0/0 | 5429 | 5 | 2 | 0 | 2 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5424): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0006 | 0/0 | 5434 | 5 | 0 | 1 | 0 | 2 | 2 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5429): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0007 | 0/0 | 5435 | 4 | 4 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5430): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0008 | 0/0 | 5433 | 3 | 2 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5428): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0009 | 0/0 | 5435 | 3 | 3 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5430): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0010 | 0/0 | 5429 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5424): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0011 | 0/0 | 5430 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5425): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0012 | 0/0 | 5429 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5424): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0013 | 0/0 | 5429 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5424): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0014 | 0/0 | 5429 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5424): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0015 | 0/0 | 5429 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5424): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0016 | 0/0 | 5429 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5424): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0017 | 0/0 | 5429 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5424): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0018 | 0/0 | 5429 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5424): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0019 | 0/0 | 5428 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5423): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0020 | 0/0 | 5429 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5424): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0021 | 0/0 | 5433 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5428): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0023 | 0/0 | 5434 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5429): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0026 | 0/0 | 5434 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5429): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0027 | 0/0 | 5433 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5428): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0028 | 0/0 | 5435 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5430): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0029 | 0/0 | 5435 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5430): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0030 | 0/0 | 5428 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5423): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0033 | 0/0 | 5429 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5424): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0034 | 0/0 | 5429 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5424): Show |
chr1 | 78485974 | 78545701 |
| a0001c0001t0035 | 0/0 | 5429 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | AGTCG others(5424): Show |
chr1 | 78485974 | 78545701 |
| a0001c0002t0001 | 0/0 | 5429 | 11 | 11 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5424): Show |
chr1 | 78485974 | 78545701 |
| a0001c0002t0002 | 0/0 | 5428 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5423): Show |
chr1 | 78485974 | 78545701 |
| a0001c0002t0022 | 0/0 | 5434 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5429): Show |
chr1 | 78485974 | 78545701 |
| a0001c0002t0024 | 0/0 | 5434 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5429): Show |
chr1 | 78485974 | 78545701 |
| a0001c0002t0025 | 0/0 | 5435 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5430): Show |
chr1 | 78485974 | 78545701 |
| a0001c0002t0031 | 0/0 | 5433 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5428): Show |
chr1 | 78485974 | 78545701 |
| a0001c0003t0001 | 0/0 | 5429 | 6 | 1 | 2 | 0 | 1 | 2 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5424): Show |
chr1 | 78485974 | 78545701 |
| a0001c0003t0002 | 0/0 | 5428 | 2 | 0 | 2 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5423): Show |
chr1 | 78485974 | 78545701 |
| a0002c0004t0001 | 0/0 | 5429 | 6 | 0 | 0 | 6 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5424): Show |
chr1 | 78485974 | 78545701 |
| a0003c0005t0001 | 0/0 | 5429 | 2 | 0 | 0 | 0 | 0 | 2 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5424): Show |
chr1 | 78485974 | 78545701 |
| a0003c0005t0002 | 0/0 | 5428 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5423): Show |
chr1 | 78485974 | 78545701 |
| a0003c0005t0010 | 0/0 | 5429 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5424): Show |
chr1 | 78485974 | 78545701 |
| a0004c0006t0032 | 0/0 | 5434 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | ACTCG others(5429): Show |
chr1 | 78485974 | 78545701 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0174 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0238 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0004g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0004g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0004g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0004g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0004g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0005g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0005g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0005g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0006g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0006g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0006g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0006g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0007g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0007g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0007g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0007g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0008g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0008g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0008g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0009g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0009g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0010g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0011g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0012g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0013g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0014g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0015g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0016g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0017g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0018g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0019g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0020g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0021g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0023g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0026g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0027g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0028g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0029g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0030g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0033g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0034g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0001t0035g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0002t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0002t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0002t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0002t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0002t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0002t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0002t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0002t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0002t0022g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0002t0024g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0002t0025g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0002t0031g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0003t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0003t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0001c0003t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0002c0004t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0002c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0002c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0002c0004t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0002c0004t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0002c0004t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0003c0005t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0003c0005t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0003c0005t0010g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| a0004c0006t0032g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0006 | EUR | GBR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0154 | EUR | GBR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0287 | EUR | GBR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00140 | hp2 | a0001 | c0001 | t0006 | g0029 | EUR | GBR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | FIN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | FIN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00597 | hp1 | a0001 | c0001 | t0018 | g0150 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0240 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01168 | hp1 | a0001 | c0001 | t0028 | g0289 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0195 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01255 | hp1 | a0001 | c0003 | t0002 | g0006 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01358 | hp2 | a0001 | c0003 | t0001 | g0263 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01433 | hp1 | a0001 | c0003 | t0002 | g0006 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0312 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01515 | hp1 | a0001 | c0003 | t0001 | g0277 | EUR | IBS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | IBS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | IBS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0044 | EUR | IBS | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0294 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0339 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0308 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01981 | hp2 | a0001 | c0001 | t0006 | g0029 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0328 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0319 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02129 | hp2 | a0003 | c0005 | t0010 | g0282 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CDX | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CDX | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | CDX | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02258 | hp2 | a0001 | c0001 | t0026 | g0255 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0225 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02602 | hp2 | a0001 | c0001 | t0006 | g0245 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02647 | hp1 | a0001 | c0001 | t0012 | g0116 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0327 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02683 | hp1 | a0001 | c0001 | t0008 | g0335 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02717 | hp1 | a0001 | c0001 | t0008 | g0337 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0315 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0334 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0014 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02809 | hp2 | a0001 | c0001 | t0023 | g0254 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0281 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02896 | hp1 | a0001 | c0001 | t0009 | g0014 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02922 | hp2 | a0001 | c0001 | t0013 | g0088 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02965 | hp2 | a0001 | c0001 | t0021 | g0280 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0320 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0314 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0248 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0266 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0283 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0105 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0330 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0340 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03209 | hp1 | a0001 | c0002 | t0025 | g0321 | AFR | MSL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | MSL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | MSL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03453 | hp2 | a0001 | c0001 | t0011 | g0239 | AFR | MSL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03486 | hp1 | a0001 | c0001 | t0009 | g0094 | AFR | MSL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0322 | AFR | MSL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03490 | hp2 | a0003 | c0005 | t0002 | g0276 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03491 | hp1 | a0003 | c0005 | t0001 | g0028 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03492 | hp2 | a0003 | c0005 | t0001 | g0028 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03516 | hp2 | a0001 | c0001 | t0029 | g0333 | AFR | ESN | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03540 | hp1 | a0001 | c0001 | t0030 | g0242 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03579 | hp1 | a0001 | c0001 | t0016 | g0241 | AFR | MSL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03579 | hp2 | a0001 | c0002 | t0031 | g0316 | AFR | MSL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0309 | SAS | STU | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | STU | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | BEB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03927 | hp2 | a0001 | c0001 | t0006 | g0244 | SAS | BEB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0313 | SAS | BEB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0268 | SAS | BEB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG04115 | hp1 | a0001 | c0001 | t0005 | g0133 | SAS | STU | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0307 | SAS | STU | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | STU | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | STU | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | STU | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | STU | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | STU | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0329 | AFR | YRI | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18522 | hp2 | a0004 | c0006 | t0032 | g0145 | AFR | YRI | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | CHB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18906 | hp1 | a0001 | c0001 | t0014 | g0288 | AFR | YRI | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | YRI | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18947 | hp1 | a0002 | c0004 | t0001 | g0157 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18970 | hp1 | a0001 | c0001 | t0010 | g0233 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18977 | hp2 | a0002 | c0004 | t0001 | g0079 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18982 | hp1 | a0002 | c0004 | t0001 | g0229 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18983 | hp2 | a0001 | c0001 | t0033 | g0200 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18984 | hp2 | a0001 | c0001 | t0017 | g0160 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19012 | hp1 | a0002 | c0004 | t0001 | g0199 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19030 | hp1 | a0001 | c0003 | t0001 | g0267 | AFR | LWK | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | LWK | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0087 | AFR | LWK | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19059 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19070 | hp2 | a0002 | c0004 | t0001 | g0173 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19075 | hp2 | a0001 | c0001 | t0034 | g0301 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19077 | hp1 | a0001 | c0001 | t0020 | g0043 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19080 | hp2 | a0001 | c0001 | t0005 | g0130 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19085 | hp2 | a0001 | c0001 | t0005 | g0132 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19088 | hp2 | a0002 | c0004 | t0001 | g0072 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0256 | AFR | YRI | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0317 | AFR | YRI | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ASW | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0325 | AFR | ASW | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA20752 | hp1 | a0001 | c0001 | t0035 | g0258 | EUR | TSI | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA20752 | hp2 | a0001 | c0001 | t0006 | g0305 | EUR | TSI | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0259 | EUR | TSI | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA20805 | hp2 | a0001 | c0001 | t0019 | g0039 | EUR | TSI | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | GIH | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | GIH | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG01123 | hp2 | a0001 | c0001 | t0015 | g0117 | AMR | CLM | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02109 | hp1 | a0001 | c0002 | t0022 | g0323 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02486 | hp1 | a0001 | c0001 | t0008 | g0338 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02486 | hp2 | a0001 | c0001 | t0027 | g0123 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0331 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | ACB | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03471 | hp1 | a0001 | c0002 | t0024 | g0324 | AFR | MSL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | MSL | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0271 | AFR | USA | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0326 | AFR | USA | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | USA | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | USA | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0299 | AFR | LWK | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0067 | AFR | LWK | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0238 | REF | REF | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0174 | REF | REF | PTGFR_chr1_78485974_78545701 | PTGFR | chr1 | 78485974 | 78545701 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:78492766 | A | T | 1 | a0003 | 4 | HG02129.hp2 HG03490.hp2 HG03491.hp1 others(1): Show |
missense_variant | MODERATE | c.23A>T | p.Gln8Leu | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/3 | 358/5429 | 23/1080 | 8/359 | chr1 | 78492766 | |||
| chr1:78493396 | T | C | 1 | a0004 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.653T>C | p.Leu218Ser | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/3 | 988/5429 | 653/1080 | 218/359 | chr1 | 78493396 | |||
| chr1:78536545 | A | G | 1 | a0002 | 6 | NA18947.hp1 NA18977.hp2 NA18982.hp1 others(3): Show |
missense_variant | MODERATE | c.938A>G | p.Lys313Arg | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 1273/5429 | 938/1080 | 313/359 | chr1 | 78536545 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:78492806 | C | T | 1 | a0001c0003 | 8 | HG00642.hp1 HG01255.hp1 HG01358.hp2 others(5): Show |
synonymous_variant | LOW | c.63C>T | p.Thr21Thr | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/3 | 398/5429 | 63/1080 | 21/359 | chr1 | 78492806 | |||
| chr1:78493178 | G | A | 2 | a0001c0002 a0004c0006 |
17 | HG02055.hp1 HG02109.hp1 HG02451.hp2 others(14): Show |
synonymous_variant | LOW | c.435G>A | p.Thr145Thr | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/3 | 770/5429 | 435/1080 | 145/359 | chr1 | 78493178 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:78490975 | C | G | 1 | a0001c0001t0035 | 1 | NA20752.hp1 | 5_prime_UTR_variant | MODIFIER | c.-334C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/3 | 1769 | chr1 | 78490975 | ||||||
| chr1:78491096 | G | T | 1 | a0001c0001t0034 | 1 | NA19075.hp2 | 5_prime_UTR_variant | MODIFIER | c.-213G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/3 | 1648 | chr1 | 78491096 | ||||||
| chr1:78491117 | A | G | 1 | a0001c0001t0033 | 1 | NA18983.hp2 | 5_prime_UTR_variant | MODIFIER | c.-192A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/3 | 1627 | chr1 | 78491117 | ||||||
| chr1:78491125 | C | T | 3 | a0001c0001t0030 a0001c0002t0031 a0004c0006t0032 |
3 | HG03540.hp1 HG03579.hp2 NA18522.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-184C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/3 | chr1 | 78491125 | |||||||
| chr1:78536859 | C | T | 16 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(13): Show |
38 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*172C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 172 | chr1 | 78536859 | ||||||
| chr1:78536904 | A | G | 14 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(11): Show |
34 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*217A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 217 | chr1 | 78536904 | ||||||
| chr1:78537277 | C | T | 14 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(11): Show |
34 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*590C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 590 | chr1 | 78537277 | ||||||
| chr1:78537346 | G | A | 4 | a0001c0001t0023 a0001c0002t0022 a0001c0002t0024 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*659G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 659 | chr1 | 78537346 | ||||||
| chr1:78537458 | C | T | 1 | a0001c0001t0020 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*771C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 771 | chr1 | 78537458 | ||||||
| chr1:78537573 | A | C | 14 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(11): Show |
34 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*886A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 886 | chr1 | 78537573 | ||||||
| chr1:78537603 | A | C | 1 | a0001c0001t0029 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*916A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 916 | chr1 | 78537603 | ||||||
| chr1:78537613 | A | G | 1 | a0001c0001t0019 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*926A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 926 | chr1 | 78537613 | ||||||
| chr1:78537614 | A | G | 2 | a0001c0001t0003 a0001c0001t0005 |
31 | HG00544.hp1 HG02015.hp1 HG02080.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*927A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 927 | chr1 | 78537614 | ||||||
| chr1:78537670 | A | G | 16 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(13): Show |
38 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*983A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 983 | chr1 | 78537670 | ||||||
| chr1:78537696 | T | C | 1 | a0001c0002t0022 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1009T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 1009 | chr1 | 78537696 | ||||||
| chr1:78537704 | G | A | 1 | a0001c0001t0019 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1017G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 1017 | chr1 | 78537704 | ||||||
| chr1:78537838 | C | G | 3 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0009 |
20 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1151C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 1151 | chr1 | 78537838 | ||||||
| chr1:78538168 | A | G | 1 | a0001c0001t0028 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1481A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 1481 | chr1 | 78538168 | ||||||
| chr1:78538482 | C | T | 1 | a0001c0001t0018 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1795C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 1795 | chr1 | 78538482 | ||||||
| chr1:78538532 | T | TA | 6 | a0001c0001t0011 a0001c0001t0023 a0001c0001t0026 others(3): Show |
6 | HG02109.hp1 HG02258.hp2 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1858dupA | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 1859 | INFO_REALIGN_3_PRIME | chr1 | 78538532 | |||||
| chr1:78538532 | T | TAA | 7 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(4): Show |
27 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1857_*1858dupAA | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 1859 | INFO_REALIGN_3_PRIME | chr1 | 78538532 | |||||
| chr1:78538532 | TA | T | 6 | a0001c0001t0002 a0001c0001t0019 a0001c0001t0030 others(3): Show |
31 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1858delA | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 1858 | INFO_REALIGN_3_PRIME | chr1 | 78538532 | |||||
| chr1:78538670 | T | C | 1 | a0001c0001t0012 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1983T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 1983 | chr1 | 78538670 | ||||||
| chr1:78538696 | T | C | 1 | a0001c0001t0013 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2009T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2009 | chr1 | 78538696 | ||||||
| chr1:78538725 | C | T | 1 | a0001c0001t0009 | 3 | HG02809.hp1 HG02896.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2038C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2038 | chr1 | 78538725 | ||||||
| chr1:78538789 | C | T | 14 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(11): Show |
34 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2102C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2102 | chr1 | 78538789 | ||||||
| chr1:78538827 | T | G | 14 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(11): Show |
34 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2140T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2140 | chr1 | 78538827 | ||||||
| chr1:78538833 | C | G | 1 | a0001c0001t0013 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2146C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2146 | chr1 | 78538833 | ||||||
| chr1:78538891 | A | C | 1 | a0001c0001t0017 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2204A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2204 | chr1 | 78538891 | ||||||
| chr1:78539032 | T | G | 1 | a0001c0001t0014 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2345T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2345 | chr1 | 78539032 | ||||||
| chr1:78539063 | A | AAGAT | 16 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(13): Show |
38 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2378_*2381dupGATA | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2382 | INFO_REALIGN_3_PRIME | chr1 | 78539063 | |||||
| chr1:78539091 | G | T | 1 | a0001c0002t0024 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2404G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2404 | chr1 | 78539091 | ||||||
| chr1:78539200 | A | G | 1 | a0001c0001t0016 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2513A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2513 | chr1 | 78539200 | ||||||
| chr1:78539235 | T | C | 14 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(11): Show |
34 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2548T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2548 | chr1 | 78539235 | ||||||
| chr1:78539618 | G | A | 1 | a0001c0001t0015 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2931G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2931 | chr1 | 78539618 | ||||||
| chr1:78539639 | G | T | 1 | a0001c0001t0021 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2952G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2952 | chr1 | 78539639 | ||||||
| chr1:78539654 | T | G | 2 | a0001c0001t0008 a0001c0001t0021 |
4 | HG02486.hp1 HG02683.hp1 HG02717.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2967T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 2967 | chr1 | 78539654 | ||||||
| chr1:78539704 | T | A | 2 | a0001c0001t0010 a0003c0005t0010 |
2 | HG02129.hp2 NA18970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3017T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 3017 | chr1 | 78539704 | ||||||
| chr1:78539796 | C | T | 2 | a0001c0001t0005 a0001c0001t0011 |
6 | HG03130.hp2 HG03195.hp1 HG03453.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3109C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 3109 | chr1 | 78539796 | ||||||
| chr1:78539799 | G | A | 10 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(7): Show |
30 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3112G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 3112 | chr1 | 78539799 | ||||||
| chr1:78539863 | C | T | 2 | a0001c0001t0008 a0001c0001t0021 |
4 | HG02486.hp1 HG02683.hp1 HG02717.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3176C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 3176 | chr1 | 78539863 | ||||||
| chr1:78539866 | T | C | 10 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(7): Show |
30 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3179T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 3179 | chr1 | 78539866 | ||||||
| chr1:78540023 | GA | G | 1 | a0001c0001t0006 | 5 | HG00140.hp2 HG01981.hp2 HG02602.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3339delA | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 3339 | INFO_REALIGN_3_PRIME | chr1 | 78540023 | |||||
| chr1:78540082 | T | A | 1 | a0001c0001t0029 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3395T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 3395 | chr1 | 78540082 | ||||||
| chr1:78540113 | T | C | 16 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(13): Show |
38 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*3426T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 3426 | chr1 | 78540113 | ||||||
| chr1:78540185 | A | G | 2 | a0001c0001t0007 a0001c0001t0027 |
5 | HG01891.hp1 HG02486.hp2 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3498A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 3/3 | 3498 | chr1 | 78540185 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:78491506 | C | G | 1 | a0001c0001t0005g0340 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-73+270C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78491506 | |||||||
| chr1:78491557 | C | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0334 a0001c0001t0001g0336 others(4): Show |
9 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-73+321C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78491557 | |||||||
| chr1:78491646 | T | C | 1 | a0001c0001t0001g0031 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-73+410T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78491646 | |||||||
| chr1:78491670 | G | T | 1 | a0001c0001t0005g0340 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-73+434G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78491670 | |||||||
| chr1:78491690 | A | T | 3 | a0001c0001t0001g0332 a0001c0001t0004g0331 a0001c0001t0029g0333 |
3 | HG02559.hp1 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-73+454A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78491690 | |||||||
| chr1:78491713 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-73+477T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78491713 | |||||||
| chr1:78491727 | G | A | 2 | a0001c0001t0001g0334 a0001c0001t0008g0335 |
2 | HG02683.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-73+491G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78491727 | |||||||
| chr1:78491756 | C | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(120): Show |
141 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.-73+520C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78491756 | |||||||
| chr1:78491784 | G | A | 3 | a0001c0001t0001g0131 a0001c0001t0005g0132 a0001c0001t0005g0133 |
3 | HG00621.hp2 HG04115.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-73+548G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78491784 | |||||||
| chr1:78491865 | G | A | 63 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(60): Show |
65 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.-73+629G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78491865 | |||||||
| chr1:78492055 | C | G | 12 | a0001c0002t0001g0009 a0001c0002t0001g0030 a0001c0002t0001g0322 others(9): Show |
15 | HG02055.hp1 HG02109.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.-72-617C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78492055 | |||||||
| chr1:78492065 | A | C | 4 | a0001c0001t0001g0318 a0001c0001t0002g0317 a0001c0001t0002g0319 others(1): Show |
4 | HG02055.hp2 HG02970.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72-607A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78492065 | |||||||
| chr1:78492174 | G | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(42): Show |
58 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-72-498G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78492174 | |||||||
| chr1:78492253 | G | T | 1 | a0001c0002t0031g0316 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-72-419G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78492253 | |||||||
| chr1:78492256 | C | T | 3 | a0001c0001t0001g0334 a0001c0001t0007g0339 a0001c0001t0008g0335 |
3 | HG01891.hp1 HG02683.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-72-416C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78492256 | |||||||
| chr1:78492293 | G | T | 2 | a0001c0001t0002g0314 a0001c0001t0002g0315 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-72-379G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78492293 | |||||||
| chr1:78492402 | T | C | 1 | a0001c0002t0031g0316 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-72-270T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78492402 | |||||||
| chr1:78492592 | C | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0297 others(18): Show |
27 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.-72-80C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 1/2 | chr1 | 78492592 | |||||||
| chr1:78493551 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.798+10T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78493551 | |||||||
| chr1:78493598 | G | C | 1 | a0001c0001t0001g0033 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.798+57G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78493598 | |||||||
| chr1:78493869 | A | G | 1 | a0001c0001t0001g0296 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.798+328A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78493869 | |||||||
| chr1:78493887 | G | GT | 38 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0286 others(35): Show |
44 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.798+347dupT | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78493887 | ||||||
| chr1:78493928 | A | T | 3 | a0001c0001t0001g0131 a0001c0001t0005g0132 a0001c0001t0005g0133 |
3 | HG00621.hp2 HG04115.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.798+387A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78493928 | |||||||
| chr1:78494001 | A | G | 2 | a0001c0001t0001g0284 a0001c0001t0001g0285 |
2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.798+460A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78494001 | |||||||
| chr1:78494029 | G | A | 5 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(2): Show |
5 | HG02074.hp1 NA18969.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.798+488G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78494029 | |||||||
| chr1:78494249 | T | C | 5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | HG01071.hp1 HG01243.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.798+708T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78494249 | |||||||
| chr1:78494314 | T | C | 2 | a0001c0002t0031g0316 a0004c0006t0032g0145 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+773T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78494314 | |||||||
| chr1:78494326 | G | T | 1 | a0001c0001t0002g0283 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.798+785G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78494326 | |||||||
| chr1:78494369 | CA | C | 7 | a0001c0001t0001g0010 a0001c0001t0001g0334 a0001c0001t0001g0336 others(4): Show |
9 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.798+836delA | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78494369 | ||||||
| chr1:78494573 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.798+1032G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78494573 | |||||||
| chr1:78494591 | G | T | 2 | a0001c0002t0031g0316 a0004c0006t0032g0145 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+1050G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78494591 | |||||||
| chr1:78494600 | T | TTTTG | 12 | a0001c0002t0001g0009 a0001c0002t0001g0030 a0001c0002t0001g0322 others(9): Show |
15 | HG02055.hp1 HG02109.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.798+1080_798+1083d others(6): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78494600 | ||||||
| chr1:78494659 | A | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(237): Show |
272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.798+1118A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78494659 | |||||||
| chr1:78494692 | G | A | 4 | a0001c0002t0001g0322 a0001c0002t0022g0323 a0001c0002t0024g0324 others(1): Show |
4 | HG02109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+1151G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78494692 | |||||||
| chr1:78494824 | T | C | 2 | a0001c0002t0031g0316 a0004c0006t0032g0145 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+1283T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78494824 | |||||||
| chr1:78494893 | C | G | 38 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0286 others(35): Show |
44 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.798+1352C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78494893 | |||||||
| chr1:78494896 | G | A | 5 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0234 others(2): Show |
5 | HG02040.hp2 NA18952.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.798+1355G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78494896 | |||||||
| chr1:78494900 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.798+1359G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78494900 | |||||||
| chr1:78495009 | C | T | 2 | a0001c0002t0031g0316 a0004c0006t0032g0145 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+1468C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78495009 | |||||||
| chr1:78495057 | G | A | 52 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0286 others(49): Show |
61 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.798+1516G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78495057 | |||||||
| chr1:78495079 | G | C | 2 | a0001c0002t0031g0316 a0004c0006t0032g0145 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+1538G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78495079 | |||||||
| chr1:78495224 | G | C | 1 | a0001c0001t0001g0297 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.798+1683G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78495224 | |||||||
| chr1:78495256 | A | C | 3 | a0001c0002t0001g0322 a0001c0002t0022g0323 a0001c0002t0024g0324 |
3 | HG02109.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.798+1715A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78495256 | |||||||
| chr1:78495511 | AT | A | 13 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(10): Show |
16 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.798+1971delT | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78495511 | |||||||
| chr1:78495635 | T | G | 1 | a0001c0001t0003g0158 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.798+2094T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78495635 | |||||||
| chr1:78495759 | T | C | 44 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0286 others(41): Show |
53 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.798+2218T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78495759 | |||||||
| chr1:78495787 | C | A | 1 | a0001c0001t0001g0298 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.798+2246C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78495787 | |||||||
| chr1:78495900 | T | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(170): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.798+2359T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78495900 | |||||||
| chr1:78495966 | A | T | 44 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0286 others(41): Show |
53 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.798+2425A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78495966 | |||||||
| chr1:78496005 | C | A | 44 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0286 others(41): Show |
53 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.798+2464C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496005 | |||||||
| chr1:78496016 | A | G | 21 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0297 others(18): Show |
27 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.798+2475A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496016 | |||||||
| chr1:78496060 | G | T | 3 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0001t0002g0086 |
3 | HG01167.hp2 HG01169.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.798+2519G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496060 | |||||||
| chr1:78496215 | G | A | 7 | a0001c0001t0001g0010 a0001c0001t0001g0334 a0001c0001t0001g0336 others(4): Show |
9 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.798+2674G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496215 | |||||||
| chr1:78496320 | A | G | 2 | a0001c0002t0031g0316 a0004c0006t0032g0145 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+2779A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496320 | |||||||
| chr1:78496372 | T | G | 1 | a0001c0001t0001g0236 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.798+2831T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496372 | |||||||
| chr1:78496430 | A | G | 2 | a0001c0002t0031g0316 a0004c0006t0032g0145 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+2889A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496430 | |||||||
| chr1:78496447 | A | G | 6 | a0001c0001t0001g0131 a0001c0001t0001g0228 a0001c0001t0001g0230 others(3): Show |
6 | HG00621.hp2 HG04115.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.798+2906A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496447 | |||||||
| chr1:78496448 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.798+2907T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496448 | |||||||
| chr1:78496555 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.798+3014G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496555 | |||||||
| chr1:78496595 | G | A | 7 | a0001c0001t0001g0010 a0001c0001t0001g0334 a0001c0001t0001g0336 others(4): Show |
9 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.798+3054G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496595 | |||||||
| chr1:78496667 | T | C | 2 | a0001c0002t0031g0316 a0004c0006t0032g0145 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+3126T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496667 | |||||||
| chr1:78496724 | A | G | 1 | a0003c0005t0010g0282 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.798+3183A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496724 | |||||||
| chr1:78496826 | A | C | 1 | a0001c0001t0001g0293 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.798+3285A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496826 | |||||||
| chr1:78496839 | T | C | 2 | a0001c0002t0031g0316 a0004c0006t0032g0145 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+3298T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496839 | |||||||
| chr1:78496936 | T | TA | 8 | a0001c0002t0001g0009 a0001c0002t0001g0030 a0001c0002t0001g0325 others(5): Show |
11 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.798+3396dupA | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78496936 | ||||||
| chr1:78496938 | T | A | 8 | a0001c0002t0001g0009 a0001c0002t0001g0030 a0001c0002t0001g0325 others(5): Show |
11 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.798+3397T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496938 | |||||||
| chr1:78496940 | T | A | 8 | a0001c0002t0001g0009 a0001c0002t0001g0030 a0001c0002t0001g0325 others(5): Show |
11 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.798+3399T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496940 | |||||||
| chr1:78496949 | C | T | 1 | a0001c0002t0025g0321 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.798+3408C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496949 | |||||||
| chr1:78496953 | G | A | 1 | a0001c0001t0001g0004 | 3 | NA18974.hp2 NA19007.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.798+3412G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496953 | |||||||
| chr1:78496989 | G | T | 4 | a0001c0002t0001g0322 a0001c0002t0022g0323 a0001c0002t0024g0324 others(1): Show |
4 | HG02109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+3448G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78496989 | |||||||
| chr1:78497065 | A | G | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.798+3524A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78497065 | |||||||
| chr1:78497170 | G | A | 3 | a0001c0002t0001g0322 a0001c0002t0022g0323 a0001c0002t0024g0324 |
3 | HG02109.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.798+3629G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78497170 | |||||||
| chr1:78497285 | C | T | 1 | a0001c0002t0024g0324 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.798+3744C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78497285 | |||||||
| chr1:78497318 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.798+3777C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78497318 | |||||||
| chr1:78497620 | A | C | 46 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0286 others(43): Show |
55 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.798+4079A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78497620 | |||||||
| chr1:78497658 | T | C | 1 | a0001c0002t0025g0321 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.798+4117T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78497658 | |||||||
| chr1:78497752 | G | A | 52 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0286 others(49): Show |
61 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.798+4211G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78497752 | |||||||
| chr1:78497798 | C | T | 1 | a0001c0001t0005g0130 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.798+4257C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78497798 | |||||||
| chr1:78497879 | C | T | 4 | a0001c0002t0001g0322 a0001c0002t0022g0323 a0001c0002t0024g0324 others(1): Show |
4 | HG02109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+4338C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78497879 | |||||||
| chr1:78498027 | T | A | 7 | a0001c0001t0001g0010 a0001c0001t0001g0334 a0001c0001t0001g0336 others(4): Show |
9 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.798+4486T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78498027 | |||||||
| chr1:78498611 | T | A | 46 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0286 others(43): Show |
55 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.798+5070T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78498611 | |||||||
| chr1:78498713 | A | C | 1 | a0001c0001t0009g0094 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.798+5172A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78498713 | |||||||
| chr1:78498857 | T | G | 52 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0286 others(49): Show |
61 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.798+5316T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78498857 | |||||||
| chr1:78499025 | C | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0297 others(18): Show |
27 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.798+5484C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78499025 | |||||||
| chr1:78499136 | A | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
272 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.798+5595A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78499136 | |||||||
| chr1:78499195 | G | C | 1 | a0001c0001t0001g0096 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.798+5654G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78499195 | |||||||
| chr1:78499207 | CTCTT | C | 4 | a0001c0002t0001g0322 a0001c0002t0022g0323 a0001c0002t0024g0324 others(1): Show |
4 | HG02109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+5671_798+5674d others(6): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78499207 | ||||||
| chr1:78499337 | A | G | 1 | a0002c0004t0001g0157 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.798+5796A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78499337 | |||||||
| chr1:78499344 | A | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
137 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.798+5803A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78499344 | |||||||
| chr1:78499358 | A | G | 3 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0083 |
3 | HG01891.hp2 HG02970.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.798+5817A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78499358 | |||||||
| chr1:78499390 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.798+5849C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78499390 | |||||||
| chr1:78499461 | T | C | 4 | a0001c0002t0001g0322 a0001c0002t0022g0323 a0001c0002t0024g0324 others(1): Show |
4 | HG02109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+5920T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78499461 | |||||||
| chr1:78499615 | G | A | 46 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0286 others(43): Show |
55 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.798+6074G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78499615 | |||||||
| chr1:78499763 | A | T | 8 | a0001c0002t0001g0009 a0001c0002t0001g0030 a0001c0002t0001g0325 others(5): Show |
11 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.798+6222A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78499763 | |||||||
| chr1:78499776 | G | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
137 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.798+6235G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78499776 | |||||||
| chr1:78500055 | T | A | 1 | a0001c0001t0001g0131 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.798+6514T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78500055 | |||||||
| chr1:78500061 | A | AT | 48 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0286 others(45): Show |
57 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.798+6530dupT | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78500061 | ||||||
| chr1:78500076 | T | A | 1 | a0001c0001t0001g0097 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.798+6535T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78500076 | |||||||
| chr1:78500093 | T | A | 55 | a0001c0001t0001g0007 a0001c0001t0001g0139 a0001c0001t0001g0231 others(52): Show |
59 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.798+6552T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78500093 | |||||||
| chr1:78500099 | T | C | 48 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0286 others(45): Show |
57 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.798+6558T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78500099 | |||||||
| chr1:78500161 | T | C | 1 | a0001c0001t0004g0299 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.798+6620T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78500161 | |||||||
| chr1:78500176 | G | A | 48 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0286 others(45): Show |
57 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.798+6635G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78500176 | |||||||
| chr1:78500232 | C | A | 1 | a0001c0001t0001g0159 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.798+6691C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78500232 | |||||||
| chr1:78500518 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.798+6977C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78500518 | |||||||
| chr1:78500650 | G | A | 8 | a0001c0002t0001g0009 a0001c0002t0001g0030 a0001c0002t0001g0325 others(5): Show |
11 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.798+7109G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78500650 | |||||||
| chr1:78500996 | A | G | 1 | a0001c0001t0002g0225 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.798+7455A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78500996 | |||||||
| chr1:78501003 | C | CT | 16 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0290 others(13): Show |
16 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.798+7472dupT | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78501003 | ||||||
| chr1:78501060 | G | T | 2 | a0001c0001t0009g0014 a0001c0001t0009g0094 |
3 | HG02809.hp1 HG02896.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.798+7519G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78501060 | |||||||
| chr1:78501117 | T | G | 2 | a0001c0001t0001g0236 a0001c0001t0001g0279 |
2 | HG02630.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.798+7576T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78501117 | |||||||
| chr1:78501357 | A | C | 1 | a0001c0001t0003g0129 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.798+7816A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78501357 | |||||||
| chr1:78501467 | G | C | 1 | a0004c0006t0032g0145 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.798+7926G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78501467 | |||||||
| chr1:78501513 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.798+7972T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78501513 | |||||||
| chr1:78501520 | G | A | 2 | a0001c0002t0001g0322 a0001c0002t0022g0323 |
2 | HG02109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.798+7979G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78501520 | |||||||
| chr1:78501648 | C | T | 2 | a0001c0002t0031g0316 a0004c0006t0032g0145 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+8107C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78501648 | |||||||
| chr1:78501743 | C | T | 2 | a0001c0002t0031g0316 a0004c0006t0032g0145 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+8202C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78501743 | |||||||
| chr1:78501783 | A | G | 4 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(1): Show |
4 | HG02572.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.798+8242A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78501783 | |||||||
| chr1:78501845 | G | A | 3 | a0001c0002t0001g0322 a0001c0002t0022g0323 a0001c0002t0024g0324 |
3 | HG02109.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.798+8304G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78501845 | |||||||
| chr1:78501963 | C | A | 1 | a0001c0001t0001g0020 | 2 | HG03491.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.798+8422C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78501963 | |||||||
| chr1:78501990 | A | G | 1 | a0001c0001t0003g0128 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.798+8449A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78501990 | |||||||
| chr1:78502055 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.798+8514G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78502055 | |||||||
| chr1:78502140 | G | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
147 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.798+8599G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78502140 | |||||||
| chr1:78502381 | C | A | 1 | a0001c0001t0001g0161 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.798+8840C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78502381 | |||||||
| chr1:78502637 | T | A | 21 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0297 others(18): Show |
27 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.798+9096T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78502637 | |||||||
| chr1:78502656 | A | G | 36 | a0001c0001t0001g0010 a0001c0001t0001g0092 a0001c0001t0001g0093 others(33): Show |
41 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.798+9115A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78502656 | |||||||
| chr1:78502724 | T | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
138 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.798+9183T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78502724 | |||||||
| chr1:78502767 | G | A | 8 | a0001c0002t0001g0009 a0001c0002t0001g0030 a0001c0002t0001g0325 others(5): Show |
11 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.798+9226G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78502767 | |||||||
| chr1:78502824 | G | A | 1 | a0001c0001t0007g0087 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.798+9283G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78502824 | |||||||
| chr1:78502833 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.798+9292C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78502833 | |||||||
| chr1:78502846 | A | C | 1 | a0001c0001t0003g0223 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.798+9305A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78502846 | |||||||
| chr1:78502862 | G | A | 16 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0290 others(13): Show |
16 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.798+9321G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78502862 | |||||||
| chr1:78503036 | C | A | 1 | a0001c0001t0001g0336 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.798+9495C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78503036 | |||||||
| chr1:78503213 | T | G | 39 | a0001c0001t0001g0010 a0001c0001t0001g0092 a0001c0001t0001g0093 others(36): Show |
44 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(41): Show |
intron_variant | MODIFIER | c.798+9672T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78503213 | |||||||
| chr1:78503233 | T | TAA | 39 | a0001c0001t0001g0010 a0001c0001t0001g0092 a0001c0001t0001g0093 others(36): Show |
44 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(41): Show |
intron_variant | MODIFIER | c.798+9692_798+9693i others(4): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78503233 | |||||||
| chr1:78503414 | A | G | 1 | a0001c0001t0003g0080 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.798+9873A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78503414 | |||||||
| chr1:78503609 | A | G | 16 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0290 others(13): Show |
16 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.798+10068A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78503609 | |||||||
| chr1:78503712 | G | A | 2 | a0001c0001t0002g0283 a0001c0001t0011g0239 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.798+10171G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78503712 | |||||||
| chr1:78503779 | A | G | 8 | a0001c0002t0001g0009 a0001c0002t0001g0030 a0001c0002t0001g0325 others(5): Show |
11 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.798+10238A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78503779 | |||||||
| chr1:78504078 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0297 others(19): Show |
28 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.798+10537G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78504078 | |||||||
| chr1:78504082 | G | C | 1 | a0001c0001t0001g0140 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.798+10541G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78504082 | |||||||
| chr1:78504104 | C | T | 4 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0001t0002g0086 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.798+10563C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78504104 | |||||||
| chr1:78504189 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.798+10648A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78504189 | |||||||
| chr1:78504237 | A | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.798+10696A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78504237 | |||||||
| chr1:78504262 | C | T | 60 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0031 others(57): Show |
71 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.798+10721C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78504262 | |||||||
| chr1:78504302 | T | C | 60 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0031 others(57): Show |
71 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.798+10761T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78504302 | |||||||
| chr1:78504360 | T | C | 1 | a0001c0001t0005g0340 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.798+10819T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78504360 | |||||||
| chr1:78504480 | T | C | 1 | a0001c0002t0025g0321 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.798+10939T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78504480 | |||||||
| chr1:78504677 | A | G | 1 | a0001c0001t0001g0222 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.798+11136A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78504677 | |||||||
| chr1:78504788 | C | T | 1 | a0001c0002t0001g0330 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.798+11247C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78504788 | |||||||
| chr1:78504817 | C | A | 2 | a0001c0002t0031g0316 a0004c0006t0032g0145 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+11276C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78504817 | |||||||
| chr1:78504895 | T | C | 1 | a0001c0003t0001g0240 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.798+11354T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78504895 | |||||||
| chr1:78505120 | C | CT | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(134): Show |
160 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.798+11598dupT | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78505120 | ||||||
| chr1:78505370 | A | G | 25 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0290 others(22): Show |
28 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.798+11829A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78505370 | |||||||
| chr1:78505440 | A | T | 1 | a0001c0001t0001g0127 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.798+11899A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78505440 | |||||||
| chr1:78505622 | G | C | 2 | a0001c0002t0031g0316 a0004c0006t0032g0145 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+12081G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78505622 | |||||||
| chr1:78505742 | A | G | 17 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(14): Show |
17 | HG00733.hp2 HG01106.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.798+12201A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78505742 | |||||||
| chr1:78505772 | G | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0334 a0001c0001t0007g0339 others(3): Show |
8 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.798+12231G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78505772 | |||||||
| chr1:78505842 | A | T | 35 | a0001c0001t0001g0010 a0001c0001t0001g0092 a0001c0001t0001g0093 others(32): Show |
40 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.798+12301A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78505842 | |||||||
| chr1:78506004 | G | T | 1 | a0002c0004t0001g0079 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.798+12463G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78506004 | |||||||
| chr1:78506099 | G | A | 1 | a0001c0001t0019g0039 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.798+12558G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78506099 | |||||||
| chr1:78506136 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.798+12595T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78506136 | |||||||
| chr1:78506158 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.798+12617G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78506158 | |||||||
| chr1:78506215 | A | G | 8 | a0001c0002t0001g0009 a0001c0002t0001g0030 a0001c0002t0001g0325 others(5): Show |
11 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.798+12674A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78506215 | |||||||
| chr1:78506242 | A | C | 57 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0031 others(54): Show |
68 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.798+12701A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78506242 | |||||||
| chr1:78506434 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.798+12893A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78506434 | |||||||
| chr1:78506540 | AT | A | 4 | a0001c0001t0002g0283 a0001c0001t0011g0239 a0001c0001t0016g0241 others(1): Show |
4 | HG03041.hp1 HG03453.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+13006delT | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78506540 | ||||||
| chr1:78506681 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.798+13140A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78506681 | |||||||
| chr1:78506833 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.798+13292G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78506833 | |||||||
| chr1:78506908 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.798+13367C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78506908 | |||||||
| chr1:78506928 | T | G | 1 | a0001c0002t0025g0321 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.798+13387T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78506928 | |||||||
| chr1:78507287 | G | T | 1 | a0001c0001t0001g0026 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.798+13746G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78507287 | |||||||
| chr1:78507343 | T | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.798+13802T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78507343 | |||||||
| chr1:78507376 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.798+13835C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78507376 | |||||||
| chr1:78507390 | T | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
138 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.798+13849T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78507390 | |||||||
| chr1:78507391 | T | G | 21 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0297 others(18): Show |
27 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.798+13850T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78507391 | |||||||
| chr1:78507712 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.798+14171C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78507712 | |||||||
| chr1:78508154 | T | C | 1 | a0001c0001t0001g0026 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.798+14613T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78508154 | |||||||
| chr1:78508588 | C | A | 1 | a0001c0001t0001g0162 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.798+15047C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78508588 | |||||||
| chr1:78508608 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.798+15067A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78508608 | |||||||
| chr1:78508805 | C | T | 1 | a0001c0001t0002g0225 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.798+15264C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78508805 | |||||||
| chr1:78508821 | G | A | 1 | a0001c0001t0009g0014 | 2 | HG02809.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.798+15280G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78508821 | |||||||
| chr1:78508957 | A | G | 2 | a0001c0001t0003g0219 a0001c0001t0003g0220 |
2 | NA18939.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.798+15416A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78508957 | |||||||
| chr1:78509050 | C | G | 8 | a0001c0002t0001g0009 a0001c0002t0001g0030 a0001c0002t0001g0325 others(5): Show |
11 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.798+15509C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78509050 | |||||||
| chr1:78509224 | G | A | 33 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0286 others(30): Show |
36 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.798+15683G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78509224 | |||||||
| chr1:78509270 | G | A | 25 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0290 others(22): Show |
28 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.798+15729G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78509270 | |||||||
| chr1:78509282 | C | T | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.798+15741C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78509282 | |||||||
| chr1:78509347 | G | A | 1 | a0001c0002t0025g0321 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.798+15806G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78509347 | |||||||
| chr1:78509476 | G | A | 3 | a0001c0001t0001g0332 a0001c0001t0004g0331 a0001c0001t0029g0333 |
3 | HG02559.hp1 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.798+15935G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78509476 | |||||||
| chr1:78509509 | T | C | 7 | a0001c0001t0001g0010 a0001c0001t0001g0334 a0001c0001t0001g0336 others(4): Show |
9 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.798+15968T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78509509 | |||||||
| chr1:78509539 | A | T | 3 | a0001c0001t0001g0298 a0001c0001t0001g0313 a0001c0001t0004g0312 |
3 | HG01496.hp2 HG02683.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.798+15998A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78509539 | |||||||
| chr1:78509593 | A | G | 1 | a0001c0001t0001g0311 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.798+16052A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78509593 | |||||||
| chr1:78509620 | G | T | 1 | a0001c0001t0001g0216 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.798+16079G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78509620 | |||||||
| chr1:78510154 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.798+16613C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510154 | |||||||
| chr1:78510170 | C | A | 2 | a0001c0001t0001g0163 a0001c0001t0003g0164 |
2 | NA19058.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.798+16629C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510170 | |||||||
| chr1:78510177 | G | A | 1 | a0001c0002t0025g0321 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.798+16636G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510177 | |||||||
| chr1:78510202 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.798+16661C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510202 | |||||||
| chr1:78510262 | G | A | 1 | a0001c0001t0002g0081 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.798+16721G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510262 | |||||||
| chr1:78510322 | T | A | 1 | a0001c0001t0001g0034 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.798+16781T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510322 | |||||||
| chr1:78510334 | C | T | 4 | a0001c0001t0001g0236 a0001c0001t0001g0279 a0001c0001t0007g0281 others(1): Show |
4 | HG02630.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.798+16793C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510334 | |||||||
| chr1:78510391 | G | A | 2 | a0001c0001t0001g0149 a0001c0001t0018g0150 |
2 | HG00597.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.798+16850G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510391 | |||||||
| chr1:78510409 | G | A | 16 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0290 others(13): Show |
16 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.798+16868G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510409 | |||||||
| chr1:78510440 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.798+16899G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510440 | |||||||
| chr1:78510525 | C | G | 9 | a0001c0001t0005g0340 a0001c0002t0001g0009 a0001c0002t0001g0030 others(6): Show |
12 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.798+16984C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510525 | |||||||
| chr1:78510598 | A | G | 4 | a0001c0001t0001g0236 a0001c0001t0001g0279 a0001c0001t0007g0281 others(1): Show |
4 | HG02630.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.798+17057A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510598 | |||||||
| chr1:78510673 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.798+17132C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510673 | |||||||
| chr1:78510674 | G | A | 16 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0290 others(13): Show |
16 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.798+17133G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510674 | |||||||
| chr1:78510761 | A | T | 1 | a0001c0001t0001g0034 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.798+17220A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510761 | |||||||
| chr1:78510885 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(240): Show |
275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.798+17344A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510885 | |||||||
| chr1:78510929 | A | G | 2 | a0001c0002t0031g0316 a0004c0006t0032g0145 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+17388A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78510929 | |||||||
| chr1:78511136 | T | C | 2 | a0001c0001t0002g0314 a0001c0001t0002g0315 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.798+17595T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78511136 | |||||||
| chr1:78511457 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.798+17916C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78511457 | |||||||
| chr1:78511562 | C | T | 3 | a0001c0002t0001g0030 a0001c0002t0001g0328 a0001c0002t0001g0329 |
4 | HG02055.hp1 HG02559.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+18021C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78511562 | |||||||
| chr1:78511581 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.798+18040G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78511581 | |||||||
| chr1:78511687 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.798+18146T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78511687 | |||||||
| chr1:78511702 | C | T | 16 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0290 others(13): Show |
16 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.798+18161C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78511702 | |||||||
| chr1:78511789 | G | T | 25 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0290 others(22): Show |
28 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.798+18248G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78511789 | |||||||
| chr1:78511833 | T | C | 1 | a0001c0001t0020g0043 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.798+18292T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78511833 | |||||||
| chr1:78511892 | G | A | 55 | a0001c0001t0001g0007 a0001c0001t0001g0139 a0001c0001t0001g0231 others(52): Show |
59 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.798+18351G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78511892 | |||||||
| chr1:78511898 | T | G | 1 | a0001c0001t0001g0221 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.798+18357T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78511898 | |||||||
| chr1:78512030 | C | T | 51 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0092 others(48): Show |
60 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.798+18489C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78512030 | |||||||
| chr1:78512100 | C | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0212 a0001c0001t0003g0211 others(1): Show |
5 | HG00544.hp1 HG02080.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.798+18559C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78512100 | |||||||
| chr1:78512105 | C | G | 1 | a0004c0006t0032g0145 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.798+18564C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78512105 | |||||||
| chr1:78512161 | T | C | 2 | a0001c0002t0031g0316 a0004c0006t0032g0145 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.798+18620T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78512161 | |||||||
| chr1:78512213 | T | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA18983.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.798+18672T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78512213 | |||||||
| chr1:78512277 | G | C | 25 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0290 others(22): Show |
28 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.798+18736G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78512277 | |||||||
| chr1:78512335 | G | A | 29 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0286 others(26): Show |
32 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.798+18794G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78512335 | |||||||
| chr1:78512625 | T | G | 4 | a0001c0002t0001g0322 a0001c0002t0022g0323 a0001c0002t0024g0324 others(1): Show |
4 | HG02109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+19084T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78512625 | |||||||
| chr1:78512752 | G | A | 1 | a0001c0001t0005g0340 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.798+19211G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78512752 | |||||||
| chr1:78512828 | C | T | 54 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0092 others(51): Show |
63 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.798+19287C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78512828 | |||||||
| chr1:78512841 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.798+19300G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78512841 | |||||||
| chr1:78512953 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0156 |
3 | HG03654.hp2 HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.798+19412C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78512953 | |||||||
| chr1:78512957 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0002g0015 |
3 | HG02615.hp2 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.798+19416T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78512957 | |||||||
| chr1:78513020 | C | A | 1 | a0001c0001t0001g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.798+19479C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78513020 | |||||||
| chr1:78513087 | G | A | 5 | a0001c0001t0001g0243 a0001c0001t0002g0283 a0001c0001t0011g0239 others(2): Show |
5 | HG01928.hp2 HG03041.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.798+19546G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78513087 | |||||||
| chr1:78513186 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.798+19645G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78513186 | |||||||
| chr1:78513196 | A | G | 1 | a0001c0002t0025g0321 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.798+19655A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78513196 | |||||||
| chr1:78513293 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.798+19752G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78513293 | |||||||
| chr1:78513487 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.798+19946G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78513487 | |||||||
| chr1:78513509 | A | G | 21 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0297 others(18): Show |
27 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.798+19968A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78513509 | |||||||
| chr1:78513556 | T | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(240): Show |
276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.798+20015T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78513556 | |||||||
| chr1:78513600 | G | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0334 a0001c0001t0001g0336 others(4): Show |
9 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.798+20059G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78513600 | |||||||
| chr1:78513713 | C | A | 29 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0286 others(26): Show |
32 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.798+20172C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78513713 | |||||||
| chr1:78513764 | C | G | 1 | a0001c0001t0001g0336 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.798+20223C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78513764 | |||||||
| chr1:78513836 | G | T | 4 | a0001c0002t0001g0322 a0001c0002t0022g0323 a0001c0002t0024g0324 others(1): Show |
4 | HG02109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+20295G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78513836 | |||||||
| chr1:78513930 | C | G | 3 | a0001c0002t0001g0322 a0001c0002t0022g0323 a0001c0002t0024g0324 |
3 | HG02109.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.798+20389C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78513930 | |||||||
| chr1:78514102 | C | T | 1 | a0001c0001t0029g0333 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.798+20561C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514102 | |||||||
| chr1:78514119 | G | A | 2 | a0001c0001t0006g0244 a0001c0001t0006g0245 |
2 | HG02602.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.798+20578G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514119 | |||||||
| chr1:78514149 | G | A | 1 | a0001c0002t0001g0322 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.798+20608G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514149 | |||||||
| chr1:78514240 | T | C | 7 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0250 others(4): Show |
7 | HG00639.hp2 HG02630.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.798+20699T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514240 | |||||||
| chr1:78514253 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.798+20712G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514253 | |||||||
| chr1:78514480 | C | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(43): Show |
60 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.798+20939C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514480 | |||||||
| chr1:78514519 | A | G | 1 | a0001c0002t0025g0321 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.798+20978A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514519 | |||||||
| chr1:78514530 | G | A | 2 | a0001c0001t0009g0014 a0001c0001t0009g0094 |
3 | HG02809.hp1 HG02896.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.798+20989G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514530 | |||||||
| chr1:78514576 | C | T | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0002t0002g0327 |
3 | HG00423.hp1 HG02523.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.798+21035C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514576 | |||||||
| chr1:78514639 | T | A | 1 | a0004c0006t0032g0145 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.798+21098T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514639 | |||||||
| chr1:78514641 | A | C | 1 | a0001c0001t0001g0298 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.798+21100A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514641 | |||||||
| chr1:78514641 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.798+21100A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514641 | |||||||
| chr1:78514731 | C | G | 54 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0092 others(51): Show |
63 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.798+21190C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514731 | |||||||
| chr1:78514791 | A | G | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.798+21250A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514791 | |||||||
| chr1:78514836 | G | A | 21 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0297 others(18): Show |
27 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.798+21295G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514836 | |||||||
| chr1:78514969 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.798+21428C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514969 | |||||||
| chr1:78514970 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.798+21429G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514970 | |||||||
| chr1:78514998 | G | A | 4 | a0001c0001t0003g0166 a0001c0001t0003g0167 a0001c0001t0003g0168 others(1): Show |
4 | NA18945.hp1 NA18956.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-21408G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78514998 | |||||||
| chr1:78515046 | A | AT | 6 | a0001c0001t0001g0236 a0001c0001t0001g0279 a0001c0001t0005g0133 others(3): Show |
6 | HG02630.hp2 HG02818.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.799-21350dupT | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78515046 | ||||||
| chr1:78515100 | G | A | 2 | a0001c0001t0023g0254 a0001c0001t0026g0255 |
2 | HG02258.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.799-21306G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78515100 | |||||||
| chr1:78515125 | A | G | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.799-21281A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78515125 | |||||||
| chr1:78515241 | A | G | 1 | a0001c0002t0025g0321 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.799-21165A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78515241 | |||||||
| chr1:78515521 | C | T | 1 | a0001c0001t0003g0310 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.799-20885C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78515521 | |||||||
| chr1:78515594 | G | A | 54 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0092 others(51): Show |
63 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.799-20812G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78515594 | |||||||
| chr1:78516235 | A | G | 1 | a0001c0002t0031g0316 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.799-20171A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78516235 | |||||||
| chr1:78516413 | C | A | 1 | a0001c0001t0001g0151 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.799-19993C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78516413 | |||||||
| chr1:78516618 | G | C | 2 | a0001c0002t0025g0321 a0004c0006t0032g0145 |
2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.799-19788G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78516618 | |||||||
| chr1:78516749 | T | A | 1 | a0001c0002t0031g0316 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.799-19657T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78516749 | |||||||
| chr1:78516999 | A | T | 3 | a0001c0002t0001g0322 a0001c0002t0022g0323 a0001c0002t0024g0324 |
3 | HG02109.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.799-19407A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78516999 | |||||||
| chr1:78517114 | T | A | 4 | a0001c0001t0001g0236 a0001c0001t0001g0279 a0001c0001t0007g0281 others(1): Show |
4 | HG02630.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-19292T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78517114 | |||||||
| chr1:78517116 | C | T | 25 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0290 others(22): Show |
28 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.799-19290C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78517116 | |||||||
| chr1:78517278 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(240): Show |
275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.799-19128A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78517278 | |||||||
| chr1:78517428 | T | C | 1 | a0004c0006t0032g0145 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.799-18978T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78517428 | |||||||
| chr1:78517488 | A | G | 1 | a0001c0001t0003g0210 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.799-18918A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78517488 | |||||||
| chr1:78517535 | G | A | 3 | a0001c0002t0001g0322 a0001c0002t0022g0323 a0001c0002t0024g0324 |
3 | HG02109.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.799-18871G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78517535 | |||||||
| chr1:78517651 | G | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0297 others(18): Show |
27 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.799-18755G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78517651 | |||||||
| chr1:78517670 | T | C | 4 | a0001c0001t0001g0236 a0001c0001t0001g0279 a0001c0001t0007g0281 others(1): Show |
4 | HG02630.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-18736T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78517670 | |||||||
| chr1:78517762 | T | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | HG02273.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.799-18644T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78517762 | |||||||
| chr1:78517880 | C | T | 3 | a0001c0002t0001g0322 a0001c0002t0022g0323 a0001c0002t0024g0324 |
3 | HG02109.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.799-18526C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78517880 | |||||||
| chr1:78517885 | A | T | 2 | a0001c0002t0025g0321 a0004c0006t0032g0145 |
2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.799-18521A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78517885 | |||||||
| chr1:78517888 | T | G | 1 | a0001c0001t0002g0256 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.799-18518T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78517888 | |||||||
| chr1:78517982 | A | T | 1 | a0001c0001t0004g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.799-18424A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78517982 | |||||||
| chr1:78518078 | G | T | 1 | a0001c0001t0001g0209 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.799-18328G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78518078 | |||||||
| chr1:78518362 | C | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0297 others(18): Show |
27 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.799-18044C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78518362 | |||||||
| chr1:78518430 | T | A | 1 | a0001c0001t0002g0015 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.799-17976T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78518430 | |||||||
| chr1:78518457 | A | G | 3 | a0001c0001t0004g0003 a0001c0001t0004g0308 a0001c0001t0004g0309 |
6 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.799-17949A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78518457 | |||||||
| chr1:78518567 | GAC | G | 18 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0131 others(15): Show |
21 | HG00621.hp2 HG01261.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.799-17787_799-1778 others(6): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78518567 | ||||||
| chr1:78518567 | GACAC | G | 41 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0146 others(38): Show |
42 | HG00438.hp2 HG00544.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.799-17789_799-1778 others(8): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78518567 | ||||||
| chr1:78518567 | GACACAC | G | 38 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0026 others(35): Show |
41 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.799-17791_799-1778 others(10): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78518567 | ||||||
| chr1:78518567 | GACACACA others(1): Show |
G | 56 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0031 others(53): Show |
67 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.799-17793_799-1778 others(12): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78518567 | ||||||
| chr1:78518567 | GACACACA others(3): Show |
G | 31 | a0001c0001t0001g0154 a0001c0001t0001g0161 a0001c0001t0001g0206 others(28): Show |
34 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.799-17795_799-1778 others(14): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78518567 | ||||||
| chr1:78518567 | GACACACA others(5): Show |
G | 16 | a0001c0001t0001g0020 a0001c0001t0001g0092 a0001c0001t0001g0093 others(13): Show |
18 | HG00140.hp2 HG00423.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.799-17797_799-1778 others(16): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78518567 | ||||||
| chr1:78518567 | GACACACA others(7): Show |
G | 8 | a0001c0001t0001g0007 a0001c0001t0001g0237 a0001c0001t0001g0273 others(5): Show |
10 | HG01069.hp2 HG01192.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.799-17799_799-1778 others(18): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78518567 | ||||||
| chr1:78518567 | GACACACA others(9): Show |
G | 3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0030g0242 |
3 | HG02886.hp1 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.799-17801_799-1778 others(20): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78518567 | ||||||
| chr1:78518567 | GACACACA others(11): Show |
G | 3 | a0001c0001t0001g0046 a0001c0001t0002g0082 a0001c0003t0001g0277 |
3 | HG01515.hp1 HG03471.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.799-17803_799-1778 others(22): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78518567 | ||||||
| chr1:78518567 | GACACACA others(13): Show |
G | 72 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(69): Show |
75 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.799-17805_799-1778 others(24): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78518567 | ||||||
| chr1:78518567 | GACACACA others(15): Show |
G | 3 | a0001c0001t0001g0097 a0001c0002t0025g0321 a0004c0006t0032g0145 |
3 | HG02698.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.799-17807_799-1778 others(26): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78518567 | ||||||
| chr1:78518567 | GACACACA others(17): Show |
G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(41): Show |
57 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.799-17809_799-1778 others(28): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78518567 | ||||||
| chr1:78518567 | GACACACA others(19): Show |
G | 1 | a0001c0001t0003g0019 | 2 | NA18972.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.799-17811_799-1778 others(30): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78518567 | ||||||
| chr1:78518739 | T | A | 1 | a0001c0001t0001g0047 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.799-17667T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78518739 | |||||||
| chr1:78518739 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.799-17667T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78518739 | |||||||
| chr1:78518903 | C | T | 21 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0297 others(18): Show |
27 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.799-17503C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78518903 | |||||||
| chr1:78518939 | C | T | 2 | a0003c0005t0001g0028 a0003c0005t0002g0276 |
3 | HG03490.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.799-17467C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78518939 | |||||||
| chr1:78518951 | C | T | 25 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0290 others(22): Show |
28 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.799-17455C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78518951 | |||||||
| chr1:78519061 | G | T | 3 | a0001c0002t0001g0322 a0001c0002t0022g0323 a0001c0002t0024g0324 |
3 | HG02109.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.799-17345G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78519061 | |||||||
| chr1:78519087 | A | C | 8 | a0001c0002t0001g0009 a0001c0002t0001g0030 a0001c0002t0001g0325 others(5): Show |
11 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.799-17319A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78519087 | |||||||
| chr1:78519106 | T | G | 1 | a0001c0001t0001g0097 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.799-17300T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78519106 | |||||||
| chr1:78519164 | A | G | 1 | a0001c0001t0003g0182 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.799-17242A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78519164 | |||||||
| chr1:78519303 | G | A | 1 | a0001c0001t0007g0087 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.799-17103G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78519303 | |||||||
| chr1:78519351 | T | C | 3 | a0001c0002t0001g0322 a0001c0002t0022g0323 a0001c0002t0024g0324 |
3 | HG02109.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.799-17055T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78519351 | |||||||
| chr1:78519404 | C | G | 1 | a0001c0001t0021g0280 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.799-17002C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78519404 | |||||||
| chr1:78519671 | C | T | 16 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0290 others(13): Show |
16 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.799-16735C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78519671 | |||||||
| chr1:78519782 | C | G | 1 | a0001c0001t0007g0271 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.799-16624C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78519782 | |||||||
| chr1:78519964 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.799-16442C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78519964 | |||||||
| chr1:78520139 | C | T | 1 | a0001c0001t0027g0123 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.799-16267C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78520139 | |||||||
| chr1:78520246 | G | A | 3 | a0001c0001t0001g0332 a0001c0001t0005g0105 a0001c0001t0027g0123 |
3 | HG02486.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.799-16160G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78520246 | |||||||
| chr1:78520375 | G | A | 2 | a0001c0001t0001g0163 a0001c0001t0003g0164 |
2 | NA19058.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.799-16031G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78520375 | |||||||
| chr1:78520745 | T | C | 3 | a0001c0002t0001g0322 a0001c0002t0022g0323 a0001c0002t0024g0324 |
3 | HG02109.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.799-15661T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78520745 | |||||||
| chr1:78520865 | G | A | 3 | a0001c0002t0001g0322 a0001c0002t0022g0323 a0001c0002t0024g0324 |
3 | HG02109.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.799-15541G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78520865 | |||||||
| chr1:78520935 | T | C | 2 | a0001c0002t0025g0321 a0004c0006t0032g0145 |
2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.799-15471T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78520935 | |||||||
| chr1:78520981 | G | A | 1 | a0001c0001t0035g0258 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.799-15425G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78520981 | |||||||
| chr1:78521027 | T | A | 3 | a0001c0002t0001g0322 a0001c0002t0022g0323 a0001c0002t0024g0324 |
3 | HG02109.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.799-15379T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521027 | |||||||
| chr1:78521042 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.799-15364C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521042 | |||||||
| chr1:78521052 | A | G | 2 | a0001c0002t0025g0321 a0004c0006t0032g0145 |
2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.799-15354A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521052 | |||||||
| chr1:78521089 | T | G | 25 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0290 others(22): Show |
28 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.799-15317T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521089 | |||||||
| chr1:78521209 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.799-15197C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521209 | |||||||
| chr1:78521211 | G | A | 1 | a0001c0002t0025g0321 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.799-15195G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521211 | |||||||
| chr1:78521269 | G | A | 34 | a0001c0001t0001g0010 a0001c0001t0001g0092 a0001c0001t0001g0093 others(31): Show |
39 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.799-15137G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521269 | |||||||
| chr1:78521434 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0106 |
3 | HG00673.hp1 HG02165.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.799-14972T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521434 | |||||||
| chr1:78521549 | G | A | 1 | a0001c0001t0001g0304 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.799-14857G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521549 | |||||||
| chr1:78521607 | T | G | 1 | a0001c0001t0001g0044 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.799-14799T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521607 | |||||||
| chr1:78521617 | T | C | 60 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0031 others(57): Show |
71 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.799-14789T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521617 | |||||||
| chr1:78521658 | A | G | 15 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(12): Show |
18 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.799-14748A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521658 | |||||||
| chr1:78521703 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0107 |
2 | NA18612.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.799-14703G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521703 | |||||||
| chr1:78521901 | G | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.799-14505G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521901 | |||||||
| chr1:78521931 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(117): Show |
137 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.799-14475G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521931 | |||||||
| chr1:78521971 | TGCA | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0042 a0001c0001t0001g0062 others(5): Show |
9 | HG00597.hp2 NA18612.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.799-14434_799-1443 others(7): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78521971 | |||||||
| chr1:78522042 | G | GTTAC | 36 | a0001c0001t0001g0010 a0001c0001t0001g0092 a0001c0001t0001g0093 others(33): Show |
41 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.799-14363_799-1436 others(8): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78522042 | ||||||
| chr1:78522091 | C | A | 1 | a0001c0001t0003g0128 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.799-14315C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78522091 | |||||||
| chr1:78522137 | C | T | 1 | a0001c0001t0001g0332 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.799-14269C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78522137 | |||||||
| chr1:78522188 | C | T | 59 | a0001c0001t0001g0007 a0001c0001t0001g0139 a0001c0001t0001g0231 others(56): Show |
63 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.799-14218C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78522188 | |||||||
| chr1:78522511 | T | A | 1 | a0001c0001t0001g0183 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.799-13895T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78522511 | |||||||
| chr1:78522655 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.799-13751C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78522655 | |||||||
| chr1:78522825 | T | A | 1 | a0001c0001t0001g0183 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.799-13581T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78522825 | |||||||
| chr1:78522860 | T | G | 27 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0290 others(24): Show |
30 | HG00140.hp1 HG01167.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.799-13546T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78522860 | |||||||
| chr1:78522946 | T | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.799-13460T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78522946 | |||||||
| chr1:78522956 | A | T | 1 | a0001c0001t0001g0183 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.799-13450A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78522956 | |||||||
| chr1:78522957 | T | A | 1 | a0001c0001t0001g0183 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.799-13449T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78522957 | |||||||
| chr1:78523100 | A | G | 1 | a0001c0002t0001g0325 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.799-13306A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523100 | |||||||
| chr1:78523271 | T | C | 2 | a0001c0001t0006g0029 a0001c0001t0006g0305 |
3 | HG00140.hp2 HG01981.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.799-13135T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523271 | |||||||
| chr1:78523327 | T | G | 2 | a0001c0001t0008g0337 a0001c0001t0008g0338 |
2 | HG02486.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.799-13079T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523327 | |||||||
| chr1:78523382 | T | C | 1 | a0001c0002t0024g0324 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.799-13024T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523382 | |||||||
| chr1:78523433 | G | C | 1 | a0001c0001t0001g0104 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.799-12973G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523433 | |||||||
| chr1:78523462 | C | T | 1 | a0001c0002t0025g0321 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.799-12944C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523462 | |||||||
| chr1:78523534 | G | A | 1 | a0003c0005t0010g0282 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.799-12872G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523534 | |||||||
| chr1:78523633 | T | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0156 |
3 | HG03654.hp2 HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.799-12773T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523633 | |||||||
| chr1:78523665 | A | G | 1 | a0001c0002t0025g0321 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.799-12741A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523665 | |||||||
| chr1:78523778 | G | T | 1 | a0004c0006t0032g0145 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.799-12628G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523778 | |||||||
| chr1:78523791 | T | A | 1 | a0001c0002t0031g0316 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.799-12615T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523791 | |||||||
| chr1:78523795 | T | C | 11 | a0001c0001t0001g0010 a0001c0001t0001g0071 a0001c0001t0001g0334 others(8): Show |
13 | HG01106.hp1 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.799-12611T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523795 | |||||||
| chr1:78523816 | A | G | 1 | a0003c0005t0010g0282 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.799-12590A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523816 | |||||||
| chr1:78523873 | A | C | 1 | a0001c0002t0025g0321 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.799-12533A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78523873 | |||||||
| chr1:78524090 | G | A | 1 | a0001c0001t0035g0258 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.799-12316G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78524090 | |||||||
| chr1:78524153 | G | A | 4 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0234 others(1): Show |
4 | NA18952.hp2 NA18970.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-12253G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78524153 | |||||||
| chr1:78524165 | A | C | 178 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(175): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.799-12241A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78524165 | |||||||
| chr1:78524321 | G | T | 1 | a0001c0001t0001g0098 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.799-12085G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78524321 | |||||||
| chr1:78524498 | C | T | 3 | a0001c0001t0001g0257 a0001c0001t0002g0006 a0001c0003t0002g0006 |
4 | HG00099.hp1 HG01175.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-11908C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78524498 | |||||||
| chr1:78524589 | T | A | 1 | a0001c0001t0018g0150 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.799-11817T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78524589 | |||||||
| chr1:78524590 | C | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(106): Show |
141 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.799-11816C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78524590 | |||||||
| chr1:78524655 | A | G | 7 | a0001c0001t0001g0010 a0001c0001t0001g0126 a0001c0001t0001g0237 others(4): Show |
9 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.799-11751A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78524655 | |||||||
| chr1:78524717 | C | G | 1 | a0001c0001t0001g0046 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.799-11689C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78524717 | |||||||
| chr1:78524889 | CT | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0126 a0001c0001t0001g0237 |
5 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.799-11514delT | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524889 | ||||||
| chr1:78524906 | A | AT | 38 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0051 others(35): Show |
39 | HG00140.hp1 HG01074.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.799-11466dupT | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | ||||||
| chr1:78524906 | A | ATT | 16 | a0001c0001t0001g0046 a0001c0001t0001g0056 a0001c0001t0001g0063 others(13): Show |
16 | HG00438.hp2 HG00733.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.799-11467_799-1146 others(6): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | ||||||
| chr1:78524906 | A | ATTT | 11 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0058 others(8): Show |
11 | HG00423.hp1 HG02129.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.799-11468_799-1146 others(7): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | ||||||
| chr1:78524906 | A | ATTTT | 10 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0038 others(7): Show |
10 | HG00438.hp1 HG03453.hp2 HG03492.hp1 others(7): Show |
intron_variant | MODIFIER | c.799-11469_799-1146 others(8): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | ||||||
| chr1:78524906 | A | ATTTTT | 9 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0077 others(6): Show |
10 | HG00733.hp2 HG02074.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.799-11470_799-1146 others(9): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | ||||||
| chr1:78524906 | AT | A | 58 | a0001c0001t0001g0007 a0001c0001t0001g0045 a0001c0001t0001g0048 others(55): Show |
61 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.799-11466delT | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | ||||||
| chr1:78524906 | ATTTTT | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0025 others(6): Show |
12 | HG01993.hp1 HG02015.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.799-11470_799-1146 others(9): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | ||||||
| chr1:78524906 | ATTTTTT | A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(26): Show |
41 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.799-11471_799-1146 others(10): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | ||||||
| chr1:78524906 | ATTTTTTT | A | 6 | a0001c0001t0001g0103 a0001c0001t0001g0112 a0001c0001t0021g0280 others(3): Show |
6 | HG01975.hp1 HG02055.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.799-11472_799-1146 others(11): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | ||||||
| chr1:78524906 | ATTTTTTT others(1): Show |
A | 9 | a0001c0001t0001g0236 a0001c0001t0001g0279 a0001c0001t0001g0332 others(6): Show |
12 | HG02258.hp2 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.799-11473_799-1146 others(12): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | ||||||
| chr1:78524906 | ATTTTTTT others(3): Show |
A | 7 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0001t0001g0306 others(4): Show |
7 | HG00597.hp1 HG02155.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.799-11475_799-1146 others(14): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | ||||||
| chr1:78524906 | ATTTTTTT others(4): Show |
A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0020 others(31): Show |
45 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.799-11476_799-1146 others(15): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | ||||||
| chr1:78524906 | ATTTTTTT others(5): Show |
A | 25 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0126 others(22): Show |
31 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.799-11477_799-1146 others(16): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | ||||||
| chr1:78524906 | ATTTTTTT others(8): Show |
A | 1 | a0001c0002t0001g0325 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.799-11480_799-1146 others(19): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | ||||||
| chr1:78524906 | ATTTTTTT others(11): Show |
A | 10 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0002g0081 others(7): Show |
10 | HG01891.hp1 HG01891.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.799-11483_799-1146 others(22): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78524906 | ||||||
| chr1:78525001 | C | T | 1 | a0001c0001t0002g0225 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.799-11405C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525001 | |||||||
| chr1:78525017 | G | A | 2 | a0001c0001t0002g0015 a0001c0001t0002g0120 |
3 | HG02622.hp1 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.799-11389G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525017 | |||||||
| chr1:78525236 | G | C | 79 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(76): Show |
99 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.799-11170G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525236 | |||||||
| chr1:78525260 | C | A | 1 | a0001c0001t0001g0092 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.799-11146C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525260 | |||||||
| chr1:78525321 | G | C | 16 | a0001c0001t0001g0103 a0001c0001t0001g0236 a0001c0001t0001g0279 others(13): Show |
19 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.799-11085G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525321 | |||||||
| chr1:78525378 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(133): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.799-11028A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525378 | |||||||
| chr1:78525454 | G | T | 1 | a0001c0001t0001g0181 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.799-10952G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525454 | |||||||
| chr1:78525512 | A | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(59): Show |
79 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.799-10894A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525512 | |||||||
| chr1:78525531 | A | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(59): Show |
79 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.799-10875A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525531 | |||||||
| chr1:78525570 | T | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(51): Show |
72 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.799-10836T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525570 | |||||||
| chr1:78525578 | A | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): Show |
151 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.799-10828A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525578 | |||||||
| chr1:78525850 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.799-10556T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525850 | |||||||
| chr1:78525867 | A | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(51): Show |
72 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.799-10539A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525867 | |||||||
| chr1:78525919 | T | C | 1 | a0001c0001t0002g0086 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.799-10487T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525919 | |||||||
| chr1:78525994 | A | G | 1 | a0001c0001t0002g0294 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.799-10412A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78525994 | |||||||
| chr1:78526056 | C | T | 4 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0011g0239 others(1): Show |
4 | HG02280.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-10350C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78526056 | |||||||
| chr1:78526058 | G | T | 4 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0011g0239 others(1): Show |
4 | HG02280.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-10348G>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78526058 | |||||||
| chr1:78526202 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.799-10204G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78526202 | |||||||
| chr1:78526264 | G | A | 1 | a0001c0001t0019g0039 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.799-10142G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78526264 | |||||||
| chr1:78526376 | C | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(59): Show |
79 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.799-10030C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78526376 | |||||||
| chr1:78526436 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.799-9970G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78526436 | |||||||
| chr1:78526494 | A | G | 18 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(15): Show |
18 | HG00733.hp2 HG01106.hp1 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.799-9912A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78526494 | |||||||
| chr1:78526517 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
190 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.799-9889A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78526517 | |||||||
| chr1:78526714 | C | G | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.799-9692C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78526714 | |||||||
| chr1:78526947 | C | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0124 |
3 | HG00621.hp1 HG02083.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.799-9459C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78526947 | |||||||
| chr1:78527132 | C | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(129): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.799-9274C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78527132 | |||||||
| chr1:78527303 | A | C | 1 | a0001c0001t0001g0013 | 2 | NA18957.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.799-9103A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78527303 | |||||||
| chr1:78527794 | T | G | 1 | a0001c0001t0002g0225 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.799-8612T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78527794 | |||||||
| chr1:78528041 | G | A | 17 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0297 others(14): Show |
23 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.799-8365G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78528041 | |||||||
| chr1:78528135 | A | C | 1 | a0001c0001t0004g0299 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.799-8271A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78528135 | |||||||
| chr1:78528156 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): Show |
151 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.799-8250G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78528156 | |||||||
| chr1:78528172 | C | G | 1 | a0001c0002t0025g0321 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.799-8234C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78528172 | |||||||
| chr1:78528216 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.799-8190T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78528216 | |||||||
| chr1:78528294 | C | CA | 58 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0001t0001g0036 others(55): Show |
58 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.799-8084dupA | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78528294 | ||||||
| chr1:78528294 | CA | C | 31 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0042 others(28): Show |
39 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.799-8084delA | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78528294 | ||||||
| chr1:78528294 | CAA | C | 44 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(41): Show |
57 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.799-8085_799-8084d others(4): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78528294 | ||||||
| chr1:78528294 | CAAA | C | 51 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(48): Show |
67 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.799-8086_799-8084d others(5): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78528294 | ||||||
| chr1:78528411 | T | G | 2 | a0001c0001t0009g0014 a0001c0001t0009g0094 |
3 | HG02809.hp1 HG02896.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.799-7995T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78528411 | |||||||
| chr1:78528428 | AG | A | 16 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0226 others(13): Show |
17 | HG01891.hp1 HG01891.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.799-7975delG | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78528428 | ||||||
| chr1:78528487 | T | C | 4 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0011g0239 others(1): Show |
4 | HG02280.hp1 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-7919T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78528487 | |||||||
| chr1:78528572 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.799-7834T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78528572 | |||||||
| chr1:78528610 | T | G | 3 | a0001c0001t0001g0236 a0001c0001t0001g0279 a0001c0001t0026g0255 |
3 | HG02258.hp2 HG02630.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.799-7796T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78528610 | |||||||
| chr1:78528755 | T | C | 16 | a0001c0001t0001g0103 a0001c0001t0001g0236 a0001c0001t0001g0279 others(13): Show |
19 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.799-7651T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78528755 | |||||||
| chr1:78528761 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.799-7645C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78528761 | |||||||
| chr1:78528908 | C | T | 1 | a0001c0002t0022g0323 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.799-7498C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78528908 | |||||||
| chr1:78528979 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): Show |
151 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.799-7427G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78528979 | |||||||
| chr1:78529198 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): Show |
151 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.799-7208G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78529198 | |||||||
| chr1:78529237 | T | C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(35): Show |
53 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.799-7169T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78529237 | |||||||
| chr1:78529244 | T | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): Show |
151 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.799-7162T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78529244 | |||||||
| chr1:78529655 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.799-6751G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78529655 | |||||||
| chr1:78529754 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.799-6652C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78529754 | |||||||
| chr1:78529793 | A | T | 1 | a0001c0002t0001g0326 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.799-6613A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78529793 | |||||||
| chr1:78529803 | C | T | 15 | a0001c0001t0001g0103 a0001c0001t0001g0236 a0001c0001t0001g0279 others(12): Show |
18 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.799-6603C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78529803 | |||||||
| chr1:78529850 | T | A | 62 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(59): Show |
79 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.799-6556T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78529850 | |||||||
| chr1:78529853 | C | T | 1 | a0001c0001t0006g0245 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.799-6553C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78529853 | |||||||
| chr1:78529946 | A | G | 1 | a0001c0001t0002g0283 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.799-6460A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78529946 | |||||||
| chr1:78529949 | T | C | 3 | a0001c0001t0001g0291 a0001c0001t0028g0289 a0001c0003t0001g0240 |
3 | HG00642.hp1 HG01168.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.799-6457T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78529949 | |||||||
| chr1:78529960 | A | C | 1 | a0001c0001t0001g0146 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.799-6446A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78529960 | |||||||
| chr1:78530095 | T | C | 2 | a0001c0001t0009g0014 a0001c0001t0009g0094 |
3 | HG02809.hp1 HG02896.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.799-6311T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78530095 | |||||||
| chr1:78530111 | TAAG | T | 62 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(59): Show |
79 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.799-6288_799-6286d others(5): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78530111 | ||||||
| chr1:78530139 | G | A | 1 | a0001c0001t0001g0189 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.799-6267G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78530139 | |||||||
| chr1:78530157 | T | G | 1 | a0003c0005t0010g0282 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.799-6249T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78530157 | |||||||
| chr1:78530253 | C | A | 17 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0297 others(14): Show |
23 | HG00140.hp2 HG00558.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.799-6153C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78530253 | |||||||
| chr1:78530337 | A | G | 28 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0031 others(25): Show |
36 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.799-6069A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78530337 | |||||||
| chr1:78530381 | T | A | 3 | a0001c0001t0001g0291 a0001c0001t0028g0289 a0001c0003t0001g0240 |
3 | HG00642.hp1 HG01168.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.799-6025T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78530381 | |||||||
| chr1:78530757 | C | A | 1 | a0001c0001t0001g0247 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.799-5649C>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78530757 | |||||||
| chr1:78530907 | C | CT | 27 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0031 others(24): Show |
35 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.799-5494dupT | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78530907 | ||||||
| chr1:78530956 | G | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0049 others(5): Show |
9 | HG00639.hp1 HG01069.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.799-5450G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78530956 | |||||||
| chr1:78530982 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.799-5424G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78530982 | |||||||
| chr1:78531176 | G | A | 1 | a0001c0001t0004g0307 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.799-5230G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78531176 | |||||||
| chr1:78531429 | T | C | 14 | a0001c0001t0001g0103 a0001c0001t0001g0236 a0001c0001t0001g0279 others(11): Show |
17 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.799-4977T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78531429 | |||||||
| chr1:78531469 | A | T | 4 | a0001c0001t0001g0178 a0001c0001t0003g0182 a0001c0001t0003g0210 others(1): Show |
4 | HG00544.hp1 HG02040.hp1 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-4937A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78531469 | |||||||
| chr1:78531776 | G | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
111 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.799-4630G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78531776 | |||||||
| chr1:78531857 | A | C | 1 | a0001c0001t0003g0019 | 2 | NA18972.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.799-4549A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78531857 | |||||||
| chr1:78531875 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.799-4531A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78531875 | |||||||
| chr1:78531903 | A | G | 2 | a0002c0004t0001g0072 a0002c0004t0001g0079 |
2 | NA18977.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.799-4503A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78531903 | |||||||
| chr1:78532020 | C | T | 1 | a0001c0001t0002g0015 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.799-4386C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532020 | |||||||
| chr1:78532228 | C | T | 11 | a0001c0001t0001g0103 a0001c0001t0001g0332 a0001c0001t0029g0333 others(8): Show |
14 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.799-4178C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532228 | |||||||
| chr1:78532313 | G | A | 2 | a0001c0001t0001g0243 a0001c0001t0030g0242 |
2 | HG01928.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.799-4093G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532313 | |||||||
| chr1:78532364 | T | TATA | 5 | a0001c0001t0001g0051 a0001c0001t0001g0058 a0001c0001t0002g0248 others(2): Show |
5 | HG01515.hp1 HG02976.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.799-4042_799-4041i others(5): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532364 | |||||||
| chr1:78532364 | T | TATATATA others(4): Show |
1 | a0001c0001t0003g0129 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.799-4042_799-4041i others(13): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532364 | |||||||
| chr1:78532364 | T | TTA | 85 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(82): Show |
88 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.799-4010_799-4009d others(4): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532364 | ||||||
| chr1:78532364 | T | TTATA | 41 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0044 others(38): Show |
43 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.799-4012_799-4009d others(6): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532364 | ||||||
| chr1:78532364 | T | TTATATA | 13 | a0001c0001t0001g0054 a0001c0001t0001g0139 a0001c0001t0001g0146 others(10): Show |
13 | HG00544.hp1 HG02080.hp1 HG02273.hp2 others(10): Show |
intron_variant | MODIFIER | c.799-4014_799-4009d others(8): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532364 | ||||||
| chr1:78532364 | T | TTATATAT others(1): Show |
12 | a0001c0001t0001g0135 a0001c0001t0001g0159 a0001c0001t0001g0162 others(9): Show |
12 | HG02015.hp2 HG02165.hp2 HG03209.hp2 others(9): Show |
intron_variant | MODIFIER | c.799-4016_799-4009d others(10): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532364 | ||||||
| chr1:78532364 | T | TTATATAT others(3): Show |
3 | a0001c0001t0003g0080 a0001c0001t0003g0197 a0001c0001t0003g0205 |
3 | NA18747.hp2 NA18965.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.799-4018_799-4009d others(12): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532364 | ||||||
| chr1:78532364 | T | TTATATAT others(5): Show |
5 | a0001c0001t0001g0178 a0001c0001t0001g0189 a0001c0001t0003g0219 others(2): Show |
5 | HG02040.hp1 NA18939.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.799-4020_799-4009d others(14): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532364 | ||||||
| chr1:78532364 | T | TTATATAT others(7): Show |
1 | a0001c0001t0003g0019 | 2 | NA18972.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.799-4022_799-4009d others(16): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532364 | ||||||
| chr1:78532364 | T | TTATATAT others(9): Show |
2 | a0001c0001t0001g0095 a0001c0002t0022g0323 |
2 | HG01109.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.799-4024_799-4009d others(18): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532364 | ||||||
| chr1:78532364 | T | TTATATAT others(11): Show |
4 | a0001c0001t0001g0286 a0001c0001t0001g0293 a0001c0001t0004g0067 others(1): Show |
4 | HG02572.hp2 NA18906.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-4026_799-4009d others(20): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532364 | ||||||
| chr1:78532364 | T | TTATATAT others(13): Show |
1 | a0001c0002t0024g0324 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.799-4028_799-4009d others(22): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532364 | ||||||
| chr1:78532364 | TTA | T | 5 | a0001c0001t0001g0171 a0001c0001t0001g0318 a0001c0001t0002g0317 others(2): Show |
5 | HG02055.hp2 HG03195.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.799-4010_799-4009d others(4): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532364 | ||||||
| chr1:78532364 | TTATA | T | 17 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0035 others(14): Show |
19 | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.799-4012_799-4009d others(6): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532364 | ||||||
| chr1:78532364 | TTATATA | T | 16 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(13): Show |
16 | HG00642.hp1 HG00733.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.799-4014_799-4009d others(8): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532364 | ||||||
| chr1:78532382 | ATATATAT others(93): Show |
A | 6 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0011g0239 others(3): Show |
6 | HG02280.hp1 HG02809.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.799-4022_799-3923d others(102): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532382 | ||||||
| chr1:78532384 | A | G | 10 | a0001c0001t0001g0103 a0001c0001t0001g0332 a0001c0002t0001g0009 others(7): Show |
13 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.799-4022A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532384 | |||||||
| chr1:78532388 | A | G | 36 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(33): Show |
51 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.799-4018A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532388 | |||||||
| chr1:78532390 | A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0020 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.799-4009_799-4008i others(30): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532390 | ||||||
| chr1:78532390 | A | ATATATAT others(19): Show |
3 | a0001c0001t0001g0002 a0001c0001t0001g0156 a0001c0001t0001g0224 |
3 | HG03831.hp1 HG03834.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.799-4009_799-4008i others(28): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532390 | ||||||
| chr1:78532390 | A | ATATATAT others(15): Show |
10 | a0001c0001t0001g0020 a0001c0001t0001g0111 a0001c0001t0001g0152 others(7): Show |
11 | HG01516.hp1 HG02083.hp1 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.799-4009_799-4008i others(24): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532390 | ||||||
| chr1:78532390 | A | ATATATAT others(13): Show |
6 | a0001c0001t0001g0002 a0001c0001t0001g0153 a0001c0001t0001g0203 others(3): Show |
6 | HG00597.hp1 HG01192.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.799-4009_799-4008i others(22): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532390 | ||||||
| chr1:78532390 | A | ATATATAT others(11): Show |
11 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(8): Show |
14 | HG00408.hp2 HG00597.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.799-4009_799-4008i others(20): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532390 | ||||||
| chr1:78532390 | A | ATATATAT others(9): Show |
4 | a0001c0001t0001g0021 a0001c0001t0001g0151 a0001c0001t0001g0154 others(1): Show |
4 | HG00099.hp2 HG00280.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-4009_799-4008i others(18): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532390 | ||||||
| chr1:78532390 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0022 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.799-4009_799-4008i others(16): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532390 | ||||||
| chr1:78532390 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0306 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.799-4009_799-4008i others(14): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532390 | ||||||
| chr1:78532390 | A | G | 4 | a0001c0001t0001g0102 a0001c0001t0001g0115 a0001c0001t0001g0300 others(1): Show |
4 | HG01496.hp2 HG02523.hp1 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-4016A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532390 | |||||||
| chr1:78532390 | ATATATAT others(69): Show |
A | 10 | a0001c0001t0001g0103 a0001c0001t0001g0332 a0001c0002t0001g0009 others(7): Show |
13 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.799-4014_799-3939d others(78): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532390 | ||||||
| chr1:78532390 | ATATATAT others(85): Show |
A | 1 | a0001c0001t0007g0271 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.799-4014_799-3923d others(94): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532390 | ||||||
| chr1:78532394 | ATATGTAT others(7): Show |
A | 1 | a0001c0001t0003g0191 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.799-4008_799-3995d others(16): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532394 | ||||||
| chr1:78532394 | ATATGTAT others(65): Show |
A | 36 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(33): Show |
51 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.799-4010_799-3939d others(74): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532394 | ||||||
| chr1:78532396 | ATGTATAT others(63): Show |
A | 4 | a0001c0001t0001g0102 a0001c0001t0001g0115 a0001c0001t0001g0300 others(1): Show |
4 | HG01496.hp2 HG02523.hp1 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-4006_799-3937d others(72): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532396 | ||||||
| chr1:78532396 | ATGTATAT others(67): Show |
A | 1 | a0001c0001t0002g0256 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.799-3996_799-3923d others(76): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532396 | ||||||
| chr1:78532398 | G | A | 18 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0226 others(15): Show |
19 | HG01891.hp1 HG01891.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.799-4008G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532398 | |||||||
| chr1:78532400 | ATATATGT others(65): Show |
A | 2 | a0001c0001t0007g0339 a0001c0001t0009g0094 |
2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.799-4000_799-3929d others(74): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532400 | ||||||
| chr1:78532402 | ATATGTGT others(39): Show |
A | 2 | a0001c0001t0026g0255 a0004c0006t0032g0145 |
2 | HG02258.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.799-4000_799-3955d others(48): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532402 | ||||||
| chr1:78532402 | ATATGTGT others(63): Show |
A | 1 | a0001c0001t0009g0014 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.799-4000_799-3931d others(72): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532402 | ||||||
| chr1:78532404 | ATGTG | A | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0002g0083 |
3 | HG02572.hp1 HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.799-4000_799-3997d others(6): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532404 | ||||||
| chr1:78532404 | ATGTGTAT others(37): Show |
A | 2 | a0001c0001t0001g0236 a0001c0001t0001g0279 |
2 | HG02630.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.799-4000_799-3957d others(46): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532404 | ||||||
| chr1:78532404 | ATGTGTAT others(61): Show |
A | 1 | a0001c0001t0005g0340 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.799-4000_799-3933d others(70): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532404 | ||||||
| chr1:78532404 | ATGTGTAT others(71): Show |
A | 1 | a0001c0001t0001g0227 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.799-3998_799-3921d others(80): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532404 | ||||||
| chr1:78532406 | G | A | 5 | a0001c0001t0001g0226 a0001c0001t0002g0081 a0001c0001t0002g0082 others(2): Show |
5 | HG01891.hp2 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.799-4000G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532406 | |||||||
| chr1:78532408 | G | A | 6 | a0001c0001t0001g0226 a0001c0001t0002g0081 a0001c0001t0002g0082 others(3): Show |
6 | HG01891.hp2 HG02809.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.799-3998G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532408 | |||||||
| chr1:78532410 | ATATATAT others(55): Show |
A | 26 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0031 others(23): Show |
34 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.799-3914_799-3853d others(64): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532410 | ||||||
| chr1:78532412 | ATATATGT others(47): Show |
A | 1 | a0001c0001t0021g0280 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.799-3992_799-3939d others(56): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532412 | ||||||
| chr1:78532414 | ATATGTGT others(51): Show |
A | 1 | a0001c0001t0002g0083 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.799-3988_799-3931d others(60): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532414 | ||||||
| chr1:78532416 | ATGTGTGT others(25): Show |
A | 1 | a0001c0001t0013g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.799-3988_799-3957d others(34): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532416 | ||||||
| chr1:78532416 | ATGTGTGT others(59): Show |
A | 4 | a0001c0001t0001g0226 a0001c0001t0002g0081 a0001c0001t0002g0082 others(1): Show |
4 | HG01891.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-3986_799-3921d others(68): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532416 | ||||||
| chr1:78532418 | G | A | 3 | a0001c0001t0001g0090 a0001c0001t0003g0191 a0001c0001t0029g0333 |
3 | HG02615.hp1 HG03516.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.799-3988G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532418 | |||||||
| chr1:78532420 | G | A | 3 | a0001c0001t0001g0090 a0001c0001t0003g0191 a0001c0001t0029g0333 |
3 | HG02615.hp1 HG03516.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.799-3986G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532420 | |||||||
| chr1:78532434 | ATATATTT others(31): Show |
A | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0029g0333 |
3 | HG02572.hp1 HG02615.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.799-3966_799-3929d others(40): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532434 | ||||||
| chr1:78532440 | T | A | 1 | a0001c0001t0003g0191 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.799-3966T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532440 | |||||||
| chr1:78532448 | G | A | 1 | a0001c0001t0003g0191 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.799-3958G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532448 | |||||||
| chr1:78532454 | G | A | 5 | a0001c0001t0001g0236 a0001c0001t0001g0279 a0001c0001t0013g0088 others(2): Show |
5 | HG02258.hp2 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.799-3952G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532454 | |||||||
| chr1:78532462 | ATTTG | A | 5 | a0001c0001t0001g0236 a0001c0001t0001g0279 a0001c0001t0013g0088 others(2): Show |
5 | HG02258.hp2 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.799-3942_799-3939d others(6): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532462 | ||||||
| chr1:78532472 | G | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(54): Show |
75 | HG00423.hp2 HG00544.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.799-3934G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532472 | |||||||
| chr1:78532472 | GTATATAT others(7): Show |
G | 1 | a0001c0001t0003g0191 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.799-3928_799-3915d others(16): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532472 | ||||||
| chr1:78532480 | G | A | 6 | a0001c0001t0002g0083 a0001c0001t0002g0256 a0001c0001t0005g0340 others(3): Show |
6 | HG01891.hp1 HG02896.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.799-3926G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532480 | |||||||
| chr1:78532482 | G | A | 6 | a0001c0001t0002g0083 a0001c0001t0002g0256 a0001c0001t0005g0340 others(3): Show |
6 | HG01891.hp1 HG02896.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.799-3924G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532482 | |||||||
| chr1:78532484 | GTA | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0042 |
3 | HG00597.hp2 NA18944.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.799-3916_799-3915d others(4): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78532484 | ||||||
| chr1:78532502 | T | A | 17 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0226 others(14): Show |
18 | HG01891.hp1 HG01891.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.799-3904T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532502 | |||||||
| chr1:78532510 | G | A | 17 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0226 others(14): Show |
18 | HG01891.hp1 HG01891.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.799-3896G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532510 | |||||||
| chr1:78532610 | G | A | 27 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0031 others(24): Show |
35 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.799-3796G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532610 | |||||||
| chr1:78532772 | A | T | 27 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0031 others(24): Show |
35 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.799-3634A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532772 | |||||||
| chr1:78532786 | A | T | 27 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0031 others(24): Show |
35 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.799-3620A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532786 | |||||||
| chr1:78532787 | T | C | 1 | a0001c0001t0023g0254 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.799-3619T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532787 | |||||||
| chr1:78532823 | A | G | 2 | a0001c0001t0023g0254 a0001c0002t0031g0316 |
2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.799-3583A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532823 | |||||||
| chr1:78532902 | T | A | 35 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0021 others(32): Show |
44 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.799-3504T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532902 | |||||||
| chr1:78532929 | G | C | 1 | a0001c0001t0002g0120 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.799-3477G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532929 | |||||||
| chr1:78532952 | T | C | 27 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0031 others(24): Show |
35 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.799-3454T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532952 | |||||||
| chr1:78532953 | A | G | 3 | a0001c0001t0001g0291 a0001c0001t0028g0289 a0001c0003t0001g0240 |
3 | HG00642.hp1 HG01168.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.799-3453A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532953 | |||||||
| chr1:78532960 | A | G | 2 | a0001c0001t0003g0080 a0001c0001t0003g0191 |
2 | NA18747.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.799-3446A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532960 | |||||||
| chr1:78532971 | G | C | 1 | a0001c0001t0001g0334 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.799-3435G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532971 | |||||||
| chr1:78532996 | A | G | 1 | a0001c0001t0029g0333 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.799-3410A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78532996 | |||||||
| chr1:78533074 | T | C | 27 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0031 others(24): Show |
35 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.799-3332T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78533074 | |||||||
| chr1:78533189 | G | A | 4 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0013g0088 others(1): Show |
4 | HG02572.hp1 HG02615.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-3217G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78533189 | |||||||
| chr1:78533403 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(176): Show |
216 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.799-3003C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78533403 | |||||||
| chr1:78533584 | G | A | 27 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0031 others(24): Show |
35 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.799-2822G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78533584 | |||||||
| chr1:78533592 | C | G | 31 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0031 others(28): Show |
39 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.799-2814C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78533592 | |||||||
| chr1:78533593 | A | G | 1 | a0001c0002t0031g0316 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.799-2813A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78533593 | |||||||
| chr1:78533666 | A | G | 1 | a0001c0002t0025g0321 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.799-2740A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78533666 | |||||||
| chr1:78533682 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(158): Show |
198 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.799-2724A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78533682 | |||||||
| chr1:78533880 | T | G | 1 | a0001c0001t0001g0218 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.799-2526T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78533880 | |||||||
| chr1:78534032 | T | C | 2 | a0001c0001t0001g0149 a0001c0001t0018g0150 |
2 | HG00597.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.799-2374T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78534032 | |||||||
| chr1:78534111 | T | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(114): Show |
144 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.799-2295T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78534111 | |||||||
| chr1:78534186 | A | G | 7 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0083 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.799-2220A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78534186 | |||||||
| chr1:78534239 | C | T | 1 | a0001c0001t0029g0333 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.799-2167C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78534239 | |||||||
| chr1:78534249 | A | C | 1 | a0001c0001t0004g0312 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.799-2157A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78534249 | |||||||
| chr1:78534297 | A | C | 6 | a0001c0001t0001g0033 a0001c0001t0001g0056 a0001c0001t0001g0076 others(3): Show |
6 | HG02738.hp1 HG02738.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.799-2109A>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78534297 | |||||||
| chr1:78534518 | T | A | 29 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0071 others(26): Show |
35 | HG00140.hp2 HG00558.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.799-1888T>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78534518 | |||||||
| chr1:78534544 | A | G | 1 | a0001c0001t0016g0241 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.799-1862A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78534544 | |||||||
| chr1:78534616 | T | C | 1 | a0001c0001t0012g0116 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.799-1790T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78534616 | |||||||
| chr1:78534697 | G | GT | 80 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(77): Show |
98 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.799-1700dupT | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 78534697 | ||||||
| chr1:78534723 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.799-1683C>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78534723 | |||||||
| chr1:78534888 | T | C | 21 | a0001c0001t0002g0015 a0001c0001t0002g0081 a0001c0001t0002g0082 others(18): Show |
22 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.799-1518T>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78534888 | |||||||
| chr1:78534931 | C | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0272 |
2 | HG02300.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.799-1475C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78534931 | |||||||
| chr1:78535272 | A | G | 1 | a0001c0001t0029g0333 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.799-1134A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78535272 | |||||||
| chr1:78535637 | C | G | 1 | a0001c0001t0029g0333 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.799-769C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78535637 | |||||||
| chr1:78535773 | A | G | 38 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0004g0003 others(35): Show |
43 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.799-633A>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78535773 | |||||||
| chr1:78535913 | C | G | 26 | a0001c0001t0004g0003 a0001c0001t0004g0067 a0001c0001t0004g0195 others(23): Show |
31 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.799-493C>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78535913 | |||||||
| chr1:78535950 | G | A | 26 | a0001c0001t0004g0003 a0001c0001t0004g0067 a0001c0001t0004g0195 others(23): Show |
31 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.799-456G>A | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78535950 | |||||||
| chr1:78535952 | G | C | 1 | a0001c0001t0011g0239 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.799-454G>C | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78535952 | |||||||
| chr1:78536235 | T | G | 37 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0004g0003 others(34): Show |
42 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.799-171T>G | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78536235 | |||||||
| chr1:78536282 | A | AC | 4 | a0001c0001t0004g0003 a0001c0001t0004g0195 a0001c0001t0004g0308 others(1): Show |
7 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.799-124_799-123ins others(1): Show |
PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78536282 | |||||||
| chr1:78536309 | A | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(73): Show |
89 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.799-97A>T | PTGFR | ENSG00000122420.10 | transcript | ENST00000370757.8 | protein_coding | 2/2 | chr1 | 78536309 |